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GCCGTGAGAGCCAGTCCAACCCTTC[A/G]TACAGTCCCATACCACTTCGAGCAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601747 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PPWD1 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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PPWD1 - peptidylprolyl isomerase domain and WD repeat containing 1 | ||||||
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There are no transcripts associated with this gene. |
TRIM23 - tripartite motif containing 23 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001656.3 | 1713 | Silent Mutation | NP_001647.1 | |||
NM_033227.2 | 1713 | Intron | NP_150230.1 | |||
NM_033228.2 | 1713 | Intron | NP_150231.1 | |||
XM_005248497.3 | 1713 | Nonsense Mutation | XP_005248554.1 | |||
XM_017009444.1 | 1713 | Intron | XP_016864933.1 |