Product Details

SNP ID
rs199701715
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.10:24591266 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGAGACTCCTGTCCTTCCAATGTTG[C/G]TGAGTAAATGATCTATGTTTGGCAC
Phenotype
MIM: 609870
Polymorphism
C/G, Transversion 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 4858 Intron NP_065875.3
XM_005252542.3 4858 Intron XP_005252599.1
XM_005252544.4 4858 Missense Mutation ACC,AGC T1360S XP_005252601.1
XM_011519602.2 4858 Missense Mutation ACC,AGC T1404S XP_011517904.1
XM_011519603.2 4858 Missense Mutation ACC,AGC T1404S XP_011517905.1
XM_011519604.2 4858 Intron XP_011517906.1
XM_011519605.2 4858 Missense Mutation ACC,AGC T1394S XP_011517907.1
XM_011519606.2 4858 Missense Mutation ACC,AGC T1336S XP_011517908.1
XM_011519607.2 4858 Intron XP_011517909.1
XM_017016459.1 4858 Missense Mutation ACC,AGC T1370S XP_016871948.1
XM_017016460.1 4858 Missense Mutation ACC,AGC T1360S XP_016871949.1
XM_017016461.1 4858 Intron XP_016871950.1

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