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CTGCTATCCTGGAAGCTGGAGGAAG[C/G]TTGGGTCTTTGTGACAGAAGGTACA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610495 MIM: 164031 | ||||||||||||||||||||
Literature Links: |
IFFO1 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 |
IFFO1 - intermediate filament family orphan 1 | ||||||
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There are no transcripts associated with this gene. |
NOP2 - NOP2 nucleolar protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001033714.2 | 2132 | Missense Mutation | CCT,GCT | P,A 668 | NP_001028886.1 | |
NM_001258308.1 | 2132 | Missense Mutation | CCT,GCT | P,A 672 | NP_001245237.1 | |
NM_001258309.1 | 2132 | Missense Mutation | CCT,GCT | P,A 705 | NP_001245238.1 | |
NM_001258310.1 | 2132 | UTR 3 | NP_001245239.1 | |||
NM_006170.3 | 2132 | Missense Mutation | CCT,GCT | P,A 668 | NP_006161.2 | |
XM_005253691.1 | 2132 | Missense Mutation | CCT,GCT | P,A 672 | XP_005253748.1 |