Product Details

SNP ID
rs141490960
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:75101876 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGAGCACTCACCCACCTGTGGGAG[C/T]ATCTGGCCCAGGCTGTGCACTTCTC
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_001007271.1 494 UTR 3 NP_001007272.1
NM_001007272.1 494 Intron NP_001007273.1
NM_001007273.1 494 Missense Mutation TAC,TGC Y90C NP_001007274.1
NM_001320842.1 494 Missense Mutation TAC,TGC Y90C NP_001307771.1
NM_001320843.1 494 UTR 5 NP_001307772.1
NM_016364.3 494 Intron NP_057448.3
XM_005269883.3 494 Missense Mutation TAC,TGC Y216C XP_005269940.1
XM_005269884.4 494 Intron XP_005269941.3
XM_005269887.1 494 Missense Mutation TAC,TGC Y90C XP_005269944.1
XM_005269890.1 494 Intron XP_005269947.1
XM_011539853.1 494 Missense Mutation TAC,TGC Y126C XP_011538155.1
XM_011539854.2 494 UTR 5 XP_011538156.1
XM_011539855.1 494 Intron XP_011538157.1
XM_011539856.2 494 UTR 5 XP_011538158.1
XM_017016313.1 494 Intron XP_016871802.1
XM_017016314.1 494 Missense Mutation TAC,TGC Y216C 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_001174156.1 494 Intron NP_001167627.1
NM_144660.2 494 Intron NP_653261.1
XM_005269541.4 494 Intron XP_005269598.1
XM_011539311.1 494 Intron XP_011537613.1
XM_011539312.2 494 Intron XP_011537614.1
XM_017015738.1 494 Intron XP_016871227.1
XM_017015739.1 494 Intron XP_016871228.1

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