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GGTAGTAGCTGATGGCCGTGTACTC[A/G]TTGAGACAGGGGGCAACCAGGCGCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 604269 MIM: 606561 | ||||||||||||||||||||
Literature Links: |
FAT2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
FAT2 - FAT atypical cadherin 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001447.2 | 13161 | Silent Mutation | AAC,AAT | N,N 4269 | NP_001438.1 | |
XM_006714761.3 | 13161 | Silent Mutation | AAC,AAT | N,N 4269 | XP_006714824.1 | |
XM_011537600.2 | 13161 | Silent Mutation | AAC,AAT | N,N 4269 | XP_011535902.1 | |
XM_011537603.2 | 13161 | Silent Mutation | AAC,AAT | N,N 4269 | XP_011535905.1 | |
XM_017009224.1 | 13161 | Silent Mutation | AAC,AAT | N,N 4269 | XP_016864713.1 | |
XM_017009225.1 | 13161 | Silent Mutation | AAC,AAT | N,N 4269 | XP_016864714.1 | |
XM_017009226.1 | 13161 | Intron | XP_016864715.1 | |||
XM_017009227.1 | 13161 | Intron | XP_016864716.1 |