Most severe consequence
21
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.
