Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [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 IPNMDB_538 (G/T), KinMutBase_NTRK1_DNA:g.19220G>T (G/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

This variation has 18 HGVS names - click the plus to show

This variation has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 11 transcripts, has 1982 individual genotypes, is associated with 5 phenotypes and is mentioned in 6 citations.

Variation displays