Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.108626296A>CCA413855015COL4A5c.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)
Xg.108626296A>GCA413855016COL4A5c.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)
Xg.108626296A>TCA413855017COL4A5c.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)
Xg.108626297A>CCA413855018COL4A5c.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)
Xg.108626297A>GCA413855020COL4A5c.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
Xg.108626297A>TCA413855019COL4A5c.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)
Xg.108626298A>CCA413855021COL4A5c.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)
Xg.108626298A>GCA517925970COL4A5c.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
Xg.108626298A>TCA413855022COL4A5c.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)
Xg.108626299G>ACA258827COL4A5c.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
Xg.108626299G>CCA258825COL4A5c.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
Xg.108626299G=CA2450698096COL4A5c.3196G= (p.Gly1066=)
n.2652G=
c.429G=
c.2872G= (p.Gly958=)
c.769G= (p.Gly257=)
c.3211G= (p.Gly1071=)
c.1531G= (p.Gly511=)
Xg.108626299G>TCA10489043COL4A5c.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
Xg.108626300G>ACA413855023COL4A5c.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
Xg.108626300G>CCA258829COL4A5c.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
Xg.108626300G=CA2450698097COL4A5c.3197G= (p.Gly1066=)
n.2653G=
c.430G=
c.2873G= (p.Gly958=)
c.770G= (p.Gly257=)
c.3212G= (p.Gly1071=)
c.1532G= (p.Gly511=)
Xg.108626300G>TCA413855024COL4A5c.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
Xg.108626301T>ACA517925979COL4A5c.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=)
Xg.108626301T>CCA517925980COL4A5c.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=)
Xg.108626301T>GCA517925982COL4A5c.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
Xg.108626301T=CA2450697562COL4A5c.3198T= (p.Gly1066=)
n.2654T=
c.431T=
c.2874T= (p.Gly958=)
c.771T= (p.Gly257=)
c.3213T= (p.Gly1071=)
c.1533T= (p.Gly511=)
Xg.108626302delCA2579676667COL4A5c.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?)
Xg.108626302G>ACA413855025COL4A5c.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)
Xg.108626302G>CCA413855026COL4A5c.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)
Xg.108626302G>TCA413855027COL4A5c.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)
Xg.108626303A>CCA413855029COL4A5c.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)
Xg.108626303A>GCA413855030COL4A5c.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)
Xg.108626303A>TCA413855028COL4A5c.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)
Xg.108626304T>ACA413855031COL4A5c.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
Xg.108626304T>CCA517925984COL4A5c.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=)
Xg.108626304T>GCA413855032COL4A5c.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)
Xg.108626305C>ACA413855033COL4A5c.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
Xg.108626305C=CA2450697564COL4A5c.3202C= (p.Pro1068=)
n.2658C=
c.435C=
c.2878C= (p.Pro960=)
c.775C= (p.Pro259=)
c.3217C= (p.Pro1073=)
c.1537C= (p.Pro513=)
Xg.108626305C>GCA413855034COL4A5c.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)
Xg.108626305C>TCA413855035COL4A5c.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)
Xg.108626306C>ACA413855036COL4A5c.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)
Xg.108626306C>GCA413855037COL4A5c.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)
Xg.108626306C>TCA413855038COL4A5c.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)
Xg.108626307T>ACA517925986COL4A5c.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
Xg.108626307T>CCA517925988COL4A5c.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=)
Xg.108626307T>GCA517925990COL4A5c.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=)
Xg.108626308G>ACA413855039COL4A5c.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)
Xg.108626308G>CCA413855040COL4A5c.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)
Xg.108626308G>TCA413855041COL4A5c.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)
Xg.108626309G>ACA413855042COL4A5c.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
Xg.108626309G>CCA413855043COL4A5c.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)
Xg.108626309G=CA2450697572COL4A5c.3206G= (p.Gly1069=)
n.2662G=
c.439G=
c.2882G= (p.Gly961=)
c.779G= (p.Gly260=)
c.3221G= (p.Gly1074=)
c.1541G= (p.Gly514=)
Xg.108626309G>TCA258832COL4A5c.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
Xg.108626310T>ACA517925992COL4A5c.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=)
Xg.108626310T>CCA517925993COL4A5c.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=)

Number of alleles fetched