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TGAGCATGTCAAACTTGATGAGCGG[C/T]GGGGCGATCACGCGCACCTCGGCGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
LRRC20 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
LRRC20 - leucine rich repeat containing 20 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278211.1 | 655 | Silent Mutation | CCA,CCG | P,P 165 | NP_001265140.1 | |
NM_001278212.1 | 655 | Silent Mutation | CCA,CCG | P,P 165 | NP_001265141.1 | |
NM_001278213.1 | 655 | Silent Mutation | CCA,CCG | P,P 115 | NP_001265142.1 | |
NM_001278214.1 | 655 | Silent Mutation | CCA,CCG | P,P 96 | NP_001265143.1 | |
NM_018205.3 | 655 | Silent Mutation | CCA,CCG | P,P 109 | NP_060675.1 | |
NM_018239.3 | 655 | Silent Mutation | CCA,CCG | P,P 115 | NP_060709.2 | |
NM_207119.2 | 655 | Silent Mutation | CCA,CCG | P,P 165 | NP_997002.1 | |
XM_017016374.1 | 655 | Silent Mutation | CCA,CCG | P,P 165 | XP_016871863.1 | |
XM_017016375.1 | 655 | Silent Mutation | CCA,CCG | P,P 165 | XP_016871864.1 |