Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCTGGGCCCTCACGGTCCACTCACC[C/T]GACTGTGGTTATTGTCCCCATATCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 187380 | ||||||||||||||||||||
Literature Links: |
TNC PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
TNC - tenascin C | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002160.3 | 7132 | Missense Mutation | CAG,CGG | Q,R 2165 | NP_002151.2 | |
XM_005251972.3 | 7132 | Missense Mutation | CAG,CGG | Q,R 2074 | XP_005252029.1 | |
XM_005251973.3 | 7132 | Missense Mutation | CAG,CGG | Q,R 1801 | XP_005252030.1 | |
XM_005251974.3 | 7132 | Missense Mutation | CAG,CGG | Q,R 1619 | XP_005252031.1 | |
XM_005251975.3 | 7132 | Missense Mutation | CAG,CGG | Q,R 1528 | XP_005252032.1 | |
XM_006717096.3 | 7132 | Missense Mutation | CAG,CGG | Q,R 2257 | XP_006717159.1 | |
XM_006717097.3 | 7132 | Missense Mutation | CAG,CGG | Q,R 2074 | XP_006717160.1 | |
XM_006717098.3 | 7132 | Missense Mutation | CAG,CGG | Q,R 1983 | XP_006717161.1 | |
XM_006717101.3 | 7132 | Missense Mutation | CAG,CGG | Q,R 1619 | XP_006717164.1 | |
XM_011518625.2 | 7132 | Missense Mutation | CAG,CGG | Q,R 1983 | XP_011516927.1 | |
XM_011518626.2 | 7132 | Missense Mutation | CAG,CGG | Q,R 1893 | XP_011516928.1 | |
XM_011518628.2 | 7132 | Missense Mutation | CAG,CGG | Q,R 1710 | XP_011516930.1 | |
XM_011518629.2 | 7132 | Missense Mutation | CAG,CGG | Q,R 1710 | XP_011516931.1 | |
XM_017014678.1 | 7132 | Missense Mutation | CAG,CGG | Q,R 2348 | XP_016870167.1 | |
XM_017014679.1 | 7132 | Missense Mutation | CAG,CGG | Q,R 2257 | XP_016870168.1 | |
XM_017014680.1 | 7132 | Missense Mutation | CAG,CGG | Q,R 2256 | XP_016870169.1 | |
XM_017014681.1 | 7132 | Missense Mutation | CAG,CGG | Q,R 1984 | XP_016870170.1 |