| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.75727753T>A | CA401039014 | ITGB4 | c.367T>A (p.Phe123Ile) n.432T>A n.367T>A c.472T>A (p.Phe158Ile) | |
| 17 | g.75727753T>C | CA401039015 | ITGB4 | c.367T>C (p.Phe123Leu) n.432T>C n.367T>C c.472T>C (p.Phe158Leu) | |
| 17 | g.75727753T>G | CA401039016 | ITGB4 | c.367T>G (p.Phe123Val) n.432T>G n.367T>G c.472T>G (p.Phe158Val) | |
| 17 | g.75727754T>A | CA401039017 | ITGB4 | c.368T>A (p.Phe123Tyr) n.433T>A n.368T>A c.473T>A (p.Phe158Tyr) | |
| 17 | g.75727754T>C | CA8768653 | ITGB4 | c.368T>C (p.Phe123Ser) n.433T>C n.368T>C c.473T>C (p.Phe158Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727754T>G | CA401039018 | ITGB4 | c.368T>G (p.Phe123Cys) n.433T>G n.368T>G c.473T>G (p.Phe158Cys) | |
| 17 | g.75727754T= | CA2275653870 | ITGB4 | c.368T= (p.Phe123=) n.433T= n.368T= c.473T= (p.Phe158=) | |
| 17 | g.75727755T>A | CA401039019 | ITGB4 | c.369T>A (p.Phe123Leu) n.434T>A n.369T>A c.474T>A (p.Phe158Leu) | |
| 17 | g.75727755T>C | CA501832183 | ITGB4 | c.369T>C (p.Phe123=) n.434T>C n.369T>C c.474T>C (p.Phe158=) | |
| 17 | g.75727755T>G | CA401039020 | ITGB4 | c.369T>G (p.Phe123Leu) n.434T>G n.369T>G c.474T>G (p.Phe158Leu) | |
| 17 | g.75727756G>A | CA401039021 | ITGB4 | c.370G>A (p.Glu124Lys) n.435G>A n.370G>A c.475G>A (p.Glu159Lys) | |
| 17 | g.75727756G>C | CA401039022 | ITGB4 | c.370G>C (p.Glu124Gln) n.435G>C n.370G>C c.475G>C (p.Glu159Gln) | COSMIC COSMIC |
| 17 | g.75727756G>T | CA401039023 | ITGB4 | c.370G>T (p.Glu124Ter) n.435G>T n.370G>T c.475G>T (p.Glu159Ter) | |
| 17 | g.75727757A>C | CA401039026 | ITGB4 | c.371A>C (p.Glu124Ala) n.436A>C n.371A>C c.476A>C (p.Glu159Ala) | gnomAD v4 |
| 17 | g.75727757A>G | CA401039025 | ITGB4 | c.371A>G (p.Glu124Gly) n.436A>G n.371A>G c.476A>G (p.Glu159Gly) | |
| 17 | g.75727757A>T | CA401039024 | ITGB4 | c.371A>T (p.Glu124Val) n.436A>T n.371A>T c.476A>T (p.Glu159Val) | |
| 17 | g.75727758G>A | CA501832184 | ITGB4 | c.372G>A (p.Glu124=) n.437G>A n.372G>A c.477G>A (p.Glu159=) | |
| 17 | g.75727758G>C | CA401039027 | ITGB4 | c.372G>C (p.Glu124Asp) n.437G>C n.372G>C c.477G>C (p.Glu159Asp) | |
| 17 | g.75727758G>T | CA401039028 | ITGB4 | c.372G>T (p.Glu124Asp) n.437G>T n.372G>T c.477G>T (p.Glu159Asp) | |
| 17 | g.75727759C>A | CA401039029 | ITGB4 | c.373C>A (p.Pro125Thr) n.438C>A n.373C>A c.478C>A (p.Pro160Thr) | |
| 17 | g.75727759C= | CA2275653871 | ITGB4 | c.373C= (p.Pro125=) n.438C= n.373C= c.478C= (p.Pro160=) | |
| 17 | g.75727759C>G | CA401039030 | ITGB4 | c.373C>G (p.Pro125Ala) n.438C>G n.373C>G c.478C>G (p.Pro160Ala) | |
| 17 | g.75727759C>T | CA401039031 | ITGB4 | c.373C>T (p.Pro125Ser) n.438C>T n.373C>T c.478C>T (p.Pro160Ser) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.75727760C>A | CA401039032 | ITGB4 | c.374C>A (p.Pro125Gln) n.439C>A n.374C>A c.479C>A (p.Pro160Gln) | |
| 17 | g.75727760C>G | CA401039033 | ITGB4 | c.374C>G (p.Pro125Arg) n.439C>G n.374C>G c.479C>G (p.Pro160Arg) | |
| 17 | g.75727760C>T | CA401039034 | ITGB4 | c.374C>T (p.Pro125Leu) n.439C>T n.374C>T c.479C>T (p.Pro160Leu) | |
| 17 | g.75727761A>C | CA501832185 | ITGB4 | c.375A>C (p.Pro125=) n.440A>C n.375A>C c.480A>C (p.Pro160=) | |
| 17 | g.75727761A>G | CA501832186 | ITGB4 | c.375A>G (p.Pro125=) n.440A>G n.375A>G c.480A>G (p.Pro160=) | |
| 17 | g.75727761A>T | CA501832187 | ITGB4 | c.375A>T (p.Pro125=) n.440A>T n.375A>T c.480A>T (p.Pro160=) | |
| 17 | g.75727762C>A | CA401039035 | ITGB4 | c.376C>A (p.Leu126Met) n.441C>A n.376C>A c.481C>A (p.Leu161Met) | |
| 17 | g.75727762C= | CA2275653872 | ITGB4 | c.376C= (p.Leu126=) n.441C= n.376C= c.481C= (p.Leu161=) | |
| 17 | g.75727762C>G | CA401039036 | ITGB4 | c.376C>G (p.Leu126Val) n.441C>G n.376C>G c.481C>G (p.Leu161Val) | |
| 17 | g.75727762C>T | CA501832188 | ITGB4 | c.376C>T (p.Leu126=) n.441C>T n.376C>T c.481C>T (p.Leu161=) | dbSNP |
| 17 | g.75727763T>A | CA401039037 | ITGB4 | c.377T>A (p.Leu126Gln) n.442T>A n.377T>A c.482T>A (p.Leu161Gln) | |
| 17 | g.75727763T>C | CA401039038 | ITGB4 | c.377T>C (p.Leu126Pro) n.442T>C n.377T>C c.482T>C (p.Leu161Pro) | |
| 17 | g.75727763T>G | CA401039039 | ITGB4 | c.377T>G (p.Leu126Arg) n.442T>G n.377T>G c.482T>G (p.Leu161Arg) | |
| 17 | g.75727764G>A | CA501832191 | ITGB4 | c.378G>A (p.Leu126=) n.443G>A n.378G>A c.483G>A (p.Leu161=) | |
| 17 | g.75727764G>C | CA501832190 | ITGB4 | c.378G>C (p.Leu126=) n.443G>C n.378G>C c.483G>C (p.Leu161=) | |
| 17 | g.75727764G>T | CA501832189 | ITGB4 | c.378G>T (p.Leu126=) n.443G>T n.378G>T c.483G>T (p.Leu161=) | |
| 17 | g.75727765G>A | CA401039040 | ITGB4 | c.379G>A (p.Glu127Lys) n.444G>A n.379G>A c.484G>A (p.Glu162Lys) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.75727765G>C | CA401039042 | ITGB4 | c.379G>C (p.Glu127Gln) n.444G>C n.379G>C c.484G>C (p.Glu162Gln) | |
| 17 | g.75727765G= | CA2275653873 | ITGB4 | c.379G= (p.Glu127=) n.444G= n.379G= c.484G= (p.Glu162=) | |
| 17 | g.75727765G>T | CA401039041 | ITGB4 | c.379G>T (p.Glu127Ter) n.444G>T n.379G>T c.484G>T (p.Glu162Ter) | |
| 17 | g.75727766A>C | CA401039043 | ITGB4 | c.380A>C (p.Glu127Ala) n.445A>C n.380A>C c.485A>C (p.Glu162Ala) | |
| 17 | g.75727766A>G | CA401039044 | ITGB4 | c.380A>G (p.Glu127Gly) n.445A>G n.380A>G c.485A>G (p.Glu162Gly) | |
| 17 | g.75727766A>T | CA401039045 | ITGB4 | c.380A>T (p.Glu127Val) n.445A>T n.380A>T c.485A>T (p.Glu162Val) | |
| 17 | g.75727767G>A | CA501832192 | ITGB4 | c.381G>A (p.Glu127=) n.446G>A n.381G>A c.486G>A (p.Glu162=) | |
| 17 | g.75727767G>C | CA401039046 | ITGB4 | c.381G>C (p.Glu127Asp) n.446G>C n.381G>C c.486G>C (p.Glu162Asp) | |
| 17 | g.75727767G>T | CA401039047 | ITGB4 | c.381G>T (p.Glu127Asp) n.446G>T n.381G>T c.486G>T (p.Glu162Asp) | |
| 17 | g.75727768A>C | CA401039048 | ITGB4 | c.382A>C (p.Ser128Arg) n.447A>C n.382A>C c.487A>C (p.Ser163Arg) |