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GTCACTCAGAAGTTTGCGTCTTACC[A/T]CTGGGTAGCTCTTAGTTCGTTCTTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602508 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
PAFAH1B2 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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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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PAFAH1B2 - platelet activating factor acetylhydrolase 1b catalytic subunit 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001184746.1 | Intron | NP_001171675.1 | ||||
NM_001184747.1 | Intron | NP_001171676.1 | ||||
NM_001184748.1 | Intron | NP_001171677.1 | ||||
NM_001309431.1 | Intron | NP_001296360.1 | ||||
NM_002572.3 | Intron | NP_002563.1 | ||||
XM_017017840.1 | Intron | XP_016873329.1 |
Set Membership: |
HapMap |