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 14:23418398 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM050708

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB MYH7_3981C_A_061711

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 8 transcripts, is associated with 3 phenotypes and is mentioned in 2 citations.

Variant displays