Original source

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

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

Chromosome X:3615831 (forward strand) | View in location tab


with COSMIC COSM108888 (G/A) ; ESP TMP_ESP_X_3533872_3533872 (G/A)

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB NC_000023.9:g.3543872G>A

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 4 transcripts, is associated with 1 phenotype and is mentioned in 1 citation.

Somatic mutation displays