Product Details

SNP ID

rs201745426

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:56207695 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTCTCCTCCAGGTTCTGAAGGTTGG[A/G]GTTGACACTGCGGATTGCACGCATG

Phenotype

Polymorphism

A/G, 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	984	Missense Mutation	CCC,TCC	P185S	NP_001229755.1
NM_005785.3	984	Missense Mutation	CCC,TCC	P185S	NP_005776.1
NM_194358.2	984	Missense Mutation	CCC,TCC	P114S	NP_919339.1
NM_194359.2	984	Missense Mutation	CCC,TCC	P185S	NP_919340.1
XM_005268561.4	984	Missense Mutation	CCC,TCC	P114S	XP_005268618.1
XM_011537734.2	984	Missense Mutation	CCC,TCC	P114S	XP_011536036.1
XM_011537735.2	984	Missense Mutation	CCC,TCC	P114S	XP_011536037.1

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