Product Details

SNP ID
rs188898027
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.X:102654465 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTGTCCTAGGCCTACATCCAAACA[A/C]GAAGCCTCTCCTAATTCTGATTTCA
Phenotype
MIM: 300417
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
ARMCX5-GPRASP2 PubMed Links

Gene Details

Gene
ARMCX5-GPRASP2
Gene Name
ARMCX5-GPRASP2 readthrough
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001199818.1 1277 Intron NP_001186747.1
Gene
GPRASP1
Gene Name
G protein-coupled receptor associated sorting protein 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001099410.1 1277 Missense Mutation CAA,CAC Q184H NP_001092880.1
NM_001099411.1 1277 Missense Mutation CAA,CAC Q184H NP_001092881.1
NM_001184727.1 1277 Missense Mutation CAA,CAC Q184H NP_001171656.1
NM_014710.4 1277 Missense Mutation CAA,CAC Q184H NP_055525.3
XM_017029981.1 1277 Missense Mutation CAA,CAC Q184H XP_016885470.1
XM_017029982.1 1277 Missense Mutation CAA,CAC Q184H XP_016885471.1

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