Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.125317748C>A | CA3071963 | FAT4 | c.1337C>A (p.Ala446Glu) c.-55+1771C>A (n.-55+1771C>A) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
4 | g.125317748C= | CA1491600645 | FAT4 | c.1337C= (p.Ala446=) c.-55+1771C= (n.-55+1771C=) | |
4 | g.125317748C>G | CA358117696 | FAT4 | c.1337C>G (p.Ala446Gly) c.-55+1771C>G (n.-55+1771C>G) | |
4 | g.125317748C>T | CA358117697 | FAT4 | c.1337C>T (p.Ala446Val) c.-55+1771C>T (n.-55+1771C>T) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
4 | g.125317749G>A | CA441367201 | FAT4 | c.1338G>A (p.Ala446=) c.-55+1772G>A (n.-55+1772G>A) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125317749G>C | CA441367202 | FAT4 | c.1338G>C (p.Ala446=) c.-55+1772G>C (n.-55+1772G>C) | |
4 | g.125317749G= | CA1491600649 | FAT4 | c.1338G= (p.Ala446=) c.-55+1772G= (n.-55+1772G=) | |
4 | g.125317749G>T | CA441367204 | FAT4 | c.1338G>T (p.Ala446=) c.-55+1772G>T (n.-55+1772G>T) | dbSNP gnomAD v4 |
4 | g.125317750C>A | CA358117699 | FAT4 | c.1339C>A (p.Pro447Thr) c.-55+1773C>A (n.-55+1773C>A) | dbSNP |
4 | g.125317750C= | CA1491600657 | FAT4 | c.1339C= (p.Pro447=) c.-55+1773C= (n.-55+1773C=) | |
4 | g.125317750C>G | CA3071964 | FAT4 | c.1339C>G (p.Pro447Ala) c.-55+1773C>G (n.-55+1773C>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317750C>T | CA358117698 | FAT4 | c.1339C>T (p.Pro447Ser) c.-55+1773C>T (n.-55+1773C>T) | |
4 | g.125317751C>A | CA358117700 | FAT4 | c.1340C>A (p.Pro447His) c.-55+1774C>A (n.-55+1774C>A) | gnomAD v4 |
4 | g.125317751C= | CA1491600669 | FAT4 | c.1340C= (p.Pro447=) c.-55+1774C= (n.-55+1774C=) | |
4 | g.125317751C>G | CA358117701 | FAT4 | c.1340C>G (p.Pro447Arg) c.-55+1774C>G (n.-55+1774C>G) | |
4 | g.125317751C>T | CA3071965 | FAT4 | c.1340C>T (p.Pro447Leu) c.-55+1774C>T (n.-55+1774C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317752C>A | CA441366471 | FAT4 | c.1341C>A (p.Pro447=) c.-55+1775C>A (n.-55+1775C>A) | |
4 | g.125317752C= | CA1491600671 | FAT4 | c.1341C= (p.Pro447=) c.-55+1775C= (n.-55+1775C=) | |
4 | g.125317752C>G | CA441366470 | FAT4 | c.1341C>G (p.Pro447=) c.-55+1775C>G (n.-55+1775C>G) | |
4 | g.125317752C>T | CA441366469 | FAT4 | c.1341C>T (p.Pro447=) c.-55+1775C>T (n.-55+1775C>T) | dbSNP |
4 | g.125317753C>A | CA358117702 | FAT4 | c.1342C>A (p.Pro448Thr) c.-55+1776C>A (n.-55+1776C>A) | |
4 | g.125317753C= | CA1491600679 | FAT4 | c.1342C= (p.Pro448=) c.-55+1776C= (n.-55+1776C=) | |
4 | g.125317753C>G | CA358117703 | FAT4 | c.1342C>G (p.Pro448Ala) c.-55+1776C>G (n.-55+1776C>G) | |
4 | g.125317753C>T | CA358117704 | FAT4 | c.1342C>T (p.Pro448Ser) c.-55+1776C>T (n.-55+1776C>T) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125317754C>A | CA358117705 | FAT4 | c.1343C>A (p.Pro448His) c.-55+1777C>A (n.-55+1777C>A) | |
4 | g.125317754C= | CA1491600686 | FAT4 | c.1343C= (p.Pro448=) c.-55+1777C= (n.-55+1777C=) | |
4 | g.125317754C>G | CA358117706 | FAT4 | c.1343C>G (p.Pro448Arg) c.-55+1777C>G (n.-55+1777C>G) | |
4 | g.125317754C>T | CA358117707 | FAT4 | c.1343C>T (p.Pro448Leu) c.-55+1777C>T (n.-55+1777C>T) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125317755del | CA2580652597 | FAT4 | c.1344del (p.Gly449AlafsTer14) c.-55+1778del (n.-55+1778del) | gnomAD v4 |
4 | g.125317755T>A | CA441366472 | FAT4 | c.1344T>A (p.Pro448=) c.-55+1778T>A (n.-55+1778T>A) | |
4 | g.125317755T>C | CA3071966 | FAT4 | c.1344T>C (p.Pro448=) c.-55+1778T>C (n.-55+1778T>C) | dbSNP ExAC gnomAD v2 |
4 | g.125317755T>G | CA441366473 | FAT4 | c.1344T>G (p.Pro448=) c.-55+1778T>G (n.-55+1778T>G) | |
4 | g.125317755T= | CA1491600692 | FAT4 | c.1344T= (p.Pro448=) c.-55+1778T= (n.-55+1778T=) | |
4 | g.125317755_125317757del | CA2541580480 | FAT4 | c.1344_1346del (p.Gly449del) c.-55+1778_-55+1780del (n.-55+1778_-55+1780del) | |
4 | g.125317756G>A | CA3071967 | FAT4 | c.1345G>A (p.Gly449Ser) c.-55+1779G>A (n.-55+1779G>A) | dbSNP ExAC gnomAD v2 COSMIC COSMIC |
4 | g.125317756G>C | CA358117708 | FAT4 | c.1345G>C (p.Gly449Arg) c.-55+1779G>C (n.-55+1779G>C) | ClinVar |
4 | g.125317756G= | CA1491600699 | FAT4 | c.1345G= (p.Gly449=) c.-55+1779G= (n.-55+1779G=) | |
4 | g.125317756G>T | CA358117709 | FAT4 | c.1345G>T (p.Gly449Cys) c.-55+1779G>T (n.-55+1779G>T) | |
4 | g.125317757G>A | CA358117712 | FAT4 | c.1346G>A (p.Gly449Asp) c.-55+1780G>A (n.-55+1780G>A) | dbSNP gnomAD v2 |
4 | g.125317757G>C | CA358117711 | FAT4 | c.1346G>C (p.Gly449Ala) c.-55+1780G>C (n.-55+1780G>C) | |
4 | g.125317757G= | CA1491600705 | FAT4 | c.1346G= (p.Gly449=) c.-55+1780G= (n.-55+1780G=) | |
4 | g.125317757G>T | CA358117710 | FAT4 | c.1346G>T (p.Gly449Val) c.-55+1780G>T (n.-55+1780G>T) | |
4 | g.125317758C>A | CA441366476 | FAT4 | c.1347C>A (p.Gly449=) c.-55+1781C>A (n.-55+1781C>A) | |
4 | g.125317758C= | CA1491600709 | FAT4 | c.1347C= (p.Gly449=) c.-55+1781C= (n.-55+1781C=) | |
4 | g.125317758C>G | CA441366474 | FAT4 | c.1347C>G (p.Gly449=) c.-55+1781C>G (n.-55+1781C>G) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.125317758C>T | CA441366475 | FAT4 | c.1347C>T (p.Gly449=) c.-55+1781C>T (n.-55+1781C>T) | |
4 | g.125317758_125317759insCCCCCCCCCCCCCCCCCCCCCCCC | CA2570850023 | FAT4 | c.1347_1348insCCCCCCCCCCCCCCCCCCCCCCCC (p.Gly449_Ala450insProProProProProProProPro) c.-55+1781_-55+1782insCCCCCCCCCCCCCCCCCCCCCCCC (n.-55+1781_-55+1782insCCCCCCCCCCCCCCCCCCCCCCCC) | |
4 | g.125317759G>A | CA358117713 | FAT4 | c.1348G>A (p.Ala450Thr) c.-55+1782G>A (n.-55+1782G>A) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125317759G>C | CA358117714 | FAT4 | c.1348G>C (p.Ala450Pro) c.-55+1782G>C (n.-55+1782G>C) | |
4 | g.125317759G= | CA1491600712 | FAT4 | c.1348G= (p.Ala450=) c.-55+1782G= (n.-55+1782G=) | |
4 | g.125317759G>T | CA3071968 | FAT4 | c.1348G>T (p.Ala450Ser) c.-55+1782G>T (n.-55+1782G>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317760C>A | CA358117715 | FAT4 | c.1349C>A (p.Ala450Glu) c.-55+1783C>A (n.-55+1783C>A) | |
4 | g.125317760C>G | CA358117716 | FAT4 | c.1349C>G (p.Ala450Gly) c.-55+1783C>G (n.-55+1783C>G) | |
4 | g.125317760C>T | CA358117717 | FAT4 | c.1349C>T (p.Ala450Val) c.-55+1783C>T (n.-55+1783C>T) | COSMIC COSMIC |
4 | g.125317761A= | CA1491600715 | FAT4 | c.1350A= (p.Ala450=) c.-55+1784A= (n.-55+1784A=) | |
4 | g.125317761A>C | CA441366480 | FAT4 | c.1350A>C (p.Ala450=) c.-55+1784A>C (n.-55+1784A>C) | |
4 | g.125317761A>G | CA3071969 | FAT4 | c.1350A>G (p.Ala450=) c.-55+1784A>G (n.-55+1784A>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125317761A>T | CA441366482 | FAT4 | c.1350A>T (p.Ala450=) c.-55+1784A>T (n.-55+1784A>T) | |
4 | g.125317762G>A | CA358117718 | FAT4 | c.1351G>A (p.Ala451Thr) c.-55+1785G>A (n.-55+1785G>A) | |
4 | g.125317762G>C | CA358117719 | FAT4 | c.1351G>C (p.Ala451Pro) c.-55+1785G>C (n.-55+1785G>C) | |
4 | g.125317762G>T | CA358117720 | FAT4 | c.1351G>T (p.Ala451Ser) c.-55+1785G>T (n.-55+1785G>T) | |
4 | g.125317763C>A | CA358117721 | FAT4 | c.1352C>A (p.Ala451Glu) c.-55+1786C>A (n.-55+1786C>A) | |
4 | g.125317763C= | CA1491600718 | FAT4 | c.1352C= (p.Ala451=) c.-55+1786C= (n.-55+1786C=) | |
4 | g.125317763C>G | CA358117722 | FAT4 | c.1352C>G (p.Ala451Gly) c.-55+1786C>G (n.-55+1786C>G) | |
4 | g.125317763C>T | CA358117723 | FAT4 | c.1352C>T (p.Ala451Val) c.-55+1786C>T (n.-55+1786C>T) | dbSNP gnomAD v2 |
4 | g.125317764A= | CA1491600721 | FAT4 | c.1353A= (p.Ala451=) c.-55+1787A= (n.-55+1787A=) | |
4 | g.125317764A>C | CA3071970 | FAT4 | c.1353A>C (p.Ala451=) c.-55+1787A>C (n.-55+1787A>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125317764A>G | CA441366489 | FAT4 | c.1353A>G (p.Ala451=) c.-55+1787A>G (n.-55+1787A>G) | |
4 | g.125317764A>T | CA441366490 | FAT4 | c.1353A>T (p.Ala451=) c.-55+1787A>T (n.-55+1787A>T) | |
4 | g.125317765G>A | CA358117725 | FAT4 | c.1354G>A (p.Val452Ile) c.-55+1788G>A (n.-55+1788G>A) | |
4 | g.125317765G>C | CA358117724 | FAT4 | c.1354G>C (p.Val452Leu) c.-55+1788G>C (n.-55+1788G>C) | |
4 | g.125317765G>T | CA358117726 | FAT4 | c.1354G>T (p.Val452Phe) c.-55+1788G>T (n.-55+1788G>T) | gnomAD v4 |
4 | g.125317766T>A | CA358117727 | FAT4 | c.1355T>A (p.Val452Asp) c.-55+1789T>A (n.-55+1789T>A) | |
4 | g.125317766T>C | CA358117729 | FAT4 | c.1355T>C (p.Val452Ala) c.-55+1789T>C (n.-55+1789T>C) | |
4 | g.125317766T>G | CA358117728 | FAT4 | c.1355T>G (p.Val452Gly) c.-55+1789T>G (n.-55+1789T>G) | |
4 | g.125317767C>A | CA441366494 | FAT4 | c.1356C>A (p.Val452=) c.-55+1790C>A (n.-55+1790C>A) | dbSNP |
4 | g.125317767C= | CA1491600723 | FAT4 | c.1356C= (p.Val452=) c.-55+1790C= (n.-55+1790C=) | |
4 | g.125317767C>G | CA441366495 | FAT4 | c.1356C>G (p.Val452=) c.-55+1790C>G (n.-55+1790C>G) | |
4 | g.125317767C>T | CA441366496 | FAT4 | c.1356C>T (p.Val452=) c.-55+1790C>T (n.-55+1790C>T) | |
4 | g.125317768C>A | CA358117730 | FAT4 | c.1357C>A (p.Gln453Lys) c.-55+1791C>A (n.-55+1791C>A) | |
4 | g.125317768C>G | CA358117732 | FAT4 | c.1357C>G (p.Gln453Glu) c.-55+1791C>G (n.-55+1791C>G) | |
4 | g.125317768C>T | CA358117731 | FAT4 | c.1357C>T (p.Gln453Ter) c.-55+1791C>T (n.-55+1791C>T) | |
4 | g.125317769A= | CA1491600729 | FAT4 | c.1358A= (p.Gln453=) c.-55+1792A= (n.-55+1792A=) | |
4 | g.125317769A>C | CA3071972 | FAT4 | c.1358A>C (p.Gln453Pro) c.-55+1792A>C (n.-55+1792A>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317769A>G | CA3071973 | FAT4 | c.1358A>G (p.Gln453Arg) c.-55+1792A>G (n.-55+1792A>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317769A>T | CA3071971 | FAT4 | c.1358A>T (p.Gln453Leu) c.-55+1792A>T (n.-55+1792A>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317770G>A | CA441366504 | FAT4 | c.1359G>A (p.Gln453=) c.-55+1793G>A (n.-55+1793G>A) | dbSNP |
4 | g.125317770G>C | CA358117733 | FAT4 | c.1359G>C (p.Gln453His) c.-55+1793G>C (n.-55+1793G>C) | |
4 | g.125317770G>T | CA358117734 | FAT4 | c.1359G>T (p.Gln453His) c.-55+1793G>T (n.-55+1793G>T) | |
4 | g.125317771G>A | CA358117735 | FAT4 | c.1360G>A (p.Ala454Thr) c.-55+1794G>A (n.-55+1794G>A) | dbSNP |
4 | g.125317771G>C | CA358117736 | FAT4 | c.1360G>C (p.Ala454Pro) c.-55+1794G>C (n.-55+1794G>C) | |
4 | g.125317771G>T | CA358117737 | FAT4 | c.1360G>T (p.Ala454Ser) c.-55+1794G>T (n.-55+1794G>T) | |
4 | g.125317772C>A | CA358117738 | FAT4 | c.1361C>A (p.Ala454Glu) c.-55+1795C>A (n.-55+1795C>A) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
4 | g.125317772C= | CA1491600737 | FAT4 | c.1361C= (p.Ala454=) c.-55+1795C= (n.-55+1795C=) | |
4 | g.125317772C>G | CA358117739 | FAT4 | c.1361C>G (p.Ala454Gly) c.-55+1795C>G (n.-55+1795C>G) | |
4 | g.125317772C>T | CA358117740 | FAT4 | c.1361C>T (p.Ala454Val) c.-55+1795C>T (n.-55+1795C>T) | gnomAD v4 |
4 | g.125317773G>A | CA441366510 | FAT4 | c.1362G>A (p.Ala454=) c.-55+1796G>A (n.-55+1796G>A) | dbSNP gnomAD v4 |
4 | g.125317773G>C | CA441366511 | FAT4 | c.1362G>C (p.Ala454=) c.-55+1796G>C (n.-55+1796G>C) | |
4 | g.125317773G= | CA1491600741 | FAT4 | c.1362G= (p.Ala454=) c.-55+1796G= (n.-55+1796G=) | |
4 | g.125317773G>T | CA441366513 | FAT4 | c.1362G>T (p.Ala454=) c.-55+1796G>T (n.-55+1796G>T) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
4 | g.125317774C>A | CA358117743 | FAT4 | c.1363C>A (p.Arg455Ser) c.-55+1797C>A (n.-55+1797C>A) | gnomAD v4 |
4 | g.125317774C= | CA1491600743 | FAT4 | c.1363C= (p.Arg455=) c.-55+1797C= (n.-55+1797C=) | |
4 | g.125317774C>G | CA358117741 | FAT4 | c.1363C>G (p.Arg455Gly) c.-55+1797C>G (n.-55+1797C>G) | |
4 | g.125317774C>T | CA358117742 | FAT4 | c.1363C>T (p.Arg455Cys) c.-55+1797C>T (n.-55+1797C>T) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125317775G>A | CA358117744 | FAT4 | c.1364G>A (p.Arg455His) c.-55+1798G>A (n.-55+1798G>A) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125317775G>C | CA358117745 | FAT4 | c.1364G>C (p.Arg455Pro) c.-55+1798G>C (n.-55+1798G>C) | |
4 | g.125317775G= | CA1491600747 | FAT4 | c.1364G= (p.Arg455=) c.-55+1798G= (n.-55+1798G=) | |
4 | g.125317775G>T | CA358117746 | FAT4 | c.1364G>T (p.Arg455Leu) c.-55+1798G>T (n.-55+1798G>T) | dbSNP gnomAD v4 |
4 | g.125317776C>A | CA441366521 | FAT4 | c.1365C>A (p.Arg455=) c.-55+1799C>A (n.-55+1799C>A) | |
4 | g.125317776C= | CA1491600749 | FAT4 | c.1365C= (p.Arg455=) c.-55+1799C= (n.-55+1799C=) | |
4 | g.125317776C>G | CA3071974 | FAT4 | c.1365C>G (p.Arg455=) c.-55+1799C>G (n.-55+1799C>G) | dbSNP ExAC gnomAD v3 gnomAD v4 |
4 | g.125317776C>T | CA441366522 | FAT4 | c.1365C>T (p.Arg455=) c.-55+1799C>T (n.-55+1799C>T) | |
4 | g.125317777T>A | CA358117747 | FAT4 | c.1366T>A (p.Ser456Thr) c.-55+1800T>A (n.-55+1800T>A) | |
4 | g.125317777T>C | CA358117748 | FAT4 | c.1366T>C (p.Ser456Pro) c.-55+1800T>C (n.-55+1800T>C) | |
4 | g.125317777T>G | CA358117749 | FAT4 | c.1366T>G (p.Ser456Ala) c.-55+1800T>G (n.-55+1800T>G) | |
4 | g.125317778C>A | CA358117750 | FAT4 | c.1367C>A (p.Ser456Tyr) c.-55+1801C>A (n.-55+1801C>A) | |
4 | g.125317778C>G | CA358117751 | FAT4 | c.1367C>G (p.Ser456Cys) c.-55+1801C>G (n.-55+1801C>G) | |
4 | g.125317778C>T | CA358117752 | FAT4 | c.1367C>T (p.Ser456Phe) c.-55+1801C>T (n.-55+1801C>T) | |
4 | g.125317779T>A | CA441366523 | FAT4 | c.1368T>A (p.Ser456=) c.-55+1802T>A (n.-55+1802T>A) | |
4 | g.125317779T>C | CA441366524 | FAT4 | c.1368T>C (p.Ser456=) c.-55+1802T>C (n.-55+1802T>C) | |
4 | g.125317779T>G | CA441366526 | FAT4 | c.1368T>G (p.Ser456=) c.-55+1802T>G (n.-55+1802T>G) | |
4 | g.125317780T>A | CA358117755 | FAT4 | c.1369T>A (p.Ser457Thr) c.-55+1803T>A (n.-55+1803T>A) | |
4 | g.125317780T>C | CA358117754 | FAT4 | c.1369T>C (p.Ser457Pro) c.-55+1803T>C (n.-55+1803T>C) | gnomAD v4 |
4 | g.125317780T>G | CA358117753 | FAT4 | c.1369T>G (p.Ser457Ala) c.-55+1803T>G (n.-55+1803T>G) | |
4 | g.125317781C>A | CA358117756 | FAT4 | c.1370C>A (p.Ser457Tyr) c.-55+1804C>A (n.-55+1804C>A) | |
4 | g.125317781C= | CA1491600753 | FAT4 | c.1370C= (p.Ser457=) c.-55+1804C= (n.-55+1804C=) | |
4 | g.125317781C>G | CA358117757 | FAT4 | c.1370C>G (p.Ser457Cys) c.-55+1804C>G (n.-55+1804C>G) | |
4 | g.125317781C>T | CA3071975 | FAT4 | c.1370C>T (p.Ser457Phe) c.-55+1804C>T (n.-55+1804C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317782T>A | CA441366530 | FAT4 | c.1371T>A (p.Ser457=) c.-55+1805T>A (n.-55+1805T>A) | |
4 | g.125317782T>C | CA441366531 | FAT4 | c.1371T>C (p.Ser457=) c.-55+1805T>C (n.-55+1805T>C) | |
4 | g.125317782T>G | CA3071976 | FAT4 | c.1371T>G (p.Ser457=) c.-55+1805T>G (n.-55+1805T>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125317782T= | CA1491600758 | FAT4 | c.1371T= (p.Ser457=) c.-55+1805T= (n.-55+1805T=) | |
4 | g.125317783G>A | CA358117758 | FAT4 | c.1372G>A (p.Val458Met) c.-55+1806G>A (n.-55+1806G>A) | gnomAD v4 |
4 | g.125317783G>C | CA358117759 | FAT4 | c.1372G>C (p.Val458Leu) c.-55+1806G>C (n.-55+1806G>C) | |
4 | g.125317783G>T | CA358117760 | FAT4 | c.1372G>T (p.Val458Leu) c.-55+1806G>T (n.-55+1806G>T) | |
4 | g.125317784T>A | CA358117761 | FAT4 | c.1373T>A (p.Val458Glu) c.-55+1807T>A (n.-55+1807T>A) | |
4 | g.125317784T>C | CA358117762 | FAT4 | c.1373T>C (p.Val458Ala) c.-55+1807T>C (n.-55+1807T>C) | |
4 | g.125317784T>G | CA358117763 | FAT4 | c.1373T>G (p.Val458Gly) c.-55+1807T>G (n.-55+1807T>G) | |
4 | g.125317785G>A | CA441366537 | FAT4 | c.1374G>A (p.Val458=) c.-55+1808G>A (n.-55+1808G>A) | |
4 | g.125317785G>C | CA441366539 | FAT4 | c.1374G>C (p.Val458=) c.-55+1808G>C (n.-55+1808G>C) | |
4 | g.125317785G>T | CA441366538 | FAT4 | c.1374G>T (p.Val458=) c.-55+1808G>T (n.-55+1808G>T) | COSMIC COSMIC |
4 | g.125317786G>A | CA358117764 | FAT4 | c.1375G>A (p.Ala459Thr) c.-55+1809G>A (n.-55+1809G>A) | |
4 | g.125317786G>C | CA358117765 | FAT4 | c.1375G>C (p.Ala459Pro) c.-55+1809G>C (n.-55+1809G>C) | |
4 | g.125317786G= | CA1491600765 | FAT4 | c.1375G= (p.Ala459=) c.-55+1809G= (n.-55+1809G=) | |
4 | g.125317786G>T | CA3071977 | FAT4 | c.1375G>T (p.Ala459Ser) c.-55+1809G>T (n.-55+1809G>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317787C>A | CA358117766 | FAT4 | c.1376C>A (p.Ala459Glu) c.-55+1810C>A (n.-55+1810C>A) | |
4 | g.125317787C>G | CA358117768 | FAT4 | c.1376C>G (p.Ala459Gly) c.-55+1810C>G (n.-55+1810C>G) | |
4 | g.125317787C>T | CA358117767 | FAT4 | c.1376C>T (p.Ala459Val) c.-55+1810C>T (n.-55+1810C>T) | gnomAD v4 |
4 | g.125317788A>C | CA441366546 | FAT4 | c.1377A>C (p.Ala459=) c.-55+1811A>C (n.-55+1811A>C) | |
4 | g.125317788A>G | CA441366547 | FAT4 | c.1377A>G (p.Ala459=) c.-55+1811A>G (n.-55+1811A>G) | |
4 | g.125317788A>T | CA441366548 | FAT4 | c.1377A>T (p.Ala459=) c.-55+1811A>T (n.-55+1811A>T) | |
4 | g.125317789A= | CA1491600769 | FAT4 | c.1378A= (p.Ser460=) c.-55+1812A= (n.-55+1812A=) | |
4 | g.125317789A>C | CA358117769 | FAT4 | c.1378A>C (p.Ser460Arg) c.-55+1812A>C (n.-55+1812A>C) | |
4 | g.125317789A>G | CA3071978 | FAT4 | c.1378A>G (p.Ser460Gly) c.-55+1812A>G (n.-55+1812A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317789A>T | CA358117770 | FAT4 | c.1378A>T (p.Ser460Cys) c.-55+1812A>T (n.-55+1812A>T) | |
4 | g.125317790G>A | CA3071979 | FAT4 | c.1379G>A (p.Ser460Asn) c.-55+1813G>A (n.-55+1813G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125317790G>C | CA358117771 | FAT4 | c.1379G>C (p.Ser460Thr) c.-55+1813G>C (n.-55+1813G>C) | |
4 | g.125317790G= | CA1491600773 | FAT4 | c.1379G= (p.Ser460=) c.-55+1813G= (n.-55+1813G=) | |
4 | g.125317790G>T | CA358117772 | FAT4 | c.1379G>T (p.Ser460Ile) c.-55+1813G>T (n.-55+1813G>T) | |
4 | g.125317791C>A | CA358117773 | FAT4 | c.1380C>A (p.Ser460Arg) c.-55+1814C>A (n.-55+1814C>A) | |
4 | g.125317791C= | CA1491600780 | FAT4 | c.1380C= (p.Ser460=) c.-55+1814C= (n.-55+1814C=) | |
4 | g.125317791C>G | CA358117774 | FAT4 | c.1380C>G (p.Ser460Arg) c.-55+1814C>G (n.-55+1814C>G) | |
4 | g.125317791C>T | CA3071980 | FAT4 | c.1380C>T (p.Ser460=) c.-55+1814C>T (n.-55+1814C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317792C>A | CA358117775 | FAT4 | c.1381C>A (p.Leu461Met) c.-55+1815C>A (n.-55+1815C>A) | |
4 | g.125317792C= | CA1491600791 | FAT4 | c.1381C= (p.Leu461=) c.-55+1815C= (n.-55+1815C=) | |
4 | g.125317792C>G | CA3071981 | FAT4 | c.1381C>G (p.Leu461Val) c.-55+1815C>G (n.-55+1815C>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317792C>T | CA441366556 | FAT4 | c.1381C>T (p.Leu461=) c.-55+1815C>T (n.-55+1815C>T) | dbSNP gnomAD v4 |
4 | g.125317793T>A | CA358117777 | FAT4 | c.1382T>A (p.Leu461Gln) c.-55+1816T>A (n.-55+1816T>A) | |
4 | g.125317793T>C | CA358117778 | FAT4 | c.1382T>C (p.Leu461Pro) c.-55+1816T>C (n.-55+1816T>C) | |
4 | g.125317793T>G | CA358117776 | FAT4 | c.1382T>G (p.Leu461Arg) c.-55+1816T>G (n.-55+1816T>G) | |
4 | g.125317794G>A | CA441366559 | FAT4 | c.1383G>A (p.Leu461=) c.-55+1817G>A (n.-55+1817G>A) | |
4 | g.125317794G>C | CA441366560 | FAT4 | c.1383G>C (p.Leu461=) c.-55+1817G>C (n.-55+1817G>C) | |
4 | g.125317794G>T | CA441366561 | FAT4 | c.1383G>T (p.Leu461=) c.-55+1817G>T (n.-55+1817G>T) | |
4 | g.125317795G>A | CA358117781 | FAT4 | c.1384G>A (p.Val462Met) c.-55+1818G>A (n.-55+1818G>A) | |
4 | g.125317795G>C | CA358117779 | FAT4 | c.1384G>C (p.Val462Leu) c.-55+1818G>C (n.-55+1818G>C) | |
4 | g.125317795G>T | CA358117780 | FAT4 | c.1384G>T (p.Val462Leu) c.-55+1818G>T (n.-55+1818G>T) | |
4 | g.125317796T>A | CA358117782 | FAT4 | c.1385T>A (p.Val462Glu) c.-55+1819T>A (n.-55+1819T>A) | |
4 | g.125317796T>C | CA358117783 | FAT4 | c.1385T>C (p.Val462Ala) c.-55+1819T>C (n.-55+1819T>C) | |
4 | g.125317796T>G | CA358117784 | FAT4 | c.1385T>G (p.Val462Gly) c.-55+1819T>G (n.-55+1819T>G) | |
4 | g.125317797G>A | CA3071982 | FAT4 | c.1386G>A (p.Val462=) c.-55+1820G>A (n.-55+1820G>A) | dbSNP ExAC gnomAD v2 |
4 | g.125317797G>C | CA441366569 | FAT4 | c.1386G>C (p.Val462=) c.-55+1820G>C (n.-55+1820G>C) | |
4 | g.125317797G= | CA1491600798 | FAT4 | c.1386G= (p.Val462=) c.-55+1820G= (n.-55+1820G=) | |
4 | g.125317797G>T | CA441366571 | FAT4 | c.1386G>T (p.Val462=) c.-55+1820G>T (n.-55+1820G>T) | |
4 | g.125317798A>C | CA358117787 | FAT4 | c.1387A>C (p.Ile463Leu) c.-55+1821A>C (n.-55+1821A>C) | gnomAD v4 |
4 | g.125317798A>G | CA358117785 | FAT4 | c.1387A>G (p.Ile463Val) c.-55+1821A>G (n.-55+1821A>G) | |
4 | g.125317798A>T | CA358117786 | FAT4 | c.1387A>T (p.Ile463Phe) c.-55+1821A>T (n.-55+1821A>T) | |
4 | g.125317799T>A | CA358117788 | FAT4 | c.1388T>A (p.Ile463Asn) c.-55+1822T>A (n.-55+1822T>A) | |
4 | g.125317799T>C | CA358117789 | FAT4 | c.1388T>C (p.Ile463Thr) c.-55+1822T>C (n.-55+1822T>C) | |
4 | g.125317799T>G | CA358117790 | FAT4 | c.1388T>G (p.Ile463Ser) c.-55+1822T>G (n.-55+1822T>G) | |
4 | g.125317803dup | CA2672009309 | FAT4 | c.1392dup (p.Val465CysfsTer2) c.-55+1826dup (n.-55+1826dup) | gnomAD v4 |
4 | g.125317802_125317803del | CA2672009310 | FAT4 | c.1391_1392del (p.Phe464CysfsTer2) c.-55+1825_-55+1826del (n.-55+1825_-55+1826del) | gnomAD v4 |
4 | g.125317800T>A | CA104864038 | FAT4 | c.1389T>A (p.Ile463=) c.-55+1823T>A (n.-55+1823T>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317800T>C | CA441366575 | FAT4 | c.1389T>C (p.Ile463=) c.-55+1823T>C (n.-55+1823T>C) | |
4 | g.125317800T>G | CA358117791 | FAT4 | c.1389T>G (p.Ile463Met) c.-55+1823T>G (n.-55+1823T>G) | |
4 | g.125317800T= | CA1491600801 | FAT4 | c.1389T= (p.Ile463=) c.-55+1823T= (n.-55+1823T=) | |
4 | g.125317801T>A | CA358117792 | FAT4 | c.1390T>A (p.Phe464Ile) c.-55+1824T>A (n.-55+1824T>A) | |
4 | g.125317801T>C | CA358117794 | FAT4 | c.1390T>C (p.Phe464Leu) c.-55+1824T>C (n.-55+1824T>C) | |
4 | g.125317801T>G | CA358117793 | FAT4 | c.1390T>G (p.Phe464Val) c.-55+1824T>G (n.-55+1824T>G) | |
4 | g.125317802T>A | CA358117795 | FAT4 | c.1391T>A (p.Phe464Tyr) c.-55+1825T>A (n.-55+1825T>A) | |
4 | g.125317802T>C | CA358117796 | FAT4 | c.1391T>C (p.Phe464Ser) c.-55+1825T>C (n.-55+1825T>C) | |
4 | g.125317802T>G | CA358117797 | FAT4 | c.1391T>G (p.Phe464Cys) c.-55+1825T>G (n.-55+1825T>G) | |
4 | g.125317803T>A | CA3071983 | FAT4 | c.1392T>A (p.Phe464Leu) c.-55+1826T>A (n.-55+1826T>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125317803T>C | CA441366580 | FAT4 | c.1392T>C (p.Phe464=) c.-55+1826T>C (n.-55+1826T>C) | |
4 | g.125317803T>G | CA358117798 | FAT4 | c.1392T>G (p.Phe464Leu) c.-55+1826T>G (n.-55+1826T>G) | |
4 | g.125317803T= | CA1491600806 | FAT4 | c.1392T= (p.Phe464=) c.-55+1826T= (n.-55+1826T=) | |
4 | g.125317804G>A | CA358117799 | FAT4 | c.1393G>A (p.Val465Ile) c.-55+1827G>A (n.-55+1827G>A) | |
4 | g.125317804G>C | CA358117800 | FAT4 | c.1393G>C (p.Val465Leu) c.-55+1827G>C (n.-55+1827G>C) | |
4 | g.125317804G>T | CA358117801 | FAT4 | c.1393G>T (p.Val465Phe) c.-55+1827G>T (n.-55+1827G>T) | gnomAD v4 |
4 | g.125317805T>A | CA358117802 | FAT4 | c.1394T>A (p.Val465Asp) c.-55+1828T>A (n.-55+1828T>A) | |
4 | g.125317805T>C | CA358117803 | FAT4 | c.1394T>C (p.Val465Ala) c.-55+1828T>C (n.-55+1828T>C) | dbSNP gnomAD v4 |
4 | g.125317805T>G | CA358117804 | FAT4 | c.1394T>G (p.Val465Gly) c.-55+1828T>G (n.-55+1828T>G) | |
4 | g.125317805T= | CA1491600809 | FAT4 | c.1394T= (p.Val465=) c.-55+1828T= (n.-55+1828T=) | |
4 | g.125317806T>A | CA441366588 | FAT4 | c.1395T>A (p.Val465=) c.-55+1829T>A (n.-55+1829T>A) | |
4 | g.125317806T>C | CA441366586 | FAT4 | c.1395T>C (p.Val465=) c.-55+1829T>C (n.-55+1829T>C) | |
4 | g.125317806T>G | CA441366585 | FAT4 | c.1395T>G (p.Val465=) c.-55+1829T>G (n.-55+1829T>G) | |
4 | g.125317807A>C | CA358117807 | FAT4 | c.1396A>C (p.Asn466His) c.-55+1830A>C (n.-55+1830A>C) | |
4 | g.125317807A>G | CA358117806 | FAT4 | c.1396A>G (p.Asn466Asp) c.-55+1830A>G (n.-55+1830A>G) | ClinVar |
4 | g.125317807A>T | CA358117805 | FAT4 | c.1396A>T (p.Asn466Tyr) c.-55+1830A>T (n.-55+1830A>T) | |
4 | g.125317808A>C | CA358117808 | FAT4 | c.1397A>C (p.Asn466Thr) c.-55+1831A>C (n.-55+1831A>C) | |
4 | g.125317808A>G | CA358117809 | FAT4 | c.1397A>G (p.Asn466Ser) c.-55+1831A>G (n.-55+1831A>G) | |
4 | g.125317808A>T | CA358117810 | FAT4 | c.1397A>T (p.Asn466Ile) c.-55+1831A>T (n.-55+1831A>T) | |
4 | g.125317809T>A | CA358117811 | FAT4 | c.1398T>A (p.Asn466Lys) c.-55+1832T>A (n.-55+1832T>A) | |
4 | g.125317809T>C | CA441366598 | FAT4 | c.1398T>C (p.Asn466=) c.-55+1832T>C (n.-55+1832T>C) | |
4 | g.125317809T>G | CA358117812 | FAT4 | c.1398T>G (p.Asn466Lys) c.-55+1832T>G (n.-55+1832T>G) | |
4 | g.125317810G>A | CA358117813 | FAT4 | c.1399G>A (p.Asp467Asn) c.-55+1833G>A (n.-55+1833G>A) | |
4 | g.125317810G>C | CA358117814 | FAT4 | c.1399G>C (p.Asp467His) c.-55+1833G>C (n.-55+1833G>C) | |
4 | g.125317810G>T | CA358117815 | FAT4 | c.1399G>T (p.Asp467Tyr) c.-55+1833G>T (n.-55+1833G>T) | |
4 | g.125317811A>C | CA358117816 | FAT4 | c.1400A>C (p.Asp467Ala) c.-55+1834A>C (n.-55+1834A>C) | |
4 | g.125317811A>G | CA358117817 | FAT4 | c.1400A>G (p.Asp467Gly) c.-55+1834A>G (n.-55+1834A>G) | gnomAD v4 |
4 | g.125317811A>T | CA358117818 | FAT4 | c.1400A>T (p.Asp467Val) c.-55+1834A>T (n.-55+1834A>T) | |
4 | g.125317812C>A | CA358117819 | FAT4 | c.1401C>A (p.Asp467Glu) c.-55+1835C>A (n.-55+1835C>A) | |
4 | g.125317812C>G | CA358117820 | FAT4 | c.1401C>G (p.Asp467Glu) c.-55+1835C>G (n.-55+1835C>G) | |
4 | g.125317812C>T | CA441366602 | FAT4 | c.1401C>T (p.Asp467=) c.-55+1835C>T (n.-55+1835C>T) | |
4 | g.125317813A>C | CA358117823 | FAT4 | c.1402A>C (p.Ile468Leu) c.-55+1836A>C (n.-55+1836A>C) | |
4 | g.125317813A>G | CA358117821 | FAT4 | c.1402A>G (p.Ile468Val) c.-55+1836A>G (n.-55+1836A>G) | gnomAD v4 |
4 | g.125317813A>T | CA358117822 | FAT4 | c.1402A>T (p.Ile468Phe) c.-55+1836A>T (n.-55+1836A>T) | |
4 | g.125317814T>A | CA358117824 | FAT4 | c.1403T>A (p.Ile468Asn) c.-55+1837T>A (n.-55+1837T>A) | |
4 | g.125317814T>C | CA358117825 | FAT4 | c.1403T>C (p.Ile468Thr) c.-55+1837T>C (n.-55+1837T>C) | |
4 | g.125317814T>G | CA358117826 | FAT4 | c.1403T>G (p.Ile468Ser) c.-55+1837T>G (n.-55+1837T>G) | |
4 | g.125317815C>A | CA441366610 | FAT4 | c.1404C>A (p.Ile468=) c.-55+1838C>A (n.-55+1838C>A) | |
4 | g.125317815C>G | CA358117827 | FAT4 | c.1404C>G (p.Ile468Met) c.-55+1838C>G (n.-55+1838C>G) | |
4 | g.125317815C>T | CA441366612 | FAT4 | c.1404C>T (p.Ile468=) c.-55+1838C>T (n.-55+1838C>T) | |
4 | g.125317816A>C | CA358117828 | FAT4 | c.1405A>C (p.Asn469His) c.-55+1839A>C (n.-55+1839A>C) | |
4 | g.125317816A>G | CA358117829 | FAT4 | c.1405A>G (p.Asn469Asp) c.-55+1839A>G (n.-55+1839A>G) | |
4 | g.125317816A>T | CA358117830 | FAT4 | c.1405A>T (p.Asn469Tyr) c.-55+1839A>T (n.-55+1839A>T) | |
4 | g.125317817A= | CA1491600812 | FAT4 | c.1406A= (p.Asn469=) c.-55+1840A= (n.-55+1840A=) | |
4 | g.125317817A>C | CA358117831 | FAT4 | c.1406A>C (p.Asn469Thr) c.-55+1840A>C (n.-55+1840A>C) | |
4 | g.125317817A>G | CA358117832 | FAT4 | c.1406A>G (p.Asn469Ser) c.-55+1840A>G (n.-55+1840A>G) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.125317817A>T | CA358117833 | FAT4 | c.1406A>T (p.Asn469Ile) c.-55+1840A>T (n.-55+1840A>T) | |
4 | g.125317818T>A | CA358117834 | FAT4 | c.1407T>A (p.Asn469Lys) c.-55+1841T>A (n.-55+1841T>A) | |
4 | g.125317818T>C | CA441366617 | FAT4 | c.1407T>C (p.Asn469=) c.-55+1841T>C (n.-55+1841T>C) | |
4 | g.125317818T>G | CA358117835 | FAT4 | c.1407T>G (p.Asn469Lys) c.-55+1841T>G (n.-55+1841T>G) | |
4 | g.125317819G>A | CA358117838 | FAT4 | c.1408G>A (p.Asp470Asn) c.-55+1842G>A (n.-55+1842G>A) | |
4 | g.125317819G>C | CA358117837 | FAT4 | c.1408G>C (p.Asp470His) c.-55+1842G>C (n.-55+1842G>C) | |
4 | g.125317819G>T | CA358117836 | FAT4 | c.1408G>T (p.Asp470Tyr) c.-55+1842G>T (n.-55+1842G>T) | |
4 | g.125317820A= | CA1491600819 | FAT4 | c.1409A= (p.Asp470=) c.-55+1843A= (n.-55+1843A=) | |
4 | g.125317820A>C | CA3071984 | FAT4 | c.1409A>C (p.Asp470Ala) c.-55+1843A>C (n.-55+1843A>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125317820A>G | CA358117840 | FAT4 | c.1409A>G (p.Asp470Gly) c.-55+1843A>G (n.-55+1843A>G) | |
4 | g.125317820A>T | CA358117839 | FAT4 | c.1409A>T (p.Asp470Val) c.-55+1843A>T (n.-55+1843A>T) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125317821C>A | CA358117841 | FAT4 | c.1410C>A (p.Asp470Glu) c.-55+1844C>A (n.-55+1844C>A) | |
4 | g.125317821C>G | CA358117842 | FAT4 | c.1410C>G (p.Asp470Glu) c.-55+1844C>G (n.-55+1844C>G) | |
4 | g.125317821C>T | CA441366627 | FAT4 | c.1410C>T (p.Asp470=) c.-55+1844C>T (n.-55+1844C>T) | |
4 | g.125317822C>A | CA358117843 | FAT4 | c.1411C>A (p.His471Asn) c.-55+1845C>A (n.-55+1845C>A) | |
4 | g.125317822C>G | CA358117844 | FAT4 | c.1411C>G (p.His471Asp) c.-55+1845C>G (n.-55+1845C>G) | |
4 | g.125317822C>T | CA358117845 | FAT4 | c.1411C>T (p.His471Tyr) c.-55+1845C>T (n.-55+1845C>T) | |
4 | g.125317823A= | CA1491600824 | FAT4 | c.1412A= (p.His471=) c.-55+1846A= (n.-55+1846A=) | |
4 | g.125317823A>C | CA358117846 | FAT4 | c.1412A>C (p.His471Pro) c.-55+1846A>C (n.-55+1846A>C) | |
4 | g.125317823A>G | CA358117847 | FAT4 | c.1412A>G (p.His471Arg) c.-55+1846A>G (n.-55+1846A>G) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
4 | g.125317823A>T | CA358117848 | FAT4 | c.1412A>T (p.His471Leu) c.-55+1846A>T (n.-55+1846A>T) | |
4 | g.125317824T>A | CA3071985 | FAT4 | c.1413T>A (p.His471Gln) c.-55+1847T>A (n.-55+1847T>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125317824T>C | CA441366630 | FAT4 | c.1413T>C (p.His471=) c.-55+1847T>C (n.-55+1847T>C) | gnomAD v4 |
4 | g.125317824T>G | CA358117849 | FAT4 | c.1413T>G (p.His471Gln) c.-55+1847T>G (n.-55+1847T>G) | COSMIC COSMIC |
4 | g.125317824T= | CA1491600831 | FAT4 | c.1413T= (p.His471=) c.-55+1847T= (n.-55+1847T=) | |
4 | g.125317825C>A | CA358117850 | FAT4 | c.1414C>A (p.Pro472Thr) c.-55+1848C>A (n.-55+1848C>A) | |
4 | g.125317825C= | CA1491600836 | FAT4 | c.1414C= (p.Pro472=) c.-55+1848C= (n.-55+1848C=) | |
4 | g.125317825C>G | CA358117851 | FAT4 | c.1414C>G (p.Pro472Ala) c.-55+1848C>G (n.-55+1848C>G) | |
4 | g.125317825C>T | CA358117852 | FAT4 | c.1414C>T (p.Pro472Ser) c.-55+1848C>T (n.-55+1848C>T) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125317826C>A | CA358117853 | FAT4 | c.1415C>A (p.Pro472His) c.-55+1849C>A (n.-55+1849C>A) | gnomAD v4 |
4 | g.125317826C= | CA1491600841 | FAT4 | c.1415C= (p.Pro472=) c.-55+1849C= (n.-55+1849C=) | |
4 | g.125317826C>G | CA358117855 | FAT4 | c.1415C>G (p.Pro472Arg) c.-55+1849C>G (n.-55+1849C>G) | |
4 | g.125317826C>T | CA358117854 | FAT4 | c.1415C>T (p.Pro472Leu) c.-55+1849C>T (n.-55+1849C>T) | dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
4 | g.125317827T>A | CA441366637 | FAT4 | c.1416T>A (p.Pro472=) c.-55+1850T>A (n.-55+1850T>A) | |
4 | g.125317827T>C | CA441366639 | FAT4 | c.1416T>C (p.Pro472=) c.-55+1850T>C (n.-55+1850T>C) | |
4 | g.125317827T>G | CA441366642 | FAT4 | c.1416T>G (p.Pro472=) c.-55+1850T>G (n.-55+1850T>G) | |
4 | g.125317828C>A | CA358117856 | FAT4 | c.1417C>A (p.Pro473Thr) c.-55+1851C>A (n.-55+1851C>A) | |
4 | g.125317828C>G | CA358117857 | FAT4 | c.1417C>G (p.Pro473Ala) c.-55+1851C>G (n.-55+1851C>G) | |
4 | g.125317828C>T | CA358117858 | FAT4 | c.1417C>T (p.Pro473Ser) c.-55+1851C>T (n.-55+1851C>T) | gnomAD v4 |
4 | g.125317829C>A | CA358117859 | FAT4 | c.1418C>A (p.Pro473His) c.-55+1852C>A (n.-55+1852C>A) | |
4 | g.125317829C>G | CA358117860 | FAT4 | c.1418C>G (p.Pro473Arg) c.-55+1852C>G (n.-55+1852C>G) | |
4 | g.125317829C>T | CA358117861 | FAT4 | c.1418C>T (p.Pro473Leu) c.-55+1852C>T (n.-55+1852C>T) | |
4 | g.125317830T>A | CA441366645 | FAT4 | c.1419T>A (p.Pro473=) c.-55+1853T>A (n.-55+1853T>A) | |
4 | g.125317830T>C | CA3071986 | FAT4 | c.1419T>C (p.Pro473=) c.-55+1853T>C (n.-55+1853T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317830T>G | CA441366646 | FAT4 | c.1419T>G (p.Pro473=) c.-55+1853T>G (n.-55+1853T>G) | |
4 | g.125317830T= | CA1491600846 | FAT4 | c.1419T= (p.Pro473=) c.-55+1853T= (n.-55+1853T=) | |
4 | g.125317831G>A | CA3071987 | FAT4 | c.1420G>A (p.Val474Ile) c.-55+1854G>A (n.-55+1854G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317831G>C | CA358117862 | FAT4 | c.1420G>C (p.Val474Leu) c.-55+1854G>C (n.-55+1854G>C) | dbSNP gnomAD v4 |
4 | g.125317831G= | CA1491600854 | FAT4 | c.1420G= (p.Val474=) c.-55+1854G= (n.-55+1854G=) | |
4 | g.125317831G>T | CA358117863 | FAT4 | c.1420G>T (p.Val474Phe) c.-55+1854G>T (n.-55+1854G>T) | |
4 | g.125317832T>A | CA358117866 | FAT4 | c.1421T>A (p.Val474Asp) c.-55+1855T>A (n.-55+1855T>A) | |
4 | g.125317832T>C | CA358117865 | FAT4 | c.1421T>C (p.Val474Ala) c.-55+1855T>C (n.-55+1855T>C) | |
4 | g.125317832T>G | CA358117864 | FAT4 | c.1421T>G (p.Val474Gly) c.-55+1855T>G (n.-55+1855T>G) | ClinVar |
4 | g.125317833C>A | CA441366655 | FAT4 | c.1422C>A (p.Val474=) c.-55+1856C>A (n.-55+1856C>A) | |
4 | g.125317833C= | CA1491600858 | FAT4 | c.1422C= (p.Val474=) c.-55+1856C= (n.-55+1856C=) | |
4 | g.125317833C>G | CA441366654 | FAT4 | c.1422C>G (p.Val474=) c.-55+1856C>G (n.-55+1856C>G) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125317833C>T | CA441366653 | FAT4 | c.1422C>T (p.Val474=) c.-55+1856C>T (n.-55+1856C>T) | |
4 | g.125317834T>A | CA358117869 | FAT4 | c.1423T>A (p.Phe475Ile) c.-55+1857T>A (n.-55+1857T>A) | |
4 | g.125317834T>C | CA358117867 | FAT4 | c.1423T>C (p.Phe475Leu) c.-55+1857T>C (n.-55+1857T>C) | |
4 | g.125317834T>G | CA358117868 | FAT4 | c.1423T>G (p.Phe475Val) c.-55+1857T>G (n.-55+1857T>G) | |
4 | g.125317835T>A | CA358117870 | FAT4 | c.1424T>A (p.Phe475Tyr) c.-55+1858T>A (n.-55+1858T>A) | |
4 | g.125317835T>C | CA358117871 | FAT4 | c.1424T>C (p.Phe475Ser) c.-55+1858T>C (n.-55+1858T>C) | |
4 | g.125317835T>G | CA358117872 | FAT4 | c.1424T>G (p.Phe475Cys) c.-55+1858T>G (n.-55+1858T>G) | |
4 | g.125317836T>A | CA358117873 | FAT4 | c.1425T>A (p.Phe475Leu) c.-55+1859T>A (n.-55+1859T>A) | |
4 | g.125317836T>C | CA441366661 | FAT4 | c.1425T>C (p.Phe475=) c.-55+1859T>C (n.-55+1859T>C) | |
4 | g.125317836T>G | CA358117874 | FAT4 | c.1425T>G (p.Phe475Leu) c.-55+1859T>G (n.-55+1859T>G) | |
4 | g.125317837T>A | CA358117875 | FAT4 | c.1426T>A (p.Ser476Thr) c.-55+1860T>A (n.-55+1860T>A) | |
4 | g.125317837T>C | CA358117876 | FAT4 | c.1426T>C (p.Ser476Pro) c.-55+1860T>C (n.-55+1860T>C) | |
4 | g.125317837T>G | CA358117877 | FAT4 | c.1426T>G (p.Ser476Ala) c.-55+1860T>G (n.-55+1860T>G) | |
4 | g.125317838C>A | CA358117878 | FAT4 | c.1427C>A (p.Ser476Ter) c.-55+1861C>A (n.-55+1861C>A) | |
4 | g.125317838C>G | CA358117879 | FAT4 | c.1427C>G (p.Ser476Ter) c.-55+1861C>G (n.-55+1861C>G) | COSMIC COSMIC |
4 | g.125317838C>T | CA358117880 | FAT4 | c.1427C>T (p.Ser476Leu) c.-55+1861C>T (n.-55+1861C>T) | |
4 | g.125317839A>C | CA441366666 | FAT4 | c.1428A>C (p.Ser476=) c.-55+1862A>C (n.-55+1862A>C) | |
4 | g.125317839A>G | CA441366672 | FAT4 | c.1428A>G (p.Ser476=) c.-55+1862A>G (n.-55+1862A>G) | |
4 | g.125317839A>T | CA441366669 | FAT4 | c.1428A>T (p.Ser476=) c.-55+1862A>T (n.-55+1862A>T) | |
4 | g.125317840C>A | CA358117883 | FAT4 | c.1429C>A (p.Gln477Lys) c.-55+1863C>A (n.-55+1863C>A) | |
4 | g.125317840C>G | CA358117881 | FAT4 | c.1429C>G (p.Gln477Glu) c.-55+1863C>G (n.-55+1863C>G) | |
4 | g.125317840C>T | CA358117882 | FAT4 | c.1429C>T (p.Gln477Ter) c.-55+1863C>T (n.-55+1863C>T) | |
4 | g.125317841A>C | CA358117884 | FAT4 | c.1430A>C (p.Gln477Pro) c.-55+1864A>C (n.-55+1864A>C) | |
4 | g.125317841A>G | CA358117885 | FAT4 | c.1430A>G (p.Gln477Arg) c.-55+1864A>G (n.-55+1864A>G) | |
4 | g.125317841A>T | CA358117886 | FAT4 | c.1430A>T (p.Gln477Leu) c.-55+1864A>T (n.-55+1864A>T) | |
4 | g.125317842G>A | CA441366677 | FAT4 | c.1431G>A (p.Gln477=) c.-55+1865G>A (n.-55+1865G>A) | |
4 | g.125317842G>C | CA358117887 | FAT4 | c.1431G>C (p.Gln477His) c.-55+1865G>C (n.-55+1865G>C) | |
4 | g.125317842G>T | CA358117888 | FAT4 | c.1431G>T (p.Gln477His) c.-55+1865G>T (n.-55+1865G>T) | |
4 | g.125317843C>A | CA358117889 | FAT4 | c.1432C>A (p.Gln478Lys) c.-55+1866C>A (n.-55+1866C>A) | COSMIC COSMIC |
4 | g.125317843C= | CA1491600863 | FAT4 | c.1432C= (p.Gln478=) c.-55+1866C= (n.-55+1866C=) | |
4 | g.125317843C>G | CA3071988 | FAT4 | c.1432C>G (p.Gln478Glu) c.-55+1866C>G (n.-55+1866C>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317843C>T | CA358117890 | FAT4 | c.1432C>T (p.Gln478Ter) c.-55+1866C>T (n.-55+1866C>T) | |
4 | g.125317844A>C | CA358117891 | FAT4 | c.1433A>C (p.Gln478Pro) c.-55+1867A>C (n.-55+1867A>C) | |
4 | g.125317844A>G | CA358117892 | FAT4 | c.1433A>G (p.Gln478Arg) c.-55+1867A>G (n.-55+1867A>G) | |
4 | g.125317844A>T | CA358117893 | FAT4 | c.1433A>T (p.Gln478Leu) c.-55+1867A>T (n.-55+1867A>T) | |
4 | g.125317845A>C | CA358117894 | FAT4 | c.1434A>C (p.Gln478His) c.-55+1868A>C (n.-55+1868A>C) | |
4 | g.125317845A>G | CA441366683 | FAT4 | c.1434A>G (p.Gln478=) c.-55+1868A>G (n.-55+1868A>G) | gnomAD v4 |
4 | g.125317845A>T | CA358117895 | FAT4 | c.1434A>T (p.Gln478His) c.-55+1868A>T (n.-55+1868A>T) | |
4 | g.125317846G>A | CA358117897 | FAT4 | c.1435G>A (p.Val479Met) c.-55+1869G>A (n.-55+1869G>A) | ClinVar |
4 | g.125317846G>C | CA358117898 | FAT4 | c.1435G>C (p.Val479Leu) c.-55+1869G>C (n.-55+1869G>C) | |
4 | g.125317846G>T | CA358117896 | FAT4 | c.1435G>T (p.Val479Leu) c.-55+1869G>T (n.-55+1869G>T) | gnomAD v4 |
4 | g.125317847T>A | CA358117899 | FAT4 | c.1436T>A (p.Val479Glu) c.-55+1870T>A (n.-55+1870T>A) | |
4 | g.125317847T>C | CA358117900 | FAT4 | c.1436T>C (p.Val479Ala) c.-55+1870T>C (n.-55+1870T>C) | |
4 | g.125317847T>G | CA358117901 | FAT4 | c.1436T>G (p.Val479Gly) c.-55+1870T>G (n.-55+1870T>G) | |
4 | g.125317848G>A | CA441366689 | FAT4 | c.1437G>A (p.Val479=) c.-55+1871G>A (n.-55+1871G>A) | gnomAD v4 |
4 | g.125317848G>C | CA441366690 | FAT4 | c.1437G>C (p.Val479=) c.-55+1871G>C (n.-55+1871G>C) | |
4 | g.125317848G>T | CA441366691 | FAT4 | c.1437G>T (p.Val479=) c.-55+1871G>T (n.-55+1871G>T) |