This variation has been flagged

Variation has more than 3 different alleles

Original source

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

T/A/C/G | Ancestral: T | Ambiguity code: N

Chromosome 4:54727437 (forward strand) | View in location tab


with COSMIC COSM1221 (T/G), COSM1216 (T/A), COSM1219 (T/C) ; HGMD-PUBLIC CM005329

Most severe consequence

This variation has 5 synonyms - click the plus to show

This variation has 24 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts.

Variation displays