Product Details

SNP ID
rs73870436
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:149818394 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGTAACTAATTTTGCAGAGCATTT[A/G]AAGGAAGGGACCATGTCTTTCTTAT
Phenotype
MIM: 609247
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
RNF13 PubMed Links

Gene Details

Gene
RNF13
Gene Name
ring finger protein 13
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_007282.4 Intron NP_009213.1
NM_183381.2 Intron NP_899237.1
XM_005247092.3 Intron XP_005247149.1
XM_011512373.2 Intron XP_011510675.1
XM_011512374.2 Intron XP_011510676.1
XM_011512376.2 Intron XP_011510678.1
XM_017005654.1 Intron XP_016861143.1
XM_017005655.1 Intron XP_016861144.1
XM_017005656.1 Intron XP_016861145.1
XM_017005657.1 Intron XP_016861146.1
XM_017005658.1 Intron XP_016861147.1
XM_017005659.1 Intron XP_016861148.1
XM_017005660.1 Intron XP_016861149.1
XM_017005661.1 Intron XP_016861150.1

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