Product Details

SNP ID
rs141678047
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:75101905 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGCCCAGGCTGTGCACTTCTCTGA[C/T]GGGCAGTTCGTGCTGCTGGCTTTCA
Phenotype
MIM: 613191 MIM: 611575
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
DUSP13 PubMed Links

Gene Details

Gene
DUSP13
Gene Name
dual specificity phosphatase 13
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001007271.1 465 UTR 3 NP_001007272.1
NM_001007272.1 465 Intron NP_001007273.1
NM_001007273.1 465 Silent Mutation CCA,CCG P80P NP_001007274.1
NM_001320842.1 465 Silent Mutation CCA,CCG P80P NP_001307771.1
NM_001320843.1 465 UTR 5 NP_001307772.1
NM_016364.3 465 Intron NP_057448.3
XM_005269883.3 465 Silent Mutation CCA,CCG P206P XP_005269940.1
XM_005269884.4 465 Intron XP_005269941.3
XM_005269887.1 465 Silent Mutation CCA,CCG P80P XP_005269944.1
XM_005269890.1 465 Intron XP_005269947.1
XM_011539853.1 465 Silent Mutation CCA,CCG P116P XP_011538155.1
XM_011539854.2 465 UTR 5 XP_011538156.1
XM_011539855.1 465 Intron XP_011538157.1
XM_011539856.2 465 UTR 5 XP_011538158.1
XM_017016313.1 465 Intron XP_016871802.1
XM_017016314.1 465 Silent Mutation CCA,CCG P206P XP_016871803.1
Gene
SAMD8
Gene Name
sterile alpha motif domain containing 8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001174156.1 465 Intron NP_001167627.1
NM_144660.2 465 Intron NP_653261.1
XM_005269541.4 465 Intron XP_005269598.1
XM_011539311.1 465 Intron XP_011537613.1
XM_011539312.2 465 Intron XP_011537614.1
XM_017015738.1 465 Intron XP_016871227.1
XM_017015739.1 465 Intron XP_016871228.1

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