Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.47286224A=CA2262605959ITGB3c.615-36A= (n.615-36A=)
c.580-36A=
17g.47286224A>CCA8623006ITGB3c.615-36A>C (n.615-36A>C)
c.580-36A>C
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.47286225G>ACA2638435524ITGB3c.615-35G>A (n.615-35G>A)
c.580-35G>A
 gnomAD v4
17g.47286226G>ACA2576302248ITGB3c.615-34G>A (n.615-34G>A)
c.580-34G>A
17g.47286226G>CCA2638435525ITGB3c.615-34G>C (n.615-34G>C)
c.580-34G>C
 gnomAD v4
17g.47286226G=CA2262605960ITGB3c.615-34G= (n.615-34G=)
c.580-34G=
17g.47286226G>TCA984234681ITGB3c.615-34G>T (n.615-34G>T)
c.580-34G>T
 dbSNP gnomAD v3 gnomAD v4
17g.47286227T>ACA8623007ITGB3c.615-33T>A (n.615-33T>A)
c.580-33T>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.47286227T=CA2262605961ITGB3c.615-33T= (n.615-33T=)
c.580-33T=
17g.47286229T>ACA984234689ITGB3c.615-31T>A (n.615-31T>A)
c.580-31T>A
 dbSNP gnomAD v3 gnomAD v4
17g.47286229T=CA2262605962ITGB3c.615-31T= (n.615-31T=)
c.580-31T=
17g.47286230C>TCA2567238456ITGB3c.615-30C>T (n.615-30C>T)
c.580-30C>T
17g.47286231T>GCA626684838ITGB3c.615-29T>G (n.615-29T>G)
c.580-29T>G
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.47286231T=CA2262605963ITGB3c.615-29T= (n.615-29T=)
c.580-29T=
17g.47286232G>ACA2638435526ITGB3c.615-28G>A (n.615-28G>A)
c.580-28G>A
 gnomAD v4
17g.47286234T>CCA2638435527ITGB3c.615-26T>C (n.615-26T>C)
c.580-26T>C
 gnomAD v4
17g.47286238A=CA2262605964ITGB3c.615-22A= (n.615-22A=)
c.580-22A=
17g.47286238A>TCA772536953ITGB3c.615-22A>T (n.615-22A>T)
c.580-22A>T
 dbSNP gnomAD v3 gnomAD v4
17g.47286239T>CCA2638435528ITGB3c.615-21T>C (n.615-21T>C)
c.580-21T>C
 gnomAD v4
17g.47286243C=CA2262605965ITGB3c.615-17C= (n.615-17C=)
c.580-17C=
17g.47286243C>TCA291224879ITGB3c.615-17C>T (n.615-17C>T)
c.580-17C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.47286244T>ACA2262605967ITGB3c.615-16T>A (n.615-16T>A)
c.580-16T>A
 dbSNP
17g.47286244T>CCA626684839ITGB3c.615-16T>C (n.615-16T>C)
c.580-16T>C
 dbSNP gnomAD v2 gnomAD v4
17g.47286244T=CA2262605966ITGB3c.615-16T= (n.615-16T=)
c.580-16T=
17g.47286245C>ACA2638435529ITGB3c.615-15C>A (n.615-15C>A)
c.580-15C>A
 gnomAD v4
17g.47286248A=CA2262605968ITGB3c.615-12A= (n.615-12A=)
c.580-12A=
17g.47286248A>GCA8623008ITGB3c.615-12A>G (n.615-12A>G)
c.580-12A>G
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.47286249T>ACA8623009ITGB3c.615-11T>A (n.615-11T>A)
c.580-11T>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.47286249T>CCA2638435530ITGB3c.615-11T>C (n.615-11T>C)
c.580-11T>C
 gnomAD v4
17g.47286249T=CA2262605969ITGB3c.615-11T= (n.615-11T=)
c.580-11T=
17g.47286250C>ACA626684840ITGB3c.615-10C>A (n.615-10C>A)
c.580-10C>A
 dbSNP gnomAD v2 gnomAD v4
17g.47286250C=CA2262605970ITGB3c.615-10C= (n.615-10C=)
c.580-10C=
17g.47286250C>GCA2638435531ITGB3c.615-10C>G (n.615-10C>G)
c.580-10C>G
 gnomAD v4
17g.47286250C>TCA2638435532ITGB3c.615-10C>T (n.615-10C>T)
c.580-10C>T
 gnomAD v4
17g.47286251C>ACA2638435533ITGB3c.615-9C>A (n.615-9C>A)
c.580-9C>A
 gnomAD v4
17g.47286251C=CA2262605971ITGB3c.615-9C= (n.615-9C=)
c.580-9C=
17g.47286251C>TCA2262605972ITGB3c.615-9C>T (n.615-9C>T)
c.580-9C>T
 ClinVar dbSNP gnomAD v4
17g.47286252C=CA2262605973ITGB3c.615-8C= (n.615-8C=)
c.580-8C=
17g.47286252C>GCA8623010ITGB3c.615-8C>G (n.615-8C>G)
c.580-8C>G
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.47286252C>TCA2638435534ITGB3c.615-8C>T (n.615-8C>T)
c.580-8C>T
 ClinVar gnomAD v4
17g.47286254C=CA2262605974ITGB3c.615-6C= (n.615-6C=)
c.580-6C=
17g.47286254C>TCA8623011ITGB3c.615-6C>T (n.615-6C>T)
c.580-6C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.47286255C>GCA2576302249ITGB3c.615-5C>G (n.615-5C>G)
c.580-5C>G
17g.47286257C>ACA2638435535ITGB3c.615-3C>A (n.615-3C>A)
c.580-3C>A
 gnomAD v4
17g.47286258A>CCA400023348ITGB3c.615-2A>C (n.615-2A>C)
c.580-2A>C
17g.47286258A>GCA400023349ITGB3c.615-2A>G (n.615-2A>G)
c.580-2A>G
17g.47286258A>TCA400023350ITGB3c.615-2A>T (n.615-2A>T)
c.580-2A>T
17g.47286259G>ACA400023351ITGB3c.615-1G>A (n.615-1G>A)
c.580-1G>A
 ClinVar gnomAD v4
17g.47286259G>CCA400023352ITGB3c.615-1G>C (n.615-1G>C)
c.580-1G>C
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.47286259G=CA2262605975ITGB3c.615-1G= (n.615-1G=)
c.580-1G=
17g.47286259G>TCA400023353ITGB3c.615-1G>T (n.615-1G>T)
c.580-1G>T
17g.47286260T>ACA400023354ITGB3c.615T>A (p.Asp205Glu)
c.580T>A
17g.47286260T>CCA500431951ITGB3c.615T>C (p.Asp205=)
c.580T>C
17g.47286260T>GCA8623012ITGB3c.615T>G (p.Asp205Glu)
c.580T>G
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.47286260T=CA2262605976ITGB3c.615T= (p.Asp205=)
c.580T=
17g.47286261A>CCA400023357ITGB3c.616A>C (p.Met206Leu)
c.581A>C
17g.47286261A>GCA400023356ITGB3c.616A>G (p.Met206Val)
c.581A>G
 gnomAD v4
17g.47286261A>TCA400023355ITGB3c.616A>T (p.Met206Leu)
c.581A>T
17g.47286261dupCA2638435536ITGB3c.616dup (p.Met206AsnfsTer19)
c.581dup
 gnomAD v4
17g.47286262T>ACA400023358ITGB3c.617T>A (p.Met206Lys)
c.582T>A
17g.47286262T>CCA400023359ITGB3c.617T>C (p.Met206Thr)
c.582T>C
 dbSNP
17g.47286262T>GCA400023360ITGB3c.617T>G (p.Met206Arg)
c.582T>G
17g.47286262T=CA2262605977ITGB3c.617T= (p.Met206=)
c.582T=
17g.47286263G>ACA400023361ITGB3c.618G>A (p.Met206Ile)
c.583G>A
17g.47286263G>CCA400023362ITGB3c.618G>C (p.Met206Ile)
c.583G>C
17g.47286263G>TCA400023363ITGB3c.618G>T (p.Met206Ile)
c.583G>T
17g.47286264A>CCA400023366ITGB3c.619A>C (p.Lys207Gln)
c.584A>C
17g.47286264A>GCA400023364ITGB3c.619A>G (p.Lys207Glu)
c.584A>G
17g.47286264A>TCA400023365ITGB3c.619A>T (p.Lys207Ter)
c.584A>T
17g.47286265A>CCA400023367ITGB3c.620A>C (p.Lys207Thr)
c.585A>C
17g.47286265A>GCA400023368ITGB3c.620A>G (p.Lys207Arg)
c.585A>G
17g.47286265A>TCA400023369ITGB3c.620A>T (p.Lys207Met)
c.585A>T
17g.47286266G>ACA500431952ITGB3c.621G>A (p.Lys207=)
c.586G>A
 ClinVar
17g.47286266G>CCA400023370ITGB3c.621G>C (p.Lys207Asn)
c.586G>C
17g.47286266G>TCA400023371ITGB3c.621G>T (p.Lys207Asn)
c.586G>T
 gnomAD v4
17g.47286267A>CCA400023372ITGB3c.622A>C (p.Thr208Pro)
c.587A>C
17g.47286267A>GCA400023374ITGB3c.622A>G (p.Thr208Ala)
c.587A>G
17g.47286267A>TCA400023373ITGB3c.622A>T (p.Thr208Ser)
c.587A>T
17g.47286268C>ACA400023375ITGB3c.623C>A (p.Thr208Asn)
c.588C>A
17g.47286268C>GCA400023376ITGB3c.623C>G (p.Thr208Ser)
c.588C>G
17g.47286268C>TCA400023377ITGB3c.623C>T (p.Thr208Ile)
c.588C>T
17g.47286269C>ACA500431953ITGB3c.624C>A (p.Thr208=)
c.589C>A
17g.47286269C>GCA500431954ITGB3c.624C>G (p.Thr208=)
c.589C>G
17g.47286269C>TCA500431955ITGB3c.624C>T (p.Thr208=)
c.589C>T
 gnomAD v4
17g.47286270A>CCA400023378ITGB3c.625A>C (p.Thr209Pro)
c.590A>C
17g.47286270A>GCA400023379ITGB3c.625A>G (p.Thr209Ala)
c.590A>G
17g.47286270A>TCA400023380ITGB3c.625A>T (p.Thr209Ser)
c.590A>T
17g.47286271C>ACA400023381ITGB3c.626C>A (p.Thr209Asn)
c.591C>A
17g.47286271C>GCA400023382ITGB3c.626C>G (p.Thr209Ser)
c.591C>G
17g.47286271C>TCA400023383ITGB3c.626C>T (p.Thr209Ile)
c.591C>T
17g.47286272C>ACA500431957ITGB3c.627C>A (p.Thr209=)
c.592C>A
17g.47286272C=CA2262605978ITGB3c.627C= (p.Thr209=)
c.592C=
17g.47286272C>GCA8623013ITGB3c.627C>G (p.Thr209=)
c.592C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.47286272C>TCA500431958ITGB3c.627C>T (p.Thr209=)
c.592C>T
17g.47286273T>ACA400023386ITGB3c.628T>A (p.Cys210Ser)
c.593T>A
17g.47286273T>CCA400023385ITGB3c.628T>C (p.Cys210Arg)
c.593T>C
17g.47286273T>GCA400023384ITGB3c.628T>G (p.Cys210Gly)
c.593T>G
17g.47286274G>ACA400023387ITGB3c.629G>A (p.Cys210Tyr)
c.594G>A
 gnomAD v4
17g.47286274G>CCA400023389ITGB3c.629G>C (p.Cys210Ser)
c.594G>C
 ClinVar dbSNP
17g.47286274G=CA2262605979ITGB3c.629G= (p.Cys210=)
c.594G=
17g.47286274G>TCA400023388ITGB3c.629G>T (p.Cys210Phe)
c.594G>T
17g.47286275C>ACA400023390ITGB3c.630C>A (p.Cys210Ter)
c.595C>A
17g.47286275C=CA2262605980ITGB3c.630C= (p.Cys210=)
c.595C=
17g.47286275C>GCA400023391ITGB3c.630C>G (p.Cys210Trp)
c.595C>G
17g.47286275C>TCA500431959ITGB3c.630C>T (p.Cys210=)
c.595C>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.47286276T>ACA400023392ITGB3c.631T>A (p.Leu211Met)
c.596T>A
17g.47286276T>CCA500431960ITGB3c.631T>C (p.Leu211=)
c.596T>C
17g.47286276T>GCA400023393ITGB3c.631T>G (p.Leu211Val)
c.596T>G
17g.47286277T>ACA400023394ITGB3c.632T>A (p.Leu211Ter)
c.597T>A
17g.47286277T>CCA400023395ITGB3c.632T>C (p.Leu211Ser)
c.597T>C
17g.47286277T>GCA400023396ITGB3c.632T>G (p.Leu211Trp)
c.597T>G
17g.47286278G>ACA8623014ITGB3c.633G>A (p.Leu211=)
c.598G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.47286278G>CCA400023397ITGB3c.633G>C (p.Leu211Phe)
c.598G>C
17g.47286278G=CA2262605981ITGB3c.633G= (p.Leu211=)
c.598G=
17g.47286278G>TCA400023398ITGB3c.633G>T (p.Leu211Phe)
c.598G>T
17g.47286279C>ACA400023401ITGB3c.634C>A (p.Pro212Thr)
c.599C>A
17g.47286279C>GCA400023400ITGB3c.634C>G (p.Pro212Ala)
c.599C>G
17g.47286279C>TCA400023399ITGB3c.634C>T (p.Pro212Ser)
c.599C>T
 gnomAD v4
17g.47286281dupCA772536995ITGB3c.636dup (p.Met213HisfsTer12)
c.601dup
 dbSNP
17g.47286280C>ACA400023402ITGB3c.635C>A (p.Pro212His)
c.600C>A
17g.47286280C=CA2262605982ITGB3c.635C= (p.Pro212=)
c.600C=
17g.47286280C>GCA400023403ITGB3c.635C>G (p.Pro212Arg)
c.600C>G
17g.47286280C>TCA291224884ITGB3c.635C>T (p.Pro212Leu)
c.600C>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.47286281C>ACA500431962ITGB3c.636C>A (p.Pro212=)
c.601C>A
 gnomAD v4
17g.47286281C>GCA500431961ITGB3c.636C>G (p.Pro212=)
c.601C>G
17g.47286281C>TCA500431963ITGB3c.636C>T (p.Pro212=)
c.601C>T
17g.47286282A=CA2262605983ITGB3c.637A= (p.Met213=)
c.602A=
17g.47286282A>CCA400023404ITGB3c.637A>C (p.Met213Leu)
c.602A>C
17g.47286282A>GCA400023405ITGB3c.637A>G (p.Met213Val)
c.602A>G
 dbSNP gnomAD v4
17g.47286282A>TCA400023406ITGB3c.637A>T (p.Met213Leu)
c.602A>T
17g.47286283T>ACA400023407ITGB3c.638T>A (p.Met213Lys)
c.603T>A
17g.47286283T>CCA400023408ITGB3c.638T>C (p.Met213Thr)
c.603T>C
 gnomAD v4
17g.47286283T>GCA400023409ITGB3c.638T>G (p.Met213Arg)
c.603T>G
17g.47286284G>ACA400023410ITGB3c.639G>A (p.Met213Ile)
c.604G>A
17g.47286284G>CCA400023411ITGB3c.639G>C (p.Met213Ile)
c.604G>C
17g.47286284G>TCA400023412ITGB3c.639G>T (p.Met213Ile)
c.604G>T
17g.47286285T>ACA400023414ITGB3c.640T>A (p.Phe214Ile)
c.605T>A
17g.47286285T>CCA400023415ITGB3c.640T>C (p.Phe214Leu)
c.605T>C
17g.47286285T>GCA400023413ITGB3c.640T>G (p.Phe214Val)
c.605T>G
17g.47286286T>ACA400023416ITGB3c.641T>A (p.Phe214Tyr)
c.606T>A
17g.47286286T>CCA400023417ITGB3c.641T>C (p.Phe214Ser)
c.606T>C
17g.47286286T>GCA400023418ITGB3c.641T>G (p.Phe214Cys)
c.606T>G
17g.47286287T>ACA400023419ITGB3c.642T>A (p.Phe214Leu)
c.607T>A
17g.47286287T>CCA500431964ITGB3c.642T>C (p.Phe214=)
c.607T>C
17g.47286287T>GCA400023420ITGB3c.642T>G (p.Phe214Leu)
c.607T>G
17g.47286288G>ACA400023423ITGB3c.643G>A (p.Gly215Ser)
c.608G>A
17g.47286288G>CCA400023422ITGB3c.643G>C (p.Gly215Arg)
c.608G>C
17g.47286288G>TCA400023421ITGB3c.643G>T (p.Gly215Cys)
c.608G>T
17g.47286289G>ACA400023424ITGB3c.644G>A (p.Gly215Asp)
c.609G>A
 gnomAD v4
17g.47286289G>CCA400023425ITGB3c.644G>C (p.Gly215Ala)
c.609G>C
17g.47286289G>TCA400023426ITGB3c.644G>T (p.Gly215Val)
c.609G>T
17g.47286290C>ACA500431967ITGB3c.645C>A (p.Gly215=)
c.610C>A
17g.47286290C>GCA500431965ITGB3c.645C>G (p.Gly215=)
c.610C>G
17g.47286290C>TCA500431966ITGB3c.645C>T (p.Gly215=)
c.610C>T
17g.47286291T>ACA400023427ITGB3c.646T>A (p.Tyr216Asn)
c.611T>A
17g.47286291T>CCA400023428ITGB3c.646T>C (p.Tyr216His)
c.611T>C
 ClinVar
17g.47286291T>GCA400023429ITGB3c.646T>G (p.Tyr216Asp)
c.611T>G
17g.47286292A=CA2262605984ITGB3c.647A= (p.Tyr216=)
c.612A=
17g.47286292A>CCA400023430ITGB3c.647A>C (p.Tyr216Ser)
c.612A>C
17g.47286292A>GCA400023432ITGB3c.647A>G (p.Tyr216Cys)
c.612A>G
 ClinVar dbSNP
17g.47286292A>TCA400023431ITGB3c.647A>T (p.Tyr216Phe)
c.612A>T
17g.47286293C>ACA400023433ITGB3c.648C>A (p.Tyr216Ter)
c.613C>A
17g.47286293C>GCA400023434ITGB3c.648C>G (p.Tyr216Ter)
c.613C>G
17g.47286293C>TCA500431968ITGB3c.648C>T (p.Tyr216=)
c.613C>T
 dbSNP
17g.47286294A>CCA400023435ITGB3c.649A>C (p.Lys217Gln)
c.614A>C
17g.47286294A>GCA400023436ITGB3c.649A>G (p.Lys217Glu)
c.614A>G
 gnomAD v4
17g.47286294A>TCA400023437ITGB3c.649A>T (p.Lys217Ter)
c.614A>T
17g.47286295A>CCA400023438ITGB3c.650A>C (p.Lys217Thr)
c.615A>C
17g.47286295A>GCA400023439ITGB3c.650A>G (p.Lys217Arg)
c.615A>G
17g.47286295A>TCA400023440ITGB3c.650A>T (p.Lys217Ile)
c.615A>T
17g.47286296A=CA2262605985ITGB3c.651A= (p.Lys217=)
c.616A=
17g.47286296A>CCA400023441ITGB3c.651A>C (p.Lys217Asn)
c.616A>C
17g.47286296A>GCA500431969ITGB3c.651A>G (p.Lys217=)
c.616A>G
 dbSNP gnomAD v3 gnomAD v4
17g.47286296A>TCA400023442ITGB3c.651A>T (p.Lys217Asn)
c.616A>T
 gnomAD v4
17g.47286297C>ACA400023443ITGB3c.652C>A (p.His218Asn)
c.617C>A
17g.47286297C>GCA400023444ITGB3c.652C>G (p.His218Asp)
c.617C>G
17g.47286297C>TCA400023445ITGB3c.652C>T (p.His218Tyr)
c.617C>T
 ClinVar dbSNP
17g.47286298A>CCA400023447ITGB3c.653A>C (p.His218Pro)
c.618A>C
17g.47286298A>GCA400023448ITGB3c.653A>G (p.His218Arg)
c.618A>G
 gnomAD v4
17g.47286298A>TCA400023446ITGB3c.653A>T (p.His218Leu)
c.618A>T
17g.47286299C>ACA400023450ITGB3c.654C>A (p.His218Gln)
c.619C>A
17g.47286299C=CA2262605986ITGB3c.654C= (p.His218=)
c.619C=
17g.47286299C>GCA400023449ITGB3c.654C>G (p.His218Gln)
c.619C>G
17g.47286299C>TCA8623015ITGB3c.654C>T (p.His218=)
c.619C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.47286300G>ACA8623016ITGB3c.655G>A (p.Val219Met)
c.620G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.47286300G>CCA400023452ITGB3c.655G>C (p.Val219Leu)
c.620G>C
 gnomAD v4
17g.47286300G=CA2262605987ITGB3c.655G= (p.Val219=)
c.620G=
17g.47286300G>TCA400023451ITGB3c.655G>T (p.Val219Leu)
c.620G>T
 gnomAD v4
17g.47286301T>ACA400023453ITGB3c.656T>A (p.Val219Glu)
c.621T>A
17g.47286301T>CCA400023455ITGB3c.656T>C (p.Val219Ala)
c.621T>C
 dbSNP gnomAD v3 gnomAD v4
17g.47286301T>GCA400023454ITGB3c.656T>G (p.Val219Gly)
c.621T>G
17g.47286301T=CA2262605988ITGB3c.656T= (p.Val219=)
c.621T=
17g.47286302G>ACA500431972ITGB3c.657G>A (p.Val219=)
c.622G>A
17g.47286302G>CCA500431971ITGB3c.657G>C (p.Val219=)
c.622G>C
 gnomAD v4
17g.47286302G>TCA500431970ITGB3c.657G>T (p.Val219=)
c.622G>T
17g.47286303C>ACA400023456ITGB3c.658C>A (p.Leu220Met)
c.623C>A
17g.47286303C>GCA400023457ITGB3c.658C>G (p.Leu220Val)
c.623C>G
17g.47286303C>TCA500431973ITGB3c.658C>T (p.Leu220=)
c.623C>T
17g.47286304T>ACA400023458ITGB3c.659T>A (p.Leu220Gln)
c.624T>A
 gnomAD v4
17g.47286304T>CCA400023459ITGB3c.659T>C (p.Leu220Pro)
c.624T>C
17g.47286304T>GCA400023460ITGB3c.659T>G (p.Leu220Arg)
c.624T>G
17g.47286305G>ACA500431975ITGB3c.660G>A (p.Leu220=)
c.625G>A
17g.47286305G>CCA500431974ITGB3c.660G>C (p.Leu220=)
c.625G>C
17g.47286305G>TCA500431976ITGB3c.660G>T (p.Leu220=)
c.625G>T
17g.47286306A>CCA400023461ITGB3c.661A>C (p.Thr221Pro)
c.626A>C
17g.47286306A>GCA400023462ITGB3c.661A>G (p.Thr221Ala)
c.626A>G
17g.47286306A>TCA400023463ITGB3c.661A>T (p.Thr221Ser)
c.626A>T
17g.47286307C>ACA400023464ITGB3c.662C>A (p.Thr221Lys)
c.627C>A
17g.47286307C=CA2262605989ITGB3c.662C= (p.Thr221=)
c.627C=
17g.47286307C>GCA400023465ITGB3c.662C>G (p.Thr221Arg)
c.627C>G
 gnomAD v4
17g.47286307C>TCA8623017ITGB3c.662C>T (p.Thr221Met)
c.627C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.47286308G>ACA8623018ITGB3c.663G>A (p.Thr221=)
c.628G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.47286308G>CCA500431977ITGB3c.663G>C (p.Thr221=)
c.628G>C
17g.47286308G=CA2262605990ITGB3c.663G= (p.Thr221=)
c.628G=
17g.47286308G>TCA500431978ITGB3c.663G>T (p.Thr221=)
c.628G>T
17g.47286308_47286312delinsGCTAACA2262605991ITGB3c.663_667delinsGCTAA (p.Thr221=)
c.628_632delinsGCTAA
17g.47286309C>ACA400023466ITGB3c.664C>A (p.Leu222Ile)
c.629C>A
17g.47286309C>GCA400023467ITGB3c.664C>G (p.Leu222Val)
c.629C>G
17g.47286309C>TCA500431979ITGB3c.664C>T (p.Leu222=)
c.629C>T
17g.47286311_47286314delCA772537044ITGB3c.666_669del (p.Asp224ArgfsTer2)
c.631_634del
 dbSNP
17g.47286310T>ACA400023468ITGB3c.665T>A (p.Leu222Gln)
c.630T>A
17g.47286310T>CCA291224887ITGB3c.665T>C (p.Leu222Pro)
c.630T>C
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.47286310T>GCA400023469ITGB3c.665T>G (p.Leu222Arg)
c.630T>G
17g.47286310T=CA2262605992ITGB3c.665T= (p.Leu222=)
c.630T=
17g.47286311A>CCA500431981ITGB3c.666A>C (p.Leu222=)
c.631A>C
17g.47286311A>GCA500431982ITGB3c.666A>G (p.Leu222=)
c.631A>G
17g.47286311A>TCA500431980ITGB3c.666A>T (p.Leu222=)
c.631A>T
 dbSNP
17g.47286312A>CCA400023470ITGB3c.667A>C (p.Thr223Pro)
c.632A>C
17g.47286312A>GCA400023471ITGB3c.667A>G (p.Thr223Ala)
c.632A>G
17g.47286312A>TCA400023472ITGB3c.667A>T (p.Thr223Ser)
c.632A>T
17g.47286313C>ACA400023473ITGB3c.668C>A (p.Thr223Asn)
c.633C>A
17g.47286313C>GCA400023474ITGB3c.668C>G (p.Thr223Ser)
c.633C>G
17g.47286313C>TCA400023475ITGB3c.668C>T (p.Thr223Ile)
c.633C>T
17g.47286314T>ACA500431985ITGB3c.669T>A (p.Thr223=)
c.634T>A
17g.47286314T>CCA500431984ITGB3c.669T>C (p.Thr223=)
c.634T>C
17g.47286314T>GCA500431983ITGB3c.669T>G (p.Thr223=)
c.634T>G
 dbSNP
17g.47286315G>ACA8623019ITGB3c.670G>A (p.Asp224Asn)
c.635G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.47286315G>CCA400023476ITGB3c.670G>C (p.Asp224His)
c.635G>C
17g.47286315G=CA2262605993ITGB3c.670G= (p.Asp224=)
c.635G=
17g.47286315G>TCA400023477ITGB3c.670G>T (p.Asp224Tyr)
c.635G>T
17g.47286316A>CCA400023479ITGB3c.671A>C (p.Asp224Ala)
c.636A>C
17g.47286316A>GCA400023480ITGB3c.671A>G (p.Asp224Gly)
c.636A>G
 gnomAD v4
17g.47286316A>TCA400023478ITGB3c.671A>T (p.Asp224Val)
c.636A>T
 gnomAD v4
17g.47286317C>ACA400023481ITGB3c.672C>A (p.Asp224Glu)
c.637C>A
17g.47286317C=CA2262605994ITGB3c.672C= (p.Asp224=)
c.637C=
17g.47286317C>GCA400023482ITGB3c.672C>G (p.Asp224Glu)
c.637C>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.47286317C>TCA8623020ITGB3c.672C>T (p.Asp224=)
c.637C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.47286318C>ACA400023483ITGB3c.673C>A (p.Gln225Lys)
c.638C>A
17g.47286318C>GCA400023484ITGB3c.673C>G (p.Gln225Glu)
c.638C>G
17g.47286318C>TCA400023485ITGB3c.673C>T (p.Gln225Ter)
c.638C>T
17g.47286319delCA915940689ITGB3c.674del (p.Gln225ArgfsTer2)
c.639del
 ClinVar dbSNP
17g.47286319A=CA2262605995ITGB3c.674A= (p.Gln225=)
c.639A=
17g.47286319A>CCA400023486ITGB3c.674A>C (p.Gln225Pro)
c.639A>C
17g.47286319A>GCA8623021ITGB3c.674A>G (p.Gln225Arg)
c.639A>G
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.47286319A>TCA400023487ITGB3c.674A>T (p.Gln225Leu)
c.639A>T
17g.47286320G>ACA500431986ITGB3c.675G>A (p.Gln225=)
c.640G>A
 dbSNP gnomAD v3 gnomAD v4
17g.47286320G>CCA400023488ITGB3c.675G>C (p.Gln225His)
c.640G>C
 gnomAD v4
17g.47286320G=CA2262605996ITGB3c.675G= (p.Gln225=)
c.640G=
17g.47286320G>TCA400023489ITGB3c.675G>T (p.Gln225His)
c.640G>T
17g.47286321G>ACA400023491ITGB3c.676G>A (p.Val226Met)
c.641G>A
17g.47286321G>CCA400023492ITGB3c.676G>C (p.Val226Leu)
c.641G>C
17g.47286321G>TCA400023490ITGB3c.676G>T (p.Val226Leu)
c.641G>T
17g.47286322T>ACA400023493ITGB3c.677T>A (p.Val226Glu)
c.642T>A
17g.47286322T>CCA400023494ITGB3c.677T>C (p.Val226Ala)
c.642T>C
17g.47286322T>GCA400023495ITGB3c.677T>G (p.Val226Gly)
c.642T>G
17g.47286323G>ACA8623022ITGB3c.678G>A (p.Val226=)
c.643G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.47286323G>CCA500431988ITGB3c.678G>C (p.Val226=)
c.643G>C
17g.47286323G=CA2262605997ITGB3c.678G= (p.Val226=)
c.643G=
17g.47286323G>TCA500431989ITGB3c.678G>T (p.Val226=)
c.643G>T
17g.47286324A>CCA400023498ITGB3c.679A>C (p.Thr227Pro)
c.644A>C
17g.47286324A>GCA400023497ITGB3c.679A>G (p.Thr227Ala)
c.644A>G
17g.47286324A>TCA400023496ITGB3c.679A>T (p.Thr227Ser)
c.644A>T

Number of alleles fetched