Original source

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

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

Chromosome 9:104822520 (forward strand) | View in location tab

Co-located

with COSMIC COSM301590 (T/C) ; HGMD-PUBLIC CM990006

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 3 HGVS names - click the plus to show

9:g.104822520T>C
ENST00000374736.5:c.2804A>G
ENSP00000363868.3:p.Asn935Ser

Variation displays