Product Details

SNP ID

rs140354506

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:40425954 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGGGGACCTGAATGGCAGCAGCAG[A/G]GAAGGCCTGAGGTATGTAGCCTGCG

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RBM47 PubMed Links

Gene Details

Gene

RBM47

Gene Name

RNA binding motif protein 47

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001098634.1	2563	Missense Mutation	CCT,TCT	P578S	NP_001092104.1
NM_019027.3	2563	Missense Mutation	CCT,TCT	P509S	NP_061900.2
XM_005248103.3	2563	Missense Mutation	CCT,TCT	P578S	XP_005248160.1
XM_005248107.3	2563	Missense Mutation	CCT,TCT	P578S	XP_005248164.1
XM_005248108.3	2563	Missense Mutation	CCT,TCT	P578S	XP_005248165.1
XM_005248109.4	2563	Missense Mutation	CCT,TCT	P578S	XP_005248166.1
XM_011513704.2	2563	Missense Mutation	CCT,TCT	P578S	XP_011512006.1
XM_011513707.2	2563	Missense Mutation	CCT,TCT	P578S	XP_011512009.1
XM_011513708.2	2563	Missense Mutation	CCT,TCT	P578S	XP_011512010.1
XM_017008304.1	2563	Missense Mutation	CCT,TCT	P578S	XP_016863793.1
XM_017008305.1	2563	Missense Mutation	CCT,TCT	P578S	XP_016863794.1
XM_017008306.1	2563	Missense Mutation	CCT,TCT	P578S	XP_016863795.1
XM_017008307.1	2563	Missense Mutation	CCT,TCT	P578S	XP_016863796.1
XM_017008308.1	2563	Missense Mutation	CCT,TCT	P578S	XP_016863797.1
XM_017008309.1	2563	Missense Mutation	CCT,TCT	P577S	XP_016863798.1
XM_017008310.1	2563	Missense Mutation	CCT,TCT	P509S	XP_016863799.1

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