Variant ID: 6-43746423-A-G

NM_001025366.2(VEGFA):c.932+150A>G

This variant was identified in 1 publication



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Germline Genetic Variants in TEK, ANGPT1, ANGPT2, MMP9, FGF2 and VEGFA Are Associated with Pathologic Complete Response to Bevacizumab in Breast Cancer Patients.

Plos One
I Makhoul, VK Todorova, ER Siegel, SW Erickson, I Dhakal, VR Raj, JY Lee, MS Orloff, RJ Griffin, RS Henry-Tillman, S Klimberg, LF Hutchins, SA Kadlubar
Publication Date: 2017

Variant appearance in text: rs3025048
PubMed Link: 28045923
PubMed Central Link
Variant Present in the following documents:
  • pone.0168550.s006.xlsx
  • pone.0168550.s005.xlsx
  • pone.0168550.s007.xlsx
View BVdb publication page


Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000230480.6 c.308+150A>G - intron_variant - 4/6
ENST00000324450.6 c.932+150A>G - intron_variant - 4/4
ENST00000372055.4 c.932+150A>G - intron_variant - 4/7
ENST00000372064.4 c.932+150A>G - intron_variant - 4/5
ENST00000372067.3 c.932+150A>G - intron_variant - 4/6
ENST00000372077.4 c.392+150A>G - intron_variant - 4/5
ENST00000413642.3 c.932+150A>G - intron_variant - 4/7
ENST00000417285.2 c.932+150A>G - intron_variant - 4/6
ENST00000425836.2 c.932+150A>G - intron_variant - 4/7
ENST00000457104.2 c.392+150A>G - intron_variant - 4/4
ENST00000476772.1 n.1605A>G - non_coding_transcript_exon_variant 4/4 -
ENST00000480614.1 n.4571+150A>G - intron_variant,non_coding_transcript_variant - 2/2
ENST00000482630.2 c.932+150A>G - intron_variant - 4/6
ENST00000493786.2 n.365+150A>G - intron_variant,non_coding_transcript_variant - 1/3
ENST00000497139.1 n.817+150A>G - intron_variant,non_coding_transcript_variant - 1/2
ENST00000518538.1 n.486+150A>G - intron_variant,non_coding_transcript_variant - 4/4
ENST00000518689.1 c.392+150A>G - intron_variant - 4/7
ENST00000518824.1 c.392+150A>G - intron_variant - 4/6
ENST00000519767.1 c.846+150A>G - intron_variant - 4/6
ENST00000520265.1 c.237+1021A>G - intron_variant - 2/3
ENST00000520948.1 c.392+150A>G - intron_variant - 4/7
ENST00000523125.1 c.392+150A>G - intron_variant - 4/6
ENST00000523873.1 c.392+150A>G - intron_variant - 4/7
ENST00000523950.1 c.392+150A>G - intron_variant - 4/6
NM_001025366.3 c.932+150A>G - intron_variant - 4/7
NM_001025367.3 c.932+150A>G - intron_variant - 4/7
NM_001025368.3 c.932+150A>G - intron_variant - 4/6
NM_001025369.3 c.932+150A>G - intron_variant - 4/6
NM_001025370.3 c.932+150A>G - intron_variant - 4/5
NM_001033756.3 c.932+150A>G - intron_variant - 4/6
NM_001171622.2 c.932+150A>G - intron_variant - 4/4
NM_001171623.1 c.392+150A>G - intron_variant - 4/7
NM_001171624.1 c.392+150A>G - intron_variant - 4/7
NM_001171625.1 c.392+150A>G - intron_variant - 4/7
NM_001171626.1 c.392+150A>G - intron_variant - 4/6
NM_001171627.1 c.392+150A>G - intron_variant - 4/6
NM_001171628.1 c.392+150A>G - intron_variant - 4/5
NM_001171629.1 c.392+150A>G - intron_variant - 4/6
NM_001171630.1 c.392+150A>G - intron_variant - 4/4
NM_001204384.1 c.392+150A>G - intron_variant - 4/6
NM_001204385.2 c.932+150A>G - intron_variant - 4/6
NM_001287044.2 c.308+150A>G - intron_variant - 4/6
NM_001317010.1 c.392+150A>G - intron_variant - 4/6
NM_003376.6 c.932+150A>G - intron_variant - 4/7