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GAGTGGCCCACAGTTAATTTTCATC[A/T]CTGGTGGGGTTGGCAGAATGTTCAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615189 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ANKRD55 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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ANKRD55 - ankyrin repeat domain 55 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024669.2 | 1299 | Missense Mutation | AGA,AGT | R,S 611 | NP_078945.2 | |
XM_011543646.1 | 1299 | Missense Mutation | AGA,AGT | R,S 384 | XP_011541948.1 | |
XM_017009852.1 | 1299 | Missense Mutation | AGA,AGT | R,S 620 | XP_016865341.1 | |
XM_017009853.1 | 1299 | Missense Mutation | AGA,AGT | R,S 611 | XP_016865342.1 | |
XM_017009854.1 | 1299 | Missense Mutation | AGA,AGT | R,S 458 | XP_016865343.1 |