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CGGGGTGGGCATCAGTACCAGGGCA[C/G]GCCAGAGATCTAAGTGACCTGAGGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606881 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FHOD1 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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FHOD1 - formin homology 2 domain containing 1 | ||||||
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There are no transcripts associated with this gene. |
LOC105369155 - uncharacterized LOC105369155 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_011523526.2 | Intron | XP_011521828.1 |
LRRC29 - leucine rich repeat containing 29 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001004055.1 | Intron | NP_001004055.1 | ||||
NM_012163.2 | Intron | NP_036295.1 | ||||
XM_017023126.1 | Intron | XP_016878615.1 | ||||
XM_017023127.1 | Intron | XP_016878616.1 | ||||
XM_017023128.1 | Intron | XP_016878617.1 | ||||
XM_017023129.1 | Intron | XP_016878618.1 | ||||
XM_017023130.1 | Intron | XP_016878619.1 | ||||
XM_017023131.1 | Intron | XP_016878620.1 | ||||
XM_017023132.1 | Intron | XP_016878621.1 | ||||
XM_017023133.1 | Intron | XP_016878622.1 | ||||
XM_017023134.1 | Intron | XP_016878623.1 |
TMEM208 - transmembrane protein 208 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318217.1 | Intron | NP_001305146.1 | ||||
NM_014187.3 | Intron | NP_054906.2 |