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AAATCTGGTGACACTATTCTTATTC[A/G]TGGTTTGGCAGATTCAGAGATGGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C9orf131 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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C9orf131 - chromosome 9 open reading frame 131 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040410.2 | 192 | Intron | NP_001035500.1 | |||
NM_001040411.2 | 192 | Intron | NP_001035501.1 | |||
NM_001040412.2 | 192 | Intron | NP_001035502.1 | |||
NM_001287391.1 | 192 | Intron | NP_001274320.1 | |||
NM_203299.3 | 192 | Missense Mutation | ATG,GTG | M,V 49 | NP_976044.2 |