Original source

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

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

Chromosome 10:72360469 (forward strand) | View in location tab

Co-located

with COSMIC COSM386287 (G/C) ; HGMD-PUBLIC CM992949 ; PhenCode PRF1base_D0067:g.3463C>T (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_079_PRF1_170280_0003, 4588

This variation has 8 HGVS names - click the plus to show

10:g.72360469G>A
ENST00000373209.2:c.190C>T
ENSP00000362305.1:p.Gln64Ter
ENST00000441259.1:c.190C>T
ENSP00000398568.1:p.Gln64Ter
LRG_94:g.7063C>T
LRG_94t1.1:c.190C>T
LRG_94p1.1:p.Gln64Ter

Variation displays