Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.135817658C>A | CA348606280 | LCT | c.1390G>T (p.Gly464Trp) | dbSNP |
2 | g.135817658C= | CA1290834880 | LCT | c.1390G= (p.Gly464=) | |
2 | g.135817658C>G | CA348606281 | LCT | c.1390G>C (p.Gly464Arg) | |
2 | g.135817658C>T | CA348606282 | LCT | c.1390G>A (p.Gly464Arg) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.135817659C>A | CA348606283 | LCT | c.1389G>T (p.Met463Ile) | dbSNP |
2 | g.135817659C= | CA1290834881 | LCT | c.1389G= (p.Met463=) | |
2 | g.135817659C>G | CA348606284 | LCT | c.1389G>C (p.Met463Ile) | |
2 | g.135817659C>T | CA348606285 | LCT | c.1389G>A (p.Met463Ile) | dbSNP gnomAD v2 |
2 | g.135817660A= | CA1290834882 | LCT | c.1388T= (p.Met463=) | |
2 | g.135817660A>C | CA348606286 | LCT | c.1388T>G (p.Met463Arg) | dbSNP |
2 | g.135817660A>G | CA348606287 | LCT | c.1388T>C (p.Met463Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817660A>T | CA348606288 | LCT | c.1388T>A (p.Met463Lys) | |
2 | g.135817661T>A | CA348606291 | LCT | c.1387A>T (p.Met463Leu) | dbSNP gnomAD v4 |
2 | g.135817661T>C | CA348606289 | LCT | c.1387A>G (p.Met463Val) | gnomAD v4 |
2 | g.135817661T>G | CA348606290 | LCT | c.1387A>C (p.Met463Leu) | |
2 | g.135817661T= | CA1290834883 | LCT | c.1387A= (p.Met463=) | |
2 | g.135817662G>A | CA429204823 | LCT | c.1386C>T (p.Pro462=) | |
2 | g.135817662G>C | CA429204822 | LCT | c.1386C>G (p.Pro462=) | |
2 | g.135817662G>T | CA429204821 | LCT | c.1386C>A (p.Pro462=) | |
2 | g.135817663G>A | CA348606292 | LCT | c.1385C>T (p.Pro462Leu) | |
2 | g.135817663G>C | CA348606293 | LCT | c.1385C>G (p.Pro462Arg) | |
2 | g.135817663G>T | CA348606294 | LCT | c.1385C>A (p.Pro462His) | |
2 | g.135817664G>A | CA348606295 | LCT | c.1384C>T (p.Pro462Ser) | |
2 | g.135817664G>C | CA348606296 | LCT | c.1384C>G (p.Pro462Ala) | |
2 | g.135817664G>T | CA348606297 | LCT | c.1384C>A (p.Pro462Thr) | |
2 | g.135817665G>A | CA429204824 | LCT | c.1383C>T (p.Phe461=) | |
2 | g.135817665G>C | CA348606298 | LCT | c.1383C>G (p.Phe461Leu) | |
2 | g.135817665G>T | CA348606299 | LCT | c.1383C>A (p.Phe461Leu) | |
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) |