Product Details

SNP ID
rs35957924
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:57782806 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGTTTATCGCGGCTAGAGAGATGT[C/T]GCTGCTGCGGTCGCTGCGCGTGTTT
Phenotype
MIM: 615258 MIM: 604723
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
METTL21B PubMed Links

Gene Details

Gene
METTL21B
Gene Name
methyltransferase like 21B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015433.2 62 Intron NP_056248.2
NM_206914.1 62 Intron NP_996797.1
Gene
TSFM
Gene Name
Ts translation elongation factor, mitochondrial
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001172695.1 62 Missense Mutation TCG,TTG S2L NP_001166166.1
NM_001172696.1 62 Missense Mutation TCG,TTG S2L NP_001166167.1
NM_001172697.1 62 Missense Mutation TCG,TTG S2L NP_001166168.1
NM_005726.5 62 Missense Mutation TCG,TTG S2L NP_005717.3

View Full Product Details