Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGATATAATGTAATGGTAGAGGTCC[A/G]TCATTTCCCCTTTGTACCAGAAGTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 176398 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PSG9 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
|
PSG9 - pregnancy specific beta-1-glycoprotein 9 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001301707.1 | 312 | Missense Mutation | ACG,ATG | T,M 73 | NP_001288636.1 | |
NM_001301708.1 | 312 | Missense Mutation | ACG,ATG | T,M 73 | NP_001288637.1 | |
NM_001301709.1 | 312 | Missense Mutation | ACG,ATG | T,M 73 | NP_001288638.1 | |
NM_002784.4 | 312 | Missense Mutation | ACG,ATG | T,M 73 | NP_002775.3 | |
XM_005259075.3 | 312 | Missense Mutation | ACG,ATG | T,M 73 | XP_005259132.1 | |
XM_017027004.1 | 312 | Missense Mutation | ACG,ATG | T,M 73 | XP_016882493.1 | |
XM_017027005.1 | 312 | Missense Mutation | ACG,ATG | T,M 73 | XP_016882494.1 | |
XM_017027006.1 | 312 | Missense Mutation | ACG,ATG | T,M 73 | XP_016882495.1 | |
XM_017027007.1 | 312 | Missense Mutation | ACG,ATG | T,M 73 | XP_016882496.1 |