Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGGTTAGGACCCAGGCCCAGATAAT[A/G]CCTGGGGCAAGGCCCAAGAATAAGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 300417 | ||||||||||||||||||||
Literature Links: |
ARMCX5-GPRASP2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
ARMCX5-GPRASP2 - ARMCX5-GPRASP2 readthrough | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001199818.1 | 866 | Intron | NP_001186747.1 |
GPRASP1 - G protein-coupled receptor associated sorting protein 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001099410.1 | 866 | Missense Mutation | ATA,ATG | I,M 47 | NP_001092880.1 | |
NM_001099411.1 | 866 | Missense Mutation | ATA,ATG | I,M 47 | NP_001092881.1 | |
NM_001184727.1 | 866 | Missense Mutation | ATA,ATG | I,M 47 | NP_001171656.1 | |
NM_014710.4 | 866 | Missense Mutation | ATA,ATG | I,M 47 | NP_055525.3 | |
XM_017029981.1 | 866 | Missense Mutation | ATA,ATG | I,M 47 | XP_016885470.1 | |
XM_017029982.1 | 866 | Missense Mutation | ATA,ATG | I,M 47 | XP_016885471.1 |