Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.108626315C>ACA413855053COL4A5c.3212C>A (p.Ser1071Ter)
n.2668C>A
c.445C>A
c.2888C>A (p.Ser963Ter)
c.785C>A (p.Ser262Ter)
c.3227C>A (p.Ser1076Ter)
c.1547C>A (p.Ser516Ter)
Xg.108626315C=CA2450697580COL4A5c.3212C= (p.Ser1071=)
n.2668C=
c.445C=
c.2888C= (p.Ser963=)
c.785C= (p.Ser262=)
c.3227C= (p.Ser1076=)
c.1547C= (p.Ser516=)
Xg.108626315C>GCA258835COL4A5c.3212C>G (p.Ser1071Ter)
n.2668C>G
c.445C>G
c.2888C>G (p.Ser963Ter)
c.785C>G (p.Ser262Ter)
c.3227C>G (p.Ser1076Ter)
c.1547C>G (p.Ser516Ter)
dbSNP
Xg.108626315C>TCA413855054COL4A5c.3212C>T (p.Ser1071Leu)
n.2668C>T
c.445C>T
c.2888C>T (p.Ser963Leu)
c.785C>T (p.Ser262Leu)
c.3227C>T (p.Ser1076Leu)
c.1547C>T (p.Ser516Leu)
Xg.108626316A>CCA517926002COL4A5c.3213A>C (p.Ser1071=)
n.2669A>C
c.446A>C
c.2889A>C (p.Ser963=)
c.786A>C (p.Ser262=)
c.3228A>C (p.Ser1076=)
c.1548A>C (p.Ser516=)
Xg.108626316A>GCA517926004COL4A5c.3213A>G (p.Ser1071=)
n.2669A>G
c.446A>G
c.2889A>G (p.Ser963=)
c.786A>G (p.Ser262=)
c.3228A>G (p.Ser1076=)
c.1548A>G (p.Ser516=)
Xg.108626316A>TCA517926005COL4A5c.3213A>T (p.Ser1071=)
n.2669A>T
c.446A>T
c.2889A>T (p.Ser963=)
c.786A>T (p.Ser262=)
c.3228A>T (p.Ser1076=)
c.1548A>T (p.Ser516=)
Xg.108626317A>CCA413855056COL4A5c.3214A>C (p.Ser1072Arg)
n.2670A>C
c.447A>C
c.2890A>C (p.Ser964Arg)
c.787A>C (p.Ser263Arg)
c.3229A>C (p.Ser1077Arg)
c.1549A>C (p.Ser517Arg)
Xg.108626317A>GCA413855057COL4A5c.3214A>G (p.Ser1072Gly)
n.2670A>G
c.447A>G
c.2890A>G (p.Ser964Gly)
c.787A>G (p.Ser263Gly)
c.3229A>G (p.Ser1077Gly)
c.1549A>G (p.Ser517Gly)
Xg.108626317A>TCA413855055COL4A5c.3214A>T (p.Ser1072Cys)
n.2670A>T
c.447A>T
c.2890A>T (p.Ser964Cys)
c.787A>T (p.Ser263Cys)
c.3229A>T (p.Ser1077Cys)
c.1549A>T (p.Ser517Cys)
Xg.108626319_108626332delCA2697544691COL4A5c.3216_3229del (p.Ser1072ArgfsTer8)
n.2672_2685del
c.449_462del
c.3216_3229del (p.Ser1072ArgfsTer?)
c.2892_2905del (p.Ser964ArgfsTer8)
c.789_802del (p.Ser263ArgfsTer8)
c.3231_3244del (p.Ser1077ArgfsTer8)
c.1551_1564del (p.Ser517ArgfsTer8)
Xg.108626318G>ACA413855059COL4A5c.3215G>A (p.Ser1072Asn)
n.2671G>A
c.448G>A
c.2891G>A (p.Ser964Asn)
c.788G>A (p.Ser263Asn)
c.3230G>A (p.Ser1077Asn)
c.1550G>A (p.Ser517Asn)
dbSNP gnomAD v3 gnomAD v4
Xg.108626318G>CCA413855060COL4A5c.3215G>C (p.Ser1072Thr)
n.2671G>C
c.448G>C
c.2891G>C (p.Ser964Thr)
c.788G>C (p.Ser263Thr)
c.3230G>C (p.Ser1077Thr)
c.1550G>C (p.Ser517Thr)
Xg.108626318G=CA2450697584COL4A5c.3215G= (p.Ser1072=)
n.2671G=
c.448G=
c.2891G= (p.Ser964=)
c.788G= (p.Ser263=)
c.3230G= (p.Ser1077=)
c.1550G= (p.Ser517=)
Xg.108626318G>TCA413855061COL4A5c.3215G>T (p.Ser1072Ile)
n.2671G>T
c.448G>T
c.2891G>T (p.Ser964Ile)
c.788G>T (p.Ser263Ile)
c.3230G>T (p.Ser1077Ile)
c.1550G>T (p.Ser517Ile)
Xg.108626319C>ACA413855062COL4A5c.3216C>A (p.Ser1072Arg)
n.2672C>A
c.449C>A
c.2892C>A (p.Ser964Arg)
c.789C>A (p.Ser263Arg)
c.3231C>A (p.Ser1077Arg)
c.1551C>A (p.Ser517Arg)
gnomAD v4
Xg.108626319C>GCA413855063COL4A5c.3216C>G (p.Ser1072Arg)
n.2672C>G
c.449C>G
c.2892C>G (p.Ser964Arg)
c.789C>G (p.Ser263Arg)
c.3231C>G (p.Ser1077Arg)
c.1551C>G (p.Ser517Arg)
Xg.108626319C>TCA517926006COL4A5c.3216C>T (p.Ser1072=)
n.2672C>T
c.449C>T
c.2892C>T (p.Ser964=)
c.789C>T (p.Ser263=)
c.3231C>T (p.Ser1077=)
c.1551C>T (p.Ser517=)
Xg.108626320A=CA2450697587COL4A5c.3217A= (p.Ile1073=)
n.2673A=
c.450A=
c.2893A= (p.Ile965=)
c.790A= (p.Ile264=)
c.3232A= (p.Ile1078=)
c.1552A= (p.Ile518=)
Xg.108626320A>CCA413855064COL4A5c.3217A>C (p.Ile1073Leu)
n.2673A>C
c.450A>C
c.2893A>C (p.Ile965Leu)
c.790A>C (p.Ile264Leu)
c.3232A>C (p.Ile1078Leu)
c.1552A>C (p.Ile518Leu)
Xg.108626320A>GCA413855065COL4A5c.3217A>G (p.Ile1073Val)
n.2673A>G
c.450A>G
c.2893A>G (p.Ile965Val)
c.790A>G (p.Ile264Val)
c.3232A>G (p.Ile1078Val)
c.1552A>G (p.Ile518Val)
dbSNP
Xg.108626320A>TCA413855066COL4A5c.3217A>T (p.Ile1073Phe)
n.2673A>T
c.450A>T
c.2893A>T (p.Ile965Phe)
c.790A>T (p.Ile264Phe)
c.3232A>T (p.Ile1078Phe)
c.1552A>T (p.Ile518Phe)
Xg.108626321T>ACA413855067COL4A5c.3218T>A (p.Ile1073Asn)
n.2674T>A
c.451T>A
c.2894T>A (p.Ile965Asn)
c.791T>A (p.Ile264Asn)
c.3233T>A (p.Ile1078Asn)
c.1553T>A (p.Ile518Asn)
Xg.108626321T>CCA413855068COL4A5c.3218T>C (p.Ile1073Thr)
n.2674T>C
c.451T>C
c.2894T>C (p.Ile965Thr)
c.791T>C (p.Ile264Thr)
c.3233T>C (p.Ile1078Thr)
c.1553T>C (p.Ile518Thr)
dbSNP gnomAD v2
Xg.108626321T>GCA413855069COL4A5c.3218T>G (p.Ile1073Ser)
n.2674T>G
c.451T>G
c.2894T>G (p.Ile965Ser)
c.791T>G (p.Ile264Ser)
c.3233T>G (p.Ile1078Ser)
c.1553T>G (p.Ile518Ser)
Xg.108626321T=CA2450697590COL4A5c.3218T= (p.Ile1073=)
n.2674T=
c.451T=
c.2894T= (p.Ile965=)
c.791T= (p.Ile264=)
c.3233T= (p.Ile1078=)
c.1553T= (p.Ile518=)
Xg.108626322T>ACA517926008COL4A5c.3219T>A (p.Ile1073=)
n.2675T>A
c.452T>A
c.2895T>A (p.Ile965=)
c.792T>A (p.Ile264=)
c.3234T>A (p.Ile1078=)
c.1554T>A (p.Ile518=)
Xg.108626322T>CCA517926009COL4A5c.3219T>C (p.Ile1073=)
n.2675T>C
c.452T>C
c.2895T>C (p.Ile965=)
c.792T>C (p.Ile264=)
c.3234T>C (p.Ile1078=)
c.1554T>C (p.Ile518=)
Xg.108626322T>GCA413855070COL4A5c.3219T>G (p.Ile1073Met)
n.2675T>G
c.452T>G
c.2895T>G (p.Ile965Met)
c.792T>G (p.Ile264Met)
c.3234T>G (p.Ile1078Met)
c.1554T>G (p.Ile518Met)
Xg.108626323G>ACA10489045COL4A5c.3220G>A (p.Gly1074Ser)
n.2676G>A
c.453G>A
c.2896G>A (p.Gly966Ser)
c.793G>A (p.Gly265Ser)
c.3235G>A (p.Gly1079Ser)
c.1555G>A (p.Gly519Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.108626323G>CCA10489046COL4A5c.3220G>C (p.Gly1074Arg)
n.2676G>C
c.453G>C
c.2896G>C (p.Gly966Arg)
c.793G>C (p.Gly265Arg)
c.3235G>C (p.Gly1079Arg)
c.1555G>C (p.Gly519Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
Xg.108626323G=CA2450697596COL4A5c.3220G= (p.Gly1074=)
n.2676G=
c.453G=
c.2896G= (p.Gly966=)
c.793G= (p.Gly265=)
c.3235G= (p.Gly1079=)
c.1555G= (p.Gly519=)
Xg.108626323G>TCA413855071COL4A5c.3220G>T (p.Gly1074Cys)
n.2676G>T
c.453G>T
c.2896G>T (p.Gly966Cys)
c.793G>T (p.Gly265Cys)
c.3235G>T (p.Gly1079Cys)
c.1555G>T (p.Gly519Cys)
gnomAD v4
Xg.108626324G>ACA413855072COL4A5c.3221G>A (p.Gly1074Asp)
n.2677G>A
c.454G>A
c.2897G>A (p.Gly966Asp)
c.794G>A (p.Gly265Asp)
c.3236G>A (p.Gly1079Asp)
c.1556G>A (p.Gly519Asp)
Xg.108626324G>CCA413855073COL4A5c.3221G>C (p.Gly1074Ala)
n.2677G>C
c.454G>C
c.2897G>C (p.Gly966Ala)
c.794G>C (p.Gly265Ala)
c.3236G>C (p.Gly1079Ala)
c.1556G>C (p.Gly519Ala)
Xg.108626324G>TCA413855074COL4A5c.3221G>T (p.Gly1074Val)
n.2677G>T
c.454G>T
c.2897G>T (p.Gly966Val)
c.794G>T (p.Gly265Val)
c.3236G>T (p.Gly1079Val)
c.1556G>T (p.Gly519Val)
Xg.108626325T>ACA517926012COL4A5c.3222T>A (p.Gly1074=)
n.2678T>A
c.455T>A
c.2898T>A (p.Gly966=)
c.795T>A (p.Gly265=)
c.3237T>A (p.Gly1079=)
c.1557T>A (p.Gly519=)
Xg.108626325T>CCA517926013COL4A5c.3222T>C (p.Gly1074=)
n.2678T>C
c.455T>C
c.2898T>C (p.Gly966=)
c.795T>C (p.Gly265=)
c.3237T>C (p.Gly1079=)
c.1557T>C (p.Gly519=)
Xg.108626325T>GCA10489047COL4A5c.3222T>G (p.Gly1074=)
n.2678T>G
c.455T>G
c.2898T>G (p.Gly966=)
c.795T>G (p.Gly265=)
c.3237T>G (p.Gly1079=)
c.1557T>G (p.Gly519=)
dbSNP ExAC gnomAD v2
Xg.108626325T=CA2450697600COL4A5c.3222T= (p.Gly1074=)
n.2678T=
c.455T=
c.2898T= (p.Gly966=)
c.795T= (p.Gly265=)
c.3237T= (p.Gly1079=)
c.1557T= (p.Gly519=)
Xg.108626326C>ACA413855075COL4A5c.3223C>A (p.Leu1075Ile)
n.2679C>A
c.456C>A
c.2899C>A (p.Leu967Ile)
c.796C>A (p.Leu266Ile)
c.3238C>A (p.Leu1080Ile)
c.1558C>A (p.Leu520Ile)
Xg.108626326C=CA2450697603COL4A5c.3223C= (p.Leu1075=)
n.2679C=
c.456C=
c.2899C= (p.Leu967=)
c.796C= (p.Leu266=)
c.3238C= (p.Leu1080=)
c.1558C= (p.Leu520=)
Xg.108626326C>GCA413855076COL4A5c.3223C>G (p.Leu1075Val)
n.2679C>G
c.456C>G
c.2899C>G (p.Leu967Val)
c.796C>G (p.Leu266Val)
c.3238C>G (p.Leu1080Val)
c.1558C>G (p.Leu520Val)
Xg.108626326C>TCA334052658COL4A5c.3223C>T (p.Leu1075Phe)
n.2679C>T
c.456C>T
c.2899C>T (p.Leu967Phe)
c.796C>T (p.Leu266Phe)
c.3238C>T (p.Leu1080Phe)
c.1558C>T (p.Leu520Phe)
dbSNP
Xg.108626327T>ACA413855077COL4A5c.3224T>A (p.Leu1075His)
n.2680T>A
c.457T>A
c.2900T>A (p.Leu967His)
c.797T>A (p.Leu266His)
c.3239T>A (p.Leu1080His)
c.1559T>A (p.Leu520His)
Xg.108626327T>CCA413855078COL4A5c.3224T>C (p.Leu1075Pro)
n.2680T>C
c.457T>C
c.2900T>C (p.Leu967Pro)
c.797T>C (p.Leu266Pro)
c.3239T>C (p.Leu1080Pro)
c.1559T>C (p.Leu520Pro)
Xg.108626327T>GCA413855079COL4A5c.3224T>G (p.Leu1075Arg)
n.2680T>G
c.457T>G
c.2900T>G (p.Leu967Arg)
c.797T>G (p.Leu266Arg)
c.3239T>G (p.Leu1080Arg)
c.1559T>G (p.Leu520Arg)
dbSNP gnomAD v2
Xg.108626327T=CA2450697604COL4A5c.3224T= (p.Leu1075=)
n.2680T=
c.457T=
c.2900T= (p.Leu967=)
c.797T= (p.Leu266=)
c.3239T= (p.Leu1080=)
c.1559T= (p.Leu520=)
Xg.108626328T>ACA517926015COL4A5c.3225T>A (p.Leu1075=)
n.2681T>A
c.458T>A
c.2901T>A (p.Leu967=)
c.798T>A (p.Leu266=)
c.3240T>A (p.Leu1080=)
c.1560T>A (p.Leu520=)
Xg.108626328T>CCA517926017COL4A5c.3225T>C (p.Leu1075=)
n.2681T>C
c.458T>C
c.2901T>C (p.Leu967=)
c.798T>C (p.Leu266=)
c.3240T>C (p.Leu1080=)
c.1560T>C (p.Leu520=)
dbSNP gnomAD v2 gnomAD v4

Number of alleles fetched