Product Details

SNP ID
rs200667147
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:19412609 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGAGAGGTTGCGCGACCCCATCTC[A/G]CTGGACTGTGGCCACGACTTCTGCA
Phenotype
MIM: 601237
Polymorphism
A/G, 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_007148.4 179 Silent Mutation TCA,TCG S69S NP_009079.2
XM_006721571.3 179 Silent Mutation TCA,TCG S69S XP_006721634.1
XM_006721572.3 179 Silent Mutation TCA,TCG S69S XP_006721635.1
XM_006721573.3 179 Silent Mutation TCA,TCG S45S XP_006721636.1

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