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CGTCAATGAGACTCTCTTTATCATC[A/G]TCTTTGGCGAGTCCCTGCTCAACGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606881 MIM: 600477 | ||||||||||||||||||||||||||||||||||||||
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. |
SLC9A5 - solute carrier family 9 member A5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001323971.1 | 2082 | Missense Mutation | ATC,GTC | I,V 206 | NP_001310900.1 | |
NM_001323972.1 | 2082 | Missense Mutation | ATC,GTC | I,V 105 | NP_001310901.1 | |
NM_001323973.1 | 2082 | Missense Mutation | ATC,GTC | I,V 206 | NP_001310902.1 | |
NM_001323974.1 | 2082 | UTR 5 | NP_001310903.1 | |||
NM_001323975.1 | 2082 | UTR 5 | NP_001310904.1 | |||
NM_004594.2 | 2082 | Missense Mutation | ATC,GTC | I,V 206 | NP_004585.1 | |
XM_017023594.1 | 2082 | Missense Mutation | ATC,GTC | I,V 206 | XP_016879083.1 |