Most severe consequence
 
Frameshift variant
Alleles
A/-|Ancestral: A
Location

Chromosome 11:68911553 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM034527, CD035789 ; PhenCode IPNMDB_890 (A/-)

HGVS names

This variant has 8 HGVS names - Show

Variants with equivalent alleles
Original source

PhenCode is a collaborative project to better understand the relationship between genotype and phenotype in humans (release 04/2014)|View in PhenCode

About this variant

This variant overlaps 5 transcripts.

Variant displays