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 | MAF: 0.01 (C)
Location

Chromosome 3:165830741 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM890021

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

3:g.165830741T>C
ENST00000482958.1:c.293A>G
ENSP00000419804.1:p.Asp98Gly
ENST00000264381.5:c.293A>G
ENSP00000264381.3:p.Asp98Gly
ENST00000479451.3:c.107+6573A>G
ENST00000488954.1:c.107+6573A>G
ENST00000497011.3:c.293A>G
ENSP00000419505.1:p.Asp98Gly

This variation has assays on 8 chips - click the plus to show

Variation displays