Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
T/A/G | Ancestral: T | Ambiguity code: D
Location

Chromosome 4:54727447 (forward strand) | View in location tab

Co-located

with COSMIC COSM1260 (T/G), COSM1257 (T/A), COSM36302 (T/C) ; HGMD-PUBLIC CM077194, CD982724 ; dbSNP rs67104871 (T/-)

Most severe consequence

This variation has 3 synonyms - click the plus to show

This variation has 16 HGVS names - click the plus to show

Variation displays