Product Details

SNP ID
rs61732945
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.10:24586048 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTCCTCTTGCGACTAGCAGCTGCA[A/G]AGATGGAGGACACAAGCAGTTCCCT
Phenotype
MIM: 609870
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
ARHGAP21 PubMed Links

Gene Details

Gene
ARHGAP21
Gene Name
Rho GTPase activating protein 21
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020824.3 4990 Intron NP_065875.3
XM_005252542.3 4990 Intron XP_005252599.1
XM_005252544.4 4990 Missense Mutation TCT,TTT S1404F XP_005252601.1
XM_011519602.2 4990 Missense Mutation TCT,TTT S1448F XP_011517904.1
XM_011519603.2 4990 Missense Mutation TCT,TTT S1448F XP_011517905.1
XM_011519604.2 4990 Intron XP_011517906.1
XM_011519605.2 4990 Missense Mutation TCT,TTT S1438F XP_011517907.1
XM_011519606.2 4990 Missense Mutation TCT,TTT S1380F XP_011517908.1
XM_011519607.2 4990 Silent Mutation CTG,TTG L1413L XP_011517909.1
XM_017016459.1 4990 Missense Mutation TCT,TTT S1414F XP_016871948.1
XM_017016460.1 4990 Missense Mutation TCT,TTT S1404F XP_016871949.1
XM_017016461.1 4990 Intron XP_016871950.1

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