Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 10:74082499 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM062022

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 27237

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

10:g.74082499C>A
ENST00000478896.2:n.332-18555C>A
ENST00000211998.5:c.829C>A
ENSP00000211998.4:p.Leu277Met
ENST00000372755.4:c.829C>A
ENSP00000361841.3:p.Leu277Met
LRG_383:g.89386C>A
LRG_383t1.1:c.829C>A
LRG_383p1.1:p.Leu277Met

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays