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GCAGTTGTGGGCGGATTCCAGAAGT[G/T]TAAAAGTGATGCTAGGAGGTACAGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 176393 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC284344 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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LOC284344 - uncharacterized LOC284344 | ||||||
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There are no transcripts associated with this gene. |
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 | 314 | Missense Mutation | AAC,CAC | N,H 26 | NP_001263424.1 | |
NM_001316339.1 | 314 | Intron | NP_001303268.1 | |||
NM_002780.4 | 314 | Missense Mutation | AAC,CAC | N,H 26 | NP_002771.2 | |
NM_213633.2 | 314 | Missense Mutation | AAC,CAC | N,H 26 | NP_998798.1 | |
XM_017026995.1 | 314 | Intron | XP_016882484.1 | |||
XM_017026996.1 | 314 | Missense Mutation | AAC,CAC | N,H 42 | XP_016882485.1 | |
XM_017026997.1 | 314 | Missense Mutation | AAC,CAC | N,H 26 | XP_016882486.1 | |
XM_017026998.1 | 314 | Intron | XP_016882487.1 | |||
XM_017026999.1 | 314 | Intron | XP_016882488.1 | |||
XM_017027000.1 | 314 | Missense Mutation | AAC,CAC | N,H 42 | XP_016882489.1 | |
XM_017027001.1 | 314 | Intron | XP_016882490.1 | |||
XM_017027002.1 | 314 | Intron | XP_016882491.1 |