Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.108668320_108668505delCA2695235652COL4A5c.3606_3790+1del
c.3282_3466+1del
c.1179_1363+1del
c.3621_3805+1del
c.1941_2125+1del
Xg.108668367_108668439delinsTTCCAGGTCCAAAGGGCGAACCAGGCTTTCACGGTTTCCCTGGTGTGCAGGGTCCCCCAGGCCCTCCTGGTTCCA2450712935COL4A5c.3653_3725delinsTTCCAGGTCCAAAGGGCGAACCAGGCTTTCACGGTTTCCCTGGTGTGCAGGGTCCCCCAGGCCCTCCTGGTTC (p.Leu1218=)
c.3329_3401delinsTTCCAGGTCCAAAGGGCGAACCAGGCTTTCACGGTTTCCCTGGTGTGCAGGGTCCCCCAGGCCCTCCTGGTTC (p.Leu1110=)
c.1226_1298delinsTTCCAGGTCCAAAGGGCGAACCAGGCTTTCACGGTTTCCCTGGTGTGCAGGGTCCCCCAGGCCCTCCTGGTTC (p.Leu409=)
c.3668_3740delinsTTCCAGGTCCAAAGGGCGAACCAGGCTTTCACGGTTTCCCTGGTGTGCAGGGTCCCCCAGGCCCTCCTGGTTC (p.Leu1223=)
c.1988_2060delinsTTCCAGGTCCAAAGGGCGAACCAGGCTTTCACGGTTTCCCTGGTGTGCAGGGTCCCCCAGGCCCTCCTGGTTC (p.Leu663=)
Xg.108668371_108668442delCA258920COL4A5c.3657_3728del (p.Gly1220_Pro1243del)
c.3333_3404del (p.Gly1112_Pro1135del)
c.1230_1301del (p.Gly411_Pro434del)
c.3672_3743del (p.Gly1225_Pro1248del)
c.1992_2063del (p.Gly665_Pro688del)
dbSNP
Xg.108668407_108668408delinsTGCA2450712951COL4A5c.3693_3694delinsTG (p.Pro1231=)
c.3369_3370delinsTG (p.Pro1123=)
c.1266_1267delinsTG (p.Pro422=)
c.3708_3709delinsTG (p.Pro1236=)
c.2028_2029delinsTG (p.Pro676=)
Xg.108668408G>ACA258932COL4A5c.3694G>A (p.Gly1232Ser)
c.3370G>A (p.Gly1124Ser)
c.1267G>A (p.Gly423Ser)
c.3709G>A (p.Gly1237Ser)
c.2029G>A (p.Gly677Ser)
dbSNP
Xg.108668408G>CCA413848789COL4A5c.3694G>C (p.Gly1232Arg)
c.3370G>C (p.Gly1124Arg)
c.1267G>C (p.Gly423Arg)
c.3709G>C (p.Gly1237Arg)
c.2029G>C (p.Gly677Arg)
Xg.108668408G=CA2450712952COL4A5c.3694G= (p.Gly1232=)
c.3370G= (p.Gly1124=)
c.1267G= (p.Gly423=)
c.3709G= (p.Gly1237=)
c.2029G= (p.Gly677=)
Xg.108668408G>TCA413848786COL4A5c.3694G>T (p.Gly1232Cys)
c.3370G>T (p.Gly1124Cys)
c.1267G>T (p.Gly423Cys)
c.3709G>T (p.Gly1237Cys)
c.2029G>T (p.Gly677Cys)
Xg.108668409delCA658659032COL4A5c.3695del (p.Gly1232ValfsTer?)
c.3371del (p.Gly1124ValfsTer?)
c.1268del (p.Gly423ValfsTer?)
c.3710del (p.Gly1237ValfsTer?)
c.2030del (p.Gly677ValfsTer?)
ClinVar dbSNP
Xg.108668409G>ACA413848793COL4A5c.3695G>A (p.Gly1232Asp)
c.3371G>A (p.Gly1124Asp)
c.1268G>A (p.Gly423Asp)
c.3710G>A (p.Gly1237Asp)
c.2030G>A (p.Gly677Asp)
Xg.108668409G>CCA413848797COL4A5c.3695G>C (p.Gly1232Ala)
c.3371G>C (p.Gly1124Ala)
c.1268G>C (p.Gly423Ala)
c.3710G>C (p.Gly1237Ala)
c.2030G>C (p.Gly677Ala)
Xg.108668409G>TCA413848795COL4A5c.3695G>T (p.Gly1232Val)
c.3371G>T (p.Gly1124Val)
c.1268G>T (p.Gly423Val)
c.3710G>T (p.Gly1237Val)
c.2030G>T (p.Gly677Val)
Xg.108668410T>ACA517922687COL4A5c.3696T>A (p.Gly1232=)
c.3372T>A (p.Gly1124=)
c.1269T>A (p.Gly423=)
c.3711T>A (p.Gly1237=)
c.2031T>A (p.Gly677=)
Xg.108668410T>CCA517922686COL4A5c.3696T>C (p.Gly1232=)
c.3372T>C (p.Gly1124=)
c.1269T>C (p.Gly423=)
c.3711T>C (p.Gly1237=)
c.2031T>C (p.Gly677=)
Xg.108668410T>GCA517922685COL4A5c.3696T>G (p.Gly1232=)
c.3372T>G (p.Gly1124=)
c.1269T>G (p.Gly423=)
c.3711T>G (p.Gly1237=)
c.2031T>G (p.Gly677=)
Xg.108668411G>ACA413848799COL4A5c.3697G>A (p.Val1233Met)
c.3373G>A (p.Val1125Met)
c.1270G>A (p.Val424Met)
c.3712G>A (p.Val1238Met)
c.2032G>A (p.Val678Met)
dbSNP
Xg.108668411G>CCA413848802COL4A5c.3697G>C (p.Val1233Leu)
c.3373G>C (p.Val1125Leu)
c.1270G>C (p.Val424Leu)
c.3712G>C (p.Val1238Leu)
c.2032G>C (p.Val678Leu)
Xg.108668411G=CA2450712953COL4A5c.3697G= (p.Val1233=)
c.3373G= (p.Val1125=)
c.1270G= (p.Val424=)
c.3712G= (p.Val1238=)
c.2032G= (p.Val678=)
Xg.108668411G>TCA413848803COL4A5c.3697G>T (p.Val1233Leu)
c.3373G>T (p.Val1125Leu)
c.1270G>T (p.Val424Leu)
c.3712G>T (p.Val1238Leu)
c.2032G>T (p.Val678Leu)
Xg.108668412T>ACA413848806COL4A5c.3698T>A (p.Val1233Glu)
c.3374T>A (p.Val1125Glu)
c.1271T>A (p.Val424Glu)
c.3713T>A (p.Val1238Glu)
c.2033T>A (p.Val678Glu)
Xg.108668412T>CCA413848807COL4A5c.3698T>C (p.Val1233Ala)
c.3374T>C (p.Val1125Ala)
c.1271T>C (p.Val424Ala)
c.3713T>C (p.Val1238Ala)
c.2033T>C (p.Val678Ala)
Xg.108668412T>GCA413848808COL4A5c.3698T>G (p.Val1233Gly)
c.3374T>G (p.Val1125Gly)
c.1271T>G (p.Val424Gly)
c.3713T>G (p.Val1238Gly)
c.2033T>G (p.Val678Gly)
Xg.108668413G>ACA517922688COL4A5c.3699G>A (p.Val1233=)
c.3375G>A (p.Val1125=)
c.1272G>A (p.Val424=)
c.3714G>A (p.Val1238=)
c.2034G>A (p.Val678=)
Xg.108668413G>CCA517922689COL4A5c.3699G>C (p.Val1233=)
c.3375G>C (p.Val1125=)
c.1272G>C (p.Val424=)
c.3714G>C (p.Val1238=)
c.2034G>C (p.Val678=)
Xg.108668413G>TCA517922690COL4A5c.3699G>T (p.Val1233=)
c.3375G>T (p.Val1125=)
c.1272G>T (p.Val424=)
c.3714G>T (p.Val1238=)
c.2034G>T (p.Val678=)
Xg.108668414C>ACA413848809COL4A5c.3700C>A (p.Gln1234Lys)
c.3376C>A (p.Gln1126Lys)
c.1273C>A (p.Gln425Lys)
c.3715C>A (p.Gln1239Lys)
c.2035C>A (p.Gln679Lys)
COSMIC COSMIC
Xg.108668414C=CA2450712954COL4A5c.3700C= (p.Gln1234=)
c.3376C= (p.Gln1126=)
c.1273C= (p.Gln425=)
c.3715C= (p.Gln1239=)
c.2035C= (p.Gln679=)
Xg.108668414C>GCA413848811COL4A5c.3700C>G (p.Gln1234Glu)
c.3376C>G (p.Gln1126Glu)
c.1273C>G (p.Gln425Glu)
c.3715C>G (p.Gln1239Glu)
c.2035C>G (p.Gln679Glu)
Xg.108668414C>TCA258935COL4A5c.3700C>T (p.Gln1234Ter)
c.3376C>T (p.Gln1126Ter)
c.1273C>T (p.Gln425Ter)
c.3715C>T (p.Gln1239Ter)
c.2035C>T (p.Gln679Ter)
dbSNP
Xg.108668415A>CCA413848816COL4A5c.3701A>C (p.Gln1234Pro)
c.3377A>C (p.Gln1126Pro)
c.1274A>C (p.Gln425Pro)
c.3716A>C (p.Gln1239Pro)
c.2036A>C (p.Gln679Pro)
Xg.108668415A>GCA413848818COL4A5c.3701A>G (p.Gln1234Arg)
c.3377A>G (p.Gln1126Arg)
c.1274A>G (p.Gln425Arg)
c.3716A>G (p.Gln1239Arg)
c.2036A>G (p.Gln679Arg)
Xg.108668415A>TCA413848820COL4A5c.3701A>T (p.Gln1234Leu)
c.3377A>T (p.Gln1126Leu)
c.1274A>T (p.Gln425Leu)
c.3716A>T (p.Gln1239Leu)
c.2036A>T (p.Gln679Leu)
Xg.108668416G>ACA517922691COL4A5c.3702G>A (p.Gln1234=)
c.3378G>A (p.Gln1126=)
c.1275G>A (p.Gln425=)
c.3717G>A (p.Gln1239=)
c.2037G>A (p.Gln679=)
Xg.108668416G>CCA413848826COL4A5c.3702G>C (p.Gln1234His)
c.3378G>C (p.Gln1126His)
c.1275G>C (p.Gln425His)
c.3717G>C (p.Gln1239His)
c.2037G>C (p.Gln679His)
Xg.108668416G>TCA413848824COL4A5c.3702G>T (p.Gln1234His)
c.3378G>T (p.Gln1126His)
c.1275G>T (p.Gln425His)
c.3717G>T (p.Gln1239His)
c.2037G>T (p.Gln679His)
Xg.108668422_108668448delCA2695235655COL4A5c.3708_3734del (p.Pro1237_Pro1245del)
c.3384_3410del (p.Pro1129_Pro1137del)
c.1281_1307del (p.Pro428_Pro436del)
c.3723_3749del (p.Pro1242_Pro1250del)
c.2043_2069del (p.Pro682_Pro690del)
Xg.108668417G>ACA413848829COL4A5c.3703G>A (p.Gly1235Ser)
c.3379G>A (p.Gly1127Ser)
c.1276G>A (p.Gly426Ser)
c.3718G>A (p.Gly1240Ser)
c.2038G>A (p.Gly680Ser)
Xg.108668417G>CCA413848832COL4A5c.3703G>C (p.Gly1235Arg)
c.3379G>C (p.Gly1127Arg)
c.1276G>C (p.Gly426Arg)
c.3718G>C (p.Gly1240Arg)
c.2038G>C (p.Gly680Arg)
Xg.108668417G>TCA413848834COL4A5c.3703G>T (p.Gly1235Cys)
c.3379G>T (p.Gly1127Cys)
c.1276G>T (p.Gly426Cys)
c.3718G>T (p.Gly1240Cys)
c.2038G>T (p.Gly680Cys)
ClinVar dbSNP
Xg.108668418G>ACA413848838COL4A5c.3704G>A (p.Gly1235Asp)
c.3380G>A (p.Gly1127Asp)
c.1277G>A (p.Gly426Asp)
c.3719G>A (p.Gly1240Asp)
c.2039G>A (p.Gly680Asp)
Xg.108668418G>CCA413848840COL4A5c.3704G>C (p.Gly1235Ala)
c.3380G>C (p.Gly1127Ala)
c.1277G>C (p.Gly426Ala)
c.3719G>C (p.Gly1240Ala)
c.2039G>C (p.Gly680Ala)
Xg.108668418G=CA2450712955COL4A5c.3704G= (p.Gly1235=)
c.3380G= (p.Gly1127=)
c.1277G= (p.Gly426=)
c.3719G= (p.Gly1240=)
c.2039G= (p.Gly680=)
Xg.108668418G>TCA413848843COL4A5c.3704G>T (p.Gly1235Val)
c.3380G>T (p.Gly1127Val)
c.1277G>T (p.Gly426Val)
c.3719G>T (p.Gly1240Val)
c.2039G>T (p.Gly680Val)
ClinVar dbSNP
Xg.108668419T>ACA517922692COL4A5c.3705T>A (p.Gly1235=)
c.3381T>A (p.Gly1127=)
c.1278T>A (p.Gly426=)
c.3720T>A (p.Gly1240=)
c.2040T>A (p.Gly680=)
Xg.108668419T>CCA517922693COL4A5c.3705T>C (p.Gly1235=)
c.3381T>C (p.Gly1127=)
c.1278T>C (p.Gly426=)
c.3720T>C (p.Gly1240=)
c.2040T>C (p.Gly680=)
Xg.108668419T>GCA517922694COL4A5c.3705T>G (p.Gly1235=)
c.3381T>G (p.Gly1127=)
c.1278T>G (p.Gly426=)
c.3720T>G (p.Gly1240=)
c.2040T>G (p.Gly680=)
Xg.108668419T=CA2450712956COL4A5c.3705T= (p.Gly1235=)
c.3381T= (p.Gly1127=)
c.1278T= (p.Gly426=)
c.3720T= (p.Gly1240=)
c.2040T= (p.Gly680=)
Xg.108668419_108668436delinsTCCCCCAGGCCCTCCTGGCA2450712957COL4A5c.3705_3722delinsTCCCCCAGGCCCTCCTGG (p.Gly1235=)
c.3381_3398delinsTCCCCCAGGCCCTCCTGG (p.Gly1127=)
c.1278_1295delinsTCCCCCAGGCCCTCCTGG (p.Gly426=)
c.3720_3737delinsTCCCCCAGGCCCTCCTGG (p.Gly1240=)
c.2040_2057delinsTCCCCCAGGCCCTCCTGG (p.Gly680=)
Xg.108668420C>ACA413848856COL4A5c.3706C>A (p.Pro1236Thr)
c.3382C>A (p.Pro1128Thr)
c.1279C>A (p.Pro427Thr)
c.3721C>A (p.Pro1241Thr)
c.2041C>A (p.Pro681Thr)
COSMIC COSMIC
Xg.108668420C=CA2450712959COL4A5c.3706C= (p.Pro1236=)
c.3382C= (p.Pro1128=)
c.1279C= (p.Pro427=)
c.3721C= (p.Pro1241=)
c.2041C= (p.Pro681=)

Number of alleles fetched