Product Details

SNP ID
rs182102288
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:19412942 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCTCTCTTCTCCTGGCCCAGGAGA[C/T]GTGTCCTGTGAGGGCGGAGCCGCTG
Phenotype
MIM: 601237
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RNF112 PubMed Links

Gene Details

Gene
RNF112
Gene Name
ring finger protein 112
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_007148.4 358 Missense Mutation ACG,ATG T129M NP_009079.2
XM_006721571.3 358 Missense Mutation ACG,ATG T129M XP_006721634.1
XM_006721572.3 358 Missense Mutation ACG,ATG T128M XP_006721635.1
XM_006721573.3 358 Missense Mutation ACG,ATG T105M XP_006721636.1

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