ZMP
LOC100332172
Ensembl ID:
Human Orthologue:
TTC37
Human Description:
tetratricopeptide repeat domain 37 [Source:HGNC Symbol;Acc:23639]
Mouse Orthologue:
Ttc37
Mouse Description:
tetratricopeptide repeat domain 37 Gene [Source:MGI Symbol;Acc:MGI:2679923]
Alleles
There are 12 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12559 | Nonsense | Available for shipment | Available now |
sa2213 | Essential Splice Site | F2 line generated | Not yet available |
sa40552 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa33706 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33705 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33704 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31475 | Essential Splice Site | Available for shipment | Available now |
sa18177 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12559
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100800 | Nonsense | 40 | 1577 | 2 | 40 |
Genomic Location (Zv9):
Chromosome 5 (position 52554320)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 50221516 |
GRCz11 | 5 | 50868109 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAATCTATTTCTCCACTTCAGGCTGTTCTAAAGCTTGAGAAGAATAACTA[T/G]AATGCCTGGGTGTTTATTGGAGTGGCAGCCACAGAGCTCCAGCAGCCGGA
Long Flanking Sequence:
TTAAATCATCTTTCTTCCCCATTCTGATGCTCTGTTTGAACTGCAGCAGATCGTCTTAATCTACTTGCCTAAATGCATTGAGTTGCTAACATGTGATTGGCTGATTAGAAATTTGTGTTAACGAGTAGTATCTAATAAAGTGGGCGATGAGTGTATAAAATACCTACATAAACACACATAAAATTACAAAAACTATGTCAAATCAAAGTTGAAACCGTGTTAGCGGCCAATGACTATAAAAATGAAACATTGTTCACAGTCAATTAAATAGTGCTAATGTTGTTTTGAAGTTATACTTACATGCAATTTCAAATTAACTATTCAAAATAGCATGGTAACGTCAAACAATATTGGGACACAAATGAACGAATGTGCAAATATAAAACTAACTTTACCTCAATTTATACCTTTCTCTTGATTGACTGAATTTATAAATGTCTTCCTCAAGTCAAATCTATTTCTCCACTTCAGGCTGTTCTAAAGCTTGAGAAGAATAACTA[T/G]AATGCCTGGGTGTTTATTGGAGTGGCAGCCACAGAGCTCCAGCAGCCGGATCAAGCACAGACTGCATACAGAAAGGCATCGGAGCTCGAGCCAGAGCAGCTGCTGGCATGGCAGGTATGTCTTCTTGATTTAACTTTAATAGAAATCTTGTGTTAAGGCAGTTTGTTTAAACGTCTTAATTTTGTATTGAAGATATTAAATGAGTATTTCTTTCACAGGGTTTAGCAAATCTGTATGAAAAAAGTGACCAAGCAGATTTCAAAGCTGAGCTTCCCAAGATTTACCAGAAACTCATTACGCTATATGAAACGTAAGTGCTCTAATGCTGAAGGGCAAATTACATTTGTTCCTCTTTATTTTTTTTATTATTGTTATTATTAGTGGTGCTTAACTACTATTAATCACATCCAAAATAAAAGTTTGCATTCAAATTAATTTGCATACAAATTTATATATAAATTTCTATATAACAACATTGTTTTGTTTTTATATATCTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2213
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000100800 | Essential Splice Site | 184 | 1577 | 5 | 40 |
Genomic Location (Zv9):
Chromosome 5 (position 52552789)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 50219985 |
GRCz11 | 5 | 50866578 |
KASP Assay ID:
554-2695.1 (used for ordering genotyping assays)
KASP Sequence:
GACTCCTGCAGGACACTGTTGACGACCAGGACAATGAAACACAGCAGCAC[G/A]TCAGAATTTCTCATATTCAAATAAAATACTCTATTTTTTCACCCAGAAAT
Long Flanking Sequence:
GATGTCCCATTTCGGTGTCATTATCAAATGAAAATGATGACAGAACATTCACATTCTTGTTCATATATAAATAAATATATGTTTAAATAAAAGCACTCTACTGCACTGGGCACCATTTGCTTCTTAACCCGTTTCTTTTTTTTTTTTTTTTTTTGCATTTGCAGCTCAGACAAAGCAAAATGTTTCGAAGTGACAAAGAAATTGGTGGAGATTTATCAGTCAGAAAAGAACTATCTACAGGTATGAGCTACAAAAAGATAAATAAAATCCTAATGTTACGGCAAATGATTTAAAGGTTCAAAATTGTGCTGATCTTTTAATTATTCAAATTTGCACAATATTTTTCAAACCCACAGGTGGCCAGAGTGTGGCGGAGGTTAATCCAGGTGAAAGAGGACGAGGAAGGGCTGGAGGATGCAGAGCTGCTGGAGCTGTGGAAGGAGATGACCAGACTCCTGCAGGACACTGTTGACGACCAGGACAATGAAACACAGCAGCAC[G/A]TCAGAATTTCTCATATTCAAATAAAATACTCTATTTTTTCACCCAGAAATACAAAATATACAAGACTTACATTTTTCATAAAGCTGACAGTGTTAGTGTTTTTTCCTCAACAGCTGATATCTGCATTTGAACGAGCTTTACAAATGACAGTAGATGTGCCCAGTGAAGCCCACAGGAGCCTTTCGCAGGATTACATTAAATGTCTTTCAAAGGTCAGCCAGCTGTATATGGTGTAAAAGCAGTAATGCGTACAATAATAATGACTGGAACAATTCGAATGTTGCATGTTTTGTGCCGTTTAGCTTCCTCATGAGGTGGCCAAGCTAAAGGAAGTATGTGACGCCACCCTGTCCCACTATCCCACACACCCATACCCTCTAGAGGCCCTCAGTGAGCACTACATCCAAACAGGTTAGTTTATTACCCTACAGAAAAAAACAAGATAAAGGCATTGTGTGTAATAATGAGTTTAACAAGTCCAAACTAACTTTACTCATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40552
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 |
---|---|---|---|---|---|
ENSDART00000100800 | Essential Splice Site | 300 | 1577 | 8 | 40 |
Genomic Location (Zv9):
Chromosome 5 (position 52548766)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 50215962 |
GRCz11 | 5 | 50862555 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTTGTCAGGATAAAAAATATGAGGATGCCATCAAAAATATTGGTCTGG[G/A]TAAGTTCATAAACACTCAGATGTTCATGAATGAATGGAGCACTAAGGTTA
Long Flanking Sequence:
ACTCCTCCACCTGGGATAAGGACTTTATTACATTCTGGAGATGGCAAACAACCTTTATTCTGGTGGAGCACCATGTCCTCCGACTTGGAGGTGCTGATTCTCATCCCTGCCGTGTCACACTCGACAGCAAACAGTCCTGTAGTTTGTATGATATAAAATAAAAACTCAAACTGGTTTGGGAAGAGAAAAGGATGAGTAAGTAATGACAATTTTTTATTTTTTTTTGGTGAAATAACCCTTTAAGCAAGATTAGGATTTTATTTAGAGGTCCATAGCATCTAAAAGCGTAAAACATAAAAAAATATGCCCCATATTTAAAAATGATAAGTAATAAATGTTGTTTTTGATTTTCTTGTCAGGTGACTGCAGTGAAGAAGCTGTTTCCTGTTTCAAGCGTCTCTTAGAACTGGATCCAAACAACTCGTATGCTCACTTTGGTCTCGGTATTAAAGCTTGTCAGGATAAAAAATATGAGGATGCCATCAAAAATATTGGTCTGG[G/A]TAAGTTCATAAACACTCAGATGTTCATGAATGAATGGAGCACTAAGGTTATAAGAAATTCATTATATCAAATTCTCCAAATGCATTTTGATCATTAAAAGTTGTTTCAATAAATCTTTTACTTAAATTCATGTTTAACTGTACAACATTAATGAAGTTCCTTGCAATTCCTAGGTATACAGTGAAAATTACAAAAAATATGTGTAACTTATTTGTTGTGTGTTTTTTTTTTTCTGCAGGACTGAAGCGTATGCGCTTCTCCATCATTGGTTGGTATAATCTTGCCCTGGCTCAGCTAAAAATGCATAAATACTCTGACAGTGCCATATCTTCCAGTCAAGGTACTGGTTATATGATTCACAGCTAACTGCTCAAGTCAGTTGCACTTAAAAACAGTTTTCAAATATGTTCCTTTTCATTTGTTCAGGGCTAAAATCGAGTGTGGGGAACGCTGATGATTGGACTCAAAAGCTCCTGAGGTTGAAACTAGAAGCTCTGGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33706
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 |
---|---|---|---|---|---|
ENSDART00000100800 | Nonsense | 471 | 1577 | 13 | 40 |
Genomic Location (Zv9):
Chromosome 5 (position 52545177)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 50212373 |
GRCz11 | 5 | 50858966 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTGTTCTTCCTGCTCGGGTCCCTTTATTGGAACATGGGAGAGGAAATA[C/T]GAAGAGACCGCAGCAAAACTCATTTACTCAAAGTGAGACACTTTAAAATC
Long Flanking Sequence:
TACCTTCTATAAAATGCTAAGGAAGTTAGTTTGTTTACCTACTGTATGTTCTTCATAATATTTTCTTTTGAATTTTTTTGAACAAGTAAATAGTATTTATTTTTTTCATTTTAGTGAACTATTCCTTTAAGAAATTGGATATTCCAAAAGCGAAGCAGTTCATAATAATGCCATTAATGCAATAATGCCACTGGAATGAAATGATTCTTGCAGGTTTCCACTGAGCTTTTGAGCTCTCACCCAGGATCTGTGGATGGTCTCACTTTGAAAGCACTTCTACATGTTGCTAAAGAACAGCACAAACAAGCTGAGGAGAGGTGTGAAACTCCACATATGCACACGCACACATGCATATATCATAAACAACTTGGGTGTAACCACCAGGCACTTATTTTCTCACTCTGTTACACAGCTTTCTAGAGGCTTTATCCAGAAGTCCAGATAGTGGGGAACTGTTCTTCCTGCTCGGGTCCCTTTATTGGAACATGGGAGAGGAAATA[C/T]GAAGAGACCGCAGCAAAACTCATTTACTCAAAGTGAGACACTTTAAAATCCTTTTATAGGACCCTGGTAAATATAATTTATTTCCCCCACATTTTGTTTTGTTTTTCCTTTTAGTTTTTATGTATTGTTTTTTAATTTTCTGTTTGAAATATATTTTTTAATTTTGATGGATATAATTTTAGTAATCAAAAACTATTATTTAATTGTTAGCAATATTTGAAATAAAAGTAAAATTTTTTTTAAGCAAAAAAGTAGCAAAAATAGTAGCAAAAAAACAAAAAAAAAATTCTCCCAAACTTTTGGGACTATTAAAGTTCTGCTACCTTAAAAAAAAAAAAAAAACTTAAAATTTAATGGGTTGTTTTAAATTAAAATTTAGGCAATGTCCTCATAAGGGAATGACAGAAGCTAAAAATAACACAATCTTCACATTTTATTAAATATTGTGCATTCAGTTAATGGAATGAACAATTAAGTATAATTCAATTTGATAAATTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33705
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100800 | Nonsense | 788 | 1577 | 19 | 40 |
Genomic Location (Zv9):
Chromosome 5 (position 52535251)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 50202447 |
GRCz11 | 5 | 50849040 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCTGATGCCAGAAGCTCCCAGTCTGTGGTGTGACCTGGGTTTGAACTA[T/G]TACCATCAATCCAGACTGCTCAGCTCTCATTATCCTGAGGAGGATCCCCA
Long Flanking Sequence:
TTGACATCACAGAAGTAAAATACATTAAATATATAAAATAAAAATCAAATTATTTCTTCCAATAATCAAGGACAAACTTTGTGAATTTGCTTGTATTTATTTAAGCAGATACAGAAACATTCATTAATTCATTTTCTTTTTGGCGTAGTCCTTTTATTAATTCGGGGTTCCCACAGTGAAATAAACCGCCAACTTATCCAGCATATGTTTTATGCAGCAGATGCCCTTCCAGCTGCAACCCATCTCTGGGAAAAGATACAAAAACATATTGAACTAATTATTAAAATGAAGACTGGAAAAATGGAAAGAAATATAAATTAGATACTGTATATAAATAAAAATACAAATGAATAGAAATAATGCCTACTGCAAAAATAAACGAATAAATGCTAATAATTTCCTCATTCTGTAATGAACCTATATTTTATTAGGTGTTTTGGTCGTGCATTAAAGCTGATGCCAGAAGCTCCCAGTCTGTGGTGTGACCTGGGTTTGAACTA[T/G]TACCATCAATCCAGACTGCTCAGCTCTCATTATCCTGAGGAGGATCCCCAGGCTCTGCTGGAGAAAGCCCTTCAGGTACTTAACCCGAATTTTTTGAATTCATAGTGATCTCATGAGTATGAGTCTTAACAGGCTGTCACTGTGATTTTGTCACTGTTCTGACAGTGTGTGAAAAAGGCAATCATGCTGGACAGTGCAAATCACACATACTGGAATGCCCTCGGGGTGGTAGCCATGACAAAGGGTAAACACAATCAGATGTGCATAATCGAATTAATCTGCATTACATAACTACAATGTGATTGGTCATTTGTGTGTTCATTATATTCTGTTTTACAATCTTAGGAATTGAAAATTTTGCACTTGCACAACACAGCTTCATCAAATCAGTCAAAGCGGAGCCAAACGTAAGTGATGCAAGAAAGGGGAACAGTTTGCTTACTTTTTAAACATTTGTGTTGATGCAAGTAATATAGAGTTGACGTCAAAATGATGAGCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33704
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 |
---|---|---|---|---|---|
ENSDART00000100800 | Essential Splice Site | 839 | 1577 | 20 | 40 |
Genomic Location (Zv9):
Chromosome 5 (position 52535006)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 50202202 |
GRCz11 | 5 | 50848795 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAAATCACACATACTGGAATGCCCTCGGGGTGGTAGCCATGACAAAGG[G/A]TAAACACAATCAGATGTGCATAATCGAATTAATCTGCATTACATAACTAC
Long Flanking Sequence:
CTGGGAAAAGATACAAAAACATATTGAACTAATTATTAAAATGAAGACTGGAAAAATGGAAAGAAATATAAATTAGATACTGTATATAAATAAAAATACAAATGAATAGAAATAATGCCTACTGCAAAAATAAACGAATAAATGCTAATAATTTCCTCATTCTGTAATGAACCTATATTTTATTAGGTGTTTTGGTCGTGCATTAAAGCTGATGCCAGAAGCTCCCAGTCTGTGGTGTGACCTGGGTTTGAACTATTACCATCAATCCAGACTGCTCAGCTCTCATTATCCTGAGGAGGATCCCCAGGCTCTGCTGGAGAAAGCCCTTCAGGTACTTAACCCGAATTTTTTGAATTCATAGTGATCTCATGAGTATGAGTCTTAACAGGCTGTCACTGTGATTTTGTCACTGTTCTGACAGTGTGTGAAAAAGGCAATCATGCTGGACAGTGCAAATCACACATACTGGAATGCCCTCGGGGTGGTAGCCATGACAAAGG[G/A]TAAACACAATCAGATGTGCATAATCGAATTAATCTGCATTACATAACTACAATGTGATTGGTCATTTGTGTGTTCATTATATTCTGTTTTACAATCTTAGGAATTGAAAATTTTGCACTTGCACAACACAGCTTCATCAAATCAGTCAAAGCGGAGCCAAACGTAAGTGATGCAAGAAAGGGGAACAGTTTGCTTACTTTTTAAACATTTGTGTTGATGCAAGTAATATAGAGTTGACGTCAAAATGATGAGCCCTCCTGTGAATGTTATTTCATTTTAAAAAATAACTCCCTAGTGTCTTAACTGATATGTTATTATTTTTAACACATTTTTAGACACAATAGTTTTAAAAACTATTTTTTTTTGTCTTTGCCATGATGAAAGTACATAATATTTTAATAGTTATTTTGCCAGGTACTATTATTCAGCTTAAATTGCTAGTTAAAGACTGAACTAGGTTTTTAGGTTAACTACACTCAAAGCATCTGTTTGTTAACTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31475
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 |
---|---|---|---|---|---|
ENSDART00000100800 | Essential Splice Site | 1009 | 1577 | 26 | 40 |
Genomic Location (Zv9):
Chromosome 5 (position 52530500)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 50197696 |
GRCz11 | 5 | 50844289 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAACACACACCTGCAGCTCAGGAAACAGGCCACTGAGGCTTATCACAGG[T/C]TTGCCCTTTCTAGCTAATTACACATGTCAAAAAAGATAATTAGGCTACCT
Long Flanking Sequence:
CTTACCCAATAAAATGATTATTAAAGTGCAACCAGTATGCTATTGATATCCTAAAATCTTTAACTTTCAAAGTAGGTAAATACGCTGAAATGGTACTATATGCACTGTAATACGCAATGTTAAAAAATCTGCATGCTTTTTGAATATGGAGCAAATAGTTATTGTATATTATTATATTATAATTCAAATAATGCACCACCCTCTTTGTTCATAAAAGCGTCTTTAGGCTGGAAATGGTTTAAATCCCATTATGGCTTGAATGATTTGAATGACTTGTAACGACTAGACGCATTTCAAAAATGTGTCTCCCATTGAATATTTAGGAAATTAATCATGTGACAATGACAAATTTGAAAGATGAAGAGAGGTAATGAAGCTCAGTGTTCTTTCTGTTTTTCACACCAGAGAGGATTCAGACAGACCCAGACGCCTTCATCATGCTCGGATACCTGAACACACACCTGCAGCTCAGGAAACAGGCCACTGAGGCTTATCACAGG[T/C]TTGCCCTTTCTAGCTAATTACACATGTCAAAAAAGATAATTAGGCTACCTGACATAATTTCATATTAATGGTTAATCTTTGGTTTTTTAATATTGCAGACATTTATATCTTATTTATTAGAAAAAATACTATAAAGTTTCTTGTATAAAGACAATGTTCATGCTGAGATGTTTTTTTCTACATATAATTCTATTGTGTTTTACACATTTTTATAGTTACTTATTTTAATATTTAGTTCCCCTCTGTGTTTATTATTAATTTTATACTAATTTTAATTAGTTAAATATTATGTGATTTTTTTTAATCTAATCTTGAGTTGTTTTTTAAATACTTAAATATTATTTTAAATATTTTATGGATGTTATTATTATTATTTTTATTGTTTTGTTCCAGCTATATTAATTTGTTTCTTTATTAAACTTTATAAAATAATGTTTTTTTTTTTTTTAATTTAGCATTTTTCTCGAAATATTTCCACTGATCCCCTGGCAGCCTCATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18177
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 |
---|---|---|---|---|---|
ENSDART00000100800 | Essential Splice Site | 1509 | 1577 | 38 | 40 |
Genomic Location (Zv9):
Chromosome 5 (position 52507193)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 50174389 |
GRCz11 | 5 | 50820982 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTCTCCTTTTTCAAGCCTTACTGCAGTTCTCCGTGAAGATGGGYGCCAG[G/T]TAGARGACTTTAAAAATAGAGCTCTTTTGTGTTTSTGTTGTATTAATTGT
Long Flanking Sequence:
TTACAGCGCCTTCAGGCTTCTCTCTTGCACATTTTCTCCCTCTAGTTTTATTTTGTCTCTCCTCCTCTCCTCCCGTCTTTAACTGTCAGCTTATTGCCTTTATTTTAGCTGACTGCAGCTTTGCCTGTTAAATTGAATTAGACACTTTGTGGCTCGCCTTTCATTACTTTTAATTAAAGTGTGTGAGCCTTCAGCGTATCCCGACTCCAGTCATATATTAGTCTGAACTGTGCCAGCTAAAATACATCTAAAATTCTTGTTTTATAAGACTTTTGTTTCTAGTTACTCATTCTATTTCATAAAGTTGATACACCAAAACTACTGAAGTAAACATTACTTAAATATATCCAACTTCACTTTTGGTTACAGGCAGGTGTTGGCGTTTCTGATTGGAAGGATCTGGTTTCTGAAGCCACAGGTGAAGTCTTAAAAATGAGCAAATCACCGGTCGCTCTCCTTTTTCAAGCCTTACTGCAGTTCTCCGTGAAGATGGGTGCCAG[G/T]TAGAAGACTTTAAAAATAGAGCTCTTTTGTGTTTGTGTTGTATTAATTGTTACCATGGTATTCGAATCAACATGTCAGATCAGTTTGACCTGTTCTGTACCATGTGTTTGCATTACATTGTTTGCTTTAGCTTGGCATTGCATTGTTAATTAACTATATTTAACCCTTATGTACTGTTCAAATTGACTACCCTTTCATATTGGTGGCACTTATCGCCCCATTTACATTCATTATAACAATATTTTTGGATTGCAAAGCCTTGACACCAAAAAATCATGCAGTCTTGTTTGTTGGTGTTTTTCCTGTTGGAAATTTTTACTGTTGATCATCAGTTTTCATCATTAACCCTTTAGTTAGGTCTTTGCAGATAAGTTTCTGAATTTTATATGGAGTTCTATGGAGTAAAACAACAAAACATAGTGTGTGCATGAATACACTTGCGTGTACTATGTTTTGAGAGCTGTGCTGCTTATTTTTGATTTTTTCAACCATATCAAGAT
Associated Phenotype:
Not determined