Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.135817360G>A | CA348605606 | LCT | c.1688C>T (p.Pro563Leu) | |
2 | g.135817360G>C | CA348605608 | LCT | c.1688C>G (p.Pro563Arg) | |
2 | g.135817360G>T | CA348605607 | LCT | c.1688C>A (p.Pro563Gln) | |
2 | g.135817361G>A | CA348605609 | LCT | c.1687C>T (p.Pro563Ser) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.135817361G>C | CA348605610 | LCT | c.1687C>G (p.Pro563Ala) | |
2 | g.135817361G= | CA1290834749 | LCT | c.1687C= (p.Pro563=) | |
2 | g.135817361G>T | CA348605611 | LCT | c.1687C>A (p.Pro563Thr) | |
2 | g.135817362G>A | CA429204480 | LCT | c.1686C>T (p.Asp562=) | |
2 | g.135817362G>C | CA348605612 | LCT | c.1686C>G (p.Asp562Glu) | |
2 | g.135817362G>T | CA348605613 | LCT | c.1686C>A (p.Asp562Glu) | |
2 | g.135817363T>A | CA348605616 | LCT | c.1685A>T (p.Asp562Val) | |
2 | g.135817363T>C | CA348605615 | LCT | c.1685A>G (p.Asp562Gly) | |
2 | g.135817363T>G | CA348605614 | LCT | c.1685A>C (p.Asp562Ala) | |
2 | g.135817364C>A | CA348605617 | LCT | c.1684G>T (p.Asp562Tyr) | |
2 | g.135817364C>G | CA348605618 | LCT | c.1684G>C (p.Asp562His) | |
2 | g.135817364C>T | CA348605619 | LCT | c.1684G>A (p.Asp562Asn) | |
2 | g.135817365A= | CA1290834750 | LCT | c.1683T= (p.Ser561=) | |
2 | g.135817365A>C | CA429204481 | LCT | c.1683T>G (p.Ser561=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817365A>G | CA429204482 | LCT | c.1683T>C (p.Ser561=) | |
2 | g.135817365A>T | CA429204483 | LCT | c.1683T>A (p.Ser561=) | |
2 | g.135817366G>A | CA348605620 | LCT | c.1682C>T (p.Ser561Phe) | |
2 | g.135817366G>C | CA348605621 | LCT | c.1682C>G (p.Ser561Cys) | dbSNP gnomAD v4 COSMIC |
2 | g.135817366G= | CA1290834751 | LCT | c.1682C= (p.Ser561=) | |
2 | g.135817366G>T | CA348605622 | LCT | c.1682C>A (p.Ser561Tyr) | |
2 | g.135817367A>C | CA348605623 | LCT | c.1681T>G (p.Ser561Ala) | |
2 | g.135817367A>G | CA348605625 | LCT | c.1681T>C (p.Ser561Pro) | |
2 | g.135817367A>T | CA348605624 | LCT | c.1681T>A (p.Ser561Thr) | |
2 | g.135817368G>A | CA429204484 | LCT | c.1680C>T (p.Ile560=) | |
2 | g.135817368G>C | CA56623340 | LCT | c.1680C>G (p.Ile560Met) | dbSNP gnomAD v4 |
2 | g.135817368G= | CA1290834752 | LCT | c.1680C= (p.Ile560=) | |
2 | g.135817368G>T | CA429204485 | LCT | c.1680C>A (p.Ile560=) | |
2 | g.135817369A>C | CA348605626 | LCT | c.1679T>G (p.Ile560Ser) | |
2 | g.135817369A>G | CA348605627 | LCT | c.1679T>C (p.Ile560Thr) | |
2 | g.135817369A>T | CA348605628 | LCT | c.1679T>A (p.Ile560Asn) | |
2 | g.135817370T>A | CA348605629 | LCT | c.1678A>T (p.Ile560Phe) | |
2 | g.135817370T>C | CA348605630 | LCT | c.1678A>G (p.Ile560Val) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.135817370T>G | CA348605631 | LCT | c.1678A>C (p.Ile560Leu) | |
2 | g.135817370T= | CA1290834753 | LCT | c.1678A= (p.Ile560=) | |
2 | g.135817371G>A | CA429204486 | LCT | c.1677C>T (p.Gly559=) | |
2 | g.135817371G>C | CA429204487 | LCT | c.1677C>G (p.Gly559=) | gnomAD v4 |
2 | g.135817371G>T | CA429204488 | LCT | c.1677C>A (p.Gly559=) | |
2 | g.135817372C>A | CA348605632 | LCT | c.1676G>T (p.Gly559Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817372C= | CA1290834754 | LCT | c.1676G= (p.Gly559=) | |
2 | g.135817372C>G | CA348605633 | LCT | c.1676G>C (p.Gly559Ala) | |
2 | g.135817372C>T | CA348605634 | LCT | c.1676G>A (p.Gly559Asp) | gnomAD v4 |
2 | g.135817373C>A | CA348605636 | LCT | c.1675G>T (p.Gly559Cys) | |
2 | g.135817373C= | CA1290834755 | LCT | c.1675G= (p.Gly559=) | |
2 | g.135817373C>G | CA348605635 | LCT | c.1675G>C (p.Gly559Arg) | COSMIC |
2 | g.135817373C>T | CA1888362 | LCT | c.1675G>A (p.Gly559Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817374G>A | CA1888363 | LCT | c.1674C>T (p.Pro558=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |