Product Details

SNP ID
rs111483466
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:120546441 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCAGTGGATCCAAGCGTTATAATC[A/G]CAAACGTGAACTTTCCTACCCCAAA
Phenotype
MIM: 615998
Polymorphism
A/G, 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_014868.4 697 Missense Mutation CAC,CGC H65R NP_055683.3
XM_005254013.2 697 Missense Mutation CAC,CGC H15R XP_005254070.1
XM_006719717.2 697 Missense Mutation CAC,CGC H65R XP_006719780.1
XM_017020282.1 697 Missense Mutation CAC,CGC H15R XP_016875771.1
XM_017020283.1 697 Missense Mutation CAC,CGC H65R XP_016875772.1

View Full Product Details