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Search Thermo Fisher Scientific
TTAATTCTTCCAACTTGTCAACATA[C/T]GCTTGTTTAGCTTGGTCCTCTCCTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610703 | ||||||||||||||||||||
Literature Links: |
HSPH1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
HSPH1 - heat shock protein family H (Hsp110) member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286503.1 | 2292 | Silent Mutation | GCA,GCG | A,A 643 | NP_001273432.1 | |
NM_001286504.1 | 2292 | Silent Mutation | GCA,GCG | A,A 689 | NP_001273433.1 | |
NM_001286505.1 | 2292 | Silent Mutation | GCA,GCG | A,A 611 | NP_001273434.1 | |
NM_006644.3 | 2292 | Silent Mutation | GCA,GCG | A,A 687 | NP_006635.2 | |
XM_005266236.1 | 2292 | Silent Mutation | GCA,GCG | A,A 645 | XP_005266293.1 | |
XM_011534887.2 | 2292 | Silent Mutation | GCA,GCG | A,A 689 | XP_011533189.1 | |
XM_011534888.1 | 2292 | Silent Mutation | GCA,GCG | A,A 609 | XP_011533190.1 | |
XM_017020361.1 | 2292 | Silent Mutation | GCA,GCG | A,A 687 | XP_016875850.1 | |
XM_017020362.1 | 2292 | Silent Mutation | GCA,GCG | A,A 645 | XP_016875851.1 | |
XM_017020363.1 | 2292 | Silent Mutation | GCA,GCG | A,A 643 | XP_016875852.1 | |
XM_017020364.1 | 2292 | Silent Mutation | GCA,GCG | A,A 565 | XP_016875853.1 |