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ATTTGGCAAGGATGTGCAGGAAGGT[A/G]GACTTCCCATCCACTGTCTTGGTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610639 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GRID2IP 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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GRID2IP - Grid2 interacting protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145118.1 | 3183 | Silent Mutation | TCC,TCT | S,S 1061 | NP_001138590.1 | |
XM_011515404.2 | 3183 | Silent Mutation | TCC,TCT | S,S 877 | XP_011513706.1 |