Product Details

SNP ID

hCV25642057

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:143629295 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCACCAGGAGGACTTCGAATGGGA[A/C]CCAAAGGAGTGGTGAATGTAATGGC

Phenotype

MIM: 300562

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

SLITRK4 PubMed Links

Gene Details

Gene

SLITRK4

Gene Name

SLIT and NTRK like family member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001184749.2	2040	Missense Mutation	GGT,GTT	G605V	NP_001171678.1
NM_001184750.2	2040	Missense Mutation	GGT,GTT	G605V	NP_001171679.1
NM_173078.4	2040	Missense Mutation	GGT,GTT	G605V	NP_775101.1

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