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CAAGTAGAAGAACATCCTTCCCCTC[A/G]GAAACTTTGGGTGGCAGGGCTTCAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 176393 MIM: 176394 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PSG4 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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PSG4 - pregnancy specific beta-1-glycoprotein 4 | ||||||
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There are no transcripts associated with this gene. |
PSG5 - pregnancy specific beta-1-glycoprotein 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130014.1 | 267 | Intron | NP_001123486.1 | |||
NM_002781.3 | 267 | Intron | NP_002772.3 | |||
XM_011527132.2 | 267 | Silent Mutation | TCC,TCT | S,S 46 | XP_011525434.1 | |
XM_017027003.1 | 267 | Intron | XP_016882492.1 |