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GATGCTGAGTCCGGAGCGCCTAGCC[A/C]TACCGGACTACGAGTATCTGGGTAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C11orf49 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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C11orf49 - chromosome 11 open reading frame 49 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001003676.2 | 133 | Missense Mutation | ATA,CTA | I,L 9 | NP_001003676.1 | |
NM_001003677.2 | 133 | Missense Mutation | ATA,CTA | I,L 9 | NP_001003677.1 | |
NM_001003678.2 | 133 | Missense Mutation | ATA,CTA | I,L 9 | NP_001003678.1 | |
NM_001278222.1 | 133 | Missense Mutation | CAT,CCT | H,P 34 | NP_001265151.1 | |
NM_024113.4 | 133 | Missense Mutation | ATA,CTA | I,L 9 | NP_077018.1 | |
XM_006718315.1 | 133 | Missense Mutation | ATA,CTA | I,L 9 | XP_006718378.1 | |
XM_011520364.2 | 133 | Missense Mutation | CAT,CCT | H,P 34 | XP_011518666.1 | |
XM_011520365.2 | 133 | Missense Mutation | ATA,CTA | I,L 9 | XP_011518667.1 | |
XM_017018276.1 | 133 | Missense Mutation | ATA,CTA | I,L 9 | XP_016873765.1 | |
XM_017018277.1 | 133 | UTR 5 | XP_016873766.1 | |||
XM_017018278.1 | 133 | UTR 5 | XP_016873767.1 | |||
XM_017018279.1 | 133 | UTR 5 | XP_016873768.1 | |||
XM_017018280.1 | 133 | UTR 5 | XP_016873769.1 | |||
XM_017018281.1 | 133 | UTR 5 | XP_016873770.1 | |||
XM_017018282.1 | 133 | UTR 5 | XP_016873771.1 |