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CTCCTCCAGGGACAGCACCTCGTCC[A/G]TACTGCTGGGTCACAGCACCGAGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 147141 MIM: 609711 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TCF3 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
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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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TCF3 - transcription factor 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001136139.2 | 1833 | Missense Mutation | ACG,ATG | T,M 531 | NP_001129611.1 | |
NM_003200.3 | 1833 | Intron | NP_003191.1 | |||
XM_006722852.3 | 1833 | Intron | XP_006722915.1 | |||
XM_006722853.3 | 1833 | Intron | XP_006722916.1 | |||
XM_006722855.3 | 1833 | Missense Mutation | ACG,ATG | T,M 560 | XP_006722918.1 | |
XM_006722856.3 | 1833 | Missense Mutation | ACG,ATG | T,M 560 | XP_006722919.1 | |
XM_006722857.3 | 1833 | Missense Mutation | ACG,ATG | T,M 559 | XP_006722920.1 | |
XM_006722858.3 | 1833 | Missense Mutation | ACG,ATG | T,M 559 | XP_006722921.1 | |
XM_011528215.2 | 1833 | Intron | XP_011526517.1 | |||
XM_011528216.2 | 1833 | Intron | XP_011526518.1 | |||
XM_011528217.2 | 1833 | Intron | XP_011526519.1 | |||
XM_011528219.2 | 1833 | Intron | XP_011526521.1 | |||
XM_011528220.2 | 1833 | Missense Mutation | ACG,ATG | T,M 560 | XP_011526522.1 | |
XM_011528221.2 | 1833 | Missense Mutation | ACG,ATG | T,M 559 | XP_011526523.1 | |
XM_011528223.2 | 1833 | Intron | XP_011526525.1 | |||
XM_011528225.2 | 1833 | Missense Mutation | ACG,ATG | T,M 530 | XP_011526527.1 | |
XM_011528226.2 | 1833 | Missense Mutation | ACG,ATG | T,M 530 | XP_011526528.1 | |
XM_011528227.2 | 1833 | Missense Mutation | ACG,ATG | T,M 480 | XP_011526529.1 | |
XM_017027177.1 | 1833 | Intron | XP_016882666.1 | |||
XM_017027178.1 | 1833 | Missense Mutation | ACG,ATG | T,M 560 | XP_016882667.1 | |
XM_017027179.1 | 1833 | Missense Mutation | ACG,ATG | T,M 559 | XP_016882668.1 | |
XM_017027180.1 | 1833 | Intron | XP_016882669.1 | |||
XM_017027181.1 | 1833 | Intron | XP_016882670.1 | |||
XM_017027182.1 | 1833 | Missense Mutation | ACG,ATG | T,M 531 | XP_016882671.1 | |
XM_017027183.1 | 1833 | Intron | XP_016882672.1 | |||
XM_017027184.1 | 1833 | Intron | XP_016882673.1 |
UQCR11 - ubiquinol-cytochrome c reductase, complex III subunit XI | ||||||
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There are no transcripts associated with this gene. |