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CAGCCTGAGAAACCTGGTCGTGTCC[A/G]TCGTCGGAAGACTAGGCGGGAACGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603074 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PAFAH1B3 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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PAFAH1B3 - platelet activating factor acetylhydrolase 1b catalytic subunit 3 | ||||||
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There are no transcripts associated with this gene. |
PRR19 - proline rich 19 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_199285.2 | 152 | Missense Mutation | CAT,CGT | H,R 21 | NP_954979.2 | |
XM_005258779.4 | 152 | Missense Mutation | CAT,CGT | H,R 73 | XP_005258836.2 | |
XM_005258780.3 | 152 | Missense Mutation | CAT,CGT | H,R 21 | XP_005258837.1 | |
XM_006723154.3 | 152 | Missense Mutation | CAT,CGT | H,R 21 | XP_006723217.1 | |
XM_011526787.1 | 152 | Missense Mutation | CAT,CGT | H,R 21 | XP_011525089.1 | |
XM_011526788.1 | 152 | Missense Mutation | CAT,CGT | H,R 21 | XP_011525090.1 | |
XM_011526789.2 | 152 | Missense Mutation | CAT,CGT | H,R 21 | XP_011525091.1 | |
XM_011526790.2 | 152 | Missense Mutation | CAT,CGT | H,R 21 | XP_011525092.1 |
TMEM145 - transmembrane protein 145 | ||||||
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There are no transcripts associated with this gene. |