Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 10:70598885 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM992953 ; PhenCode PRF1base_D0067:g.5291G>A (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4592, 2010_April_001_083_PRF1_170280_0007

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

10:g.70598885C>T
ENST00000373209.2:c.836G>A
ENSP00000362305.1:p.Cys279Tyr
ENST00000441259.1:c.836G>A
ENSP00000398568.1:p.Cys279Tyr
LRG_94:g.8891G>A
LRG_94t1:c.836G>A
LRG_94p1:p.Cys279Tyr

Variation displays