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GGTTAGGATCAGCACCATGGTCCAG[A/G]AGCAGCTGCACTGGAAACAGGCAAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613383 MIM: 603692 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ANKRD54 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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ANKRD54 - ankyrin repeat domain 54 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_138797.2 | 980 | Silent Mutation | CTC,CTT | L,L 162 | NP_620152.1 | |
XM_006724136.1 | 980 | Missense Mutation | TCC,TTC | S,F 44 | XP_006724199.1 | |
XM_006724137.1 | 980 | Missense Mutation | TCC,TTC | S,F 31 | XP_006724200.1 | |
XM_011529877.2 | 980 | Missense Mutation | TCC,TTC | S,F 181 | XP_011528179.1 | |
XM_011529878.2 | 980 | Missense Mutation | TCC,TTC | S,F 116 | XP_011528180.1 | |
XM_011529879.2 | 980 | Silent Mutation | CTC,CTT | L,L 64 | XP_011528181.1 | |
XM_011529880.2 | 980 | Missense Mutation | TCC,TTC | S,F 31 | XP_011528182.1 | |
XM_011529882.2 | 980 | Silent Mutation | CTC,CTT | L,L 42 | XP_011528184.1 | |
XM_011529883.2 | 980 | Silent Mutation | CTC,CTT | L,L 29 | XP_011528185.1 | |
XM_011529884.2 | 980 | Silent Mutation | CTC,CTT | L,L 29 | XP_011528186.1 | |
XM_017028590.1 | 980 | Silent Mutation | CTC,CTT | L,L 97 | XP_016884079.1 | |
XM_017028591.1 | 980 | Silent Mutation | CTC,CTT | L,L 42 | XP_016884080.1 | |
XM_017028593.1 | 980 | Silent Mutation | CTC,CTT | L,L 42 | XP_016884082.1 |
GALR3 - galanin receptor 3 | ||||||
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There are no transcripts associated with this gene. |