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TTCCCCACAGACCCCAAGGCTAGCA[A/G]CTGGGGGTAAGGGGGGCCGATGGCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 123841 MIM: 601272 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PPIB 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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PPIB - peptidylprolyl isomerase B | ||||||
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There are no transcripts associated with this gene. |
SNX1 - sorting nexin 1 | ||||||
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There are no transcripts associated with this gene. |
SNX22 - sorting nexin 22 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024798.2 | 347 | Missense Mutation | AAC,AGC | N,S 118 | NP_079074.2 | |
XM_005254677.3 | 347 | Missense Mutation | AAC,AGC | N,S 90 | XP_005254734.1 | |
XM_017022581.1 | 347 | Missense Mutation | AAC,AGC | N,S 90 | XP_016878070.1 |