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 | MAF: < 0.01 (T)
Location

Chromosome 1:173914725 (forward strand) | View in location tab

Co-located

with COSMIC COSM899818 (C/T) ; HGMD-PUBLIC CM890016

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

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

1:g.173914725C>T
ENST00000494024.1:n.462G>A
ENST00000367698.3:c.236G>A
ENSP00000356671.3:p.Arg79His
ENST00000617423.1:c.236G>A
ENSP00000478688.1:p.Arg79His

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni5

Variation displays