Original source

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

Alleles
C/A/T | Ancestral: C | Ambiguity code: H
Location

Chromosome 9:104818830 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM021044

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

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

Variant allele A
9:g.104818830C>A
ENST00000374736.4:c.3295G>T
ENSP00000363868.3:p.Asp1099Tyr

Variant allele T
9:g.104818830C>T
ENST00000374736.4:c.3295G>A
ENSP00000363868.3:p.Asp1099Asn

Variation displays