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CTGGTCAGCTTCCTCACCTTTGACC[G/T]GCTCCATAGGTAAGTGGGCAGCAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C20orf141 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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C20orf141 - chromosome 20 open reading frame 141 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256538.1 | 425 | Missense Mutation | CGG,CTG | R,L 84 | NP_001243467.1 | |
NM_080739.2 | 425 | Missense Mutation | CGG,CTG | R,L 84 | NP_542777.1 |
TMEM239 - transmembrane protein 239 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001167670.2 | 425 | Intron | NP_001161142.1 | |||
NM_001318207.1 | 425 | Intron | NP_001305136.1 | |||
XM_011529128.2 | 425 | Intron | XP_011527430.1 | |||
XM_011529129.2 | 425 | Intron | XP_011527431.1 |