Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Co-located

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

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

This variant has 38 HGVS names - click the plus to show

About this variant

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

Variant displays