Busch Lab

ZMP

si:ch211-120k19.2

Ensembl ID:
ENSDARG00000073732
ZFIN ID:
ZDB-GENE-100921-1
Human Orthologue:
MYH14
Human Description:
myosin, heavy chain 14, non-muscle [Source:HGNC Symbol;Acc:23212]
Mouse Orthologue:
Myh14
Mouse Description:
myosin, heavy polypeptide 14 Gene [Source:MGI Symbol;Acc:MGI:1919210]

Alleles

There are 8 alleles of this gene:

Allele Name Consequence Status Availability
sa15579 Essential Splice Site Available for shipment Available now
sa17178 Nonsense Available for shipment Available now
sa16888 Nonsense Available for shipment Available now
sa45571 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa36084 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa36085 Nonsense Mutation detected in F1 DNA Not yet available
sa44846 Nonsense Mutation detected in F1 DNA Not yet available
sa22798 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa15579
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000047409 Essential Splice Site 175 2020 4 42
ENSDART00000142155 Essential Splice Site 175 2007 5 41
Genomic Location (Zv9):
Chromosome 16 (position 18938522)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 16968845
GRCz11 16 16876822
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGTTCATGTNATKCTAATGTCCTTCCTCTTTCTGTTTTTTTTTTYACTC[A/T]GACCGAGAAGATCAGTCTATCCTCTGCACGTGAGTTTCCACTGCCTRYGC
Long Flanking Sequence:
TAAAAGAATGGTGATTTGTCAGCACTTCACTGAAAAAAGTGAAACTACTGTGTCTTTCATTCAAATGACATTTTTATTTTAAAAAATGTTTTTTGATTTTAACCTATTTCATTCAACTTGCCCTAAAGAGAACAAATTTAAACAAACCCCCTAGGAAAAAGCAAACTGAAAAAGAAATAATTGATTGGATTTACTACCTTTTTTAAGGTAAGTGGTGGCAAACAATTTATATGGACTGGATTGAAACAAACAGATTAAATGTAGTAAAGTTTAACTTAAAGTGTTTGTCTTTGATTCAGCCAATATAAATTTTTTACAAACAATTTCCTTAATAACTTTAGTTAATCCAATGAATCTTATTTTCTGTGTAGTATTTTTACTTTAAACCTGCAGTTTTCATATCATGTGACCACATGAAAAAGTTGCTGTTTATGTGCTATTTGGTTTTTATGTGTTCATGTATTCTAATGTCCTTCCTCTTTCTGTTTTTTTTTTCACTC[A/T]GACCGAGAAGATCAGTCTATCCTCTGCACGTGAGTTTCCACTGCCTGTGCCCATTGTATACATTTACTGACTTTTATTAGCACATGTCTAATTTTGTTCCAAATGTTTTCTTTTAAGTCACCTGCCAGTATTTGTTTTAAGAACTCTGAAAATAGTCCGATCAGGTTTTACAGCAGAAGGTCATTTATTTGTTCTGTTTGTGTATATGTGTGTGCAGAGGGGAATCCGGTGCAGGAAAAACAGAAAACACCAAAAAAGTGATTCAGTATTTGGCACATGTGGCATCTTCACACAAGTCTGGTACTCTGGGGCGACCCAAAGACACTGTTGTACAGGTGAGGACTGCCGTCTTTTGGGAGCAAAACTCTAAACTCTAAACTTTTGGGTGCATAAAAGCAACAGTTCCTGCTTTTCTGAAACAAGCCAGCATACCTATTTTTTGAGTTATTGCTTCTCTTTCTTTCATTCTATAATAATAACTAAAGCATCTGTTACGGTTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17178
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
ENSDART00000047409 Nonsense 236 2020 7 42
ENSDART00000142155 Nonsense 232 2007 7 41
Genomic Location (Zv9):
Chromosome 16 (position 18945051)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 16975374
GRCz11 16 16883351
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
RGCTATTCTTCTTTTGTTGTGCYTAGGGGGAGCTGGAAAKACAGTTACTG[C/T]AAGCAAACCCCAKTCTTGAGGCCTTCGGMAAYGCCAAGACTGTCAAAAAC
Long Flanking Sequence:
TAGAAAGTGAAATTTAGGACATTATAAGAGATTTAAAAACCGGGCCAGACGAGAAGGTCTCGCGGGCACAGAAAAAAAACTGGTAAACAAGAGATTTTCTTCTACTTAATTGATTGCTGATGTTTGGCTATATAGAGTGGATATATATGTATATGGCTAAAAAAAACAACTAGATCTCAGAACTAGTTTATCCACCCACACGCAACCTTACAATGCATCTGCACTCCTTTAGGAGATTCTTCCCACACTTTAAAAAGCACTGAGTTAATATTTGGGTTATGATTAGTGTAGAGTAATCTCATATTAACAGAAGTAATAAGTCTCTAGTTAGAGTGTGTGTGTGTGTGTGTGTGTGTTTGAGAAAGAGTGTGAGGGTCTGCTTGGCTGCAGTCATACAGTATGCTGATGCTGGGCTTTTAGCTGAATGTGAGTTATATTCTTGCACTGAAGGGCTATTCTTCTTTTGTTGTGCCTAGGGGGAGCTGGAAAGACAGTTACTG[C/T]AAGCAAACCCCATTCTTGAGGCCTTCGGCAACGCCAAGACTGTCAAAAACGATAACTCTTCCAGATTTGTAAGCCCTGAATCGCCACAGCTAACACACAGAGTTAGATCTTGAGTTTGTGATTTGCTCTGAACTGACATGTATTTTTTATTTGTTACAGGGCAAATTCATCAGAATCAATTTTGATGTTGCTGGATATATTGTTGGTGCTAATATTGAGACTTGTATCCTTCATAATCCCTAAAATTCATTTAAACAGCTGATAATTGCAGAAAAGTTGCAAAATAATGTAGTTGTGAGAAAAGTACTGGCATTTTTGTTGCAGGTACTGCTATAATTATTTTGCCCGTACTATGTTTGTTTACAGATGTTACTTTATATTTTTTGATAAAATACCAAAATGCTAAGAAAGAATTTAAGGCCATTCTGCTGTATTTTTAATGTAAATTATTAGTATTTTGCTAAAAATTAGTTTTATGAAAAGCTTTAGTTTTAGTTTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16888
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
ENSDART00000047409 Nonsense 831 2020 20 42
ENSDART00000142155 Nonsense 827 2007 20 41
Genomic Location (Zv9):
Chromosome 16 (position 18968434)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 16998757
GRCz11 16 16906734
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGMACCGTATTTTAACGAYTATGTTTTTCAGGGCATTCCATAAGAAGCAG[C/T]AGCAGCTTAGTGCTCTGCGGGTGATGCAGAGAAATTGTGCTGCRTATCTG
Long Flanking Sequence:
GTACAGTGCTCAGCATAATTGAGTACAGCCAATCTTGAAATTTTTTTATTCATTTTTCAGTGAATGTACACAATGCATTTTGATGCATTTAAACAAAACACATTTATTGAACAGATATACTTATTAACCTAATATTTTAGTCACCAAACATATTGAGAAATTAAAATTAAATTCAAGCAAAATCTTGCAAAAAAAAAAAGACTATTTTAACTAAATTATTACATTGTATGCTTCTCTTGATATCTCCTCGTTTTAAATTTGTATTTGATATTTTTCTATAACATTAATTTGGTTGTACTAGTTTTTTGACCGTTATCGTATTGTTAGATAAGATCCAGATTTGGCTTCAGTACTGCCTAATCTAATGTATATGCATAAATATAATATTGTATAGCTTCCTATTAAAATATGAATTTAAAAGGTTTGTGAGGGGTGTACTTATATATGCTGAGAACCGTATTTTAACGATTATGTTTTTCAGGGCATTCCATAAGAAGCAG[C/T]AGCAGCTTAGTGCTCTGCGGGTGATGCAGAGAAATTGTGCTGCATATCTGAAGCTCAGAAACTGGCAGTGGTGGAGACTCTTCACCAAGGTAACACAAATTACTACACAAGGTTATAAACATAAAATTAGTAATGGGCTTAGTAAAGAAATGTATCTTTATTAGTTAGAGTATATGACAGTAATTTTTTACATTGCAAAAATGCTTTTCGTATTTAAAGGTTTTGTCTTGTTTTTTAGTCCAAATATCTAACAATTCTTCAATCAAGAAGCATTTTTTAGATGATCAACAATATTGCTTACCCCATTGGCAGATTATTTTTCTTGTTTTAAGTAAAAACTAATTTAAATGTAAAAAAACTTAACTTTGACATTATGTTTATGAAAACAAGACAATAAAATGTTTCTTGATTTAAGACTTTTTTAGATATTAGGGCTAAAAAAAAACTAAGAAAGGCATTTTTTGCAGTGTATTTATTGTCTCATTGCATATTCAGAACTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45571
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
ENSDART00000047409 Essential Splice Site 904 2020 21 42
ENSDART00000142155 Essential Splice Site 900 2007 21 41
Genomic Location (Zv9):
Chromosome 16 (position 18970053)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 17000376
GRCz11 16 16908353
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGTAAACTAGAGCTTGACTTTACTGAACTGGACAAGAAAAACCAACAG[G/A]TAACTTTCTTTCCGTGTTTCCTTGCGTGTTGGTTTATTTGCTTGATTTCC
Long Flanking Sequence:
TTATCTGTTATTATCCATGTTGAACAGCTTTTTCTCATTATTATTTTTGTACAAACTATTATAGATTTTTTTATGTTTCTTTAAATTTTGAAGGATTTGAAATTAAATGTCTCAATGCATGCCTCCTGAATAAAAAATATAAAATATGTGGTCCATTGTTTTAACTAATTTAATTAAGCATAGTTTATCAAGCTGTTCTAATATGTCACAAATATTTCACCTAAAAGAAGTGTTCAAAAATATATTTGTAATATTATTTAAAAATAATTAAGTGGCATATTAAATGATTGCATAATACAGTATAATGTCAGGTGGAAATAGTACATTAATGTGATGTGGAGTGAATTCAACTGTGATCCCTCCTGCAGGTGAAGCCCTTGTTGCAGGTGACCCGTCAGGATGAAGAGATTCAAGCTCGGGAAGCACAGCTTCAGAAAGCCAAAGACAAGCTGAGTAAACTAGAGCTTGACTTTACTGAACTGGACAAGAAAAACCAACAG[G/A]TAACTTTCTTTCCGTGTTTCCTTGCGTGTTGGTTTATTTGCTTGATTTCCACACTGATCTTGATGTCCTCTTGACAGCTGATTGAGGAGAAGTCAGTCTTGACCGACCAGCTGCAGGCCGAGGCAGAGTTATTCGCGGAAGCAGAGGAAATGAGAGCACGGCTGGCCAATCGCAAACAGGAGCTTGAAGATGTGTTGGGGGAGCTTGAGAGCCGATTGGAGGAGGAAGAAGAGAGGACTGTTCAGCTGACCAATGAGAAGAAGAGGATCCAGCAACATGTGCAGGTTTGCAGGATGGTTCTGTTGCTGTCTAACTACAGATGTTCGATTTCAGTTTTTTTTTTTTTTTTTTTTTTGATAGTTTCTCTTTAGGGGTTGTTTTCAATCATGTAGGTCTAAAGGGGAATACCAAATTTCAAAGGAGATATAAATATTAAATAACTACATATGTTGGACATGATCCTAATATCATGAAGACCGCAGAGTTTTCTACTGAAATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36084
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
ENSDART00000047409 Essential Splice Site 973 2020 22 42
ENSDART00000142155 Essential Splice Site 969 2007 22 41
Genomic Location (Zv9):
Chromosome 16 (position 18970338)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 17000661
GRCz11 16 16908638
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACTGTTCAGCTGACCAATGAGAAGAAGAGGATCCAGCAACATGTGCAG[G/A]TTTGCAGGATGGTTCTGTTGCTGTCTAACTACAGATGTTCGATTTCAGTT
Long Flanking Sequence:
GATTGCATAATACAGTATAATGTCAGGTGGAAATAGTACATTAATGTGATGTGGAGTGAATTCAACTGTGATCCCTCCTGCAGGTGAAGCCCTTGTTGCAGGTGACCCGTCAGGATGAAGAGATTCAAGCTCGGGAAGCACAGCTTCAGAAAGCCAAAGACAAGCTGAGTAAACTAGAGCTTGACTTTACTGAACTGGACAAGAAAAACCAACAGGTAACTTTCTTTCCGTGTTTCCTTGCGTGTTGGTTTATTTGCTTGATTTCCACACTGATCTTGATGTCCTCTTGACAGCTGATTGAGGAGAAGTCAGTCTTGACCGACCAGCTGCAGGCCGAGGCAGAGTTATTCGCGGAAGCAGAGGAAATGAGAGCACGGCTGGCCAATCGCAAACAGGAGCTTGAAGATGTGTTGGGGGAGCTTGAGAGCCGATTGGAGGAGGAAGAAGAGAGGACTGTTCAGCTGACCAATGAGAAGAAGAGGATCCAGCAACATGTGCAG[G/A]TTTGCAGGATGGTTCTGTTGCTGTCTAACTACAGATGTTCGATTTCAGTTTTTTTTTTTTTTTTTTTTTTGATAGTTTCTCTTTAGGGGTTGTTTTCAATCATGTAGGTCTAAAGGGGAATACCAAATTTCAAAGGAGATATAAATATTAAATAACTACATATGTTGGACATGATCCTAATATCATGAAGACCGCAGAGTTTTCTACTGAAATAAATTATACTTGCCTGTCATCGAGGAGGTAGATACTGTATAAGCTATTATGTTACATGAAAAAGTACTGTCGTAAATACTATAGTGTTTGGAAGCATACTATACCATACTTTTATTGTTGCTGTGGTACGACACAACTGTAGTAATAAACAAATTATTCAGGCTTCAGTTTTCTAAGCTAAAATTATACACCATCACAATGCACCACAGTTTACACCAACGTTACAGTATTTATTACCGTTTATCAGTTTACTATGGATGTTTACAGTTTAATTTGAACTTGAATTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36085
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
ENSDART00000047409 Nonsense 1079 2020 25 42
ENSDART00000142155 Nonsense 1075 2007 25 41
Genomic Location (Zv9):
Chromosome 16 (position 18975842)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 17006165
GRCz11 16 16914142
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTGAAAAGGGAAGAGCAGGGTCGTCTGGAACAGGAGAAGTGGAAGCGG[C/T]GAATGGAAGGAGAAGCAGTGGAGGCTCAAGAGCAGCTATCTGACATGAGC
Long Flanking Sequence:
CTGGAAGGGCATCCGTTGTGTCGACCCCAGATTAATAAAGTAACTAAGCTGAAAAGAAAATGAATGAATGAATTATCTTAAGATAACAATTTTTTCCCATATTTTACTACTTAATTTGCAATATACTATTTAGCTTAAAGGGTAATAAGGCTCAATTAAGTTAATAATGTTAACTAGTAAGGTTAATTAGGCAATTCATTTTTGTTATAATACAGGTATATATATAAACAGGTCGTGAGTGCTAAGGGGAGGTAGCCATGCGTAGAGAGAGTACACCCTAATAGGGTTTGTATTTTGTCGGACATGATCTGTATGAACCATCACAGCATGGAAAAGAATGAAGTCCATCTTTTGCTTTTCACATGATGTAATAAGTACACCAAATAACATTTTCATTGTTAAGTGGACTCTTATAAACATAACATAAAATAACATTTTCTTCTTTAGAGCGTCTGAAAAGGGAAGAGCAGGGTCGTCTGGAACAGGAGAAGTGGAAGCGG[C/T]GAATGGAAGGAGAAGCAGTGGAGGCTCAAGAGCAGCTATCTGACATGAGCTTACTCGTCACTGAGCTGAGAGGAAGCCTGAGCCAGAGAGAAAAAGAGATCACCACATTACAGACAAGGTATTCACAAAGTCAATAATAAATCTGGGTTAATTAATCATGGTTTCCATAAGTCATGGATTTTCTTGAATACTAGGGAACTTTAAAAGGTGCATTCCAGAAAGTCATCCCATTTATATCAGGGATTTAAAATTCCTATTTACCAAAATTTCTAATTATTGCGACCAAAAATTAAAAAAATGGTGCCAAATTTTATCAAAATAAAAAATTAGAAATAACATTTGTGGCAGTATTTGTAGCATTTCTTGTGTTGTTTTGAAAGGAAAAATACACAAATGTACATATCTTAGTTCATTACATTTTTGATCTGAAGAATTAGTCCATGTAATGTATATAAAGAGAATAAGACAAAAAGAGAATTTTCTTACCTCTTAACATAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44846
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
ENSDART00000047409 Nonsense 1673 2020 35 42
ENSDART00000142155 Nonsense 1669 2007 35 41
Genomic Location (Zv9):
Chromosome 16 (position 18990070)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 17020393
GRCz11 16 16928370
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATCCCTGATGTGAACATTTTGATGTGTTCCTGTGTGTTTTTTAAGACT[C/T]AGATGAAGGAGCTTATTCGTGAGCTTGACGAAACCAAGTTGGCTCGAGAT
Long Flanking Sequence:
TGAGACTGAAGCTGTTTTATTTTATTTGATTTTATTTAATGTTGTAACTCAAGTCACTGTTTTTGTTTCTTGTTTGTATTCTTCAGTAATTGTAATTATTAACAGCAGGTGTTCATCAGTGTCTGAATTCACTCATTAGTGTTCATTAAAACTGTCAGGTGAACTATATTAGTTAACTAGTGTATGAAATAGTGAACAAGGACACAAAGTGTGATTTCAAACACAGACTTCAAAACATCGAATCTGAACTCTGTTAGCTCACAGTTTTCTGCAGTTGGTTTCTTTCTCGAAAACAAAAATGTTACCCAGAAAGCACTGTTTTTAACAGAATATTACTGTTTTAGTGAAAAAACATTATTTTACCGTAGAATCTGACCGTTTTTTAACAGCAATTTTTTACAGTGTATAATTTATTCAGGAACCTGATTTTGCTAACAGGCTGACAGTTGAAAATCCCTGATGTGAACATTTTGATGTGTTCCTGTGTGTTTTTTAAGACT[C/T]AGATGAAGGAGCTTATTCGTGAGCTTGACGAAACCAAGTTGGCTCGAGATGAGATTGTTGCCCAATCAAAGGACAGCGAAAAGCGTCTGCAGACATTGGAGGCAGAACTATTGCAGCTGACAGAGGTGAGTTAATCTGTCATTGCAACCCAATATAACTGTGAGCTTCTTCCTCATTTTTATCTTTCCATTCTCTGTTGTTTTTTCAGGATCTATCTGTTTCTGAGAGGCAGAAGAGGCAAGCCCAGCAGGAAAGAGATGAAATGGCAGATGAAATCATCAACAATGCAACTGGAAAGTCAGTATCTGTTTAAGATAATTGTTTTTCTTTTACACAGAAAAATAAATCATTAAGCAACTCCGAGAAAAAAAACACAACTATACTAATCAGCACAATTGTTTGTGGGCCAATATTGATAATACAATATTATTTAAGTAAGAAATCAGAACTACAGTTATTTCTAAAGTATCCTTTTCTCACAACTATTTTTATTGAACATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22798
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000047409 Essential Splice Site 1949 2020 40 42
ENSDART00000142155 Essential Splice Site 1945 2007 40 41

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 16 (position 18996330)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 17026653
GRCz11 16 16934630
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCATGCAGAGCATGAACCGCGAGCTCAACACTCTCCGCTCCCAACTCAG[G/A]TAAGGACAATGACAGTTATGACTGTGTGTTCGCCGTTTTGTGTATGGAGC
Long Flanking Sequence:
GCTGCATAAAACATGTGCTGGATAAGTTGGCGGTTTATTCCGCAGTGGCGACCCCAGATTATTAAAGGAACTTAGCCGAAAAGAAAACGAATTAATGAATATTAAGTTTGTTTGTTTGAATAAATTTGACCAAGTCATCTAGTTTGAGTTCAATCGCATTAAAATAATCAACTCAAATTAACAGATTATAACTTCTTAAAAAAAATGGACTCATTCCACAATCCCTTACAAATGATTTCTTTGCTATGTACCTAATCTTATATAGTCAACTTGGCTGTGGTTACACTTGGAGCATTTTTACATTATAAAATCTCTCTATTTTTGTAGTTGGATAAGTCTATGGGGCGCCTCCGTCAACTGAAGAGGCAGCTAGAGGAGGTAGAAGAAGAGAACTCTCGCTCCAATGCCCAGCGCAGGAAACTACAGCGAGAGCTGGAGGAAATGAGCGACAGCATGCAGAGCATGAACCGCGAGCTCAACACTCTCCGCTCCCAACTCAG[G/A]TAAGGACAATGACAGTTATGACTGTGTGTTCGCCGTTTTGTGTATGGAGCAAAAACAAACAACAACTAGCTAGCTTTTTTTAGCTGACTCAGGCTCATAATTTCCTGATATACAAGGGAATATATTGTGTATATGATGTTTAATAGTATTTAAAAATATAAATAAATATCTATATATATATATATATATATATATATATATATATTTATATAGTTAAATTTTTTCAGATTCGTCAAACGGCTATAAAAACAAACATACCTACTTTTCAGAGTCTACTGTATATGATAAATCTTATCAGATCTAGATCATCACTAGATCCAAAATTGCTTGCCGCTGGAATTTGATACATTAAATGTTTTCGTGTGAAACTTTTGTTGTTGTTTTAAATAAATTTACTATTAGTGAATTTCATGTTTTACTGCATGTTTATTCACTCACTTACTCATTTAATGTGTCTGATTGTGTGTCCATCTATATTTGTGCGTTTGTCTCCTACACCC
Associated Phenotype:
Not determined