ZMP
KIAA1797
Ensembl ID:
Description:
KIAA1797 [Source:HGNC Symbol;Acc:23377]
Human Orthologue:
KIAA1797
Human Description:
KIAA1797 [Source:HGNC Symbol;Acc:23377]
Mouse Orthologue:
BC057079
Mouse Description:
cDNA sequence BC057079 Gene [Source:MGI Symbol;Acc:MGI:2676921]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa26920 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa40858 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20893 | Essential Splice Site | Available for shipment | Available now |
sa10081 | Essential Splice Site | Available for shipment | Available now |
sa18867 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40859 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34032 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa34033 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa26920
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037846 | Essential Splice Site | 299 | 1797 | 10 | 49 |
Genomic Location (Zv9):
Chromosome 7 (position 20128283)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 18661312 |
GRCz11 | 7 | 18913579 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATGTCTCTGCTTCACACACTCCACCACATTATACCTGCACATGCAGAG[G/A]TGAATGCACACACACTGCAATAACAATGCTTTTCTTACTTCGATTTTTGA
Long Flanking Sequence:
CTATTGACTGATACTGTAATTCACTGACATAAATTAGTTGGGAAACATAATCGAGAAACATATATTAGTCTTTAATGTTGTGCTGTATTAGGATTTACAGCTAACATATATTGTGTTTTTCAAATATTATAGTTCAAACTAGTGCATTTTTTATTCTCACATGTTAGTCACTTTTTTATAAGTACATATGTTGAATAAATAATAGGTAATATTACATACAATCATTAAAAGATAATAATTAAAAATAAATTATTTCTGTCTCACACTTGTTTTTCTAAATTGTGCCCTGTCAGGTGGACAGTGTAACTGCAGTGGTGGAGTTGAGCTCGTTTGCCGAGTCTCTGACAGCGGCTCTGATCAGCCATCCAGAGCTCTGGAGGAAGGAACTGACCCGGCTGGCTCTCCAGCTCCTGTGTGCCTGTCAGCTCACAATTCATCTGGGAGGAGAGCTGATGTCTCTGCTTCACACACTCCACCACATTATACCTGCACATGCAGAG[G/A]TGAATGCACACACACTGCAATAACAATGCTTTTCTTACTTCGATTTTTGACATGTTCATTTAGTTTGGTTAGTACTGTAGTTGTTAGTACGTAAACACATGGCTCTCGGTGTTCACAGCAACCCAAATTCAATTCAATTAAAGGTGAAAACGCCCTTCTCGTATTTTGTGATTCACAACTGTTTTACATTTATTTACGGTTGCGAATTGCATTATGGGACCTTGATCTCTGCTCTGACAACTTTTGATGTTGCAAATTCAACTCTACAGTTTAACAAAGTGACTTTTATTGACATTTTAGTTGTTTGAAATAATTTAATGTATAAGAAATAGTATAGAGAGAAATAAGAAAATAGAGAGTCTGTAAAATAATAGAGTGTCTACTGGCAGTTTATTACAAGGTATTTGTAGTTTAACATACAACACCAACCCAGACAATATATGACTTTAAACTATTAAAAATTTTCATAAATGTCCCTTTATTAATTTTTCAAAGTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40858
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037846 | Essential Splice Site | 328 | 1797 | 11 | 49 |
Genomic Location (Zv9):
Chromosome 7 (position 20130266)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 18663295 |
GRCz11 | 7 | 18915562 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCCTGCTGAATGCCTCTGTCTCTCAGCAAACGGCGCTCCTAGATCTTG[G/A]TAAAACCCCTCTTGCTCTCTGAAGCCTTCATATTGACACGCCACGCTTCA
Long Flanking Sequence:
TCAACTGAGAATTTGGTTTAGAACAGTCACTGTCGTCTTTGTGCTTCCCCGTTTTCACTAACATTGCTGTAGTACAAAATAGAAATATGAAGTTGTACTAACTTATATGTAATATGTTTCCACAAATCAAAACATATTCTGTTTTACAGTTCTATCTAATTGCTTTCGTTAACAAAATGCCGATTAAAAAAGTGTTCGTTTTTTTTCTTCACAGGGAAGGGCAAAGTTATTATTATTATGTATTTGCTGCAGTTGTACTCTCTGTGTGATCTCTACAAATCTTCTCCTCTCATCTTTATAATGGTGTTGTTTGTGCAGCGTTGTCTATCTGAAAGCGATTTGCATTCAGCATTCCCTCTGCGACTCCATCTGTGTCAAAGCATTTGTCTGATTGTGCTCCATCTAATTGTAGGAACTCCCGGCTGAGCAAGTGATCATGGGAATCTCGCTGCTCCTGCTGAATGCCTCTGTCTCTCAGCAAACGGCGCTCCTAGATCTTG[G/A]TAAAACCCCTCTTGCTCTCTGAAGCCTTCATATTGACACGCCACGCTTCATTTACACAAAGGATGCCTAAAAAACAAGGAGTTTTTTTGTATCAAATTGTTTGATTTGCTATTATAATTTTTTTTATTGCAAAAACTGCTTTTGTTACTCAAGTAAAAATTATGTTTCCAGAAAATATGAATGTTCCTAAAACAAGCAAAAAATAAAGTAAATATCTGCCATTAAGATAAGCAAAAAATGATTGCTGCCTAAAATGTTTTAGTTGAATTAAATTAAAGATGCAGTATATAAGTTTGACTTGCAGTGGTTGAACTAGGAATTGCATTTCTGGATCAAAACAAACACAAGTGGAGGTTGCCAGATTGAGAACTAACAAGACTGATTTAAATCGTGTTCTTAATAAAAGCAACGGCATATGATAGAAGGAATATTTTACATATTGAAAGGAGTTTGTGTTCTAACCAGCACCTCGAATTGATATAATAGAGACAGCTTCTTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20893
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037846 | Essential Splice Site | 518 | 1797 | 15 | 49 |
Genomic Location (Zv9):
Chromosome 7 (position 20150230)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 18683259 |
GRCz11 | 7 | 18935526 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTGTCTCTCTCTGTTCTCTATACTCTGCCCAAACTGGGAACTCATAAG[G/A]TAAAGCCATTACGATGCACAACATGAACCATTAATCTCATAAGAGAATAC
Long Flanking Sequence:
TTTTCTGCGCGCATTGTTATTTATTTGGTAAAAAAATGTATCTTTTCATTTACACAAAAAAGCCACAATATTCTTAACTACGCTCCTCTTATTAGTTTGCTACAAGGGAATGATATACAAAAACAAAGGCCCGGCCCTTATCAATACTCTGTTTCAGAAGTACATCAATATATAAAATGATTTTTAGCAACTTTCAGTTCACGTAGACTTTAACATGGATAAAATATCATTTGGGAGGCAAAAAAATGCGATAACACGCAATACTGTAAATTTGTATAATTGTATAATTATATTTAAACTAATTTTTAATGAAAAATTAAATCTAAGAAAAGGAACTCCTAATGTTCTTAAATATGTGTTAATTGTTTGCTTAATTGTCTGATGTGCACCTCCAGGTTCCGTGTCTGCTCCCTGTGCTGATGTTCAAGCTCAGCAGAGTATCTGATCCAGCTCTGTCTCTCTCTGTTCTCTATACTCTGCCCAAACTGGGAACTCATAAG[G/A]TAAAGCCATTACGATGCACAACATGAACCATTAATCTCATAAGAGAATACAGAAACTCAATCAATACATGTTTTTTCAGCAAATGTTTTCTGTTTTTGAATGTTTGTGTAAAGAAAGCAGATACATTTTTACGTAACCATTCTTTCGCTAAATAGTAGTTTACGGTTTACGGTTAATATTATTCTGTCATTTTTATCCAGAAAAAGATTTTGGGTGTTTCTTTTGATCACTTATCACTCATATTTTAGAAAACAATTTGAAGAGCAACAGAGTTTCTATGGGTCATGTAATTGTTTTATATTTTTTTTCTAAGTCATGGAATATCAGAAACTTTTGTTTGTGGCTTCAGAGTTTAATTTTCATTTATCAAAACGGCATTTTCTATATCGTGTAATGTTTTTTTGTCTCATTTTTTTCACATATTTTTTTTTTTTAGTAGTAAATATTATAAATTTATTCTTTTATTCTTTTCCTGCTCATCAGTTGGCAGTCACTTAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10081
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037846 | Essential Splice Site | 518 | 1797 | 15 | 49 |
Genomic Location (Zv9):
Chromosome 7 (position 20150231)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 18683260 |
GRCz11 | 7 | 18935527 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGTCTCTCTCTGTTCTCTATACTCTGCCCAAACTGGGAACTCATAAGG[T/C]AAAGCCATTACGATGCACARCAYGAACCATTWATCTCATAAGWGAATACW
Long Flanking Sequence:
TTTCTGCGCGCATTGTTATTTATTTGGTAAAAAAATGTATCTTTTCATTTACACAAAAAAGCCACAATATTCTTAACTACGCTCCTCTTATTAGTTTGCTACAAGGGAATGATATACAAAAACAAAGGCCCGGCCCTTATCAATACTCTGTTTCAGAAGTACATCAATATATAAAATGATTTTTAGCAACTTTCAGTTCACGTAGACTTTAACATGGATAAAATATCATTTGGGAGGCAAAAAAATGCGATAACACGCAATACTGTAAATTTGTATAATTGTATAATTATATTTAAACTAATTTTTAATGAAAAATTAAATCTAAGAAAAGGAACTCCTAATGTTCTTAAATATGTGTTAATTGTTTGCTTAATTGTCTGATGTGCACCTCCAGGTTCCGTGTCTGCTCCCTGTGCTGATGTTCAAGCTCAGCAGAGTATCTGATCCAGCTCTGTCTCTCTCTGTTCTCTATACTCTGCCCAAACTGGGAACTCATAAGG[T/C]AAAGCCATTACGATGCACAACATGAACCATTAATCTCATAAGAGAATACAGAAACTCAATCAATACATGTTTTTTCAGCAAATGTTTTCTGTTTTTGAATGTTTGTGTAAAGAAAGCAGATACATTTTTACGTAACCATTCTTTCGCTAAATAGTAGTTTACGGTTTACGGTTAATATTATTCTGTCATTTTTATCCAGAAAAAGATTTTGGGTGTTTCTTTTGATCACTTATCACTCATATTTTAGAAAACAATTTGAAGAGCAACAGAGTTTCTATGGGTCATGTAATTGTTTTATATTTTTTTTCTAAGTCATGGAATATCAGAAACTTTTGTTTGTGGCTTCAGAGTTTAATTTTCATTTATCAAAACGGCATTTTCTATATCGTGTAATGTTTTTTTGTCTCATTTTTTTCACATATTTTTTTTTTTTAGTAGTAAATATTATAAATTTATTCTTTTATTCTTTTCCTGCTCATCAGTTGGCAGTCACTTAGGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18867
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037846 | Nonsense | 675 | 1797 | 19 | 49 |
Genomic Location (Zv9):
Chromosome 7 (position 20156781)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 18689810 |
GRCz11 | 7 | 18942077 |
KASP Assay ID:
2259-8622.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCGCTGGTCCTGAAGGCCACAGCTGAACTTCTGGCATTAGTACCAGATT[T/A]AAATGTCAAAACAGAGGAATATGAGGCACGAGACCATCACCGTACTTTCT
Long Flanking Sequence:
ATTTTATGTGAACCAGTCATGACAGTATGGAACCGCCATCACAGATTTCCAGAACATCTCTGCACTGGTTTGATCTCATTCATTCTCTGTGTTTGCTATAATGTGCATTCTGTTCCAGGCCGTACCAGCATGGAGGAGACATGCTGGCTGCCATCAGAGACACACTGCTGCAGTTCTCCCGGAAAGACCAGGCCACCCCTGTGGCTCTGGCACTGCAGGCCTTACAGGAGCTCTGTAGAGCTGAGGTCAGTCTTCAGAGAGTCACACTGAACACATTCACATGCACACCAATCAGCTTATTGACAGGACATGTTTTTTTAGTGTACAGGCTAATCAATAAGGTAACACTGCATTAAACGTTTGCATTCTCCTTTCATATTTTTGGCTTCAGGTAGTTGATATCTGCTCTACATGGAAGGCTCTTTCTCCTAAGCTCCTCTCTGACACCAGACCGCTGGTCCTGAAGGCCACAGCTGAACTTCTGGCATTAGTACCAGATT[T/A]AAATGTCAAAACAGAGGAATATGAGGCACGAGACCATCACCGTACTTTCTCATTGCCATATATGTGTGGTATTTCTAGCTTCACATTTCATATACACTGCAGGACAAATGACTTCAAGCTTTATGTCCTTTTCCCCTACAGAAATTCGGAAGCGAGGCAGTGGGTGTTTTATGGGGCTACGCTCTTAGTCAGGTGAGTGCTGACATTTGCAAATGGTAATGAAGAGTAGGGATGGGCAGGACGGTTTACTAGTCATCCAACAATAGTTTCTAAAAGTCATTGTGCCGTTTTATGTGTCCGTGTATAGGTAGACATGTTTTAGTTGCTTCTCTGTGTCTAATTGTGGTTATTTGATTGGTTCAAAATTAGTTTGGCTCAAATACTGTAAAAGGGGAAGAAATAACCTGTAATACAAAGATGCTGTTTTAGCAAGAAAACTTGTCTTTTACTTTCACTTTCAAATTCGAGATGTTTTTGCTGGAGGTTGATATGTAAATTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40859
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037846 | Nonsense | 739 | 1797 | 22 | 49 |
Genomic Location (Zv9):
Chromosome 7 (position 20159911)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 18692940 |
GRCz11 | 7 | 18945207 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGGGGATCTTGCTTTCAGGCTAGGCCCATACCCAAGCAACCTGAAGTC[G/T]AGGATGAAGTGAAGCAAAATGAGGAGGAGAATGAGGAGGAGGAAGATATT
Long Flanking Sequence:
TATTTCAAAATATTGCAAAATGTCTATTTACCTATTTATTTTCAAACTGTTAGATTACCAAAATGTGCACATATATTTAATTATATTAATTATAATTTTATATAAAGTACATGTTCATAATTGGCCATATATTAGGTTACTGTACTGGCCACAAAACAGACAATTAATAAATATAATCACAGTTATTTCTTAGACAATTAATCATCAGCCATTATAATCCTGACAGCCCAATATCTACTATACCTTTGCTAAAAAATAAATAAAAAAAACGGTATAATTTAAATTTTTTTTCTGGCTTTATCAGGACTCAGTGGTTGCAAGCCAGGGTTTTAAAGCTCTTTCTGAATACCCTGAATCATCTCACACCATTCTGCACTTACCAGAGCAGGTGAGAACATCTACAGAATGTCTTCGCATTGTTTTTGTGTTTTATTTATTGTATCTGTCTGTAATGGGGATCTTGCTTTCAGGCTAGGCCCATACCCAAGCAACCTGAAGTC[G/T]AGGATGAAGTGAAGCAAAATGAGGAGGAGAATGAGGAGGAGGAAGATATTTCAGTGCCAGGAGCATCATATGTGAAGCTCGTTTCTCTCACATCTTTATCTGTTTTACCAGGTATAAATAAAAGAATATATTGTGCATCAATTAATAGCGCTTTACTTTTTCCACATTTTTAGCAGCTTAATTGGAGTTAATCTGTGGTAAATTCAGTTGATTGGACATGATTTGAAAAGGCACACACCTGTGTATATAAGGTCTCAGGGTTGACAGTGCATGTCAAGCACAAACCAAGCATGAAGACAAAGGAATTGTCTGTAGACCTCAGAGACAGAATTGTGTTCAGGTACAAGGCTGGGGAAGGTTACAGAAAAATTTCTGCTGCTCTAAAAGTTGCAATGAGTGCCTCCATCATCATCTGTAAGTGGAAGATGATTGGAACCACCAGGACTCTTCCAAGAGCTGGCCGGCCATCTAAGTTGAGTGATCGGGGGAGGGCCTTAGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34032
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037846 | Essential Splice Site | 1229 | 1797 | 33 | 49 |
Genomic Location (Zv9):
Chromosome 7 (position 20175534)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 18708563 |
GRCz11 | 7 | 18960830 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGGAAAGCATGAACACTCTTCGCGCCCTGACCGAGGAAAGTCAACAGG[T/C]GAGAGAGACCTCGAACTGACTGTTTCACAACCAGTATCATACGCTAAGAT
Long Flanking Sequence:
TATTAATGAATGGTTTATTGGGACAGGACCATCTGAGAGTGCAAAAAAACATCTAAATGCTGAGAAAATCTGCATTAAAGTTAAATGCTTGGCAATGCACAATACTAATAAAAAATGTACCAAGTGAAATTTACACAATATCCTTATGGAGCTTGATTTTTTTTACTTAATATTCTAATGATTTTTGGCATCAAATAAAAATCATCAAATAAAGATCATTTTGATTTATAATGTATTTTTCCCCCTACTTCTAAAGAAATATACATGTCCTGCGTTAGGATAGTTTTGTGGTCTAATATTTAACAAAATATTTATATTTTTACAAAAGCCTCCATCTAAATTCATCCATTTCTTGTGTCTATTTTTGTCTGTATGTCAGGTTGTAGCCTATTCTGTGGCATGTGTGGGAGTTTCAGCATTTAGTGCAGGCATTATTGAGGCCAGTAAAGCAGAGGAAAGCATGAACACTCTTCGCGCCCTGACCGAGGAAAGTCAACAGG[T/C]GAGAGAGACCTCGAACTGACTGTTTCACAACCAGTATCATACGCTAAGATAAAATACTTTAGGATTTGACCTCTAGGTCAATTAGTTTGATCTTTCAACTAATGCCTTGTACATACACACACTTGCAGTCTTGGTCACTTGAGAGTGCTTGCATTCAGCAGAAAGTTTATATAAAGGTTATGGTATTTGATTAAGATTTGAGGGCATTTTTGATGTTCTGATAGCGAATCCTATGAATCACTTTCTATCCTGCATCGGAATTTCACGATTCATCAGTGGTGTCATGTGATGTCTTGAGAATGAAATAAATGGTGATTTTTTTTTTCATGGAAAACTTTTCTATACAAGTTAACTAATCACTGCAATGATATATACTGTAATATATTTTATTTCATAATTGCACTTCATATGCAAATAATTTGAAACAGCTTTTTATTACATAATTTAAGATGCATAAATGACTTCATGTCTATTTTTACTGTAAATAAAAGTTTTAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34033
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037846 | Nonsense | 1658 | 1797 | 46 | 49 |
Genomic Location (Zv9):
Chromosome 7 (position 20191285)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 18727916 |
GRCz11 | 7 | 18980183 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGAATGGAGTGGCTGCTGGAGTTAATGGGCCACATCAGAAATGTGGCATA[T/A]GGATCTCCCTCTGTTAAATGTGTGGATGTTCTACAGGTATTTGCATTTCT
Long Flanking Sequence:
AGTTGTAAAAATGGCTTTTGCATTATTGGAATATATTCCTTTATTTTATTTGAATCAATTTCTTAATGATGAAATACAGTTGCAAATTTTTTTTTAACAAAATTGAAAAAGAAATGCAAATCCTGATACTAATATTCCAAAAAAAAAAAAATGACAATGTGTTAATTCATATCTAAGCTATTCTTGTTTCAAAAAATAACTTTAGTCTAATATAATTTGAATATATTGAATTGTTTTAAAAAGTAAAATACAAAGTGTATTAAAATTAAAAAGTTCTAATGGAAAAAAATATTAAATGAGCTATGAACTAAAATTATGTGTTTGTTAAACCAAAATATTTTATTTGGTTTTCCTGAAAAGTAAAATAATTATAAAAAAACTGTATGTTTCCTGTATTTACTGTATGTTTCAGAAAGTGAGGTGTTTTGTTTGTTCTCAGGGGTCTCGAAACGAATGGAGTGGCTGCTGGAGTTAATGGGCCACATCAGAAATGTGGCATA[T/A]GGATCTCCCTCTGTTAAATGTGTGGATGTTCTACAGGTATTTGCATTTCTTTACCCTCACTTTACAATCAGATGTGAGTGTGTCTATCTGAAGTGCAGTTACTGCTCTCTGAAAAGCATTTCTCTATACTTAAAGGTCTCATGAAGTGCTTTGAAATGTGTTATTTTATTTAAAGTTGACGTAATCTAAAACATGGAGGGTGGGACATAGAGTAGCTTCTCCCCCTTTTTCGAAAACAGCCAAGATAATTTTGTTTTTATCACAGCTCTGCCAGTGAGAGTGGTTGAGCAAATAAGAAGCTTTCTGAAGGAGGCAGAACATGTCAGATACTAGACTGCATTTGATTGGTTAGAAGATTTGACGAGAACCTGAAGTATGAGGTGATGTCAAATTATCTGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCAGGGCACAGATTTCCTCCTC
Associated Phenotype:
Not determined