ZMP
polr1a
Ensembl ID:
ZFIN ID:
Description:
DNA-directed RNA polymerase [Source:UniProtKB/TrEMBL;Acc:Q7SXQ2]
Human Orthologue:
POLR1A
Human Description:
polymerase (RNA) I polypeptide A, 194kDa [Source:HGNC Symbol;Acc:17264]
Mouse Orthologue:
Polr1a
Mouse Description:
polymerase (RNA) I polypeptide A Gene [Source:MGI Symbol;Acc:MGI:1096397]
Alleles
There are 10 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa45512 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa12570 | Nonsense | Available for shipment | Available now |
| sa2745 | Essential Splice Site | F2 line generated | Not yet available |
| sa22458 | Essential Splice Site | Available for shipment | Available now |
| sa22459 | Nonsense | Available for shipment | Available now |
| sa1376 | Nonsense | Available for shipment | Available now |
| sa22460 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45512
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
|---|---|---|---|---|---|
| ENSDART00000044708 | Nonsense | 97 | 810 | 3 | 17 |
| ENSDART00000114501 | Nonsense | 97 | 1710 | 3 | 36 |
| ENSDART00000123326 | Nonsense | 97 | 1684 | 3 | 34 |
Genomic Location (Zv9):
Chromosome 14 (position 20098061)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 15862796 |
| GRCz11 | 14 | 16168359 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACGTTATCGTATCACTCACTCCTAATTGTTTTTGTTGCAGAAATTATA[T/A]TTACTCATCCGGGGTTCATGCCTGTCATGTCACATACTGAAGTGTCCAAG
Long Flanking Sequence:
CTAATTAGGACAATCAGATCCAGAAACAATTTTGTTGCCAATTGTCAGTAGAAAAGAAGCCAAATAACTTTGCTCTTAATTACCGCCAATCAACATTGCTCAAAATTGTTTTGTGTATCATCAGCATTACTTTAGTTAATTGGAGATATAAGTAGTTTTACTTGCATATCGAATTTCTAGTGTTTATTGAAATCATCAATTGTTTTAGTGGACACTGTTTTTCTGCTGTTGTTGCTTACTGTACTGTAAAAATCGAAAAATGGGGCATTCATTGTCTGGTGGGTTTCTGCTAATGACACCTTGCTTAAGTAGTGTATAATATTTTTTTGTATACTTGTTTATTTAGATGCATTTATTTAGATGTGGTGAAAAATGTCTTGGTTTAGACCCTTGCAACATAGTCTTTTAAAGATTTGTGATAAGATTGTGGATCTTGATCCAGCCTAAACAAAACGTTATCGTATCACTCACTCCTAATTGTTTTTGTTGCAGAAATTATA[T/A]TTACTCATCCGGGGTTCATGCCTGTCATGTCACATACTGAAGTGTCCAAGAGCAGCTATTCATTTACTGCTGTGCCAGCTGAAGCTCCTGGACGTGGGGGCCATGAAGGAGGTGTTTGAGATTGAAAACGTTCTCAATCAGGTCAGAAATTCCCAACAGTCTCGCGTCATTAAAGGAAAAAGGCATCATTAATTAGACTACAGTGCTTTTATATTGTGTTTTTGTTGTCTCTCTTAGTTTTTGGAATCCAACCCCAGCCCACCTGGAGAAGAAATCCAAGAAACTCTGAATGACTTTGTTAAACCCATCCTCGAAACCAGAAAAGACAAGCAACACACTGACCCTGTGAGTTTGAAACTCATCTGTTTTGTCTTTTATATTAATCATATTTGTATATATATTTTTACATCTTAAACATTTATGACTTCAGGTCAAGCACATCTGTGAGAAAAAGTCCAGTCTCATTACCAGTTTCTGGAGAATACATATGGGCCCAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12570
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044708 | Nonsense | 112 | 810 | 3 | 17 |
| ENSDART00000114501 | Nonsense | 112 | 1710 | 3 | 36 |
| ENSDART00000123326 | Nonsense | 112 | 1684 | 3 | 34 |
Genomic Location (Zv9):
Chromosome 14 (position 20098106)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 15862841 |
| GRCz11 | 14 | 16168404 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTATATTTACTCATCCGGGGTTCATGCCTGTCATGTCACATACTGAAGTG[T/A]CCAAGAGCAGCTATTCAYTTACTGCTGTGCCAGCTGAAGCTCCTGGACGT
Long Flanking Sequence:
CAGTAGAAAAGAAGCCAAATAACTTTGCTCTTAATTACCGCCAATCAACATTGCTCAAAATTGTTTTGTGTATCATCAGCATTACTTTAGTTAATTGGAGATATAAGTAGTTTTACTTGCATATCGAATTTCTAGTGTTTATTGAAATCATCAATTGTTTTAGTGGACACTGTTTTTCTGCTGTTGTTGCTTACTGTACTGTAAAAATCGAAAAATGGGGCATTCATTGTCTGGTGGGTTTCTGCTAATGACACCTTGCTTAAGTAGTGTATAATATTTTTTTGTATACTTGTTTATTTAGATGCATTTATTTAGATGTGGTGAAAAATGTCTTGGTTTAGACCCTTGCAACATAGTCTTTTAAAGATTTGTGATAAGATTGTGGATCTTGATCCAGCCTAAACAAAACGTTATCGTATCACTCACTCCTAATTGTTTTTGTTGCAGAAATTATATTTACTCATCCGGGGTTCATGCCTGTCATGTCACATACTGAAGTG[T/A]CCAAGAGCAGCTATTCATTTACTGCTGTGCCAGCTGAAGCTCCTGGACGTGGGGGCCATGAAGGAGGTGTTTGAGATTGAAAACGTTCTCAATCAGGTCAGAAATTCCCAACAGTCTCGCGTCATTAAAGGAAAAAGGCATCATTAATTAGACTACAGTGCTTTTATATTGTGTTTTTGTTGTCTCTCTTAGTTTTTGGAATCCAACCCCAGCCCACCTGGAGAAGAAATCCAAGAAACTCTGAATGACTTTGTTAAACCCATCCTCGAAACCAGAAAAGACAAGCAACACACTGACCCTGTGAGTTTGAAACTCATCTGTTTTGTCTTTTATATTAATCATATTTGTATATATATTTTTACATCTTAAACATTTATGACTTCAGGTCAAGCACATCTGTGAGAAAAAGTCCAGTCTCATTACCAGTTTCTGGAGAATACATATGGGCCCAAAAAAATGCCAGAATTGCAAGTAAGCTGATCTTTTCCTTCATCTTAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2745
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
|---|---|---|---|---|---|
| ENSDART00000044708 | Essential Splice Site | 264 | 810 | 7 | 17 |
| ENSDART00000114501 | Essential Splice Site | 276 | 1710 | 8 | 36 |
| ENSDART00000123326 | Essential Splice Site | 264 | 1684 | 7 | 34 |
Genomic Location (Zv9):
Chromosome 14 (position 20102256)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 15866991 |
| GRCz11 | 14 | 16172554 |
KASP Assay ID:
554-2769.1 (used for ordering genotyping assays)
KASP Sequence:
GACTCCGAGTGTGGCACGAGAACACATCATCAAACTTTGGGAGACAGAAG[G/A]TAGGATTGATTGAGTTTATTTATCATTTCTTTTTGGTTTTACAGTGCAAA
Long Flanking Sequence:
GGTGCAGCTTCCAATCCTCGTCGATGTAGAGCAAAGTAAGGCTTAAGAATGAGTCCATCTTCCTACTTGACCAGAGATCAGATAGAAATCAGCCACAGCTTTTAACAGAGCGCTGTCACGTGATATGTAGGGAACGTAATTGAAAAAAATCAACCTGGAAAAATTAGATCGATTACAAGTTCGGATGATTTCAATTACTTTTCAATTAATCGCCCAGCCCTAGTGGAGTGTTTTTTTTAAATATGTATATACAAGAGACTTTTGTGACAGTGAAGTTGAATTCAGACTAGTATAGTGCATAAAATCTCATGCATAATGGGATCCTGTGATTTTTATTTTTTAATTATTATTATTTTTTTAAATTGAGATCTTTAGGAGTTGGCGTTTGTAAACATCTATTCATTTACCATTGCTTTCAGATGATTCCCAATTGACCAAACGTATATTCCTGACTCCGAGTGTGGCACGAGAACACATCATCAAACTTTGGGAGACAGAAG[G/A]TAGGATTGATTGAGTTTATTTATCATTTCTTTTTGGTTTTACAGTGCAAATGTAATAGGTTTTCTGAAATAATTCATTATGACTTTCAGGTTTTTTCCTGAAGCATTTGTTCTCAGGGTTTGACATGGACAACTCTGATAATGGCTTTAATCCTGAAGTTTTTTTCTTGGAGCTGCTGGTGGTTCCTCCATGCAGGTCAGCTTTTCAGTGTTTGTACTAGGGCTGCACAATGTATAATTTTAGCATTAAAATTGGATTTTACAATGTTTTTTTTAGTATTTTTCAAATGTTAAGTTGTATTTCTAGCTGAGCAGGAGCTACAGCACATAAGAGTTGTGGAGTCACTGCAGAGTTTAACCAGAATACAGTGAAAGTTTATTATGTGCATGTGTTTTTAAAGCCTGGGTGAGCATTCAGATACAAGAAACTTTAACTTTTATTATACTCCTTTAAGCAATGAAAACTAAGCAGTGTTTTTTTTTTTTACATTTGATTAATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22458
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044708 | Essential Splice Site | 530 | 810 | 12 | 17 |
| ENSDART00000114501 | Essential Splice Site | 542 | 1710 | 13 | 36 |
| ENSDART00000123326 | Essential Splice Site | 521 | 1684 | 12 | 34 |
Genomic Location (Zv9):
Chromosome 14 (position 20110197)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 15874932 |
| GRCz11 | 14 | 16180495 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAACTCCTGACACCCAGCACTGGCCAGCACAGGATACCCATGAAAATTG[T/A]GAGTCGGTTATCTTTGACAGAAACACACTGTTTTTGACATACATTTCAGT
Long Flanking Sequence:
AATACCAATTGAACTTAAGTCTAGTCTCGTAAATGCATGTGTGGACCTGCACCTGTGCCTTGATATACGCCCCTTCCATGTTCTTTCAGCCCCTTCCATTTCAGCTGATCCGCGTATCTCTAATACACATTGACATATTTTGGAGGAGGCATGAAACTAGCTTCCCATTGTCTGCACTGAAATATCAAATTACAAAAGTATTTGATTGTGATTTTTGCTGTTTTGTTTAATTGTTTTTTTTTTTTATTATTTATTATTATGGTTCCTCTAGGTTTTTGCTACCAAGTTGACATATCCTCAACCTGTGACACCCTGGAACGTAAAGGAAATGAGGCAGGCAGTGCTGAATGGACCCAACATCCACCCTGGAGCCACCATGGTTGTTAATGAAGACGGGTCCCGCACTATTCTCAGCAGTACCAATCAGACCCAAAGAGAAGCTGTCGCCAAACAACTCCTGACACCCAGCACTGGCCAGCACAGGATACCCATGAAAATTG[T/A]GAGTCGGTTATCTTTGACAGAAACACACTGTTTTTGACATACATTTCAGTGTCACTACTTTTCTCAATATCTGTGCCGTTTGTTAACAAATCTAATATCTTTAAACCCCTTTGCACTTATTTTTACCTAATTATCCCAACGACTCCCTTATGATTTGTTCAGTGATTCAATTGTTCCCAAACTTCTCCTTAGCACAATGCTAATCTGCTGTGATTGGTCCGATGACCCAGTCTGTTGTGATTGGTCAACCGGTTTCAACACGATTCAGAGAAACGCCTATCATGGCTATGAAGTAGCAAAGAGTGTGTGAGAACCCAATACAGATATACATTAAAGCAATTCAGTTAAACACCACCATATTACTCTACTCATAACCCTAACCCCAAGTAATAACAACGACACACATTCAGTATTAATCCACACAGTGGCAAAGTTGAACTATGTTGAAAATTGACAGCACCATGCATGTGAGGAACAGCTGATGGTTGCCATAGCAAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22459
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044708 | Nonsense | 781 | 810 | 16 | 17 |
| ENSDART00000114501 | Nonsense | 793 | 1710 | 17 | 36 |
| ENSDART00000123326 | Nonsense | 772 | 1684 | 16 | 34 |
Genomic Location (Zv9):
Chromosome 14 (position 20115244)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 15879979 |
| GRCz11 | 14 | 16185542 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGACTAGTGGGAAACTGCTTAGCTGTCTGGCACGGCTCTTCACTGCCTA[T/A]CTGCAGCTTTACCGCGGGTTTACTTTGGGTAAATCCACATCGATGCCAAC
Long Flanking Sequence:
CCAAACAAACCACGCCAAAAGGAAAAATGAACTCTAGTGCGATTCTACCGAACAAGATAAGGCAGATGTGAAAACCCTTTGACACCTTTTTCATCCAAGTTTTCCCCAGAGATTTTCAGTCAGGTTTTAATTGAGACTTTAGGCTAGCCATTTTAATATATTCAGCTTCAAAGAATGGTTTTACTCTATTTGCTGTGTGACAGTGGACGATTCCCTGCATAAAATTAATTAATTAGTATCCGATTGACTTCTTAGTTTGCATACTACAGCTTAAAAGACTTGCCTGTAGCAGTTTATCTTGACTGTTCCCTGGTATTATTGATTCTTATATGCTCTGTTTGTCAGGTGGTCATTCGTCAGGGAGAGCTCTTGATGGGGGTTCTGGATAAAGCTCACTATGGGAGCTCAGCGTATGGTCTGGTCCACTGCTGCTATGAACTCTATGGAGGAGAGACTAGTGGGAAACTGCTTAGCTGTCTGGCACGGCTCTTCACTGCCTA[T/A]CTGCAGCTTTACCGCGGGTTTACTTTGGGTAAATCCACATCGATGCCAACCCATCTTGTTAAACAGAGAGCTGTAAAATTATTTTGTATTAATCTGTCATTTGTGTCTGATAGGTGTGGAGGACATTCTTGTAAAGGATGGAGCCAACAAACAAAGAAAAAAAATCATCAAAAAGTCAGTCACATGTGGCTCCAAGGTGAATTACTCAGATCCAGCACTCACTCTTTGTGCCTTTTTGAAATATGTAAATCAGTGTTTTGAAAAATGAGTAGTTCTTTTAAATAATGAAATGTATATTAACTTTCAGAAATATGTGCTCAATCTGCTCAAATTGATGAAATTTTGCTAGAAATTTTATTAATATATTACTAATTGTAATATTACTACAGAATGGTTGTTGACACATTGTCATTTTAAACAAAAACTAAAAAAACTAAATTTGTAAATTATGGATAATTTATGCACCTATCTGGTCTAGATCTTATTTGTGTAATGTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1376
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044708 | None | None | 810 | None | 17 |
| ENSDART00000114501 | Nonsense | 1487 | 1710 | 32 | 36 |
| ENSDART00000123326 | Nonsense | 1461 | 1684 | 30 | 34 |
Genomic Location (Zv9):
Chromosome 14 (position 20133691)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 15898426 |
| GRCz11 | 14 | 16203989 |
KASP Assay ID:
554-1288.1 (used for ordering genotyping assays)
KASP Sequence:
CTACTGAGAGCCAACAGAGAGTTAACTCTGAACAGCCGAAGGGAAGCTCA[C/T]AGGGCTCAGTGAGGATCAACTCTGTGCTGCAGTTAAGCGCTGCTATTGAG
Long Flanking Sequence:
TTACAACCAAGATATGACCCTATTTCATGTATAATATGGGCTCTTTAAAAATTCAGTACTGATTGGTATCAAATTCCAGTATTGTGACAAACACTATTGTTTTTCATAATATTTGTTTTATCTACTATGGATGTCAATTGTTAGCAGTTTCCACCATTTTCTAGAATATATTTTTTGTTTTTGAACAGAAAAAAAAGTTTGAAACCATTTAAGGTTAAAGTACAGTAAATGGTGAGATGTCGTCAATTTTTGTGTTATATAGTGTAATCCTTCTATATTTTATTTCAGACATGTACATTTTATAGCACAAGAGCTAGTAAAGTTGTATTGTCTGTGCTGTGATTCCTCAGGTAGACTATGAGAGCGAGGAGGGAGAGGAAGGCAGTGATCAGGAGCAGGAGGAAGTGGCTGAGGAACAGGAGGCGTCTCAGGAGGTCTCTGAGGAAGGGTCTACTGAGAGCCAACAGAGAGTTAACTCTGAACAGCCGAAGGGAAGCTCA[C/T]AGGGCTCAGTGAGGATCAACTCTGTGCTGCAGTTAAGCGCTGCTATTGAGGACTACAAATATGACACCAAAAAAGGACTGTGGTGTGAGGTGTGTATAAATAAATTGATCTTCATTTAGGGTCGTTGTTATTGAAACATTTCAGAGTCTTTGAGAGTGCATTGGATGGATTTGTAATAGTTTTTTTTAATGCTGTAGTCTTCCAGTATCAATTAGTTATATGTAGTATCAGTGTTTACCAGACCAGCAGTGTTCGGTAGAGTTACTTTTAAAAGTAATGCATTACAATGTTGAGTCACTCCCCAAAGAAGTATCTAGTTAAGTTACTTAGTTACTTTTTATGGTAAGTAATGCTTTAACTTACTTTTGAGTTATTTTTGCGTTGCGAACTTGTTTTTTTTTTCTGTTTTAATTAAAGGAGCTCTGCGATTAACAACGCACTGTATAACCTACACCTATTTACCTTAAAAAACACATTAAAATATATATTTTAGAATAATG
Associated Phenotype:
This allele has been associated with this phenotype by genetic linkage analysis and may not be causal.
See FAQs for more info.
See FAQs for more info.
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Hatching:Long-pec ZFS:0000033 |
blood ZFA:0000007 |
quality PATO:0000001 |
abnormal PATO:0000460 |
| Hatching:Long-pec ZFS:0000033 |
brain ZFA:0000008 |
quality PATO:0000001 |
abnormal PATO:0000460 |
| Hatching:Long-pec ZFS:0000033 |
extension ZFA:0000106 |
decreased size PATO:0000587 |
abnormal PATO:0000460 |
| Hatching:Long-pec ZFS:0000033 |
eye ZFA:0000107 |
decreased size PATO:0000587 |
abnormal PATO:0000460 |
| Hatching:Long-pec ZFS:0000033 |
hindbrain ZFA:0000029 |
hydrocephalic PATO:0001853 |
abnormal PATO:0000460 |
| Hatching:Long-pec ZFS:0000033 |
inner ear ZFA:0000217 |
decreased size PATO:0000587 |
abnormal PATO:0000460 |
| Hatching:Long-pec ZFS:0000033 |
melanocyte ZFA:0009091 |
quality PATO:0000001 |
abnormal PATO:0000460 |
Mutation Details
Allele Name:
sa22460
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044708 | None | None | 810 | None | 17 |
| ENSDART00000114501 | Nonsense | 1537 | 1710 | 33 | 36 |
| ENSDART00000123326 | Nonsense | 1511 | 1684 | 31 | 34 |
Genomic Location (Zv9):
Chromosome 14 (position 20137672)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 15902407 |
| GRCz11 | 14 | 16207970 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATGCCGATCACTAAAGTGCACTTTGACCTCACCTCAGTGGTGGTGAAA[C/T]AGGCTCAGAACGCGGTCATCATGGAGACCAAGGGCATCACGCGCTGTTTG
Long Flanking Sequence:
AATCAAAGCAGCAAATTACACTGAAGAATGAAAACTCCATCACATTAAAAGATTGCATTCTTAAGTACTTTTTATGAATTATTATCTATTACTTAACATTATTATGTTTTGTGTATTACATGCTTGCCAACAATTATTTAAATGCTAACTAATGCAGTGCGTTACCACATTTGCCATATTACAGGACGTATATGTTGTATATAAATGACTGTAATAGACAGAGATATTTGCATAAATTCAAATTGCAGCTATATATAATGTATGTATATTTAGGTATGCATACTGATTATGTAAGTGTATGTGTGTGTGTGTCATTTGTGATAGTACCCATATTTAATCAAATTTGCAAATAAAAAATTCAAAGAAGAGTATCGGTATTTCTCAACAATTGATGGTAAACGTGTTGCTATTCATAATGCTTTGCTGTGTCTGTTTAACAGTTAACCCTGGTCATGCCGATCACTAAAGTGCACTTTGACCTCACCTCAGTGGTGGTGAAA[C/T]AGGCTCAGAACGCGGTCATCATGGAGACCAAGGGCATCACGCGCTGTTTGTTAAATGAAGTGACCAGAAAAGACGGAAGCAAAGAGATTATGCTCAACACAGAAGGCATCAACATTCATGAGATGTTCAAATATGCTGATGTAAGTCAAATACACCATATACAGGGCTTGACATTAACTTTTTTGTTCACCAGCCACTGTTCTAGTTGGGAAAATATGTTTTATATGCATAAATTTGACTTTAATGTACTAAAATGACTTGATTTAGATGGTGTGTTTTGTCCACATGCCTTCTCATTCACTTAACTTCTTGTGTGTATTGTGTATTAGCTTGCTCAGTGTGCATGAGCAAATGGGTTGTCGCAATGCAATCAGTTTTTATTTCTATTATTTATGACTTTTCAGGGCTCAAGATTAAGGATTTACTAAATTTTTCTCTGACCACACCAAATAAGTATTTCTAGCCACAATGTTTTATTGTGTCAAAACAAGGAAAATATC
Associated Phenotype:
Not determined