Product Details

SNP ID
rs9998092
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:40423286 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTAAAATAAGGTCTTGCGATTGCTT[C/T]AAAGAAAGCTTTATTTACTACATAC
Phenotype
Polymorphism
C/T, 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 4798 UTR 3 NP_001092104.1
NM_019027.3 4798 UTR 3 NP_061900.2
XM_005248103.3 4798 UTR 3 XP_005248160.1
XM_005248107.3 4798 Intron XP_005248164.1
XM_005248108.3 4798 Intron XP_005248165.1
XM_005248109.4 4798 Intron XP_005248166.1
XM_011513704.2 4798 Intron XP_011512006.1
XM_011513707.2 4798 Intron XP_011512009.1
XM_011513708.2 4798 Intron XP_011512010.1
XM_017008304.1 4798 Intron XP_016863793.1
XM_017008305.1 4798 Intron XP_016863794.1
XM_017008306.1 4798 Intron XP_016863795.1
XM_017008307.1 4798 Intron XP_016863796.1
XM_017008308.1 4798 Intron XP_016863797.1
XM_017008309.1 4798 Intron XP_016863798.1
XM_017008310.1 4798 Intron XP_016863799.1

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