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rs4646149 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: X:15581590 (GRCh38)
X:15599713 (GRCh37)
Canonical SPDI:: NC_000023.11:15581589:G:A,NC_000023.11:15581589:G:C,NC_000023.11:15581589:G:T
Gene:: ACE2 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
T=0./0 (HapMap)
T=0.00371/14 (1000Genomes)
T=0.00416/20 (1000Genomes_30X)
T=0.02353/4 (PharmGKB)
G=0.5/1 (SGDP_PRJ)
HGVS:: NC_000023.11:g.15581590G>A, NC_000023.11:g.15581590G>C, NC_000023.11:g.15581590G>T, NC_000023.10:g.15599713G>A, NC_000023.10:g.15599713G>C, NC_000023.10:g.15599713G>T, NG_012575.3:g.30621C>T, NG_012575.3:g.30621C>G, NG_012575.3:g.30621C>A, NG_012575.2:g.25569C>T, NG_012575.2:g.25569C>G, NG_012575.2:g.25569C>A

Supplemental Content

4646149[uid] (1)
SNP
Bos taurus chromosome 1 genomic contig, reference assembly (based on Btau_3.1), ...
Bos taurus chromosome 1 genomic contig, reference assembly (based on Btau_3.1), whole genome shotgun sequence
gi|119879628|ref|NW_001493888.1|Bt1 8_3

Nucleotide
Bos taurus integrin subunit beta 5 (ITGB5), mRNA
Bos taurus integrin subunit beta 5 (ITGB5), mRNA
gi|31340754|ref|NM_174679.2|

Nucleotide
10989589[uid] (1)
SNP
43470589[uid] (0)
SNP

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