Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTCCGGGGCCTAGGGGGATGCCTGA[A/C]CAACAGAGGCTCTGCAGGCTCTGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611510 MIM: 607720 | ||||||||||||||||||||
Literature Links: |
CENPT 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 |
CENPT - centromere protein T | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_025082.3 | 1716 | Missense Mutation | GTC,TTC | V,F 438 | NP_079358.3 | |
XM_006721277.2 | 1716 | Missense Mutation | GTC,TTC | V,F 335 | XP_006721340.1 | |
XM_011523344.1 | 1716 | Missense Mutation | GTC,TTC | V,F 335 | XP_011521646.1 | |
XM_011523345.1 | 1716 | Missense Mutation | GTC,TTC | V,F 191 | XP_011521647.1 | |
XM_017023712.1 | 1716 | Missense Mutation | GTC,TTC | V,F 335 | XP_016879201.1 | |
XM_017023713.1 | 1716 | Missense Mutation | GTC,TTC | V,F 196 | XP_016879202.1 | |
XM_017023714.1 | 1716 | Missense Mutation | GTC,TTC | V,F 196 | XP_016879203.1 | |
XM_017023715.1 | 1716 | Missense Mutation | GTC,TTC | V,F 196 | XP_016879204.1 | |
XM_017023716.1 | 1716 | Missense Mutation | GTC,TTC | V,F 191 | XP_016879205.1 | |
XM_017023717.1 | 1716 | Missense Mutation | GTC,TTC | V,F 191 | XP_016879206.1 |