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TCTTATTTTGGAGAAAGATGGAGAC[A/G]ATAATCCTGTCTGTCGACTGCCAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
LRRCC1 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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LRRCC1 - leucine rich repeat and coiled-coil centrosomal protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_033402.4 | 389 | Missense Mutation | AAT,GAT | N,D 174 | NP_208325.3 | |
XM_005251318.3 | 389 | Missense Mutation | AAT,GAT | N,D 81 | XP_005251375.1 | |
XM_005251319.4 | 389 | Silent Mutation | ACA,ACG | T,T 3 | XP_005251376.1 | |
XM_005251320.3 | 389 | Silent Mutation | ACA,ACG | T,T 3 | XP_005251377.1 | |
XM_005251322.3 | 389 | UTR 5 | XP_005251379.1 | |||
XM_017013920.1 | 389 | Missense Mutation | AAT,GAT | N,D 174 | XP_016869409.1 | |
XM_017013921.1 | 389 | Missense Mutation | AAT,GAT | N,D 174 | XP_016869410.1 | |
XM_017013922.1 | 389 | Missense Mutation | AAT,GAT | N,D 174 | XP_016869411.1 | |
XM_017013923.1 | 389 | Missense Mutation | AAT,GAT | N,D 81 | XP_016869412.1 | |
XM_017013924.1 | 389 | Missense Mutation | AAT,GAT | N,D 174 | XP_016869413.1 | |
XM_017013925.1 | 389 | UTR 5 | XP_016869414.1 | |||
XM_017013926.1 | 389 | UTR 5 | XP_016869415.1 | |||
XM_017013927.1 | 389 | UTR 5 | XP_016869416.1 | |||
XM_017013928.1 | 389 | UTR 5 | XP_016869417.1 |