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TGACTTCTGGATTGGGCTCAGGAGG[C/T]GTGAGGAGAAACAAAGCAATAGCAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C11orf88 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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C11orf88 - chromosome 11 open reading frame 88 | ||||||
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There are no transcripts associated with this gene. |
LAYN - layilin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001258390.1 | 667 | Missense Mutation | CGT,TGT | R,C 111 | NP_001245319.1 | |
NM_001258391.1 | 667 | Silent Mutation | GGC,GGT | G,G 10 | NP_001245320.1 | |
NM_001318799.1 | 667 | UTR 5 | NP_001305728.1 | |||
NM_178834.4 | 667 | Missense Mutation | CGT,TGT | R,C 103 | NP_849156.1 | |
XM_006718769.3 | 667 | UTR 5 | XP_006718832.1 | |||
XM_006718770.3 | 667 | Silent Mutation | GGC,GGT | G,G 10 | XP_006718833.1 |