Product Details

SNP ID
rs74105323
Assay Type
Functionally tested
NCBI dbSNP Submissions
5
Location
Chr.1:95244131 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTCATGAAAAATAAATTGACATTT[C/G]AGACAAAAGTTTGAACTTGCTGGTG
Phenotype
MIM: 615875
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
RWDD3 PubMed Links

Gene Details

Gene
RWDD3
Gene Name
RWD domain containing 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001128142.1 Intron NP_001121614.1
NM_001199682.1 Intron NP_001186611.1
NM_001278247.1 Intron NP_001265176.1
NM_001278248.1 Intron NP_001265177.1
NM_015485.4 Intron NP_056300.2
Gene
TMEM56-RWDD3
Gene Name
TMEM56-RWDD3 readthrough
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001199691.1 Intron NP_001186620.1

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