Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.48 (T)
Location

Chromosome 7:95308134 (forward strand) | View in location tab

Co-located

with COSMIC COSM150330 (T/C) ; HGMD-PUBLIC CM930596

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

This variation has 4 HGVS names - click the plus to show

7:g.95308134T>C
ENST00000222381.5:c.575A>G
ENSP00000222381.3:p.Gln192Arg
ENST00000433729.1:c.*300A>G

This variation has assays on 9 chips - click the plus to show

Variation displays