Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.03 (T)
Location

Chromosome 20:62819980 (forward strand) | View in location tab

Co-located

with COSMIC COSM1559579 (C/G) ; HGMD-PUBLIC CM014050

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 7 HGVS names - click the plus to show

20:g.62819980C>T
ENST00000489045.2:n.353C>T
ENST00000343916.4:c.307C>T
ENSP00000341640.3:p.Arg103Trp
ENST00000477612.2:n.303C>T
ENST00000452372.1:c.196C>T
ENSP00000394280.1:p.Arg66Trp

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni2.5

Variation displays