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CCCTCAGATCTGTTAGCTGTGACCC[A/G]TAGATTGGGGGAGGGAGGAAAGCCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609785 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TFCP2L1 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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TFCP2L1 - transcription factor CP2-like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014553.2 | 6366 | UTR 3 | NP_055368.1 | |||
XM_017003902.1 | 6366 | UTR 3 | XP_016859391.1 | |||
XM_017003903.1 | 6366 | UTR 3 | XP_016859392.1 | |||
XM_017003904.1 | 6366 | Intron | XP_016859393.1 | |||
XM_017003905.1 | 6366 | Intron | XP_016859394.1 |