Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.135817652C>A | CA1888395 | LCT | c.1396G>T (p.Gly466Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817652C= | CA1290834876 | LCT | c.1396G= (p.Gly466=) | |
2 | g.135817652C>G | CA1888394 | LCT | c.1396G>C (p.Gly466Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135817652C>T | CA348606268 | LCT | c.1396G>A (p.Gly466Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817653G>A | CA1888396 | LCT | c.1395C>T (p.His465=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.135817653G>C | CA348606269 | LCT | c.1395C>G (p.His465Gln) | dbSNP |
2 | g.135817653G= | CA1290834877 | LCT | c.1395C= (p.His465=) | |
2 | g.135817653G>T | CA348606270 | LCT | c.1395C>A (p.His465Gln) | dbSNP gnomAD v4 |
2 | g.135817654T>A | CA348606271 | LCT | c.1394A>T (p.His465Leu) | |
2 | g.135817654T>C | CA348606272 | LCT | c.1394A>G (p.His465Arg) | gnomAD v4 |
2 | g.135817654T>G | CA348606273 | LCT | c.1394A>C (p.His465Pro) | |
2 | g.135817655G>A | CA348606276 | LCT | c.1393C>T (p.His465Tyr) | dbSNP |
2 | g.135817655G>C | CA348606275 | LCT | c.1393C>G (p.His465Asp) | |
2 | g.135817655G= | CA1290834878 | LCT | c.1393C= (p.His465=) | |
2 | g.135817655G>T | CA348606274 | LCT | c.1393C>A (p.His465Asn) | |
2 | g.135817656C>A | CA1888397 | LCT | c.1392G>T (p.Gly464=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817656C= | CA1290834879 | LCT | c.1392G= (p.Gly464=) | |
2 | g.135817656C>G | CA429204813 | LCT | c.1392G>C (p.Gly464=) | |
2 | g.135817656C>T | CA429204814 | LCT | c.1392G>A (p.Gly464=) | COSMIC |
2 | g.135817657C>A | CA348606277 | LCT | c.1391G>T (p.Gly464Val) | |
2 | g.135817657C>G | CA348606278 | LCT | c.1391G>C (p.Gly464Ala) | |
2 | g.135817657C>T | CA348606279 | LCT | c.1391G>A (p.Gly464Glu) | |
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) |