UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.75727667C>A | CA401038848 | ITGB4 | c.281C>A (p.Thr94Asn) n.346C>A n.281C>A c.386C>A (p.Thr129Asn) | |
| 17 | g.75727667C= | CA2275653822 | ITGB4 | c.281C= (p.Thr94=) n.346C= n.281C= c.386C= (p.Thr129=) | |
| 17 | g.75727667C>G | CA401038845 | ITGB4 | c.281C>G (p.Thr94Ser) n.346C>G n.281C>G c.386C>G (p.Thr129Ser) | dbSNP |
| 17 | g.75727667C>T | CA401038847 | ITGB4 | c.281C>T (p.Thr94Ile) n.346C>T n.281C>T c.386C>T (p.Thr129Ile) | |
| 17 | g.75727667_75727668delinsTT | CA645599090 | ITGB4 | c.281_282delinsTT (p.Thr94Ile) n.346_347delinsTT n.281_282delinsTT c.386_387delinsTT (p.Thr129Ile) | COSMIC COSMIC |
| 17 | g.75727668C>A | CA502047877 | ITGB4 | c.282C>A (p.Thr94=) n.347C>A n.282C>A c.387C>A (p.Thr129=) | |
| 17 | g.75727668C= | CA2275653823 | ITGB4 | c.282C= (p.Thr94=) n.347C= n.282C= c.387C= (p.Thr129=) | |
| 17 | g.75727668C>G | CA502047878 | ITGB4 | c.282C>G (p.Thr94=) n.347C>G n.282C>G c.387C>G (p.Thr129=) | |
| 17 | g.75727668C>T | CA8768624 | ITGB4 | c.282C>T (p.Thr94=) n.347C>T n.282C>T c.387C>T (p.Thr129=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727669A= | CA2275653824 | ITGB4 | c.283A= (p.Thr95=) n.348A= n.283A= c.388A= (p.Thr130=) | |
| 17 | g.75727669A>C | CA401038850 | ITGB4 | c.283A>C (p.Thr95Pro) n.348A>C n.283A>C c.388A>C (p.Thr130Pro) | dbSNP |
| 17 | g.75727669A>G | CA401038852 | ITGB4 | c.283A>G (p.Thr95Ala) n.348A>G n.283A>G c.388A>G (p.Thr130Ala) | |
| 17 | g.75727669A>T | CA401038854 | ITGB4 | c.283A>T (p.Thr95Ser) n.348A>T n.283A>T c.388A>T (p.Thr130Ser) | |
| 17 | g.75727670C>A | CA401038855 | ITGB4 | c.284C>A (p.Thr95Asn) n.349C>A n.284C>A c.389C>A (p.Thr130Asn) | |
| 17 | g.75727670C= | CA2275653825 | ITGB4 | c.284C= (p.Thr95=) n.349C= n.284C= c.389C= (p.Thr130=) | |
| 17 | g.75727670C>G | CA401038856 | ITGB4 | c.284C>G (p.Thr95Ser) n.349C>G n.284C>G c.389C>G (p.Thr130Ser) | gnomAD v4 |
| 17 | g.75727670C>T | CA401038857 | ITGB4 | c.284C>T (p.Thr95Ile) n.349C>T n.284C>T c.389C>T (p.Thr130Ile) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727671C>A | CA502047883 | ITGB4 | c.285C>A (p.Thr95=) n.350C>A n.285C>A c.390C>A (p.Thr130=) | gnomAD v4 |
| 17 | g.75727671C= | CA2275653826 | ITGB4 | c.285C= (p.Thr95=) n.350C= n.285C= c.390C= (p.Thr130=) | |
| 17 | g.75727671C>G | CA502047884 | ITGB4 | c.285C>G (p.Thr95=) n.350C>G n.285C>G c.390C>G (p.Thr130=) | dbSNP |
| 17 | g.75727671C>T | CA8768625 | ITGB4 | c.285C>T (p.Thr95=) n.350C>T n.285C>T c.390C>T (p.Thr130=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 17 | g.75727672C>A | CA401038858 | ITGB4 | c.286C>A (p.Leu96Met) n.351C>A n.286C>A c.391C>A (p.Leu131Met) | |
| 17 | g.75727672C>G | CA401038859 | ITGB4 | c.286C>G (p.Leu96Val) n.351C>G n.286C>G c.391C>G (p.Leu131Val) | gnomAD v4 |
| 17 | g.75727672C>T | CA502047889 | ITGB4 | c.286C>T (p.Leu96=) n.351C>T n.286C>T c.391C>T (p.Leu131=) | |
| 17 | g.75727673T>A | CA401038862 | ITGB4 | c.287T>A (p.Leu96Gln) n.352T>A n.287T>A c.392T>A (p.Leu131Gln) | |
| 17 | g.75727673T>C | CA401038861 | ITGB4 | c.287T>C (p.Leu96Pro) n.352T>C n.287T>C c.392T>C (p.Leu131Pro) | |
| 17 | g.75727673T>G | CA401038860 | ITGB4 | c.287T>G (p.Leu96Arg) n.352T>G n.287T>G c.392T>G (p.Leu131Arg) | |
| 17 | g.75727674G>A | CA502047891 | ITGB4 | c.288G>A (p.Leu96=) n.353G>A n.288G>A c.393G>A (p.Leu131=) | dbSNP gnomAD v4 |
| 17 | g.75727674G>C | CA502047892 | ITGB4 | c.288G>C (p.Leu96=) n.353G>C n.288G>C c.393G>C (p.Leu131=) | |
| 17 | g.75727674G= | CA2275653827 | ITGB4 | c.288G= (p.Leu96=) n.353G= n.288G= c.393G= (p.Leu131=) | |
| 17 | g.75727674G>T | CA502047893 | ITGB4 | c.288G>T (p.Leu96=) n.353G>T n.288G>T c.393G>T (p.Leu131=) | |
| 17 | g.75727675C>A | CA502047898 | ITGB4 | c.289C>A (p.Arg97=) n.354C>A n.289C>A c.394C>A (p.Arg132=) | ClinVar gnomAD v4 |
| 17 | g.75727675C= | CA2275653828 | ITGB4 | c.289C= (p.Arg97=) n.354C= n.289C= c.394C= (p.Arg132=) | |
| 17 | g.75727675C>G | CA401038863 | ITGB4 | c.289C>G (p.Arg97Gly) n.354C>G n.289C>G c.394C>G (p.Arg132Gly) | |
| 17 | g.75727675C>T | CA8768626 | ITGB4 | c.289C>T (p.Arg97Trp) n.354C>T n.289C>T c.394C>T (p.Arg132Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727676G>A | CA8768627 | ITGB4 | c.290G>A (p.Arg97Gln) n.355G>A n.290G>A c.395G>A (p.Arg132Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727676G>C | CA401038864 | ITGB4 | c.290G>C (p.Arg97Pro) n.355G>C n.290G>C c.395G>C (p.Arg132Pro) | |
| 17 | g.75727676G= | CA2275653829 | ITGB4 | c.290G= (p.Arg97=) n.355G= n.290G= c.395G= (p.Arg132=) | |
| 17 | g.75727676G>T | CA401038865 | ITGB4 | c.290G>T (p.Arg97Leu) n.355G>T n.290G>T c.395G>T (p.Arg132Leu) | |
| 17 | g.75727677G>A | CA502047901 | ITGB4 | c.291G>A (p.Arg97=) n.356G>A n.291G>A c.396G>A (p.Arg132=) | ClinVar dbSNP gnomAD v2 |
| 17 | g.75727677G>C | CA502047903 | ITGB4 | c.291G>C (p.Arg97=) n.356G>C n.291G>C c.396G>C (p.Arg132=) | dbSNP gnomAD v4 |
| 17 | g.75727677G= | CA2275653830 | ITGB4 | c.291G= (p.Arg97=) n.356G= n.291G= c.396G= (p.Arg132=) | |
| 17 | g.75727677G>T | CA502047904 | ITGB4 | c.291G>T (p.Arg97=) n.356G>T n.291G>T c.396G>T (p.Arg132=) | gnomAD v4 |
| 17 | g.75727678C>A | CA401038867 | ITGB4 | c.292C>A (p.Arg98Ser) n.357C>A n.292C>A c.397C>A (p.Arg133Ser) | gnomAD v4 |
| 17 | g.75727678C= | CA2275653831 | ITGB4 | c.292C= (p.Arg98=) n.357C= n.292C= c.397C= (p.Arg133=) | |
| 17 | g.75727678C>G | CA401038866 | ITGB4 | c.292C>G (p.Arg98Gly) n.357C>G n.292C>G c.397C>G (p.Arg133Gly) | |
| 17 | g.75727678C>T | CA8768628 | ITGB4 | c.292C>T (p.Arg98Cys) n.357C>T n.292C>T c.397C>T (p.Arg133Cys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 17 | g.75727679G>A | CA8768629 | ITGB4 | c.293G>A (p.Arg98His) n.358G>A n.293G>A c.398G>A (p.Arg133His) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727679G>C | CA401038868 | ITGB4 | c.293G>C (p.Arg98Pro) n.358G>C n.293G>C c.398G>C (p.Arg133Pro) | |
| 17 | g.75727679G= | CA2275653832 | ITGB4 | c.293G= (p.Arg98=) n.358G= n.293G= c.398G= (p.Arg133=) | |
| 17 | g.75727679G>T | CA401038869 | ITGB4 | c.293G>T (p.Arg98Leu) n.358G>T n.293G>T c.398G>T (p.Arg133Leu) | dbSNP gnomAD v4 |
| 17 | g.75727680C>A | CA502047911 | ITGB4 | c.294C>A (p.Arg98=) n.359C>A n.294C>A c.399C>A (p.Arg133=) | |
| 17 | g.75727680C>G | CA502047913 | ITGB4 | c.294C>G (p.Arg98=) n.359C>G n.294C>G c.399C>G (p.Arg133=) | |
| 17 | g.75727680C>T | CA502047915 | ITGB4 | c.294C>T (p.Arg98=) n.359C>T n.294C>T c.399C>T (p.Arg133=) | |
| 17 | g.75727681A>C | CA401038870 | ITGB4 | c.295A>C (p.Ser99Arg) n.360A>C n.295A>C c.400A>C (p.Ser134Arg) | |
| 17 | g.75727681A>G | CA401038871 | ITGB4 | c.295A>G (p.Ser99Gly) n.360A>G n.295A>G c.400A>G (p.Ser134Gly) | |
| 17 | g.75727681A>T | CA401038872 | ITGB4 | c.295A>T (p.Ser99Cys) n.360A>T n.295A>T c.400A>T (p.Ser134Cys) | |
| 17 | g.75727682G>A | CA401038873 | ITGB4 | c.296G>A (p.Ser99Asn) n.361G>A n.296G>A c.401G>A (p.Ser134Asn) | dbSNP gnomAD v2 |
| 17 | g.75727682G>C | CA401038875 | ITGB4 | c.296G>C (p.Ser99Thr) n.361G>C n.296G>C c.401G>C (p.Ser134Thr) | dbSNP gnomAD v2 |
| 17 | g.75727682G= | CA2275653833 | ITGB4 | c.296G= (p.Ser99=) n.361G= n.296G= c.401G= (p.Ser134=) | |
| 17 | g.75727682G>T | CA401038874 | ITGB4 | c.296G>T (p.Ser99Ile) n.361G>T n.296G>T c.401G>T (p.Ser134Ile) | |
| 17 | g.75727683C>A | CA401038876 | ITGB4 | c.297C>A (p.Ser99Arg) n.362C>A n.297C>A c.402C>A (p.Ser134Arg) | |
| 17 | g.75727683C>G | CA401038877 | ITGB4 | c.297C>G (p.Ser99Arg) n.362C>G n.297C>G c.402C>G (p.Ser134Arg) | |
| 17 | g.75727683C>T | CA502047919 | ITGB4 | c.297C>T (p.Ser99=) n.362C>T n.297C>T c.402C>T (p.Ser134=) | |
| 17 | g.75727684C>A | CA401038878 | ITGB4 | c.298C>A (p.Gln100Lys) n.363C>A n.298C>A c.403C>A (p.Gln135Lys) | |
| 17 | g.75727684C>G | CA401038879 | ITGB4 | c.298C>G (p.Gln100Glu) n.363C>G n.298C>G c.403C>G (p.Gln135Glu) | |
| 17 | g.75727684C>T | CA401038880 | ITGB4 | c.298C>T (p.Gln100Ter) n.363C>T n.298C>T c.403C>T (p.Gln135Ter) | |
| 17 | g.75727685A= | CA2275653834 | ITGB4 | c.299A= (p.Gln100=) n.364A= n.299A= c.404A= (p.Gln135=) | |
| 17 | g.75727685A>C | CA401038881 | ITGB4 | c.299A>C (p.Gln100Pro) n.364A>C n.299A>C c.404A>C (p.Gln135Pro) | |
| 17 | g.75727685A>G | CA8768630 | ITGB4 | c.299A>G (p.Gln100Arg) n.364A>G n.299A>G c.404A>G (p.Gln135Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727685A>T | CA401038882 | ITGB4 | c.299A>T (p.Gln100Leu) n.364A>T n.299A>T c.404A>T (p.Gln135Leu) | gnomAD v4 |
| 17 | g.75727686G>A | CA502047925 | ITGB4 | c.300G>A (p.Gln100=) n.365G>A n.300G>A c.405G>A (p.Gln135=) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.75727686G>C | CA401038883 | ITGB4 | c.300G>C (p.Gln100His) n.365G>C n.300G>C c.405G>C (p.Gln135His) | dbSNP gnomAD v2 |
| 17 | g.75727686G= | CA2275653835 | ITGB4 | c.300G= (p.Gln100=) n.365G= n.300G= c.405G= (p.Gln135=) | |
| 17 | g.75727686G>T | CA401038884 | ITGB4 | c.300G>T (p.Gln100His) n.365G>T n.300G>T c.405G>T (p.Gln135His) | |
| 17 | g.75727687A>C | CA401038887 | ITGB4 | c.301A>C (p.Met101Leu) n.366A>C n.301A>C c.406A>C (p.Met136Leu) | |
| 17 | g.75727687A>G | CA401038886 | ITGB4 | c.301A>G (p.Met101Val) n.366A>G n.301A>G c.406A>G (p.Met136Val) | |
| 17 | g.75727687A>T | CA401038885 | ITGB4 | c.301A>T (p.Met101Leu) n.366A>T n.301A>T c.406A>T (p.Met136Leu) | |
| 17 | g.75727688T>A | CA401038888 | ITGB4 | c.302T>A (p.Met101Lys) n.367T>A n.302T>A c.407T>A (p.Met136Lys) | |
| 17 | g.75727688T>C | CA401038890 | ITGB4 | c.302T>C (p.Met101Thr) n.367T>C n.302T>C c.407T>C (p.Met136Thr) | |
| 17 | g.75727688T>G | CA401038889 | ITGB4 | c.302T>G (p.Met101Arg) n.367T>G n.302T>G c.407T>G (p.Met136Arg) | |
| 17 | g.75727689G>A | CA401038891 | ITGB4 | c.303G>A (p.Met101Ile) n.368G>A n.303G>A c.408G>A (p.Met136Ile) | |
| 17 | g.75727689G>C | CA401038893 | ITGB4 | c.303G>C (p.Met101Ile) n.368G>C n.303G>C c.408G>C (p.Met136Ile) | |
| 17 | g.75727689G>T | CA401038892 | ITGB4 | c.303G>T (p.Met101Ile) n.368G>T n.303G>T c.408G>T (p.Met136Ile) | |
| 17 | g.75727690T>A | CA401038894 | ITGB4 | c.304T>A (p.Ser102Thr) n.369T>A n.304T>A c.409T>A (p.Ser137Thr) | |
| 17 | g.75727690T>C | CA401038895 | ITGB4 | c.304T>C (p.Ser102Pro) n.369T>C n.304T>C c.409T>C (p.Ser137Pro) | COSMIC COSMIC |
| 17 | g.75727690T>G | CA401038896 | ITGB4 | c.304T>G (p.Ser102Ala) n.369T>G n.304T>G c.409T>G (p.Ser137Ala) | |
| 17 | g.75727690T= | CA2275653836 | ITGB4 | c.304T= (p.Ser102=) n.369T= n.304T= c.409T= (p.Ser137=) | |
| 17 | g.75727691C>A | CA401038897 | ITGB4 | c.305C>A (p.Ser102Tyr) n.370C>A n.305C>A c.410C>A (p.Ser137Tyr) | dbSNP |
| 17 | g.75727691C= | CA2275653837 | ITGB4 | c.305C= (p.Ser102=) n.370C= n.305C= c.410C= (p.Ser137=) | |
| 17 | g.75727691C>G | CA8768632 | ITGB4 | c.305C>G (p.Ser102Cys) n.370C>G n.305C>G c.410C>G (p.Ser137Cys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.75727691C>T | CA8768631 | ITGB4 | c.305C>T (p.Ser102Phe) n.370C>T n.305C>T c.410C>T (p.Ser137Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727696dup | CA627595788 | ITGB4 | c.310dup (p.Gln104ProfsTer11) n.375dup n.310dup c.415dup (p.Gln139ProfsTer11) | ClinVar dbSNP gnomAD v2 |
| 17 | g.75727696del | CA2639874239 | ITGB4 | c.310del (p.Gln104LysfsTer?) n.375del n.310del c.415del (p.Gln139LysfsTer?) | gnomAD v4 |
| 17 | g.75727692C>A | CA294058535 | ITGB4 | c.306C>A (p.Ser102=) n.371C>A n.306C>A c.411C>A (p.Ser137=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727692C= | CA2275653838 | ITGB4 | c.306C= (p.Ser102=) n.371C= n.306C= c.411C= (p.Ser137=) | |
| 17 | g.75727692C>G | CA502047933 | ITGB4 | c.306C>G (p.Ser102=) n.371C>G n.306C>G c.411C>G (p.Ser137=) | dbSNP |
| 17 | g.75727692C>T | CA8768633 | ITGB4 | c.306C>T (p.Ser102=) n.371C>T n.306C>T c.411C>T (p.Ser137=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727693C>A | CA401038898 | ITGB4 | c.307C>A (p.Pro103Thr) n.372C>A n.307C>A c.412C>A (p.Pro138Thr) | gnomAD v4 |
| 17 | g.75727693C= | CA2275653839 | ITGB4 | c.307C= (p.Pro103=) n.372C= n.307C= c.412C= (p.Pro138=) | |
| 17 | g.75727693C>G | CA401038899 | ITGB4 | c.307C>G (p.Pro103Ala) n.372C>G n.307C>G c.412C>G (p.Pro138Ala) | |
| 17 | g.75727693C>T | CA8768634 | ITGB4 | c.307C>T (p.Pro103Ser) n.372C>T n.307C>T c.412C>T (p.Pro138Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.75727694C>A | CA401038900 | ITGB4 | c.308C>A (p.Pro103His) n.373C>A n.308C>A c.413C>A (p.Pro138His) | |
| 17 | g.75727694C= | CA2275653840 | ITGB4 | c.308C= (p.Pro103=) n.373C= n.308C= c.413C= (p.Pro138=) | |
| 17 | g.75727694C>G | CA401038901 | ITGB4 | c.308C>G (p.Pro103Arg) n.373C>G n.308C>G c.413C>G (p.Pro138Arg) | |
| 17 | g.75727694C>T | CA401038902 | ITGB4 | c.308C>T (p.Pro103Leu) n.373C>T n.308C>T c.413C>T (p.Pro138Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.75727695C>A | CA8768635 | ITGB4 | c.309C>A (p.Pro103=) n.374C>A n.309C>A c.414C>A (p.Pro138=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 17 | g.75727695C= | CA2275653841 | ITGB4 | c.309C= (p.Pro103=) n.374C= n.309C= c.414C= (p.Pro138=) | |
| 17 | g.75727695C>G | CA502047938 | ITGB4 | c.309C>G (p.Pro103=) n.374C>G n.309C>G c.414C>G (p.Pro138=) | ClinVar |
| 17 | g.75727695C>T | CA294058549 | ITGB4 | c.309C>T (p.Pro103=) n.374C>T n.309C>T c.414C>T (p.Pro138=) | ClinVar dbSNP |
| 17 | g.75727695_75727696delinsAG | CA891863035 | ITGB4 | c.309_310delinsAG (p.Gln104Glu) n.374_375delinsAG n.309_310delinsAG c.414_415delinsAG (p.Gln139Glu) | ClinVar dbSNP |
| 17 | g.75727695_75727696delinsCC | CA2275653842 | ITGB4 | c.309_310delinsCC (p.Pro103=) n.374_375delinsCC n.309_310delinsCC c.414_415delinsCC (p.Pro138=) | |
| 17 | g.75727696C>A | CA401038903 | ITGB4 | c.310C>A (p.Gln104Lys) n.375C>A n.310C>A c.415C>A (p.Gln139Lys) | |
| 17 | g.75727696C= | CA2275653843 | ITGB4 | c.310C= (p.Gln104=) n.375C= n.310C= c.415C= (p.Gln139=) | |
| 17 | g.75727696C>G | CA8768636 | ITGB4 | c.310C>G (p.Gln104Glu) n.375C>G n.310C>G c.415C>G (p.Gln139Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727696C>T | CA401038904 | ITGB4 | c.310C>T (p.Gln104Ter) n.375C>T n.310C>T c.415C>T (p.Gln139Ter) | ClinVar gnomAD v4 |
| 17 | g.75727697A>C | CA401038905 | ITGB4 | c.311A>C (p.Gln104Pro) n.376A>C n.311A>C c.416A>C (p.Gln139Pro) | |
| 17 | g.75727697A>G | CA401038906 | ITGB4 | c.311A>G (p.Gln104Arg) n.376A>G n.311A>G c.416A>G (p.Gln139Arg) | gnomAD v4 |
| 17 | g.75727697A>T | CA401038907 | ITGB4 | c.311A>T (p.Gln104Leu) n.376A>T n.311A>T c.416A>T (p.Gln139Leu) | |
| 17 | g.75727698A= | CA2275653844 | ITGB4 | c.312A= (p.Gln104=) n.377A= n.312A= c.417A= (p.Gln139=) | |
| 17 | g.75727698A>C | CA401038908 | ITGB4 | c.312A>C (p.Gln104His) n.377A>C n.312A>C c.417A>C (p.Gln139His) | |
| 17 | g.75727698A>G | CA8768637 | ITGB4 | c.312A>G (p.Gln104=) n.377A>G n.312A>G c.417A>G (p.Gln139=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727698A>T | CA401038909 | ITGB4 | c.312A>T (p.Gln104His) n.377A>T n.312A>T c.417A>T (p.Gln139His) | |
| 17 | g.75727699G>A | CA401038910 | ITGB4 | c.313G>A (p.Gly105Ser) n.378G>A n.313G>A c.418G>A (p.Gly140Ser) | gnomAD v4 |
| 17 | g.75727699G>C | CA401038911 | ITGB4 | c.313G>C (p.Gly105Arg) n.378G>C n.313G>C c.418G>C (p.Gly140Arg) | |
| 17 | g.75727699G>T | CA401038912 | ITGB4 | c.313G>T (p.Gly105Cys) n.378G>T n.313G>T c.418G>T (p.Gly140Cys) | |
| 17 | g.75727700G>A | CA401038915 | ITGB4 | c.314G>A (p.Gly105Asp) n.379G>A n.314G>A c.419G>A (p.Gly140Asp) | |
| 17 | g.75727700G>C | CA401038914 | ITGB4 | c.314G>C (p.Gly105Ala) n.379G>C n.314G>C c.419G>C (p.Gly140Ala) | |
| 17 | g.75727700G>T | CA401038913 | ITGB4 | c.314G>T (p.Gly105Val) n.379G>T n.314G>T c.419G>T (p.Gly140Val) | |
| 17 | g.75727701C>A | CA502047950 | ITGB4 | c.315C>A (p.Gly105=) n.380C>A n.315C>A c.420C>A (p.Gly140=) | |
| 17 | g.75727701C>G | CA502047951 | ITGB4 | c.315C>G (p.Gly105=) n.380C>G n.315C>G c.420C>G (p.Gly140=) | |
| 17 | g.75727701C>T | CA502047952 | ITGB4 | c.315C>T (p.Gly105=) n.380C>T n.315C>T c.420C>T (p.Gly140=) | gnomAD v4 |
| 17 | g.75727702C>A | CA401038916 | ITGB4 | c.316C>A (p.Leu106Met) n.381C>A n.316C>A c.421C>A (p.Leu141Met) | |
| 17 | g.75727702C>G | CA401038917 | ITGB4 | c.316C>G (p.Leu106Val) n.381C>G n.316C>G c.421C>G (p.Leu141Val) | |
| 17 | g.75727702C>T | CA502047968 | ITGB4 | c.316C>T (p.Leu106=) n.381C>T n.316C>T c.421C>T (p.Leu141=) | |
| 17 | g.75727703T>A | CA401038918 | ITGB4 | c.317T>A (p.Leu106Gln) n.382T>A n.317T>A c.422T>A (p.Leu141Gln) | |
| 17 | g.75727703T>C | CA401038919 | ITGB4 | c.317T>C (p.Leu106Pro) n.382T>C n.317T>C c.422T>C (p.Leu141Pro) | |
| 17 | g.75727703T>G | CA401038920 | ITGB4 | c.317T>G (p.Leu106Arg) n.382T>G n.317T>G c.422T>G (p.Leu141Arg) | |
| 17 | g.75727704G>A | CA502047973 | ITGB4 | c.318G>A (p.Leu106=) n.383G>A n.318G>A c.423G>A (p.Leu141=) | |
| 17 | g.75727704G>C | CA502047975 | ITGB4 | c.318G>C (p.Leu106=) n.383G>C n.318G>C c.423G>C (p.Leu141=) | |
| 17 | g.75727704G>T | CA502047974 | ITGB4 | c.318G>T (p.Leu106=) n.383G>T n.318G>T c.423G>T (p.Leu141=) | |
| 17 | g.75727705C>A | CA502047976 | ITGB4 | c.319C>A (p.Arg107=) n.384C>A n.319C>A c.424C>A (p.Arg142=) | dbSNP gnomAD v4 |
| 17 | g.75727705C= | CA2275653845 | ITGB4 | c.319C= (p.Arg107=) n.384C= n.319C= c.424C= (p.Arg142=) | |
| 17 | g.75727705C>G | CA401038921 | ITGB4 | c.319C>G (p.Arg107Gly) n.384C>G n.319C>G c.424C>G (p.Arg142Gly) | dbSNP |
| 17 | g.75727705C>T | CA8768638 | ITGB4 | c.319C>T (p.Arg107Trp) n.384C>T n.319C>T c.424C>T (p.Arg142Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727706G>A | CA8768639 | ITGB4 | c.320G>A (p.Arg107Gln) n.385G>A n.320G>A c.425G>A (p.Arg142Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727706G>C | CA401038922 | ITGB4 | c.320G>C (p.Arg107Pro) n.385G>C n.320G>C c.425G>C (p.Arg142Pro) | |
| 17 | g.75727706G= | CA2275653846 | ITGB4 | c.320G= (p.Arg107=) n.385G= n.320G= c.425G= (p.Arg142=) | |
| 17 | g.75727706G>T | CA401038923 | ITGB4 | c.320G>T (p.Arg107Leu) n.385G>T n.320G>T c.425G>T (p.Arg142Leu) | |
| 17 | g.75727707G>A | CA502047983 | ITGB4 | c.321G>A (p.Arg107=) n.386G>A n.321G>A c.426G>A (p.Arg142=) | gnomAD v4 |
| 17 | g.75727707G>C | CA502047984 | ITGB4 | c.321G>C (p.Arg107=) n.386G>C n.321G>C c.426G>C (p.Arg142=) | |
| 17 | g.75727707G>T | CA502047985 | ITGB4 | c.321G>T (p.Arg107=) n.386G>T n.321G>T c.426G>T (p.Arg142=) | |
| 17 | g.75727708G>A | CA401038924 | ITGB4 | c.322G>A (p.Val108Ile) n.387G>A n.322G>A c.427G>A (p.Val143Ile) | |
| 17 | g.75727708G>C | CA401038925 | ITGB4 | c.322G>C (p.Val108Leu) n.387G>C n.322G>C c.427G>C (p.Val143Leu) | |
| 17 | g.75727708G>T | CA401038926 | ITGB4 | c.322G>T (p.Val108Phe) n.387G>T n.322G>T c.427G>T (p.Val143Phe) | |
| 17 | g.75727709T>A | CA401038929 | ITGB4 | c.323T>A (p.Val108Asp) n.388T>A n.323T>A c.428T>A (p.Val143Asp) | |
| 17 | g.75727709T>C | CA401038927 | ITGB4 | c.323T>C (p.Val108Ala) n.388T>C n.323T>C c.428T>C (p.Val143Ala) | dbSNP gnomAD v4 COSMIC |
| 17 | g.75727709T>G | CA401038928 | ITGB4 | c.323T>G (p.Val108Gly) n.388T>G n.323T>G c.428T>G (p.Val143Gly) | |
| 17 | g.75727709T= | CA2275653847 | ITGB4 | c.323T= (p.Val108=) n.388T= n.323T= c.428T= (p.Val143=) | |
| 17 | g.75727710C>A | CA501832150 | ITGB4 | c.324C>A (p.Val108=) n.389C>A n.324C>A c.429C>A (p.Val143=) | |
| 17 | g.75727710C>G | CA501832151 | ITGB4 | c.324C>G (p.Val108=) n.389C>G n.324C>G c.429C>G (p.Val143=) | gnomAD v4 |
| 17 | g.75727710C>T | CA501832152 | ITGB4 | c.324C>T (p.Val108=) n.389C>T n.324C>T c.429C>T (p.Val143=) | |
| 17 | g.75727711C>A | CA401038930 | ITGB4 | c.325C>A (p.Arg109Ser) n.390C>A n.325C>A c.430C>A (p.Arg144Ser) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.75727711C= | CA2275653848 | ITGB4 | c.325C= (p.Arg109=) n.390C= n.325C= c.430C= (p.Arg144=) | |
| 17 | g.75727711C>G | CA401038931 | ITGB4 | c.325C>G (p.Arg109Gly) n.390C>G n.325C>G c.430C>G (p.Arg144Gly) | |
| 17 | g.75727711C>T | CA8768640 | ITGB4 | c.325C>T (p.Arg109Cys) n.390C>T n.325C>T c.430C>T (p.Arg144Cys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.75727712G>A | CA294058590 | ITGB4 | c.326G>A (p.Arg109His) n.391G>A n.326G>A c.431G>A (p.Arg144His) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 17 | g.75727712G>C | CA401038932 | ITGB4 | c.326G>C (p.Arg109Pro) n.391G>C n.326G>C c.431G>C (p.Arg144Pro) | |
| 17 | g.75727712G= | CA2275653849 | ITGB4 | c.326G= (p.Arg109=) n.391G= n.326G= c.431G= (p.Arg144=) | |
| 17 | g.75727712G>T | CA401038933 | ITGB4 | c.326G>T (p.Arg109Leu) n.391G>T n.326G>T c.431G>T (p.Arg144Leu) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.75727713T>A | CA501832155 | ITGB4 | c.327T>A (p.Arg109=) n.392T>A n.327T>A c.432T>A (p.Arg144=) | |
| 17 | g.75727713T>C | CA501832156 | ITGB4 | c.327T>C (p.Arg109=) n.392T>C n.327T>C c.432T>C (p.Arg144=) | |
| 17 | g.75727713T>G | CA501832158 | ITGB4 | c.327T>G (p.Arg109=) n.392T>G n.327T>G c.432T>G (p.Arg144=) | |
| 17 | g.75727714C>A | CA401038934 | ITGB4 | c.328C>A (p.Leu110Met) n.393C>A n.328C>A c.433C>A (p.Leu145Met) | |
| 17 | g.75727714C= | CA2275653850 | ITGB4 | c.328C= (p.Leu110=) n.393C= n.328C= c.433C= (p.Leu145=) | |
| 17 | g.75727714C>G | CA401038935 | ITGB4 | c.328C>G (p.Leu110Val) n.393C>G n.328C>G c.433C>G (p.Leu145Val) | |
| 17 | g.75727714C>T | CA8768641 | ITGB4 | c.328C>T (p.Leu110=) n.393C>T n.328C>T c.433C>T (p.Leu145=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727715_75727722del | CA2739268382 | ITGB4 | c.329_336del (p.Leu110ArgfsTer2) n.394_401del n.329_336del c.434_441del (p.Leu145ArgfsTer2) | ClinVar |
| 17 | g.75727715T>A | CA401038936 | ITGB4 | c.329T>A (p.Leu110Gln) n.394T>A n.329T>A c.434T>A (p.Leu145Gln) | |
| 17 | g.75727715T>C | CA401038937 | ITGB4 | c.329T>C (p.Leu110Pro) n.394T>C n.329T>C c.434T>C (p.Leu145Pro) | |
| 17 | g.75727715T>G | CA8768642 | ITGB4 | c.329T>G (p.Leu110Arg) n.394T>G n.329T>G c.434T>G (p.Leu145Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.75727715T= | CA2275653851 | ITGB4 | c.329T= (p.Leu110=) n.394T= n.329T= c.434T= (p.Leu145=) | |
| 17 | g.75727716G>A | CA501832159 | ITGB4 | c.330G>A (p.Leu110=) n.395G>A n.330G>A c.435G>A (p.Leu145=) | |
| 17 | g.75727716G>C | CA501832160 | ITGB4 | c.330G>C (p.Leu110=) n.395G>C n.330G>C c.435G>C (p.Leu145=) | |
| 17 | g.75727716G>T | CA501832161 | ITGB4 | c.330G>T (p.Leu110=) n.395G>T n.330G>T c.435G>T (p.Leu145=) | |
| 17 | g.75727717C>A | CA501832162 | ITGB4 | c.331C>A (p.Arg111=) n.396C>A n.331C>A c.436C>A (p.Arg146=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.75727717C= | CA2275653852 | ITGB4 | c.331C= (p.Arg111=) n.396C= n.331C= c.436C= (p.Arg146=) | |
| 17 | g.75727717C>G | CA401038938 | ITGB4 | c.331C>G (p.Arg111Gly) n.396C>G n.331C>G c.436C>G (p.Arg146Gly) | |
| 17 | g.75727717C>T | CA8768643 | ITGB4 | c.331C>T (p.Arg111Trp) n.396C>T n.331C>T c.436C>T (p.Arg146Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727718G>A | CA8768644 | ITGB4 | c.332G>A (p.Arg111Gln) n.397G>A n.332G>A c.437G>A (p.Arg146Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727718G>C | CA401038939 | ITGB4 | c.332G>C (p.Arg111Pro) n.397G>C n.332G>C c.437G>C (p.Arg146Pro) | |
| 17 | g.75727718G= | CA2275653853 | ITGB4 | c.332G= (p.Arg111=) n.397G= n.332G= c.437G= (p.Arg146=) | |
| 17 | g.75727718G>T | CA401038940 | ITGB4 | c.332G>T (p.Arg111Leu) n.397G>T n.332G>T c.437G>T (p.Arg146Leu) | dbSNP |
| 17 | g.75727719G>A | CA8768645 | ITGB4 | c.333G>A (p.Arg111=) n.398G>A n.333G>A c.438G>A (p.Arg146=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.75727719G>C | CA501832163 | ITGB4 | c.333G>C (p.Arg111=) n.398G>C n.333G>C c.438G>C (p.Arg146=) | |
| 17 | g.75727719G= | CA2275653854 | ITGB4 | c.333G= (p.Arg111=) n.398G= n.333G= c.438G= (p.Arg146=) | |
| 17 | g.75727719G>T | CA501832164 | ITGB4 | c.333G>T (p.Arg111=) n.398G>T n.333G>T c.438G>T (p.Arg146=) | |
| 17 | g.75727720C>A | CA401038941 | ITGB4 | c.334C>A (p.Pro112Thr) n.399C>A n.334C>A c.439C>A (p.Pro147Thr) | |
| 17 | g.75727720C= | CA2275653855 | ITGB4 | c.334C= (p.Pro112=) n.399C= n.334C= c.439C= (p.Pro147=) | |
| 17 | g.75727720C>G | CA401038942 | ITGB4 | c.334C>G (p.Pro112Ala) n.399C>G n.334C>G c.439C>G (p.Pro147Ala) | |
| 17 | g.75727720C>T | CA401038943 | ITGB4 | c.334C>T (p.Pro112Ser) n.399C>T n.334C>T c.439C>T (p.Pro147Ser) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.75727721C>A | CA401038944 | ITGB4 | c.335C>A (p.Pro112His) n.400C>A n.335C>A c.440C>A (p.Pro147His) | |
| 17 | g.75727721C>G | CA401038945 | ITGB4 | c.335C>G (p.Pro112Arg) n.400C>G n.335C>G c.440C>G (p.Pro147Arg) | |
| 17 | g.75727721C>T | CA401038946 | ITGB4 | c.335C>T (p.Pro112Leu) n.400C>T n.335C>T c.440C>T (p.Pro147Leu) | |
| 17 | g.75727722C>A | CA501832165 | ITGB4 | c.336C>A (p.Pro112=) n.401C>A n.336C>A c.441C>A (p.Pro147=) | |
| 17 | g.75727722C= | CA2275653856 | ITGB4 | c.336C= (p.Pro112=) n.401C= n.336C= c.441C= (p.Pro147=) | |
| 17 | g.75727722C>G | CA501832166 | ITGB4 | c.336C>G (p.Pro112=) n.401C>G n.336C>G c.441C>G (p.Pro147=) | |
| 17 | g.75727722C>T | CA8768646 | ITGB4 | c.336C>T (p.Pro112=) n.401C>T n.336C>T c.441C>T (p.Pro147=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727723G>A | CA294058617 | ITGB4 | c.337G>A (p.Gly113Ser) n.402G>A n.337G>A c.442G>A (p.Gly148Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 17 | g.75727723G>C | CA401038947 | ITGB4 | c.337G>C (p.Gly113Arg) n.402G>C n.337G>C c.442G>C (p.Gly148Arg) | |
| 17 | g.75727723G= | CA2275653857 | ITGB4 | c.337G= (p.Gly113=) n.402G= n.337G= c.442G= (p.Gly148=) | |
| 17 | g.75727723G>T | CA401038948 | ITGB4 | c.337G>T (p.Gly113Cys) n.402G>T n.337G>T c.442G>T (p.Gly148Cys) | |
| 17 | g.75727724G>A | CA401038951 | ITGB4 | c.338G>A (p.Gly113Asp) n.403G>A n.338G>A c.443G>A (p.Gly148Asp) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.75727724G>C | CA401038950 | ITGB4 | c.338G>C (p.Gly113Ala) n.403G>C n.338G>C c.443G>C (p.Gly148Ala) | dbSNP gnomAD v4 |
| 17 | g.75727724G= | CA2275653858 | ITGB4 | c.338G= (p.Gly113=) n.403G= n.338G= c.443G= (p.Gly148=) | |
| 17 | g.75727724G>T | CA401038949 | ITGB4 | c.338G>T (p.Gly113Val) n.403G>T n.338G>T c.443G>T (p.Gly148Val) | |
| 17 | g.75727725T>A | CA501832168 | ITGB4 | c.339T>A (p.Gly113=) n.404T>A n.339T>A c.444T>A (p.Gly148=) | |
| 17 | g.75727725T>C | CA501832169 | ITGB4 | c.339T>C (p.Gly113=) n.404T>C n.339T>C c.444T>C (p.Gly148=) | |
| 17 | g.75727725T>G | CA501832167 | ITGB4 | c.339T>G (p.Gly113=) n.404T>G n.339T>G c.444T>G (p.Gly148=) | dbSNP |
| 17 | g.75727725T= | CA2275653859 | ITGB4 | c.339T= (p.Gly113=) n.404T= n.339T= c.444T= (p.Gly148=) | |
| 17 | g.75727726G>A | CA401038952 | ITGB4 | c.340G>A (p.Glu114Lys) n.405G>A n.340G>A c.445G>A (p.Glu149Lys) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.75727726G>C | CA401038953 | ITGB4 | c.340G>C (p.Glu114Gln) n.405G>C n.340G>C c.445G>C (p.Glu149Gln) | |
| 17 | g.75727726G= | CA2275653860 | ITGB4 | c.340G= (p.Glu114=) n.405G= n.340G= c.445G= (p.Glu149=) | |
| 17 | g.75727726G>T | CA401038954 | ITGB4 | c.340G>T (p.Glu114Ter) n.405G>T n.340G>T c.445G>T (p.Glu149Ter) | |
| 17 | g.75727727A>C | CA401038955 | ITGB4 | c.341A>C (p.Glu114Ala) n.406A>C n.341A>C c.446A>C (p.Glu149Ala) | |
| 17 | g.75727727A>G | CA401038956 | ITGB4 | c.341A>G (p.Glu114Gly) n.406A>G n.341A>G c.446A>G (p.Glu149Gly) | |
| 17 | g.75727727A>T | CA401038957 | ITGB4 | c.341A>T (p.Glu114Val) n.406A>T n.341A>T c.446A>T (p.Glu149Val) | |
| 17 | g.75727728G>A | CA501832170 | ITGB4 | c.342G>A (p.Glu114=) n.407G>A n.342G>A c.447G>A (p.Glu149=) | |
| 17 | g.75727728G>C | CA401038958 | ITGB4 | c.342G>C (p.Glu114Asp) n.407G>C n.342G>C c.447G>C (p.Glu149Asp) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.75727728G= | CA2275653861 | ITGB4 | c.342G= (p.Glu114=) n.407G= n.342G= c.447G= (p.Glu149=) | |
| 17 | g.75727728G>T | CA401038959 | ITGB4 | c.342G>T (p.Glu114Asp) n.407G>T n.342G>T c.447G>T (p.Glu149Asp) | |
| 17 | g.75727729G>A | CA401038960 | ITGB4 | c.343G>A (p.Glu115Lys) n.408G>A n.343G>A c.448G>A (p.Glu150Lys) | gnomAD v4 |
| 17 | g.75727729G>C | CA401038961 | ITGB4 | c.343G>C (p.Glu115Gln) n.408G>C n.343G>C c.448G>C (p.Glu150Gln) | |
| 17 | g.75727729G>T | CA401038962 | ITGB4 | c.343G>T (p.Glu115Ter) n.408G>T n.343G>T c.448G>T (p.Glu150Ter) | |
| 17 | g.75727730A>C | CA401038963 | ITGB4 | c.344A>C (p.Glu115Ala) n.409A>C n.344A>C c.449A>C (p.Glu150Ala) | |
| 17 | g.75727730A>G | CA401038964 | ITGB4 | c.344A>G (p.Glu115Gly) n.409A>G n.344A>G c.449A>G (p.Glu150Gly) | gnomAD v4 |
| 17 | g.75727730A>T | CA401038965 | ITGB4 | c.344A>T (p.Glu115Val) n.409A>T n.344A>T c.449A>T (p.Glu150Val) | |
| 17 | g.75727731G>A | CA8768647 | ITGB4 | c.345G>A (p.Glu115=) n.410G>A n.345G>A c.450G>A (p.Glu150=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727731G>C | CA401038967 | ITGB4 | c.345G>C (p.Glu115Asp) n.410G>C n.345G>C c.450G>C (p.Glu150Asp) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.75727731G= | CA2275653862 | ITGB4 | c.345G= (p.Glu115=) n.410G= n.345G= c.450G= (p.Glu150=) | |
| 17 | g.75727731G>T | CA401038966 | ITGB4 | c.345G>T (p.Glu115Asp) n.410G>T n.345G>T c.450G>T (p.Glu150Asp) | |
| 17 | g.75727732C>A | CA8768649 | ITGB4 | c.346C>A (p.Arg116=) n.411C>A n.346C>A c.451C>A (p.Arg151=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727732C= | CA2275653863 | ITGB4 | c.346C= (p.Arg116=) n.411C= n.346C= c.451C= (p.Arg151=) | |
| 17 | g.75727732C>G | CA401038968 | ITGB4 | c.346C>G (p.Arg116Gly) n.411C>G n.346C>G c.451C>G (p.Arg151Gly) | |
| 17 | g.75727732C>T | CA8768648 | ITGB4 | c.346C>T (p.Arg116Trp) n.411C>T n.346C>T c.451C>T (p.Arg151Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727733G>A | CA401038969 | ITGB4 | c.347G>A (p.Arg116Gln) n.412G>A n.347G>A c.452G>A (p.Arg151Gln) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727733G>C | CA401038970 | ITGB4 | c.347G>C (p.Arg116Pro) n.412G>C n.347G>C c.452G>C (p.Arg151Pro) | gnomAD v4 |
| 17 | g.75727733G= | CA2275653864 | ITGB4 | c.347G= (p.Arg116=) n.412G= n.347G= c.452G= (p.Arg151=) | |
| 17 | g.75727733G>T | CA401038971 | ITGB4 | c.347G>T (p.Arg116Leu) n.412G>T n.347G>T c.452G>T (p.Arg151Leu) | |
| 17 | g.75727734G>A | CA501832171 | ITGB4 | c.348G>A (p.Arg116=) n.413G>A n.348G>A c.453G>A (p.Arg151=) | gnomAD v4 COSMIC COSMIC |
| 17 | g.75727734G>C | CA501832172 | ITGB4 | c.348G>C (p.Arg116=) n.413G>C n.348G>C c.453G>C (p.Arg151=) | |
| 17 | g.75727734G>T | CA501832173 | ITGB4 | c.348G>T (p.Arg116=) n.413G>T n.348G>T c.453G>T (p.Arg151=) | |
| 17 | g.75727735C>A | CA401038974 | ITGB4 | c.349C>A (p.His117Asn) n.414C>A n.349C>A c.454C>A (p.His152Asn) | |
| 17 | g.75727735C>G | CA401038972 | ITGB4 | c.349C>G (p.His117Asp) n.414C>G n.349C>G c.454C>G (p.His152Asp) | |
| 17 | g.75727735C>T | CA401038973 | ITGB4 | c.349C>T (p.His117Tyr) n.414C>T n.349C>T c.454C>T (p.His152Tyr) | |
| 17 | g.75727736A>C | CA401038975 | ITGB4 | c.350A>C (p.His117Pro) n.415A>C n.350A>C c.455A>C (p.His152Pro) | |
| 17 | g.75727736A>G | CA401038976 | ITGB4 | c.350A>G (p.His117Arg) n.415A>G n.350A>G c.455A>G (p.His152Arg) | |
| 17 | g.75727736A>T | CA401038977 | ITGB4 | c.350A>T (p.His117Leu) n.415A>T n.350A>T c.455A>T (p.His152Leu) | |
| 17 | g.75727737T>A | CA401038978 | ITGB4 | c.351T>A (p.His117Gln) n.416T>A n.351T>A c.456T>A (p.His152Gln) | |
| 17 | g.75727737T>C | CA501832174 | ITGB4 | c.351T>C (p.His117=) n.416T>C n.351T>C c.456T>C (p.His152=) | dbSNP |
| 17 | g.75727737T>G | CA401038979 | ITGB4 | c.351T>G (p.His117Gln) n.416T>G n.351T>G c.456T>G (p.His152Gln) | |
| 17 | g.75727738T>A | CA401038980 | ITGB4 | c.352T>A (p.Phe118Ile) n.417T>A n.352T>A c.457T>A (p.Phe153Ile) | |
| 17 | g.75727738T>C | CA401038982 | ITGB4 | c.352T>C (p.Phe118Leu) n.417T>C n.352T>C c.457T>C (p.Phe153Leu) | |
| 17 | g.75727738T>G | CA401038981 | ITGB4 | c.352T>G (p.Phe118Val) n.417T>G n.352T>G c.457T>G (p.Phe153Val) | |
| 17 | g.75727739T>A | CA401038983 | ITGB4 | c.353T>A (p.Phe118Tyr) n.418T>A n.353T>A c.458T>A (p.Phe153Tyr) | |
| 17 | g.75727739T>C | CA401038984 | ITGB4 | c.353T>C (p.Phe118Ser) n.418T>C n.353T>C c.458T>C (p.Phe153Ser) | |
| 17 | g.75727739T>G | CA401038985 | ITGB4 | c.353T>G (p.Phe118Cys) n.418T>G n.353T>G c.458T>G (p.Phe153Cys) | |
| 17 | g.75727740T>A | CA401038986 | ITGB4 | c.354T>A (p.Phe118Leu) n.419T>A n.354T>A c.459T>A (p.Phe153Leu) | |
| 17 | g.75727740T>C | CA501832175 | ITGB4 | c.354T>C (p.Phe118=) n.419T>C n.354T>C c.459T>C (p.Phe153=) | |
| 17 | g.75727740T>G | CA401038987 | ITGB4 | c.354T>G (p.Phe118Leu) n.419T>G n.354T>G c.459T>G (p.Phe153Leu) | |
| 17 | g.75727741G>A | CA401038988 | ITGB4 | c.355G>A (p.Glu119Lys) n.420G>A n.355G>A c.460G>A (p.Glu154Lys) | |
| 17 | g.75727741G>C | CA401038989 | ITGB4 | c.355G>C (p.Glu119Gln) n.420G>C n.355G>C c.460G>C (p.Glu154Gln) | |
| 17 | g.75727741G>T | CA401038990 | ITGB4 | c.355G>T (p.Glu119Ter) n.420G>T n.355G>T c.460G>T (p.Glu154Ter) | |
| 17 | g.75727742A>C | CA401038991 | ITGB4 | c.356A>C (p.Glu119Ala) n.421A>C n.356A>C c.461A>C (p.Glu154Ala) | |
| 17 | g.75727742A>G | CA401038992 | ITGB4 | c.356A>G (p.Glu119Gly) n.421A>G n.356A>G c.461A>G (p.Glu154Gly) | |
| 17 | g.75727742A>T | CA401038993 | ITGB4 | c.356A>T (p.Glu119Val) n.421A>T n.356A>T c.461A>T (p.Glu154Val) | |
| 17 | g.75727743G>A | CA8768650 | ITGB4 | c.357G>A (p.Glu119=) n.422G>A n.357G>A c.462G>A (p.Glu154=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.75727743G>C | CA401038995 | ITGB4 | c.357G>C (p.Glu119Asp) n.422G>C n.357G>C c.462G>C (p.Glu154Asp) | |
| 17 | g.75727743G= | CA2275653865 | ITGB4 | c.357G= (p.Glu119=) n.422G= n.357G= c.462G= (p.Glu154=) | |
| 17 | g.75727743G>T | CA401038994 | ITGB4 | c.357G>T (p.Glu119Asp) n.422G>T n.357G>T c.462G>T (p.Glu154Asp) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.75727744C>A | CA401038996 | ITGB4 | c.358C>A (p.Leu120Met) n.423C>A n.358C>A c.463C>A (p.Leu155Met) | |
| 17 | g.75727744C= | CA2275653866 | ITGB4 | c.358C= (p.Leu120=) n.423C= n.358C= c.463C= (p.Leu155=) | |
| 17 | g.75727744C>G | CA401038997 | ITGB4 | c.358C>G (p.Leu120Val) n.423C>G n.358C>G c.463C>G (p.Leu155Val) | |
| 17 | g.75727744C>T | CA8768651 | ITGB4 | c.358C>T (p.Leu120=) n.423C>T n.358C>T c.463C>T (p.Leu155=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.75727745T>A | CA401038998 | ITGB4 | c.359T>A (p.Leu120Gln) n.424T>A n.359T>A c.464T>A (p.Leu155Gln) | |
| 17 | g.75727745T>C | CA8768652 | ITGB4 | c.359T>C (p.Leu120Pro) n.424T>C n.359T>C c.464T>C (p.Leu155Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.75727745T>G | CA401038999 | ITGB4 | c.359T>G (p.Leu120Arg) n.424T>G n.359T>G c.464T>G (p.Leu155Arg) | |
| 17 | g.75727745T= | CA2275653867 | ITGB4 | c.359T= (p.Leu120=) n.424T= n.359T= c.464T= (p.Leu155=) | |
| 17 | g.75727745_75727748delinsTGGA | CA2275653868 | ITGB4 | c.359_362delinsTGGA (p.Leu120=) n.424_427delinsTGGA n.359_362delinsTGGA c.464_467delinsTGGA (p.Leu155=) | |
| 17 | g.75727746G>A | CA501832178 | ITGB4 | c.360G>A (p.Leu120=) n.425G>A n.360G>A c.465G>A (p.Leu155=) | |
| 17 | g.75727746G>C | CA501832177 | ITGB4 | c.360G>C (p.Leu120=) n.425G>C n.360G>C c.465G>C (p.Leu155=) | |
| 17 | g.75727746G>T | CA501832176 | ITGB4 | c.360G>T (p.Leu120=) n.425G>T n.360G>T c.465G>T (p.Leu155=) | |
| 17 | g.75727748_75727750del | CA986368822 | ITGB4 | c.362_364del (p.Glu121del) n.427_429del n.362_364del c.467_469del (p.Glu156del) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.75727747G>A | CA401039000 | ITGB4 | c.361G>A (p.Glu121Lys) n.426G>A n.361G>A c.466G>A (p.Glu156Lys) | dbSNP gnomAD v4 |
| 17 | g.75727747G>C | CA401039001 | ITGB4 | c.361G>C (p.Glu121Gln) n.426G>C n.361G>C c.466G>C (p.Glu156Gln) | |
| 17 | g.75727747G= | CA2275653869 | ITGB4 | c.361G= (p.Glu121=) n.426G= n.361G= c.466G= (p.Glu156=) | |
| 17 | g.75727747G>T | CA401039002 | ITGB4 | c.361G>T (p.Glu121Ter) n.426G>T n.361G>T c.466G>T (p.Glu156Ter) | |
| 17 | g.75727748A>C | CA401039003 | ITGB4 | c.362A>C (p.Glu121Ala) n.427A>C n.362A>C c.467A>C (p.Glu156Ala) | |
| 17 | g.75727748A>G | CA401039004 | ITGB4 | c.362A>G (p.Glu121Gly) n.427A>G n.362A>G c.467A>G (p.Glu156Gly) | |
| 17 | g.75727748A>T | CA401039005 | ITGB4 | c.362A>T (p.Glu121Val) n.427A>T n.362A>T c.467A>T (p.Glu156Val) | |
| 17 | g.75727749G>A | CA501832179 | ITGB4 | c.363G>A (p.Glu121=) n.428G>A n.363G>A c.468G>A (p.Glu156=) | |
| 17 | g.75727749G>C | CA401039006 | ITGB4 | c.363G>C (p.Glu121Asp) n.428G>C n.363G>C c.468G>C (p.Glu156Asp) | |
| 17 | g.75727749G>T | CA401039007 | ITGB4 | c.363G>T (p.Glu121Asp) n.428G>T n.363G>T c.468G>T (p.Glu156Asp) | |
| 17 | g.75727750G>A | CA401039008 | ITGB4 | c.364G>A (p.Val122Met) n.429G>A n.364G>A c.469G>A (p.Val157Met) | |
| 17 | g.75727750G>C | CA401039009 | ITGB4 | c.364G>C (p.Val122Leu) n.429G>C n.364G>C c.469G>C (p.Val157Leu) | |
| 17 | g.75727750G>T | CA401039010 | ITGB4 | c.364G>T (p.Val122Leu) n.429G>T n.364G>T c.469G>T (p.Val157Leu) | gnomAD v4 |
| 17 | g.75727751T>A | CA401039013 | ITGB4 | c.365T>A (p.Val122Glu) n.430T>A n.365T>A c.470T>A (p.Val157Glu) | |
| 17 | g.75727751T>C | CA401039012 | ITGB4 | c.365T>C (p.Val122Ala) n.430T>C n.365T>C c.470T>C (p.Val157Ala) | |
| 17 | g.75727751T>G | CA401039011 | ITGB4 | c.365T>G (p.Val122Gly) n.430T>G n.365T>G c.470T>G (p.Val157Gly) | |
| 17 | g.75727752G>A | CA501832180 | ITGB4 | c.366G>A (p.Val122=) n.431G>A n.366G>A c.471G>A (p.Val157=) | ClinVar |
| 17 | g.75727752G>C | CA501832181 | ITGB4 | c.366G>C (p.Val122=) n.431G>C n.366G>C c.471G>C (p.Val157=) | gnomAD v4 |
| 17 | g.75727752G>T | CA501832182 | ITGB4 | c.366G>T (p.Val122=) n.431G>T n.366G>T c.471G>T (p.Val157=) | |
| 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) |