Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CACGCGCCACGTCCACCTTGAATGT[C/G]GGCTTCAGCTCTGGTGGTGTGGGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602297 MIM: 612661 | ||||||||||||||||||||
Literature Links: |
EFNB3 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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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 |
EFNB3 - ephrin B3 | ||||||
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There are no transcripts associated with this gene. |
WRAP53 - WD repeat containing antisense to TP53 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001143990.1 | 1692 | Missense Mutation | CGG,GGG | R,G 513 | NP_001137462.1 | |
NM_001143991.1 | 1692 | Missense Mutation | CGG,GGG | R,G 513 | NP_001137463.1 | |
NM_001143992.1 | 1692 | Missense Mutation | CGG,GGG | R,G 513 | NP_001137464.1 | |
NM_018081.2 | 1692 | Missense Mutation | CGG,GGG | R,G 513 | NP_060551.2 | |
XM_011523952.2 | 1692 | Missense Mutation | CGG,GGG | R,G 300 | XP_011522254.1 | |
XM_017024812.1 | 1692 | Intron | XP_016880301.1 |