Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTTGTAACCAGGGATTTGGTGCGCG[A/G]GGCTTCACAGGCTGCAGAGAAACAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
HEATR4 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 |
HEATR4 - HEAT repeat containing 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001220484.1 | 3686 | Silent Mutation | CCC,CCT | P,P 952 | NP_001207413.1 | |
NM_203309.2 | 3686 | Silent Mutation | CCC,CCT | P,P 952 | NP_976054.2 | |
XM_006720143.2 | 3686 | Silent Mutation | CCC,CCT | P,P 952 | XP_006720206.1 | |
XM_011536760.2 | 3686 | Silent Mutation | CCC,CCT | P,P 952 | XP_011535062.1 | |
XM_011536761.2 | 3686 | Intron | XP_011535063.1 | |||
XM_017021289.1 | 3686 | Silent Mutation | CCC,CCT | P,P 952 | XP_016876778.1 |