Product Details

SNP ID
rs10257317
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:102806609 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGCTTGAGAAGAGTCCACAGGCCC[C/T]TACAAGCGGTCCCTGTTCTGTCTCA
Phenotype
MIM: 609080
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FAM185A PubMed Links

Gene Details

Gene
FAM185A
Gene Name
family with sequence similarity 185 member A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001145268.1 Intron NP_001138740.1
NM_001145269.1 Intron NP_001138741.1
XM_006715896.3 Intron XP_006715959.1
XM_011515922.2 Intron XP_011514224.1
XM_011515923.2 Intron XP_011514225.1
XM_011515924.2 Intron XP_011514226.1
XM_011515925.2 Intron XP_011514227.1
XM_011515926.2 Intron XP_011514228.1
XM_017011846.1 Intron XP_016867335.1
XM_017011847.1 Intron XP_016867336.1
XM_017011848.1 Intron XP_016867337.1
XM_017011849.1 Intron XP_016867338.1
Gene
FBXL13
Gene Name
F-box and leucine rich repeat protein 13
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001111038.1 Intron NP_001104508.1
NM_001287150.1 Intron NP_001274079.1
NM_145032.3 Intron NP_659469.3
XM_005250205.3 Intron XP_005250262.1
XM_005250207.3 Intron XP_005250264.1
XM_005250208.3 Intron XP_005250265.1
XM_005250209.2 Intron XP_005250266.1
XM_006715898.2 Intron XP_006715961.1
XM_011515928.2 Intron XP_011514230.1
XM_011515929.2 Intron XP_011514231.1
XM_011515930.2 Intron XP_011514232.1
XM_011515932.2 Intron XP_011514234.1
XM_017011850.1 Intron XP_016867339.1
XM_017011851.1 Intron XP_016867340.1
XM_017011852.1 Intron XP_016867341.1
XM_017011853.1 Intron XP_016867342.1

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