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TGCCAGCCTAGTGAGACACCCTCAG[A/G]TTGGGTGAGATAAAAAGCGGGGGCT
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 187380 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC101928748 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)
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SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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LOC101928748 - uncharacterized LOC101928748 | ||||||
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There are no transcripts associated with this gene. |
TNC - tenascin C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002160.3 | Intron | NP_002151.2 | ||||
XM_005251972.3 | Intron | XP_005252029.1 | ||||
XM_005251973.3 | Intron | XP_005252030.1 | ||||
XM_005251974.3 | Intron | XP_005252031.1 | ||||
XM_005251975.3 | Intron | XP_005252032.1 | ||||
XM_006717096.3 | Intron | XP_006717159.1 | ||||
XM_006717097.3 | Intron | XP_006717160.1 | ||||
XM_006717098.3 | Intron | XP_006717161.1 | ||||
XM_006717101.3 | Intron | XP_006717164.1 | ||||
XM_011518625.2 | Intron | XP_011516927.1 | ||||
XM_011518626.2 | Intron | XP_011516928.1 | ||||
XM_011518628.2 | Intron | XP_011516930.1 | ||||
XM_011518629.2 | Intron | XP_011516931.1 | ||||
XM_017014678.1 | Intron | XP_016870167.1 | ||||
XM_017014679.1 | Intron | XP_016870168.1 | ||||
XM_017014680.1 | Intron | XP_016870169.1 | ||||
XM_017014681.1 | Intron | XP_016870170.1 |
Set Membership: |
HapMap |