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CAAGTAGAAGAACATCCTTCCCCTC[A/G]GAAACTTTGGGTGGCTGGGCTTCAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 176398 | ||||||||||||||||||||
Literature Links: |
PSG9 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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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 |
PSG9 - pregnancy specific beta-1-glycoprotein 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001301707.1 | 232 | Silent Mutation | TCC,TCT | S,S 46 | NP_001288636.1 | |
NM_001301708.1 | 232 | Silent Mutation | TCC,TCT | S,S 46 | NP_001288637.1 | |
NM_001301709.1 | 232 | Silent Mutation | TCC,TCT | S,S 46 | NP_001288638.1 | |
NM_002784.4 | 232 | Silent Mutation | TCC,TCT | S,S 46 | NP_002775.3 | |
XM_005259075.3 | 232 | Silent Mutation | TCC,TCT | S,S 46 | XP_005259132.1 | |
XM_017027004.1 | 232 | Silent Mutation | TCC,TCT | S,S 46 | XP_016882493.1 | |
XM_017027005.1 | 232 | Silent Mutation | TCC,TCT | S,S 46 | XP_016882494.1 | |
XM_017027006.1 | 232 | Silent Mutation | TCC,TCT | S,S 46 | XP_016882495.1 | |
XM_017027007.1 | 232 | Silent Mutation | TCC,TCT | S,S 46 | XP_016882496.1 |