Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 186982 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
TCP11 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)
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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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TCP11 - t-complex 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001093728.2 | 1347 | Missense Mutation | CGC,GGC | R,G 358 | NP_001087197.1 | |
NM_001261817.1 | 1347 | Missense Mutation | CGC,GGC | R,G 353 | NP_001248746.1 | |
NM_001261818.1 | 1347 | Missense Mutation | CGC,GGC | R,G 312 | NP_001248747.1 | |
NM_001261819.1 | 1347 | Missense Mutation | CGC,GGC | R,G 307 | NP_001248748.1 | |
NM_001261820.1 | 1347 | Missense Mutation | CGC,GGC | R,G 282 | NP_001248749.1 | |
NM_001261821.1 | 1347 | Missense Mutation | CGC,GGC | R,G 282 | NP_001248750.1 | |
NM_018679.5 | 1347 | Missense Mutation | CGC,GGC | R,G 283 | NP_061149.1 | |
XM_005249339.2 | 1347 | Missense Mutation | CGC,GGC | R,G 204 | XP_005249396.1 | |
XM_011514830.1 | 1347 | Missense Mutation | CGC,GGC | R,G 461 | XP_011513132.1 | |
XM_011514831.1 | 1347 | Missense Mutation | CGC,GGC | R,G 204 | XP_011513133.1 | |
XM_011514832.1 | 1347 | Missense Mutation | CGC,GGC | R,G 204 | XP_011513134.1 |
Set Membership: |
HapMap |