Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602699 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
NFATC4 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)
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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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NFATC4 - nuclear factor of activated T-cells 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001136022.2 | 1058 | Missense Mutation | AAC,AGC | N,S 309 | NP_001129494.1 | |
NM_001198965.1 | 1058 | Missense Mutation | AAC,AGC | N,S 246 | NP_001185894.1 | |
NM_001198966.2 | 1058 | Missense Mutation | AAC,AGC | N,S 176 | NP_001185895.1 | |
NM_001198967.2 | 1058 | Missense Mutation | AAC,AGC | N,S 309 | NP_001185896.1 | |
NM_001288802.1 | 1058 | Missense Mutation | AAC,AGC | N,S 234 | NP_001275731.1 | |
NM_001320043.1 | 1058 | Missense Mutation | AAC,AGC | N,S 309 | NP_001306972.1 | |
NM_004554.4 | 1058 | Missense Mutation | AAC,AGC | N,S 246 | NP_004545.2 | |
XM_011536797.2 | 1058 | Missense Mutation | AAC,AGC | N,S 234 | XP_011535099.1 | |
XM_011536798.1 | 1058 | Missense Mutation | AAC,AGC | N,S 223 | XP_011535100.1 | |
XM_011536799.2 | 1058 | Missense Mutation | AAC,AGC | N,S 234 | XP_011535101.1 |
Set Membership: |
HapMap |