Busch Lab

ZMP

ABCC1

Ensembl ID:
ENSDARG00000059874
Description:
ATP-binding cassette, sub-family C (CFTR/MRP), member 1 [Source:HGNC Symbol;Acc:51]
Human Orthologue:
ABCC1
Human Description:
ATP-binding cassette, sub-family C (CFTR/MRP), member 1 [Source:HGNC Symbol;Acc:51]
Mouse Orthologue:
Abcc1
Mouse Description:
ATP-binding cassette, sub-family C (CFTR/MRP), member 1 Gene [Source:MGI Symbol;Acc:MGI:102676]

Alleles

There are 8 alleles of this gene:

Allele Name Consequence Status Availability
sa10834 Nonsense Available for shipment Available now
sa45145 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa33242 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa40113 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa6039 Nonsense Mutation detected in F1 DNA Not yet available
sa2103 Essential Splice Site F2 line generated Not yet available
sa33241 Nonsense Mutation detected in F1 DNA Not yet available
sa40112 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa10834
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083659 Nonsense 53 1529 2 34
Genomic Location (Zv9):
Chromosome 3 (position 36473717)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 36575387
GRCz11 3 36717245
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGCTGGTTTGGATACCCTGTCTCTACCTCTGGCTTTTTGCACCACTCTA[C/A]ATCCTATACCTCAAAAGCCATGATCGCGGATACATATGCATGACCCACCT
Long Flanking Sequence:
TGATCTGTTATTCTCATTAATTTATTGATCTATTTTTTTTCTCCTCAGAGACAGCAGGGTTATGGGAACACATGCTTCCTGCAGAGAACAAGATTAGATTTTCTTTGTAAGGAAAAGGTTTAGTTAATGTTTTAGAAGTTACTACTTAAAGAAGACTCTCAGCTCTGCTCTATTGCGTAGAAAAAAACATCCTTGACTTTGGTTCTCAGAAGGCTCCTCGCAGAAGTCCTGAAGTGTTTGTTCCTTGCACACATCATTAGTTCTTTGTGTGCTTTACTACTCGTCTGAGATCACAGTGTCCACTTCAATAATTGCTTTGTTTCCATGTTTCATCTAAAGAATTTCTAGAGATGTGGAGAAAGGAATGAAGCCCTCTTGTCTTGTTTTCAGGATTGGAACCGGACATGGCAAACATACTATCCAGACCTGACCCCATGTTTCCAGAACACTGTGCTGGTTTGGATACCCTGTCTCTACCTCTGGCTTTTTGCACCACTCTA[C/A]ATCCTATACCTCAAAAGCCATGATCGCGGATACATATGCATGACCCACCTCAACAGAGCCAAAACAGTGAGTACAGTAAACAACTCTGTTTGCGTGTTGCAGCCTGCTTTGTGAATGTGTTTCCTGATAACTCTGTCAAGGTCAACAGGGGTTTGAAGGTCATGTGACTCTCCTCCACCAGGTTATCGGGTTTACCCTATGGCTTATCTGCTGGGCAGATGTTTTCTACTCTTTCTGGGAAAGAAGCCACGGGGCTACAGTAGCCCCAGTCTACCTAGTCAGCCCCACAATGCTTGGTGTTACAATGGTGAGACCCGTTCTTTCACAAAAGGAAGAGCTGAGCTAAACTGCTTTGCCTGTAATTTACTTTGCATTGATTTCATATTCAAATGACATACATGTATTTTCCTTGAAGGGAGGAAATAGATTTCTTTATAGATGGTAGCATGGTCTGCTCATGTTCATGTATGTCTTTCAGTTGCTGGCTACTTTCTTGATCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45145
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083659 Essential Splice Site 75 1529 2 34
Genomic Location (Zv9):
Chromosome 3 (position 36473649)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 36575455
GRCz11 3 36717313
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATGATCGCGGATACATATGCATGACCCACCTCAACAGAGCCAAAACAG[T/C]GAGTACAGTAAACAACTCTGTTTGCGTGTTGCAGCCTGCTTTGTGAATGT
Long Flanking Sequence:
CACATGCTTCCTGCAGAGAACAAGATTAGATTTTCTTTGTAAGGAAAAGGTTTAGTTAATGTTTTAGAAGTTACTACTTAAAGAAGACTCTCAGCTCTGCTCTATTGCGTAGAAAAAAACATCCTTGACTTTGGTTCTCAGAAGGCTCCTCGCAGAAGTCCTGAAGTGTTTGTTCCTTGCACACATCATTAGTTCTTTGTGTGCTTTACTACTCGTCTGAGATCACAGTGTCCACTTCAATAATTGCTTTGTTTCCATGTTTCATCTAAAGAATTTCTAGAGATGTGGAGAAAGGAATGAAGCCCTCTTGTCTTGTTTTCAGGATTGGAACCGGACATGGCAAACATACTATCCAGACCTGACCCCATGTTTCCAGAACACTGTGCTGGTTTGGATACCCTGTCTCTACCTCTGGCTTTTTGCACCACTCTACATCCTATACCTCAAAAGCCATGATCGCGGATACATATGCATGACCCACCTCAACAGAGCCAAAACAG[T/C]GAGTACAGTAAACAACTCTGTTTGCGTGTTGCAGCCTGCTTTGTGAATGTGTTTCCTGATAACTCTGTCAAGGTCAACAGGGGTTTGAAGGTCATGTGACTCTCCTCCACCAGGTTATCGGGTTTACCCTATGGCTTATCTGCTGGGCAGATGTTTTCTACTCTTTCTGGGAAAGAAGCCACGGGGCTACAGTAGCCCCAGTCTACCTAGTCAGCCCCACAATGCTTGGTGTTACAATGGTGAGACCCGTTCTTTCACAAAAGGAAGAGCTGAGCTAAACTGCTTTGCCTGTAATTTACTTTGCATTGATTTCATATTCAAATGACATACATGTATTTTCCTTGAAGGGAGGAAATAGATTTCTTTATAGATGGTAGCATGGTCTGCTCATGTTCATGTATGTCTTTCAGTTGCTGGCTACTTTCTTGATCCAGTACGAGCGGATGAAGGGGGTCCAGTCCTCAGGAGTGATGCTCAATTTTTGGCTGATCACTATAGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33242
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
ENSDART00000083659 Essential Splice Site 405 1529 9 34
Genomic Location (Zv9):
Chromosome 3 (position 36469300)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 36579804
GRCz11 3 36721662
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACTGGCATGAGGTTACGCACAGCCATAGTTGGTGCTGTATACAGAAAA[G/A]TAAGTGTAGTTTTAATTGATTGATTGATAAAAATGCATGACATGCATTAA
Long Flanking Sequence:
CCTTCCCTCAGCGTTTTCACAGTCATGTGGCTAGAAATGACTTTAACTCAGTAGGAAGGCCTCGATGTCAAAACAACAGCTGTGGCTCTTAAAAGGGCTTCAATGAAGAGTTAGTTTTGGCATGTTGGAAGTTATGCCATCAAATTGTGCACTGGACCATGTTTAAATCCGCTTAATCTCTTGAAAATAACACTTGAACTCACGGCAGAGAGCCTTTAACCAGTTTGCCCAGTTTTCACACACTTGAATCTTGGATATTTGCATTCTTCTTGTGGTGAAGAGGACTGACATACAGTATTAAATTTGGTCTATTGTATCTTAGGCTGCTGATCCTGTTTGTGAATGATTCAAGTGCCCCCACCTGGCATGGCTACTTCTACACTGCCCTGCTGTTCGTTTGTACCTGCTTGCAAACACTCATTCTTCAGAAATATTTCCACGTTTGCTTTGTGACTGGCATGAGGTTACGCACAGCCATAGTTGGTGCTGTATACAGAAAA[G/A]TAAGTGTAGTTTTAATTGATTGATTGATAAAAATGCATGACATGCATTAATTATGAAGTGTAATAAGCTAATATTAATATTTATATTTCTTTTTATTTTTAGATATTAAAAAAAGCATAAATAATACATTTGTTCAATATCAGTGTGTAAAAATTTGGTTCTCAGAAATTTTATTGAATTATTAATGAATTAATTTGTTAATTTATTAAAGTTTTAAAATTGGTTACTAGTTTAGGGTTCAATGCTAAGGATTTTTTTTAATGACCCAATTTTTTACTTGCCCTACCAAAATTTTTAATATCCCCACCTACAAAAAAGGAAAAGTTAATAGCTCTTTTTTTAGCCACATATTTTAAATTATGTGTCAAAAATAACGTCTGTGATTCTAGAATTTAATTATTTTATAAATGTTAATAAATGCATAATATGCAAAATTAAGTGTTATGCAACCAAAATAAACAGTATGGAAAATGTGCAGGTATTTTATTGCGGTTCTGAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40113
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
ENSDART00000083659 Essential Splice Site 459 1529 10 34
Genomic Location (Zv9):
Chromosome 3 (position 36467859)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 36581245
GRCz11 3 36723103
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGGTCAGCACCTTTGCAGGTTATCCTGGCTCTATACTTTCTGTGGCAG[G/A]TATGTAAAGAGATTTTGAATTGTATAAACTGTGTGTTTGTTTCATTCAAC
Long Flanking Sequence:
TGCAGTCCTTATTGTTGTGCCCTGTAGTTTCAATTTGGCATCTCATGCTCACTCAAGCTGTATTTAATCAATCAAATATGTTAAATTTTATGTAAAAAATAAATAAACATATATCATTACAATGTAAAATTTTTGTTTTCTATTTGAATATATTTTAATGTAAAATATCCTATTATTAGTAAAGCAGTGTTGAAAACCTTAAAATTTACATTCAACATGCAACTTTATTTAGGATTCTAAAAAGACTGCAGCATGTATTTAAATGCATTTTTATTGTGCATTATATATGTCTTCACTGTCAATTTTAATCCATTTAAATTTATTCGGAATTTTTTAAGGCCTTAGTGATTACCAATGCTGCCCGGCGAACATCCACAGTTGGAGAGATTGTGAATCTGATGTCTGTAGACGCGCAGCGGTTCATGGACCTCATTACATATATCAATATGATTTGGTCAGCACCTTTGCAGGTTATCCTGGCTCTATACTTTCTGTGGCAG[G/A]TATGTAAAGAGATTTTGAATTGTATAAACTGTGTGTTTGTTTCATTCAACATCACTAATGCCTGTATTATTTTCCCTCTCTTTTTTTAAATCAGAATTTGGGTGCTTCAGTGCTCGCAGGAGTTGCCGTAATGGTGCTAATGGTTCCTCTAAATGCGGTCATTGCCATGAAAACTAAAACCTACCAGGTTTTTTGCACCTCTGTTCCTGCATGACAGGTTTATTTACCTCAAAATGTTGTTAATCAGATCATGTTTGGTAATCTGAAGCACTCACCCACAGGTTGCCCAAATGAAAAGCAAGGACAATAGGATCAAGCTTATGAATGAGGTGCTGAATGGCATTAAAGTGCTTAAACTCTACGCATGGGAACTTGCTTTCAAAGGCAAAGTATCTGCTATCCGAGAGAGTGAATTGCGTGTGCTGAAGAAAATGGCTTACCTTGGTGCTATTTCCACCTTTACTTGGGTCTGCGCGCCGTTTTTGGTAAGTGGCTCTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6039
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083659 Nonsense 679 1529 16 34
Genomic Location (Zv9):
Chromosome 3 (position 36464405)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 36584699
GRCz11 3 36726557
KASP Assay ID:
554-3872.1 (used for ordering genotyping assays)
KASP Sequence:
TGTAAGTATCCCTGAGGGGGCGCTGGTTGCTGTGGTGGGGCATGTGGGTT[C/A]GGGGAAGTCCTCTCTGCTTTCAGCTTTGCTGGGAGAGATGCATAAGCAAG
Long Flanking Sequence:
ACATTATTGCGGTTACACCGAGCAGAACCAGTGAAACAGGCTACTGAGGACATGACAGGCAAGTACATGTGCATGAACTCCATTACAGGAAAAATGTCAAACCCCAGAGCAATTGTAATCTGATGAATCTACGTTGATGTTAATGAGAGGGATGATGAAATTTGGGTCGCCGTTTTCCTTTTCAATCTTGATTTCTGCCACATCTACTTCAAATTAAGGATTGAAATGTTTAATTTGTCTTGCATTATTGCTCATTTTAAATTCAGTTGTTAATATCAGAGCACTCTATTATCACGTGAATGAAGAAATCATAATGAATGGAAGAATAGATGAACAAATGAAACCTTTTTTCTTGCAATACTGCATGTGTCCACAGGTGATTAAACAGTTAATTCTTTGTATCTGATTTAGTTTTATTCTCTCTTTCTCTCTACCTCCCTCCAGGATCAATGTAAGTATCCCTGAGGGGGCGCTGGTTGCTGTGGTGGGGCATGTGGGTT[C/A]GGGGAAGTCCTCTCTGCTTTCAGCTTTGCTGGGAGAGATGCATAAGCAAGAAGGATCGGTCTCGATCAAGGTACAGAGTCAGACCTTTGTCCTTGTGCTCCCTATTGAATTTCTTTGTAGTGAAGTCAACTGAAATGATGTTGTGTGAGGGCAGTGGCTCTTCTAATGGAGTGCTGCATTGTATTTAAGTTTAAAAGTATAGATACTGCTTTATAAAAAATAAATAAAAGACCACTTAGAAGTTTTCTGGATATGTTAATAATAGGTACATTGTTCATTTGTGTTTTATTTTATAAAGCACAGATAACAAATTTAGCATTTAGAGAATTTATTTGTAAAAAAAAAAAAAAAGTCAATAGAAAGTGAAAAAACAGACACATGCATGTATAAATCAGAAATTTGGCTTTTTTGTTTGTCCCCTTTTCCTTTAATGACAGCAGCACTCAAGCTGCTTGAACTTCACATGATTTGAAAATGATCCAGAAAGCATCTTGTGCCTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2103
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083659 Essential Splice Site 903 1529 21 34
Genomic Location (Zv9):
Chromosome 3 (position 36457413)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 36591691
GRCz11 3 36733549
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAAATATTTTGTATGAGTTTCAAACGATATGGTCACCTCACCAGCCTAA[T/G]AAAAACAAAAATGTTTTTCAATGTTTAAAAATCTTTAGTTGTTATATTTA
Long Flanking Sequence:
CAGTACAGTATTTAACAGTTATTCCTGTACTGCAAAGCTGAACTTACAAAACATTACATCAAACCATCCTTCAGAAATCTTTTAATATGTGCCAATTTTAATAAGCCAGTTTTAGAATGACATTGATGCATTTTAGATTAGGTTTAATTTTATTGTCATTACACATGTGGAAGGCAACAAAATGCAGTTTAGGTCTAACCAGGAGTGCAATAGCAGCAAGTGCAGGATACAGGTATAAGTTATAAAGTGCAATTATAGAAAAACTATGGATAATATTTACAGATGGATGTACTATGAACATTATATACAGGTTGTATTAACTATGATCAGAGATTTACAAAAGATGAATATATGTACAGGATTTTTGGGGTCCCTCAGTGAATAAAATGTACAAATGTACAAAACCCTTTAGTGAATAAAATGTACAAAAGAACAACATTCATTTATAAAGGAAATATTTTGTATGAGTTTCAAACGATATGGTCACCTCACCAGCCTAA[T/G]AAAAACAAAAATGTTTTTCAATGTTTAAAAATCTTTAGTTGTTATATTTAAAGTATTCAGTCACAGGCTGCTTTCGATGAAAATGATTCTTTTTTTCAAGTTTATAAAACAAACCATCTAAAATATTGTGTAATAATTTCTTAGATTTGTTTTTAATTAAAATAACTTGAAAATATGGTGTAAAATTCACACACAATAGTGTAAATGGTCATTTTAATTTTTATAAATAGGAAAAGCTCTTTGCTGTGTGCTGGACCGTTACATTCATCATTCTTTATTAGCATGGTGGATATATTTTAAAATGTCTGGTCATCAGCAATCTTTTCACTGTAACAGTTCCTTATTTGTCTGATTGTGTGTGAGGTGCTGGACTCTGTTACAGTACAGTCTGCTGGTGATTCTTCTAAACTTAACTCTCACCTTAGACCCTAAAAGGTTGTTTTACCTTCATTCATTTTTACAGAAATTCTCATTTCAATTGGCTTGAGAGGTGTTGTTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33241
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
ENSDART00000083659 Nonsense 943 1529 23 34
Genomic Location (Zv9):
Chromosome 3 (position 36455481)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 36593623
GRCz11 3 36735481
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCTAATGATGATGCTGCTGCAACAAAGACCAAATCTGCAGAAGCTTCC[C/T]GACTGACCGAAGCAGACAAGGCCAACACTGGCAGAGTATGAGCCAACCGT
Long Flanking Sequence:
ACTGCAGGTACTCTATGCATTTTATGCCATAGTAAAAAAAGAAATCATGTTCTTTGATAAGCTATGGTTTGCCTTTTTTTGCCAAATAATTTGTCAGATAAATATCTCAACCGAGTTTAGTGTTTTCCAATATAATTTTCATCTTATATTTTGAGGGTTTCTTCTTCTTGTTCTTCTTCTTGTTCTTGTTCTTGTTCTTGTTGTTCTTCTTCTTCTCCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTATATTTAGGCTATTAAAAGTAAATGCTGTACACTTACTGTTTGTCCTAGATAATCTGATTGTTAGTTGGGCTTTATGTAACAATCATTTACCATTTGACATTTATTAACCTGTTGTTTTTCTGTGTCCTTTAGGCAGAGTCAGATCTCTCTTAATGCAACTGGTGCAGGTAAAACCACACAGAAAACTGAAGCTAATGATGATGCTGCTGCAACAAAGACCAAATCTGCAGAAGCTTCC[C/T]GACTGACCGAAGCAGACAAGGCCAACACTGGCAGAGTATGAGCCAACCGTCTCCTTATGTCAGGACATATTGTTTGTCTGTTTCTGAAAACAACTAATAGTTTGTTGTAAAATCATAGAATTTGAGTCATGTAAATTGAAATGTTTCAAGTTGATTTTGATGTTTTCTAAGTAATATTTTTTTGTGTAGGTGAAGCTGTCTGTGTTTTGGGAATACATGAAGGCTATCGGCTTGCCGCTGTCCATCTTCAGCATCTTTCTGTTCTTCTGTCATCATCTCTCCTCTCTGGGCTCAAACTACTGGCTCAGTCTCTGGACAGATGACCCTGTTGTCAACAACACACAGCCCAAAAGAGAGATGCGTTTAGGGGTTTATGGAGCTCTGGGAATTTCACAAGGTGATTTCACTTCTTTGGTTGTGTGTTTTTGTGTGACATTGCATATATTTGCATTATAATTTGTGAACAACGTTAATGATTTGACTATTTTTACTGAAGGTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40112
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083659 Nonsense 1056 1529 25 34
Genomic Location (Zv9):
Chromosome 3 (position 36454206)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 36594898
GRCz11 3 36736756
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTAGCCTCCCGCTACCTGCACCAGACAATGCTCTATAACGTCCTGAGAT[C/G]ACCCATGTCTTTCTTTGAACGCACACCCAGCGGCAACCTGGTCAACCGCT
Long Flanking Sequence:
AAATGTTGATAATTATATTTTTTGTTGATCAATCATTGTCAATCATTAAAACATTTAGATTTTAGATTTTCATTTTTTTGTCAGACAGATATTTTTGATGAATGCAGTTTAGTATAACCCTTCTTTCTTCAATATATTTTAATAAGCACAAGTCAGAATATATTTGTTGTTTTATTTGTACCTAAATAAGTTACAATGAATGAAACATTTTTGCCAGATTTTGCCATTTTATTTTTACAAATGTTATTTGAAATCTTAAAGGAGACACTTCACTTTACTTTACTTTCATTTAATGTATGAAATATGATTTATTTATTTATTTTGTCCCATGCATATTGTATGTATCTTTATTAAATTGGTTCTAAATCCAGCTTTTTAAACTTTTGTTTGTTTTTCTCTGACAGGCATTGCTGTGTTCTGCTATTCTGTGTCGGTGTCTGTCGGTGGGATCTTAGCCTCCCGCTACCTGCACCAGACAATGCTCTATAACGTCCTGAGAT[C/G]ACCCATGTCTTTCTTTGAACGCACACCCAGCGGCAACCTGGTCAACCGCTTTGCCAAAGAGACGGACACGATCGACTCAGTCATACCTAGCATCATAAAAATGTTCATGGGCTCCATGTTCAATGTTTTGGGCTCATGTGCAGTCATCCTCATCGCCACTCCATTGGTAGCCATCATCATTCCACCATTGGGCCTGCTGTACTTCTTTGTACAGGTCAGTCAGTTTTTTAACCTCTTGTTACACAGTGTTATTGCAGTATGACATTTAGAAATTCATTCGAAGTTTAGTCATTTCCTGGCTCTCTGTTTGTCTCTAGCGTTTCTATGTGGCGTCCTCTCGTCAAATGAAGCGACTGGAGTCTGTGAGCCGCTCTCCAGTCTACACACACTTCAATGAGACGCTGCTGGGCACTAGTGTGATCAGAGCGTTTGGAGAGCAGCAGCGCTTCATCAAGGAGAGTGACGGCAGAGTGGACCACAACCAGAAAGCTTATTTCCCC
Associated Phenotype:
Not determined