Original source

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

C/A/T | Ancestral: C | Ambiguity code: H

Chromosome 4:154585711 (forward strand) | View in location tab


with COSMIC COSM1579303 (C/T), COSM1637833 (C/A) ; HGMD-PUBLIC CM0910627, CM930250

Most severe consequence
Evidence status

Clinical significance


LSDB 1934

This variation has 22 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12

About this variant

This variant overlaps 10 transcripts and is associated with 2 phenotypes.

Variation displays