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Select item 29949171.

rs2994917 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 1:120116693 (GRCh38)
1:120659278 (GRCh37)
Canonical SPDI:: NC_000001.11:120116692:G:C,NC_000001.11:120116692:G:T
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000013/2 (GnomAD_genomes)
T=0.010951/32 (KOREAN)
HGVS:: NC_000001.11:g.120116693G>C, NC_000001.11:g.120116693G>T, NW_003871056.3:g.188267G>C, NW_003871056.3:g.188267G>T, NC_000001.10:g.120659278G>C, NC_000001.10:g.120659278G>T

2994917[uid] (1)
SNP
1048598[uid] (1)
SNP
1048597[uid] (1)
SNP
11547853[uid] (1)
SNP
Homo sapiens NFKB inhibitor like 1 (NFKBIL1), transcript variant 1, mRNA
Homo sapiens NFKB inhibitor like 1 (NFKBIL1), transcript variant 1, mRNA
gi|1519311412|ref|NM_005007.4|

Nucleotide

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