Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/G/T | Ancestral: C | Ambiguity code: B
Location

Chromosome 10:87933147 (forward strand) | View in location tab

Co-located

with COSMIC COSM5329 (C/A), COSM5219 (C/G), COSM5152 (C/T), COSM308347 (C/-) ; HGMD-PUBLIC CM094223, CM971273

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB Cosmic:5152, 10473, Cosmic:5219

This variation has 18 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and is associated with 5 phenotypes.

Variation displays