Product Details

SNP ID

rs150070833

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:56208169 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCGTGTCTTGGGGCCTACCTGCTC[C/T]GCCAGCTGGTGTTTGTGTTCAGCTG

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

RNF41 PubMed Links

Gene Details

Gene

RNF41

Gene Name

ring finger protein 41

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001242826.1	923	Silent Mutation	GCA,GCG	A164A	NP_001229755.1
NM_005785.3	923	Silent Mutation	GCA,GCG	A164A	NP_005776.1
NM_194358.2	923	Silent Mutation	GCA,GCG	A93A	NP_919339.1
NM_194359.2	923	Silent Mutation	GCA,GCG	A164A	NP_919340.1
XM_005268561.4	923	Silent Mutation	GCA,GCG	A93A	XP_005268618.1
XM_011537734.2	923	Silent Mutation	GCA,GCG	A93A	XP_011536036.1
XM_011537735.2	923	Silent Mutation	GCA,GCG	A93A	XP_011536037.1

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