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GTGGGCAGGTATGAGAATGCATCTT[C/G]GTGAAGTTGAGCCAGCACAGTCAAT
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 | |||
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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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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 | 13769 | UTR 3 | NP_001438.1 | |||
XM_006714761.3 | 13769 | UTR 3 | XP_006714824.1 | |||
XM_011537600.2 | 13769 | UTR 3 | XP_011535902.1 | |||
XM_011537603.2 | 13769 | UTR 3 | XP_011535905.1 | |||
XM_017009224.1 | 13769 | UTR 3 | XP_016864713.1 | |||
XM_017009225.1 | 13769 | UTR 3 | XP_016864714.1 | |||
XM_017009226.1 | 13769 | Intron | XP_016864715.1 | |||
XM_017009227.1 | 13769 | Intron | XP_016864716.1 |