Product Details

SNP ID
rs142294903
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:76736993 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTCGTGAAAGCGAACGAAGGCGAA[A/G]CCGCGGGACTCCTTGGTGTAGCGGT
Phenotype
MIM: 615262 MIM: 600813
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
METTL23 PubMed Links
Additional Information
For this assay, SNP(s) [rs237057] are located under a primer 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
METTL23
Gene Name
methyltransferase like 23
There are no transcripts associated with this gene.

Gene
MFSD11
Gene Name
major facilitator superfamily domain containing 11
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001242532.1 419 Intron NP_001229461.1
NM_001242533.1 419 Intron NP_001229462.1
NM_001242534.1 419 UTR 5 NP_001229463.1
NM_001242535.1 419 Intron NP_001229464.1
NM_001242536.1 419 Intron NP_001229465.1
NM_001242537.1 419 Intron NP_001229466.1
NM_024311.3 419 Intron NP_077287.1
XM_011525236.2 419 Intron XP_011523538.1
XM_011525237.2 419 Intron XP_011523539.2
XM_011525238.2 419 Intron XP_011523540.2
XM_011525239.2 419 Intron XP_011523541.2
XM_011525240.2 419 Intron XP_011523542.2
XM_011525241.2 419 Intron XP_011523543.2
XM_011525242.1 419 Intron XP_011523544.1
XM_011525244.1 419 Intron XP_011523546.1
XM_011525247.2 419 Intron XP_011523549.2
XM_017025065.1 419 Intron XP_016880554.1
XM_017025066.1 419 Intron XP_016880555.1
XM_017025067.1 419 Intron XP_016880556.1
XM_017025068.1 419 Intron XP_016880557.1
XM_017025069.1 419 Intron XP_016880558.1
XM_017025070.1 419 Intron XP_016880559.1
XM_017025071.1 419 Intron XP_016880560.1
Gene
MIR636
Gene Name
microRNA 636
There are no transcripts associated with this gene.

Gene
SRSF2
Gene Name
serine and arginine rich splicing factor 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001195427.1 419 Silent Mutation GGC,GGT G56G NP_001182356.1
NM_003016.4 419 Silent Mutation GGC,GGT G56G NP_003007.2
XM_017024942.1 419 Silent Mutation GGC,GGT G56G XP_016880431.1

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