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CCTGCAGCAGCTGCAGAGCTGTCAC[A/G]CTGAACTGATTCCACCATGTCCGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600735 MIM: 601555 MIM: 604631 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IFI35 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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IFI35 - interferon induced protein 35 | ||||||
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There are no transcripts associated with this gene. |
RND2 - Rho family GTPase 2 | ||||||
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There are no transcripts associated with this gene. |
VAT1 - vesicle amine transport 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006373.3 | 1050 | Silent Mutation | AGC,AGT | S,S 310 | NP_006364.2 |