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- SNP ID:
- rs80332987
- Gene
-
WDFY4 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.10: 48730240 - 48730240 on Build GRCh38
- Polymorphism:
- A/C, Transversion substitution
- Context Sequence [VIC/FAM]:
TAAAGGCAGAAATGACAGTCTGGGG[A/C]ATAAATGGTGGCCTGGAAGGCTGGG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 613316
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Literature Links: |
WDFY4 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
| WDFY4 - WDFY family member 4 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_020945.1 | Intron | NP_065996.1 | ||||
| XM_005270004.3 | Intron | XP_005270061.1 | ||||
| XM_011539986.2 | Intron | XP_011538288.2 | ||||
| XM_011539987.2 | Intron | XP_011538289.2 | ||||
| XM_011539988.2 | Intron | XP_011538290.1 | ||||
| XM_011539990.2 | Intron | XP_011538292.1 | ||||
| XM_011539991.2 | Intron | XP_011538293.1 | ||||
| XM_011539992.2 | Intron | XP_011538294.1 | ||||
| XM_017016463.1 | Intron | XP_016871952.1 | ||||
| XM_017016464.1 | Intron | XP_016871953.1 | ||||
| XM_017016465.1 | Intron | XP_016871954.1 | ||||
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