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GAAAATGTACCTATTGAACAGATTC[C/T]ACTTGTGAAGGTTAGTAAGAAATTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
DTWD1 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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DTWD1 - DTW domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001144955.1 | 450 | Missense Mutation | CCA,CTA | P,L 85 | NP_001138427.1 | |
NM_020234.5 | 450 | Missense Mutation | CCA,CTA | P,L 85 | NP_064619.2 | |
XM_011521815.1 | 450 | Missense Mutation | CCA,CTA | P,L 85 | XP_011520117.1 | |
XM_017022419.1 | 450 | Missense Mutation | CCA,CTA | P,L 85 | XP_016877908.1 | |
XM_017022420.1 | 450 | Missense Mutation | CCA,CTA | P,L 85 | XP_016877909.1 | |
XM_017022421.1 | 450 | Missense Mutation | CCA,CTA | P,L 85 | XP_016877910.1 | |
XM_017022422.1 | 450 | Missense Mutation | CCA,CTA | P,L 85 | XP_016877911.1 | |
XM_017022423.1 | 450 | Missense Mutation | CCA,CTA | P,L 85 | XP_016877912.1 | |
XM_017022424.1 | 450 | Missense Mutation | CCA,CTA | P,L 85 | XP_016877913.1 | |
XM_017022425.1 | 450 | Missense Mutation | CCA,CTA | P,L 85 | XP_016877914.1 | |
XM_017022426.1 | 450 | Missense Mutation | CCA,CTA | P,L 85 | XP_016877915.1 | |
XM_017022427.1 | 450 | UTR 5 | XP_016877916.1 | |||
XM_017022428.1 | 450 | UTR 5 | XP_016877917.1 | |||
XM_017022429.1 | 450 | UTR 5 | XP_016877918.1 | |||
XM_017022430.1 | 450 | UTR 5 | XP_016877919.1 | |||
XM_017022431.1 | 450 | Intron | XP_016877920.1 |
FAM227B - family with sequence similarity 227 member B | ||||||
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There are no transcripts associated with this gene. |