Original source

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

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

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


with COSMIC COSM1260 (T/G), COSM36302 (T/C), COSM1257 (T/A) ; 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

About this variant

This variant overlaps 8 transcripts.

Variation displays