Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
47 submissions
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Phenotype: |
MIM: 613466 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
KLHDC9 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) - Not Available | ||||||
SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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KLHDC9 - kelch domain containing 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001007255.2 | 989 | Missense Mutation | AAC,AGC | N,S 288 | NP_001007256.1 | |
NM_152366.4 | 989 | Missense Mutation | ACT,GCT | T,A 282 | NP_689579.3 |
PFDN2 - prefoldin subunit 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_012394.3 | 989 | Intron | NP_036526.2 | |||
XM_011509624.2 | 989 | Intron | XP_011507926.1 |
Set Membership: |
HapMap JSNP |