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ATGTCTGAAAACCTTGACAAGTCCA[A/G]TGTAAATGAAGCAGGAAAATCAAAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
TCP11L1 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 |
TCP11L1 - t-complex 11 like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145541.1 | 425 | Missense Mutation | AAT,AGT | N,S 9 | NP_001139013.1 | |
NM_018393.3 | 425 | Missense Mutation | AAT,AGT | N,S 9 | NP_060863.3 | |
XM_011520204.2 | 425 | Missense Mutation | AAT,AGT | N,S 9 | XP_011518506.1 | |
XM_011520205.2 | 425 | Missense Mutation | AAT,AGT | N,S 9 | XP_011518507.1 | |
XM_011520206.2 | 425 | Missense Mutation | AAT,AGT | N,S 9 | XP_011518508.1 | |
XM_011520207.2 | 425 | Missense Mutation | AAT,AGT | N,S 9 | XP_011518509.1 | |
XM_017017989.1 | 425 | Missense Mutation | AAT,AGT | N,S 9 | XP_016873478.1 | |
XM_017017990.1 | 425 | Missense Mutation | AAT,AGT | N,S 9 | XP_016873479.1 | |
XM_017017991.1 | 425 | Intron | XP_016873480.1 | |||
XM_017017992.1 | 425 | Intron | XP_016873481.1 |