Product Details

SNP ID
rs146802529
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:120546418 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTTGCTTTCAGATGGAAAGAACTC[C/T]AGTGGATCCAAGCGTTATAATCGCA
Phenotype
MIM: 615998
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RNF10 PubMed Links

Gene Details

Gene
RNF10
Gene Name
ring finger protein 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014868.4 674 Silent Mutation TCC,TCT S57S NP_055683.3
XM_005254013.2 674 Silent Mutation TCC,TCT S7S XP_005254070.1
XM_006719717.2 674 Silent Mutation TCC,TCT S57S XP_006719780.1
XM_017020282.1 674 Silent Mutation TCC,TCT S7S XP_016875771.1
XM_017020283.1 674 Silent Mutation TCC,TCT S57S XP_016875772.1

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