Product Details

SNP ID
rs17849462
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:76737116 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTAGGTCAGGTTGTCCACCTTGAG[A/G]GAGGTCATACCCTCCACATCGGGAG
Phenotype
MIM: 615262 MIM: 600813
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
METTL23 PubMed Links

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_001242532.1 296 Intron NP_001229461.1
NM_001242533.1 296 Intron NP_001229462.1
NM_001242534.1 296 Intron NP_001229463.1
NM_001242535.1 296 Intron NP_001229464.1
NM_001242536.1 296 Intron NP_001229465.1
NM_001242537.1 296 Intron NP_001229466.1
NM_024311.3 296 Intron NP_077287.1
XM_011525236.2 296 Intron XP_011523538.1
XM_011525237.2 296 Intron XP_011523539.2
XM_011525238.2 296 Intron XP_011523540.2
XM_011525239.2 296 Intron XP_011523541.2
XM_011525240.2 296 Intron XP_011523542.2
XM_011525241.2 296 Intron XP_011523543.2
XM_011525242.1 296 Intron XP_011523544.1
XM_011525244.1 296 Intron XP_011523546.1
XM_011525247.2 296 Intron XP_011523549.2
XM_017025065.1 296 Intron XP_016880554.1
XM_017025066.1 296 Intron XP_016880555.1
XM_017025067.1 296 Intron XP_016880556.1
XM_017025068.1 296 Intron XP_016880557.1
XM_017025069.1 296 Intron XP_016880558.1
XM_017025070.1 296 Intron XP_016880559.1
XM_017025071.1 296 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_001195427.1 296 Silent Mutation TCC,TCT S15S NP_001182356.1
NM_003016.4 296 Silent Mutation TCC,TCT S15S NP_003007.2
XM_017024942.1 296 Silent Mutation TCC,TCT S15S XP_016880431.1

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