Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 5:1278750 (forward strand) | View in location tab

Co-located

with COSMIC COSM299794 (G/A), COSM299795 (G/A) ; HGMD-PUBLIC CM066607

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_198253.2:c.2177C>T

This variation has 13 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays