Product Details

SNP ID
rs151285118
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:48431253 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGAACCAAGAATGGAGTTATACGGG[C/G]GCAGCCCTCTCCTTTAGGTTGGTTA
Phenotype
MIM: 610585 MIM: 601158
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
ARHGAP22 PubMed Links

Gene Details

Gene
ARHGAP22
Gene Name
Rho GTPase activating protein 22
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001256024.1 1353 Intron NP_001242953.1
NM_001256025.2 1353 Intron NP_001242954.1
NM_001256026.1 1353 Intron NP_001242955.1
NM_021226.3 1353 Intron NP_067049.2
XM_005270014.3 1353 Intron XP_005270071.1
XM_011540002.1 1353 Intron XP_011538304.1
XM_011540003.1 1353 Intron XP_011538305.1
XM_011540004.1 1353 Intron XP_011538306.1
XM_011540005.1 1353 Intron XP_011538307.1
XM_011540006.1 1353 Intron XP_011538308.1
XM_011540007.2 1353 Intron XP_011538309.1
XM_011540011.2 1353 Intron XP_011538313.1
XM_011540012.2 1353 Intron XP_011538314.1
XM_011540013.2 1353 Intron XP_011538315.1
XM_011540015.2 1353 Intron XP_011538317.1
XM_017016470.1 1353 Intron XP_016871959.1
XM_017016471.1 1353 Intron XP_016871960.1
XM_017016472.1 1353 Intron XP_016871961.1
XM_017016473.1 1353 Intron XP_016871962.1
XM_017016474.1 1353 Intron XP_016871963.1
XM_017016475.1 1353 Intron XP_016871964.1
XM_017016476.1 1353 Intron XP_016871965.1
XM_017016477.1 1353 Intron XP_016871966.1
Gene
MAPK8
Gene Name
mitogen-activated protein kinase 8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001278547.1 1353 Missense Mutation GCG,GGG A374G NP_001265476.1
NM_001278548.1 1353 Missense Mutation GCG,GGG A298G NP_001265477.1
NM_001323302.1 1353 Missense Mutation GCG,GGG A374G NP_001310231.1
NM_001323320.1 1353 Missense Mutation GCG,GGG A298G NP_001310249.1
NM_001323321.1 1353 Missense Mutation GCG,GGG A374G NP_001310250.1
NM_001323322.1 1353 Missense Mutation GCG,GGG A374G NP_001310251.1
NM_001323323.1 1353 Missense Mutation GCG,GGG A374G NP_001310252.1
NM_001323324.1 1353 Missense Mutation GCG,GGG A374G NP_001310253.1
NM_001323325.1 1353 Missense Mutation GCG,GGG A374G NP_001310254.1
NM_001323326.1 1353 Missense Mutation GCG,GGG A374G NP_001310255.1
NM_001323327.1 1353 Missense Mutation GCG,GGG A374G NP_001310256.1
NM_001323328.1 1353 Missense Mutation GCG,GGG A374G NP_001310257.1
NM_001323329.1 1353 Missense Mutation GCG,GGG A374G NP_001310258.1
NM_001323330.1 1353 Missense Mutation GCG,GGG A374G NP_001310259.1
NM_001323331.1 1353 Missense Mutation GCG,GGG A374G NP_001310260.1
NM_139046.3 1353 Missense Mutation GCG,GGG A374G NP_620634.1
NM_139049.3 1353 Missense Mutation GCG,GGG A374G NP_620637.1

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