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GGTCTGCCACCGTGATCCTCGGGGT[C/G]ACCTCCTCGGTGCCCTCCCTGCCAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
FAM71F2 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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FAM71F2 - family with sequence similarity 71 member F2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001012454.5 | 348 | Silent Mutation | GTC,GTG | V,V 81 | NP_001012457.3 | |
NM_001128926.3 | 348 | Silent Mutation | GTC,GTG | V,V 72 | NP_001122398.1 | |
NM_001290254.1 | 348 | UTR 5 | NP_001277183.1 | |||
NM_001290255.1 | 348 | UTR 5 | NP_001277184.1 | |||
XM_011516128.2 | 348 | Silent Mutation | GTC,GTG | V,V 81 | XP_011514430.1 | |
XM_011516129.2 | 348 | Silent Mutation | GTC,GTG | V,V 81 | XP_011514431.1 | |
XM_011516130.2 | 348 | Silent Mutation | GTC,GTG | V,V 81 | XP_011514432.1 | |
XM_011516131.2 | 348 | Silent Mutation | GTC,GTG | V,V 81 | XP_011514433.1 | |
XM_011516132.2 | 348 | Silent Mutation | GTC,GTG | V,V 72 | XP_011514434.1 | |
XM_011516134.2 | 348 | UTR 5 | XP_011514436.1 | |||
XM_011516135.2 | 348 | UTR 5 | XP_011514437.1 | |||
XM_011516136.2 | 348 | UTR 5 | XP_011514438.1 | |||
XM_017012147.1 | 348 | UTR 5 | XP_016867636.1 | |||
XM_017012149.1 | 348 | Silent Mutation | GTC,GTG | V,V 81 | XP_016867638.1 |