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CGCTTTCGGGGAGGTAGGGATGCCA[C/T]GTCCATGCCTTGGAGAGAAGAGGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
SFT2D3 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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SFT2D3 - SFT2 domain containing 3 | ||||||
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There are no transcripts associated with this gene. |
WDR33 - WD repeat domain 33 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001006622.2 | 3872 | Intron | NP_001006623.1 | |||
NM_001006623.2 | 3872 | Intron | NP_001006624.1 | |||
NM_018383.4 | 3872 | Missense Mutation | ATG,GTG | M,V 1225 | NP_060853.3 | |
XM_005263697.2 | 3872 | Silent Mutation | ACA,ACG | T,T 1078 | XP_005263754.1 | |
XM_011511436.1 | 3872 | Missense Mutation | ATG,GTG | M,V 1225 | XP_011509738.1 | |
XM_017004435.1 | 3872 | Intron | XP_016859924.1 | |||
XM_017004436.1 | 3872 | Intron | XP_016859925.1 |