Annotation Detail
Information
- Associated Genes
- VEGFA POLR1C
- Associated Variants
-
VEGFA c.-94C>G
(
ENST00000372067.8,
ENST00000425836.9,
ENST00000672860.3 )
VEGFA c.-94C>G ( ENST00000372067.8, ENST00000425836.9, ENST00000672860.3 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_003376.6(VEGFA):c.-94C>G AND not provided
- ClinVar Allele ID
- 27262
- ClinVar RefSeq Alternation Syntax
- NM_001025366.3:c.-94C>G
- ClinVar RefSeq Alternation Syntax
- NM_001171623.2:c.-634C>G
- ClinVar RefSeq Alternation Syntax
- NM_001171625.2:c.-634C>G
- ClinVar RefSeq Alternation Syntax
- NM_001025368.3:c.-94C>G
- ClinVar RefSeq Alternation Syntax
- NM_001204385.2:c.-94C>G
- ClinVar RefSeq Alternation Syntax
- NM_001033756.3:c.-94C>G
- ClinVar RefSeq Alternation Syntax
- NM_001171626.2:c.-634C>G
- ClinVar RefSeq Alternation Syntax
- NM_001171627.2:c.-634C>G
- ClinVar RefSeq Alternation Syntax
- NM_001171630.2:c.-634C>G
- ClinVar RefSeq Alternation Syntax
- NM_001171622.2:c.-94C>G
- ClinVar RefSeq Alternation Syntax
- NM_001171628.2:c.-634C>G
- ClinVar RefSeq Alternation Syntax
- NM_001204384.2:c.-634C>G
- ClinVar RefSeq Alternation Syntax
- NM_001317010.2:c.-634C>G
- ClinVar RefSeq Alternation Syntax
- NM_001171629.2:c.-634C>G
- ClinVar RefSeq Alternation Syntax
- NM_001025367.3:c.-94C>G
- ClinVar RefSeq Alternation Syntax
- NM_001025370.3:c.-94C>G
- ClinVar RefSeq Alternation Syntax
- NM_001025369.3:c.-94C>G
- ClinVar RefSeq Alternation Syntax
- NM_001318876.2:c.945+241342C>G
- ClinVar RefSeq Alternation Syntax
- NM_003376.6:c.-94C>G
- ClinVar RefSeq Alternation Syntax
- NM_001171624.2:c.-634C>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2021-06-19
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001618210
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs