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 2:15945879 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM056658

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4416, 2010_April_001_091_MYCN_164840_0002

This variation has 3 HGVS names - click the plus to show

2:g.15945879C>A
ENST00000281043.3:c.1177C>A
ENSP00000281043.3:p.Arg393Ser

Variation displays