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GACAAGTAGAGGTTTTCTCCTGAAC[A/G]GTAATAGGTGAATGAAGGGTAAATG
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 |
---|---|---|
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 |
PSG4 - pregnancy specific beta-1-glycoprotein 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001276495.1 | 992 | Missense Mutation | CGT,TGT | R,C 252 | NP_001263424.1 | |
NM_001316339.1 | 992 | Missense Mutation | CGT,TGT | R,C 223 | NP_001303268.1 | |
NM_002780.4 | 992 | Missense Mutation | CGT,TGT | R,C 345 | NP_002771.2 | |
NM_213633.2 | 992 | Missense Mutation | CGT,TGT | R,C 252 | NP_998798.1 | |
XM_017026995.1 | 992 | Intron | XP_016882484.1 | |||
XM_017026996.1 | 992 | Missense Mutation | CGT,TGT | R,C 361 | XP_016882485.1 | |
XM_017026997.1 | 992 | Missense Mutation | CGT,TGT | R,C 345 | XP_016882486.1 | |
XM_017026998.1 | 992 | Intron | XP_016882487.1 | |||
XM_017026999.1 | 992 | Intron | XP_016882488.1 | |||
XM_017027000.1 | 992 | Missense Mutation | CGT,TGT | R,C 268 | XP_016882489.1 | |
XM_017027001.1 | 992 | Intron | XP_016882490.1 | |||
XM_017027002.1 | 992 | Intron | XP_016882491.1 |
PSG5 - pregnancy specific beta-1-glycoprotein 5 | ||||||
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There are no transcripts associated with this gene. |