Product Details

SNP ID

rs4682357

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:112095870 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCCCAGCCTCACCTAGAGCAGTTCC[A/G]TAGGCATTTTTTGGGGATGATCTTC

Phenotype

MIM: 611956

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

C3orf52 PubMed Links

Gene Details

Gene

C3orf52

Gene Name

chromosome 3 open reading frame 52

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001171747.1		Intron			NP_001165218.1
NM_024616.2		Intron			NP_078892.2
XM_011513133.2		Intron			XP_011511435.1
XM_017007181.1		Intron			XP_016862670.1

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