Product Details

SNP ID
rs35475086
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:123368814 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATTTGGGGTTTCATTCATTATCTTG[A/G]CAAAAATAGTGTCAATGAAGTCCCA
Phenotype
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
GRAMD1B PubMed Links
Additional Information
For this assay, SNP(s) [rs112379089] 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
GRAMD1B
Gene Name
GRAM domain containing 1B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286563.1 Intron NP_001273492.1
NM_001286564.1 Intron NP_001273493.1
NM_020716.2 Intron NP_065767.1
XM_005271619.4 Intron XP_005271676.1
XM_005271621.4 Intron XP_005271678.1
XM_005271623.4 Intron XP_005271680.1
XM_005271624.4 Intron XP_005271681.2
XM_006718892.3 Intron XP_006718955.1
XM_011542926.2 Intron XP_011541228.1
XM_011542929.2 Intron XP_011541231.1
XM_011542930.2 Intron XP_011541232.1
XM_011542931.2 Intron XP_011541233.1
XM_011542933.1 Intron XP_011541235.1
XM_017018034.1 Intron XP_016873523.1
XM_017018035.1 Intron XP_016873524.1
XM_017018036.1 Intron XP_016873525.1
XM_017018037.1 Intron XP_016873526.1
XM_017018038.1 Intron XP_016873527.1
XM_017018039.1 Intron XP_016873528.1
XM_017018040.1 Intron XP_016873529.1
XM_017018041.1 Intron XP_016873530.1
XM_017018042.1 Intron XP_016873531.1
XM_017018043.1 Intron XP_016873532.1
XM_017018044.1 Intron XP_016873533.1
XM_017018045.1 Intron XP_016873534.1
XM_017018046.1 Intron XP_016873535.1
XM_017018047.1 Intron XP_016873536.1
XM_017018048.1 Intron XP_016873537.1
XM_017018049.1 Intron XP_016873538.1
XM_017018050.1 Intron XP_016873539.1
XM_017018051.1 Intron XP_016873540.1

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