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- SNP ID:
- rs768801020
- Gene
-
WDFY3 - Gene Name
- WD repeat and FYVE domain containing 3
- Set Membership:
- -
- Chromosome Location:
- Chr.4: 84828131 - 84828131 on Build GRCh38
- Polymorphism:
- T/C, Transition substitution
- Context Sequence [VIC/FAM]:
GAAGGAAGGGAGGGAGACAAGTAAG[T/C]TTACAAAACAGTGGTGTCTTATAAT
Genomic Map
Back To TopAssay Details
Species: |
Human |
dbSNP Submissions: |
NA
|
Phenotype: |
|
Literature Links: |
WDFY3 PubMed Links |
Allele Nomenclature: |
|
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 |
| WDFY3 - WD repeat and FYVE domain containing 3 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_014991.4 | Intron | NP_055806.2 | ||||
| XM_005262858.4 | Intron | XP_005262915.1 | ||||
| XM_011531757.2 | Intron | XP_011530059.1 | ||||
| XM_011531759.2 | Intron | XP_011530061.1 | ||||
| XM_011531760.2 | Intron | XP_011530062.1 | ||||
| XM_011531761.2 | Intron | XP_011530063.1 | ||||
| XM_011531762.2 | Intron | XP_011530064.1 | ||||
| XM_011531763.2 | Intron | XP_011530065.1 | ||||
| XM_011531764.2 | Intron | XP_011530066.1 | ||||
| XM_011531765.2 | Intron | XP_011530067.1 | ||||
| XM_011531766.2 | Intron | XP_011530068.1 | ||||
| XM_011531767.2 | Intron | XP_011530069.1 | ||||
| XM_017007906.1 | Intron | XP_016863395.1 | ||||
| XM_017007907.1 | Intron | XP_016863396.1 | ||||
| XM_017007908.1 | Intron | XP_016863397.1 | ||||
| XM_017007909.1 | Intron | XP_016863398.1 | ||||
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