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ATACACTGAACTTCGTCAATGTCCA[C/T]GTCCTCCACCTGCATGAACTTCAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613713 MIM: 176895 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PCID2 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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PCID2 - PCI domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001127202.3 | 1652 | Missense Mutation | ATG,GTG | M,V 355 | NP_001120674.1 | |
NM_001127203.3 | 1652 | Missense Mutation | ATG,GTG | M,V 355 | NP_001120675.1 | |
NM_001258213.2 | 1652 | Missense Mutation | ATG,GTG | M,V 353 | NP_001245142.1 | |
NM_001320655.1 | 1652 | Missense Mutation | ATG,GTG | M,V 353 | NP_001307584.1 | |
NM_001320656.1 | 1652 | Missense Mutation | ATG,GTG | M,V 409 | NP_001307585.1 | |
NM_001320657.1 | 1652 | Missense Mutation | ATG,GTG | M,V 355 | NP_001307586.1 | |
NM_001320659.1 | 1652 | Missense Mutation | ATG,GTG | M,V 355 | NP_001307588.1 | |
NM_001320660.1 | 1652 | Missense Mutation | ATG,GTG | M,V 353 | NP_001307589.1 | |
NM_018386.4 | 1652 | Missense Mutation | ATG,GTG | M,V 355 | NP_060856.2 | |
XM_005268325.3 | 1652 | Intron | XP_005268382.1 | |||
XM_017020664.1 | 1652 | Missense Mutation | ATG,GTG | M,V 353 | XP_016876153.1 | |
XM_017020665.1 | 1652 | Missense Mutation | ATG,GTG | M,V 313 | XP_016876154.1 | |
XM_017020666.1 | 1652 | Missense Mutation | ATG,GTG | M,V 313 | XP_016876155.1 | |
XM_017020667.1 | 1652 | Missense Mutation | ATG,GTG | M,V 188 | XP_016876156.1 | |
XM_017020668.1 | 1652 | Missense Mutation | ATG,GTG | M,V 188 | XP_016876157.1 | |
XM_017020669.1 | 1652 | Missense Mutation | ATG,GTG | M,V 188 | XP_016876158.1 | |
XM_017020670.1 | 1652 | Missense Mutation | ATG,GTG | M,V 188 | XP_016876159.1 | |
XM_017020671.1 | 1652 | Missense Mutation | ATG,GTG | M,V 188 | XP_016876160.1 | |
XM_017020672.1 | 1652 | Missense Mutation | ATG,GTG | M,V 188 | XP_016876161.1 |
PROZ - protein Z, vitamin K dependent plasma glycoprotein | ||||||
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There are no transcripts associated with this gene. |