ZMP
thbs3a
Ensembl ID:
ZFIN ID:
Description:
Thrombospondin-3a [Source:UniProtKB/Swiss-Prot;Acc:Q8JHW2]
Human Orthologue:
THBS3
Human Description:
thrombospondin 3 [Source:HGNC Symbol;Acc:11787]
Mouse Orthologue:
Thbs3
Mouse Description:
thrombospondin 3 Gene [Source:MGI Symbol;Acc:MGI:98739]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6444 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42799 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17435 | Nonsense | Available for shipment | Available now |
sa10527 | Essential Splice Site | Available for shipment | Available now |
sa22930 | Nonsense | Available for shipment | Available now |
sa9297 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10346 | Nonsense | Available for shipment | Available now |
sa17001 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa6444
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 |
---|---|---|---|---|---|
ENSDART00000057305 | Nonsense | 27 | 962 | 1 | 23 |
Genomic Location (Zv9):
Chromosome 16 (position 45771219)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 43029409 |
GRCz11 | 16 | 42933167 |
KASP Assay ID:
554-5071.1 (used for ordering genotyping assays)
KASP Sequence:
TCAGTCTGGTCGTGTTGATGTYCGTCTGGKCAGCACAGAGCGACAAGAAA[C/T]AAGACGTGCCAGGTAWTTTTTCTCTCTTTCTAAACTTCGAGTAATGAACT
Long Flanking Sequence:
TGATACCAACACGAATAGGCTAACTGTCCGTTCATTTAATGGGTTTTATGGTTCACTAAAATCAAACACGTTAATTTTTCGCTCTAAAGACGGCGTCTTTATCATCTACGTTTTTAGTTACTTTATTAGTTAAGTATACCCTAATTAACGTTCACAAACACGTTTAGTTATAATTTACAGCCCTGAACGCGTCTCGGGTAAACGGCCCCCTGCAATCCATCATGCTTGAGTGTTTTACAAGAGAATAAAGTGTTGTAGGATGGTGATGAGGGCGGATTCAGCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTGTGAGCGCAGGTTTGCTCTATTATATTCCGTCTTTCAATGCATCGCTGACGGATCTGTTCTGGATATTTTCTGCACCACTTTTGCGTGTATTTTTGTAAACATGAAACAAATGTTTGTACACATTTGGGTCAGTCTGGTCGTGTTGATGTCCGTCTGGTCAGCACAGAGCGACAAGAAA[C/T]AAGACGTGCCAGGTAATTTTTCTCTCTTTCTAAACTTCGAGTAATGAACTATCTTACGTACTTGAAATAGCTATATTTTGTCTTTGTAACTGTATATTTTTCATTATTGTCTCTGCTTAATTTGCATTCACTCAGTTTTTTAAATTTGTCTTCACTCGGTTTCGAGAACGTTTGAAGAACATTTGACCTTCCGTTTTATGAAAGCTACTATAGAAAAAAGTACATTTACACCGTTTCAATTTTCATATTGCAGTATAGGCTATATTGTTGTAAAAACGTATAACTTTCAAATTGGACTGTACTACTGAATGTAGTCTAATTGTCCAACAATTAAAATGAATGTGAGTTGGAGCTTTCAAAAAGAGTATAACAGTTTAATAAAAGTGACTCATTCATATGGGACTCTATTCAAAACTTTGAGTCATCATTGAGTCCATGAGCTATTTCATCTGAACAGTCTGAATGATTCATTCACAAAAATCGGTCTGATTCGGGCTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42799
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 |
---|---|---|---|---|---|
ENSDART00000057305 | Nonsense | 330 | 962 | 9 | 23 |
Genomic Location (Zv9):
Chromosome 16 (position 45758472)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 43016662 |
GRCz11 | 16 | 42920420 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGATCATTGTGTTTCACTTCATCAGTGTTCAGAGGCTCAGCCGTGTTA[T/A]ACACCGGGTGCTTGTGTCAATACTGCAAGAGGTTTTACCTGTGAGTCGTG
Long Flanking Sequence:
TTCGGCTAGAATAAAAGCAGTTTTAATTTTTTAAAAGCGTTTAAGGTGAATATTGTTAGCTTTCTTAAAGAAATATTTGTTTTCGACTGTCCACAGATCAAACCTTTGTTATACAATGACATGGAAAATTACCCTACCTTGCCTAATTAACCTTATTAACCTAGTTAAATGTCACTTTAAATGTTTTTTGAAAAATATCTAGACAAATATTATTTACTGTCATCATGGCAAAGAAAAAAGATTTCCGTTATTAGAAATAAGTTATTAAAACTATTATGTTTAGAAATGTGTTAAATAAAATGTTCTTTCCGTTAAACAGAAATTGGGGAAACATATACAAGGGGGGCTAATAATTCAGGGGTAGGCTAATAATTCTGACTTCAACTGTAAAGTGATTATGTTGTTTAAGTTGAATTTTTAATTATTTTGAGCGTATTTTGAGTTATTGAATGTGATCATTGTGTTTCACTTCATCAGTGTTCAGAGGCTCAGCCGTGTTA[T/A]ACACCGGGTGCTTGTGTCAATACTGCAAGAGGTTTTACCTGTGAGTCGTGTCCCCCTGGCATGTGGGGTCCACCTTTGTCTGGAGTCGGTGTGGAGTATGCTAAGAGTCACCGTCAGGTACAGGGCATTTGCATTATTGAAAATACTGTAAAAACTGTGATATTGTGGAATATTATCAGAGTTACTACAGCTTTCAGAGTCAAATTATCAATCAGAAATCACTCTATTATGCTGATATGGTCCAATGATGTTTATTTGGAATTTCTGTAACATTATATGGAACGTAAAAAGTAAAATTAGCAGGAAAAAATGTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTAATCAACCAAATGTTATGGAGGGACACTTCAATGTAAAAGTCTTCTATGGTTTTGTGTATAAGACTTCATATACACTGTGAAATATTAATGTGTAATGTGAATGGGACGCTGACAAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17435
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 |
---|---|---|---|---|---|
ENSDART00000057305 | Nonsense | 344 | 962 | 9 | 23 |
Genomic Location (Zv9):
Chromosome 16 (position 45758430)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 43016620 |
GRCz11 | 16 | 42920378 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCGTGTTATACACCGGGTGCTTGTGTCAATACTGCAAGAGGTTTTACCTG[T/A]GAGTCRTGTCCCCCTGGCATGTGGGGTCCRCCTTTGTCTGGAGTSGGWGT
Long Flanking Sequence:
AAGGTGAATATTGTTAGCTTTCTTAAAGAAATATTTGTTTTCGACTGTCCACAGATCAAACCTTTGTTATACAATGACATGGAAAATTACCCTACCTTGCCTAATTAACCTTATTAACCTAGTTAAATGTCACTTTAAATGTTTTTTGAAAAATATCTAGACAAATATTATTTACTGTCATCATGGCAAAGAAAAAAGATTTCCGTTATTAGAAATAAGTTATTAAAACTATTATGTTTAGAAATGTGTTAAATAAAATGTTCTTTCCGTTAAACAGAAATTGGGGAAACATATACAAGGGGGGCTAATAATTCAGGGGTAGGCTAATAATTCTGACTTCAACTGTAAAGTGATTATGTTGTTTAAGTTGAATTTTTAATTATTTTGAGCGTATTTTGAGTTATTGAATGTGATCATTGTGTTTCACTTCATCAGTGTTCAGAGGCTCAGCCGTGTTATACACCGGGTGCTTGTGTCAATACTGCAAGAGGTTTTACCTG[T/A]GAGTCGTGTCCCCCTGGCATGTGGGGTCCACCTTTGTCTGGAGTCGGTGTGGAGTATGCTAAGAGTCACCGTCAGGTACAGGGCATTTGCATTATTGAAAATACTGTAAAAACTGTGATATTGTGGAATATTATCAGAGTTACTACAGCTTTCAGAGTCAAATTATCAATCAGAAATCACTCTATTATGCTGATATGGTCCAATGATGTTTATTTGGAATTTCTGTAACATTATATGGAACGTAAAAAGTAAAATTAGCAGGAAAAAATGTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTAATCAACCAAATGTTATGGAGGGACACTTCAATGTAAAAGTCTTCTATGGTTTTGTGTATAAGACTTCATATACACTGTGAAATATTAATGTGTAATGTGAATGGGACGCTGACAAGGGAGGTCGGATCCAAACGCAGGATTTATGTAGCAGAATAGGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10527
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057305 | Essential Splice Site | 572 | 962 | 15 | 23 |
Genomic Location (Zv9):
Chromosome 16 (position 45750735)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 43008925 |
GRCz11 | 16 | 42912683 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACTGTTTTGTGTTTTYACAGCATCATCTTGAGTGGATGTGATGTTTTGC[A/T]GGGATTCAGAATGTTCTGGATAACTGTCCTAAAGTGCCGAACCCGATGCA
Long Flanking Sequence:
TGTTGTTTTAGTTTTTATTAATTTTCAGTTTACAATTTTGGGGCTTCAACTTATTTCTGATAGTTGGAAAGACATAATGTTTTAATCTCACAATTTTCTCACAATTTAAAGAAGTCAAAATTGCTTGAGATCAGATATCAGAAAACAAACTAATATAAATTTTCTTTTCATTGTTTTTTAATGTATTCATAAATGCTTCAGATCTTATTCTTATAAAATAACAAAGGAACACTGCATCAAACATGTCTGTGTTATTTCTTCAGGATAACTGTCGTTTGGTCTCCAATAAAGACCAGCAGAACTCGGACACAGATTCGTTCGGAGACGCGTGTGATAACTGTCCCACCGTTCCCAACATCGACCAGAAAGACACTGATAGCAACGGAGAGGGAGACGCTTGTGATGACGACATTGATGGAGATGGTAAAAAATGTTCAGCTCTATGGATTGGACTGTTTTGTGTTTTTACAGCATCATCTTGAGTGGATGTGATGTTTTGC[A/T]GGGATTCAGAATGTTCTGGATAACTGTCCTAAAGTGCCGAACCCGATGCAGACGGACCGAGACAGAGACGGAGTGGGAGATGCGTGTGACAGCTGTCCTGAGATCAGCAACCCCATGCAGGTACTGAAGCACAGCTTATATTAGTGCTGGGCAAAGATTAATTGCATCCAAAATAAACGTTTGTTTTGACAAACAATCGTTATACAATAAATTGCCTAATTACCCTATCCTGCCTAGTTAACCTGATTAACCGAGTTAAGCCTTTAAACGTCACGTATAAAAGTGTCTTGAAAAAATATCTAGTAAAATATTATTTACTGTCATCATGGCAAAGATCAAATAAATCGGTTATTAGAAATGAGTTATTAAAACTATTATGTTTAGAAATGTGTTATAAATCTTTTCTCCGTTAAACCTAAATTGGGGAGAAAAAATAAACAGGCGGGCTTATAATTTTACTATGTCTACTATGTTGTTGTAACGCCGGGGGAGTGACAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22930
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 |
---|---|---|---|---|---|
ENSDART00000057305 | Nonsense | 580 | 962 | 15 | 23 |
Genomic Location (Zv9):
Chromosome 16 (position 45750708)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 43008898 |
GRCz11 | 16 | 42912656 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTGAGTGGATGTGATGTTTTGCAGGGATTCAGAATGTTCTGGATAACTG[T/A]CCTAAAGTGCCGAACCCGATGCAGACGGACCGAGACAGAGACGGAGTGGG
Long Flanking Sequence:
GTTTACAATTTTGGGGCTTCAACTTATTTCTGATAGTTGGAAAGACATAATGTTTTAATCTCACAATTTTCTCACAATTTAAAGAAGTCAAAATTGCTTGAGATCAGATATCAGAAAACAAACTAATATAAATTTTCTTTTCATTGTTTTTTAATGTATTCATAAATGCTTCAGATCTTATTCTTATAAAATAACAAAGGAACACTGCATCAAACATGTCTGTGTTATTTCTTCAGGATAACTGTCGTTTGGTCTCCAATAAAGACCAGCAGAACTCGGACACAGATTCGTTCGGAGACGCGTGTGATAACTGTCCCACCGTTCCCAACATCGACCAGAAAGACACTGATAGCAACGGAGAGGGAGACGCTTGTGATGACGACATTGATGGAGATGGTAAAAAATGTTCAGCTCTATGGATTGGACTGTTTTGTGTTTTTACAGCATCATCTTGAGTGGATGTGATGTTTTGCAGGGATTCAGAATGTTCTGGATAACTG[T/A]CCTAAAGTGCCGAACCCGATGCAGACGGACCGAGACAGAGACGGAGTGGGAGATGCGTGTGACAGCTGTCCTGAGATCAGCAACCCCATGCAGGTACTGAAGCACAGCTTATATTAGTGCTGGGCAAAGATTAATTGCATCCAAAATAAACGTTTGTTTTGACAAACAATCGTTATACAATAAATTGCCTAATTACCCTATCCTGCCTAGTTAACCTGATTAACCGAGTTAAGCCTTTAAACGTCACGTATAAAAGTGTCTTGAAAAAATATCTAGTAAAATATTATTTACTGTCATCATGGCAAAGATCAAATAAATCGGTTATTAGAAATGAGTTATTAAAACTATTATGTTTAGAAATGTGTTATAAATCTTTTCTCCGTTAAACCTAAATTGGGGAGAAAAAATAAACAGGCGGGCTTATAATTTTACTATGTCTACTATGTTGTTGTAACGCCGGGGGAGTGACAGAGACAACTGGAGGTAAGATCCACAATGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9297
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057305 | Nonsense | 814 | 962 | 20 | 23 |
ENSDART00000057305 | Nonsense | 814 | 962 | 20 | 23 |
Genomic Location (Zv9):
Chromosome 16 (position 45744811)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 43003001 |
GRCz11 | 16 | 42906759 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCTTCATCTTCGGCTACCAGGATTCATCTAGTTTCTACGTGGTGATGTG[G/A]AAGCAGACCGAACAGACRTACTGGCAGTCCATCCCATTCAGAGCCATGGC
Long Flanking Sequence:
AAAATTAATATAATCTTGGATTCACTTCAAAAAAGTAACCAAATGTGTTACTTAGTTCCTTTTTAAATAAATTGTGTGTAATCAGTGTTGGAGAAAGTTACTTTTGAAAGTAATGCATTACAATATTGAGTTTGGAAGCACTCTAGGGTGAGTAAATAGTGAGTAAATTGTCAATTTGGGTGAACCATCCCTTTGAATGTGGTGTGTAATTGGCAATACTGTAGTGCTCATATTAACAGATGAATTTGGGTTTCAGGGAATGGAAATAGTTCAGACCATGAACAGTGACCCTGGACTGGCAGTGGGTGAGTCTGGATTCAGATTTGAGCTGCTGAACGCAGAGCATATGCTCAAAACATGATTCACCTCTCCGCAGGTTATACAGCGTTTAACGGCGTGGACTTTGAGGGAACATTTCACGTGAACACAGTGACCGACGATGACTATGCCGGCTTCATCTTCGGCTACCAGGATTCATCTAGTTTCTACGTGGTGATGTG[G/A]AAGCAGACCGAACAGACGTACTGGCAGTCCATCCCATTCAGAGCCATGGCTGAACCGGGCCTGCAGCTCAAGGTAAAAAAAAAAATACTGCTAAATTACATTCATTACAAACTTTCACTGAAATATATTGACTCGCTAATGATCATGTGACCTCTCTTGGAGTGGAATTTCAAGACGTTGTGTTTGTGTAGGCAGTGAAGTCTCGTACTGGTCCTGGTGAGTTTCTTCGTAACGCTCTGTGGCATGCTGGAGATACTGATGGAGAGGTGAAGCTGCTGTGGAAAGACCCACGAAACGTCGGCTGGCTGGATAAAACATCGTATCGGTGGCAGCTCAGCCATCGGCCTCAGGTCGGATACATCAGGTGAGACTTCCAGCGACAGATTAAACAATACTGTTTGGGGACAGATAGTTTTTAAATAATGAATACTTGATTTTTGCAAGGACACATCAACTGAATTAAACTGCTGTAAAAATGCATCAGAAAAAAAAACTATCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10346
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057305 | Nonsense | 814 | 962 | 20 | 23 |
ENSDART00000057305 | Nonsense | 814 | 962 | 20 | 23 |
Genomic Location (Zv9):
Chromosome 16 (position 45744811)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 43003001 |
GRCz11 | 16 | 42906759 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCTTCATCTTCGGCTACCAGGATTCATCTAGTTTCTACGTGGTGATGTG[G/A]AAGCAGACCGAACAGACRTACTGGCAGTCCATCCCATTCAGAGCCATGGC
Long Flanking Sequence:
AAAATTAATATAATCTTGGATTCACTTCAAAAAAGTAACCAAATGTGTTACTTAGTTCCTTTTTAAATAAATTGTGTGTAATCAGTGTTGGAGAAAGTTACTTTTGAAAGTAATGCATTACAATATTGAGTTTGGAAGCACTCTAGGGTGAGTAAATAGTGAGTAAATTGTCAATTTGGGTGAACCATCCCTTTGAATGTGGTGTGTAATTGGCAATACTGTAGTGCTCATATTAACAGATGAATTTGGGTTTCAGGGAATGGAAATAGTTCAGACCATGAACAGTGACCCTGGACTGGCAGTGGGTGAGTCTGGATTCAGATTTGAGCTGCTGAACGCAGAGCATATGCTCAAAACATGATTCACCTCTCCGCAGGTTATACAGCGTTTAACGGCGTGGACTTTGAGGGAACATTTCACGTGAACACAGTGACCGACGATGACTATGCCGGCTTCATCTTCGGCTACCAGGATTCATCTAGTTTCTACGTGGTGATGTG[G/A]AAGCAGACCGAACAGACGTACTGGCAGTCCATCCCATTCAGAGCCATGGCTGAACCGGGCCTGCAGCTCAAGGTAAAAAAAAAAATACTGCTAAATTACATTCATTACAAACTTTCACTGAAATATATTGACTCGCTAATGATCATGTGACCTCTCTTGGAGTGGAATTTCAAGACGTTGTGTTTGTGTAGGCAGTGAAGTCTCGTACTGGTCCTGGTGAGTTTCTTCGTAACGCTCTGTGGCATGCTGGAGATACTGATGGAGAGGTGAAGCTGCTGTGGAAAGACCCACGAAACGTCGGCTGGCTGGATAAAACATCGTATCGGTGGCAGCTCAGCCATCGGCCTCAGGTCGGATACATCAGGTGAGACTTCCAGCGACAGATTAAACAATACTGTTTGGGGACAGATAGTTTTTAAATAATGAATACTTGATTTTTGCAAGGACACATCAACTGAATTAAACTGCTGTAAAAATGCATCAGAAAAAAAAACTATCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17001
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057305 | Nonsense | 872 | 962 | 21 | 23 |
Genomic Location (Zv9):
Chromosome 16 (position 45744520)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 43002710 |
GRCz11 | 16 | 42906468 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCATGCTGGAGATACTGATGGAGAGGTGAAGCTGCTGTGGAAAGACCCA[C/T]GAAACGTCGGCTGGCTGGATAAAACATCGTATCGGTGGCAGCTCAGCCAT
Long Flanking Sequence:
TGGACTGGCAGTGGGTGAGTCTGGATTCAGATTTGAGCTGCTGAACGCAGAGCATATGCTCAAAACATGATTCACCTCTCCGCAGGTTATACAGCGTTTAACGGCGTGGACTTTGAGGGAACATTTCACGTGAACACAGTGACCGACGATGACTATGCCGGCTTCATCTTCGGCTACCAGGATTCATCTAGTTTCTACGTGGTGATGTGGAAGCAGACCGAACAGACGTACTGGCAGTCCATCCCATTCAGAGCCATGGCTGAACCGGGCCTGCAGCTCAAGGTAAAAAAAAAAATACTGCTAAATTACATTCATTACAAACTTTCACTGAAATATATTGACTCGCTAATGATCATGTGACCTCTCTTGGAGTGGAATTTCAAGACGTTGTGTTTGTGTAGGCAGTGAAGTCTCGTACTGGTCCTGGTGAGTTTCTTCGTAACGCTCTGTGGCATGCTGGAGATACTGATGGAGAGGTGAAGCTGCTGTGGAAAGACCCA[C/T]GAAACGTCGGCTGGCTGGATAAAACATCGTATCGGTGGCAGCTCAGCCATCGGCCTCAGGTCGGATACATCAGGTGAGACTTCCAGCGACAGATTAAACAATACTGTTTGGGGACAGATAGTTTTTAAATAATGAATACTTGATTTTTGCAAGGACACATCAACTGAATTAAACTGCTGTAAAAATGCATCAGAAAAAAAAACTATCACTTTGATCACCTGATCAAAACTACTAAATATTTTTATTAATTACAGGATTTTAAATATTTAATTGTCAAATTCAAGTAACTGTGGACTGGATTTGTTTACCTTTTATCACAGTTTTGGATATGTGATAAAAGATTAGTAACAACATTGGCTTTGATGCAATTTTATTTTTTGTGCAGCATAAGAGTTTCAGTTTTTTCTCCCTAAGTGACTGTTTTTGCCCCATTGTTTTTTTTTATTATAACCACGTTTTTTTTAATTGCAAAGCCATGATATCTTATAATGATGCATTAT
Associated Phenotype:
Not determined