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SNP ID

rs143849049

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:82043191 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAAGATGCGGATGGCCTGAGTGACC[A/G]CGGTGTGGCAGACCGGGCACTCGGG

Phenotype

MIM: 611008

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MEX3B PubMed Links

Gene Details

Gene

MEX3B

Gene Name

mex-3 RNA binding family member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032246.4	2117	Missense Mutation	GCG,GTG	A560V	NP_115622.2

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