This variant has been flagged

Variation has more than 3 different alleles

Original source

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

C/A/G/T | Ancestral: C | Ambiguity code: N

Chromosome 14:28768479 (forward strand) | View in location tab


with HGMD-PUBLIC CM100366 ; PhenCode RettBASE_FOXG1:c.1200C>G (C/G)

Most severe consequence
Stop gained
Evidence status

Clinical significance


This variant has 2 synonyms - Show

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 21 transcripts, 1 regulatory feature and is associated with 3 phenotypes.

Variant displays