Busch Lab

ZMP

TANC2 (2 of 2)

Ensembl ID:
ENSDARG00000079004
Description:
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2 [Source:HGNC Symbol;Acc:30212]
Human Orthologue:
TANC2
Human Description:
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2 [Source:HGNC Symbol;Acc:30212]
Mouse Orthologue:
Tanc2
Mouse Description:
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2 Gene [Source:MGI Symbol;Acc:MG

Alleles

There are 11 alleles of this gene:

Allele Name Consequence Status Availability
sa38868 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa35185 Nonsense Mutation detected in F1 DNA Not yet available
sa14210 Essential Splice Site Available for shipment Available now
sa38867 Nonsense Mutation detected in F1 DNA Not yet available
sa35184 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa45445 Nonsense Mutation detected in F1 DNA Not yet available
sa6228 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa45444 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa38868
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109164 Essential Splice Site 218 1720 5 28
Genomic Location (Zv9):
Chromosome 12 (position 3944407)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 3238833
GRCz11 12 3350473
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTGTGTGTTTAAATGTGTGTGTAATGTGTATTTTTCATGCTGTTTTC[A/G]GTGCGCTTGGCTCCGTATCGACTGCAGGACATCGCTCTGAAGCCGCTGCT
Long Flanking Sequence:
AGAAGATAATATAATATAATATAATATAATACCTGTTTTATAGTGATCTGATCAGCTGTAGTTTGAAATTACGCTGGGTTATTCCTCCTCCAGACGGTCTCTGTCGCCATCTTGTGGCGGAACGTCAACCATCTTTGCTCTGCTCAGTATGACTTATTTCTAATGACTCTTTATTTAACAATGTGTTTATTACAAACATACATTTAATTTTTAAACAATTATGTAATTAATTATTTGTCGTTTAACGTATTTACATTTCGTTTTAATATCATATTATTATTTTTTAATTCATGTAATTAACAAATAATATTTTAATTGACTAATTCATTGCTATTTTTTCTGTAACCATATGCTTAGCAAACAGAAAACGTGTCCGAAGTGCCTGAATATTTGTCATGTTGTGAGAGGTTTCTGTCTGTTGATTGTTTTTAATGTATTGTGGGTTGCATGTGTGTGTGTGTTTAAATGTGTGTGTAATGTGTATTTTTCATGCTGTTTTC[A/G]GTGCGCTTGGCTCCGTATCGACTGCAGGACATCGCTCTGAAGCCGCTGCTGTTCGAGGTGCCGAGCATCACCATGGACTCTGTGTTCACGGGCCGCGATTGGCTCTTTCAGGAGATCGACGCTTGTCTGCGCTCCACACACTCGGGCTCCAGCGCCGGCGTGGTTTTGGTGGGAAACATCGGATTTGGGAAAACAGCCATAATCTCACGGCTGGTGGCTCTGAGCTGCCATGGGAATCGCATGAGACAGATCGCCTCCGACAGCCCACAGGCATCGCCAAAACGTGAGATTCACAAGTCCCCTGTCAGACCGAGTGGCACATTCATTCATTCAAATTCATTCATTCATTCATTCATTCATTCAACTTTTATAAAGGTCCCTTGAAGTAAATGGAAGACAAAAATTAAAAATAAATAAATGTGTATATTAAAATATATACAGTTGAAGGGAAATTTATTAGCCCTGCTGTGAAATTTTTATTATTATGATGTATGATATAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35185
Status:
Mutation detected in F1 DNA
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
ENSDART00000109164 Nonsense 224 1720 5 28
Genomic Location (Zv9):
Chromosome 12 (position 3944388)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 3238814
GRCz11 12 3350454
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTGTAATGTGTATTTTTCATGCTGTTTTCAGTGCGCTTGGCTCCGTAT[C/T]GACTGCAGGACATCGCTCTGAAGCCGCTGCTGTTCGAGGTGCCGAGCATC
Long Flanking Sequence:
TATAATATAATACCTGTTTTATAGTGATCTGATCAGCTGTAGTTTGAAATTACGCTGGGTTATTCCTCCTCCAGACGGTCTCTGTCGCCATCTTGTGGCGGAACGTCAACCATCTTTGCTCTGCTCAGTATGACTTATTTCTAATGACTCTTTATTTAACAATGTGTTTATTACAAACATACATTTAATTTTTAAACAATTATGTAATTAATTATTTGTCGTTTAACGTATTTACATTTCGTTTTAATATCATATTATTATTTTTTAATTCATGTAATTAACAAATAATATTTTAATTGACTAATTCATTGCTATTTTTTCTGTAACCATATGCTTAGCAAACAGAAAACGTGTCCGAAGTGCCTGAATATTTGTCATGTTGTGAGAGGTTTCTGTCTGTTGATTGTTTTTAATGTATTGTGGGTTGCATGTGTGTGTGTGTTTAAATGTGTGTGTAATGTGTATTTTTCATGCTGTTTTCAGTGCGCTTGGCTCCGTAT[C/T]GACTGCAGGACATCGCTCTGAAGCCGCTGCTGTTCGAGGTGCCGAGCATCACCATGGACTCTGTGTTCACGGGCCGCGATTGGCTCTTTCAGGAGATCGACGCTTGTCTGCGCTCCACACACTCGGGCTCCAGCGCCGGCGTGGTTTTGGTGGGAAACATCGGATTTGGGAAAACAGCCATAATCTCACGGCTGGTGGCTCTGAGCTGCCATGGGAATCGCATGAGACAGATCGCCTCCGACAGCCCACAGGCATCGCCAAAACGTGAGATTCACAAGTCCCCTGTCAGACCGAGTGGCACATTCATTCATTCAAATTCATTCATTCATTCATTCATTCATTCAACTTTTATAAAGGTCCCTTGAAGTAAATGGAAGACAAAAATTAAAAATAAATAAATGTGTATATTAAAATATATACAGTTGAAGGGAAATTTATTAGCCCTGCTGTGAAATTTTTATTATTATGATGTATGATATATAGAATTATTGTTTGTGTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14210
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109164 Essential Splice Site 312 1720 5 28
Genomic Location (Zv9):
Chromosome 12 (position 3944122)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 3238548
GRCz11 12 3350188
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATCGCATGAGACAGATCGCCTCCGACAGCCCACAGGCATCGCCAAAACG[T/A]GAGATTCACAAGTCCCCTGTCAGACCRAGTGGCACATTNNNCATTCATTCANN
Long Flanking Sequence:
AATTCATGTAATTAACAAATAATATTTTAATTGACTAATTCATTGCTATTTTTTCTGTAACCATATGCTTAGCAAACAGAAAACGTGTCCGAAGTGCCTGAATATTTGTCATGTTGTGAGAGGTTTCTGTCTGTTGATTGTTTTTAATGTATTGTGGGTTGCATGTGTGTGTGTGTTTAAATGTGTGTGTAATGTGTATTTTTCATGCTGTTTTCAGTGCGCTTGGCTCCGTATCGACTGCAGGACATCGCTCTGAAGCCGCTGCTGTTCGAGGTGCCGAGCATCACCATGGACTCTGTGTTCACGGGCCGCGATTGGCTCTTTCAGGAGATCGACGCTTGTCTGCGCTCCACACACTCGGGCTCCAGCGCCGGCGTGGTTTTGGTGGGAAACATCGGATTTGGGAAAACAGCCATAATCTCACGGCTGGTGGCTCTGAGCTGCCATGGGAATCGCATGAGACAGATCGCCTCCGACAGCCCACAGGCATCGCCAAAACG[T/A]GAGATTCACAAGTCCCCTGTCAGACCGAGTGGCACATTCATTCATTCAAATTCATTCATTCATTCATTCATTCATTCAACTTTTATAAAGGTCCCTTGAAGTAAATGGAAGACAAAAATTAAAAATAAATAAATGTGTATATTAAAATATATACAGTTGAAGGGAAATTTATTAGCCCTGCTGTGAAATTTTTATTATTATGATGTATGATATATAGAATTATTGTTTGTGTGTGTGTGTAGATGGAGATGGCATCCCTCTCTCACAGCCTCAGCCTTCCCATGGTACACTGGGTGGAGGAAGCTGTCCGGGAACTCCAGAGATGAGGAGGAGGCAGGAGGAGGCCATGAGGAGACTCGCCGCTCAGGTACAAACAAACACACACAACACGCGCACACATGCACACACGCACATAATCCTGCTGTTTACACATGATTGGACGCTTTAGAATAAAACAAAACAACCAATTAAATTGAATTAAATATTATTTTAAACACAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38867
Status:
Mutation detected in F1 DNA
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
ENSDART00000109164 Nonsense 500 1720 9 28
Genomic Location (Zv9):
Chromosome 12 (position 3927207)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 3221633
GRCz11 12 3333273
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTTCTTTTCAGGAAATCACCAAACCTCTGCCGTTCCACCAAATCTCTT[T/A]GGACGCTCTGGAGGAAAACGACGCCATCGATCACGACCTGCAAGGCTACA
Long Flanking Sequence:
CGGATTCCATGATCTATGCTAAGCTAAGCTAAATGTGCTCCTGCAAAACCCGAAGAATGTCTGAATGGATTGAAAAACTTTAGGGGACCTATTTCCAAAAAAAAGTGCAGTGTTCCTTTAAACCTCTGGTTGTTTTCAGTCATTTTAGACCAAAAATGGATGTTAATTACTATATAAGTATTAATAATTACCACAAAACCTTCTGAAAATTAAAAAATAATATAGAAAAAATGTAATTAAACAAAAATAAATGTAATTGATTTAGCTTAAGACAAAACAGAAAGTTCTTTACAGGAATTCGTCCCTTTTTGACCAACTAAGACCACCAGTGTGATTCCCAAATAAGGGACACCAGAGGGATAAAAACATTCCACGCATATGCTCAATTGTGCAAAATCTTATTCTAAACACACCAATGAGCCTGCCTTGTTGACGTTTCTTATCTCTCACCTCTTCTTTTCAGGAAATCACCAAACCTCTGCCGTTCCACCAAATCTCTT[T/A]GGACGCTCTGGAGGAAAACGACGCCATCGATCACGACCTGCAAGGCTACATCCTCCACCGCATCCATAGCAGTGCTGAGATCCAGAACAACATCTCGCTGAATGGCAAGATGGACAACAGCAGCTTCGGCAAGCTCAGCTCCCACCTCAAGGCCCTCAGTCAGGGCTCCTTCCTCTACCTGAAGCTCACCTTCGACCTGATTGAGCGCGGATACCTGGTGCTCAAGAGCTCCAACTACAAGGTGGTCCCGGTCAGTTTGGCGGAGGTCTACCTGCTGCAGTGTAACATGAGGTTCCCCACGCAGTCGTCTTTCGAGAGGGCTCTGCCACTGCTTAATGTGGGCCTGGCTTCATTGCACCCGCTCACCGACGAACAGATCTACCAGGCCATCAATGGTGGCTCCGTCAAGGGGACTCTGGACTGGGACGACTTCCAGCAGAGGATGGAGAACCTGTCTGTGTTCTTGGTGAAGAGGCGGGACGGCACGCGCATGTTCGTTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35184
Status:
Mutation detected in F1 DNA
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
ENSDART00000109164 Essential Splice Site 846 1720 13 28
Genomic Location (Zv9):
Chromosome 12 (position 3922470)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 3216896
GRCz11 12 3328536
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGCCGGACACCTCAGCATCGTCACCTCACTCTGCAAGAGGAAAGCAAAG[G/A]TACACCCGTCTCTGAACTGTAGAGTGGATAATATTTGACTAGAAATTTTT
Long Flanking Sequence:
ATCACCCAACCTGCTTTAAGCTGGTATCAAACCGGCAACCTTCCGCATGGGACTTGGGTGCTCTACCAAGGAGGCTAAAGACTATGGCCTTTAGCGTCTGTTGCTAGAGCACCTTTACAGGTCAGAGGTGTGAGGTTTACCTGCACAGCACTTACTAGCTGGCCTCCGATACATAAAATGATCCATTTGGGCCAGCAACCAGCATTCTTCAAAACATCTTCATTTTTGGGTGAACTGTCCCTTTAAATTGTAATTGTGTTCAGGTGTCCCGGCTGCTGATCCTGGGTGGTGCGAATGTGAACTACCGTACGGAGGTGCTGAACAACGCTCCAGTGCTGTGTGTTCATGCTCATCTGGGCTACGCAGACATGGTGAATCTGCTGCTGGAGAATGGAGCCGGTGTGGATTCGCCGTCTGAGAGTGGACTCACTCCACTGGGCTACGCGGCCGCCGCCGGACACCTCAGCATCGTCACCTCACTCTGCAAGAGGAAAGCAAAG[G/A]TACACCCGTCTCTGAACTGTAGAGTGGATAATATTTGACTAGAAATTTTTCAAGATACTAGTATTTGGCTTAAAGTTACTTTAACTAGGTTAATTAGGCTAAAGTTAGAGTCATTGTATAACAGTGGTTTATTTTGTAGACAATCCAAAACAAATTGCTTAAGGGGGCTAATAATATTGAGCTTAAAATGGATTTTAAAAGATTAAAAACTTTTATTCAAGCCAAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAATTATTATTAGACATTAGTGATGGAAGTTCGGATCATTTTACTGACTCGGATCTTTAAGGTCTTGTACATCGAGATGAACGAATCTTTTTTCGAGTCATTTCGTTCATTTGGTTCAATTTGCCAAAATATGATTCAAATGTTATGAATTGCTTCCAAACACATCTACAACTAGCCCAAAAGGTTGATCACACGACAAATAAGTCATAAACTGAATACTATAGGAAGGAGAAAATAATAATTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45445
Status:
Mutation detected in F1 DNA
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
ENSDART00000109164 Nonsense 928 1720 16 28
Genomic Location (Zv9):
Chromosome 12 (position 3918969)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 3213395
GRCz11 12 3325035
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTATCTCTTGGACTTGCCTGAGAGGGATGAAGAGGACATTCAACGCGCA[C/T]AGATTAACAGCTGTGACACCCTGTGGGGTGAAACAGGTAAATGAGATTTT
Long Flanking Sequence:
CCATCCCCCACCCCACCAGATGCCACGCCCTCGCCCACACAGGCCACGCCCACAGAATCTCCACCCTCAGGCCCAGAACAGCAGGAGGATCCAGCAGAGACGCCTCAAGAAGAAGAGCAGAATCGGGAAGAGTCTCCAAAAGAAGAGGTTGAAAAACAGACGCAGGAGGACACACAGGCTGAGCGCTCCTCGTCTCCATCATCTGTGAGCTTTAATAAGAGCATCGCCATCCAGCAGGCCCTTATAGCTGCCGCCAGCATGGGTTACACTGAGGTAAAGTACTCTGGGTGTTGTGTGTATACATATTTGCATCGCTTTGACCGTTTGTCTGTAGGTATGAAAACAGGAAAGCAAGACCAAATCTAGAAATCCTAGTTTGGATGTGTTTTGCGAGACCAAACGGACACTCTTACTAATTGAGCGTGTGTGTGTGTGTCTTTAAGATTGTGTCTTATCTCTTGGACTTGCCTGAGAGGGATGAAGAGGACATTCAACGCGCA[C/T]AGATTAACAGCTGTGACACCCTGTGGGGTGAAACAGGTAAATGAGATTTTTTTTCATGCTATGAATGTGTCTCAAGTGACTGATTTACAACACTTTAAATATACTGGTTTGCGGTGACACCGTGCCTCAGTGGTTAGCACTGTGGCCTCACAGCAAGAAGGTCACTGGTTCGAGTTCCGGCTGGATCAGTTGTCATTTGTGTGTGAAGTTTGCCCTTGTAGCCCACCTCGTGTTGGTGTGGGTTTCCTCCAGGTGCCCTGGTTTGCCCCACAGTCCAAAGATATATGGTACAGATGAATTAGGTAAACAAAATTTGCCTTAGTGTGCGAGTGTGTGTGAATGCGAGTGTATGGGGCATCCACTGTGTAAAAGTTACATGAATGGGACTAAGCTGAAGGAAAATGAATGTATGAATGTATTTTTTGCTCTTAATTTGCATATTTTTGCACTTTTGCATCATAAATATGAGTATTGTAAGTACTGTAAGTTCACACAGAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6228
Status:
Mutation detected in F1 DNA
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
ENSDART00000109164 Essential Splice Site 939 1720 16 28
Genomic Location (Zv9):
Chromosome 12 (position 3918932)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 3213358
GRCz11 12 3324998
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATTCAACGCGCACAGATTAACWGCTGTGACACCCTGTGGGGTGAAACAG[G/A]TAAATGAGMTTWTTTTTCATGCTATRAATKTGTCTCAAGTGACTGATTTA
Long Flanking Sequence:
CACAGGCCACGCCCACAGAATCTCCACCCTCAGGCCCAGAACAGCAGGAGGATCCAGCAGAGACGCCTCAAGAAGAAGAGCAGAATCGGGAAGAGTCTCCAAAAGAAGAGGTTGAAAAACAGACGCAGGAGGACACACAGGCTGAGCGCTCCTCGTCTCCATCATCTGTGAGCTTTAATAAGAGCATCGCCATCCAGCAGGCCCTTATAGCTGCCGCCAGCATGGGTTACACTGAGGTAAAGTACTCTGGGTGTTGTGTGTATACATATTTGCATCGCTTTGACCGTTTGTCTGTAGGTATGAAAACAGGAAAGCAAGACCAAATCTAGAAATCCTAGTTTGGATGTGTTTTGCGAGACCAAACGGACACTCTTACTAATTGAGCGTGTGTGTGTGTGTCTTTAAGATTGTGTCTTATCTCTTGGACTTGCCTGAGAGGGATGAAGAGGACATTCAACGCGCACAGATTAACAGCTGTGACACCCTGTGGGGTGAAACAG[G/A]TAAATGAGATTTTTTTTCATGCTATGAATGTGTCTCAAGTGACTGATTTACAACACTTTAAATATACTGGTTTGCGGTGACACCGTGCCTCAGTGGTTAGCACTGTGGCCTCACAGCAAGAAGGTCACTGGTTCGAGTTCCGGCTGGATCAGTTGTCATTTGTGTGTGAAGTTTGCCCTTGTAGCCCACCTCGTGTTGGTGTGGGTTTCCTCCAGGTGCCCTGGTTTGCCCCACAGTCCAAAGATATATGGTACAGATGAATTAGGTAAACAAAATTTGCCTTAGTGTGCGAGTGTGTGTGAATGCGAGTGTATGGGGCATCCACTGTGTAAAAGTTACATGAATGGGACTAAGCTGAAGGAAAATGAATGTATGAATGTATTTTTTGCTCTTAATTTGCATATTTTTGCACTTTTGCATCATAAATATGAGTATTGTAAGTACTGTAAGTTCACACAGAAAAACTACCTAAACTGTTTCACATATGGTCTCAGTAATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45444
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109164 Essential Splice Site 1337 1720 24 28
Genomic Location (Zv9):
Chromosome 12 (position 3910234)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 3204660
GRCz11 12 3316300
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAACCTGTCCAAGACTTGTTTGAGGATGATGACTTCCTGGAACAAGAG[C/T]TAGAGGCTGTGTCTATTGGTCTTGCTTCTGATATTCGCTCAAACACTTCG
Long Flanking Sequence:
TCCAATAAGTTTTTATTGAACATACTTTCTTGGTTGCAGGACTTTGGAATGGCAGAGGAGTTTGCTACCAAGGCTCTGGAACTCAAGCCTAAGTCCTATGAGGCGTTTTACGCTAGAGCCCGTGCCAAACGGAGCAGCAGGTAGGTACCTCTTATTACTTTTCTTCATTCCACTTCAAGTTACTTAAGGGTGGTTTAATAATTCCATTGCCAACCCATAGGCAATTCGCTGAAGCACTAGATGACCTGAGGGAAGCCATAAAACTATGTCCCAACAATCGGGAAATCCAGCGCCTCCTCCAGCGTGTGGAAGAAGAGTACAGACAAGTGACCCAATCAGAAGAGCTAGAGCTTGAGCCACCTCCATCTCCACCACCATCTCCTTTACCAGTGGAAGAAGACGAGGAGCCCCCTCGTCACACTCCTCCTCCTGAACCAAGACTTGATGACATGGAACCTGTCCAAGACTTGTTTGAGGATGATGACTTCCTGGAACAAGAG[C/T]TAGAGGCTGTGTCTATTGGTCTTGCTTCTGATATTCGCTCAAACACTTCGAGTCTTGCCATCATTCGTAGTCCACCCCTTTCTCCTGCCCATCATGACACTGGCTACCTATCTGGGGGGCAGGCCTTTGAGTTCCACCCAAGCTCCTCTTCTATGTCATCTCCTACTCATCATAGTTACCAGTCAACTTCCCCTTGTATTTCCCCAACACATCAGAACTCCCACTATCGCCAGAGTCCACCCCACACCTCACCTGCCCACCAGTCCTCCTACCGTTTCAGCCCGCCACCCATGGGTGGTGGAGGGAACCAAGGGATGGACTATCAGAGTCCTCCACCGTCTCCTCTTCGACGTGGGGTTCCATTCCGAGCCAGCCCTCCAGTTGAGAGTGTGTGTATATATCGTTCCCAGTCTGGCTCTCCAGTCCGCTACCAGCAGGAGCCTTTACCTAGCCGTCCCAAATCTCCACTTTTGAAGATGAGCAGTCAGCGATCCTTCCAG
Associated Phenotype:
Not determined