Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.48589405C>ACA352724355COL7A1c.2236G>T (p.Asp746Tyr)
n.2272G>T
3g.48589405C>GCA352724360COL7A1c.2236G>C (p.Asp746His)
n.2272G>C
COSMIC
3g.48589405C>TCA352724364COL7A1c.2236G>A (p.Asp746Asn)
n.2272G>A
3g.48589406T>ACA433617717COL7A1c.2235A>T (p.Pro745=)
n.2271A>T
3g.48589406T>CCA433617718COL7A1c.2235A>G (p.Pro745=)
n.2271A>G
3g.48589406T>GCA433617719COL7A1c.2235A>C (p.Pro745=)
n.2271A>C
3g.48589407G>ACA352724367COL7A1c.2234C>T (p.Pro745Leu)
n.2270C>T
3g.48589407G>CCA352724370COL7A1c.2234C>G (p.Pro745Arg)
n.2270C>G
3g.48589407G=CA1363091089COL7A1c.2234C= (p.Pro745=)
n.2270C=
3g.48589407G>TCA352724376COL7A1c.2234C>A (p.Pro745Gln)
n.2270C>A
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.48589408G>ACA352724381COL7A1c.2233C>T (p.Pro745Ser)
n.2269C>T
3g.48589408G>CCA2380962COL7A1c.2233C>G (p.Pro745Ala)
n.2269C>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.48589408G=CA1363091091COL7A1c.2233C= (p.Pro745=)
n.2269C=
3g.48589408G>TCA352724388COL7A1c.2233C>A (p.Pro745Thr)
n.2269C>A
3g.48589409C>ACA352724393COL7A1c.2232G>T (p.Glu744Asp)
n.2268G>T
3g.48589409C>GCA352724398COL7A1c.2232G>C (p.Glu744Asp)
n.2268G>C
3g.48589409C>TCA433617722COL7A1c.2232G>A (p.Glu744=)
n.2268G>A
3g.48589410T>ACA352724402COL7A1c.2231A>T (p.Glu744Val)
n.2267A>T
3g.48589410T>CCA352724405COL7A1c.2231A>G (p.Glu744Gly)
n.2267A>G
gnomAD v4
3g.48589410T>GCA352724410COL7A1c.2231A>C (p.Glu744Ala)
n.2267A>C
3g.48589411C>ACA352724413COL7A1c.2230G>T (p.Glu744Ter)
n.2266G>T
3g.48589411C>GCA352724416COL7A1c.2230G>C (p.Glu744Gln)
n.2266G>C
3g.48589411C>TCA352724423COL7A1c.2230G>A (p.Glu744Lys)
n.2266G>A
gnomAD v4
3g.48589412C>ACA433617724COL7A1c.2229G>T (p.Leu743=)
n.2265G>T
3g.48589412C=CA1363091094COL7A1c.2229G= (p.Leu743=)
n.2265G=
3g.48589412C>GCA433617725COL7A1c.2229G>C (p.Leu743=)
n.2265G>C
3g.48589412C>TCA433617726COL7A1c.2229G>A (p.Leu743=)
n.2265G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.48589413A>CCA352724428COL7A1c.2228T>G (p.Leu743Arg)
n.2264T>G
3g.48589413A>GCA352724432COL7A1c.2228T>C (p.Leu743Pro)
n.2264T>C
gnomAD v4
3g.48589413A>TCA352724435COL7A1c.2228T>A (p.Leu743Gln)
n.2264T>A
3g.48589414G>ACA433617729COL7A1c.2227C>T (p.Leu743=)
n.2263C>T
3g.48589414G>CCA352724442COL7A1c.2227C>G (p.Leu743Val)
n.2263C>G
dbSNP gnomAD v4
3g.48589414G=CA1363091097COL7A1c.2227C= (p.Leu743=)
n.2263C=
3g.48589414G>TCA352724446COL7A1c.2227C>A (p.Leu743Met)
n.2263C>A
3g.48589415T>ACA433617731COL7A1c.2226A>T (p.Gly742=)
n.2262A>T
3g.48589415T>CCA433617732COL7A1c.2226A>G (p.Gly742=)
n.2262A>G
3g.48589415T>GCA433617733COL7A1c.2226A>C (p.Gly742=)
n.2262A>C
3g.48589419_48589422dupCA16042453COL7A1c.2223_2226dup (p.Leu743TrpfsTer7)
n.2259_2262dup
ClinVar dbSNP
3g.48589416C>ACA352724457COL7A1c.2225G>T (p.Gly742Val)
n.2261G>T
gnomAD v4
3g.48589416C>GCA352724463COL7A1c.2225G>C (p.Gly742Ala)
n.2261G>C
3g.48589416C>TCA352724460COL7A1c.2225G>A (p.Gly742Glu)
n.2261G>A
3g.48589417C>ACA352724488COL7A1c.2224G>T (p.Gly742Ter)
n.2260G>T
COSMIC
3g.48589417C>GCA352724490COL7A1c.2224G>C (p.Gly742Arg)
n.2260G>C
3g.48589417C>TCA352724494COL7A1c.2224G>A (p.Gly742Arg)
n.2260G>A
gnomAD v4
3g.48589418A>CCA352724500COL7A1c.2223T>G (p.Asp741Glu)
n.2259T>G
gnomAD v4
3g.48589418A>GCA433617736COL7A1c.2223T>C (p.Asp741=)
n.2259T>C
ClinVar dbSNP gnomAD v4
3g.48589418A>TCA352724505COL7A1c.2223T>A (p.Asp741Glu)
n.2259T>A
3g.48589419T>ACA352724516COL7A1c.2222A>T (p.Asp741Val)
n.2258A>T
3g.48589419T>CCA352724537COL7A1c.2222A>G (p.Asp741Gly)
n.2258A>G
3g.48589419T>GCA352724539COL7A1c.2222A>C (p.Asp741Ala)
n.2258A>C

Number of alleles fetched