Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.108580728C>ACA413926468COL4A5c.881C>A (p.Pro294Gln)
c.557C>A (p.Pro186Gln)
c.896C>A (p.Pro299Gln)
Xg.108580728C>GCA413926471COL4A5c.881C>G (p.Pro294Arg)
c.557C>G (p.Pro186Arg)
c.896C>G (p.Pro299Arg)
Xg.108580728C>TCA413926469COL4A5c.881C>T (p.Pro294Leu)
c.557C>T (p.Pro186Leu)
c.896C>T (p.Pro299Leu)
Xg.108580729A>CCA517991908COL4A5c.882A>C (p.Pro294=)
c.558A>C (p.Pro186=)
c.897A>C (p.Pro299=)
Xg.108580729A>GCA517991909COL4A5c.882A>G (p.Pro294=)
c.558A>G (p.Pro186=)
c.897A>G (p.Pro299=)
ClinVar
Xg.108580729A>TCA517991910COL4A5c.882A>T (p.Pro294=)
c.558A>T (p.Pro186=)
c.897A>T (p.Pro299=)
Xg.108580730G>ACA413926474COL4A5c.883G>A (p.Gly295Ser)
c.559G>A (p.Gly187Ser)
c.898G>A (p.Gly300Ser)
ClinVar dbSNP
Xg.108580730G>CCA413926477COL4A5c.883G>C (p.Gly295Arg)
c.559G>C (p.Gly187Arg)
c.898G>C (p.Gly300Arg)
Xg.108580730G>TCA413926480COL4A5c.883G>T (p.Gly295Cys)
c.559G>T (p.Gly187Cys)
c.898G>T (p.Gly300Cys)
Xg.108580731G>ACA258346COL4A5c.884G>A (p.Gly295Asp)
c.560G>A (p.Gly187Asp)
c.899G>A (p.Gly300Asp)
ClinVar dbSNP
Xg.108580731G>CCA413926488COL4A5c.884G>C (p.Gly295Ala)
c.560G>C (p.Gly187Ala)
c.899G>C (p.Gly300Ala)
Xg.108580731G=CA2450683103COL4A5c.884G= (p.Gly295=)
c.560G= (p.Gly187=)
c.899G= (p.Gly300=)
Xg.108580731G>TCA413926493COL4A5c.884G>T (p.Gly295Val)
c.560G>T (p.Gly187Val)
c.899G>T (p.Gly300Val)
Xg.108580732delCA2695235192COL4A5c.885del (p.Arg297GlufsTer?)
c.561del (p.Arg189GlufsTer?)
c.900del (p.Arg302GlufsTer?)
Xg.108580732C>ACA517991911COL4A5c.885C>A (p.Gly295=)
c.561C>A (p.Gly187=)
c.900C>A (p.Gly300=)
COSMIC COSMIC
Xg.108580732C>GCA517991912COL4A5c.885C>G (p.Gly295=)
c.561C>G (p.Gly187=)
c.900C>G (p.Gly300=)
Xg.108580732C>TCA517991913COL4A5c.885C>T (p.Gly295=)
c.561C>T (p.Gly187=)
c.900C>T (p.Gly300=)
Xg.108580733A>CCA413926496COL4A5c.886A>C (p.Lys296Gln)
c.562A>C (p.Lys188Gln)
c.901A>C (p.Lys301Gln)
Xg.108580733A>GCA413926498COL4A5c.886A>G (p.Lys296Glu)
c.562A>G (p.Lys188Glu)
c.901A>G (p.Lys301Glu)
Xg.108580733A>TCA413926504COL4A5c.886A>T (p.Lys296Ter)
c.562A>T (p.Lys188Ter)
c.901A>T (p.Lys301Ter)
Xg.108580735_108580736delCA2695235193COL4A5c.888_889del (p.Gly298Ter)
c.564_565del (p.Gly190Ter)
c.903_904del (p.Gly303Ter)
Xg.108580734A>CCA413926509COL4A5c.887A>C (p.Lys296Thr)
c.563A>C (p.Lys188Thr)
c.902A>C (p.Lys301Thr)
Xg.108580734A>GCA413926518COL4A5c.887A>G (p.Lys296Arg)
c.563A>G (p.Lys188Arg)
c.902A>G (p.Lys301Arg)
gnomAD v4
Xg.108580734A>TCA413926522COL4A5c.887A>T (p.Lys296Ile)
c.563A>T (p.Lys188Ile)
c.902A>T (p.Lys301Ile)
Xg.108580735A>CCA413926524COL4A5c.888A>C (p.Lys296Asn)
c.564A>C (p.Lys188Asn)
c.903A>C (p.Lys301Asn)
Xg.108580735A>GCA517991914COL4A5c.888A>G (p.Lys296=)
c.564A>G (p.Lys188=)
c.903A>G (p.Lys301=)
Xg.108580735A>TCA413926527COL4A5c.888A>T (p.Lys296Asn)
c.564A>T (p.Lys188Asn)
c.903A>T (p.Lys301Asn)
Xg.108580736A>CCA517991915COL4A5c.889A>C (p.Arg297=)
c.565A>C (p.Arg189=)
c.904A>C (p.Arg302=)
gnomAD v4
Xg.108580736A>GCA413926554COL4A5c.889A>G (p.Arg297Gly)
c.565A>G (p.Arg189Gly)
c.904A>G (p.Arg302Gly)
Xg.108580736A>TCA413926557COL4A5c.889A>T (p.Arg297Ter)
c.565A>T (p.Arg189Ter)
c.904A>T (p.Arg302Ter)
Xg.108580738_108580739delCA2580612293COL4A5c.891_891+1del
c.567_567+1del
c.906_906+1del
ClinVar
Xg.108580737G>ACA413926559COL4A5c.890G>A (p.Arg297Lys)
c.566G>A (p.Arg189Lys)
c.905G>A (p.Arg302Lys)
Xg.108580737G>CCA413926561COL4A5c.890G>C (p.Arg297Thr)
c.566G>C (p.Arg189Thr)
c.905G>C (p.Arg302Thr)
Xg.108580737G>TCA413926564COL4A5c.890G>T (p.Arg297Ile)
c.566G>T (p.Arg189Ile)
c.905G>T (p.Arg302Ile)
Xg.108580738A=CA2450683104COL4A5c.891A= (p.Arg297=)
c.567A= (p.Arg189=)
c.906A= (p.Arg302=)
Xg.108580738A>CCA413926573COL4A5c.891A>C (p.Arg297Ser)
c.567A>C (p.Arg189Ser)
c.906A>C (p.Arg302Ser)
Xg.108580738A>GCA517991916COL4A5c.891A>G (p.Arg297=)
c.567A>G (p.Arg189=)
c.906A>G (p.Arg302=)
Xg.108580738A>TCA413926575COL4A5c.891A>T (p.Arg297Ser)
c.567A>T (p.Arg189Ser)
c.906A>T (p.Arg302Ser)
dbSNP gnomAD v4
Xg.108580739G>ACA258348COL4A5c.891+1G>A (n.891+1G>A)
c.567+1G>A (n.567+1G>A)
c.906+1G>A (n.906+1G>A)
ClinVar dbSNP
Xg.108580739G>CCA413926592COL4A5c.891+1G>C (n.891+1G>C)
c.567+1G>C (n.567+1G>C)
c.906+1G>C (n.906+1G>C)
Xg.108580739G=CA2450683105COL4A5c.891+1G= (n.891+1G=)
c.567+1G= (n.567+1G=)
c.906+1G= (n.906+1G=)
Xg.108580739G>TCA413926601COL4A5c.891+1G>T (n.891+1G>T)
c.567+1G>T (n.567+1G>T)
c.906+1G>T (n.906+1G>T)
ClinVar dbSNP
Xg.108580740delCA2739273686COL4A5c.891+2del (n.891+2del)
c.567+2del (n.567+2del)
c.906+2del (n.906+2del)
ClinVar
Xg.108580740T>ACA413926608COL4A5c.891+2T>A (n.891+2T>A)
c.567+2T>A (n.567+2T>A)
c.906+2T>A (n.906+2T>A)
ClinVar dbSNP
Xg.108580740T>CCA413926606COL4A5c.891+2T>C (n.891+2T>C)
c.567+2T>C (n.567+2T>C)
c.906+2T>C (n.906+2T>C)
Xg.108580740T>GCA413926604COL4A5c.891+2T>G (n.891+2T>G)
c.567+2T>G (n.567+2T>G)
c.906+2T>G (n.906+2T>G)
Xg.108580741A>GCA2579675981COL4A5c.891+3A>G (n.891+3A>G)
c.567+3A>G (n.567+3A>G)
c.906+3A>G (n.906+3A>G)
Xg.108580742A=CA2450683106COL4A5c.891+4A= (n.891+4A=)
c.567+4A= (n.567+4A=)
c.906+4A= (n.906+4A=)
Xg.108580742A>CCA2450683107COL4A5c.891+4A>C (n.891+4A>C)
c.567+4A>C (n.567+4A>C)
c.906+4A>C (n.906+4A>C)
dbSNP
Xg.108580742A>GCA645608363COL4A5c.891+4A>G (n.891+4A>G)
c.567+4A>G (n.567+4A>G)
c.906+4A>G (n.906+4A>G)
dbSNP COSMIC COSMIC

Number of alleles fetched