Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.108668320_108668505del | CA2695235652 | COL4A5 | c.3606_3790+1del c.3282_3466+1del c.1179_1363+1del c.3621_3805+1del c.1941_2125+1del | |
X | g.108668367_108668439delinsTTCCAGGTCCAAAGGGCGAACCAGGCTTTCACGGTTTCCCTGGTGTGCAGGGTCCCCCAGGCCCTCCTGGTTC | CA2450712935 | COL4A5 | c.3653_3725delinsTTCCAGGTCCAAAGGGCGAACCAGGCTTTCACGGTTTCCCTGGTGTGCAGGGTCCCCCAGGCCCTCCTGGTTC (p.Leu1218=) c.3329_3401delinsTTCCAGGTCCAAAGGGCGAACCAGGCTTTCACGGTTTCCCTGGTGTGCAGGGTCCCCCAGGCCCTCCTGGTTC (p.Leu1110=) c.1226_1298delinsTTCCAGGTCCAAAGGGCGAACCAGGCTTTCACGGTTTCCCTGGTGTGCAGGGTCCCCCAGGCCCTCCTGGTTC (p.Leu409=) c.3668_3740delinsTTCCAGGTCCAAAGGGCGAACCAGGCTTTCACGGTTTCCCTGGTGTGCAGGGTCCCCCAGGCCCTCCTGGTTC (p.Leu1223=) c.1988_2060delinsTTCCAGGTCCAAAGGGCGAACCAGGCTTTCACGGTTTCCCTGGTGTGCAGGGTCCCCCAGGCCCTCCTGGTTC (p.Leu663=) | |
X | g.108668371_108668442del | CA258920 | COL4A5 | c.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 |
X | g.108668409del | CA658659032 | COL4A5 | c.3695del (p.Gly1232ValfsTer?) c.3371del (p.Gly1124ValfsTer?) c.1268del (p.Gly423ValfsTer?) c.3710del (p.Gly1237ValfsTer?) c.2030del (p.Gly677ValfsTer?) | ClinVar dbSNP |
X | g.108668409G>A | CA413848793 | COL4A5 | c.3695G>A (p.Gly1232Asp) c.3371G>A (p.Gly1124Asp) c.1268G>A (p.Gly423Asp) c.3710G>A (p.Gly1237Asp) c.2030G>A (p.Gly677Asp) | ClinVar |
X | g.108668409G>C | CA413848797 | COL4A5 | c.3695G>C (p.Gly1232Ala) c.3371G>C (p.Gly1124Ala) c.1268G>C (p.Gly423Ala) c.3710G>C (p.Gly1237Ala) c.2030G>C (p.Gly677Ala) | |
X | g.108668409G>T | CA413848795 | COL4A5 | c.3695G>T (p.Gly1232Val) c.3371G>T (p.Gly1124Val) c.1268G>T (p.Gly423Val) c.3710G>T (p.Gly1237Val) c.2030G>T (p.Gly677Val) | |
X | g.108668410T>A | CA517922687 | COL4A5 | c.3696T>A (p.Gly1232=) c.3372T>A (p.Gly1124=) c.1269T>A (p.Gly423=) c.3711T>A (p.Gly1237=) c.2031T>A (p.Gly677=) | |
X | g.108668410T>C | CA517922686 | COL4A5 | c.3696T>C (p.Gly1232=) c.3372T>C (p.Gly1124=) c.1269T>C (p.Gly423=) c.3711T>C (p.Gly1237=) c.2031T>C (p.Gly677=) | ClinVar |
X | g.108668410T>G | CA517922685 | COL4A5 | c.3696T>G (p.Gly1232=) c.3372T>G (p.Gly1124=) c.1269T>G (p.Gly423=) c.3711T>G (p.Gly1237=) c.2031T>G (p.Gly677=) | |
X | g.108668411G>A | CA413848799 | COL4A5 | c.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 |
X | g.108668411G>C | CA413848802 | COL4A5 | c.3697G>C (p.Val1233Leu) c.3373G>C (p.Val1125Leu) c.1270G>C (p.Val424Leu) c.3712G>C (p.Val1238Leu) c.2032G>C (p.Val678Leu) | |
X | g.108668411G= | CA2450712953 | COL4A5 | c.3697G= (p.Val1233=) c.3373G= (p.Val1125=) c.1270G= (p.Val424=) c.3712G= (p.Val1238=) c.2032G= (p.Val678=) | |
X | g.108668411G>T | CA413848803 | COL4A5 | c.3697G>T (p.Val1233Leu) c.3373G>T (p.Val1125Leu) c.1270G>T (p.Val424Leu) c.3712G>T (p.Val1238Leu) c.2032G>T (p.Val678Leu) | |
X | g.108668412T>A | CA413848806 | COL4A5 | c.3698T>A (p.Val1233Glu) c.3374T>A (p.Val1125Glu) c.1271T>A (p.Val424Glu) c.3713T>A (p.Val1238Glu) c.2033T>A (p.Val678Glu) | |
X | g.108668412T>C | CA413848807 | COL4A5 | c.3698T>C (p.Val1233Ala) c.3374T>C (p.Val1125Ala) c.1271T>C (p.Val424Ala) c.3713T>C (p.Val1238Ala) c.2033T>C (p.Val678Ala) | |
X | g.108668412T>G | CA413848808 | COL4A5 | c.3698T>G (p.Val1233Gly) c.3374T>G (p.Val1125Gly) c.1271T>G (p.Val424Gly) c.3713T>G (p.Val1238Gly) c.2033T>G (p.Val678Gly) | |
X | g.108668413G>A | CA517922688 | COL4A5 | c.3699G>A (p.Val1233=) c.3375G>A (p.Val1125=) c.1272G>A (p.Val424=) c.3714G>A (p.Val1238=) c.2034G>A (p.Val678=) | ClinVar |
X | g.108668413G>C | CA517922689 | COL4A5 | c.3699G>C (p.Val1233=) c.3375G>C (p.Val1125=) c.1272G>C (p.Val424=) c.3714G>C (p.Val1238=) c.2034G>C (p.Val678=) | |
X | g.108668413G>T | CA517922690 | COL4A5 | c.3699G>T (p.Val1233=) c.3375G>T (p.Val1125=) c.1272G>T (p.Val424=) c.3714G>T (p.Val1238=) c.2034G>T (p.Val678=) | |
X | g.108668414C>A | CA413848809 | COL4A5 | c.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 |
X | g.108668414C= | CA2450712954 | COL4A5 | c.3700C= (p.Gln1234=) c.3376C= (p.Gln1126=) c.1273C= (p.Gln425=) c.3715C= (p.Gln1239=) c.2035C= (p.Gln679=) | |
X | g.108668414C>G | CA413848811 | COL4A5 | c.3700C>G (p.Gln1234Glu) c.3376C>G (p.Gln1126Glu) c.1273C>G (p.Gln425Glu) c.3715C>G (p.Gln1239Glu) c.2035C>G (p.Gln679Glu) | |
X | g.108668414C>T | CA258935 | COL4A5 | c.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 |
X | g.108668415A>C | CA413848816 | COL4A5 | c.3701A>C (p.Gln1234Pro) c.3377A>C (p.Gln1126Pro) c.1274A>C (p.Gln425Pro) c.3716A>C (p.Gln1239Pro) c.2036A>C (p.Gln679Pro) | |
X | g.108668415A>G | CA413848818 | COL4A5 | c.3701A>G (p.Gln1234Arg) c.3377A>G (p.Gln1126Arg) c.1274A>G (p.Gln425Arg) c.3716A>G (p.Gln1239Arg) c.2036A>G (p.Gln679Arg) | |
X | g.108668415A>T | CA413848820 | COL4A5 | c.3701A>T (p.Gln1234Leu) c.3377A>T (p.Gln1126Leu) c.1274A>T (p.Gln425Leu) c.3716A>T (p.Gln1239Leu) c.2036A>T (p.Gln679Leu) | |
X | g.108668416G>A | CA517922691 | COL4A5 | c.3702G>A (p.Gln1234=) c.3378G>A (p.Gln1126=) c.1275G>A (p.Gln425=) c.3717G>A (p.Gln1239=) c.2037G>A (p.Gln679=) | |
X | g.108668416G>C | CA413848826 | COL4A5 | c.3702G>C (p.Gln1234His) c.3378G>C (p.Gln1126His) c.1275G>C (p.Gln425His) c.3717G>C (p.Gln1239His) c.2037G>C (p.Gln679His) | |
X | g.108668416G>T | CA413848824 | COL4A5 | c.3702G>T (p.Gln1234His) c.3378G>T (p.Gln1126His) c.1275G>T (p.Gln425His) c.3717G>T (p.Gln1239His) c.2037G>T (p.Gln679His) | |
X | g.108668422_108668448del | CA2695235655 | COL4A5 | c.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) | |
X | g.108668417G>A | CA413848829 | COL4A5 | c.3703G>A (p.Gly1235Ser) c.3379G>A (p.Gly1127Ser) c.1276G>A (p.Gly426Ser) c.3718G>A (p.Gly1240Ser) c.2038G>A (p.Gly680Ser) | |
X | g.108668417G>C | CA413848832 | COL4A5 | c.3703G>C (p.Gly1235Arg) c.3379G>C (p.Gly1127Arg) c.1276G>C (p.Gly426Arg) c.3718G>C (p.Gly1240Arg) c.2038G>C (p.Gly680Arg) | |
X | g.108668417G>T | CA413848834 | COL4A5 | c.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 |
X | g.108668418G>A | CA413848838 | COL4A5 | c.3704G>A (p.Gly1235Asp) c.3380G>A (p.Gly1127Asp) c.1277G>A (p.Gly426Asp) c.3719G>A (p.Gly1240Asp) c.2039G>A (p.Gly680Asp) | |
X | g.108668418G>C | CA413848840 | COL4A5 | c.3704G>C (p.Gly1235Ala) c.3380G>C (p.Gly1127Ala) c.1277G>C (p.Gly426Ala) c.3719G>C (p.Gly1240Ala) c.2039G>C (p.Gly680Ala) | ClinVar |
X | g.108668418G= | CA2450712955 | COL4A5 | c.3704G= (p.Gly1235=) c.3380G= (p.Gly1127=) c.1277G= (p.Gly426=) c.3719G= (p.Gly1240=) c.2039G= (p.Gly680=) | |
X | g.108668418G>T | CA413848843 | COL4A5 | c.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 |
X | g.108668419T>A | CA517922692 | COL4A5 | c.3705T>A (p.Gly1235=) c.3381T>A (p.Gly1127=) c.1278T>A (p.Gly426=) c.3720T>A (p.Gly1240=) c.2040T>A (p.Gly680=) | |
X | g.108668419T>C | CA517922693 | COL4A5 | c.3705T>C (p.Gly1235=) c.3381T>C (p.Gly1127=) c.1278T>C (p.Gly426=) c.3720T>C (p.Gly1240=) c.2040T>C (p.Gly680=) | |
X | g.108668419T>G | CA517922694 | COL4A5 | c.3705T>G (p.Gly1235=) c.3381T>G (p.Gly1127=) c.1278T>G (p.Gly426=) c.3720T>G (p.Gly1240=) c.2040T>G (p.Gly680=) | |
X | g.108668419T= | CA2450712956 | COL4A5 | c.3705T= (p.Gly1235=) c.3381T= (p.Gly1127=) c.1278T= (p.Gly426=) c.3720T= (p.Gly1240=) c.2040T= (p.Gly680=) | |
X | g.108668419_108668436delinsTCCCCCAGGCCCTCCTGG | CA2450712957 | COL4A5 | c.3705_3722delinsTCCCCCAGGCCCTCCTGG (p.Gly1235=) c.3381_3398delinsTCCCCCAGGCCCTCCTGG (p.Gly1127=) c.1278_1295delinsTCCCCCAGGCCCTCCTGG (p.Gly426=) c.3720_3737delinsTCCCCCAGGCCCTCCTGG (p.Gly1240=) c.2040_2057delinsTCCCCCAGGCCCTCCTGG (p.Gly680=) | |
X | g.108668420C>A | CA413848856 | COL4A5 | c.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 |
X | g.108668420C= | CA2450712959 | COL4A5 | c.3706C= (p.Pro1236=) c.3382C= (p.Pro1128=) c.1279C= (p.Pro427=) c.3721C= (p.Pro1241=) c.2041C= (p.Pro681=) | |
X | g.108668420C>G | CA413848855 | COL4A5 | c.3706C>G (p.Pro1236Ala) c.3382C>G (p.Pro1128Ala) c.1279C>G (p.Pro427Ala) c.3721C>G (p.Pro1241Ala) c.2041C>G (p.Pro681Ala) | ClinVar dbSNP gnomAD v4 |
X | g.108668420C>T | CA413848852 | COL4A5 | c.3706C>T (p.Pro1236Ser) c.3382C>T (p.Pro1128Ser) c.1279C>T (p.Pro427Ser) c.3721C>T (p.Pro1241Ser) c.2041C>T (p.Pro681Ser) | dbSNP gnomAD v4 |
X | g.108668423_108668424dup | CA258941 | COL4A5 | c.3709_3710dup (p.Gly1238GlnfsTer?) c.3385_3386dup (p.Gly1130GlnfsTer?) c.1282_1283dup (p.Gly429GlnfsTer?) c.3724_3725dup (p.Gly1243GlnfsTer?) c.2044_2045dup (p.Gly683GlnfsTer?) | dbSNP |
X | g.108668424del | CA2695235656 | COL4A5 | c.3710del (p.Pro1237GlnfsTer?) c.3386del (p.Pro1129GlnfsTer?) c.1283del (p.Pro428GlnfsTer?) c.3725del (p.Pro1242GlnfsTer?) c.2045del (p.Pro682GlnfsTer?) | |
X | g.108668420_108668433del | CA2573159109 | COL4A5 | c.3706_3719del (p.Pro1236TrpfsTer11) c.3382_3395del (p.Pro1128TrpfsTer11) c.1279_1292del (p.Pro427TrpfsTer11) c.3721_3734del (p.Pro1241TrpfsTer11) c.2041_2054del (p.Pro681TrpfsTer11) | dbSNP |