Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCTTTGCTCGCTTGGCTTGCTCGAA[C/T]GGCAGTTTCTAGACGCACTTTCAAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
HEATR5B 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 |
HEATR5B - HEAT repeat containing 5B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_019024.2 | 6681 | Missense Mutation | ATT,GTT | I,V 2039 | NP_061897.1 | |
XM_006712034.2 | 6681 | Missense Mutation | ATT,GTT | I,V 2038 | XP_006712097.1 | |
XM_006712035.3 | 6681 | Missense Mutation | ATT,GTT | I,V 2027 | XP_006712098.1 | |
XM_011532934.2 | 6681 | Missense Mutation | ATT,GTT | I,V 2039 | XP_011531236.1 | |
XM_011532935.2 | 6681 | Missense Mutation | ATT,GTT | I,V 1422 | XP_011531237.1 | |
XM_017004378.1 | 6681 | Missense Mutation | ATT,GTT | I,V 1950 | XP_016859867.1 | |
XM_017004379.1 | 6681 | Missense Mutation | ATT,GTT | I,V 1914 | XP_016859868.1 | |
XM_017004380.1 | 6681 | Missense Mutation | ATT,GTT | I,V 1914 | XP_016859869.1 |