Product Details

SNP ID

rs112245487

Assay Type

Functionally Tested

NCBI dbSNP Submissions

6

Location

Chr.1:171783898 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCAGATGAGCTTCTTGAAGATGGA[C/T]ATGACGCAGATGGAGTTTCCTGATG

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

METTL13 PubMed Links

Additional Information

For this assay, SNP(s) [rs2232816] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

METTL13

Gene Name

methyltransferase like 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001007239.1	326	Silent Mutation	GAC,GAT	D104D	NP_001007240.1
NM_014955.2	326	Silent Mutation	GAC,GAT	D18D	NP_055770.1
NM_015935.4	326	Silent Mutation	GAC,GAT	D104D	NP_057019.3
XM_017001455.1	326	Silent Mutation	GAC,GAT	D18D	XP_016856944.1
XM_017001456.1	326	Silent Mutation	GAC,GAT	D18D	XP_016856945.1
XM_017001457.1	326	Silent Mutation	GAC,GAT	D18D	XP_016856946.1
XM_017001458.1	326	Silent Mutation	GAC,GAT	D104D	XP_016856947.1
XM_017001459.1	326	Silent Mutation	GAC,GAT	D18D	XP_016856948.1

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