Product Details

SNP ID

rs201914636

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:58155597 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTGTGTGGGCCTGGTAGTAGCCGC[A/C]TGGGTGGGGGGCTTTGTCCACTCCA

Phenotype

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

MSX2P1 PubMed Links

Gene Details

Gene

MSX2P1

Gene Name

msh homeobox 2 pseudogene 1

There are no transcripts associated with this gene.

Gene

OR4D1

Gene Name

olfactory receptor family 4 subfamily D member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012374.1	444	Silent Mutation	GCA,GCC	A148A	NP_036506.1

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