Most severe consequence
28
intron variant
Alleles
A/T|Ancestral: A|Highest population MAF: 0.39
Change tolerance
CADD: T:8.431|GERP: -4.93
Location
Chromosome 4:61996246 (forward strand)|VCF:4 61996246 rs56038622 A T
Co-located variant
COSMIC COSV72229370
Evidence status 
HGVS names
This variant has 5 HGVS names - Show
Synonyms
This variant has 2 synonyms - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 156)|View in dbSNP
About this variant
This variant has predicted consequences for 4 transcripts, has 3009 sample genotypes and is mentioned in 2 citations.
