Original source

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

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

Chromosome 1:158655080 (forward strand) | View in location tab

Co-located

with COSMIC COSM1335249 (G/A) ; HGMD-PUBLIC CM910358, CM910359

Most severe consequence
Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 10 HGVS names - click the plus to show

Variation displays