Product Details

SNP ID
rs6795918
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:151435472 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CACATTTTAGGCTGAGATGGGGCTA[A/G]CTGAAAGTCAGTGTGATGAAAACCC
Phenotype
MIM: 611318
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
IGSF10 PubMed Links
Additional Information
For this assay, SNP(s) [rs112829133] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
IGSF10
Gene Name
immunoglobulin superfamily member 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001178145.1 9898 Intron NP_001171616.1
NM_001178146.1 9898 Intron NP_001171617.1
NM_178822.4 9898 Intron NP_849144.2
XM_011512708.2 9898 UTR 3 XP_011511010.1
XM_011512709.2 9898 UTR 3 XP_011511011.1
Gene
MED12L
Gene Name
mediator complex subunit 12 like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_053002.5 9898 UTR 3 NP_443728.3
XM_006713487.3 9898 Intron XP_006713550.1
XM_011512390.2 9898 UTR 3 XP_011510692.1
XM_011512394.2 9898 Intron XP_011510696.1
XM_011512399.2 9898 Intron XP_011510701.1
XM_017005676.1 9898 UTR 3 XP_016861165.1
XM_017005677.1 9898 UTR 3 XP_016861166.1
XM_017005678.1 9898 UTR 3 XP_016861167.1
XM_017005679.1 9898 UTR 3 XP_016861168.1
XM_017005680.1 9898 UTR 3 XP_016861169.1
XM_017005681.1 9898 Intron XP_016861170.1

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