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TGGTGTCCAGATTTTGCCGGGATGT[C/G]GAAACAGAGTTGATGACCGAGGAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600743 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LINC01569 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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LINC01569 - long intergenic non-protein coding RNA 1569 | ||||||
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There are no transcripts associated with this gene. |
LOC105371063 - putative uncharacterized protein encoded by LINC00596 | ||||||
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There are no transcripts associated with this gene. |
TFAP4 - transcription factor AP-4 (activating enhancer binding protein 4) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003223.2 | 1179 | Silent Mutation | TCC,TCG | S,S 263 | NP_003214.1 | |
XM_011522633.2 | 1179 | Silent Mutation | TCC,TCG | S,S 250 | XP_011520935.1 | |
XM_011522635.2 | 1179 | Silent Mutation | TCC,TCG | S,S 203 | XP_011520937.1 |