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GCCACCACACCACTGACCAGCTCCA[C/T]CTCACCATCCAGGTAGCCCAGGTGG
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 1123 | Missense Mutation | ATG,GTG | M,V 335 | NP_006364.2 |