Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 5:13754203 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM020274

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11779

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

5:g.13754203C>G
ENST00000265104.4:c.10555G>C
ENSP00000265104.4:p.Gly3519Arg

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays