Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.151001605A>C | CA369857289 | NOS3 | c.1490A>C (p.Lys497Thr) c.872A>C (p.Lys291Thr) | |
7 | g.151001605A>G | CA369857291 | NOS3 | c.1490A>G (p.Lys497Arg) c.872A>G (p.Lys291Arg) | gnomAD v4 |
7 | g.151001605A>T | CA369857292 | NOS3 | c.1490A>T (p.Lys497Ile) c.872A>T (p.Lys291Ile) | |
7 | g.151001606A>C | CA369857294 | NOS3 | c.1491A>C (p.Lys497Asn) c.873A>C (p.Lys291Asn) | |
7 | g.151001606A>G | CA458649404 | NOS3 | c.1491A>G (p.Lys497=) c.873A>G (p.Lys291=) | |
7 | g.151001606A>T | CA369857296 | NOS3 | c.1491A>T (p.Lys497Asn) c.873A>T (p.Lys291Asn) | |
7 | g.151001607G>A | CA4566986 | NOS3 | c.1492G>A (p.Glu498Lys) c.874G>A (p.Glu292Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151001607G>C | CA369857299 | NOS3 | c.1492G>C (p.Glu498Gln) c.874G>C (p.Glu292Gln) | |
7 | g.151001607G= | CA1752441074 | NOS3 | c.1492G= (p.Glu498=) c.874G= (p.Glu292=) | |
7 | g.151001607G>T | CA369857301 | NOS3 | c.1492G>T (p.Glu498Ter) c.874G>T (p.Glu292Ter) | |
7 | g.151001608A>C | CA369857303 | NOS3 | c.1493A>C (p.Glu498Ala) c.875A>C (p.Glu292Ala) | |
7 | g.151001608A>G | CA369857305 | NOS3 | c.1493A>G (p.Glu498Gly) c.875A>G (p.Glu292Gly) | |
7 | g.151001608A>T | CA369857307 | NOS3 | c.1493A>T (p.Glu498Val) c.875A>T (p.Glu292Val) | |
7 | g.151001609A>C | CA369857310 | NOS3 | c.1494A>C (p.Glu498Asp) c.876A>C (p.Glu292Asp) | gnomAD v4 |
7 | g.151001609A>G | CA458649406 | NOS3 | c.1494A>G (p.Glu498=) c.876A>G (p.Glu292=) | COSMIC |
7 | g.151001609A>T | CA369857311 | NOS3 | c.1494A>T (p.Glu498Asp) c.876A>T (p.Glu292Asp) | |
7 | g.151001610G>A | CA369857317 | NOS3 | c.1495G>A (p.Val499Met) c.877G>A (p.Val293Met) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.151001610G>C | CA369857319 | NOS3 | c.1495G>C (p.Val499Leu) c.877G>C (p.Val293Leu) | |
7 | g.151001610G= | CA1752441078 | NOS3 | c.1495G= (p.Val499=) c.877G= (p.Val293=) | |
7 | g.151001610G>T | CA369857315 | NOS3 | c.1495G>T (p.Val499Leu) c.877G>T (p.Val293Leu) | |
7 | g.151001611T>A | CA369857323 | NOS3 | c.1496T>A (p.Val499Glu) c.878T>A (p.Val293Glu) | gnomAD v4 |
7 | g.151001611T>C | CA369857327 | NOS3 | c.1496T>C (p.Val499Ala) c.878T>C (p.Val293Ala) | |
7 | g.151001611T>G | CA369857325 | NOS3 | c.1496T>G (p.Val499Gly) c.878T>G (p.Val293Gly) | |
7 | g.151001612G>A | CA458649410 | NOS3 | c.1497G>A (p.Val499=) c.879G>A (p.Val293=) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.151001612G>C | CA458649411 | NOS3 | c.1497G>C (p.Val499=) c.879G>C (p.Val293=) | |
7 | g.151001612G= | CA1752441087 | NOS3 | c.1497G= (p.Val499=) c.879G= (p.Val293=) | |
7 | g.151001612G>T | CA458649412 | NOS3 | c.1497G>T (p.Val499=) c.879G>T (p.Val293=) | |
7 | g.151001613G>A | CA369857329 | NOS3 | c.1498G>A (p.Ala500Thr) c.880G>A (p.Ala294Thr) | |
7 | g.151001613G>C | CA369857333 | NOS3 | c.1498G>C (p.Ala500Pro) c.880G>C (p.Ala294Pro) | |
7 | g.151001613G>T | CA369857331 | NOS3 | c.1498G>T (p.Ala500Ser) c.880G>T (p.Ala294Ser) | |
7 | g.151001614C>A | CA369857336 | NOS3 | c.1499C>A (p.Ala500Asp) c.881C>A (p.Ala294Asp) | |
7 | g.151001614C= | CA1752441089 | NOS3 | c.1499C= (p.Ala500=) c.881C= (p.Ala294=) | |
7 | g.151001614C>G | CA369857340 | NOS3 | c.1499C>G (p.Ala500Gly) c.881C>G (p.Ala294Gly) | |
7 | g.151001614C>T | CA169072636 | NOS3 | c.1499C>T (p.Ala500Val) c.881C>T (p.Ala294Val) | dbSNP |
7 | g.151001615C>A | CA4566987 | NOS3 | c.1500C>A (p.Ala500=) c.882C>A (p.Ala294=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151001615C= | CA1752441105 | NOS3 | c.1500C= (p.Ala500=) c.882C= (p.Ala294=) | |
7 | g.151001615C>G | CA458649415 | NOS3 | c.1500C>G (p.Ala500=) c.882C>G (p.Ala294=) | |
7 | g.151001615C>T | CA458649414 | NOS3 | c.1500C>T (p.Ala500=) c.882C>T (p.Ala294=) | |
7 | g.151001616A>C | CA369857343 | NOS3 | c.1501A>C (p.Asn501His) c.883A>C (p.Asn295His) | |
7 | g.151001616A>G | CA369857345 | NOS3 | c.1501A>G (p.Asn501Asp) c.883A>G (p.Asn295Asp) | |
7 | g.151001616A>T | CA369857347 | NOS3 | c.1501A>T (p.Asn501Tyr) c.883A>T (p.Asn295Tyr) | |
7 | g.151001617A>C | CA369857349 | NOS3 | c.1502A>C (p.Asn501Thr) c.884A>C (p.Asn295Thr) | |
7 | g.151001617A>G | CA369857351 | NOS3 | c.1502A>G (p.Asn501Ser) c.884A>G (p.Asn295Ser) | |
7 | g.151001617A>T | CA369857353 | NOS3 | c.1502A>T (p.Asn501Ile) c.884A>T (p.Asn295Ile) | |
7 | g.151001618G>A | CA369857356 | NOS3 | c.1502+1G>A (n.1502+1G>A) c.884+1G>A (n.884+1G>A) | |
7 | g.151001618G>C | CA369857358 | NOS3 | c.1502+1G>C (n.1502+1G>C) c.884+1G>C (n.884+1G>C) | |
7 | g.151001618G>T | CA369857361 | NOS3 | c.1502+1G>T (n.1502+1G>T) c.884+1G>T (n.884+1G>T) | |
7 | g.151001619T>A | CA369857363 | NOS3 | c.1502+2T>A (n.1502+2T>A) c.884+2T>A (n.884+2T>A) | |
7 | g.151001619T>C | CA369857365 | NOS3 | c.1502+2T>C (n.1502+2T>C) c.884+2T>C (n.884+2T>C) | gnomAD v4 |
7 | g.151001619T>G | CA369857366 | NOS3 | c.1502+2T>G (n.1502+2T>G) c.884+2T>G (n.884+2T>G) | gnomAD v4 |