Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

Chromosome 18:52752126 (forward strand)|View in location tab

Co-located variant


Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB NC_000018.8:g.48532494G>A

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and is mentioned in 1 citation.

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Somatic mutation displays