Product Details

SNP ID
rs200769821
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:8625720 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGACGAGGTCACCTTTAGGAGCGAC[A/G]CTGTGCTGTCAGATGTCCACCTCTA
Phenotype
MIM: 615261
Polymorphism
A/G, 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_024109.3 316 Missense Mutation ACT,GCT T19A NP_077014.3
XM_005255570.3 316 Missense Mutation ACT,GCT T19A XP_005255627.1
XM_005255571.2 316 Missense Mutation ACT,GCT T19A XP_005255628.1
XM_011522657.2 316 Missense Mutation ACT,GCT T19A XP_011520959.1
XM_017023659.1 316 Missense Mutation ACT,GCT T19A XP_016879148.1
XM_017023660.1 316 Missense Mutation ACT,GCT T19A XP_016879149.1
XM_017023661.1 316 Missense Mutation ACT,GCT T19A XP_016879150.1
XM_017023662.1 316 UTR 5 XP_016879151.1

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