Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 17:15230931 (forward strand) | View in location tab

Co-located

with COSMIC COSM1493766 (G/A) ; HGMD-PUBLIC CM000029, CM991060 ; PhenCode IPNMDB_32 (G/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 13 HGVS names - click the plus to show

Variation displays