Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 9:107584801 (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.107584801T>C
ENST00000374736.3:c.2804A>G
ENSP00000363868.3:p.Asn935Ser

Variation displays