Product Details

SNP ID

rs12840364

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:80353147 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCATCTTGCCAGCAGCCCTTGTTTA[C/G]TTTTTAATTGGTTTGTCTTATTCTT

Phenotype

MIM: 300976

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

FAM46D PubMed Links

Gene Details

Gene

FAM46D

Gene Name

family with sequence similarity 46 member D

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001170574.1		Intron			NP_001164045.1
NM_152630.4		Intron			NP_689843.1

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