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CGGGGAATGAAACTGTATGGGAACA[A/G]TGGAGTGAGCAGTACTGCAAAGCTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612483 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAT3 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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FAT3 - FAT atypical cadherin 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001008781.2 | 864 | Missense Mutation | AAT,AGT | N,S 244 | NP_001008781.2 | |
XM_017017178.1 | 864 | Missense Mutation | AAT,AGT | N,S 244 | XP_016872667.1 | |
XM_017017179.1 | 864 | Missense Mutation | AAT,AGT | N,S 244 | XP_016872668.1 | |
XM_017017180.1 | 864 | Missense Mutation | AAT,AGT | N,S 244 | XP_016872669.1 | |
XM_017017181.1 | 864 | Missense Mutation | AAT,AGT | N,S 244 | XP_016872670.1 | |
XM_017017182.1 | 864 | Missense Mutation | AAT,AGT | N,S 244 | XP_016872671.1 | |
XM_017017183.1 | 864 | Missense Mutation | AAT,AGT | N,S 244 | XP_016872672.1 | |
XM_017017184.1 | 864 | Missense Mutation | AAT,AGT | N,S 244 | XP_016872673.1 | |
XM_017017185.1 | 864 | Intron | XP_016872674.1 | |||
XM_017017186.1 | 864 | Intron | XP_016872675.1 | |||
XM_017017187.1 | 864 | Intron | XP_016872676.1 |