Product Details

SNP ID
rs150226280
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:128968978 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCGGGCAGGAAGGCCCCTTGACCCA[A/G]CGCTGTAGCATAGGTCCTGCTCTGT
Phenotype
MIM: 608541
Polymorphism
A/G, Transition 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 5371 Silent Mutation CTG,TTG L2065L NP_001136157.1
NM_014715.3 5371 Silent Mutation CTG,TTG L1716L NP_055530.2
XM_005271736.4 5371 Silent Mutation CTG,TTG L2079L XP_005271793.2
XM_011543072.2 5371 Silent Mutation CTG,TTG L2039L XP_011541374.1
XM_011543073.2 5371 Silent Mutation CTG,TTG L2052L XP_011541375.2
XM_011543075.2 5371 Silent Mutation CTG,TTG L1740L XP_011541377.1
XM_017018595.1 5371 Silent Mutation CTG,TTG L2039L XP_016874084.1
XM_017018596.1 5371 Silent Mutation CTG,TTG L1986L XP_016874085.1
XM_017018597.1 5371 Intron XP_016874086.1

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