Product Details

SNP ID
rs201355689
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:102654473 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGCCTACATCCAAACAAGAAGCCT[C/G]TCCTAATTCTGATTTCAAATGGGTA
Phenotype
MIM: 300417
Polymorphism
C/G, 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 1285 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 1285 Missense Mutation TCT,TGT S187C NP_001092880.1
NM_001099411.1 1285 Missense Mutation TCT,TGT S187C NP_001092881.1
NM_001184727.1 1285 Missense Mutation TCT,TGT S187C NP_001171656.1
NM_014710.4 1285 Missense Mutation TCT,TGT S187C NP_055525.3
XM_017029981.1 1285 Missense Mutation TCT,TGT S187C XP_016885470.1
XM_017029982.1 1285 Missense Mutation TCT,TGT S187C XP_016885471.1

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