Busch Lab

ZMP

si:ch211-287b5.1

Ensembl ID:
ENSDARG00000002880
ZFIN ID:
ZDB-GENE-060503-41
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q1LUH6]
Human Orthologue:
CCDC132
Human Description:
coiled-coil domain containing 132 [Source:HGNC Symbol;Acc:25956]
Mouse Orthologue:
Ccdc132
Mouse Description:
coiled-coil domain containing 132 Gene [Source:MGI Symbol;Acc:MGI:1920538]

Alleles

There are 8 alleles of this gene:

Allele Name Consequence Status Availability
sa10581 Nonsense Available for shipment Available now
sa32255 Essential Splice Site Available for shipment Available now
sa23579 Nonsense Available for shipment Available now
sa43334 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa29252 Nonsense Mutation detected in F1 DNA Not yet available
sa3030 Nonsense F2 line generated Not yet available

Mutation Details

Allele Name:
sa10581
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017917 Nonsense 43 314 3 12
ENSDART00000110699 Nonsense 43 965 3 28
Genomic Location (Zv9):
Chromosome 19 (position 41356264)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 40808802
GRCz11 19 40395922
KASP Assay ID:
2261-3613.1 (used for ordering genotyping assays)
KASP Sequence:
TCTCATTTYTTTTGCTTTTCACACAGGAGGAGCTGAGGGAGCTGAGAGAG[C/T]AGCCCAMSGATCCACAGGCAGAAMAAGAAATCATTGACAGCATAGAGGAA
Long Flanking Sequence:
GCAAAACTCAACTGTGTAAAACTCGAATTACTCTATATCCCAAAAAAGTGGAGTTTTCTTTTAAACCTTGCCTCTGCATTCGCTCTGGGAAGCCAGTGTGACTCAGTAAGTTTATCTCAGTTTGGGTCGCACCATTGTTTTAACCACATTGCATCACGGCATGTGAATCAAGCGTAATGAGCCTCTCAGCAATTTTCTTCAAAGAAAAGAGGACGACTTTGTTTCTTCAAGCTGTTTTGAGTGAAATTGATGTTCTTGTGCTGATCCTCATTAAGGTTCATGAAGGGTGTTCCTCAGGGACGGGTGCTAAGACCACTTAATCTTTGCACTTGGCTTGGCTGTAAGCCAGACTTGAAAATTAATCAATGCTCAGACCCCGTGCTTAGGTGCGAGGCAAGCTTCCCAATGATAGCGTCCCAGAAGCACAGAGATTTCCCTGCCAATACTCATTCTCATTTCTTTTGCTTTTCACACAGGAGGAGCTGAGGGAGCTGAGAGAG[C/T]AGCCCACGGATCCACAGGCAGAACAAGAAATCATTGACAGCATAGAGGAAGTCTACTACTCCAGCGACTCGTTTGACATGGTTCAATATGAACTTGAGGTGTGTGTATGAGAGAATACATATTGCTTGTTGTTGTTTGTTTAACCCTCCTGCACATCTCAAGTCTAACAGTGGGGTTTAGGTCAACTAGGGGTCAATTCTTGTAAAATAAATGGAGCTCTTTCCAAATTTGAGCTCAGTAAGTCTTGTCATCGCCAACCAGGGTGTCCGTGGGGTCCTAAAAAAGTATTAAAAGTTGATAAGTCATTCATTGATTCATTCATTTTCTGCGTAGTCCCTTTATTAATCCGGGGTCGCCACAGCGGAATGAACCGCCAACTTATCCAGCACATGTTTTACGCATAGGATGCCTTTCCAGCTGCAACCCCTCTACGAAACATCCATTCACACTCATACACTACGGACAATTTAGCTTATTCAATTTACCTGTACCGCATGTCT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa29251
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017917 None None 314 None 12
ENSDART00000110699 Essential Splice Site 455 965 17 28
Genomic Location (Zv9):
Chromosome 19 (position 41508844)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 40961199
GRCz11 19 40548319
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGGGTCTCCAGCTCACAAAAGCCAACCTCTTGTCATTTCTCCCCTACA[G/T]AACTCGCCTGGAGGAGCTGCGAATGTTTCTTGAAAATGAAACGTGGGAAT
Long Flanking Sequence:
CGCCGTGTCGCCATTAACACATTTTGCCATTACAATACACATTGTGCCCTCTGGCTTAGAGGACAAAACGATCCACTTTCCCTTCAAGTGCTTTGAAAATGATGCATTTAAAATATCATGCATTGAAGTCATAACTACAGATGGTATTTCGAATGTCAAACGCCCTGCTGTTGGCTACACTTTATTCAAATTTAGAGAGCTTATAGCAACTTATAATCAGGTGGTATGTTCTATAGAGATTAGTTGAGGACTTCGTTTTGTTGCATTCATTGTGAATTATAATGCCGGTTTTTGACATTTTGCACAAGCCTTTTGGTATTGACCTTGTCTGGCAGCGGGCCACTTTGACACTCATTGTAGCAGGACGTACCTCTAACCTTCTTCACCCATCGACTTTTCCTTGGATCGTTTTTTTTGCCAGCCCATTTCATTTTCATTGAGTTGAATGGCAAAGGGTCTCCAGCTCACAAAAGCCAACCTCTTGTCATTTCTCCCCTACA[G/T]AACTCGCCTGGAGGAGCTGCGAATGTTTCTTGAAAATGAAACGTGGGAATTGTGCCCTGTGAAGTCCAACTTCAGTATCGCCCAGCTCCACGTAAGCCTTAATGTCATTGAGAGTTGTTTAAATTGATGAATTACAAATCAGATTACTGTAATTGAGTAGTTTTCCTCAGGAATTGTATTTTGCATTGATAAAGCCTTGTTTAGACTGCATGACTTTAAACATCGGCAGATCGCTGTGCCGTTCAAACTACATCACCGGATTTTGTCTTTAAATCACTGTTGTGTTCATACTACACAACACTTCGTAAATGATCTACAAGATGGGGTCACACTACATGATCCGACAACAACTCGTTCGCCAACAGCTCAGTCAAGCTACCAATCCACAGCCAATGAAATGTTGAGGGAGGAGCCGGCAGAAAAACTGAATACTATTGGCTGCTTGTGTGCTGATTACATCCCTGACAGCGTTTCAAACTTCTCTGAAAGCTTTCAAGGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32255
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
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017917 None None 314 None 12
ENSDART00000110699 Essential Splice Site 544 965 18 28
Genomic Location (Zv9):
Chromosome 19 (position 41512606)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 40964961
GRCz11 19 40552081
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATAGACAACAAAGAAGAGGAGACTGAGGACGTCCTGGCTTCTAATGGGG[T/C]ATATAGTAGTTTGAATGATGGTCATGTTATGTACAGTTTTATATACTGTT
Long Flanking Sequence:
TGATGCGCAGAGTGGTTGAACTATGAGAACTATGCTATTGTGCTTTCACCTTTGCATCTTAGTTCTTGTTTTTTATGACTAGTATATTCAGAATTTTCAATACAAATCTTAATGCATCTGTAATATTTATCAAATACTCCTTGAATGGTTAATAAACACAAACACGCAGTATCATTAAATCCAGTCTTTCACTGCTGATGGCGCAAACACAAATTAATACATCGTTAGCAAACAAACAACATACTCAAAAAACAAGTGCAGGTGGGTGTTTTCATGACCTGTCTTTTAGTTGTTTGATCTGCATGTTTCTCTTCTTTTTCAGGAGTTTAAGTTCATGGGTCAGTGTCGTTCTCCTTCAGTGTCTCCCAGCAGGCAGCCAGAATCCACAGATCTGCTGGAGCTTTCTCTGTTCGAGCAGTACCTGGAGGGTGGAAACCCCTTCGAGATGCAGATAGACAACAAAGAAGAGGAGACTGAGGACGTCCTGGCTTCTAATGGGG[T/C]ATATAGTAGTTTGAATGATGGTCATGTTATGTACAGTTTTATATACTGTTGAATATACAATTATTAGCCCTTACTGAATTATTAGTCCTCCTGTATAATTTCCCTCTAATTTTTGTTTAACGGAAAGATTTTTTTTTTCAATTTCTAAACATAATAGTTTTAATAACTCATTTCTAATAACTGATTTATTTCATCTTTGCCATGATGACAGTACATAGTATTTTACTAGATATTAAGAGTGATATTTAAAGGGTTACCTAGGTTAATTAGGTAAGTTAGAGTTGAGCTTAAAATGTTTTTTTTTTTTTTATCAAAAGCTGCTTTTATTCTAGCTGAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAAATATTATAGGAAATACTGTAAAAAATCCCTTGCCCTGTTAAACATCATTTCGGAAATATTTAAAAAAGAAACAATTCACAGGAGGGCTAATAATTATGTCTTTAACAGTAGATGGTGAAGGGTGAGTAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23579
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017917 None None 314 None 12
ENSDART00000110699 Nonsense 646 965 21 28
Genomic Location (Zv9):
Chromosome 19 (position 41525869)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 40978224
GRCz11 19 40565344
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCCCATCGCCTTTGATGTCATCCACTGTGTGTCTCAGCTCTTTGATTA[T/G]TACCTGTATGCCGTCTACACCTTCTTCGGCCGCAATGACATGGTATGCAT
Long Flanking Sequence:
ATTTTTAAAGTGACATTTAAAGACTTAATTAGGTTAACTAGGCAGGTTAGGGTAATTAGGCAAGTATTTATATAATGACAGACTATTGAAAAAAAAGAAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACATACACATATACACACATGATAAATGCACTTTATTAATGCACATTACATTACATTCCTTTGTTTTTCTTATTTGAACAATAAGACGTTTCCAAAATATGTATTTTAAAAATGACACAGAAGCTTTGTGGTTGTACTATATATTCCACCCTGTGTATTTACCCTTTTTGTGTATCTCACGTATCTTTTCCTGATTTGTTTTTCTTTGATAGGGAAATACATGCAGATGATGAACATCCTGAAGCCCATCGCCTTTGATGTCATCCACTGTGTGTCTCAGCTCTTTGATTA[T/G]TACCTGTATGCCGTCTACACCTTCTTCGGCCGCAATGACATGGTATGCATTTCAAAAAGCATTGCCTTTCTCCTCCCGGGTTCGTTGTTATTACTTAACATTATGAAATATTTATTATATGCAATTGGAATCTTGCTGTGCTGTTTTGTCTGGAAGGTACATGTTCATTAAGAAAAGCTTTCCCGTATACCCTCATAGTTTTTTTTTCCCCTCTAATGTTTGCAAGGCCTTTGGGCACTGTTCTATAATTATTTCAATTATCATGTGAGCGAGTGTTTAGGCTTTGAGTTTTCCTCAGGAGGCTGGACTTTGAACATCAAAGACAGGTGTAAATGGCTGTTTCTCTTGCGTTCTTGTGAATGAACTCAGAAGACCACAAGCTGTGAGAGTTGAGATACTGAGATCTTCGTGTGGGTCACATGGAAGTTTAAATAGAAAGTAATTGAAACATCACAACATTCATGCAGTGCATTATTATTTTATTTTTATTTTTCAATATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43334
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
ENSDART00000017917 None None 314 None 12
ENSDART00000110699 Essential Splice Site 687 965 22 28
Genomic Location (Zv9):
Chromosome 19 (position 41548586)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 41000941
GRCz11 19 40588061
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGATTGAGGACCACTCTCAGCCGAATCCAGGAGAGCCTAATAGACATG[G/A]TGAGTAAAACATGACTCGTTTAATGCACTCTTTCAGTTTTCCCCCTGTCT
Long Flanking Sequence:
TTCGAGTGTGGTCCTGATAAATCTTTGTTTGAAGGGGTTGTATAGTATACCCAATAGGTTTCTTCCCAGCTCTGCTGCCTGGCCCCTAATTATGGAGAAATAGTAGTAAGAATATAAATAGAAAATAAAAGAAATTATAACAAAATATTTAAAGACTTTTGATATAGAGTATCTGGCTGTAGATAAAAGTATGAAAAAAAATTCTCGAGGTTTCCTATAAGGGTTGGGTTTAGAACACACAATACATTTTGTCAACGACGAGTCCTCATCAACCACCAAAACAAGTATGTGTGTTTGTGCCATTTTTAGGATATGATCAGTAGCATGTATCCTTTCAAGTTTGGGTTTGTGAAGTGTGTGTATTCCCAGTGGTCAATAAAATCTCTTTCACACGCAGTGTGTTCTGCTCTCACCTACAGTATGAATCCTCTGGCCTGGGTTTGATCAGCAGCAGATTGAGGACCACTCTCAGCCGAATCCAGGAGAGCCTAATAGACATG[G/A]TGAGTAAAACATGACTCGTTTAATGCACTCTTTCAGTTTTCCCCCTGTCTCTCTTACTCCAATGGTTCATCTGTTGGTCTCTAATACATAACCATTATAAATCCAAGTGGAAATGCATTTATCCGAGTCCCTTATAGCCTCTCATTGGGCCTGTCATCTTTTGCCCCTTCCTACTTTCAGCCGCAGCATCCACAGGTGAGTTAATCACACTTCCATGGCCCTGCGCTCTTGTAATAAATGTCCTTTGGTTTCCATGGCTGCACCCATTACGGCTCTCTGGGCCAAAGGTTTGATACCCACAATGCACCATAAACCTCTATTTGCAGCACAAATGGCCAGTCATTATATGGGATCCTTTTCCCCCAGATGTCTGAGTGTCAAAGAGCACAACGAGGTACTTATTTGCAGTATTCAATCAGGCTTGAGAGTTGTAGTGTTCCGTCTGAGATTATGGGCTGTTTCTACCTGGTATTAACATTCAATTTCAGTGATTTGATTAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa29252
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017917 None None 314 None 12
ENSDART00000110699 Nonsense 776 965 25 28

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 19 (position 41613297)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 41065551
GRCz11 19 40652671
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGACATTTTCCGCTGCTGTTTTCTCTACAGACTGTATCAACGGCCAGC[G/T]AGCTCCGCAAGCCCATTTACTGGATCGTGGCAGCCAAAGCCATAGATTAT
Long Flanking Sequence:
CTGTCAGTTCGTCTTTCTGTTCGTCTGACTGTCTGTCAGGCTGTTCGTCCGTCCGTCCGTCTGTTTGTCTGTCTATCTGTCTGTCTGTCTGTCTAATGCAGCAGACTGAAAATGCAAGCTTGTGCAATGAGTTTTACATGGATGCTGTGTTCTAAAGTTCAAGCTTGGTGTACTCTGTTCTGTGAAATGAATTTACATATTGTTCTATTAGTCCCTTTTGGAAATCACTTTTGATAAACACACCTGTCATGTGATTCAATCTAAAAGAATTCCTGACCTCTGCATAAAGTAGTACATTTCAGGATTTACATTTCAATATGCAGTTTACATTTCAAGCACAAGCCACTTTCAGCATGACTTTCACAACTTGTTAGTTTTTGGATAATCGACAAATACTAAACTGCATTTATCACCCCTGATGTCTGGCGGTTATGTATAGGAGCTCTTAATTTTGACATTTTCCGCTGCTGTTTTCTCTACAGACTGTATCAACGGCCAGC[G/T]AGCTCCGCAAGCCCATTTACTGGATCGTGGCAGCCAAAGCCATAGATTATGAGCAGATGCTGCTGCTGATGGCTGGAGTGAAATGGGACATTAAAGAGATAATGTCACAGCACAACGTCTACGTGGATGTCCTTTTAAAGGTAATGTGTTTGTGTGCGCAGCGGTCTTTATGTGCAACGATAATGTGTTGTTCATTACACACTAGAGGAGAGAGCAGGTGGGAGAATATCAGTAGAGATTAGCCAACCTTTACTTCATCTATCCACCTTTTTCCTACAGCTCCGTGATTTTTGGCGTGAACTATGTTGGCGTGAACTTCTGTTAAGCTGTGAACAGTCAGTGAAGTGTTATTAAAAACTGGGGTGGTATTGTTCTGCTCACAGTTCATCAAAACAAATTTTACTATGCAATATTAAAGACATGTTAATGTGACTGTATTGTAAAGAATATACAGTGGGGGAAATACGTAGGGTTGGGTATCGTTTAGGGTTATTTCGATA
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa5651
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017917 None None 314 None 12
ENSDART00000110699 Nonsense 950 965 28 28
ENSDART00000017917 None None 314 None 12
ENSDART00000110699 Nonsense 950 965 28 28

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 19 (position 41645988)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 41098242
GRCz11 19 40685362
KASP Assay ID:
554-3435.1 (used for ordering genotyping assays)
KASP Sequence:
TGACTAACCTGGTCAACGTCTGCCTCGGGTCCCACATCAACAAGAAAGCA[C/T]GACAGAAACTCCTCGCAGCCATTGATGACATTGACCGGCCCAAAAGATAA
Long Flanking Sequence:
TAAAATAAAAAGGGATAATAATTAAAAATGGTGAATGCAATTTAAAAAAAATTTAAATAATAATTTAAAAATAATGCAAATGAAGGGTAGCTTATAATAATTCGTTTAAACAAAATCACATTTTATTCTTTTCTTAGAAGTGCCTTGTCAAACCTTTTTATGCTAATGTTCGGATCAAACATTCTTGCATATACTGTAAAAATCGAATCTCATATTCTAATGAAGCATTAGCATATTTTATAAATGACGCATCACTAAATGTTTGCCTTTTAAATGTCAAGACAAACGCTGGCTTGGCTCCAAATGTGCTTGTGATGTTGCTTAGTAAGGCATATCCTGCAAGACTGGCTTTAATTCTCCATTAAAGAGATGTATGGTTATGACTGTCATCTCCGCTCGATTTATCACCAGTTTGTTTTGTATTTACCCAGGAGTACTCGATGAAGCAGCTGACTAACCTGGTCAACGTCTGCCTCGGGTCCCACATCAACAAGAAAGCA[C/T]GACAGAAACTCCTCGCAGCCATTGATGACATTGACCGGCCCAAAAGATAAATCACTGTCATCAAAAATACACCACAAAAGTCACACACACCTACACTGTTACGCGTCCCGTATCTGTCTTGCGTGGTCTGCAGTTTGTTTGTCAACCATGAAAACGTTTACGGTTTCTGTTTGCGTTTTGTTAGGAATGTAAGCAGGACGTGCTGTGACTACATATGAAGCGGCTGTAAAAGATAATGGGTAATGAAAGTGTTATCAGCATCACTTGAATCACAACATGAGTGAATGTCTCAGGCGCTGTTAAACCCTAATTTAAGCAGAGCTGTGGATGAGCAGCTGAATTTTTCCTTGTTGAGGAATATATGAGGGTTTTGTAGCATGAGGCTTTTTAATATGGTATAAAGACGTCCTTTAAAGGGACAGTACACTCAAAAATGAAAATGTTGTCATTTAATCATCTTCCACTTATTCCAAACTTGTATGGGTCACTTTGTACTGTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa3030
Status:
F2 line generated
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
ENSDART00000017917 None None 314 None 12
ENSDART00000110699 Nonsense 950 965 28 28
ENSDART00000017917 None None 314 None 12
ENSDART00000110699 Nonsense 950 965 28 28

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 19 (position 41645988)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 41098242
GRCz11 19 40685362
KASP Assay ID:
554-3435.1 (used for ordering genotyping assays)
KASP Sequence:
TGACTAACCTGGTCAACGTCTGCCTCGGGTCCCACATCAACAAGAAAGCA[C/T]GACAGAAACTCCTCGCAGCCATTGATGACATTGACCGGCCCAAAAGATAA
Long Flanking Sequence:
TAAAATAAAAAGGGATAATAATTAAAAATGGTGAATGCAATTTAAAAAAAATTTAAATAATAATTTAAAAATAATGCAAATGAAGGGTAGCTTATAATAATTCGTTTAAACAAAATCACATTTTATTCTTTTCTTAGAAGTGCCTTGTCAAACCTTTTTATGCTAATGTTCGGATCAAACATTCTTGCATATACTGTAAAAATCGAATCTCATATTCTAATGAAGCATTAGCATATTTTATAAATGACGCATCACTAAATGTTTGCCTTTTAAATGTCAAGACAAACGCTGGCTTGGCTCCAAATGTGCTTGTGATGTTGCTTAGTAAGGCATATCCTGCAAGACTGGCTTTAATTCTCCATTAAAGAGATGTATGGTTATGACTGTCATCTCCGCTCGATTTATCACCAGTTTGTTTTGTATTTACCCAGGAGTACTCGATGAAGCAGCTGACTAACCTGGTCAACGTCTGCCTCGGGTCCCACATCAACAAGAAAGCA[C/T]GACAGAAACTCCTCGCAGCCATTGATGACATTGACCGGCCCAAAAGATAAATCACTGTCATCAAAAATACACCACAAAAGTCACACACACCTACACTGTTACGCGTCCCGTATCTGTCTTGCGTGGTCTGCAGTTTGTTTGTCAACCATGAAAACGTTTACGGTTTCTGTTTGCGTTTTGTTAGGAATGTAAGCAGGACGTGCTGTGACTACATATGAAGCGGCTGTAAAAGATAATGGGTAATGAAAGTGTTATCAGCATCACTTGAATCACAACATGAGTGAATGTCTCAGGCGCTGTTAAACCCTAATTTAAGCAGAGCTGTGGATGAGCAGCTGAATTTTTCCTTGTTGAGGAATATATGAGGGTTTTGTAGCATGAGGCTTTTTAATATGGTATAAAGACGTCCTTTAAAGGGACAGTACACTCAAAAATGAAAATGTTGTCATTTAATCATCTTCCACTTATTCCAAACTTGTATGGGTCACTTTGTACTGTTG
Associated Phenotype:
Not determined