ZMP
DOCK3
Ensembl ID:
Description:
dedicator of cytokinesis 3 [Source:HGNC Symbol;Acc:2989]
Human Orthologue:
DOCK3
Human Description:
dedicator of cytokinesis 3 [Source:HGNC Symbol;Acc:2989]
Mouse Orthologue:
Dock3
Mouse Description:
dedicator of cyto-kinesis 3 Gene [Source:MGI Symbol;Acc:MGI:2429763]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18344 | Essential Splice Site | Available for shipment | Available now |
sa24207 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24208 | Nonsense | Available for shipment | Available now |
sa1627 | Essential Splice Site | Available for shipment | Available now |
sa37557 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa9819 | Essential Splice Site | Available for shipment | Available now |
sa37558 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13650 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18344
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 |
---|---|---|---|---|---|
ENSDART00000092090 | Essential Splice Site | 497 | 1938 | 13 | 57 |
Genomic Location (Zv9):
Chromosome 22 (position 34948130)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 32187827 |
GRCz11 | 22 | 32142451 |
KASP Assay ID:
2261-7023.1 (used for ordering genotyping assays)
KASP Sequence:
AACCCTCTGGATAWCAACRCAACTCTCTTCCACCAAACTAACACAGAATG[G/A]TAACATACTAAAGCCAYGTTCACATGTACACTGRTATTTTAYAAATKACN
Long Flanking Sequence:
TGCTAACTAAATAAATTATAGTGTTTTAGTTCATTTTGTGTTGTTTTTAGTTGTAACATTATACAATAAGGTTGTATTAATTAATGTAATCTTTGCTCATTTTAGATCATGAAAATAAAGTTAACTCCGGCACATTAATGCTAACAAGCACGAAGTTGGATTTTAGTAACACATTAGTAAATGTCGAGCTATGATTGATAACATAACCTAATGAAACCTCAATGAAAAGTGTGACCTTTGTTAATCTTGTTAATGACAATAACAAAGATACAGGGCATTGCACGTTCAAATGACCTTTAAAATTGTCTTGTGTATGTGTGTTGATCAGTGTGATGAAAACACCACCTTCAGTAACCACGCGCTGTACCTGGGCCTGCCCTGCTGTAAAGATGACTTCAACGGCTGCCCGAACATCCCGTCCAGCCTCATATTCCAGCGCAGCACGAAGGAAACCCTCTGGATATCAACACAACTCTCTTCCACCAAACTAACACAGAATG[G/A]TAACATACTAAAGCCACGTTCACATGTACACTGGTATTTTATAAATTACTTTTTCTCGTCTTCGTTTTTAACAATATTAAATTAATTAAATTTGATGATTACAATTCAGTTCAGTTCATCTTTGATTCTATAGCGCTTTAAGTTGTGTCAAAGCAGCTTCACATAGACGATTGTAGTCAATTGAAACAGTGTCAGTCCAGTTTTCAGTGTTTAAGTTCAGTTTGGTTCAGTTTAGTTCAGTTCAGCTTATCATCCACGGCTGATAGTCCAAACACTGAAGAGCAAATCCATCCATGCGCAGCTCCACAAGTCCCAAACTATGCAAGACAGTGGTGACAGTGGCGAGGAAAAAACTTCACTAATTGGCAAAAGTGAAGGATAAAAAACCTTGAGAGAAACCAGGCTTAGTTGGGCACAACTATTTCTCCTATGGCCAAACGTCTTGTGCAGAGCTCTAAGCGCTGGAGGCTGGAGAACGCCGGACGTCAGTGAAAACTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24207
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092090 | Nonsense | 841 | 1938 | 24 | 57 |
Genomic Location (Zv9):
Chromosome 22 (position 34975471)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 32215168 |
GRCz11 | 22 | 32169792 |
KASP Assay ID:
2261-7024.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGTAAATTCACTAAGAATATACTGTAATAACATTACATGTTTGCAAACA[C/T]AACTCATTTTGTTTATAAAGTGTCTAGGGACTCCACTGACCCAAGGTTTG
Long Flanking Sequence:
ATGTCTTCGTGTGGGTGAACTTCATGAAAACTGCGAATAAAGTACATATTTTAAGAACACAATAAAAAAGATTGGACCATTACATTTATTTTGTTTTTTGGTTCAACTTTCTTTATGTAAAATTTAAATACATAGTTGTTTTTGCGTAAAATAAGGCCGTGATGTTTCTTGTCAGGCTTCATGAGACTCACCCGCGCATGCTTGTCTTATTCTTGTTTTTTTGTCTCCTGCATTTAGTTTGTTTTAACACCTGCTGGGAAAACTCAACAGTAACTATCTAAAACACATGCATACTCAGATCTACACATTTGATGTCTTCTTACACATTTATTTTGTTTTCAATGTTATTTGTGGATGTATTTAGGATAGATCTCTTTCAAACAAAACCCAGCAGAAACTAGTCATGTTTATGTGTCTGTTTAGTTAAAAGAAGCAAGGAAAGTCCAGATGGGGTAAATTCACTAAGAATATACTGTAATAACATTACATGTTTGCAAACA[C/T]AACTCATTTTGTTTATAAAGTGTCTAGGGACTCCACTGACCCAAGGTTTGCAATAGTGCGAGTAGATCGTGAGTATATTGCAGTGTGTAATATACATTCAGTATATTTTGTTACAAAAAGTAAAAAAAATACTTTATTTGGGTTATTTTGGGATTTGTTTTGCTCTTGTGCCATTGTAATTTAATTATTGTGATCCATCCATAATAGATATGTGCACGTGATGTAGCTATGCACTAGTTTTATATAAGTTTATATTGGTTACGTGATGGACATTGCGCTCTTTGCTCTCATTAACATGCTTAAATACCTGTGCTATATGACAATACTAAAACTGTTTAGGTCCTCGTGTATGTGATTTAAAATTTGGGACTCTACTGAAGTCTGTTCTGAAATGAAAGTGTCAGACTTGACATCATTCGCTAGGGTTTTTAATGCCGCGCGACTCGCATTGCTAGGTGAAAACTACCTGCTTACACTGCAGACACGAGAACACAGATCCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24208
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092090 | Nonsense | 1146 | 1938 | 35 | 57 |
Genomic Location (Zv9):
Chromosome 22 (position 34998359)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 32238056 |
GRCz11 | 22 | 32192680 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTGACCTGAGAGTCACATGATCTGGACGTTTACAGAATTTCTACAAGT[C/A]GGAGATCAATAAGGAGGAGATGTACATCCGATACATTCATAAGCTGTGTG
Long Flanking Sequence:
CCTACGTCAAGCAAATTGTGCTGAAATCAGGAAAAGATATGCGTAATCTGAATTAATTGTGCAGTATTTAAACCTTAAATTGAATGCTTGGTCAATAAATATTTGGATGTTTAGTAACCCTGGCCCACACATCTTAAATAGATGGATGTATCACTGCAGCAAGAGCATACAACGTTCCTGTTCAGTCTATCATATGTAATCTAAAAGCAAACAGTAGAAATCTCTTTATAAGTTGCATAGAAAGCAGCCAATCAGATTCAGACTTCATATTGTGCATATATATGATCATTGGGCGTGGCATCTGTAACTACTGAGACGTCCTGTTTCTGTTGTTGGCAGAGATTGCATGAAAGGTGATGAGACGGAAAACAAGAAGATCGGTTGCACGGTCAACCTGCTGGTGAGTTTGAGCTTTCATAATAAACATGACGCAGCTTTGTGAGCAAGCTGAACTGACCTGAGAGTCACATGATCTGGACGTTTACAGAATTTCTACAAGT[C/A]GGAGATCAATAAGGAGGAGATGTACATCCGATACATTCATAAGCTGTGTGACATGCACCTGCAGGCGGAAAACTACACAGGTGAGACACTTCATCTTACTGCAGGGGTGTCCAAACTCGATCTTGAAGGCCCGGTGTCCTGCAGATTTTAGCTCCAAGGGTCCGTTCTTCGTACCTCACTTAAATGATCTAAGATGATTTGGCAGATTCTGGATCTTTTGATCTTGATAACTGATCTCTCGCTAATATGGTTCTTCAAACAAGTTCGCGAATCAGATTAGAATGTCTGGATGAACTGATCTGAGATCGCTGCGTGTGTTGTGAAGGACAGATCTATCGATCCTCGAAATCATGATCAGCAATGCAACGATTGGCTGACGGCACAGCAGCGTAATGACATCATCTGATTAATATTCAATTATCCATGTGAGCAAAATTACATCAAATTAGCAGTAAACGGTTTGTTAAATATGACACGCAATAACCTTCCACATTTGTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1627
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 |
---|---|---|---|---|---|
ENSDART00000092090 | Essential Splice Site | 1389 | 1938 | 40 | 57 |
Genomic Location (Zv9):
Chromosome 22 (position 35009609)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 32249306 |
GRCz11 | 22 | 32203930 |
KASP Assay ID:
554-1568.1 (used for ordering genotyping assays)
KASP Sequence:
ATGACCGACCATTCCACAAGGGTCCTAAAGACCGGGAGAATGAGTTCAAG[G/A]TAAAATTATGCCTCTCTTCACTTSTGGATTATGATGAACCGCATGTTACT
Long Flanking Sequence:
TATTTATGCATTAGTTTATTTTATTATGATGTGCACTCCTTATTTTTTAGCAAAAATATTTTTTTAAAGATGTATGTTTGACGTGTTTGCCTTCATTGACAGGACAGTATATAAACAGGAAGTGAAGGTGGAGAGAGCAAGGGAGGAAGGATTATAGAAAGGTCCACATGCCAAGATTTAAATGTGGGATGCCTGAAGCGCAGTTGGTGCAATCAGTGCAGACAATGACATAAACTCTTGACAGCATTCTTATTTCCAGTTTGATTTATTCGCCTATACTACAAGTTGAAAAAAAACAGTAGCGGTGTTTTGCCTTGACATAAGCTTTGCTAGACCTCCAGATCTACGCCGTGTCTGCAGTTCCTGAAAACATGGACGTTCTTCAGATGGACCGCGTGCCCGACCGCATCAAGAGCTTTTACAGAGTCAACAACGTCCGACGATTCAGATATGACCGACCATTCCACAAGGGTCCTAAAGACCGGGAGAATGAGTTCAAG[G/A]TAAAATTATGCCTCTCTTCACTTCTGGATTATGATGAACCGCATGTTACTTAAAGTGTTGTTGTGTTTTCAGAGTCTATGGATCGAGCGAACCACACTAATCCTCACCCACCCTCTGCCCGGCATATCCCGCTGGTTTGAAGTGGACAAGCGAGAGCTGGTGGGTTAATCTGCATAATCTTTAATGTGATCAGCTCGTTTACATGAATATTCTTAACCTGTTTGTGCTTAAAGTGATAATTCACCCTTAATTATAATAATCATTACTGAATTATGCACTACTTATACTTATTTTTAGCCCTTTTCATTTCCCTTTTTTTATATGTTACTCTAAATTACAAGGGAACATTCATCCATATTTTGACATTTGATAAAGGTGATTTAAAACATTAAAGAAGATACTTTACTTGTATTTGATATGCTTTCTATGTATGTAAACTCGAATGGGAAAATACTGCAGTAATCCATAGTAAATATTTTTTAAATCATACTATAAAATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37557
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 |
---|---|---|---|---|---|
ENSDART00000092090 | Essential Splice Site | 1698 | 1938 | 51 | 57 |
Genomic Location (Zv9):
Chromosome 22 (position 35020839)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 32260536 |
GRCz11 | 22 | 32215160 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGATCGGCCCAGTAGTGCCATGTACCCCAATATAACTGAGAATGGACAG[G/A]TGGTGTGTTTACCTTTCAAACAATTAATTTAGTTTAAAATTCATCAAACT
Long Flanking Sequence:
TTGCCCTCAAACTAAGAACGAAAAATAATTTTGAAGAACTTTGAAGTATACCAGGGCCTTAAACCAAAGAAACCACTCACAACCCTCGCAACTCCCTGACAACCCTTCAAAACAGCTTAGCTTCTGCAGAACAACACCATTAGCCAGGATCAACACTACGAACTAACAAAAACACTGAAGATGATCTTTTCTGTTTTCCCCATGTAACCTTTCAGCCCAGTCCATCGTCATCCAGCTTGAGTTCGACGCATTCAGCTCCGTCTCAGATGATCAACTCAGGGCACGGCAGCATCAGAGGTAAACACCAATAACGTTTTCATATTAACATCAGGATTAACGTTCACGATTCCCAAATTGAGATTACTTTTAAACTATTTCCAGTTGGATCCCCATCACTACCTGACAGATACAGACACAATCGGGAGATGTTGATGCTTCTGCCACCGCACAGGGATCGGCCCAGTAGTGCCATGTACCCCAATATAACTGAGAATGGACAG[G/A]TGGTGTGTTTACCTTTCAAACAATTAATTTAGTTTAAAATTCATCAAACTATCTGGAACTAAGTTTTGAAGGTGAGATGATGTCAGCAATAAATGTTTATTTCCCTTTTTTTCACCAGCCTACTAATCATCAGAGGGCTCTGTATCATCAAGTCATTGGTCCCTGCAAACCTTGCAGTGACCCCAATCTTTCGGTGGCTGATAAAGGTATGACTGGGTGTGTATAATTCTCTGAACCCACTGTAACTCACAATCTCCTGATTGTGCAGAATTACAATCCATGCTCTATCTGAAATCCCCCCCAACTCTGAATGATTTTTTGAATATGCAACAATTCTGGCGTAATATCCTGACCATGTAAATCTGATATGTTTGTTGGTGAACAGCGTGCTTAAGTTGGTCACCCTCCTGTACCAGCTACAAAACATCCTCTCTTGTTAGGCTAGTTTAGCAGCCGGCTGGTAACAAACCTTTGATCAGACCTACCTGAGATATCTGGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9819
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092090 | Essential Splice Site | 1771 | 1938 | 55 | 57 |
Genomic Location (Zv9):
Chromosome 22 (position 35023923)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 32263620 |
GRCz11 | 22 | 32218244 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGCATGTCCGCGMTAGCATTCCACGATGTCTAATGTCCTGTTAACCTCA[G/T]ATGTCCCCACCTGTTCTCCAGCCAAAACACCCAGAGCCGAATTGTCCGCC
Long Flanking Sequence:
TAGTCTTTTAATTTTGATTATTATAATAATATGCATCCTGTCAACTACCCGAATGTGTCTAAAAAGTAGCCTCCTCCTTTTCATTTCAGTAGATTTCCCTACATCTAAAACATCAATCCTTTGCTGTTAGCATAAATCCTCACATGATTGAGTAATTTCCTGGTCATTCCCTCTATCCCAGCCATTACCCTCCTCTGAACGTCAGCTAAGTTCAGAAAGAGTCCTTGATAGTGCTTGCTGAGTGAGCGCATGCCGACCTGTGTGCGGGCAAGTATATACCGGCGTGTGCTCTTTCCAACCCTGGTTGTCCAACTGTGTCTCCCCCTTTAGGACACTTCTCGATGCACTTTGATGCTTTCCACCACCAGATCAACGAACTCCCTCCAGCTCTCCCCGCGCGCTCCTTAAGAAAGGTATCCTCCGCCTAGATGTGTCCTGTTAGTGCTCATCATGCATGTCCGCGCTAGCATTCCACGATGTCTAATGTCCTGTTAACCTCA[G/T]ATGTCCCCACCTGTTCTCCAGCCAAAACACCCAGAGCCGAATTGTCCGCCAGTCTGCTTTTGGTTATAATTGGGTTGTTCTTGTCCCTAAGATGCTGAAAGTGTTTGGGTTCATTATGTAATTGTTTCATGTGCATCTGTATATGTGCGCATCTATAGAGCAATTTGTGTGTATGTGTGTGCATATGTGTGCTTGAGATTGTCGCTTCTCCATTATGAACTGGAGATCAGTAGGATGCAAGTGAAGGATGATGACTATAGGGTGACTGATAAAGTCAAATCTGCTTCCGTCATCCAGAGACCTAAACTTCAGGTCAGAGAGTAGCTTTAAATCAGAAGTGCTGAAGCCTGCTCCTGAAAAACAACTTGCTATTTTGATTGATATACCAGAAGTAGCCATAGAATTAAATTGGGTTTGTTTGGCAGTGTTTGCTTTAAATTTACTGCTTATGATGGGAAAGTCCTTGTGCCCAAGTGATAGGACAAACATTCTGTTAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37558
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 |
---|---|---|---|---|---|
ENSDART00000092090 | Essential Splice Site | 1791 | 1938 | 55 | 57 |
Genomic Location (Zv9):
Chromosome 22 (position 35023987)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 32263684 |
GRCz11 | 22 | 32218308 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTCCAGCCAAAACACCCAGAGCCGAATTGTCCGCCAGTCTGCTTTTGG[T/C]TATAATTGGGTTGTTCTTGTCCCTAAGATGCTGAAAGTGTTTGGGTTCAT
Long Flanking Sequence:
AGTAGCCTCCTCCTTTTCATTTCAGTAGATTTCCCTACATCTAAAACATCAATCCTTTGCTGTTAGCATAAATCCTCACATGATTGAGTAATTTCCTGGTCATTCCCTCTATCCCAGCCATTACCCTCCTCTGAACGTCAGCTAAGTTCAGAAAGAGTCCTTGATAGTGCTTGCTGAGTGAGCGCATGCCGACCTGTGTGCGGGCAAGTATATACCGGCGTGTGCTCTTTCCAACCCTGGTTGTCCAACTGTGTCTCCCCCTTTAGGACACTTCTCGATGCACTTTGATGCTTTCCACCACCAGATCAACGAACTCCCTCCAGCTCTCCCCGCGCGCTCCTTAAGAAAGGTATCCTCCGCCTAGATGTGTCCTGTTAGTGCTCATCATGCATGTCCGCGCTAGCATTCCACGATGTCTAATGTCCTGTTAACCTCAGATGTCCCCACCTGTTCTCCAGCCAAAACACCCAGAGCCGAATTGTCCGCCAGTCTGCTTTTGG[T/C]TATAATTGGGTTGTTCTTGTCCCTAAGATGCTGAAAGTGTTTGGGTTCATTATGTAATTGTTTCATGTGCATCTGTATATGTGCGCATCTATAGAGCAATTTGTGTGTATGTGTGTGCATATGTGTGCTTGAGATTGTCGCTTCTCCATTATGAACTGGAGATCAGTAGGATGCAAGTGAAGGATGATGACTATAGGGTGACTGATAAAGTCAAATCTGCTTCCGTCATCCAGAGACCTAAACTTCAGGTCAGAGAGTAGCTTTAAATCAGAAGTGCTGAAGCCTGCTCCTGAAAAACAACTTGCTATTTTGATTGATATACCAGAAGTAGCCATAGAATTAAATTGGGTTTGTTTGGCAGTGTTTGCTTTAAATTTACTGCTTATGATGGGAAAGTCCTTGTGCCCAAGTGATAGGACAAACATTCTGTTAAAAAAGGGCATACTTCAAATTAAAGCTACATTAAAGCAATACTCTAATTTTAATTAAAAAATAAGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13650
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092090 | Nonsense | 1870 | 1938 | 56 | 57 |
Genomic Location (Zv9):
Chromosome 22 (position 35025722)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 32265419 |
GRCz11 | 22 | 32220043 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGACCACAGACACGGAAGAGGCAGAAAGTCCCTATCTCCCCGTACGCTA[C/A]AGCGTCTCCGAGCCTGAAGTTCTGGACCCTCTCAAGCCMGCTCCATGCCG
Long Flanking Sequence:
TAAATTATGGAACTATGGGGCCATTTTAATTTTAAATGAACTATTTCTTTAACAATATTTCCACTGTCAAATGTGGAGATCATTAGAACTTAATGTGGTTAAAACTTCAACCTGTAGGATGGAAGTTCTCCAGGAGTTGGATTTAGCTGCCTTGCTCTTAGATCACCTGAATGTCATCCTACTGGTCTTACATTTGAACGTTGCATTTAAAAAAGGTGTTAATAATGCAGTGTAATGTTGACCTTGTTTACCTTTCCTTACCAGTCGCCCCTGCACCCTATACCTGCCTCACCCACCAGTCCACAGTCGGGGCTGGATGGCAGTAACTCCACCTTATCCGGCAGCGCCAGCAGTGGTGTCTCCTCCTTGAGTGAGAGCAACTTCGCCCAGTCCTCCTCTGAGCCTCCAGCTCGAGCCGACACCTTGGACTCGATGCCGAGCAGCCAGGCCTGGACCACAGACACGGAAGAGGCAGAAAGTCCCTATCTCCCCGTACGCTA[C/A]AGCGTCTCCGAGCCTGAAGTTCTGGACCCTCTCAAGCCCGCTCCATGCCGTAGTCACTCAGCCCCGTTGGGTGTAACCCCAGGGATACCCTCTGATGGCCACCACCACCATCACCTCCATCTCCACCATCACCACCCACACGCAGTGCACATCACCCACCCTCACTACCACCACCACGAGCCTGCACCCGCACTGCCTCCCAAACCTTACCTGAGGGAAGGGTGCATCCCTGAAGAGGACCTGAGGCCAGTTCCGAGGCCTATGCCACGCAAGATCTCCCAGCCTTTGCTTACTACCAAGGAGGAACAGGCCAAGGTGGCCTGGGAACATGGCATTAGTGAAGAATAGACGAAGAATAACCTGGACTGTAAGCTTTGGCATGATTTGTGGCAGGATTTTGGGAAAGTCCCCAAAAATTATTCATTTGAACCTTCTCTGCTCCCAGTATACCCAGTGTAGGTCTTTTCAACCTTTTAAGAAGTGCTTGCCATGTTACAGAG
Associated Phenotype:
Not determined