| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.87566118A>C | CA368090384 | ABCB1 | c.654T>G (p.Ile218Met) c.462T>G (p.Ile154Met) c.864T>G (p.Ile288Met) | |
| 7 | g.87566118A>G | CA456372044 | ABCB1 | c.654T>C (p.Ile218=) c.462T>C (p.Ile154=) c.864T>C (p.Ile288=) | |
| 7 | g.87566118A>T | CA456372045 | ABCB1 | c.654T>A (p.Ile218=) c.462T>A (p.Ile154=) c.864T>A (p.Ile288=) | COSMIC |
| 7 | g.87566119A>C | CA368090385 | ABCB1 | c.653T>G (p.Ile218Ser) c.461T>G (p.Ile154Ser) c.863T>G (p.Ile288Ser) | COSMIC |
| 7 | g.87566119A>G | CA368090387 | ABCB1 | c.653T>C (p.Ile218Thr) c.461T>C (p.Ile154Thr) c.863T>C (p.Ile288Thr) | |
| 7 | g.87566119A>T | CA368090386 | ABCB1 | c.653T>A (p.Ile218Asn) c.461T>A (p.Ile154Asn) c.863T>A (p.Ile288Asn) | |
| 7 | g.87566120T>A | CA368090388 | ABCB1 | c.652A>T (p.Ile218Phe) c.460A>T (p.Ile154Phe) c.862A>T (p.Ile288Phe) | |
| 7 | g.87566120T>C | CA368090389 | ABCB1 | c.652A>G (p.Ile218Val) c.460A>G (p.Ile154Val) c.862A>G (p.Ile288Val) | |
| 7 | g.87566120T>G | CA368090390 | ABCB1 | c.652A>C (p.Ile218Leu) c.460A>C (p.Ile154Leu) c.862A>C (p.Ile288Leu) | |
| 7 | g.87566121C>A | CA456372048 | ABCB1 | c.651G>T (p.Val217=) c.459G>T (p.Val153=) c.861G>T (p.Val287=) | |
| 7 | g.87566121C>G | CA456372049 | ABCB1 | c.651G>C (p.Val217=) c.459G>C (p.Val153=) c.861G>C (p.Val287=) | |
| 7 | g.87566121C>T | CA456372050 | ABCB1 | c.651G>A (p.Val217=) c.459G>A (p.Val153=) c.861G>A (p.Val287=) | |
| 7 | g.87566122A>C | CA368090391 | ABCB1 | c.650T>G (p.Val217Gly) c.458T>G (p.Val153Gly) c.860T>G (p.Val287Gly) | |
| 7 | g.87566122A>G | CA368090392 | ABCB1 | c.650T>C (p.Val217Ala) c.458T>C (p.Val153Ala) c.860T>C (p.Val287Ala) | |
| 7 | g.87566122A>T | CA368090393 | ABCB1 | c.650T>A (p.Val217Glu) c.458T>A (p.Val153Glu) c.860T>A (p.Val287Glu) | |
| 7 | g.87566123C>A | CA368090394 | ABCB1 | c.649G>T (p.Val217Leu) c.457G>T (p.Val153Leu) c.859G>T (p.Val287Leu) | |
| 7 | g.87566123C= | CA1723648113 | ABCB1 | c.649G= (p.Val217=) c.457G= (p.Val153=) c.859G= (p.Val287=) | |
| 7 | g.87566123C>G | CA368090395 | ABCB1 | c.649G>C (p.Val217Leu) c.457G>C (p.Val153Leu) c.859G>C (p.Val287Leu) | |
| 7 | g.87566123C>T | CA368090396 | ABCB1 | c.649G>A (p.Val217Met) c.457G>A (p.Val153Met) c.859G>A (p.Val287Met) | dbSNP gnomAD v4 |
| 7 | g.87566124A>C | CA456372052 | ABCB1 | c.648T>G (p.Leu216=) c.456T>G (p.Leu152=) c.858T>G (p.Leu286=) | |
| 7 | g.87566124A>G | CA456372053 | ABCB1 | c.648T>C (p.Leu216=) c.456T>C (p.Leu152=) c.858T>C (p.Leu286=) | |
| 7 | g.87566124A>T | CA456372054 | ABCB1 | c.648T>A (p.Leu216=) c.456T>A (p.Leu152=) c.858T>A (p.Leu286=) | |
| 7 | g.87566125A>C | CA368090397 | ABCB1 | c.647T>G (p.Leu216Arg) c.455T>G (p.Leu152Arg) c.857T>G (p.Leu286Arg) | |
| 7 | g.87566125A>G | CA368090398 | ABCB1 | c.647T>C (p.Leu216Pro) c.455T>C (p.Leu152Pro) c.857T>C (p.Leu286Pro) | |
| 7 | g.87566125A>T | CA368090399 | ABCB1 | c.647T>A (p.Leu216His) c.455T>A (p.Leu152His) c.857T>A (p.Leu286His) | |
| 7 | g.87566126G>A | CA368090401 | ABCB1 | c.646C>T (p.Leu216Phe) c.454C>T (p.Leu152Phe) c.856C>T (p.Leu286Phe) | COSMIC |
| 7 | g.87566126G>C | CA368090402 | ABCB1 | c.646C>G (p.Leu216Val) c.454C>G (p.Leu152Val) c.856C>G (p.Leu286Val) | |
| 7 | g.87566126G>T | CA368090400 | ABCB1 | c.646C>A (p.Leu216Ile) c.454C>A (p.Leu152Ile) c.856C>A (p.Leu286Ile) | |
| 7 | g.87566127G>A | CA456372058 | ABCB1 | c.645C>T (p.Thr215=) c.453C>T (p.Thr151=) c.855C>T (p.Thr285=) | gnomAD v4 |
| 7 | g.87566127G>C | CA456372059 | ABCB1 | c.645C>G (p.Thr215=) c.453C>G (p.Thr151=) c.855C>G (p.Thr285=) | |
| 7 | g.87566127G>T | CA456372060 | ABCB1 | c.645C>A (p.Thr215=) c.453C>A (p.Thr151=) c.855C>A (p.Thr285=) | gnomAD v4 |
| 7 | g.87566128G>A | CA162470415 | ABCB1 | c.644C>T (p.Thr215Ile) c.452C>T (p.Thr151Ile) c.854C>T (p.Thr285Ile) | dbSNP |
| 7 | g.87566128G>C | CA368090403 | ABCB1 | c.644C>G (p.Thr215Ser) c.452C>G (p.Thr151Ser) c.854C>G (p.Thr285Ser) | gnomAD v4 |
| 7 | g.87566128G= | CA1723648116 | ABCB1 | c.644C= (p.Thr215=) c.452C= (p.Thr151=) c.854C= (p.Thr285=) | |
| 7 | g.87566128G>T | CA368090404 | ABCB1 | c.644C>A (p.Thr215Asn) c.452C>A (p.Thr151Asn) c.854C>A (p.Thr285Asn) | |
| 7 | g.87566129T>A | CA368090405 | ABCB1 | c.643A>T (p.Thr215Ser) c.451A>T (p.Thr151Ser) c.853A>T (p.Thr285Ser) | |
| 7 | g.87566129T>C | CA368090406 | ABCB1 | c.643A>G (p.Thr215Ala) c.451A>G (p.Thr151Ala) c.853A>G (p.Thr285Ala) | |
| 7 | g.87566129T>G | CA368090407 | ABCB1 | c.643A>C (p.Thr215Pro) c.451A>C (p.Thr151Pro) c.853A>C (p.Thr285Pro) | |
| 7 | g.87566130T>A | CA456372065 | ABCB1 | c.642A>T (p.Leu214=) c.450A>T (p.Leu150=) c.852A>T (p.Leu284=) | |
| 7 | g.87566130T>C | CA456372062 | ABCB1 | c.642A>G (p.Leu214=) c.450A>G (p.Leu150=) c.852A>G (p.Leu284=) | |
| 7 | g.87566130T>G | CA456372064 | ABCB1 | c.642A>C (p.Leu214=) c.450A>C (p.Leu150=) c.852A>C (p.Leu284=) | |
| 7 | g.87566131A>C | CA368090408 | ABCB1 | c.641T>G (p.Leu214Arg) c.449T>G (p.Leu150Arg) c.851T>G (p.Leu284Arg) | |
| 7 | g.87566131A>G | CA368090409 | ABCB1 | c.641T>C (p.Leu214Pro) c.449T>C (p.Leu150Pro) c.851T>C (p.Leu284Pro) | |
| 7 | g.87566131A>T | CA368090410 | ABCB1 | c.641T>A (p.Leu214Gln) c.449T>A (p.Leu150Gln) c.851T>A (p.Leu284Gln) | |
| 7 | g.87566132G>A | CA456372068 | ABCB1 | c.640C>T (p.Leu214=) c.448C>T (p.Leu150=) c.850C>T (p.Leu284=) | gnomAD v4 |
| 7 | g.87566132G>C | CA368090411 | ABCB1 | c.640C>G (p.Leu214Val) c.448C>G (p.Leu150Val) c.850C>G (p.Leu284Val) | |
| 7 | g.87566132G>T | CA368090412 | ABCB1 | c.640C>A (p.Leu214Ile) c.448C>A (p.Leu150Ile) c.850C>A (p.Leu284Ile) | |
| 7 | g.87566133C>A | CA368090413 | ABCB1 | c.639G>T (p.Lys213Asn) c.447G>T (p.Lys149Asn) c.849G>T (p.Lys283Asn) | |
| 7 | g.87566133C>G | CA368090414 | ABCB1 | c.639G>C (p.Lys213Asn) c.447G>C (p.Lys149Asn) c.849G>C (p.Lys283Asn) | |
| 7 | g.87566133C>T | CA456372069 | ABCB1 | c.639G>A (p.Lys213=) c.447G>A (p.Lys149=) c.849G>A (p.Lys283=) |