Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.125317649A>C | CA358117490 | FAT4 | c.1238A>C (p.Lys413Thr) c.-55+1672A>C (n.-55+1672A>C) | |
4 | g.125317649A>G | CA358117491 | FAT4 | c.1238A>G (p.Lys413Arg) c.-55+1672A>G (n.-55+1672A>G) | |
4 | g.125317649A>T | CA358117492 | FAT4 | c.1238A>T (p.Lys413Ile) c.-55+1672A>T (n.-55+1672A>T) | |
4 | g.125317650A>C | CA358117493 | FAT4 | c.1239A>C (p.Lys413Asn) c.-55+1673A>C (n.-55+1673A>C) | |
4 | g.125317650A>G | CA441366875 | FAT4 | c.1239A>G (p.Lys413=) c.-55+1673A>G (n.-55+1673A>G) | |
4 | g.125317650A>T | CA358117494 | FAT4 | c.1239A>T (p.Lys413Asn) c.-55+1673A>T (n.-55+1673A>T) | |
4 | g.125317651G>A | CA358117495 | FAT4 | c.1240G>A (p.Val414Met) c.-55+1674G>A (n.-55+1674G>A) | |
4 | g.125317651G>C | CA358117496 | FAT4 | c.1240G>C (p.Val414Leu) c.-55+1674G>C (n.-55+1674G>C) | gnomAD v4 |
4 | g.125317651G>T | CA358117497 | FAT4 | c.1240G>T (p.Val414Leu) c.-55+1674G>T (n.-55+1674G>T) | |
4 | g.125317652T>A | CA358117499 | FAT4 | c.1241T>A (p.Val414Glu) c.-55+1675T>A (n.-55+1675T>A) | |
4 | g.125317652T>C | CA3071946 | FAT4 | c.1241T>C (p.Val414Ala) c.-55+1675T>C (n.-55+1675T>C) | dbSNP ExAC gnomAD v2 |
4 | g.125317652T>G | CA358117498 | FAT4 | c.1241T>G (p.Val414Gly) c.-55+1675T>G (n.-55+1675T>G) | |
4 | g.125317652T= | CA1491600364 | FAT4 | c.1241T= (p.Val414=) c.-55+1675T= (n.-55+1675T=) | |
4 | g.125317653G>A | CA441366887 | FAT4 | c.1242G>A (p.Val414=) c.-55+1676G>A (n.-55+1676G>A) | |
4 | g.125317653G>C | CA441366889 | FAT4 | c.1242G>C (p.Val414=) c.-55+1676G>C (n.-55+1676G>C) | |
4 | g.125317653G>T | CA441366890 | FAT4 | c.1242G>T (p.Val414=) c.-55+1676G>T (n.-55+1676G>T) | |
4 | g.125317654C>A | CA358117501 | FAT4 | c.1243C>A (p.Pro415Thr) c.-55+1677C>A (n.-55+1677C>A) | |
4 | g.125317654C>G | CA358117500 | FAT4 | c.1243C>G (p.Pro415Ala) c.-55+1677C>G (n.-55+1677C>G) | |
4 | g.125317654C>T | CA358117502 | FAT4 | c.1243C>T (p.Pro415Ser) c.-55+1677C>T (n.-55+1677C>T) | gnomAD v4 COSMIC COSMIC |
4 | g.125317655C>A | CA358117503 | FAT4 | c.1244C>A (p.Pro415Gln) c.-55+1678C>A (n.-55+1678C>A) | |
4 | g.125317655C= | CA1491600368 | FAT4 | c.1244C= (p.Pro415=) c.-55+1678C= (n.-55+1678C=) | |
4 | g.125317655C>G | CA3071947 | FAT4 | c.1244C>G (p.Pro415Arg) c.-55+1678C>G (n.-55+1678C>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317655C>T | CA104862065 | FAT4 | c.1244C>T (p.Pro415Leu) c.-55+1678C>T (n.-55+1678C>T) | dbSNP |
4 | g.125317656G>A | CA441366900 | FAT4 | c.1245G>A (p.Pro415=) c.-55+1679G>A (n.-55+1679G>A) | dbSNP COSMIC COSMIC |
4 | g.125317656G>C | CA441366901 | FAT4 | c.1245G>C (p.Pro415=) c.-55+1679G>C (n.-55+1679G>C) | |
4 | g.125317656G= | CA1491600376 | FAT4 | c.1245G= (p.Pro415=) c.-55+1679G= (n.-55+1679G=) | |
4 | g.125317656G>T | CA441366902 | FAT4 | c.1245G>T (p.Pro415=) c.-55+1679G>T (n.-55+1679G>T) | ClinVar dbSNP gnomAD v4 |
4 | g.125317657A>C | CA358117504 | FAT4 | c.1246A>C (p.Asn416His) c.-55+1680A>C (n.-55+1680A>C) | |
4 | g.125317657A>G | CA358117506 | FAT4 | c.1246A>G (p.Asn416Asp) c.-55+1680A>G (n.-55+1680A>G) | |
4 | g.125317657A>T | CA358117505 | FAT4 | c.1246A>T (p.Asn416Tyr) c.-55+1680A>T (n.-55+1680A>T) | |
4 | g.125317658A>C | CA358117507 | FAT4 | c.1247A>C (p.Asn416Thr) c.-55+1681A>C (n.-55+1681A>C) | |
4 | g.125317658A>G | CA358117508 | FAT4 | c.1247A>G (p.Asn416Ser) c.-55+1681A>G (n.-55+1681A>G) | |
4 | g.125317658A>T | CA358117509 | FAT4 | c.1247A>T (p.Asn416Ile) c.-55+1681A>T (n.-55+1681A>T) | |
4 | g.125317659C>A | CA358117510 | FAT4 | c.1248C>A (p.Asn416Lys) c.-55+1682C>A (n.-55+1682C>A) | |
4 | g.125317659C= | CA1491600381 | FAT4 | c.1248C= (p.Asn416=) c.-55+1682C= (n.-55+1682C=) | |
4 | g.125317659C>G | CA358117511 | FAT4 | c.1248C>G (p.Asn416Lys) c.-55+1682C>G (n.-55+1682C>G) | |
4 | g.125317659C>T | CA3071948 | FAT4 | c.1248C>T (p.Asn416=) c.-55+1682C>T (n.-55+1682C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317660C>A | CA358117512 | FAT4 | c.1249C>A (p.Leu417Met) c.-55+1683C>A (n.-55+1683C>A) | |
4 | g.125317660C= | CA1491600394 | FAT4 | c.1249C= (p.Leu417=) c.-55+1683C= (n.-55+1683C=) | |
4 | g.125317660C>G | CA358117513 | FAT4 | c.1249C>G (p.Leu417Val) c.-55+1683C>G (n.-55+1683C>G) | |
4 | g.125317660C>T | CA441366916 | FAT4 | c.1249C>T (p.Leu417=) c.-55+1683C>T (n.-55+1683C>T) | dbSNP |
4 | g.125317661T>A | CA358117514 | FAT4 | c.1250T>A (p.Leu417Gln) c.-55+1684T>A (n.-55+1684T>A) | |
4 | g.125317661T>C | CA358117515 | FAT4 | c.1250T>C (p.Leu417Pro) c.-55+1684T>C (n.-55+1684T>C) | dbSNP |
4 | g.125317661T>G | CA358117516 | FAT4 | c.1250T>G (p.Leu417Arg) c.-55+1684T>G (n.-55+1684T>G) | |
4 | g.125317661T= | CA1491600403 | FAT4 | c.1250T= (p.Leu417=) c.-55+1684T= (n.-55+1684T=) | |
4 | g.125317662G>A | CA441366922 | FAT4 | c.1251G>A (p.Leu417=) c.-55+1685G>A (n.-55+1685G>A) | |
4 | g.125317662G>C | CA441366920 | FAT4 | c.1251G>C (p.Leu417=) c.-55+1685G>C (n.-55+1685G>C) | |
4 | g.125317662G>T | CA441366918 | FAT4 | c.1251G>T (p.Leu417=) c.-55+1685G>T (n.-55+1685G>T) | |
4 | g.125317663A= | CA1491600407 | FAT4 | c.1252A= (p.Ser418=) c.-55+1686A= (n.-55+1686A=) | |
4 | g.125317663A>C | CA358117519 | FAT4 | c.1252A>C (p.Ser418Arg) c.-55+1686A>C (n.-55+1686A>C) |