Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.135817552T>A | CA348606042 | LCT | c.1496A>T (p.Asp499Val) | |
2 | g.135817552T>C | CA348606043 | LCT | c.1496A>G (p.Asp499Gly) | |
2 | g.135817552T>G | CA348606044 | LCT | c.1496A>C (p.Asp499Ala) | dbSNP |
2 | g.135817552T= | CA1290834827 | LCT | c.1496A= (p.Asp499=) | |
2 | g.135817553C>A | CA348606045 | LCT | c.1495G>T (p.Asp499Tyr) | COSMIC |
2 | g.135817553C>G | CA348606047 | LCT | c.1495G>C (p.Asp499His) | |
2 | g.135817553C>T | CA348606046 | LCT | c.1495G>A (p.Asp499Asn) | |
2 | g.135817554C>A | CA348606048 | LCT | c.1494G>T (p.Trp498Cys) | |
2 | g.135817554C>G | CA348606049 | LCT | c.1494G>C (p.Trp498Cys) | |
2 | g.135817554C>T | CA348606050 | LCT | c.1494G>A (p.Trp498Ter) | |
2 | g.135817555C>A | CA348606051 | LCT | c.1493G>T (p.Trp498Leu) | |
2 | g.135817555C= | CA1290834828 | LCT | c.1493G= (p.Trp498=) | |
2 | g.135817555C>G | CA348606052 | LCT | c.1493G>C (p.Trp498Ser) | |
2 | g.135817555C>T | CA348606053 | LCT | c.1493G>A (p.Trp498Ter) | dbSNP |
2 | g.135817556A= | CA1290834829 | LCT | c.1492T= (p.Trp498=) | |
2 | g.135817556A>C | CA348606054 | LCT | c.1492T>G (p.Trp498Gly) | |
2 | g.135817556A>G | CA348606055 | LCT | c.1492T>C (p.Trp498Arg) | dbSNP |
2 | g.135817556A>T | CA348606056 | LCT | c.1492T>A (p.Trp498Arg) | |
2 | g.135817557G>A | CA429204621 | LCT | c.1491C>T (p.His497=) | gnomAD v4 |
2 | g.135817557G>C | CA348606057 | LCT | c.1491C>G (p.His497Gln) | |
2 | g.135817557G>T | CA348606058 | LCT | c.1491C>A (p.His497Gln) | |
2 | g.135817558T>A | CA348606060 | LCT | c.1490A>T (p.His497Leu) | |
2 | g.135817558T>C | CA348606061 | LCT | c.1490A>G (p.His497Arg) | |
2 | g.135817558T>G | CA348606059 | LCT | c.1490A>C (p.His497Pro) | |
2 | g.135817559G>A | CA348606064 | LCT | c.1489C>T (p.His497Tyr) | gnomAD v4 |
2 | g.135817559G>C | CA348606062 | LCT | c.1489C>G (p.His497Asp) | |
2 | g.135817559G>T | CA348606063 | LCT | c.1489C>A (p.His497Asn) | |
2 | g.135817560G>A | CA429204625 | LCT | c.1488C>T (p.Phe496=) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
2 | g.135817560G>C | CA348606065 | LCT | c.1488C>G (p.Phe496Leu) | |
2 | g.135817560G= | CA1290834830 | LCT | c.1488C= (p.Phe496=) | |
2 | g.135817560G>T | CA348606066 | LCT | c.1488C>A (p.Phe496Leu) | COSMIC |
2 | g.135817561A>C | CA348606067 | LCT | c.1487T>G (p.Phe496Cys) | |
2 | g.135817561A>G | CA348606068 | LCT | c.1487T>C (p.Phe496Ser) | |
2 | g.135817561A>T | CA348606069 | LCT | c.1487T>A (p.Phe496Tyr) | dbSNP |
2 | g.135817562A>C | CA348606070 | LCT | c.1486T>G (p.Phe496Val) | |
2 | g.135817562A>G | CA348606071 | LCT | c.1486T>C (p.Phe496Leu) | |
2 | g.135817562A>T | CA348606072 | LCT | c.1486T>A (p.Phe496Ile) | |
2 | g.135817563C>A | CA429204627 | LCT | c.1485G>T (p.Leu495=) | |
2 | g.135817563C>G | CA429204628 | LCT | c.1485G>C (p.Leu495=) | dbSNP |
2 | g.135817563C>T | CA429204630 | LCT | c.1485G>A (p.Leu495=) | gnomAD v4 |
2 | g.135817564A>C | CA348606073 | LCT | c.1484T>G (p.Leu495Arg) | |
2 | g.135817564A>G | CA348606074 | LCT | c.1484T>C (p.Leu495Pro) | |
2 | g.135817564A>T | CA348606075 | LCT | c.1484T>A (p.Leu495Gln) | |
2 | g.135817565G>A | CA429204633 | LCT | c.1483C>T (p.Leu495=) | |
2 | g.135817565G>C | CA348606077 | LCT | c.1483C>G (p.Leu495Val) | |
2 | g.135817565G= | CA1290834831 | LCT | c.1483C= (p.Leu495=) | |
2 | g.135817565G>T | CA348606076 | LCT | c.1483C>A (p.Leu495Met) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.135817566C>A | CA429204634 | LCT | c.1482G>T (p.Thr494=) | dbSNP |
2 | g.135817566C= | CA1290834832 | LCT | c.1482G= (p.Thr494=) | |
2 | g.135817566C>G | CA429204635 | LCT | c.1482G>C (p.Thr494=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |