Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTAGGGGTTCCATTCATGACACCGG[C/G]AGACTGTGCACCTGTGAACAAGAAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 602977 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GP2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
GP2 - glycoprotein 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001007240.2 | 1456 | Missense Mutation | CCC,GCC | P,A 508 | NP_001007241.2 | |
NM_001007241.2 | 1456 | Missense Mutation | CCC,GCC | P,A 361 | NP_001007242.2 | |
NM_001007242.2 | 1456 | Missense Mutation | CCC,GCC | P,A 358 | NP_001007243.2 | |
NM_001502.3 | 1456 | Missense Mutation | CCC,GCC | P,A 505 | NP_001493.2 | |
XM_017023155.1 | 1456 | Missense Mutation | CCC,GCC | P,A 486 | XP_016878644.1 |