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CTGCTGTTGTAAGGTTCCATCCTCC[A/G]TGTGTTGTACCAGTCACTGCCCAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C9orf24 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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C9orf24 - chromosome 9 open reading frame 24 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001252195.1 | 546 | Intron | NP_001239124.1 | |||
NM_032596.3 | 546 | Missense Mutation | CGG,TGG | R,W 110 | NP_115985.2 | |
NM_147168.1 | 546 | Intron | NP_671697.1 | |||
NM_147169.2 | 546 | Intron | NP_671698.1 | |||
XM_005251616.4 | 546 | Missense Mutation | CGG,TGG | R,W 110 | XP_005251673.1 | |
XM_005251618.4 | 546 | Intron | XP_005251675.1 | |||
XM_011518055.2 | 546 | Intron | XP_011516357.1 |
KIAA1161 - KIAA1161 | ||||||
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There are no transcripts associated with this gene. |