Product Details

SNP ID

rs17118378

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:56208214 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAGCTGACGTCTTCTCCAGCTCTGC[A/G]ATGCGTGTCTGCTGCTGCTGTACCA

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	878	Silent Mutation	ATC,ATT	I149I	NP_001229755.1
NM_005785.3	878	Silent Mutation	ATC,ATT	I149I	NP_005776.1
NM_194358.2	878	Silent Mutation	ATC,ATT	I78I	NP_919339.1
NM_194359.2	878	Silent Mutation	ATC,ATT	I149I	NP_919340.1
XM_005268561.4	878	Silent Mutation	ATC,ATT	I78I	XP_005268618.1
XM_011537734.2	878	Silent Mutation	ATC,ATT	I78I	XP_011536036.1
XM_011537735.2	878	Silent Mutation	ATC,ATT	I78I	XP_011536037.1

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