Busch Lab

ZMP

NR_023325.1

Ensembl ID:
ENSDARG00000030945
Description:
wu:fj53g11 (wu:fj53g11), non-coding RNA [Source:RefSeq DNA;Acc:NR_023325]
Human Orthologue:
KIAA0100
Human Description:
KIAA0100 [Source:HGNC Symbol;Acc:28960]
Mouse Orthologue:
2610507B11Rik
Mouse Description:
RIKEN cDNA 2610507B11 gene Gene [Source:MGI Symbol;Acc:MGI:1919753]

Alleles

There are 10 alleles of this gene:

Allele Name Consequence Status Availability
sa14495 Nonsense Available for shipment Available now
sa17554 Essential Splice Site Available for shipment Available now
sa10040 Nonsense Available for shipment Available now
sa16334 Nonsense Available for shipment Available now
sa16877 Nonsense Available for shipment Available now
sa16463 Nonsense Available for shipment Available now
sa1105 Nonsense F2 line generated Not yet available
sa24979 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa14495
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091772 Nonsense 98 2218 4 39
Genomic Location (Zv9):
Chromosome 15 (position 15192367)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 16237330
GRCz11 15 16173352
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGGAGGTTTTTGGCGCTGTGTGTTGGTGAGGCCCGGGTCCGCTTCGACT[T/A]GCAGGAACCCTTTAGGCCCCGGGTCCCAAACAAAAAWGAGGAGAATCCAA
Long Flanking Sequence:
AAAACTGTGACTTGTTTAAGAATATTTTGACGATAAAAACATATTTTAACAGAATTTGTATTTTTAAATGATATTTGAAAACATTTTTATTCAGGATATATTTTAAGGGAAATGATTGTGTCTTCTGGAAAAATGTTAGAACATTTGTCTTTAACCAAACTAAAAGATTGTATATGACTCCCTTCAATGTTTTTTTTGTGGAATGTATGTTTGTTGAGAAACAGATGTGTATGTTATATATTGTTTATTTAGTACAGGTTTTACCATGAAATAAATAAAATAATTAATTTTTCTCTTTTTCTCTTTTTTTTTCCAGGAAATTGACAGGATATGGATTTCTTGTAAAATAGTTAACCCAGACCTGCCGTAAGTATCATTACGAATGTAGTTAGCATAAATGTAGTCAAAGAAATATAGTAGATCAATTTTAATGATTCTGCTGATTGTTTTTAGGAGGTTTTTGGCGCTGTGTGTTGGTGAGGCCCGGGTCCGCTTCGACT[T/A]GCAGGAACCCTTTAGGCCCCGGGTCCCAAACAAAAAAGAGGAGAATCCAAAAAAGCCTCCTCCTCTCAGTCCCTCTACCCTGCACTTCCTCTCTCAGGTGAGCAGCATGTAACACTTGACTGTTGTTGTACAGCAATTCATGCTCCGTACATGTTTAATACCACAGAATATCATTCAGCAGGAAATTAAATACAGTTTTAGTAATGTACTTGCACAGGAAGTAACTGTAAAAAAAATGCTGGGTTCCACACATTTCATTTAACAATTAAAGGGCCATGAAACCCCCTTGTTTCAGCAGGGTTTTTTCACACCTCTATTTTGGAAAAAGTCAGGAAAGCAGGCGTGTCCAGCTCTGTTTAGGGGGAGTGTCAGAGGTTGGAAAGAGGGTAGGTCCGTAAAAATTTGCATAAAAATGGGAGTTTTGGTTTGTGCACACGCTGATTTTCACATAGGCATAGACAAACACTCAGACACAGAAGAGAAAGACAGTGACTGTGTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17554
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091772 Essential Splice Site 337 2218 9 39
Genomic Location (Zv9):
Chromosome 15 (position 15186336)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 16231299
GRCz11 15 16167321
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTCCTGAGCTCAGTTTCCCACAGAGCCGCCTGGAGCTTCTGCTGGAGGG[T/C]GAGTTTGAAAACACACTCTTTATCACTGTTATTATTGCWCTGGACGCACT
Long Flanking Sequence:
TCATTTGAGAAAATTTGAAAAAGAAATAAAAATTCACAGCTGGGCTAATAACTTTGATTTCAACTACATATCAAAAAGGTTTTGAATGGTTTTAATTTTGATTAACTACAATAATCCTGCTGTAAATGCAGCTCTGTTTAAGCCTTTTTTTATGTGTGTATCTCTTTGTAGATGACCAAGAAGACTCTTACATCCAAACAGACTCAATTGAGCGCCTTCACAGCCTGATTCCACAGAACGTCAACGTGGATTTTGAAAACACTAATATCACACTCTCCATGCACAGTCAGAAGAGGTGAGCAGTGACGCTTGAGCCATTTTCATCACCATCAAATATTGTGTTTGAGCTCTAAATATCTGCATCTTCTTCACAGACATCTGAACTGGACTTTAAAGTCTCTGAAGCTGGGTTATGATCGCAATGATGAGCAGCTTCCTCTGAAATCTTTCACTCCTGAGCTCAGTTTCCCACAGAGCCGCCTGGAGCTTCTGCTGGAGGG[T/C]GAGTTTGAAAACACACTCTTTATCACTGTTATTATTGCACTGGACGCACTCTTAAACCTAAATATTATTGTACTTGCTGTTTTTCAGATGGTCTCTTGCTGTCACAAAGCAGACAGAGGATTATATGTCTGAACACTCTAAGAACGATACTGCATGTGAGTTGCTTTGCAGCTTTCTATTATCACTGGGTACTAGGGATGTAACGGTATCAGAATTTTACGGTACGGTAATACCTCGGTATCAATGTCACGGTACAGTATTTATTGAATCATTTACAGGAAAAAACAAAACTTATGAAAATACTCCAAAAAAGTGGCAAAAGTGTCAATGACATACAAATTAGCCATCTATCTGTAAGCTTTGAAACAGGAACTTCAATTTTAATAACAAAAAAAATATTAAACCATGTAAAAAAAAAAAAATAAAGTTTTTAATTTAGTATTGTTGAAAACTCATCACATTCAACATTTAATCACTCACTCACTTAGATAGAGATGGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10040
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091772 Nonsense 975 2218 16 39
Genomic Location (Zv9):
Chromosome 15 (position 15171427)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 16216390
GRCz11 15 16152412
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGTGGCACTTGCAGATCAGTCTTTGCATGGCCCAGAGCAGATCCGAGAG[C/T]AGCTGCGGGACATCGATGGTGTCAGCCCCTTCCCCAGAGATGGCCTGCAG
Long Flanking Sequence:
CGCCCAGCCTTGCCATAGAGTTCCCTTATCAGTACAATTTCTCAGACACCTTCGACAAGGCCATCAGTGTGCAGAAGTGGTTGAAGACCCTACATGGTGGCGTCATTCAATCAGAAGAACCCTCTCGGCTACCACCGGACCTGCTGATCCGCATCAACCAGTTCTCCTTTGTGTTCCTGGACGACGTTTTCGAGATCAAGCTGCGCGACAATTACGAGCTCATGAAGGACGAAAGCAAGGAGAGCGCCAAGCGTCTGCAGCTGCTGGATAAGAAAGTTGCAGAGTTGCGCAAGCAGCATGGCGAGCTTCTGCCGGCCCGGAAGATTGAAGAGCTCTACACATCACTTGAGCGCAAGCACATCGAGATCTACATTCAGCGGTCCCGGCGTTTGTACGCTAACACACCCATGCGCAAGTCTCTGCTCACGTGGACGGTGTCAGAGTTGGAGCTGGTGGCACTTGCAGATCAGTCTTTGCATGGCCCAGAGCAGATCCGAGAG[C/T]AGCTGCGGGACATCGATGGTGTCAGCCCCTTCCCCAGAGATGGCCTGCAGCTGGTGGTCCAGTGGTGTCGTGCTTTTAAATTCAATCTAAATGCATTCCTGGGTAAGTCAATACTGGGGTGTGTAATCCTGCTTCTGACTCTAGTAATAGTAAGATCTGAAAAGATCTGAAGTCGCATACTTTTTTGTTACTATAAACAATGTAGTAAGCAGTGGTGTAAAGTACCAACTTACACATACTCCTCAAGCTACTGTAAGTAGTTTTTCGCTGGAATTGTAATTTACTAAGTAGTTTTAAAAATATTTACTATTACTTTCCCTGAAATACATTTTTAGTGCTGTATCGGTACCTTTACTGCACTAATTTCCTTTGACCTGCAGTCAGTACATTTTTTTTTCTTGTTAATGGTGATTGGCTAAAGTAGAAAAAACAGTCCTACAATTCTTTTACATCATATTAAACAATTTCAAGTAGGTCTGTGTGATTAATTGAAATTTAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16334
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091772 Nonsense 1357 2218 23 39
Genomic Location (Zv9):
Chromosome 15 (position 15163157)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 16208120
GRCz11 15 16144142
KASP Assay ID:
2260-8252.1 (used for ordering genotyping assays)
KASP Sequence:
TTTMTGCTGAAATGATGGATGCCTGTTTTCTAGCTGGCACTGTGATGAGA[C/T]GACTGATCTCTGAGTGGAACGTCACTCAGATGGTGAGCGATCTCTCTCTG
Long Flanking Sequence:
TACAGTAATACAGTAGCAAATGCATTTTGAGATATATATACACATCCAAATGGCTCTTTACAAAAATGCATTTGCTAAAACAAATCAGAAATGGCTCTTTGCTAAAAAAAAGGTTCCCGACCCCTCCTTTAGCCCCTTTATAAGTCTATAATTCTTCAATTAAACTTTGTGAAACCTGCATAATCCCTGTTCAAAATATTTTACCAGCTGAGACGATTTAAAGAGAGTTTTGTGATTTAAATTTAATCTAGAGTAAAACTGTAGAGTAAAACTGTGTTTAATGTCCTACTGCAGGTCCACTACTGGGCTTCGTTTGCTCAGCAGAGAGGCATTCAGGTGGAGTGCAGTAAAGGTCACGTCTTCACCAGAGGAGCACAGAGGCTCATTCCACAGGGTGAGAAAGCAAAGAGCATTCAGTCACACTTTCGACACCTCACAGACTGTTAAAATTTTCTGCTGAAATGATGGATGCCTGTTTTCTAGCTGGCACTGTGATGAGA[C/T]GACTGATCTCTGAGTGGAACGTCACTCAGATGGTGAGCGATCTCTCTCTGGTCACCGTGCACCTTATGGCCTCCACATGGGATGAGACAGCCGACCATCAGATCAACGCCCAGGTGAAGAAAACCCACCTGCTCAGCCTTTCCTCACTCAGCTACCAGAGACAGAGCAACCGTATTGAGGAGGTGAGACACTTCTGTGCAACATTCATCCATCGGAAGTAATATTTCACTATTTGGATGTAATAAGTGGTGGACATTAATTAAGTATTTTTACTTCACTACAAAATGCTGTATTTTTTATTTTACTACATCTTGGATTCATGTAGATGAGTAAAACAGTATTTTAAATGGAGAAATGGACGTCTGGTTTGGTAAAGTGGCAATGTAATGGCCACATTATTACATGTAATTTCTTCACAACACATCCTATTTTACCAGTATATCCAATTCGATATACCTGATTTGTCTGAAAATAATTAAAAAAATCTTAATCTAAAGTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16877
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
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091772 Nonsense 1569 2218 25 39
Genomic Location (Zv9):
Chromosome 15 (position 15160950)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 16205913
GRCz11 15 16141935
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACTGATGATGTTTACAACCGCAACTGGTTCATAGAGCTCGTCAATGGA[C/T]AGGTAAGTATTAAAGGTGCCAYARAATGAACATTTAGGTACAGCTATAAG
Long Flanking Sequence:
GACCTAAGGGCCTCCTGGACCACCACCAACAGGAATATTGCATTTGGCTTGTATGATGGCTACAAGAAAGCTGCCGTTCTGAAGAGGAACCTCTCAACAGAGGCTTTGAAGGGGCTACGGATCGATACGCAGGTGCAGACGAAAAAGCTAAAGCGATCCATGTCCAGCTATTCCTCAAACACAGCTCCTGCTACACCGGTCATCACTGCAGCCACCCGCCCAGAGAAGAGCCAGAATGAAGGTACAAAAATGTGGTGCTGCTGTAGCTTATTTGTGAGGTTTTGTGAGGTGGATCTTCATTGATCTTTTTTGCTCCAGCTAATCTGTTTTTGTGGTTCTTTTCAGGAACATCCATGCTGCAGAAGCTTATTGAGGAGACTGATAAGTTTGTGGTCTTCTCTGAAGAGGATGCAGGAGTGAGTGATCAGCTCTGTGGAATTGCCGCATGCCAGACTGATGATGTTTACAACCGCAACTGGTTCATAGAGCTCGTCAATGGA[C/T]AGGTAAGTATTAAAGGTGCCATAAAATGAACATTTAGGTACAGCTATAAGTTCCGAATAAGGAAATGAAGTGAGCCTCAAATATCATTGTTTCCTCATTCTCGTGTAAATTTTCTGAATGTTTAATCCTGGTGAAAAAAACAGCCCAATCAGAACAAAACCATTACAGACCGTTATGTTGTACTCAGGATCTTTAATATGCACACCCCAGGCAGCTTTTGATTGGCCACAAAGTTTCATATTGAGATTACAGCAATGATCTTTTTTTAAACTTATTTTTAAGTTAATTTAAGCTTGTATTATGCTTACTATGTATTTGAGACTCTTATTTTGAAAACGTGACAGGCTTTAGGGAAAAGTAAAGGTGCAGCAGGTCCCATGCATGCCACCCAGCCTTGTTTATAGTGTGTCAGAATGCTGAATGGCAAGAAATAAGGATTAAAAGTGTATTTAAAGAGGAATAAGATCTTTTTAATAGTGGTGGGCAAAGCGAGGCTTCGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16463
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
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091772 Nonsense 1647 2218 27 39
Genomic Location (Zv9):
Chromosome 15 (position 15158040)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 16203003
GRCz11 15 16139025
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCAATMCCATTTTGTGAACCTGCAGGTGAAGAACATTGAGGAAYACAGA[C/T]AGAGGAATCTGGACTCAGTGCTGGAGCTGATGGAGAGCGGTCAGGCTGTT
Long Flanking Sequence:
GGGTTGAAAATGGACTTACCTAAGCCACATGCCTACTATGTAGTTATCAGAGAACAGTTGAATATATTGTATCAATGCATTCTAAGGCACATAAACTTTTGAGAGCAGTAACTCATAGTTGAAGGTTCTGTTTAATCAGATCTAAGCATCTTACTCTGTACGTTGTGTTCAGATGATGCTGCGAGGCACTGAGACCGCCGGCTGTGTGCTGGTATCTGCCGCCAAGGCTCAGCTACTGCAGTGTGAACACCACCCTGCTTGGTACAGCGACACCCTCAAGCAGAAGACCACCTGGACTTGCCTACTGGATGGTATGCAGTACTTTGCCACCATGGAACAAAACCCCTCTGAGCAAGAGGACTGGCAGCTTTGGCTTGAGGTGGGTTGAGATGTCTAGATATCAGTCAAATCCCATTTATGATAAAGAAAACTTTGGGTAAACTTACAGCGACCAATCCCATTTTGTGAACCTGCAGGTGAAGAACATTGAGGAACACAGA[C/T]AGAGGAATCTGGACTCAGTGCTGGAGCTGATGGAGAGCGGTCAGGCTGTTGGAGGAATGGTCAGCACCACCACAGGTGTGCCTTTTTAATGCTCATTTAAAAGTTTGTTATTCTATTTTTGAGGCCTGTGTAACCCCACCTACACCAATTAACCTACTCTAAGCTGGGATCAAACCGCCGACCTTCGACATTGGAGTCGGTTGCTTTACCAAAGAGGCTAAAGACCATGGCCTCTAGCATCTGTCACTAGAACACCTTTACGAGTCAGAGGAGTGAGGTTTACCTGCAGAGGACTTCACTAGCTGGCCTCTGCTACACTCACCCTCCTTAAACCTCACTCCCTTCCGATTACGGCACCAATGTAACCCTGCCAGTCCTACACCACCAAACCCGCTCTGAGCTGGGATCGAACCGGTGACCTTTCACATGGGAGTTGGTTGTTCTATCAAGGCTGGCTTCTGCTACACCTGCTAGAATTTGCATGATTAAAAATCTTTCCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1105
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091772 Nonsense 2033 2218 35 39
Genomic Location (Zv9):
Chromosome 15 (position 15148986)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 16193949
GRCz11 15 16129971
KASP Assay ID:
554-1007.1 (used for ordering genotyping assays)
KASP Sequence:
CTGGAAGAAATGTGGAAGAGGAAGAAGTTGGGGATGAGGAGGACAAGTTC[A/T]GATTGGTTACTACAGGTTTGTCAACATGGTTACTTTTTTTTTTTTCNNGTAA
Long Flanking Sequence:
TTACTTTCTAATTTGTTATTACAGGCGTTGCATTCCACTTTTACTTTTTTATGTCTCTTTTTTTTTCTAAATTTATTTTTGTATGAGTTTGACCAGCAGACTATTTAACCATGTCCATGTTTTCTGTGTTCCATGTTTACTTCAGTCAGGCGTGTGTAATTATGCTAATGTTGTGTATTGTAGGTGGTTTTGCGTCCTCAGAGTCCCTGCCAATCAGGACGTCAGCTCGCTCTCCGTATCTTCAGTAAAGTCCGCCCCCCAGTAGGAGGGATCTCCGTCAAAGAGCACTTTGAGGTCACTATACTGAAATCCCAGTGTTGATGAATTATTCGCAATAGTAGTTATTATATGATTAGTTCATTAATGTATTTATGTTGTAGGTAAATGTGGTACCACTCACCATTCAGCTCATGTACCAGTTCTTCAAGAGGATGATGGGATTTTTCTTTCCTGGAAGAAATGTGGAAGAGGAAGAAGTTGGGGATGAGGAGGACAAGTTC[A/T]GATTGGTTACTACAGGTTTGTCAACATGGTTACTTTTTTTTTTTTCGTAAATATGAGGTAATCACCTTCCACAACAGGGACATTCGACTGTTAAATCATTTATTATAACTCAAGAAGTAGAGTACAGTGAGTACAGTGAACTCATTGTTATGTTCAAGAAACCAGTCTGAGATGATTCACAATTTGACATGAAGTGTTATCCTGCTGGAAGTAGCCATCAGAAGATGAGTACACTGTGGTCATAAAGGGAAGAACACAGTCAGCAACAATATTCGGGTAGGCTGTGGCATTGATTGGATGCTCAATTGGTACTAATGGGCCCAAAGTGTGCCAAGAAAATATCCCTCACACCATTACACCACCACCACCACCAGCCTGAACCATTGATACAAGGCAGGATGGATCCTCCATGATTTCATGTTGTTGATGCCACACTCTGACCCTATCATTCAAATGTTGAAGCAGAAATTGAGACTCATCAGATCAGGCAACGTTTTTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24979
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
ENSDART00000091772 Essential Splice Site 2157 2218 38 39
Genomic Location (Zv9):
Chromosome 15 (position 15144783)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 16189746
GRCz11 15 16125768
KASP Assay ID:
554-7866.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTCGCTATGGCTGTGAAAAGAGACAGTCGGAAAGCGCTAGTTGCACAG[G/A]TAATCACTAGACAGAAAATCAACCTTTAAAGGTGCTCGATGTACAATTCA
Long Flanking Sequence:
TATCACTCAGTATTTATGCATTTGCCTTGAAATGAAAAAGGTTTACCCAAATAGCCATCAAAATTGTAAATATAGTAAGTAATATTTAATAATGTGTATGTGTATTGTGGCTTTCAAATTACAATACTTAAAAAAAATGTGTCTAGTTAAGTACATTGTTGATCAGTCAATTACCATGAGGGAGTATTTTATACTGGTTTGCTTAAACATATTTGCAAATTGAAGCCGATTTTATAGATCTGAGTTTATAAACAACTAAAAGTCATTTTACCTTCCCAGCAAAAGCATTTAAAAGCTAATACTTAATTAATCACAAGCTCTAGTGAAGTGTGACTGTAAGCATTTCTCTTGTGGTGTATGTATAGGGAGAGAAGAGCAGCGTAGACTGGAAGGATCTGAATCTTGTTCTGCCCTGTTTGGAGTATCACAACAACACCTGGACCTGGCTGGACTTCGCTATGGCTGTGAAAAGAGACAGTCGGAAAGCGCTAGTTGCACAG[G/A]TAATCACTAGACAGAAAATCAACCTTTAAAGGTGCTCGATGTACAATTCAGAAATCCTACAACTTATTGTGTTTGACAGCTTATTGTCCTTTATTCACTCTCATGGGGCTTGGCGATAAATCTCATAAAACTCAAATCACGATATAAGTCATCAACTCACATCCTGATGATAAACGATATACATCACAAATTATTGACCACATGTAAAGCAGTGTTTATTTTTTACATTTATAGTATTTACTCAGGGATTTGCTAATTTATATATGTTTGTTTTTCTCACTTTAAAAAGAATTTCAGGAAAATGCTTGATTAAAAATGTAGAAATGTAAATTAAATATTAATAAAGTATAAAACATTTCTCAAAAACCTATGATTACATGTCCAACATAAAATTCATCAGACATACACTACCTGACAAAAGTCTTGTTTTCAGTCCCAGTTATAAGAGCAACAAATGATAACTTGACTTCTAGTTGATCTTTTGGAAAACTGGCAGAGAA
Associated Phenotype:
Not determined