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
Location

Chromosome 5:41842685 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM005410

Most severe consequence
Clinical significance

Synonyms

LSDB 10159

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

5:g.41842685C>T
ENST00000509987.1:c.103G>A
ENSP00000425348.1:p.Val35Met
ENST00000196371.7:c.661G>A
ENSP00000196371.5:p.Val221Met
ENST00000514723.1:n.73G>A

Variation displays