Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.108626296A>C | CA413855015 | COL4A5 | c.3193A>C (p.Lys1065Gln) n.2649A>C c.426A>C c.2869A>C (p.Lys957Gln) c.766A>C (p.Lys256Gln) c.3208A>C (p.Lys1070Gln) c.1528A>C (p.Lys510Gln) | |
X | g.108626296A>G | CA413855016 | COL4A5 | c.3193A>G (p.Lys1065Glu) n.2649A>G c.426A>G c.2869A>G (p.Lys957Glu) c.766A>G (p.Lys256Glu) c.3208A>G (p.Lys1070Glu) c.1528A>G (p.Lys510Glu) | |
X | g.108626296A>T | CA413855017 | COL4A5 | c.3193A>T (p.Lys1065Ter) n.2649A>T c.426A>T c.2869A>T (p.Lys957Ter) c.766A>T (p.Lys256Ter) c.3208A>T (p.Lys1070Ter) c.1528A>T (p.Lys510Ter) | |
X | g.108626297A>C | CA413855018 | COL4A5 | c.3194A>C (p.Lys1065Thr) n.2650A>C c.427A>C c.2870A>C (p.Lys957Thr) c.767A>C (p.Lys256Thr) c.3209A>C (p.Lys1070Thr) c.1529A>C (p.Lys510Thr) | |
X | g.108626297A>G | CA413855020 | COL4A5 | c.3194A>G (p.Lys1065Arg) n.2650A>G c.427A>G c.2870A>G (p.Lys957Arg) c.767A>G (p.Lys256Arg) c.3209A>G (p.Lys1070Arg) c.1529A>G (p.Lys510Arg) | ClinVar |
X | g.108626297A>T | CA413855019 | COL4A5 | c.3194A>T (p.Lys1065Ile) n.2650A>T c.427A>T c.2870A>T (p.Lys957Ile) c.767A>T (p.Lys256Ile) c.3209A>T (p.Lys1070Ile) c.1529A>T (p.Lys510Ile) | |
X | g.108626298A>C | CA413855021 | COL4A5 | c.3195A>C (p.Lys1065Asn) n.2651A>C c.428A>C c.2871A>C (p.Lys957Asn) c.768A>C (p.Lys256Asn) c.3210A>C (p.Lys1070Asn) c.1530A>C (p.Lys510Asn) | |
X | g.108626298A>G | CA517925970 | COL4A5 | c.3195A>G (p.Lys1065=) n.2651A>G c.428A>G c.2871A>G (p.Lys957=) c.768A>G (p.Lys256=) c.3210A>G (p.Lys1070=) c.1530A>G (p.Lys510=) | gnomAD v4 |
X | g.108626298A>T | CA413855022 | COL4A5 | c.3195A>T (p.Lys1065Asn) n.2651A>T c.428A>T c.2871A>T (p.Lys957Asn) c.768A>T (p.Lys256Asn) c.3210A>T (p.Lys1070Asn) c.1530A>T (p.Lys510Asn) | |
X | g.108626299G>A | CA258827 | COL4A5 | c.3196G>A (p.Gly1066Ser) n.2652G>A c.429G>A c.2872G>A (p.Gly958Ser) c.769G>A (p.Gly257Ser) c.3211G>A (p.Gly1071Ser) c.1531G>A (p.Gly511Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.108626299G>C | CA258825 | COL4A5 | c.3196G>C (p.Gly1066Arg) n.2652G>C c.429G>C c.2872G>C (p.Gly958Arg) c.769G>C (p.Gly257Arg) c.3211G>C (p.Gly1071Arg) c.1531G>C (p.Gly511Arg) | dbSNP |
X | g.108626299G= | CA2450698096 | COL4A5 | c.3196G= (p.Gly1066=) n.2652G= c.429G= c.2872G= (p.Gly958=) c.769G= (p.Gly257=) c.3211G= (p.Gly1071=) c.1531G= (p.Gly511=) | |
X | g.108626299G>T | CA10489043 | COL4A5 | c.3196G>T (p.Gly1066Cys) n.2652G>T c.429G>T c.2872G>T (p.Gly958Cys) c.769G>T (p.Gly257Cys) c.3211G>T (p.Gly1071Cys) c.1531G>T (p.Gly511Cys) | dbSNP ExAC |
X | g.108626300G>A | CA413855023 | COL4A5 | c.3197G>A (p.Gly1066Asp) n.2653G>A c.430G>A c.2873G>A (p.Gly958Asp) c.770G>A (p.Gly257Asp) c.3212G>A (p.Gly1071Asp) c.1532G>A (p.Gly511Asp) | ClinVar dbSNP |
X | g.108626300G>C | CA258829 | COL4A5 | c.3197G>C (p.Gly1066Ala) n.2653G>C c.430G>C c.2873G>C (p.Gly958Ala) c.770G>C (p.Gly257Ala) c.3212G>C (p.Gly1071Ala) c.1532G>C (p.Gly511Ala) | dbSNP |
X | g.108626300G= | CA2450698097 | COL4A5 | c.3197G= (p.Gly1066=) n.2653G= c.430G= c.2873G= (p.Gly958=) c.770G= (p.Gly257=) c.3212G= (p.Gly1071=) c.1532G= (p.Gly511=) | |
X | g.108626300G>T | CA413855024 | COL4A5 | c.3197G>T (p.Gly1066Val) n.2653G>T c.430G>T c.2873G>T (p.Gly958Val) c.770G>T (p.Gly257Val) c.3212G>T (p.Gly1071Val) c.1532G>T (p.Gly511Val) | ClinVar dbSNP |
X | g.108626301T>A | CA517925979 | COL4A5 | c.3198T>A (p.Gly1066=) n.2654T>A c.431T>A c.2874T>A (p.Gly958=) c.771T>A (p.Gly257=) c.3213T>A (p.Gly1071=) c.1533T>A (p.Gly511=) | |
X | g.108626301T>C | CA517925980 | COL4A5 | c.3198T>C (p.Gly1066=) n.2654T>C c.431T>C c.2874T>C (p.Gly958=) c.771T>C (p.Gly257=) c.3213T>C (p.Gly1071=) c.1533T>C (p.Gly511=) | |
X | g.108626301T>G | CA517925982 | COL4A5 | c.3198T>G (p.Gly1066=) n.2654T>G c.431T>G c.2874T>G (p.Gly958=) c.771T>G (p.Gly257=) c.3213T>G (p.Gly1071=) c.1533T>G (p.Gly511=) | dbSNP gnomAD v2 gnomAD v4 |
X | g.108626301T= | CA2450697562 | COL4A5 | c.3198T= (p.Gly1066=) n.2654T= c.431T= c.2874T= (p.Gly958=) c.771T= (p.Gly257=) c.3213T= (p.Gly1071=) c.1533T= (p.Gly511=) | |
X | g.108626302del | CA2579676667 | COL4A5 | c.3199del (p.Asp1067IlefsTer?) n.2655del c.432del c.3199del (p.Asp1067IlefsTer17) c.2875del (p.Asp959IlefsTer?) c.772del (p.Asp258IlefsTer?) c.3214del (p.Asp1072IlefsTer?) c.1534del (p.Asp512IlefsTer?) | |
X | g.108626302G>A | CA413855025 | COL4A5 | c.3199G>A (p.Asp1067Asn) n.2655G>A c.432G>A c.2875G>A (p.Asp959Asn) c.772G>A (p.Asp258Asn) c.3214G>A (p.Asp1072Asn) c.1534G>A (p.Asp512Asn) | |
X | g.108626302G>C | CA413855026 | COL4A5 | c.3199G>C (p.Asp1067His) n.2655G>C c.432G>C c.2875G>C (p.Asp959His) c.772G>C (p.Asp258His) c.3214G>C (p.Asp1072His) c.1534G>C (p.Asp512His) | |
X | g.108626302G>T | CA413855027 | COL4A5 | c.3199G>T (p.Asp1067Tyr) n.2655G>T c.432G>T c.2875G>T (p.Asp959Tyr) c.772G>T (p.Asp258Tyr) c.3214G>T (p.Asp1072Tyr) c.1534G>T (p.Asp512Tyr) | |
X | g.108626303A>C | CA413855029 | COL4A5 | c.3200A>C (p.Asp1067Ala) n.2656A>C c.433A>C c.2876A>C (p.Asp959Ala) c.773A>C (p.Asp258Ala) c.3215A>C (p.Asp1072Ala) c.1535A>C (p.Asp512Ala) | |
X | g.108626303A>G | CA413855030 | COL4A5 | c.3200A>G (p.Asp1067Gly) n.2656A>G c.433A>G c.2876A>G (p.Asp959Gly) c.773A>G (p.Asp258Gly) c.3215A>G (p.Asp1072Gly) c.1535A>G (p.Asp512Gly) | |
X | g.108626303A>T | CA413855028 | COL4A5 | c.3200A>T (p.Asp1067Val) n.2656A>T c.433A>T c.2876A>T (p.Asp959Val) c.773A>T (p.Asp258Val) c.3215A>T (p.Asp1072Val) c.1535A>T (p.Asp512Val) | |
X | g.108626304T>A | CA413855031 | COL4A5 | c.3201T>A (p.Asp1067Glu) n.2657T>A c.434T>A c.2877T>A (p.Asp959Glu) c.774T>A (p.Asp258Glu) c.3216T>A (p.Asp1072Glu) c.1536T>A (p.Asp512Glu) | gnomAD v4 |
X | g.108626304T>C | CA517925984 | COL4A5 | c.3201T>C (p.Asp1067=) n.2657T>C c.434T>C c.2877T>C (p.Asp959=) c.774T>C (p.Asp258=) c.3216T>C (p.Asp1072=) c.1536T>C (p.Asp512=) | |
X | g.108626304T>G | CA413855032 | COL4A5 | c.3201T>G (p.Asp1067Glu) n.2657T>G c.434T>G c.2877T>G (p.Asp959Glu) c.774T>G (p.Asp258Glu) c.3216T>G (p.Asp1072Glu) c.1536T>G (p.Asp512Glu) | |
X | g.108626305C>A | CA413855033 | COL4A5 | c.3202C>A (p.Pro1068Thr) n.2658C>A c.435C>A c.2878C>A (p.Pro960Thr) c.775C>A (p.Pro259Thr) c.3217C>A (p.Pro1073Thr) c.1537C>A (p.Pro513Thr) | dbSNP gnomAD v3 gnomAD v4 |
X | g.108626305C= | CA2450697564 | COL4A5 | c.3202C= (p.Pro1068=) n.2658C= c.435C= c.2878C= (p.Pro960=) c.775C= (p.Pro259=) c.3217C= (p.Pro1073=) c.1537C= (p.Pro513=) | |
X | g.108626305C>G | CA413855034 | COL4A5 | c.3202C>G (p.Pro1068Ala) n.2658C>G c.435C>G c.2878C>G (p.Pro960Ala) c.775C>G (p.Pro259Ala) c.3217C>G (p.Pro1073Ala) c.1537C>G (p.Pro513Ala) | |
X | g.108626305C>T | CA413855035 | COL4A5 | c.3202C>T (p.Pro1068Ser) n.2658C>T c.435C>T c.2878C>T (p.Pro960Ser) c.775C>T (p.Pro259Ser) c.3217C>T (p.Pro1073Ser) c.1537C>T (p.Pro513Ser) | |
X | g.108626306C>A | CA413855036 | COL4A5 | c.3203C>A (p.Pro1068His) n.2659C>A c.436C>A c.2879C>A (p.Pro960His) c.776C>A (p.Pro259His) c.3218C>A (p.Pro1073His) c.1538C>A (p.Pro513His) | |
X | g.108626306C>G | CA413855037 | COL4A5 | c.3203C>G (p.Pro1068Arg) n.2659C>G c.436C>G c.2879C>G (p.Pro960Arg) c.776C>G (p.Pro259Arg) c.3218C>G (p.Pro1073Arg) c.1538C>G (p.Pro513Arg) | |
X | g.108626306C>T | CA413855038 | COL4A5 | c.3203C>T (p.Pro1068Leu) n.2659C>T c.436C>T c.2879C>T (p.Pro960Leu) c.776C>T (p.Pro259Leu) c.3218C>T (p.Pro1073Leu) c.1538C>T (p.Pro513Leu) | |
X | g.108626307T>A | CA517925986 | COL4A5 | c.3204T>A (p.Pro1068=) n.2660T>A c.437T>A c.2880T>A (p.Pro960=) c.777T>A (p.Pro259=) c.3219T>A (p.Pro1073=) c.1539T>A (p.Pro513=) | gnomAD v4 |
X | g.108626307T>C | CA517925988 | COL4A5 | c.3204T>C (p.Pro1068=) n.2660T>C c.437T>C c.2880T>C (p.Pro960=) c.777T>C (p.Pro259=) c.3219T>C (p.Pro1073=) c.1539T>C (p.Pro513=) | |
X | g.108626307T>G | CA517925990 | COL4A5 | c.3204T>G (p.Pro1068=) n.2660T>G c.437T>G c.2880T>G (p.Pro960=) c.777T>G (p.Pro259=) c.3219T>G (p.Pro1073=) c.1539T>G (p.Pro513=) | |
X | g.108626308G>A | CA413855039 | COL4A5 | c.3205G>A (p.Gly1069Ser) n.2661G>A c.438G>A c.2881G>A (p.Gly961Ser) c.778G>A (p.Gly260Ser) c.3220G>A (p.Gly1074Ser) c.1540G>A (p.Gly514Ser) | |
X | g.108626308G>C | CA413855040 | COL4A5 | c.3205G>C (p.Gly1069Arg) n.2661G>C c.438G>C c.2881G>C (p.Gly961Arg) c.778G>C (p.Gly260Arg) c.3220G>C (p.Gly1074Arg) c.1540G>C (p.Gly514Arg) | |
X | g.108626308G>T | CA413855041 | COL4A5 | c.3205G>T (p.Gly1069Cys) n.2661G>T c.438G>T c.2881G>T (p.Gly961Cys) c.778G>T (p.Gly260Cys) c.3220G>T (p.Gly1074Cys) c.1540G>T (p.Gly514Cys) | |
X | g.108626309G>A | CA413855042 | COL4A5 | c.3206G>A (p.Gly1069Asp) n.2662G>A c.439G>A c.2882G>A (p.Gly961Asp) c.779G>A (p.Gly260Asp) c.3221G>A (p.Gly1074Asp) c.1541G>A (p.Gly514Asp) | gnomAD v4 |
X | g.108626309G>C | CA413855043 | COL4A5 | c.3206G>C (p.Gly1069Ala) n.2662G>C c.439G>C c.2882G>C (p.Gly961Ala) c.779G>C (p.Gly260Ala) c.3221G>C (p.Gly1074Ala) c.1541G>C (p.Gly514Ala) | |
X | g.108626309G= | CA2450697572 | COL4A5 | c.3206G= (p.Gly1069=) n.2662G= c.439G= c.2882G= (p.Gly961=) c.779G= (p.Gly260=) c.3221G= (p.Gly1074=) c.1541G= (p.Gly514=) | |
X | g.108626309G>T | CA258832 | COL4A5 | c.3206G>T (p.Gly1069Val) n.2662G>T c.439G>T c.2882G>T (p.Gly961Val) c.779G>T (p.Gly260Val) c.3221G>T (p.Gly1074Val) c.1541G>T (p.Gly514Val) | ClinVar dbSNP |
X | g.108626310T>A | CA517925992 | COL4A5 | c.3207T>A (p.Gly1069=) n.2663T>A c.440T>A c.2883T>A (p.Gly961=) c.780T>A (p.Gly260=) c.3222T>A (p.Gly1074=) c.1542T>A (p.Gly514=) | |
X | g.108626310T>C | CA517925993 | COL4A5 | c.3207T>C (p.Gly1069=) n.2663T>C c.440T>C c.2883T>C (p.Gly961=) c.780T>C (p.Gly260=) c.3222T>C (p.Gly1074=) c.1542T>C (p.Gly514=) |