Original source

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

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

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

Co-located variants

COSMIC COSM4023189 ; 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

Synonyms

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