Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AATGAAGCAGGAAAATCAAAATCCA[A/G]TGATTCTGAGGAAGGCCTCGAAGAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||||||||||||||||||||
Literature Links: |
TCP11L1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
TCP11L1 - t-complex 11 like 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145541.1 | 455 | Missense Mutation | AAT,AGT | N,S 19 | NP_001139013.1 | |
NM_018393.3 | 455 | Missense Mutation | AAT,AGT | N,S 19 | NP_060863.3 | |
XM_011520204.2 | 455 | Missense Mutation | AAT,AGT | N,S 19 | XP_011518506.1 | |
XM_011520205.2 | 455 | Missense Mutation | AAT,AGT | N,S 19 | XP_011518507.1 | |
XM_011520206.2 | 455 | Missense Mutation | AAT,AGT | N,S 19 | XP_011518508.1 | |
XM_011520207.2 | 455 | Missense Mutation | AAT,AGT | N,S 19 | XP_011518509.1 | |
XM_017017989.1 | 455 | Missense Mutation | AAT,AGT | N,S 19 | XP_016873478.1 | |
XM_017017990.1 | 455 | Missense Mutation | AAT,AGT | N,S 19 | XP_016873479.1 | |
XM_017017991.1 | 455 | Intron | XP_016873480.1 | |||
XM_017017992.1 | 455 | Intron | XP_016873481.1 |