Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCTCCTGACTGAGTATCAAAAGGCC[C/T]GGGATTTTCTAGTTCGAGCCCAGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604839 | ||||||||||||||||||||
Literature Links: |
FKBP6 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 |
FKBP6 - FK506 binding protein 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135211.2 | 938 | Missense Mutation | CGG,TGG | R,W 268 | NP_001128683.1 | |
NM_001281304.1 | 938 | Missense Mutation | CGG,TGG | R,W 243 | NP_001268233.1 | |
NM_003602.4 | 938 | Missense Mutation | CGG,TGG | R,W 273 | NP_003593.3 | |
XM_006716153.2 | 938 | Missense Mutation | CGG,TGG | R,W 228 | XP_006716216.1 | |
XM_017012741.1 | 938 | Missense Mutation | CGG,TGG | R,W 263 | XP_016868230.1 | |
XM_017012742.1 | 938 | UTR 3 | XP_016868231.1 |