Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCCATATCTCCCCATCAGGTTGACA[C/T]GGTGACAGTTCCTGTACCAGAAAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 187380 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TNC 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
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
TNC - tenascin C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002160.3 | 7090 | Missense Mutation | CAT,CGT | H,R 2151 | NP_002151.2 | |
XM_005251972.3 | 7090 | Missense Mutation | CAT,CGT | H,R 2060 | XP_005252029.1 | |
XM_005251973.3 | 7090 | Missense Mutation | CAT,CGT | H,R 1787 | XP_005252030.1 | |
XM_005251974.3 | 7090 | Missense Mutation | CAT,CGT | H,R 1605 | XP_005252031.1 | |
XM_005251975.3 | 7090 | Missense Mutation | CAT,CGT | H,R 1514 | XP_005252032.1 | |
XM_006717096.3 | 7090 | Missense Mutation | CAT,CGT | H,R 2243 | XP_006717159.1 | |
XM_006717097.3 | 7090 | Missense Mutation | CAT,CGT | H,R 2060 | XP_006717160.1 | |
XM_006717098.3 | 7090 | Missense Mutation | CAT,CGT | H,R 1969 | XP_006717161.1 | |
XM_006717101.3 | 7090 | Missense Mutation | CAT,CGT | H,R 1605 | XP_006717164.1 | |
XM_011518625.2 | 7090 | Missense Mutation | CAT,CGT | H,R 1969 | XP_011516927.1 | |
XM_011518626.2 | 7090 | Missense Mutation | CAT,CGT | H,R 1879 | XP_011516928.1 | |
XM_011518628.2 | 7090 | Missense Mutation | CAT,CGT | H,R 1696 | XP_011516930.1 | |
XM_011518629.2 | 7090 | Missense Mutation | CAT,CGT | H,R 1696 | XP_011516931.1 | |
XM_017014678.1 | 7090 | Missense Mutation | CAT,CGT | H,R 2334 | XP_016870167.1 | |
XM_017014679.1 | 7090 | Missense Mutation | CAT,CGT | H,R 2243 | XP_016870168.1 | |
XM_017014680.1 | 7090 | Missense Mutation | CAT,CGT | H,R 2242 | XP_016870169.1 | |
XM_017014681.1 | 7090 | Missense Mutation | CAT,CGT | H,R 1970 | XP_016870170.1 |