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CACCTGAGCGGCTGCTACCTCTTGC[C/T]GGAGGCAGTTTCTTCTGGCCTCACC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615370 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ANKS6 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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ANKS6 - ankyrin repeat and sterile alpha motif domain containing 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_173551.4 | 1482 | UTR 3 | NP_775822.3 | |||
XM_005251793.4 | 1482 | Missense Mutation | AGC,GGC | S,G 884 | XP_005251850.1 | |
XM_005251794.4 | 1482 | Missense Mutation | AGC,GGC | S,G 883 | XP_005251851.1 | |
XM_006716998.3 | 1482 | UTR 3 | XP_006717061.1 | |||
XM_006716999.2 | 1482 | Missense Mutation | AGC,GGC | S,G 826 | XP_006717062.1 | |
XM_011518357.2 | 1482 | Missense Mutation | AGC,GGC | S,G 554 | XP_011516659.1 | |
XM_017014445.1 | 1482 | UTR 3 | XP_016869934.1 | |||
XM_017014446.1 | 1482 | Missense Mutation | AGC,GGC | S,G 790 | XP_016869935.1 | |
XM_017014447.1 | 1482 | Missense Mutation | AGC,GGC | S,G 467 | XP_016869936.1 |