Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATTTTTGGTTTCGGTTGTGTTACAA[C/T]GGGTTCACATGTGTTGTTCAATTCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 610703 | ||||||||||||||||||||
Literature Links: |
HSPH1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286503.1 | 2626 | Missense Mutation | ATT,GTT | I,V 755 | NP_001273432.1 | |
NM_001286504.1 | 2626 | Missense Mutation | ATT,GTT | I,V 801 | NP_001273433.1 | |
NM_001286505.1 | 2626 | Missense Mutation | ATT,GTT | I,V 723 | NP_001273434.1 | |
NM_006644.3 | 2626 | Missense Mutation | ATT,GTT | I,V 799 | NP_006635.2 | |
XM_005266236.1 | 2626 | Missense Mutation | ATT,GTT | I,V 757 | XP_005266293.1 | |
XM_011534887.2 | 2626 | Missense Mutation | ATT,GTT | I,V 801 | XP_011533189.1 | |
XM_011534888.1 | 2626 | Missense Mutation | ATT,GTT | I,V 721 | XP_011533190.1 | |
XM_017020361.1 | 2626 | Missense Mutation | ATT,GTT | I,V 799 | XP_016875850.1 | |
XM_017020362.1 | 2626 | Missense Mutation | ATT,GTT | I,V 757 | XP_016875851.1 | |
XM_017020363.1 | 2626 | Missense Mutation | ATT,GTT | I,V 755 | XP_016875852.1 | |
XM_017020364.1 | 2626 | Missense Mutation | ATT,GTT | I,V 677 | XP_016875853.1 |