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CCTGAGCCTAATCAAGGTGGCCAGC[C/G]CCTTGGACCGCGAGCGCATCCCTTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612411 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAT4 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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FAT4 - FAT atypical cadherin 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001291285.1 | 1273 | Missense Mutation | CCC,GCC | P,A 425 | NP_001278214.1 | |
NM_001291303.1 | 1273 | Missense Mutation | CCC,GCC | P,A 425 | NP_001278232.1 | |
NM_024582.4 | 1273 | Missense Mutation | CCC,GCC | P,A 425 | NP_078858.4 | |
XM_011532236.2 | 1273 | Missense Mutation | CCC,GCC | P,A 425 | XP_011530538.1 | |
XM_011532237.2 | 1273 | Intron | XP_011530539.1 |