Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TACCTGCACTACCTCAGTGAGCGAG[A/G]TGCCTGTAAGATCCTCATCGCAGAC
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 | |||
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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
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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CENPT - centromere protein T | ||||||
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There are no transcripts associated with this gene. |
TSNAXIP1 - translin associated factor X interacting protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001288990.1 | 572 | Missense Mutation | GAT,GGT | D,G 246 | NP_001275919.1 | |
NM_001288991.1 | 572 | Missense Mutation | GAT,GGT | D,G 177 | NP_001275920.1 | |
NM_001288992.1 | 572 | UTR 5 | NP_001275921.1 | |||
NM_001288993.1 | 572 | UTR 5 | NP_001275922.1 | |||
NM_001288994.1 | 572 | UTR 5 | NP_001275923.1 | |||
NM_018430.3 | 572 | Missense Mutation | GAT,GGT | D,G 192 | NP_060900.2 | |
XM_005256049.4 | 572 | Missense Mutation | GAT,GGT | D,G 246 | XP_005256106.1 | |
XM_011523230.2 | 572 | Missense Mutation | GAT,GGT | D,G 246 | XP_011521532.1 | |
XM_011523231.2 | 572 | Missense Mutation | GAT,GGT | D,G 246 | XP_011521533.1 | |
XM_011523232.2 | 572 | Missense Mutation | GAT,GGT | D,G 246 | XP_011521534.1 | |
XM_011523233.2 | 572 | Missense Mutation | GAT,GGT | D,G 246 | XP_011521535.1 | |
XM_011523234.2 | 572 | Missense Mutation | GAT,GGT | D,G 246 | XP_011521536.1 | |
XM_011523235.1 | 572 | Missense Mutation | GAT,GGT | D,G 192 | XP_011521537.1 | |
XM_011523236.2 | 572 | Missense Mutation | GAT,GGT | D,G 177 | XP_011521538.1 | |
XM_011523237.2 | 572 | Missense Mutation | GAT,GGT | D,G 166 | XP_011521539.1 | |
XM_011523238.1 | 572 | Missense Mutation | GAT,GGT | D,G 158 | XP_011521540.1 | |
XM_011523239.1 | 572 | Missense Mutation | GAT,GGT | D,G 149 | XP_011521541.1 | |
XM_011523240.1 | 572 | Missense Mutation | GAT,GGT | D,G 88 | XP_011521542.1 | |
XM_011523241.1 | 572 | Missense Mutation | GAT,GGT | D,G 56 | XP_011521543.1 | |
XM_011523242.1 | 572 | Missense Mutation | GAT,GGT | D,G 56 | XP_011521544.1 | |
XM_011523243.1 | 572 | UTR 5 | XP_011521545.1 | |||
XM_017023445.1 | 572 | Missense Mutation | GAT,GGT | D,G 177 | XP_016878934.1 | |
XM_017023446.1 | 572 | Missense Mutation | GAT,GGT | D,G 158 | XP_016878935.1 | |
XM_017023447.1 | 572 | Missense Mutation | GAT,GGT | D,G 177 | XP_016878936.1 | |
XM_017023448.1 | 572 | Missense Mutation | GAT,GGT | D,G 158 | XP_016878937.1 | |
XM_017023449.1 | 572 | Missense Mutation | GAT,GGT | D,G 177 | XP_016878938.1 | |
XM_017023450.1 | 572 | Missense Mutation | GAT,GGT | D,G 88 | XP_016878939.1 | |
XM_017023451.1 | 572 | Missense Mutation | GAT,GGT | D,G 88 | XP_016878940.1 | |
XM_017023452.1 | 572 | Missense Mutation | GAT,GGT | D,G 56 | XP_016878941.1 | |
XM_017023453.1 | 572 | Missense Mutation | GAT,GGT | D,G 56 | XP_016878942.1 | |
XM_017023454.1 | 572 | Missense Mutation | GAT,GGT | D,G 56 | XP_016878943.1 | |
XM_017023455.1 | 572 | Missense Mutation | GAT,GGT | D,G 56 | XP_016878944.1 |