Product Details

SNP ID
hCV25616446
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.20:49945330 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGCCCTTGTTTGGGACTATATTTT[C/G]CCTGTTGCAAGGTCCTCACTAACTT
Phenotype
MIM: 612451
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
RNF114 PubMed Links

Gene Details

Gene
RNF114
Gene Name
ring finger protein 114
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018683.3 Intron NP_061153.1

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