Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCCGAGCGCAGGGTGCGCCGCCTAC[C/T]GCTGCTGGTGCAGGGCAAGGGCGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602438 MIM: 605235 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HSF4 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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HSF4 - heat shock transcription factor 4 | ||||||
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There are no transcripts associated with this gene. |
KIAA0895L - KIAA0895 like | ||||||
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There are no transcripts associated with this gene. |
NOL3 - nucleolar protein 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001185057.2 | 387 | Missense Mutation | CCG,CTG | P,L 62 | NP_001171986.1 | |
NM_001276307.1 | 387 | Missense Mutation | CCG,CTG | P,L 62 | NP_001263236.1 | |
NM_001276309.1 | 387 | Missense Mutation | CCG,CTG | P,L 62 | NP_001263238.1 | |
NM_001276311.1 | 387 | Intron | NP_001263240.1 | |||
NM_001276312.1 | 387 | Missense Mutation | CCG,CTG | P,L 62 | NP_001263241.1 | |
NM_001276319.1 | 387 | Missense Mutation | CCG,CTG | P,L 124 | NP_001263248.1 | |
NM_003946.6 | 387 | Missense Mutation | CCG,CTG | P,L 62 | NP_003937.1 | |
XM_005256217.2 | 387 | Missense Mutation | CCG,CTG | P,L 124 | XP_005256274.1 | |
XM_005256219.3 | 387 | Intron | XP_005256276.1 | |||
XM_011523424.2 | 387 | Missense Mutation | CCG,CTG | P,L 62 | XP_011521726.1 | |
XM_017023843.1 | 387 | Missense Mutation | CCG,CTG | P,L 124 | XP_016879332.1 |