Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTCGATCCTGTGATTCAAGGGGGAT[C/T]CATTTTCGTCTTCTTTGGTGTCCGA
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610331 MIM: 603426 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
HES6 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)
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EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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HES6 - hes family bHLH transcription factor 6 | ||||||
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There are no transcripts associated with this gene. |
LOC101927958 - uncharacterized LOC101927958 | ||||||
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There are no transcripts associated with this gene. |
PER2 - period circadian clock 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022817.2 | 3906 | Missense Mutation | GAA,GGA | E,G 1244 | NP_073728.1 | |
XM_005246111.4 | 3906 | Missense Mutation | GAA,GGA | E,G 1244 | XP_005246168.1 | |
XM_006712824.3 | 3906 | Missense Mutation | GAA,GGA | E,G 1244 | XP_006712887.1 |
Set Membership: |
HapMap |