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CAAGTGAGGAGTAGCCTTTATTGGG[A/G]ACGACCAGCCTAGGTGAAGAATTTC
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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There are no transcripts associated with this gene. |
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 | 385 | Silent Mutation | GTC,GTT | V,V 91 | NP_001171869.1 | |
NM_001184941.1 | 385 | Silent Mutation | GTC,GTT | V,V 91 | NP_001171870.1 | |
NM_001184942.1 | 385 | Silent Mutation | GTC,GTT | V,V 80 | NP_001171871.1 | |
NM_001184943.1 | 385 | Silent Mutation | GTC,GTT | V,V 74 | NP_001171872.1 | |
NM_001184945.1 | 385 | Silent Mutation | GTC,GTT | V,V 63 | NP_001171874.1 | |
NM_147202.1 | 385 | Silent Mutation | GTC,GTT | V,V 74 | NP_671735.1 | |
XM_005251402.4 | 385 | Silent Mutation | GTC,GTT | V,V 50 | XP_005251459.1 | |
XM_011517797.2 | 385 | Silent Mutation | GTC,GTT | V,V 80 | XP_011516099.1 | |
XM_011517798.2 | 385 | Silent Mutation | GTC,GTT | V,V 63 | XP_011516100.1 | |
XM_011517799.2 | 385 | Silent Mutation | GTC,GTT | V,V 22 | XP_011516101.1 |