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- SNP ID:
- rs755276560
- Gene
-
WDFY2 - Gene Name
- WD repeat and FYVE domain containing 2
- Set Membership:
- -
- Chromosome Location:
- Chr.13: 51637568 - 51637568 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
GAAAGAGGTCCCGATCCAGACCCCA[A/G]GAGAGGGTTCTTGGATCTCTTGCAA
Genomic Map
Back To TopAssay Details
Species: |
Human |
dbSNP Submissions: |
NA
|
Phenotype: |
MIM: 610418
|
Literature Links: |
WDFY2 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 |
| WDFY2 - WD repeat and FYVE domain containing 2 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_052950.3 | Intron | NP_443182.1 | ||||
| XM_011534914.1 | Intron | XP_011533216.1 | ||||
| XM_011534915.2 | Intron | XP_011533217.1 | ||||
| XM_017020386.1 | Intron | XP_016875875.1 | ||||
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