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GCGCGGGAGCGGAGCCGGGTCAGGA[C/T]GCTGCGCCAGGCCTTCTTGGCCTTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609635 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TCF23 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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TCF23 - transcription factor 23 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_175769.2 | 329 | Missense Mutation | ACG,ATG | T,M 91 | NP_786951.1 | |
XM_005264159.4 | 329 | Missense Mutation | ACG,ATG | T,M 91 | XP_005264216.1 |