Product Details

SNP ID
rs200317291
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:8625716 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCATGGACGAGGTCACCTTTAGGAG[C/T]GACACTGTGCTGTCAGATGTCCACC
Phenotype
MIM: 615261
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
METTL22 PubMed Links

Gene Details

Gene
METTL22
Gene Name
methyltransferase like 22
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_024109.3 312 Silent Mutation AGC,AGT S17S NP_077014.3
XM_005255570.3 312 Silent Mutation AGC,AGT S17S XP_005255627.1
XM_005255571.2 312 Silent Mutation AGC,AGT S17S XP_005255628.1
XM_011522657.2 312 Silent Mutation AGC,AGT S17S XP_011520959.1
XM_017023659.1 312 Silent Mutation AGC,AGT S17S XP_016879148.1
XM_017023660.1 312 Silent Mutation AGC,AGT S17S XP_016879149.1
XM_017023661.1 312 Silent Mutation AGC,AGT S17S XP_016879150.1
XM_017023662.1 312 UTR 5 XP_016879151.1

View Full Product Details