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GCAGAAAACATTCTTTCAAATTTTC[C/T]AGTTTGGGCACTCATTTCATGAATA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
15 submissions
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Phenotype: |
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Literature Links: |
C1orf141 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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C1orf141 - chromosome 1 open reading frame 141 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001276351.1 | 1266 | Missense Mutation | AGA,GGA | R,G 345 | NP_001263280.1 | |
NM_001276352.1 | 1266 | UTR 3 | NP_001263281.1 | |||
XM_011541465.2 | 1266 | Missense Mutation | AGA,GGA | R,G 416 | XP_011539767.1 | |
XM_011541466.2 | 1266 | Missense Mutation | AGA,GGA | R,G 416 | XP_011539768.1 | |
XM_011541467.1 | 1266 | Missense Mutation | AGA,GGA | R,G 403 | XP_011539769.1 | |
XM_011541469.1 | 1266 | Missense Mutation | AGA,GGA | R,G 278 | XP_011539771.1 | |
XM_011541472.1 | 1266 | Intron | XP_011539774.1 | |||
XM_011541473.2 | 1266 | Intron | XP_011539775.1 | |||
XM_011541475.1 | 1266 | Intron | XP_011539777.1 | |||
XM_017001276.1 | 1266 | Missense Mutation | AGA,GGA | R,G 416 | XP_016856765.1 | |
XM_017001277.1 | 1266 | Intron | XP_016856766.1 |