| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.88118157_88118159delinsTAA | CA1474610994 | ABCG2 | c.791_793delinsTTA (p.Leu264=) | |
| 4 | g.88118158A>C | CA440269496 | ABCG2 | c.792T>G (p.Leu264=) | |
| 4 | g.88118158A>G | CA440269501 | ABCG2 | c.792T>C (p.Leu264=) | |
| 4 | g.88118158A>T | CA440269500 | ABCG2 | c.792T>A (p.Leu264=) | |
| 4 | g.88118158_88118159del | CA129178 | ABCG2 | c.791_792del (p.Leu264HisfsTer14) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.88118158_88118160del | CA2671372873 | ABCG2 | c.790_792del (p.Leu264del) | gnomAD v4 |
| 4 | g.88118159A= | CA1474610996 | ABCG2 | c.791T= (p.Leu264=) | |
| 4 | g.88118159A>C | CA3004809 | ABCG2 | c.791T>G (p.Leu264Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.88118159A>G | CA357627733 | ABCG2 | c.791T>C (p.Leu264Pro) | COSMIC COSMIC |
| 4 | g.88118159A>T | CA357627734 | ABCG2 | c.791T>A (p.Leu264His) | |
| 4 | g.88118159_88118160del | CA357627735 | ABCG2 | c.790_791del (p.Leu264TyrfsTer14) | |
| 4 | g.88118160G>A | CA357627736 | ABCG2 | c.790C>T (p.Leu264Phe) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.88118160G>C | CA3004810 | ABCG2 | c.790C>G (p.Leu264Val) | dbSNP ExAC |
| 4 | g.88118160G= | CA1474610997 | ABCG2 | c.790C= (p.Leu264=) | |
| 4 | g.88118160G>T | CA100889503 | ABCG2 | c.790C>A (p.Leu264Ile) | dbSNP |
| 4 | g.88118161T>A | CA357627737 | ABCG2 | c.789A>T (p.Arg263Ser) | |
| 4 | g.88118161T>C | CA440269511 | ABCG2 | c.789A>G (p.Arg263=) | dbSNP gnomAD v4 |
| 4 | g.88118161T>G | CA357627738 | ABCG2 | c.789A>C (p.Arg263Ser) | |
| 4 | g.88118161T= | CA1474610998 | ABCG2 | c.789A= (p.Arg263=) | |
| 4 | g.88118162C>A | CA357627739 | ABCG2 | c.788G>T (p.Arg263Ile) | gnomAD v4 |
| 4 | g.88118162C>G | CA357627740 | ABCG2 | c.788G>C (p.Arg263Thr) | |
| 4 | g.88118162C>T | CA357627741 | ABCG2 | c.788G>A (p.Arg263Lys) | |
| 4 | g.88118163T>A | CA357627742 | ABCG2 | c.787A>T (p.Arg263Ter) | |
| 4 | g.88118163T>C | CA357627743 | ABCG2 | c.787A>G (p.Arg263Gly) | |
| 4 | g.88118163T>G | CA440269517 | ABCG2 | c.787A>C (p.Arg263=) | gnomAD v4 |
| 4 | g.88118164T>A | CA3004811 | ABCG2 | c.786A>T (p.Gly262=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.88118164T>C | CA440269521 | ABCG2 | c.786A>G (p.Gly262=) | |
| 4 | g.88118164T>G | CA440269523 | ABCG2 | c.786A>C (p.Gly262=) | |
| 4 | g.88118164T= | CA1474610999 | ABCG2 | c.786A= (p.Gly262=) | |
| 4 | g.88118165C>A | CA357627744 | ABCG2 | c.785G>T (p.Gly262Val) | |
| 4 | g.88118165C>G | CA357627745 | ABCG2 | c.785G>C (p.Gly262Ala) | |
| 4 | g.88118165C>T | CA357627746 | ABCG2 | c.785G>A (p.Gly262Glu) | COSMIC COSMIC |
| 4 | g.88118166C>A | CA3004812 | ABCG2 | c.784G>T (p.Gly262Ter) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.88118166C= | CA1474611000 | ABCG2 | c.784G= (p.Gly262=) | |
| 4 | g.88118166C>G | CA357627748 | ABCG2 | c.784G>C (p.Gly262Arg) | |
| 4 | g.88118166C>T | CA357627747 | ABCG2 | c.784G>A (p.Gly262Arg) | |
| 4 | g.88118167T>A | CA440269533 | ABCG2 | c.783A>T (p.Ser261=) | |
| 4 | g.88118167T>C | CA440269529 | ABCG2 | c.783A>G (p.Ser261=) | |
| 4 | g.88118167T>G | CA440269531 | ABCG2 | c.783A>C (p.Ser261=) | |
| 4 | g.88118168G>A | CA357627749 | ABCG2 | c.782C>T (p.Ser261Leu) | COSMIC COSMIC |
| 4 | g.88118168G>C | CA357627750 | ABCG2 | c.782C>G (p.Ser261Ter) | |
| 4 | g.88118168G>T | CA357627751 | ABCG2 | c.782C>A (p.Ser261Ter) | |
| 4 | g.88118169A>C | CA357627753 | ABCG2 | c.781T>G (p.Ser261Ala) | |
| 4 | g.88118169A>G | CA357627754 | ABCG2 | c.781T>C (p.Ser261Pro) | |
| 4 | g.88118169A>T | CA357627755 | ABCG2 | c.781T>A (p.Ser261Thr) | |
| 4 | g.88118170G>A | CA100889517 | ABCG2 | c.780C>T (p.Ala260=) | dbSNP gnomAD v4 |
| 4 | g.88118170G>C | CA440269538 | ABCG2 | c.780C>G (p.Ala260=) | |
| 4 | g.88118170G= | CA1474611001 | ABCG2 | c.780C= (p.Ala260=) | |
| 4 | g.88118170G>T | CA440269540 | ABCG2 | c.780C>A (p.Ala260=) | |
| 4 | g.88118171G>A | CA357627756 | ABCG2 | c.779C>T (p.Ala260Val) |