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TCTCACTTCACCTATCTTCTATGGC[C/T]GCCCCATAGCCATACTGCCCATTAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
DNAJC22 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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DNAJC22 - DnaJ heat shock protein family (Hsp40) member C22 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001304944.1 | 1184 | Missense Mutation | CGC,TGC | R,C 148 | NP_001291873.1 | |
NM_024902.3 | 1184 | Missense Mutation | CGC,TGC | R,C 148 | NP_079178.2 | |
XM_005269155.2 | 1184 | Missense Mutation | CGC,TGC | R,C 148 | XP_005269212.1 | |
XM_005269156.2 | 1184 | Missense Mutation | CGC,TGC | R,C 148 | XP_005269213.1 | |
XM_005269157.2 | 1184 | Missense Mutation | CGC,TGC | R,C 148 | XP_005269214.1 |