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CGCTGTCCGCAGTCCTTAGCGGGAT[A/G]ATAATGTCACTGGGCTCTGAGCCGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600527 | ||||||||||||||||||||
Literature Links: |
EFNB2 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 |
EFNB2 - ephrin B2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004093.3 | 946 | Silent Mutation | ATC,ATT | I,I 290 | NP_004084.1 | |
XM_017020406.1 | 946 | Silent Mutation | ATC,ATT | I,I 292 | XP_016875895.1 |