Product Details

SNP ID
rs61995873
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:100992588 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TATCGAGTATTCATCAACTGGTCTC[A/C]ATTTCCTGAACACATTCACTGTATC
Phenotype
MIM: 615936
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
ARHGAP42 PubMed Links

Gene Details

Gene
ARHGAP42
Gene Name
Rho GTPase activating protein 42
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_152432.2 509 Intron NP_689645.2
XM_011542615.2 509 UTR 3 XP_011540917.1
XM_011542616.2 509 UTR 3 XP_011540918.1
XM_011542617.2 509 UTR 3 XP_011540919.1
XM_017017237.1 509 UTR 3 XP_016872726.1
XM_017017238.1 509 UTR 3 XP_016872727.1
Gene
TMEM133
Gene Name
transmembrane protein 133
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_032021.2 509 Missense Mutation AAT,CAT N94H NP_114410.1

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