Original source

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


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

Most severe consequence
protein altering variant
Evidence status

Clinical significance


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

This variant has 5 HGVS names - click the plus to show

About this variant

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

Variant displays