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- SNP ID:
- rs73248508
- Gene
-
EFNB3WRAP53 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.17: 7701770 - 7701770 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
CCACGGCCCGGCCTGGCCGAGACTG[C/T]GAGGTCCGAGCCACATTTGGTAAGC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 602297
MIM: 612661
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Literature Links: |
EFNB3 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
|
| EFNB3 - ephrin B3 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| WRAP53 - WD repeat containing antisense to TP53 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001143990.1 | 1091 | Silent Mutation | TGC,TGT | C,C 312 | NP_001137462.1 | |
| NM_001143991.1 | 1091 | Silent Mutation | TGC,TGT | C,C 312 | NP_001137463.1 | |
| NM_001143992.1 | 1091 | Silent Mutation | TGC,TGT | C,C 312 | NP_001137464.1 | |
| NM_018081.2 | 1091 | Silent Mutation | TGC,TGT | C,C 312 | NP_060551.2 | |
| XM_011523952.2 | 1091 | Silent Mutation | TGC,TGT | C,C 99 | XP_011522254.1 | |
| XM_017024812.1 | 1091 | UTR 3 | XP_016880301.1 | |||
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