Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.103937267A>G | CA2793448844 | PDGFD | c.772+6185T>C (n.772+6185T>C) c.754+6185T>C (n.754+6185T>C) | |
11 | g.103937269C= | CA1996762702 | PDGFD | c.772+6183G= (n.772+6183G=) c.754+6183G= (n.754+6183G=) | |
11 | g.103937269C>T | CA601294178 | PDGFD | c.772+6183G>A (n.772+6183G>A) c.754+6183G>A (n.754+6183G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.103937271A>C | CA2724771187 | PDGFD | c.772+6181T>G (n.772+6181T>G) c.754+6181T>G (n.754+6181T>G) | dbSNP |
11 | g.103937274C= | CA1996762703 | PDGFD | c.772+6178G= (n.772+6178G=) c.754+6178G= (n.754+6178G=) | |
11 | g.103937274C>T | CA941703509 | PDGFD | c.772+6178G>A (n.772+6178G>A) c.754+6178G>A (n.754+6178G>A) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.103937276C= | CA1996762704 | PDGFD | c.772+6176G= (n.772+6176G=) c.754+6176G= (n.754+6176G=) | |
11 | g.103937276C>G | CA227642630 | PDGFD | c.772+6176G>C (n.772+6176G>C) c.754+6176G>C (n.754+6176G>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.103937276C>T | CA671011005 | PDGFD | c.772+6176G>A (n.772+6176G>A) c.754+6176G>A (n.754+6176G>A) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.103937283T>G | CA671011006 | PDGFD | c.772+6169A>C (n.772+6169A>C) c.754+6169A>C (n.754+6169A>C) | dbSNP |
11 | g.103937283T= | CA1996762705 | PDGFD | c.772+6169A= (n.772+6169A=) c.754+6169A= (n.754+6169A=) | |
11 | g.103937284G= | CA1996762706 | PDGFD | c.772+6168C= (n.772+6168C=) c.754+6168C= (n.754+6168C=) | |
11 | g.103937286_103937290dup | CA671011008 | PDGFD | c.772+6163_772+6167dup (n.772+6163_772+6167dup) c.754+6163_754+6167dup (n.754+6163_754+6167dup) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.103937288A>G | CA2516145168 | PDGFD | c.772+6164T>C (n.772+6164T>C) c.754+6164T>C (n.754+6164T>C) | |
11 | g.103937290A= | CA1996762707 | PDGFD | c.772+6162T= (n.772+6162T=) c.754+6162T= (n.754+6162T=) | |
11 | g.103937290A>C | CA671011012 | PDGFD | c.772+6162T>G (n.772+6162T>G) c.754+6162T>G (n.754+6162T>G) | dbSNP |
11 | g.103937297C>A | CA2519160917 | PDGFD | c.772+6155G>T (n.772+6155G>T) c.754+6155G>T (n.754+6155G>T) | |
11 | g.103937297C= | CA1996762708 | PDGFD | c.772+6155G= (n.772+6155G=) c.754+6155G= (n.754+6155G=) | |
11 | g.103937297C>G | CA671011018 | PDGFD | c.772+6155G>C (n.772+6155G>C) c.754+6155G>C (n.754+6155G>C) | dbSNP |
11 | g.103937297C>T | CA671011017 | PDGFD | c.772+6155G>A (n.772+6155G>A) c.754+6155G>A (n.754+6155G>A) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.103937300C= | CA1996762709 | PDGFD | c.772+6152G= (n.772+6152G=) c.754+6152G= (n.754+6152G=) | |
11 | g.103937300C>T | CA671011019 | PDGFD | c.772+6152G>A (n.772+6152G>A) c.754+6152G>A (n.754+6152G>A) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.103937301C= | CA1996762710 | PDGFD | c.772+6151G= (n.772+6151G=) c.754+6151G= (n.754+6151G=) | |
11 | g.103937301C>T | CA227642631 | PDGFD | c.772+6151G>A (n.772+6151G>A) c.754+6151G>A (n.754+6151G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.103937302T>C | CA227642632 | PDGFD | c.772+6150A>G (n.772+6150A>G) c.754+6150A>G (n.754+6150A>G) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.103937302T= | CA1996762711 | PDGFD | c.772+6150A= (n.772+6150A=) c.754+6150A= (n.754+6150A=) | |
11 | g.103937303T>C | CA1996762713 | PDGFD | c.772+6149A>G (n.772+6149A>G) c.754+6149A>G (n.754+6149A>G) | dbSNP |
11 | g.103937303T= | CA1996762712 | PDGFD | c.772+6149A= (n.772+6149A=) c.754+6149A= (n.754+6149A=) | |
11 | g.103937304G>A | CA671011033 | PDGFD | c.772+6148C>T (n.772+6148C>T) c.754+6148C>T (n.754+6148C>T) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.103937304G= | CA1996762714 | PDGFD | c.772+6148C= (n.772+6148C=) c.754+6148C= (n.754+6148C=) | |
11 | g.103937307A= | CA1996762715 | PDGFD | c.772+6145T= (n.772+6145T=) c.754+6145T= (n.754+6145T=) | |
11 | g.103937307A>G | CA227642633 | PDGFD | c.772+6145T>C (n.772+6145T>C) c.754+6145T>C (n.754+6145T>C) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.103937309T>C | CA1996762717 | PDGFD | c.772+6143A>G (n.772+6143A>G) c.754+6143A>G (n.754+6143A>G) | dbSNP |
11 | g.103937309T= | CA1996762716 | PDGFD | c.772+6143A= (n.772+6143A=) c.754+6143A= (n.754+6143A=) | |
11 | g.103937310A= | CA1996762718 | PDGFD | c.772+6142T= (n.772+6142T=) c.754+6142T= (n.754+6142T=) | |
11 | g.103937310A>T | CA227642634 | PDGFD | c.772+6142T>A (n.772+6142T>A) c.754+6142T>A (n.754+6142T>A) | dbSNP |
11 | g.103937311T>G | CA671011036 | PDGFD | c.772+6141A>C (n.772+6141A>C) c.754+6141A>C (n.754+6141A>C) | dbSNP |
11 | g.103937311T= | CA1996762719 | PDGFD | c.772+6141A= (n.772+6141A=) c.754+6141A= (n.754+6141A=) | |
11 | g.103937312G>A | CA227642635 | PDGFD | c.772+6140C>T (n.772+6140C>T) c.754+6140C>T (n.754+6140C>T) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.103937312G= | CA1996762720 | PDGFD | c.772+6140C= (n.772+6140C=) c.754+6140C= (n.754+6140C=) | |
11 | g.103937314C= | CA1996762721 | PDGFD | c.772+6138G= (n.772+6138G=) c.754+6138G= (n.754+6138G=) | |
11 | g.103937314C>G | CA227642636 | PDGFD | c.772+6138G>C (n.772+6138G>C) c.754+6138G>C (n.754+6138G>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.103937315C>T | CA2724771203 | PDGFD | c.772+6137G>A (n.772+6137G>A) c.754+6137G>A (n.754+6137G>A) | dbSNP |
11 | g.103937317G>C | CA601294180 | PDGFD | c.772+6135C>G (n.772+6135C>G) c.754+6135C>G (n.754+6135C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.103937317G= | CA1996762722 | PDGFD | c.772+6135C= (n.772+6135C=) c.754+6135C= (n.754+6135C=) | |
11 | g.103937318G>C | CA227642637 | PDGFD | c.772+6134C>G (n.772+6134C>G) c.754+6134C>G (n.754+6134C>G) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.103937318G= | CA1996762723 | PDGFD | c.772+6134C= (n.772+6134C=) c.754+6134C= (n.754+6134C=) | |
11 | g.103937327T>C | CA1996762725 | PDGFD | c.772+6125A>G (n.772+6125A>G) c.754+6125A>G (n.754+6125A>G) | dbSNP |
11 | g.103937327T= | CA1996762724 | PDGFD | c.772+6125A= (n.772+6125A=) c.754+6125A= (n.754+6125A=) | |
11 | g.103937329G>A | CA601294181 | PDGFD | c.772+6123C>T (n.772+6123C>T) c.754+6123C>T (n.754+6123C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.103937329G= | CA1996762726 | PDGFD | c.772+6123C= (n.772+6123C=) c.754+6123C= (n.754+6123C=) | |
11 | g.103937330G>A | CA671011043 | PDGFD | c.772+6122C>T (n.772+6122C>T) c.754+6122C>T (n.754+6122C>T) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.103937330G>C | CA2793448845 | PDGFD | c.772+6122C>G (n.772+6122C>G) c.754+6122C>G (n.754+6122C>G) | |
11 | g.103937330G= | CA1996762727 | PDGFD | c.772+6122C= (n.772+6122C=) c.754+6122C= (n.754+6122C=) | |
11 | g.103937334A= | CA1996762728 | PDGFD | c.772+6118T= (n.772+6118T=) c.754+6118T= (n.754+6118T=) | |
11 | g.103937334A>G | CA227642638 | PDGFD | c.772+6118T>C (n.772+6118T>C) c.754+6118T>C (n.754+6118T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.103937339C= | CA1996762729 | PDGFD | c.772+6113G= (n.772+6113G=) c.754+6113G= (n.754+6113G=) | |
11 | g.103937339C>T | CA941703540 | PDGFD | c.772+6113G>A (n.772+6113G>A) c.754+6113G>A (n.754+6113G>A) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.103937340T>C | CA671011049 | PDGFD | c.772+6112A>G (n.772+6112A>G) c.754+6112A>G (n.754+6112A>G) | dbSNP |
11 | g.103937340T= | CA1996762730 | PDGFD | c.772+6112A= (n.772+6112A=) c.754+6112A= (n.754+6112A=) | |
11 | g.103937341A= | CA1996762731 | PDGFD | c.772+6111T= (n.772+6111T=) c.754+6111T= (n.754+6111T=) | |
11 | g.103937341A>C | CA2724648835 | PDGFD | c.772+6111T>G (n.772+6111T>G) c.754+6111T>G (n.754+6111T>G) | dbSNP |
11 | g.103937341A>G | CA941703546 | PDGFD | c.772+6111T>C (n.772+6111T>C) c.754+6111T>C (n.754+6111T>C) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.103937342T>C | CA941703567 | PDGFD | c.772+6110A>G (n.772+6110A>G) c.754+6110A>G (n.754+6110A>G) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.103937342T= | CA1996762732 | PDGFD | c.772+6110A= (n.772+6110A=) c.754+6110A= (n.754+6110A=) | |
11 | g.103937343C= | CA1996762733 | PDGFD | c.772+6109G= (n.772+6109G=) c.754+6109G= (n.754+6109G=) | |
11 | g.103937343C>T | CA941703569 | PDGFD | c.772+6109G>A (n.772+6109G>A) c.754+6109G>A (n.754+6109G>A) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.103937348T>A | CA941703573 | PDGFD | c.772+6104A>T (n.772+6104A>T) c.754+6104A>T (n.754+6104A>T) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.103937348T>C | CA1996762734 | PDGFD | c.772+6104A>G (n.772+6104A>G) c.754+6104A>G (n.754+6104A>G) | dbSNP |
11 | g.103937348T>G | CA227642639 | PDGFD | c.772+6104A>C (n.772+6104A>C) c.754+6104A>C (n.754+6104A>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.103937348T= | CA1996762735 | PDGFD | c.772+6104A= (n.772+6104A=) c.754+6104A= (n.754+6104A=) | |
11 | g.103937352A= | CA1996762736 | PDGFD | c.772+6100T= (n.772+6100T=) c.754+6100T= (n.754+6100T=) | |
11 | g.103937352A>C | CA1996762737 | PDGFD | c.772+6100T>G (n.772+6100T>G) c.754+6100T>G (n.754+6100T>G) | dbSNP |
11 | g.103937354G>C | CA227642640 | PDGFD | c.772+6098C>G (n.772+6098C>G) c.754+6098C>G (n.754+6098C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.103937354G= | CA1996762738 | PDGFD | c.772+6098C= (n.772+6098C=) c.754+6098C= (n.754+6098C=) | |
11 | g.103937360T>A | CA1996762740 | PDGFD | c.772+6092A>T (n.772+6092A>T) c.754+6092A>T (n.754+6092A>T) | dbSNP |
11 | g.103937360T= | CA1996762739 | PDGFD | c.772+6092A= (n.772+6092A=) c.754+6092A= (n.754+6092A=) | |
11 | g.103937363T>C | CA1996762742 | PDGFD | c.772+6089A>G (n.772+6089A>G) c.754+6089A>G (n.754+6089A>G) | dbSNP |
11 | g.103937363T= | CA1996762741 | PDGFD | c.772+6089A= (n.772+6089A=) c.754+6089A= (n.754+6089A=) | |
11 | g.103937365C= | CA1996762743 | PDGFD | c.772+6087G= (n.772+6087G=) c.754+6087G= (n.754+6087G=) | |
11 | g.103937365C>G | CA601294184 | PDGFD | c.772+6087G>C (n.772+6087G>C) c.754+6087G>C (n.754+6087G>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.103937365C>T | CA1996762744 | PDGFD | c.772+6087G>A (n.772+6087G>A) c.754+6087G>A (n.754+6087G>A) | dbSNP |