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Select item 102058331.

rs10205833 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 2:37179537 (GRCh38)
2:37406680 (GRCh37)
Canonical SPDI:: NC_000002.12:37179536:C:A,NC_000002.12:37179536:C:G,NC_000002.12:37179536:C:T
Gene:: SULT6B1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.26877/13109 (ALFA)
T=0./0 (KOREAN)
G=0.205993/110 (MGP)
C=0.208469/128 (Vietnamese)
G=0.226852/49 (Qatari)
C=0.236238/1708 (Korea4K)
G=0.236473/236 (GoNL)
G=0.249731/3248 (GoESP)
G=0.25/76 (FINRISK)
G=0.257654/993 (ALSPAC)
G=0.259821/1164 (Estonian)
C=0.260498/20174 (TOMMO)
G=0.264024/979 (TWINSUK)
G=0.271667/163 (NorthernSweden)
G=0.279167/67 (PharmGKB)
C=0.286842/109 (SGDP_PRJ)
G=0.294234/43825 (GnomAD_genomes)
G=0.310537/82196 (TOPMED)
G=0.347957/42226 (ExAC)
G=0.35/14 (GENOME_DK)
C=0.368421/14 (Siberian)
G=0.418645/2681 (1000Genomes_30X)
G=0.42492/2128 (1000Genomes)
HGVS:: NC_000002.12:g.37179537C>A, NC_000002.12:g.37179537C>G, NC_000002.12:g.37179537C>T, NC_000002.11:g.37406680C>A, NC_000002.11:g.37406680C>G, NC_000002.11:g.37406680C>T, NM_001032377.2:c.336G>T, NM_001032377.2:c.336G>C, NM_001032377.2:c.336G>A, NM_001032377.1:c.336G>T, NM_001032377.1:c.336G>C, NM_001032377.1:c.336G>A, NM_001367551.1:c.450G>T, NM_001367551.1:c.450G>C, NM_001367551.1:c.450G>A, NP_001027549.1:p.Leu112Phe, NP_001027549.1:p.Leu112Phe, NP_001354480.1:p.Leu150Phe, NP_001354480.1:p.Leu150Phe

dbSNP