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Select item 10647331.

rs1064733 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 22:50739384 (GRCh38)
22:51177812 (GRCh37)
Canonical SPDI:: NC_000022.11:50739383:C:A,NC_000022.11:50739383:C:G,NC_000022.11:50739383:C:T
Gene:: ACR (Varview), LOC105373100 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,missense_variant,coding_sequence_variant
Clinical significance:: uncertain-significance
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000078/14 (ALFA)
G=0./0 (HapMap)
T=0.000039/3 (TOMMO)
T=0.000047/7 (GnomAD_genomes)
T=0.000076/20 (TOPMED)
T=0.000077/1 (GoESP)
T=0.000079/9 (ExAC)
T=0.000127/10 (PAGE_STUDY)
T=0.000156/1 (1000Genomes_30X)
T=0.0002/1 (1000Genomes)
HGVS:: NC_000022.11:g.50739384C>A, NC_000022.11:g.50739384C>G, NC_000022.11:g.50739384C>T, NC_000022.10:g.51177812C>A, NC_000022.10:g.51177812C>G, NC_000022.10:g.51177812C>T, NW_015148969.2:g.75504C>A, NW_015148969.2:g.75504C>G, NW_015148969.2:g.75504C>T, NM_001097.3:c.191C>A, NM_001097.3:c.191C>G, NM_001097.3:c.191C>T, NM_001097.2:c.191C>A, NM_001097.2:c.191C>G, NM_001097.2:c.191C>T, NP_001088.2:p.Thr64Lys, NP_001088.2:p.Thr64Arg, NP_001088.2:p.Thr64Met

dbSNP