ZMP
LOC100333724
Ensembl ID:
Human Orthologue:
ITPR1
Human Description:
inositol 1,4,5-triphosphate receptor, type 1 [Source:HGNC Symbol;Acc:6180]
Mouse Orthologue:
Itpr1
Mouse Description:
inositol 1,4,5-triphosphate receptor 1 Gene [Source:MGI Symbol;Acc:MGI:96623]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10895 | Nonsense | Available for shipment | Available now |
sa31844 | Essential Splice Site | Available for shipment | Available now |
sa35136 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21954 | Essential Splice Site | Available for shipment | Available now |
sa21953 | Nonsense | Available for shipment | Available now |
sa12719 | Nonsense | Available for shipment | Available now |
sa27817 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21952 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10895
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031993 | Nonsense | 235 | 2782 | 7 | 61 |
Genomic Location (Zv9):
Chromosome 11 (position 36810974)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 35708202 |
GRCz11 | 11 | 35970185 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAAGATTGTTTTATTTAWGAAGTGGAGCGACAACAAGGAGGCYATTCTT[A/T]AAGGGGTAGATGACCTATGAAATGTCATTTTTTTNYAAGATATGATGCTT
Long Flanking Sequence:
TTTTTACACAGTTTTTTTTAACTACCTCACACGTTTCTGTTAATATTATTAAAGCAATGGCTAATCAGAGATGTAGTTCTGTTGAGCTGCATACTTTCAAATTCTCTCACCATCAGCACCAGCAAACTCCTGAAACTATGAACTAAGGGAATCATTTTGCGGCGTCAGTGATTAAAACTGGAGTTTCAGCATAACTAATGCTTGACTAACGACACAGACGGACATGTTCTGACGAGACATTCCTTCAATTAAAATGATTTTATTTGTAATCAATTTATAAACAGATGTTGTCCACAAATCCTGAATCTGAACATCCTGACTCTTTATGCTCTGGTAACTCTCATTTCAGAGCCAGAATGACTCTGTAGTGTGAAATGTAGTTTGTATTAAGTGCTGTTTTTTCCCTCTGTGTTTCTCCTCAGGTGAACTCGGTGAACTGCAACACGAGCTGGAAGATTGTTTTATTTATGAAGTGGAGCGACAACAAGGAGGCTATTCTT[A/T]AAGGGGTAGATGACCTATGAAATGTCATTTTTTTTCAAGATATGATGCTTCTGTAGTAATTGCATCTCTGTGGTTGTTTAGGGGGACGTTGTTCGGCTGTTTCACGCGGAGCAGGAGAAGTTTCTGACCTGCGATGAGCACCGGAAGAAGCAGCACGTGTTTTTGAGAACCACCGGCCGTCAGTCCGCCACCTCTGCCACCAGCAGCAAAGCATTGTGGGAAATAGAGGTGAGTTTTAAAGTTGTATCTGTCGGGGTGATTGTCACAGATTAACACAACCTAAATGAGTTTGGCCTGAATATAATGTGAATCTGGCTGAATAGATTGAAGTAGTGGGAGTATAAACAGTGCTGTATAAGGAGTTGTAAAAAATAAAGCTGCAAGCAGCGATGAAAGGGACCTCGCACCTGGGTTTAAGCTGACATATATATATATATATACACCATTCTTCATATATAAATAGACTTCAACTATATATATATATATATATATATATATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31844
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031993 | Essential Splice Site | 342 | 2782 | 11 | 61 |
Genomic Location (Zv9):
Chromosome 11 (position 36806290)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 35703518 |
GRCz11 | 11 | 35965501 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTGTTTCCTGCTTCAGGTGGCAGATTTTTCACCCTTTAACTTCCAGG[T/C]ACAGTCAATCTCTCAAACGGCTCTCACTACTGTACCTTCATGTTCATCTC
Long Flanking Sequence:
ACTTGTCAGTGATTACTGGTCTTTAAAAATAGTTTCTGCTACAATCAAAAGCATTTTTAAGAGCGATGAACACCTGTTATTTACAATAGGACCAAAATTTTGCATTTAGTGCACTTGAAGCTTTTCAGAAGGGGAAATACTGTGTTAATGTCAAGTCTTCAAAAAAAAAAAAAAGATGAAAAAATCTTGCTATGCAGGTAAACCATGTTCAAAGATCAGGCCCTGACTATCTTGATTAGCTTGTGCCCACAAGTCTATCAGTTTCCTGCTGATTTCTCAGATTTCGTTGCACAATTTAAGGATGTTTTTGGTGTCTTTTTGCATTCACAGGTCAATCCTGACTATGAGGAAGAATCGCAGGAATCCCGTTCATCTGTAAGCAGTCAAATAGCTGTCGTTCTTGTGTTTGTGCTTTTGCTTTGTGTGAAGGCAAATAAACTGTTGGCTGTGTTTCTGTTTCCTGCTTCAGGTGGCAGATTTTTCACCCTTTAACTTCCAGG[T/C]ACAGTCAATCTCTCAAACGGCTCTCACTACTGTACCTTCATGTTCATCTCAGATGCCTAAATCAAAAGATGCCTCTTATCTTGAAGTTTTGTGCAGCATTGTGCTTTTGTCAAGTGTTTGTGCATTTTGTGCCATTTAAAAATTTCATTTGATTTTCTTTTTAGGCTTTGGTGGTTTTCTTTGGTTCTCATTTAACAAATGATTATAACTATTATTTAAATCTGTAGATACAGTGGGTTATAATTAAAGGGGTGGTCCAGAATTTATTTTAAGGCTTGGTTGTGTTTATAAGATGCAAAGCAATGTGTGCTCATGCTTCACTTTACTTTTTTTTCATCTTACTTTGATTATATACAGCTACTCCGCTATCATGAAAACGACATATTTCCTAGTAACGACATATTTCCTAGTTCCTCCAAAGGCCCGCCCTCAAGAGACTCTGATTAGTCAGAAATCATAATGTGCTGTGATTCGTGGATCGGTTCCATGTCACCAGGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35136
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031993 | Essential Splice Site | 987 | 2782 | 23 | 61 |
Genomic Location (Zv9):
Chromosome 11 (position 36775444)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 35672672 |
GRCz11 | 11 | 35934655 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACATTCTGGTGATGGATACCAAGCTAAAAATCATAGAGATATTACAGG[T/C]GATTACAAACATTAAATAGTGGAACATGGAATAGCAATTAAATTTCAATA
Long Flanking Sequence:
CCTCATTTACTTCGGCTTTTACAACTTCAGCGACTTGTTACGTTTGACGAAGATCCTTTTGGCCATTTTGGACTGCGTTCATGTCAGCACCATTTATCCCATCAACAAGATGGAAAAAGGAGATGAGTCCAAAAGTAAATCTTCACACTCTTGATCTTTAATATTATAATAATTTAGGTTTATTTGGTAGATCAGCAGCTCAACTTTCAATATTGATATTGTGTATTATAATCAGACAATTGCTAATTGTTTGAAACAGATATGTTGCCTGAGAGGTGTTTAACAATTGGTTGGTTTTATTTCTGCAGGTAGTAATGTAATGAAGTCCATTCATGGTGTTGGTGAGCTGATGACTCAGGTGGTGCTGAGAGGAGGCGGATTCTTACCCACAACCCCTACAACACCTCCAGATGGAGATGTAGTGAAGACCCAGACAGAACCAGAGAAAGAAGACATTCTGGTGATGGATACCAAGCTAAAAATCATAGAGATATTACAGG[T/C]GATTACAAACATTAAATAGTGGAACATGGAATAGCAATTAAATTTCAATAAAAAATAAATAAATAAATAAACATTTTATTTTAAGCATTGCTATTCTGTGGTTTTATAGCGCTTAAAATATTTATTTATTTATTTATTTATATTTTAATCATTGCTACTCTATTGTTTTATAAGGCTTAAAATATTTATTTATTTATTTATTTATATTTTAATCATTGCTACTCTATTGTTTTATAGGGCTTAAAATATTTATTTATTTATATTTTAATCATTGCTATTATATGTTTTTTTAGGGCTTAAATGTTTTATTTTATTTTAATCATTGCTATTCAATGGTTTTATAGGGCTTAAAATATTTTATTTTATTTTACTTTATTTTAGACTTTTGGGACTTCAGCCTGAGGAACCCTAATTTCAGCAGTTAGTAAAAACAGAGTAGAAATCTGTTAACATTTTTTTTGTCATGTCTCTCTTGTTATTCAGTTCATTCTGAATGTTCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21954
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 |
---|---|---|---|---|---|
ENSDART00000031993 | Essential Splice Site | 1188 | 2782 | 28 | 61 |
Genomic Location (Zv9):
Chromosome 11 (position 36771129)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 35668357 |
GRCz11 | 11 | 35930340 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAAAGACGGACGGAAATGGCAGTGACAATTACAGAGACGTAAAAGAGG[T/A]AAAGTGTCTTTCACACGCACGCACATTTAGCTTTGTGTAGCAGTCAGCGG
Long Flanking Sequence:
ACAATCCTTTAAAACATTTTTTTGTTTTATTTAATTTTAGAACTTCTTAAATAGAGCTTTAACTTACATTTGTTAATAATTATGTTATTATTAACATGATTATTAGTATTATATTTTAATAATTACAGTTAACTTAAAATCTAACAATATTGCATGATATAACATTTATAAATATTAAAATAATTCATAAAAAATATTTTATGTAATTAACTACCTGGCTGTAGCCTAATTTGATATAATTGGTAAAATACATTAATATATTTTGTATTTTGTAAGCTGTCTTATGTTCTGTTTTTGTAAGGTCTATTTTATTTTAAAACTTCTCTCACCTTTTCTTTGGGACCTTGAAACTGTTATTAATTAAATTCAATGCATCATTCACACTTCATCCACACACTTTATTTAGCCCTCGTGTTTATTCCTTTTCTAGAGGGACTCTGGCTCAGACAAAAAAAAGACGGACGGAAATGGCAGTGACAATTACAGAGACGTAAAAGAGG[T/A]AAAGTGTCTTTCACACGCACGCACATTTAGCTTTGTGTAGCAGTCAGCGGTTATATTGCCATTCACCATAAACACTGGCAAAGCTATTTATGTGGCCTCCTTTTCTAAAGTTGATCTAATTAGCCAGTGCTGAAGTGTTCATCTAGAGGAATTAACTCCACATGAACTGTCGAAGAGTGTTTGAGCTCTTCTTTTTCTCCTGTTTGAAATAAACCCAAATATACATAAAAGACACTTTTGAAATGTTGTTTTTAAGACCAGGCATTAACAGACTTAATATTCCAGATGCCGAATCGGTCACTTTTGGTTGACTCATTTGTACAGTGCTCAACATAAATAAGTAAACATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTTTCAGTGAATATAGGTCATCTATTTTGTGCATTTGAACAAAGCAGATTTATCAAACAGATATATTTATTAACAATAGTGTTTTAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21953
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031993 | Nonsense | 1468 | 2782 | 33 | 61 |
Genomic Location (Zv9):
Chromosome 11 (position 36757565)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 35654793 |
GRCz11 | 11 | 35916776 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAGCAATCACATGTGGAAGCTCTTTGAAAACTTTCTGGTCGACATATG[C/A]AGGGTAACGAAAGCTTATTCGGGGATTTTTAGCAACCCCAATTATTTGTT
Long Flanking Sequence:
GTATTTAAAAATGGAAATAACATACATATTTTGACCTGTACTTGAACTAAGTTCTACTTTTTGGATATAGATTGTTATTTCACTGATTAAACATGTATTACTAAAAAATAGGCTAAACTTAGTTATTTAAAACCTAGTGGCAAAAGTGGTACAGGTTTAAAATGGCATTAATTAGTACTGTGGGTATGCAGAGCAATGTTCTTGAACCCATATCAAATGTTTCTAGTTCTAAATATGCCTGACTATTTTTTATTTAATTTTTCTATGAAATTATCCTCACACTGAATGACATTTTAATTGGTGTCTTTTGTAAGTCATACTAAATATGTGTGATATAATCGTTTTCATACTTGAAAACTTCTTTACATCCCATCTTAGGTCAAAATAGCATACATCAACTTCCTGAACCATTGCTACGTGGACACAGAGGTGGAAATGAAGGAGATTTACACCAGCAATCACATGTGGAAGCTCTTTGAAAACTTTCTGGTCGACATATG[C/A]AGGGTAACGAAAGCTTATTCGGGGATTTTTAGCAACCCCAATTATTTGTTTAGCTGTGAAGTACAAAAAAAGTACCAATCTCTTGCTCGCTATCTTGAAACCAACATCAATTAAATGTTGCTGATTGCCTGTGTTTTTCAAAAAGACAAAAAGGAGTGATTCAATTTGTGTGGTATTATATGGGTTTGATGTATGATTTCTTATCATCTGAAACTGATGTGACATTTATTTTGGTGCAGGAAAGACGTGAATGAGTGTTTGTTCTGACTGTACAAATACCTCAATCTCTTAATTATTCTCCTTTCTATGGTTGTTTTCATCCAGGTCTGCAACAATACAAGTGACCGCAAACATGCTGACACGACACTAGAAAGCTACGTGACTGAAACCGTGATGAGTATTGTGACGACATTTTTCAGCTCCCCTTTCTCCGACCAGAGCACTAGTTTACAGGTAATGACCCCAATACAGCACAACATGTAAATATATATACTTGGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12719
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 |
---|---|---|---|---|---|
ENSDART00000031993 | Nonsense | 1883 | 2782 | 44 | 61 |
Genomic Location (Zv9):
Chromosome 11 (position 36685802)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 35583030 |
GRCz11 | 11 | 35845013 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTCAGAGAAGTTCTTYAAGGTGTTTTACGAGCGRATGAAACTCGCCCAG[C/T]AGGAGATCAAGGCCACAGTGACGGTGAACACCAGCGATCTAKSCAGCAAA
Long Flanking Sequence:
CATAAACTGTTATCAATTGTACAAAGATCTCACAAAGATAATATAATAATAGTTTATGTAATAATATAGATATATAATTATAGGTTTTATTGTATTTTGCTGTATATTATTGTAATATACAATAATATTGTTATTAAGGCATATATAATATTACAGTGCAACTAAACTTACAATTACATGTATTTATCTTGTTTATTTATCATGGTTTTGGAATTTAACTTGTTTATTAGTATAATTTGTGCTTAGATGTCAGTAATTGTTTGATTTTTATCTCATTCTAAAGGTCTAATATTATTATTATGATAAACTAAATGTTGACTATTATTTGTGCACAAAAATGTCCAGATTCAGGGGAAAAGACTTTTTTTTTTTTGTATACATCTATACACAGTATCTGTCTTCTTACCTTCCTACAGCGGTCGTTCTTCTGCCGCTTGACGGGTGATAATAAGTCAGAGAAGTTCTTTAAGGTGTTTTACGAGCGGATGAAACTCGCCCAG[C/T]AGGAGATCAAGGCCACAGTGACGGTGAACACCAGCGATCTAGGCAGCAAACGCAAAGATGAGGACACCAATGATAAGGATGTACAATCACGCAAGAAAGGTCAGGACTAATCGTAACAAGTAGTCGAAATCTAATGATCTAAAGTTTTGCAATTAGTTAATCGCCACGTCTATGCTATATTGAAAAAAAGTGATATGCTATAGCATGCTAAATAGTGTCATAATCAATATGTGGACTGATTTATTGACCTTAAAATTGTTTTTTTAAAAAATGAAAAACTGCTTGAGTGCATTATAAACTACAGACAAATGCACATCATGCTACACAAACATAATCCTCTCTATCTCTCAGTCAAAGATGTGGCTGTTATAACCGAAGAAGTGCGAGAGCAGCTACTAGAAGCCTCTACGGTCACTAAGAAGGCCTTCAGCACTTACAGAAGAGAAGCGGACGCGGATGAGCATCTGAATGCTACGGAGGGACCAAGCAGCACAGCTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27817
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031993 | Essential Splice Site | 2337 | 2782 | 52 | 61 |
Genomic Location (Zv9):
Chromosome 11 (position 36670273)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 35567501 |
GRCz11 | 11 | 35829484 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTTGGTAGCATTCTTCTATCCACTGGAAGGTGGAGGTGTCCGTGGAGG[T/C]GAGACAAATTTTTTTTTTTATGTTTGACGTGAAGTTTTATGTGTAATATT
Long Flanking Sequence:
TGGTCATCTGGATACTTGAAGTATTAATTAACATTTCTTAGATAGTATTGTGAGGGATGCAGCCATCAAAACTCAAATGTATTGCAATTTGGATTTCCTCCACTAGGTGCATGAATGTTCACACTAGAGTATTCGCAACTGAATTTGAACATTAACAGAAAGTTCCAATAAAACTCTATAACTGTCGGTTTATGCCAGAACCACTTGTGTGAAGCTCTGACATGGTGTGCATCAGGGCTTTAGTGTTAGACCCTTTTATTTTTGTGATAGTATCCAAATGAACATTGTGGGATGATGTGTTTTGTGTTGTGTTGGTGTGCATTGTCTTTTAACACTTGGAATTGAATTTTTAACTTGCTGCCTCCTCCAGCTCAGCCCATCCTGTACTGGTGTTCCCGTAACATGTCCTTTTGGAGCAGCATTTCCTTTAACCTCGCCGTCCTCATGAACCTCTTGGTAGCATTCTTCTATCCACTGGAAGGTGGAGGTGTCCGTGGAGG[T/C]GAGACAAATTTTTTTTTTTATGTTTGACGTGAAGTTTTATGTGTAATATTAAACTGATTTTTACAGTGGTGGAAAAATATTGAACACGTCACCATTATTCTCAGAAAACATTTTTAAAGGTGCTGTTGACTTGAAATTTTTACTGGATGTTGGTAACAACTAAATAAATCCATGTATGCAAAAAACCCATTTCAAATTAGTTTACAAATGAAGTTATATTTAATAAAAAAGTATTGAACACATGAAGAAAGGGAGGTGTAGAAAGGCAGGGAAAACCCAGACAGAAGTTGAAATTTCTCTGTAGTTCTTTAGCAGCCCTCTGCCCTTCGTCATTGTAAATTAGCTGCTTCAGTCCAACATCTACATTAGCAGGATGATAAGGATGAAACCAGAGTGGACATTTCAGCAAGACAATGATCCCAAACACAGCCAAGGAAACTCTCAAATGGTTTCAGGGAAAGAATGTTGAATTTTTATGTGTGTATTGTTTGGGCTTTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21952
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031993 | Essential Splice Site | 2450 | 2782 | 54 | 61 |
Genomic Location (Zv9):
Chromosome 11 (position 36655247)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 35552475 |
GRCz11 | 11 | 35814458 |
KASP Assay ID:
2260-4544.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATATGCAGCCTTGGGGTCTTCGTTCACGTCTTCTTCTATAGTTTACTT[G/T]TGAGTACAAACACAAGCGCTCATTCACTCCAGCTCATCTTTCACACATCG
Long Flanking Sequence:
CCTCCTTGCTGAAGGAATGATTTAAGTTTCCAAAATAAAAGAGATTGTATTTTTTCCTGCAAAACTCAAAATGAGCTTACATCTTTTTATTATATTCAAAACATTTGAAGTTTATTTTTTTCTTTTGCTTTAGAAAAATCAGCAGAAAGCTTATGTTCAAATAATGACATCTCATTAACTTTATGGAAACATCTTATAACTGTCACATTAAAAAACACTTCAATCTCAGGTTGCATTCAATTGTAGGCTACTAAAATAACTGTTCTCATTGTTGCTTATCATTACACAAGAGAGAGAGCTAAAAATCTGTGGTCAAACTTTGCTGTTGTTTTCAGGTGGGCAATAAAGTGATCTTCCTAATGAGTTTTGTGGGCAATCGGGGCACGTTCACGAGAGGATACAAGGCCATGATCATGGACGTGGAGTTCCTGTATCATCTGCTGTACCTCATCATATGCAGCCTTGGGGTCTTCGTTCACGTCTTCTTCTATAGTTTACTT[G/T]TGAGTACAAACACAAGCGCTCATTCACTCCAGCTCATCTTTCACACATCGACCTCTGACCTCTCACACTTTCACTGACACTGTTTCCCAGTTCTGGGTTGGGGCTGGAAGGGCATCCGCTGCGTAAAACATATGCCGGATTAGTTGCTGATTCATTCCTCTGTGGTGACCCCTAATAAATAAGACACTAAGCCAAAGGAGAGTGAATGAATGAACTATTCTGTTTAGAAATCTTCTTACTATTAAACAAAACTATACTGGAGGGCTAATAATTTTGAACGGCTAATAATTCTGACTTCAACTGTATTTTTAGAATGGGCGTCTCTTCTAACACACACACACACACACACACATACACACAAGCACACACACACACACACACGCGCTTTCATTCACCCCATCCCAGCTTTAACATATGGACGTCTCTTCTAACTCTGACCTCTGACCTCTCGCACTTTCACCGACACTGTATACACACACACACACACACACACACACACA
Associated Phenotype:
Not determined