Original source

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

G/T | Ancestral: G | Ambiguity code: K | MAF: 0.02 (T)

Chromosome 1:156879154 (forward strand) | View in location tab


with COSMIC COSM3750441 (G/T), COSM3750442 (G/T) ; HGMD-PUBLIC CM990978 ; PhenCode KinMutBase_NTRK1_DNA:g.19220G>T (G/T), IPNMDB_538 (G/T)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 6 synonyms - Show

HGVS names

This variant has 18 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 11 transcripts, has 3393 sample genotypes, is associated with 5 phenotypes and is mentioned in 6 citations.

Variant displays