Product Details

SNP ID
rs7130954
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:123362601 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCAGTGATGTACTACCTACCTACTC[C/T]CCCACCCCATGAGTTGCTGAGCTCA
Phenotype
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
GRAMD1B PubMed Links

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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