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CTTGATGGAGGTGGGAGCCCTGTAG[C/G]AGTCACTGTAGGTACTGATAGGGGT
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 |
---|---|---|
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 |
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 | 271 | Intron | NP_001239124.1 | |||
NM_032596.3 | 271 | Missense Mutation | TCC,TGC | S,C 18 | NP_115985.2 | |
NM_147168.1 | 271 | Intron | NP_671697.1 | |||
NM_147169.2 | 271 | Intron | NP_671698.1 | |||
XM_005251616.4 | 271 | Missense Mutation | TCC,TGC | S,C 18 | XP_005251673.1 | |
XM_005251618.4 | 271 | Intron | XP_005251675.1 | |||
XM_011518055.2 | 271 | Intron | XP_011516357.1 |
FAM219A - family with sequence similarity 219 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001184940.1 | 271 | Intron | NP_001171869.1 | |||
NM_001184941.1 | 271 | Intron | NP_001171870.1 | |||
NM_001184942.1 | 271 | Intron | NP_001171871.1 | |||
NM_001184943.1 | 271 | Intron | NP_001171872.1 | |||
NM_001184945.1 | 271 | Intron | NP_001171874.1 | |||
NM_147202.1 | 271 | Intron | NP_671735.1 | |||
XM_005251402.4 | 271 | Intron | XP_005251459.1 | |||
XM_011517797.2 | 271 | Intron | XP_011516099.1 | |||
XM_011517798.2 | 271 | Intron | XP_011516100.1 | |||
XM_011517799.2 | 271 | Intron | XP_011516101.1 |