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 10:72358804 (forward strand) | View in location tab

Co-located

with COSMIC COSM920026 (G/A) ; HGMD-PUBLIC CM992951 ; PhenCode PRF1base_D0067:g.5128C>T (G/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

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

10:g.72358804G>A
ENST00000373209.2:c.673C>T
ENSP00000362305.1:p.Arg225Trp
ENST00000441259.1:c.673C>T
ENSP00000398568.1:p.Arg225Trp
LRG_94:g.8728C>T
LRG_94t1.1:c.673C>T
LRG_94p1.1:p.Arg225Trp

Variation displays