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GTCTCATTGCTATATTGAGAGGGGC[A/G]GCTAATGTCATAGGTGTGGGTAGAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606747 | ||||||||||||||||||||
Literature Links: |
VEZF1 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 |
VEZF1 - vascular endothelial zinc finger 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_007146.2 | 1832 | Silent Mutation | GCC,GCT | A,A 495 | NP_009077.2 | |
XM_005257643.1 | 1832 | Silent Mutation | GCC,GCT | A,A 501 | XP_005257700.1 | |
XM_005257644.4 | 1832 | Silent Mutation | GCC,GCT | A,A 492 | XP_005257701.1 | |
XM_017025017.1 | 1832 | Silent Mutation | GCC,GCT | A,A 486 | XP_016880506.1 | |
XM_017025018.1 | 1832 | Silent Mutation | GCC,GCT | A,A 486 | XP_016880507.1 |