2 | g.135817666A>C | CA348606300 | LCT | c.1382T>G (p.Phe461Cys)
| |
2 | g.135817666A>G | CA348606301 | LCT | c.1382T>C (p.Phe461Ser)
| |
2 | g.135817666A>T | CA348606302 | LCT | c.1382T>A (p.Phe461Tyr)
| |
2 | g.135817667A>C | CA348606305 | LCT | c.1381T>G (p.Phe461Val)
| |
2 | g.135817667A>G | CA348606304 | LCT | c.1381T>C (p.Phe461Leu)
| |
2 | g.135817667A>T | CA348606303 | LCT | c.1381T>A (p.Phe461Ile)
| |
2 | g.135817668G>A | CA429204826 | LCT | c.1380C>T (p.Ile460=)
| |
2 | g.135817668G>C | CA348606306 | LCT | c.1380C>G (p.Ile460Met)
| |
2 | g.135817668G>T | CA429204827 | LCT | c.1380C>A (p.Ile460=)
| |
2 | g.135817669A>C | CA348606307 | LCT | c.1379T>G (p.Ile460Ser)
| |
2 | g.135817669A>G | CA348606308 | LCT | c.1379T>C (p.Ile460Thr)
| |
2 | g.135817669A>T | CA348606309 | LCT | c.1379T>A (p.Ile460Asn)
| |
2 | g.135817670T>A | CA348606310 | LCT | c.1378A>T (p.Ile460Phe)
| |
2 | g.135817670T>C | CA348606311 | LCT | c.1378A>G (p.Ile460Val)
| |
2 | g.135817670T>G | CA348606312 | LCT | c.1378A>C (p.Ile460Leu)
| gnomAD v4 |
2 | g.135817671C>A | CA429204829 | LCT | c.1377G>T (p.Arg459=)
| |
2 | g.135817671C= | CA1290834884 | LCT | c.1377G= (p.Arg459=)
| |
2 | g.135817671C>G | CA429204831 | LCT | c.1377G>C (p.Arg459=)
| dbSNP |
2 | g.135817671C>T | CA429204832 | LCT | c.1377G>A (p.Arg459=)
| |
2 | g.135817672C>A | CA348606315 | LCT | c.1376G>T (p.Arg459Leu)
| dbSNP gnomAD v2 |
2 | g.135817672C= | CA1290834885 | LCT | c.1376G= (p.Arg459=)
| |
2 | g.135817672C>G | CA348606313 | LCT | c.1376G>C (p.Arg459Pro)
| |
2 | g.135817672C>T | CA348606314 | LCT | c.1376G>A (p.Arg459Gln)
| dbSNP gnomAD v3 gnomAD v4 |
2 | g.135817673G>A | CA1888398 | LCT | c.1375C>T (p.Arg459Trp)
| dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
2 | g.135817673G>C | CA348606316 | LCT | c.1375C>G (p.Arg459Gly)
| |
2 | g.135817673G= | CA1290834886 | LCT | c.1375C= (p.Arg459=)
| |
2 | g.135817673G>T | CA429204837 | LCT | c.1375C>A (p.Arg459=)
| |
2 | g.135817674G>A | CA429204840 | LCT | c.1374C>T (p.Ser458=)
| gnomAD v4 |
2 | g.135817674G>C | CA429204839 | LCT | c.1374C>G (p.Ser458=)
| |
2 | g.135817674G>T | CA429204838 | LCT | c.1374C>A (p.Ser458=)
| |
2 | g.135817675G>A | CA348606317 | LCT | c.1373C>T (p.Ser458Phe)
| dbSNP gnomAD v2 gnomAD v4 COSMIC |
2 | g.135817675G>C | CA348606318 | LCT | c.1373C>G (p.Ser458Cys)
| |
2 | g.135817675G= | CA1290834887 | LCT | c.1373C= (p.Ser458=)
| |
2 | g.135817675G>T | CA348606319 | LCT | c.1373C>A (p.Ser458Tyr)
| gnomAD v4 |
2 | g.135817676A>C | CA348606320 | LCT | c.1372T>G (p.Ser458Ala)
| |
2 | g.135817676A>G | CA348606322 | LCT | c.1372T>C (p.Ser458Pro)
| |
2 | g.135817676A>T | CA348606321 | LCT | c.1372T>A (p.Ser458Thr)
| |
2 | g.135817677C>A | CA348606323 | LCT | c.1371G>T (p.Trp457Cys)
| |
2 | g.135817677C>G | CA348606324 | LCT | c.1371G>C (p.Trp457Cys)
| |
2 | g.135817677C>T | CA348606325 | LCT | c.1371G>A (p.Trp457Ter)
| gnomAD v4 |
2 | g.135817678C>A | CA348606326 | LCT | c.1370G>T (p.Trp457Leu)
| |
2 | g.135817678C>G | CA348606327 | LCT | c.1370G>C (p.Trp457Ser)
| |
2 | g.135817678C>T | CA348606328 | LCT | c.1370G>A (p.Trp457Ter)
| |
2 | g.135817679A>C | CA348606329 | LCT | c.1369T>G (p.Trp457Gly)
| |
2 | g.135817679A>G | CA348606330 | LCT | c.1369T>C (p.Trp457Arg)
| |
2 | g.135817679A>T | CA348606331 | LCT | c.1369T>A (p.Trp457Arg)
| |
2 | g.135817680G>A | CA429204844 | LCT | c.1368C>T (p.Ser456=)
| |
2 | g.135817680G>C | CA429204845 | LCT | c.1368C>G (p.Ser456=)
| |
2 | g.135817680G>T | CA429204847 | LCT | c.1368C>A (p.Ser456=)
| |
2 | g.135817681G>A | CA348606332 | LCT | c.1367C>T (p.Ser456Phe)
| |
2 | g.135817681G>C | CA348606333 | LCT | c.1367C>G (p.Ser456Cys)
| dbSNP gnomAD v2 gnomAD v4 |
2 | g.135817681G= | CA1290834888 | LCT | c.1367C= (p.Ser456=)
| |
2 | g.135817681G>T | CA348606334 | LCT | c.1367C>A (p.Ser456Tyr)
| |
2 | g.135817682A>C | CA348606335 | LCT | c.1366T>G (p.Ser456Ala)
| |
2 | g.135817682A>G | CA348606337 | LCT | c.1366T>C (p.Ser456Pro)
| |
2 | g.135817682A>T | CA348606336 | LCT | c.1366T>A (p.Ser456Thr)
| |
2 | g.135817683G>A | CA429204849 | LCT | c.1365C>T (p.Ile455=)
| gnomAD v4 |
2 | g.135817683G>C | CA348606338 | LCT | c.1365C>G (p.Ile455Met)
| |
2 | g.135817683G>T | CA429204851 | LCT | c.1365C>A (p.Ile455=)
| |
2 | g.135817684A>C | CA348606339 | LCT | c.1364T>G (p.Ile455Ser)
| |
2 | g.135817684A>G | CA348606340 | LCT | c.1364T>C (p.Ile455Thr)
| |
2 | g.135817684A>T | CA348606341 | LCT | c.1364T>A (p.Ile455Asn)
| |
2 | g.135817685T>A | CA348606342 | LCT | c.1363A>T (p.Ile455Phe)
| |
2 | g.135817685T>C | CA348606343 | LCT | c.1363A>G (p.Ile455Val)
| |
2 | g.135817685T>G | CA348606344 | LCT | c.1363A>C (p.Ile455Leu)
| gnomAD v4 |
2 | g.135817685_135817691delinsTGGAGAA | CA1290834889 | LCT | c.1357_1363delinsTTCTCCA (p.Phe453=)
| |
2 | g.135817686G>A | CA429204853 | LCT | c.1362C>T (p.Ser454=)
| |
2 | g.135817686G>C | CA429204854 | LCT | c.1362C>G (p.Ser454=)
| |
2 | g.135817686G>T | CA429204855 | LCT | c.1362C>A (p.Ser454=)
| |
2 | g.135817686_135817691del | CA1888399 | LCT | c.1357_1362del (p.Phe453_Ser454del)
| dbSNP ExAC gnomAD v2 |
2 | g.135817687G>A | CA348606345 | LCT | c.1361C>T (p.Ser454Phe)
| |
2 | g.135817687G>C | CA348606346 | LCT | c.1361C>G (p.Ser454Cys)
| |
2 | g.135817687G>T | CA348606347 | LCT | c.1361C>A (p.Ser454Tyr)
| |
2 | g.135817688A>C | CA348606348 | LCT | c.1360T>G (p.Ser454Ala)
| gnomAD v4 |
2 | g.135817688A>G | CA348606349 | LCT | c.1360T>C (p.Ser454Pro)
| |
2 | g.135817688A>T | CA348606350 | LCT | c.1360T>A (p.Ser454Thr)
| |
2 | g.135817689G>A | CA429204859 | LCT | c.1359C>T (p.Phe453=)
| COSMIC |
2 | g.135817689G>C | CA348606351 | LCT | c.1359C>G (p.Phe453Leu)
| |
2 | g.135817689G>T | CA348606352 | LCT | c.1359C>A (p.Phe453Leu)
| gnomAD v4 |
2 | g.135817690A>C | CA348606353 | LCT | c.1358T>G (p.Phe453Cys)
| |
2 | g.135817690A>G | CA348606354 | LCT | c.1358T>C (p.Phe453Ser)
| |
2 | g.135817690A>T | CA348606355 | LCT | c.1358T>A (p.Phe453Tyr)
| |
2 | g.135817691A>C | CA348606356 | LCT | c.1357T>G (p.Phe453Val)
| |
2 | g.135817691A>G | CA348606357 | LCT | c.1357T>C (p.Phe453Leu)
| |
2 | g.135817691A>T | CA348606358 | LCT | c.1357T>A (p.Phe453Ile)
| |
2 | g.135817692C>A | CA348606359 | LCT | c.1356G>T (p.Lys452Asn)
| COSMIC |
2 | g.135817692C>G | CA348606360 | LCT | c.1356G>C (p.Lys452Asn)
| |
2 | g.135817692C>T | CA429204860 | LCT | c.1356G>A (p.Lys452=)
| dbSNP |
2 | g.135817693T>A | CA348606361 | LCT | c.1355A>T (p.Lys452Met)
| |
2 | g.135817693T>C | CA348606362 | LCT | c.1355A>G (p.Lys452Arg)
| |
2 | g.135817693T>G | CA348606363 | LCT | c.1355A>C (p.Lys452Thr)
| |
2 | g.135817694T>A | CA348606364 | LCT | c.1354A>T (p.Lys452Ter)
| |
2 | g.135817694T>C | CA348606366 | LCT | c.1354A>G (p.Lys452Glu)
| |
2 | g.135817694T>G | CA348606365 | LCT | c.1354A>C (p.Lys452Gln)
| |
2 | g.135817695G>A | CA429204863 | LCT | c.1353C>T (p.Tyr451=)
| |
2 | g.135817695G>C | CA348606367 | LCT | c.1353C>G (p.Tyr451Ter)
| |
2 | g.135817695G>T | CA348606368 | LCT | c.1353C>A (p.Tyr451Ter)
| |
2 | g.135817696T>A | CA348606369 | LCT | c.1352A>T (p.Tyr451Phe)
| COSMIC |
2 | g.135817696T>C | CA348606371 | LCT | c.1352A>G (p.Tyr451Cys)
| |
2 | g.135817696T>G | CA348606370 | LCT | c.1352A>C (p.Tyr451Ser)
| |
2 | g.135817697A>C | CA348606372 | LCT | c.1351T>G (p.Tyr451Asp)
| |
2 | g.135817697A>G | CA348606374 | LCT | c.1351T>C (p.Tyr451His)
| |
2 | g.135817697A>T | CA348606373 | LCT | c.1351T>A (p.Tyr451Asn)
| |
2 | g.135817698C>A | CA429204870 | LCT | c.1350G>T (p.Val450=)
| |
2 | g.135817698C= | CA1290834891 | LCT | c.1350G= (p.Val450=)
| |
2 | g.135817698C>G | CA429204871 | LCT | c.1350G>C (p.Val450=)
| |
2 | g.135817698C>T | CA1888400 | LCT | c.1350G>A (p.Val450=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135817698_135817699delinsCA | CA1290834890 | LCT | c.1349_1350delinsTG (p.Val450=)
| |
2 | g.135817699del | CA1888401 | LCT | c.1349del (p.Val450GlyfsTer?)
| dbSNP ExAC gnomAD v3 gnomAD v4 |
2 | g.135817699A>C | CA348606375 | LCT | c.1349T>G (p.Val450Gly)
| |
2 | g.135817699A>G | CA348606376 | LCT | c.1349T>C (p.Val450Ala)
| |
2 | g.135817699A>T | CA348606377 | LCT | c.1349T>A (p.Val450Glu)
| |
2 | g.135817700C>A | CA348606378 | LCT | c.1348G>T (p.Val450Leu)
| |
2 | g.135817700C>G | CA348606379 | LCT | c.1348G>C (p.Val450Leu)
| |
2 | g.135817700C>T | CA348606380 | LCT | c.1348G>A (p.Val450Met)
| gnomAD v4 |
2 | g.135817701del | CA348606381 | LCT | c.1348del (p.Val450CysfsTer?)
| |
2 | g.135817701C>A | CA348606382 | LCT | c.1347G>T (p.Gln449His)
| |
2 | g.135817701C>G | CA348606383 | LCT | c.1347G>C (p.Gln449His)
| |
2 | g.135817701C>T | CA429204877 | LCT | c.1347G>A (p.Gln449=)
| gnomAD v4 |
2 | g.135817702T>A | CA348606385 | LCT | c.1346A>T (p.Gln449Leu)
| |
2 | g.135817702T>C | CA1888402 | LCT | c.1346A>G (p.Gln449Arg)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135817702T>G | CA348606384 | LCT | c.1346A>C (p.Gln449Pro)
| |
2 | g.135817702T= | CA1290834892 | LCT | c.1346A= (p.Gln449=)
| |
2 | g.135817703G>A | CA348606386 | LCT | c.1345C>T (p.Gln449Ter)
| dbSNP |
2 | g.135817703G>C | CA348606387 | LCT | c.1345C>G (p.Gln449Glu)
| |
2 | g.135817703G= | CA1290834893 | LCT | c.1345C= (p.Gln449=)
| |
2 | g.135817703G>T | CA348606388 | LCT | c.1345C>A (p.Gln449Lys)
| gnomAD v4 |
2 | g.135817704A= | CA1290834894 | LCT | c.1344T= (p.Ala448=)
| |
2 | g.135817704A>C | CA429204881 | LCT | c.1344T>G (p.Ala448=)
| |
2 | g.135817704A>G | CA429204882 | LCT | c.1344T>C (p.Ala448=)
| dbSNP |
2 | g.135817704A>T | CA429204883 | LCT | c.1344T>A (p.Ala448=)
| |
2 | g.135817705G>A | CA348606389 | LCT | c.1343C>T (p.Ala448Val)
| |
2 | g.135817705G>C | CA348606390 | LCT | c.1343C>G (p.Ala448Gly)
| |
2 | g.135817705G>T | CA348606391 | LCT | c.1343C>A (p.Ala448Asp)
| |
2 | g.135817706C>A | CA348606392 | LCT | c.1342G>T (p.Ala448Ser)
| gnomAD v4 |
2 | g.135817706C>G | CA348606393 | LCT | c.1342G>C (p.Ala448Pro)
| |
2 | g.135817706C>T | CA348606394 | LCT | c.1342G>A (p.Ala448Thr)
| |
2 | g.135817707C>A | CA429204889 | LCT | c.1341G>T (p.Arg447=)
| |
2 | g.135817707C>G | CA429204888 | LCT | c.1341G>C (p.Arg447=)
| |
2 | g.135817707C>T | CA429204887 | LCT | c.1341G>A (p.Arg447=)
| |
2 | g.135817708C>A | CA348606395 | LCT | c.1340G>T (p.Arg447Leu)
| |
2 | g.135817708C= | CA1290834895 | LCT | c.1340G= (p.Arg447=)
| |
2 | g.135817708C>G | CA348606396 | LCT | c.1340G>C (p.Arg447Pro)
| |
2 | g.135817708C>T | CA1888403 | LCT | c.1340G>A (p.Arg447Gln)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.135817709G>A | CA56623581 | LCT | c.1339C>T (p.Arg447Trp)
| dbSNP gnomAD v4 |
2 | g.135817709G>C | CA348606397 | LCT | c.1339C>G (p.Arg447Gly)
| |
2 | g.135817709G= | CA1290834896 | LCT | c.1339C= (p.Arg447=)
| |
2 | g.135817709G>T | CA429204891 | LCT | c.1339C>A (p.Arg447=)
| |
2 | g.135817710G>A | CA429204892 | LCT | c.1338C>T (p.Leu446=)
| |
2 | g.135817710G>C | CA429204893 | LCT | c.1338C>G (p.Leu446=)
| |
2 | g.135817710G>T | CA429204894 | LCT | c.1338C>A (p.Leu446=)
| |
2 | g.135817711A>C | CA348606398 | LCT | c.1337T>G (p.Leu446Arg)
| |
2 | g.135817711A>G | CA348606399 | LCT | c.1337T>C (p.Leu446Pro)
| |
2 | g.135817711A>T | CA348606400 | LCT | c.1337T>A (p.Leu446His)
| |
2 | g.135817711_135817712delinsAG | CA1290834897 | LCT | c.1336_1337delinsCT (p.Leu446=)
| |
2 | g.135817712G>A | CA348606401 | LCT | c.1336C>T (p.Leu446Phe)
| gnomAD v4 |
2 | g.135817712G>C | CA348606402 | LCT | c.1336C>G (p.Leu446Val)
| |
2 | g.135817712G>T | CA348606403 | LCT | c.1336C>A (p.Leu446Ile)
| |
2 | g.135817713dup | CA1290834898 | LCT | c.1336dup (p.Leu446ProfsTer?)
| dbSNP |
2 | g.135817713del | CA1888404 | LCT | c.1336del (p.Leu446SerfsTer?)
| dbSNP ExAC |
2 | g.135817713G>A | CA429204898 | LCT | c.1335C>T (p.Gly445=)
| |
2 | g.135817713G>C | CA429204899 | LCT | c.1335C>G (p.Gly445=)
| |
2 | g.135817713G>T | CA429204900 | LCT | c.1335C>A (p.Gly445=)
| |
2 | g.135817714C>A | CA348606404 | LCT | c.1334G>T (p.Gly445Val)
| |
2 | g.135817714C>G | CA348606405 | LCT | c.1334G>C (p.Gly445Ala)
| |
2 | g.135817714C>T | CA348606406 | LCT | c.1334G>A (p.Gly445Asp)
| COSMIC |
2 | g.135817715C>A | CA348606407 | LCT | c.1333G>T (p.Gly445Cys)
| |
2 | g.135817715C= | CA1290834899 | LCT | c.1333G= (p.Gly445=)
| |
2 | g.135817715C>G | CA348606408 | LCT | c.1333G>C (p.Gly445Arg)
| |
2 | g.135817715C>T | CA348606409 | LCT | c.1333G>A (p.Gly445Ser)
| dbSNP gnomAD v2 gnomAD v4 COSMIC |
2 | g.135817716G>A | CA1888405 | LCT | c.1332C>T (p.Cys444=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817716G>C | CA348606410 | LCT | c.1332C>G (p.Cys444Trp)
| |
2 | g.135817716G= | CA1290834900 | LCT | c.1332C= (p.Cys444=)
| |
2 | g.135817716G>T | CA348606411 | LCT | c.1332C>A (p.Cys444Ter)
| |
2 | g.135817717C>A | CA348606412 | LCT | c.1331G>T (p.Cys444Phe)
| |
2 | g.135817717C>G | CA348606413 | LCT | c.1331G>C (p.Cys444Ser)
| |
2 | g.135817717C>T | CA348606414 | LCT | c.1331G>A (p.Cys444Tyr)
| |
2 | g.135817718A= | CA1290834901 | LCT | c.1330T= (p.Cys444=)
| |
2 | g.135817718A>C | CA348606415 | LCT | c.1330T>G (p.Cys444Gly)
| |
2 | g.135817718A>G | CA348606416 | LCT | c.1330T>C (p.Cys444Arg)
| dbSNP |
2 | g.135817718A>T | CA56623587 | LCT | c.1330T>A (p.Cys444Ser)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817719A>C | CA429204904 | LCT | c.1329T>G (p.Leu443=)
| |
2 | g.135817719A>G | CA429204905 | LCT | c.1329T>C (p.Leu443=)
| |
2 | g.135817719A>T | CA429204906 | LCT | c.1329T>A (p.Leu443=)
| |
2 | g.135817720A>C | CA348606417 | LCT | c.1328T>G (p.Leu443Arg)
| |
2 | g.135817720A>G | CA348606418 | LCT | c.1328T>C (p.Leu443Pro)
| |
2 | g.135817720A>T | CA348606419 | LCT | c.1328T>A (p.Leu443His)
| |
2 | g.135817721G>A | CA348606420 | LCT | c.1327C>T (p.Leu443Phe)
| |
2 | g.135817721G>C | CA348606421 | LCT | c.1327C>G (p.Leu443Val)
| |
2 | g.135817721G>T | CA348606422 | LCT | c.1327C>A (p.Leu443Ile)
| COSMIC |
2 | g.135817722C>A | CA429204913 | LCT | c.1326G>T (p.Leu442=)
| |
2 | g.135817722C= | CA1290834902 | LCT | c.1326G= (p.Leu442=)
| |
2 | g.135817722C>G | CA429204912 | LCT | c.1326G>C (p.Leu442=)
| dbSNP |
2 | g.135817722C>T | CA429204911 | LCT | c.1326G>A (p.Leu442=)
| dbSNP gnomAD v3 gnomAD v4 |
2 | g.135817723A>C | CA348606425 | LCT | c.1325T>G (p.Leu442Arg)
| |
2 | g.135817723A>G | CA348606424 | LCT | c.1325T>C (p.Leu442Pro)
| |
2 | g.135817723A>T | CA348606423 | LCT | c.1325T>A (p.Leu442Gln)
| gnomAD v4 |
2 | g.135817724G>A | CA429204915 | LCT | c.1324C>T (p.Leu442=)
| |
2 | g.135817724G>C | CA348606426 | LCT | c.1324C>G (p.Leu442Val)
| |
2 | g.135817724G= | CA1290834903 | LCT | c.1324C= (p.Leu442=)
| |
2 | g.135817724G>T | CA348606427 | LCT | c.1324C>A (p.Leu442Met)
| dbSNP gnomAD v4 |
2 | g.135817725G>A | CA429204916 | LCT | c.1323C>T (p.Ala441=)
| |
2 | g.135817725G>C | CA429204917 | LCT | c.1323C>G (p.Ala441=)
| |
2 | g.135817725G>T | CA429204919 | LCT | c.1323C>A (p.Ala441=)
| |
2 | g.135817726G>A | CA348606428 | LCT | c.1322C>T (p.Ala441Val)
| |
2 | g.135817726G>C | CA348606429 | LCT | c.1322C>G (p.Ala441Gly)
| |
2 | g.135817726G>T | CA348606430 | LCT | c.1322C>A (p.Ala441Asp)
| |
2 | g.135817727C>A | CA348606431 | LCT | c.1321G>T (p.Ala441Ser)
| dbSNP gnomAD v3 gnomAD v4 |
2 | g.135817727C= | CA1290834904 | LCT | c.1321G= (p.Ala441=)
| |
2 | g.135817727C>G | CA348606432 | LCT | c.1321G>C (p.Ala441Pro)
| gnomAD v4 |
2 | g.135817727C>T | CA1888406 | LCT | c.1321G>A (p.Ala441Thr)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.135817728G>A | CA429204922 | LCT | c.1320C>T (p.Val440=)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.135817728G>C | CA429204924 | LCT | c.1320C>G (p.Val440=)
| dbSNP |
2 | g.135817728G= | CA1290834905 | LCT | c.1320C= (p.Val440=)
| |
2 | g.135817728G>T | CA429204923 | LCT | c.1320C>A (p.Val440=)
| |
2 | g.135817729A>C | CA348606433 | LCT | c.1319T>G (p.Val440Gly)
| |
2 | g.135817729A>G | CA348606434 | LCT | c.1319T>C (p.Val440Ala)
| |
2 | g.135817729A>T | CA348606435 | LCT | c.1319T>A (p.Val440Asp)
| |
2 | g.135817730C>A | CA348606436 | LCT | c.1318G>T (p.Val440Phe)
| |
2 | g.135817730C= | CA1290834906 | LCT | c.1318G= (p.Val440=)
| |
2 | g.135817730C>G | CA348606437 | LCT | c.1318G>C (p.Val440Leu)
| |
2 | g.135817730C>T | CA1888407 | LCT | c.1318G>A (p.Val440Ile)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817731G>A | CA1888408 | LCT | c.1317C>T (p.Asp439=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817731G>C | CA348606439 | LCT | c.1317C>G (p.Asp439Glu)
| |
2 | g.135817731G= | CA1290834907 | LCT | c.1317C= (p.Asp439=)
| |
2 | g.135817731G>T | CA348606438 | LCT | c.1317C>A (p.Asp439Glu)
| |
2 | g.135817732T>A | CA348606440 | LCT | c.1316A>T (p.Asp439Val)
| |
2 | g.135817732T>C | CA348606441 | LCT | c.1316A>G (p.Asp439Gly)
| |
2 | g.135817732T>G | CA348606442 | LCT | c.1316A>C (p.Asp439Ala)
| |
2 | g.135817733C>A | CA348606443 | LCT | c.1315G>T (p.Asp439Tyr)
| |
2 | g.135817733C>G | CA348606444 | LCT | c.1315G>C (p.Asp439His)
| |
2 | g.135817733C>T | CA348606445 | LCT | c.1315G>A (p.Asp439Asn)
| |
2 | g.135817734A>C | CA429204932 | LCT | c.1314T>G (p.Ser438=)
| |
2 | g.135817734A>G | CA429204933 | LCT | c.1314T>C (p.Ser438=)
| |
2 | g.135817734A>T | CA429204934 | LCT | c.1314T>A (p.Ser438=)
| |
2 | g.135817735G>A | CA348606446 | LCT | c.1313C>T (p.Ser438Phe)
| dbSNP gnomAD v4 |
2 | g.135817735G>C | CA56623593 | LCT | c.1313C>G (p.Ser438Cys)
| dbSNP |
2 | g.135817735G= | CA1290834908 | LCT | c.1313C= (p.Ser438=)
| |
2 | g.135817735G>T | CA348606447 | LCT | c.1313C>A (p.Ser438Tyr)
| |
2 | g.135817736A= | CA1290834909 | LCT | c.1312T= (p.Ser438=)
| |
2 | g.135817736A>C | CA56623594 | LCT | c.1312T>G (p.Ser438Ala)
| dbSNP |
2 | g.135817736A>G | CA348606448 | LCT | c.1312T>C (p.Ser438Pro)
| |
2 | g.135817736A>T | CA348606449 | LCT | c.1312T>A (p.Ser438Thr)
| dbSNP |
2 | g.135817737G>A | CA429204940 | LCT | c.1311C>T (p.Ala437=)
| gnomAD v4 |
2 | g.135817737G>C | CA429204936 | LCT | c.1311C>G (p.Ala437=)
| |
2 | g.135817737G>T | CA429204938 | LCT | c.1311C>A (p.Ala437=)
| |
2 | g.135817738G>A | CA348606452 | LCT | c.1310C>T (p.Ala437Val)
| gnomAD v4 |
2 | g.135817738G>C | CA348606451 | LCT | c.1310C>G (p.Ala437Gly)
| |
2 | g.135817738G= | CA1290834910 | LCT | c.1310C= (p.Ala437=)
| |
2 | g.135817738G>T | CA348606450 | LCT | c.1310C>A (p.Ala437Asp)
| dbSNP |
2 | g.135817739C>A | CA348606453 | LCT | c.1309G>T (p.Ala437Ser)
| |
2 | g.135817739C= | CA1290834911 | LCT | c.1309G= (p.Ala437=)
| |
2 | g.135817739C>G | CA348606454 | LCT | c.1309G>C (p.Ala437Pro)
| |
2 | g.135817739C>T | CA1888409 | LCT | c.1309G>A (p.Ala437Thr)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817740T>A | CA429204943 | LCT | c.1308A>T (p.Val436=)
| |
2 | g.135817740T>C | CA429204944 | LCT | c.1308A>G (p.Val436=)
| dbSNP |
2 | g.135817740T>G | CA429204945 | LCT | c.1308A>C (p.Val436=)
| |
2 | g.135817740T= | CA1290834912 | LCT | c.1308A= (p.Val436=)
| |
2 | g.135817741A>C | CA348606455 | LCT | c.1307T>G (p.Val436Gly)
| |
2 | g.135817741A>G | CA348606456 | LCT | c.1307T>C (p.Val436Ala)
| |
2 | g.135817741A>T | CA348606457 | LCT | c.1307T>A (p.Val436Glu)
| |
2 | g.135817742C>A | CA348606460 | LCT | c.1306G>T (p.Val436Leu)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817742C= | CA1290834913 | LCT | c.1306G= (p.Val436=)
| |
2 | g.135817742C>G | CA348606458 | LCT | c.1306G>C (p.Val436Leu)
| |
2 | g.135817742C>T | CA348606459 | LCT | c.1306G>A (p.Val436Ile)
| gnomAD v4 |
2 | g.135817743C>A | CA348606461 | LCT | c.1305G>T (p.Lys435Asn)
| |
2 | g.135817743C= | CA1290834914 | LCT | c.1305G= (p.Lys435=)
| |
2 | g.135817743C>G | CA348606462 | LCT | c.1305G>C (p.Lys435Asn)
| |
2 | g.135817743C>T | CA429204948 | LCT | c.1305G>A (p.Lys435=)
| dbSNP |
2 | g.135817744T>A | CA348606463 | LCT | c.1304A>T (p.Lys435Met)
| |
2 | g.135817744T>C | CA348606464 | LCT | c.1304A>G (p.Lys435Arg)
| |
2 | g.135817744T>G | CA348606465 | LCT | c.1304A>C (p.Lys435Thr)
| |
2 | g.135817745T>A | CA348606466 | LCT | c.1303A>T (p.Lys435Ter)
| |
2 | g.135817745T>C | CA348606468 | LCT | c.1303A>G (p.Lys435Glu)
| |
2 | g.135817745T>G | CA348606467 | LCT | c.1303A>C (p.Lys435Gln)
| |
2 | g.135817746G>A | CA429204952 | LCT | c.1302C>T (p.His434=)
| dbSNP gnomAD v2 gnomAD v4 COSMIC |
2 | g.135817746G>C | CA348606469 | LCT | c.1302C>G (p.His434Gln)
| |
2 | g.135817746G= | CA1290834915 | LCT | c.1302C= (p.His434=)
| |
2 | g.135817746G>T | CA348606470 | LCT | c.1302C>A (p.His434Gln)
| gnomAD v4 |
2 | g.135817747T>A | CA348606471 | LCT | c.1301A>T (p.His434Leu)
| |
2 | g.135817747T>C | CA348606472 | LCT | c.1301A>G (p.His434Arg)
| dbSNP gnomAD v3 gnomAD v4 |
2 | g.135817747T>G | CA348606473 | LCT | c.1301A>C (p.His434Pro)
| |
2 | g.135817747T= | CA1290834916 | LCT | c.1301A= (p.His434=)
| |
2 | g.135817748G>A | CA348606474 | LCT | c.1300C>T (p.His434Tyr)
| |
2 | g.135817748G>C | CA348606475 | LCT | c.1300C>G (p.His434Asp)
| |
2 | g.135817748G>T | CA348606476 | LCT | c.1300C>A (p.His434Asn)
| |
2 | g.135817749G>A | CA429204958 | LCT | c.1299C>T (p.Tyr433=)
| |
2 | g.135817749G>C | CA348606477 | LCT | c.1299C>G (p.Tyr433Ter)
| |
2 | g.135817749G>T | CA348606478 | LCT | c.1299C>A (p.Tyr433Ter)
| |
2 | g.135817750T>A | CA348606481 | LCT | c.1298A>T (p.Tyr433Phe)
| |
2 | g.135817750T>C | CA348606480 | LCT | c.1298A>G (p.Tyr433Cys)
| |
2 | g.135817750T>G | CA348606479 | LCT | c.1298A>C (p.Tyr433Ser)
| |
2 | g.135817751A>C | CA348606482 | LCT | c.1297T>G (p.Tyr433Asp)
| |
2 | g.135817751A>G | CA348606484 | LCT | c.1297T>C (p.Tyr433His)
| |
2 | g.135817751A>T | CA348606483 | LCT | c.1297T>A (p.Tyr433Asn)
| |
2 | g.135817752A= | CA1290834917 | LCT | c.1296T= (p.Ser432=)
| |
2 | g.135817752A>C | CA348606485 | LCT | c.1296T>G (p.Ser432Arg)
| |
2 | g.135817752A>G | CA1888410 | LCT | c.1296T>C (p.Ser432=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817752A>T | CA348606486 | LCT | c.1296T>A (p.Ser432Arg)
| |
2 | g.135817753C>A | CA348606487 | LCT | c.1295G>T (p.Ser432Ile)
| |
2 | g.135817753C>G | CA348606488 | LCT | c.1295G>C (p.Ser432Thr)
| |
2 | g.135817753C>T | CA348606489 | LCT | c.1295G>A (p.Ser432Asn)
| |
2 | g.135817754T>A | CA348606492 | LCT | c.1294A>T (p.Ser432Cys)
| |
2 | g.135817754T>C | CA348606490 | LCT | c.1294A>G (p.Ser432Gly)
| |
2 | g.135817754T>G | CA348606491 | LCT | c.1294A>C (p.Ser432Arg)
| |
2 | g.135817755G>A | CA429204966 | LCT | c.1293C>T (p.Asp431=)
| gnomAD v4 |
2 | g.135817755G>C | CA348606493 | LCT | c.1293C>G (p.Asp431Glu)
| |
2 | g.135817755G>T | CA348606494 | LCT | c.1293C>A (p.Asp431Glu)
| |
2 | g.135817756T>A | CA348606495 | LCT | c.1292A>T (p.Asp431Val)
| |
2 | g.135817756T>C | CA348606496 | LCT | c.1292A>G (p.Asp431Gly)
| |
2 | g.135817756T>G | CA348606497 | LCT | c.1292A>C (p.Asp431Ala)
| |
2 | g.135817757C>A | CA348606499 | LCT | c.1291G>T (p.Asp431Tyr)
| |
2 | g.135817757C= | CA1290834918 | LCT | c.1291G= (p.Asp431=)
| |
2 | g.135817757C>G | CA348606498 | LCT | c.1291G>C (p.Asp431His)
| |
2 | g.135817757C>T | CA1888411 | LCT | c.1291G>A (p.Asp431Asn)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.135817757dup | CA2842163412 | LCT | c.1291dup (p.Asp431GlyfsTer9)
| |
2 | g.135817758G>A | CA1888412 | LCT | c.1290C>T (p.Ser430=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135817758G>C | CA348606500 | LCT | c.1290C>G (p.Ser430Arg)
| |
2 | g.135817758G= | CA1290834919 | LCT | c.1290C= (p.Ser430=)
| |
2 | g.135817758G>T | CA348606501 | LCT | c.1290C>A (p.Ser430Arg)
| |
2 | g.135817759C>A | CA348606502 | LCT | c.1289G>T (p.Ser430Ile)
| |
2 | g.135817759C>G | CA348606503 | LCT | c.1289G>C (p.Ser430Thr)
| |
2 | g.135817759C>T | CA348606504 | LCT | c.1289G>A (p.Ser430Asn)
| |
2 | g.135817760T>A | CA348606505 | LCT | c.1288A>T (p.Ser430Cys)
| |
2 | g.135817760T>C | CA348606506 | LCT | c.1288A>G (p.Ser430Gly)
| |
2 | g.135817760T>G | CA348606507 | LCT | c.1288A>C (p.Ser430Arg)
| |
2 | g.135817761G>A | CA429204976 | LCT | c.1287C>T (p.Ala429=)
| |
2 | g.135817761G>C | CA429204977 | LCT | c.1287C>G (p.Ala429=)
| |
2 | g.135817761G>T | CA429204979 | LCT | c.1287C>A (p.Ala429=)
| |
2 | g.135817762G>A | CA348606508 | LCT | c.1286C>T (p.Ala429Val)
| |
2 | g.135817762G>C | CA348606509 | LCT | c.1286C>G (p.Ala429Gly)
| |
2 | g.135817762G>T | CA348606510 | LCT | c.1286C>A (p.Ala429Asp)
| |
2 | g.135817763C>A | CA348606511 | LCT | c.1285G>T (p.Ala429Ser)
| |
2 | g.135817763C>G | CA348606513 | LCT | c.1285G>C (p.Ala429Pro)
| |
2 | g.135817763C>T | CA348606512 | LCT | c.1285G>A (p.Ala429Thr)
| |
2 | g.135817764C>A | CA429204981 | LCT | c.1284G>T (p.Val428=)
| |
2 | g.135817764C= | CA1290834920 | LCT | c.1284G= (p.Val428=)
| |
2 | g.135817764C>G | CA429204983 | LCT | c.1284G>C (p.Val428=)
| |
2 | g.135817764C>T | CA429204982 | LCT | c.1284G>A (p.Val428=)
| dbSNP |
2 | g.135817765A>C | CA348606514 | LCT | c.1283T>G (p.Val428Gly)
| |
2 | g.135817765A>G | CA348606515 | LCT | c.1283T>C (p.Val428Ala)
| |
2 | g.135817765A>T | CA348606516 | LCT | c.1283T>A (p.Val428Glu)
| |
2 | g.135817766C>A | CA348606517 | LCT | c.1282G>T (p.Val428Leu)
| |
2 | g.135817766C= | CA1290834921 | LCT | c.1282G= (p.Val428=)
| |
2 | g.135817766C>G | CA348606518 | LCT | c.1282G>C (p.Val428Leu)
| |
2 | g.135817766C>T | CA1888413 | LCT | c.1282G>A (p.Val428Met)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |