Original source

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

Alleles
-/GGT
Location

Chromosome 10: between 77982170 and 77982171 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CI117051

Most severe consequence
 
protein altering variant
Evidence status

Clinical significance

Synonyms

LSDB NM_007055.3:c.3742insACC, NM_007055.3:c.3742_3743insACC

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and is associated with 1 phenotype.

Variant displays