Product Details

SNP ID
rs200741943
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:128969002 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AACGCTGTAGCATAGGTCCTGCTCT[G/T]TGGATGGGGAAAGCCAGGGGGCACA
Phenotype
MIM: 608541
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
ARHGAP32 PubMed Links

Gene Details

Gene
ARHGAP32
Gene Name
Rho GTPase activating protein 32
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001142685.1 5347 Missense Mutation NP_001136157.1
NM_014715.3 5347 Missense Mutation NP_055530.2
XM_005271736.4 5347 Nonsense Mutation XP_005271793.2
XM_011543072.2 5347 Nonsense Mutation XP_011541374.1
XM_011543073.2 5347 Missense Mutation XP_011541375.2
XM_011543075.2 5347 Nonsense Mutation XP_011541377.1
XM_017018595.1 5347 Nonsense Mutation XP_016874084.1
XM_017018596.1 5347 Nonsense Mutation XP_016874085.1
XM_017018597.1 5347 Intron XP_016874086.1

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