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GCCCATGCTTTGATTTTTTACATCA[A/G]ACTTTATTGAGGTGTAACTTACAGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603621 MIM: 615216 MIM: 609172 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FOXH1 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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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FOXH1 - forkhead box H1 | ||||||
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There are no transcripts associated with this gene. |
KIFC2 - kinesin family member C2 | ||||||
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There are no transcripts associated with this gene. |
PPP1R16A - protein phosphatase 1 regulatory subunit 16A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_005272350.2 | Intron | XP_005272407.1 | ||||
XM_011517349.2 | Intron | XP_011515651.1 | ||||
XM_017013912.1 | Intron | XP_016869401.1 | ||||
XM_017013913.1 | Intron | XP_016869402.1 | ||||
XM_017013914.1 | Intron | XP_016869403.1 | ||||
XM_017013915.1 | Intron | XP_016869404.1 |