Product Details

SNP ID
rs141740706
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:30663442 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCAGGGGCTCGTGGGATGGCTCACA[A/G]TGGAATCATCAAACGGACTTCCTTC
Phenotype
MIM: 611446
Polymorphism
A/G, Transition 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 1304 Silent Mutation CTG,TTG L188L NP_001291723.1
NM_001304795.1 1304 Silent Mutation CTG,TTG L188L NP_001291724.1
NM_001304796.1 1304 UTR 3 NP_001291725.1
NM_152511.4 1304 Silent Mutation CTG,TTG L188L NP_689724.3
XM_005261368.4 1304 Silent Mutation CTG,TTG L188L XP_005261425.1
XM_006724148.3 1304 Silent Mutation CTG,TTG L188L XP_006724211.1
XM_011529920.2 1304 Silent Mutation CTG,TTG L188L XP_011528222.1
XM_011529921.2 1304 Silent Mutation CTG,TTG L188L XP_011528223.1
XM_017028627.1 1304 Silent Mutation CTG,TTG L188L XP_016884116.1
XM_017028628.1 1304 Silent Mutation CTG,TTG L188L 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 1304 Intron NP_001001479.1
NM_001318370.1 1304 Intron NP_001305299.1
NM_001318371.1 1304 Intron NP_001305300.1
XM_017028794.1 1304 Intron XP_016884283.1
XM_017028795.1 1304 Intron XP_016884284.1

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