Product Details

SNP ID
rs200350819
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.22:30663459 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCTCACAGTGGAATCATCAAACGG[A/T]CTTCCTTCTCATAGATGTCAGGGAT
Phenotype
MIM: 611446
Polymorphism
A/T, Transversion Substitution
Allele Nomenclature
Literature Links
DUSP18 PubMed Links

Gene Details

Gene
DUSP18
Gene Name
dual specificity phosphatase 18
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001304794.1 1287 Missense Mutation GAC,GTC D182V NP_001291723.1
NM_001304795.1 1287 Missense Mutation GAC,GTC D182V NP_001291724.1
NM_001304796.1 1287 UTR 3 NP_001291725.1
NM_152511.4 1287 Missense Mutation GAC,GTC D182V NP_689724.3
XM_005261368.4 1287 Missense Mutation GAC,GTC D182V XP_005261425.1
XM_006724148.3 1287 Missense Mutation GAC,GTC D182V XP_006724211.1
XM_011529920.2 1287 Missense Mutation GAC,GTC D182V XP_011528222.1
XM_011529921.2 1287 Missense Mutation GAC,GTC D182V XP_011528223.1
XM_017028627.1 1287 Missense Mutation GAC,GTC D182V XP_016884116.1
XM_017028628.1 1287 Missense Mutation GAC,GTC D182V XP_016884117.1
Gene
SLC35E4
Gene Name
solute carrier family 35 member E4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001001479.3 1287 Intron NP_001001479.1
NM_001318370.1 1287 Intron NP_001305299.1
NM_001318371.1 1287 Intron NP_001305300.1
XM_017028794.1 1287 Intron XP_016884283.1
XM_017028795.1 1287 Intron XP_016884284.1

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