Original source

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

G/A/T | Ancestral: G | Ambiguity code: D

Chromosome 1:156138660 (forward strand) | View in location tab


with COSMIC COSM4023189 (G/A) ; HGMD-PUBLIC CM020736 ; PhenCode HIFD_LMNA:c.1871G>A (G/A), LMNA:c.1871G>T (G/T)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 38 HGVS names - Show

About this variant

This variant overlaps 48 transcripts, has 2 sample genotypes and is associated with 1 phenotype.

Variant displays