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CCTGTGCTGCCTGCGGTTCTCGACT[C/T]ACCACTCCCCAAATGTCTTCCCTGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600489 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NFATC1 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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NFATC1 - nuclear factor of activated T-cells 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278669.1 | Intron | NP_001265598.1 | ||||
NM_001278670.1 | Intron | NP_001265599.1 | ||||
NM_001278672.1 | Intron | NP_001265601.1 | ||||
NM_001278673.1 | Intron | NP_001265602.1 | ||||
NM_001278675.1 | Intron | NP_001265604.1 | ||||
NM_006162.4 | Intron | NP_006153.2 | ||||
NM_172387.2 | Intron | NP_765975.1 | ||||
NM_172388.2 | Intron | NP_765976.1 | ||||
NM_172389.2 | Intron | NP_765977.1 | ||||
NM_172390.2 | Intron | NP_765978.1 | ||||
XM_017025783.1 | Intron | XP_016881272.1 |