ZMP
fat2
Ensembl ID:
Human Orthologue:
FAT2
Human Description:
FAT tumor suppressor homolog 2 (Drosophila) [Source:HGNC Symbol;Acc:3596]
Mouse Orthologue:
Fat2
Mouse Description:
FAT tumor suppressor homolog 2 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2685369]
Alleles
There are 16 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22485 | Nonsense | Available for shipment | Available now |
sa22484 | Nonsense | Available for shipment | Available now |
sa22483 | Nonsense | Available for shipment | Available now |
sa16670 | Nonsense | Available for shipment | Available now |
sa13608 | Nonsense | Available for shipment | Available now |
sa31986 | Essential Splice Site | Available for shipment | Available now |
sa22482 | Nonsense | Available for shipment | Available now |
sa15091 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22485
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014149 | Nonsense | 323 | 4342 | 1 | 23 |
Genomic Location (Zv9):
Chromosome 14 (position 27180635)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 25873837 |
GRCz11 | 14 | 26171082 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTTTTATGATGGTGGCTTTCAGCTGGTCTCAACAAAATTTATTGACTG[G/A]TCACAGAACCCATTAGGACTAAACATTTCTCTTCAGGCCAAAGACAGAAG
Long Flanking Sequence:
GTGGTAATTAAGGAGGACACACCAATCAAGTCGAGCCTGGTGAGAGTGAGTGCAACGGATGCTGATATTGGCAGCAATGCTGAATTTTATTACTCATTCACCACTAGATCACACCCGTTTGCTGTTGATCCTTTCACGGGGACTGTTACACTTGTCAAGAGACTTGACACCAGTCAGAGAGATAGGTATGACCTGACAGTGCTGGCAGAGGACAGGAAAAAGAAAATCTCTGGTGTGCAGAAATTTGGAAATGTAGCAACGGTTGTTGTGAAGATCCAAAAAGTAGAAAAGAATTTCACCCTTATTTCACCAACCACTGCAGAGAGTCTGCTAACGATCGATGACAAAATAAGTGTAAACATCAAGATGGAACCTAAAGAGAAGGAAAACACAGCATCTTTAAGTATAGTTAAAGGAGATCCATTGAATTGCTTTCAGATTATTCCCTCAGCCTTTTATGATGGTGGCTTTCAGCTGGTCTCAACAAAATTTATTGACTG[G/A]TCACAGAACCCATTAGGACTAAACATTTCTCTTCAGGCCAAAGACAGAAGCAACCCTCCTTTGCTAACTCCAATAAAAACTGTGCACATTCCACCTCCTCTTCAAATAAAACCCTTGAGGTTTGAACAAGAACTTTACTATGTAACTCTCAGTGAATTTTCTCCACCAAAAACTCATGTGGTTAGAGTTTCTGTTGGGTTGAGTTTAAAAAACACGACATTCAGCATTCAAGAAAACCCAGATAGCTATAAGTTCAAAATCAGTGCCAAAACTGGTGTAATTGTGACTTCTCAGTCTCTTGACTTTGAAAACCGAAATCATTATGAGTTTGATGTCACAGCAAATGATGGGGAAGCAGTTACTCGTGTCATTGTGGATATAACTGATGAAAATGATAATGCCCCTAGTTTCACTTTACCCTCATACCAGGCTTCTCTGCCTGAAAATGTGCGAATCGGAACAAGTGTCTTATCTGTCTCTGCTATTGATGTGGACAAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22484
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014149 | Nonsense | 757 | 4342 | 1 | 23 |
Genomic Location (Zv9):
Chromosome 14 (position 27179335)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 25872537 |
GRCz11 | 14 | 26169782 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGATAATGACTCTGGATTTAACGGAAAGCTTGTCTATTCAATTTCAAGT[G/T]GAAATGAGGACGGATGCTTTACTATCGATGTGAACGCAGGGGATCTGAAG
Long Flanking Sequence:
CACTTGATTTGGATGAGCTGCAGCAGATCGTATACAGGATAGAGTCTGGAAATGATGATGGACTGTTTTCAATTGACCCTGTTTCTGGCATCATCAAACTGGCTAAGGCCATTCCATCAAACTACAAAGACACAGAAAATTCTTTATATACACTTAAAATAACAGCAACAGATGGCACATATATTGCAGACCCCAACACTGTGACTGTGAGCATCACAGACAATGGCGAAGGTGCCATCACACATTGCGAGGAGACCGGAATTACTAGGCAGTTGACAGAAAAGCTTATTGAGTCCTTTAGGCCATCTCTTAACATAAAAGAAGAGGAGTCCATCTCAGATGTTCATATAATTAACCAGCACTCACCGAAATTTGTCATTAGCACGCCAGGCTCAATTGACATCAGGGAAGACTTTGCTCTCAATAGATCTGTGTTGCAGTTTAATGCCACTGATAATGACTCTGGATTTAACGGAAAGCTTGTCTATTCAATTTCAAGT[G/T]GAAATGAGGACGGATGCTTTACTATCGATGTGAACGCAGGGGATCTGAAGGTTATTTGCGCTTTGGACAGAGAGCAGAAAGAGTTTTACATTCTCAACATAACAGTCTATGACTTGGGATATCCGCAAACCTCTACATGGAAACTTCTTGCTGTTAATATTCTTGATGCAAATGATAATCCTCCATTATTTTCTCAGTCAAGATATGTTGTAACCATCCCAGAAAACACAGAGGTTGACAAAAGCATCTTCAAAGTCAATGCAGTCGACTTCGACTTGGATAACAATGGAGCATTTAAATATTCGCTGTTTACCTTCACAGATTTGTTTCAGATAGAGGAAGACACAGGGGTGGTGAAGGTAATCGGGCCTTTGGATAGGGAAACCTTCAGGAGATATGACCTAACAATTGAGGCCAGAGATCAGGCCAAACCGGATCCACAACTTTTCTCATTTACAGATGTGGTTGTTGTTCTGGAGGACATCAATGACAATCCTCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22483
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014149 | Nonsense | 948 | 4342 | 1 | 23 |
Genomic Location (Zv9):
Chromosome 14 (position 27178762)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 25871964 |
GRCz11 | 14 | 26169209 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATCAAAGTTCCTGAGGATGTTCCTCCAGGCACAGTGCTGCTATGGGTT[G/T]AAAGTTTTGATTTAGATCTGGAGAGCGGCGGTGTCATAAGCTACAACCTG
Long Flanking Sequence:
AGCAGAAAGAGTTTTACATTCTCAACATAACAGTCTATGACTTGGGATATCCGCAAACCTCTACATGGAAACTTCTTGCTGTTAATATTCTTGATGCAAATGATAATCCTCCATTATTTTCTCAGTCAAGATATGTTGTAACCATCCCAGAAAACACAGAGGTTGACAAAAGCATCTTCAAAGTCAATGCAGTCGACTTCGACTTGGATAACAATGGAGCATTTAAATATTCGCTGTTTACCTTCACAGATTTGTTTCAGATAGAGGAAGACACAGGGGTGGTGAAGGTAATCGGGCCTTTGGATAGGGAAACCTTCAGGAGATATGACCTAACAATTGAGGCCAGAGATCAGGCCAAACCGGATCCACAACTTTTCTCATTTACAGATGTGGTTGTTGTTCTGGAGGACATCAATGACAATCCTCCAAAGTTTGTACCCACAGTCTACAAGATCAAAGTTCCTGAGGATGTTCCTCCAGGCACAGTGCTGCTATGGGTT[G/T]AAAGTTTTGATTTAGATCTGGAGAGCGGCGGTGTCATAAGCTACAACCTGAAAAACAGCGAATCAGGAACGTTTTTTCTTGATACATCCACAGGTTCTTTGACTTTGGAGCGGGAATTAGACTTCGAAAAGCGGCAGTTTTATAATTTAACAGTTCGAGCTGTTGACCATGGAAAGCCCCGGTCTTTATCATCTTCGTGTTTTATTGAGATTGAAGTATTAGATGTCAATGAAAACCTGAACCGGCCTCTCTTTGGTGAAATGGTGCATACAGCAGCCGTTATGGAGGATGCTAAAATAGGAACCTCAGTCTTAACACTAACTGCTGTAGATAACGACCTGGGACGAGATGGAGTTGTCAGATACTACATCCATGATGGCTCAGGGCTCGGCGTCTTCACGGTTGATGAAGAAACAGGTATGCGAGTGAATACATTATTTAAAATACACTTTGCACACTTTACTTTGACAGGAAAATACATCATGGATATTACTGACCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16670
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014149 | Nonsense | 1019 | 4342 | 1 | 23 |
Genomic Location (Zv9):
Chromosome 14 (position 27178549)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 25871751 |
GRCz11 | 14 | 26168996 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGACCATGGAAAGCCCCGKTCTTTRTCATCTTCGTGTTTTATTGAGATT[G/T]AAGTATTAGATGTCAATGAAAACCWGAACCGGCCTCTCTTTGGTGAAATG
Long Flanking Sequence:
ATGGAGCATTTAAATATTCGCTGTTTACCTTCACAGATTTGTTTCAGATAGAGGAAGACACAGGGGTGGTGAAGGTAATCGGGCCTTTGGATAGGGAAACCTTCAGGAGATATGACCTAACAATTGAGGCCAGAGATCAGGCCAAACCGGATCCACAACTTTTCTCATTTACAGATGTGGTTGTTGTTCTGGAGGACATCAATGACAATCCTCCAAAGTTTGTACCCACAGTCTACAAGATCAAAGTTCCTGAGGATGTTCCTCCAGGCACAGTGCTGCTATGGGTTGAAAGTTTTGATTTAGATCTGGAGAGCGGCGGTGTCATAAGCTACAACCTGAAAAACAGCGAATCAGGAACGTTTTTTCTTGATACATCCACAGGTTCTTTGACTTTGGAGCGGGAATTAGACTTCGAAAAGCGGCAGTTTTATAATTTAACAGTTCGAGCTGTTGACCATGGAAAGCCCCGGTCTTTATCATCTTCGTGTTTTATTGAGATT[G/T]AAGTATTAGATGTCAATGAAAACCTGAACCGGCCTCTCTTTGGTGAAATGGTGCATACAGCAGCCGTTATGGAGGATGCTAAAATAGGAACCTCAGTCTTAACACTAACTGCTGTAGATAACGACCTGGGACGAGATGGAGTTGTCAGATACTACATCCATGATGGCTCAGGGCTCGGCGTCTTCACGGTTGATGAAGAAACAGGTATGCGAGTGAATACATTATTTAAAATACACTTTGCACACTTTACTTTGACAGGAAAATACATCATGGATATTACTGACCTTCTATTTTACAGTTGCCTTTAGCACATTGGGTCAAGACTGCATGTATAGACATTTCCAGAAAGTTTATTGGCATAACTAACACATGTAAAGACAAAGCGATAAATGGCTTTTTCTGAAAGATTGTAAGAATTTGAAAAGCTATTACTTCAACACCACCTGCCACATTACATGCATTACTCTTTTCTTAAGTACATAATTATTGGGTTGAGTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13608
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 |
---|---|---|---|---|---|
ENSDART00000014149 | Nonsense | 2338 | 4342 | 9 | 23 |
Genomic Location (Zv9):
Chromosome 14 (position 27163869)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 25857071 |
GRCz11 | 14 | 26154316 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTAAGTGGAGTTTTGRTGACTACACAAGTATTGGACTAYGAARGTACA[C/T]AGCAGTYTACTTTAAAAGTGAAAGCCACAGATAAAGGGGTACCACCGCTG
Long Flanking Sequence:
GCATGTACTACCCGTTGAAATTACCTGAGAATATTACTCCTTTTACAACAATCCTGCATGTGCAGGCAAGAAATCCAGAAGGATACCGCCTTATCTACAATCTAGAGGAAGACAACGCCTCCAGGTTATTTAACATCGATTTCAAAACTGGGGTCTTAAGTGTCACTGATTTCCTAGACTTTGAGAGTGAAACAAAGCATATTTTGACTGTTCGTGCCACTGATTCCGTGTCTGGTACATTTGCTGAAGCCAAAGTAGAGATTGACGTGGAAGATATAAACGACAATGCCCCAGTCTTCCAGAATCTTTCTTATGTTGCAGATGTGTTTGAGGGCCTTCCAATAGGCACATCTGTTTTACAAGTCTCAGCTGTTGACAGAGATGCAGACAAGAATGCAGAGGCAACTTACCAACTGATTGACAAAGAGAGTCATTTTTTCGAAATTGACCCTCTAAGTGGAGTTTTGGTGACTACACAAGTATTGGACTATGAAAGTACA[C/T]AGCAGTTTACTTTAAAAGTGAAAGCCACAGATAAAGGGGTACCACCGCTGAGTGGTGAGGCTCACATTATTGTGAACGTCATAGATGTTAATGACAACCCTCCAGATTTTAGCGAGCCATCTTATCGGGCATCTCTTGATGAAATGGCCACTTGTGGCAACATCGTTATCAAAGTTCAAGCATCAGACCCCGATAGTAAGGATGACCTTCAATATAAGATTCTGTCAGGCAATGAAGGCCGATATTTCGCTATTAATGAATCATCTGGACTCATCTCATTCTCTAATGTGTGCAAGAGAAACTTGGATCCATTTTATAACCTCACAGTTGCAGTTTCAGACGGTGTGTTTCAGAAGACTGCCCCCGTTAACATTGACATGACAAATGGCAACAAATACAGCCCCTATTTTACCCAGAACATTTACGAGGCAGATCTGGCAGAGAATGCAGAAGTGGGAACTCGTGTGATCAGACTGGCTGCTATTGACCCAGACGATGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31986
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 |
---|---|---|---|---|---|
ENSDART00000014149 | Essential Splice Site | 3006 | 4342 | 10 | 23 |
Genomic Location (Zv9):
Chromosome 14 (position 27160475)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 25853677 |
GRCz11 | 14 | 26150922 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGGTCCATGTTCTTGACCTCAATGACAACAGTCCTTTCTGTGAGCAA[G/T]TAAGTATGCACTTATTCACTTATTCACTAGGGGCCTCTGCACAGAAATGA
Long Flanking Sequence:
GTGACAAACTGTACATGTTGTATCCGTTTTATATCTTCTAAACGCAAATGTTGTCACTGTTTTGGAGAGCACTAGCTTATAGATATCCTAAAATCTAACAATACTAATTCTAACATCTAACGTTATTTTTATTTTATGGGACCTTTAAAGAAACTGACTTCTGTTATTCCTCTGTGCAGTCTGGTTTTATAGTTCAGCTTTGAAATTTTATTTTTTCTTTGACTGTTGCATAAACAATTTTGCATTGGTAAAGTTGTGTATTTTGGTTTTAAGCAAATACCTTTGGTGTTTCAATCCCTAAAGATGGAGACCCGCTGGGCCAGTTTTCAGTCACAGCGGTAGGGGAGGAGTGGACGGTGATTTCCAAAAGTCCACTTGACAGAGAGGACAAAGACAAATACACTCTAAAAATAATAGCCACGGATGGAAGGTTTCAAACCTCTGCCAATGTGGAGGTCCATGTTCTTGACCTCAATGACAACAGTCCTTTCTGTGAGCAA[G/T]TAAGTATGCACTTATTCACTTATTCACTAGGGGCCTCTGCACAGAAATGAATAAACAAGCAAAACAAAAAACAAAACAAAACAAATAAATGTAGGAAAAACTAAATGATGGCATAGTATCCAGGACTGTTTGGGAAAAAAAAGAAAGAAATGCATTTGTTAAAAAAAAATTCATTCACTAAACATTACCCTCAAATATAAAATCATTCATGCTAGCACATGCTACAGTAGGAATTGTAAAAGTGTTTTGCTTGTTCAGAAAATACAACAGAAAGTTGATTGGTGGCAAACTATTTGATTAGTAAATTAGACCCACATGGAAAATATTTATTTAATAACTTTTACCCTTTTTTTTACAGTTGCAGTACACTGAAGCAGTCATGGAGAATTCTTCATCAGGCAAGGTTATCCTGAAGATCTCTGCTTCAGATCCGGACATTGGAACAAATGGTCAGGTGTCATTCACTCTTCATGGACCTAATGCAGACAAGTTCCATCTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22482
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014149 | Nonsense | 3529 | 4342 | 18 | 23 |
Genomic Location (Zv9):
Chromosome 14 (position 27137624)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 25830826 |
GRCz11 | 14 | 26128071 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATCAACATCACAGAGCAGAGCCGGTATCCACCTACTGTGAATCCGCTT[G/T]AGATTTTCATCACCACTGCTGGTGGTCCAATCTTGAAGAGTGTCATCAGC
Long Flanking Sequence:
GACAGCATGCCAAACAGGCTTTATAATCAATCATTAGCTAAGTGTGAACTCTTGAAACGGTTTTAGTTACAGTACATTCTAAAAGGTTTATGGTTCCCATTAACGTTTTTCAAAATATCTGCTTCAATCTGCTTCAATCTTTAACAGAAGAACAAACACATGCCATACAGGTTTGGAACAATATGAAAGTGAATAAATGATGACACAGTCTTTCATTTCTAAATGAATCACACCTTCAAACAGAATAGAACGAGTACAGTAGTGGTTGTAAACTTGATTGCTATCTGTGAACCAGTGACTTTACCACCATCTTCAATAATTTAAAGAGATACCTTAAAGGTCAGTGCACTGTTCACATGTCACAATACTTTTTTTCACACTTCACATAAATATCATCTCCACAGGTCACTGACAGCGGCCACCCTCCACTGTCCTCTATCTGCGTGGTGAAGATCAACATCACAGAGCAGAGCCGGTATCCACCTACTGTGAATCCGCTT[G/T]AGATTTTCATCACCACTGCTGGTGGTCCAATCTTGAAGAGTGTCATCAGCAAGCTGCACGCTACTGACCAAGATCCCCAAGATGTACTGTCCTACAAGCTGGTCTCCGAGGGCCAGGACAAAGGCCTGTTTTCTGTGGACACAGTTGATGGAAAGATTGTAGTGGAGAAGAACCTGGATCCAGGCCTGTATCACTTGAACGTGAGCGTGACCGACGGGAAATTTAGCATCTGGGCTGGAGTGAAGGTCCATGTTTGGGCTGCCACTCAGCAAAACCTGGATCAGGGCTTCACACTGCAGTTGGCTGGAATTTCTGCAGAAGAATTCGTCTCTGACCACTGGAGAGGCCTCCAACGCAGCCTGGCTCAGGAGTTAAACATACCCCGACAAGAGTTGCACATCGCCAGCTTGCAACAGCAGCCAAACTCTGTCAACACTGAGGTTTTGCTGGTCCGGCGTGCTCAGGATGGTTCCGTTAAGTCTGTGCCTGTTCAACGTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15091
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 |
---|---|---|---|---|---|
ENSDART00000014149 | Nonsense | 4285 | 4342 | 23 | 23 |
Genomic Location (Zv9):
Chromosome 14 (position 27116186)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 25809388 |
GRCz11 | 14 | 26106633 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTGCCCTAATGAGTACACTGCCATAAGCTACTACCCTACCCAGCACGCT[C/T]GAAGCCTGGACAACGTCTCCAGCGGCTATAAGAGACTCAGTGTGCGTCTG
Long Flanking Sequence:
CTGTGGCGACCTCCGAAATAGAGACCAAGCTGGAGGAAAATGAATGAATACTACTGACTCCAAACCTTTTGAACAGCATAAAACATTGAAACAGCACAAACTGTAAAATATGTCCAGAACAAATGTTGTCCGACAAGCCTTATTTACCATCACCGCACTAATGAGCCCTTACTTAAAAAGAACTAATCATTTTTCAACTTTTCTCATTCACAGTGTATCCAGCTGACCCTGACTACTATGGTCGACCCGCCGTTCAGGAGTTCCCTCAATTTGACATTGTGGAAAGCACCTACTCCAATACTTCCACCGAGTCGCGCAGAAACTCTCGCTTCGGAGGTTTTCCTTTCCCGTTGGACCGCGCCGACCGCCGAGCTCCATTACCCCCATGTTACAGCAATCAAAATCTCGATGACTTCTTAGGGCCTGACGGACTGCCGCTGCCTCGCTCTCAGTGCCCTAATGAGTACACTGCCATAAGCTACTACCCTACCCAGCACGCT[C/T]GAAGCCTGGACAACGTCTCCAGCGGCTATAAGAGACTCAGTGTGCGTCTGAGCGTAGCACAGCCTTCCTATGCGGACAGCACACGGCCTGGATCCACTAGAAGGACGTCTCGCAGTTATGCTGGCTCAGATAGGGTGGAGAGCGACTACGGCAGCTGCGAGGAGGTCATGTTTTAGCCAGACGAAAGAGGATCAAAGGTCCCATATGAGAGGGGTTACGGAGGGGAAGGTCATCGTACTTATAGTATATGAAGCTCAATGGCTGAAAGCCGCAGAAGCACTATCAGTATTATTAGTCACTTTCAGGGAAAAAGTATATATGGCTGTGTGGAATGCAAGTTTCCTTGCTGTTTCTTCCTTTTATGCGCCTGTAGAATTAATGCATGGCGGTAAAACAGTCTACAGTGTGGTAGTAAATGATGTTGTTGCTGTGTAGAGATCATGCGCCCTTGTTTGGTGTTGCGAGGTAACATTTTTGACAAGAAAAAACAACTGAATAAG
Associated Phenotype:
Not determined