Product Details

SNP ID
rs147622918
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:129905639 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACCCGACCGAGTAGCGTAGCTTACC[A/G]AAGTAACCGCCTTCACCTGGCCAGT
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
PRDM10 PubMed Links

Gene Details

Gene
PRDM10
Gene Name
PR domain 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020228.2 5270 Missense Mutation TCG,TTG S1093L NP_064613.2
NM_199437.1 5270 Missense Mutation TCG,TTG S1089L NP_955469.1
NM_199438.1 5270 Missense Mutation TCG,TTG S994L NP_955470.1
NM_199439.1 5270 Missense Mutation TCG,TTG S956L NP_955471.1
XM_011542912.2 5270 Missense Mutation TCG,TTG S1076L XP_011541214.1
XM_017018023.1 5270 Missense Mutation TCG,TTG S990L XP_016873512.1

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