Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.48583061A=CA1363080203COL7A1c.4483-13T= (p.=)
n.400-13T=
c.4510-13T= (p.=)
n.4546-13T=
n.4519-13T=
3g.48583061A>GCA1363080204COL7A1c.4483-13T>C (p.=)
n.400-13T>C
c.4510-13T>C (p.=)
n.4546-13T>C
n.4519-13T>C
3g.48583064A=CA1363080206COL7A1c.4483-16T= (p.=)
n.400-16T=
c.4510-16T= (p.=)
n.4546-16T=
n.4519-16T=
3g.48583065G>ACA542792450COL7A1c.4483-17C>T (p.=)
n.400-17C>T
c.4510-17C>T (p.=)
n.4546-17C>T
n.4519-17C>T
gnomAD
3g.48583065G=CA1363080209COL7A1c.4483-17C= (p.=)
n.400-17C=
c.4510-17C= (p.=)
n.4546-17C=
n.4519-17C=
3g.48583066dupCA2379996COL7A1c.4483-17dup (p.=)
n.400-17dup
c.4510-17dup (p.=)
n.4546-17dup
n.4519-17dup
ClinVar dbSNP ExAC gnomAD
3g.48583068C>ACA2379997COL7A1c.4483-20G>T (p.=)
n.400-20G>T
c.4510-20G>T (p.=)
n.4546-20G>T
n.4519-20G>T
dbSNP ExAC gnomAD
3g.48583068C=CA1363080210COL7A1c.4483-20G= (p.=)
n.400-20G=
c.4510-20G= (p.=)
n.4546-20G=
n.4519-20G=
3g.48583076A=CA1363080211COL7A1c.4483-28T= (p.=)
n.400-28T=
c.4510-28T= (p.=)
n.4546-28T=
n.4519-28T=
3g.48583076A>GCA1363080212COL7A1c.4483-28T>C (p.=)
n.400-28T>C
c.4510-28T>C (p.=)
n.4546-28T>C
n.4519-28T>C
3g.48583078T>GCA542792451COL7A1c.4483-30A>C (p.=)
n.400-30A>C
c.4510-30A>C (p.=)
n.4546-30A>C
n.4519-30A>C
gnomAD
3g.48583078T=CA1363080214COL7A1c.4483-30A= (p.=)
n.400-30A=
c.4510-30A= (p.=)
n.4546-30A=
n.4519-30A=
3g.48583078_48583079insCCA1363080219COL7A1c.4483-31_4483-30insG (p.=)
n.400-31_400-30insG
c.4510-31_4510-30insG (p.=)
n.4546-31_4546-30insG
n.4519-31_4519-30insG
dbSNP
3g.48583079_48583080delinsTGCA1363080220COL7A1c.4483-32_4483-31delinsCA (p.=)
n.400-32_400-31delinsCA
c.4510-32_4510-31delinsCA (p.=)
n.4546-32_4546-31delinsCA
n.4519-32_4519-31delinsCA
3g.48583080G>ACA542792452COL7A1c.4483-32C>T (p.=)
n.400-32C>T
c.4510-32C>T (p.=)
n.4546-32C>T
n.4519-32C>T
gnomAD
3g.48583080G=CA1363080222COL7A1c.4483-32C= (p.=)
n.400-32C=
c.4510-32C= (p.=)
n.4546-32C=
n.4519-32C=
3g.48583082delCA2379998COL7A1c.4483-32del (p.=)
n.400-32del
c.4510-32del (p.=)
n.4546-32del
n.4519-32del
dbSNP ExAC gnomAD
3g.48583082G>ACA2379999COL7A1c.4483-34C>T (p.=)
n.400-34C>T
c.4510-34C>T (p.=)
n.4546-34C>T
n.4519-34C>T
dbSNP ExAC gnomAD
3g.48583082G=CA1363080225COL7A1c.4483-34C= (p.=)
n.400-34C=
c.4510-34C= (p.=)
n.4546-34C=
n.4519-34C=
3g.48583083C=CA1363080227COL7A1c.4483-35G= (p.=)
n.400-35G=
c.4510-35G= (p.=)
n.4546-35G=
n.4519-35G=
3g.48583083C>TCA73980383COL7A1c.4483-35G>A (p.=)
n.400-35G>A
c.4510-35G>A (p.=)
n.4546-35G>A
n.4519-35G>A
dbSNP
3g.48583085C=CA1363080229COL7A1c.4483-37G= (p.=)
n.400-37G=
c.4510-37G= (p.=)
n.4546-37G=
n.4519-37G=
3g.48583085C>TCA1363080230COL7A1c.4483-37G>A (p.=)
n.400-37G>A
c.4510-37G>A (p.=)
n.4546-37G>A
n.4519-37G>A
3g.48583088A=CA1363080234COL7A1c.4483-40T= (p.=)
n.400-40T=
c.4510-40T= (p.=)
n.4546-40T=
n.4519-40T=
3g.48583088A>CCA2380000COL7A1c.4483-40T>G (p.=)
n.400-40T>G
c.4510-40T>G (p.=)
n.4546-40T>G
n.4519-40T>G
dbSNP ExAC gnomAD
3g.48583091C=CA1363080237COL7A1c.4482+36G= (p.=)
n.399+36G=
c.4509+36G= (p.=)
n.4545+36G=
n.4518+36G=
3g.48583091C>TCA1363080238COL7A1c.4482+36G>A (p.=)
n.399+36G>A
c.4509+36G>A (p.=)
n.4545+36G>A
n.4518+36G>A
3g.48583092T>ACA73980387COL7A1c.4482+35A>T (p.=)
n.399+35A>T
c.4509+35A>T (p.=)
n.4545+35A>T
n.4518+35A>T
dbSNP
3g.48583092T=CA1363080239COL7A1c.4482+35A= (p.=)
n.399+35A=
c.4509+35A= (p.=)
n.4545+35A=
n.4518+35A=
3g.48583093C=CA1363080240COL7A1c.4482+34G= (p.=)
n.399+34G=
c.4509+34G= (p.=)
n.4545+34G=
n.4518+34G=
3g.48583093C>TCA2380001COL7A1c.4482+34G>A (p.=)
n.399+34G>A
c.4509+34G>A (p.=)
n.4545+34G>A
n.4518+34G>A
dbSNP ExAC gnomAD
3g.48583094C=CA1363080243COL7A1c.4482+33G= (p.=)
n.399+33G=
c.4509+33G= (p.=)
n.4545+33G=
n.4518+33G=
3g.48583094C>GCA542792453COL7A1c.4482+33G>C (p.=)
n.399+33G>C
c.4509+33G>C (p.=)
n.4545+33G>C
n.4518+33G>C
gnomAD
3g.48583094C>TCA73980391COL7A1c.4482+33G>A (p.=)
n.399+33G>A
c.4509+33G>A (p.=)
n.4545+33G>A
n.4518+33G>A
dbSNP
3g.48583096G>CCA1363080247COL7A1c.4482+31C>G (p.=)
n.399+31C>G
c.4509+31C>G (p.=)
n.4545+31C>G
n.4518+31C>G
3g.48583096G=CA1363080246COL7A1c.4482+31C= (p.=)
n.399+31C=
c.4509+31C= (p.=)
n.4545+31C=
n.4518+31C=
3g.48583097G>CCA73980395COL7A1c.4482+30C>G (p.=)
n.399+30C>G
c.4509+30C>G (p.=)
n.4545+30C>G
n.4518+30C>G
dbSNP
3g.48583097G=CA1363080250COL7A1c.4482+30C= (p.=)
n.399+30C=
c.4509+30C= (p.=)
n.4545+30C=
n.4518+30C=
3g.48583098_48583099delinsGCCA1363080252COL7A1c.4482+28_4482+29delinsGC (p.=)
n.399+28_399+29delinsGC
c.4509+28_4509+29delinsGC (p.=)
n.4545+28_4545+29delinsGC
n.4518+28_4518+29delinsGC
3g.48583101delCA542792454COL7A1c.4482+28del (p.=)
n.399+28del
c.4509+28del (p.=)
n.4545+28del
n.4518+28del
dbSNP gnomAD
3g.48583100C=CA1363080255COL7A1c.4482+27G= (p.=)
n.399+27G=
c.4509+27G= (p.=)
n.4545+27G=
n.4518+27G=
3g.48583100C>GCA2380002COL7A1c.4482+27G>C (p.=)
n.399+27G>C
c.4509+27G>C (p.=)
n.4545+27G>C
n.4518+27G>C
dbSNP ExAC gnomAD
3g.48583101C=CA1363080258COL7A1c.4482+26G= (p.=)
n.399+26G=
c.4509+26G= (p.=)
n.4545+26G=
n.4518+26G=
3g.48583101C>TCA907757573COL7A1c.4482+26G>A (p.=)
n.399+26G>A
c.4509+26G>A (p.=)
n.4545+26G>A
n.4518+26G>A
3g.48583103T>CCA433542324COL7A1c.4482+24A>G (p.=)
n.399+24A>G
c.4509+24A>G (p.=)
n.4545+24A>G
n.4518+24A>G
3g.48583105G=CA1363080260COL7A1c.4482+22C= (p.=)
n.399+22C=
c.4509+22C= (p.=)
n.4545+22C=
n.4518+22C=
3g.48583105G>TCA1363080263COL7A1c.4482+22C>A (p.=)
n.399+22C>A
c.4509+22C>A (p.=)
n.4545+22C>A
n.4518+22C>A
3g.48583107A=CA1363080270COL7A1c.4482+20T= (p.=)
n.399+20T=
c.4509+20T= (p.=)
n.4545+20T=
n.4518+20T=
3g.48583107A>CCA1363080267COL7A1c.4482+20T>G (p.=)
n.399+20T>G
c.4509+20T>G (p.=)
n.4545+20T>G
n.4518+20T>G
3g.48583107A>GCA542792455COL7A1c.4482+20T>C (p.=)
n.399+20T>C
c.4509+20T>C (p.=)
n.4545+20T>C
n.4518+20T>C
gnomAD

Number of alleles fetched