This variant has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A/C/T | Ancestral: G | Ambiguity code: N | MAF: < 0.01 (A)
Location

Chromosome 1:156881590 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM990981 ; PhenCode IPNMDB_447 (G/C), KinMutBase_NTRK1_DNA:g.21656G>C (G/C)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

This variant has 57 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip, Illumina_HumanOmni5

About this variant

This variant overlaps 30 transcripts, has 2506 sample genotypes and is associated with 3 phenotypes.

Variant displays