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 10:70598417 (forward strand) | View in location tab

Co-located

with COSMIC COSM685468 (G/T) ; HGMD-PUBLIC CM030491 ; PhenCode PRF1base_D0067:g.5759C>T (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4595, 2010_April_001_086_PRF1_170280_0010

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

10:g.70598417G>A
ENST00000373209.2:c.1304C>T
ENSP00000362305.1:p.Thr435Met
ENST00000441259.1:c.1304C>T
ENSP00000398568.1:p.Thr435Met
LRG_94:g.9359C>T
LRG_94t1.1:c.1304C>T
LRG_94p1.1:p.Thr435Met

Variation displays