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Human (GRCh37.p13)
Most severe consequence
 
intron variant
Alleles
G/A/C|Ancestral: G|MAF: 0.35 (A)|Highest population MAF: 0.48
Change tolerance
CADD: A:0.019, C:0.012
Location

Chromosome 2:127844161 (forward strand)|VCF:2  127844161  rs10929006  G  A,C

Co-located variant

COSMIC COSV52122972

Evidence status

HGVS names

This variant has 24 HGVS names - Show

Synonyms

ClinGen Allele Registry CA11082104 (A), CA756622533 (C)

Original source

Variants (including SNPs and indels) imported from dbSNP (release 154)|View in dbSNP

About this variant

This variant overlaps 11 transcripts and has 2504 sample genotypes.

Variant displays