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 13:23324452 (forward strand) | View in location tab

Co-located

with COSMIC COSM1365850 (G/A) ; HGMD-PUBLIC HM040058 ; PhenCode SGCG:c.787G>A (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_064_SGCG_608896_0008, 16019, NC_000013.9:g.22796591G>A

This variation has 6 HGVS names - click the plus to show

13:g.23324452G>A
ENST00000218867.3:c.787G>A
ENSP00000218867.3:p.Glu263Lys
LRG_207:g.148532G>A
LRG_207t1:c.787G>A
LRG_207p1:p.Glu263Lys

Variation displays