Original source

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

C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.02 (T)

Chromosome 1:156879126 (forward strand)|View in location tab

Co-located variants

COSMIC COSM5019976, COSM5019975 ; HGMD-PUBLIC CM990977 ; PhenCode KinMutBase_NTRK1_DNA:g.19192C>T (C/T)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 5 synonyms - Show

HGVS names

This variant has 18 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_ExomeChip

About this variant

This variant overlaps 11 transcripts, has 2866 sample genotypes, is associated with 5 phenotypes and is mentioned in 9 citations.

Variant displays