Product Details

SNP ID
rs145460879
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:75105823 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGCATGAGGTAGGCCAGGACCAGC[A/G]TGGCAGAGCGGCTCACGCCCACCAC
Phenotype
MIM: 613191 MIM: 611575
Polymorphism
A/G, 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_001007271.1 468 Missense Mutation ACG,ATG T138M NP_001007272.1
NM_001007272.1 468 Intron NP_001007273.1
NM_001007273.1 468 Intron NP_001007274.1
NM_001320842.1 468 Intron NP_001307771.1
NM_001320843.1 468 Intron NP_001307772.1
NM_016364.3 468 Intron NP_057448.3
XM_005269883.3 468 Silent Mutation CAC,CAT H65H XP_005269940.1
XM_005269884.4 468 Intron XP_005269941.3
XM_005269887.1 468 Intron XP_005269944.1
XM_005269890.1 468 Intron XP_005269947.1
XM_011539853.1 468 UTR 5 XP_011538155.1
XM_011539854.2 468 Intron XP_011538156.1
XM_011539855.1 468 Intron XP_011538157.1
XM_011539856.2 468 Intron XP_011538158.1
XM_017016313.1 468 Intron XP_016871802.1
XM_017016314.1 468 Silent Mutation CAC,CAT H65H 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_001174156.1 468 Intron NP_001167627.1
NM_144660.2 468 Intron NP_653261.1
XM_005269541.4 468 Intron XP_005269598.1
XM_011539311.1 468 Intron XP_011537613.1
XM_011539312.2 468 Intron XP_011537614.1
XM_017015738.1 468 Intron XP_016871227.1
XM_017015739.1 468 Intron XP_016871228.1

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