Product Details

SNP ID
rs77240208
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:149813021 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GACGCCTGCCCCACCCTGCTCTTCC[C/T]TTCCAGGGAAGACGGATCACGCGGC
Phenotype
MIM: 609247
Polymorphism
C/T, 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_007282.4 283 UTR 5 NP_009213.1
NM_183381.2 283 UTR 5 NP_899237.1
XM_005247092.3 283 UTR 5 XP_005247149.1
XM_011512373.2 283 UTR 5 XP_011510675.1
XM_011512374.2 283 UTR 5 XP_011510676.1
XM_011512376.2 283 Intron XP_011510678.1
XM_017005654.1 283 UTR 5 XP_016861143.1
XM_017005655.1 283 UTR 5 XP_016861144.1
XM_017005656.1 283 UTR 5 XP_016861145.1
XM_017005657.1 283 UTR 5 XP_016861146.1
XM_017005658.1 283 UTR 5 XP_016861147.1
XM_017005659.1 283 UTR 5 XP_016861148.1
XM_017005660.1 283 UTR 5 XP_016861149.1
XM_017005661.1 283 Intron XP_016861150.1

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