Original source

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

C/A | Ancestral: C | Ambiguity code: M | MAF: 0.15 (A)

Chromosome 19:33301725 (forward strand) | View in location tab


with COSMIC COSM3756627 (C/A)

Most severe consequence
Evidence status

Clinical significance


LSDB NM_004364.3:c.690G>T

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 1093 individual genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variation displays