Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.108668310_108668317delCA920430367COL4A5c.3605-9_3605-2del (n.3605-9_3605-2del)
c.3281-9_3281-2del (n.3281-9_3281-2del)
c.1178-9_1178-2del (n.1178-9_1178-2del)
c.3620-9_3620-2del (n.3620-9_3620-2del)
c.1940-9_1940-2del (n.1940-9_1940-2del)
dbSNP
Xg.108668317A=CA2450712911COL4A5c.3605-2A= (n.3605-2A=)
c.3281-2A= (n.3281-2A=)
c.1178-2A= (n.1178-2A=)
c.3620-2A= (n.3620-2A=)
c.1940-2A= (n.1940-2A=)
Xg.108668317A>CCA413848308COL4A5c.3605-2A>C (n.3605-2A>C)
c.3281-2A>C (n.3281-2A>C)
c.1178-2A>C (n.1178-2A>C)
c.3620-2A>C (n.3620-2A>C)
c.1940-2A>C (n.1940-2A>C)
Xg.108668317A>GCA258905COL4A5c.3605-2A>G (n.3605-2A>G)
c.3281-2A>G (n.3281-2A>G)
c.1178-2A>G (n.1178-2A>G)
c.3620-2A>G (n.3620-2A>G)
c.1940-2A>G (n.1940-2A>G)
ClinVar dbSNP
Xg.108668317A>TCA413848311COL4A5c.3605-2A>T (n.3605-2A>T)
c.3281-2A>T (n.3281-2A>T)
c.1178-2A>T (n.1178-2A>T)
c.3620-2A>T (n.3620-2A>T)
c.1940-2A>T (n.1940-2A>T)
Xg.108668320_108668505delCA2695235652COL4A5c.3606_3790+1del
c.3282_3466+1del
c.1179_1363+1del
c.3621_3805+1del
c.1941_2125+1del
Xg.108668318G>ACA258906COL4A5c.3605-1G>A (n.3605-1G>A)
c.3281-1G>A (n.3281-1G>A)
c.1178-1G>A (n.1178-1G>A)
c.3620-1G>A (n.3620-1G>A)
c.1940-1G>A (n.1940-1G>A)
dbSNP
Xg.108668318G>CCA413848313COL4A5c.3605-1G>C (n.3605-1G>C)
c.3281-1G>C (n.3281-1G>C)
c.1178-1G>C (n.1178-1G>C)
c.3620-1G>C (n.3620-1G>C)
c.1940-1G>C (n.1940-1G>C)
Xg.108668318G=CA2450712912COL4A5c.3605-1G= (n.3605-1G=)
c.3281-1G= (n.3281-1G=)
c.1178-1G= (n.1178-1G=)
c.3620-1G= (n.3620-1G=)
c.1940-1G= (n.1940-1G=)
Xg.108668318G>TCA413848316COL4A5c.3605-1G>T (n.3605-1G>T)
c.3281-1G>T (n.3281-1G>T)
c.1178-1G>T (n.1178-1G>T)
c.3620-1G>T (n.3620-1G>T)
c.1940-1G>T (n.1940-1G>T)
Xg.108668319G>ACA413848319COL4A5c.3605G>A (p.Gly1202Asp)
c.3281G>A (p.Gly1094Asp)
c.1178G>A (p.Gly393Asp)
c.3620G>A (p.Gly1207Asp)
c.1940G>A (p.Gly647Asp)
ClinVar dbSNP
Xg.108668319G>CCA413848321COL4A5c.3605G>C (p.Gly1202Ala)
c.3281G>C (p.Gly1094Ala)
c.1178G>C (p.Gly393Ala)
c.3620G>C (p.Gly1207Ala)
c.1940G>C (p.Gly647Ala)
Xg.108668319G=CA2450712913COL4A5c.3605G= (p.Gly1202=)
c.3281G= (p.Gly1094=)
c.1178G= (p.Gly393=)
c.3620G= (p.Gly1207=)
c.1940G= (p.Gly647=)
Xg.108668319G>TCA413848323COL4A5c.3605G>T (p.Gly1202Val)
c.3281G>T (p.Gly1094Val)
c.1178G>T (p.Gly393Val)
c.3620G>T (p.Gly1207Val)
c.1940G>T (p.Gly647Val)
ClinVar dbSNP
Xg.108668320C>ACA517922544COL4A5c.3606C>A (p.Gly1202=)
c.3282C>A (p.Gly1094=)
c.1179C>A (p.Gly393=)
c.3621C>A (p.Gly1207=)
c.1941C>A (p.Gly647=)
Xg.108668320C>GCA517922545COL4A5c.3606C>G (p.Gly1202=)
c.3282C>G (p.Gly1094=)
c.1179C>G (p.Gly393=)
c.3621C>G (p.Gly1207=)
c.1941C>G (p.Gly647=)
Xg.108668320C>TCA517922546COL4A5c.3606C>T (p.Gly1202=)
c.3282C>T (p.Gly1094=)
c.1179C>T (p.Gly393=)
c.3621C>T (p.Gly1207=)
c.1941C>T (p.Gly647=)
gnomAD v4
Xg.108668321C>ACA413848325COL4A5c.3607C>A (p.Gln1203Lys)
c.3283C>A (p.Gln1095Lys)
c.1180C>A (p.Gln394Lys)
c.3622C>A (p.Gln1208Lys)
c.1942C>A (p.Gln648Lys)
Xg.108668321C>GCA413848327COL4A5c.3607C>G (p.Gln1203Glu)
c.3283C>G (p.Gln1095Glu)
c.1180C>G (p.Gln394Glu)
c.3622C>G (p.Gln1208Glu)
c.1942C>G (p.Gln648Glu)
Xg.108668321C>TCA413848330COL4A5c.3607C>T (p.Gln1203Ter)
c.3283C>T (p.Gln1095Ter)
c.1180C>T (p.Gln394Ter)
c.3622C>T (p.Gln1208Ter)
c.1942C>T (p.Gln648Ter)
Xg.108668322A>CCA413848332COL4A5c.3608A>C (p.Gln1203Pro)
c.3284A>C (p.Gln1095Pro)
c.1181A>C (p.Gln394Pro)
c.3623A>C (p.Gln1208Pro)
c.1943A>C (p.Gln648Pro)
Xg.108668322A>GCA413848334COL4A5c.3608A>G (p.Gln1203Arg)
c.3284A>G (p.Gln1095Arg)
c.1181A>G (p.Gln394Arg)
c.3623A>G (p.Gln1208Arg)
c.1943A>G (p.Gln648Arg)
Xg.108668322A>TCA413848336COL4A5c.3608A>T (p.Gln1203Leu)
c.3284A>T (p.Gln1095Leu)
c.1181A>T (p.Gln394Leu)
c.3623A>T (p.Gln1208Leu)
c.1943A>T (p.Gln648Leu)
Xg.108668325delCA2579676916COL4A5c.3611del (p.Lys1204ArgfsTer?)
c.3287del (p.Lys1096ArgfsTer?)
c.1184del (p.Lys395ArgfsTer?)
c.3626del (p.Lys1209ArgfsTer?)
c.1946del (p.Lys649ArgfsTer?)
Xg.108668323A=CA2450712914COL4A5c.3609A= (p.Gln1203=)
c.3285A= (p.Gln1095=)
c.1182A= (p.Gln394=)
c.3624A= (p.Gln1208=)
c.1944A= (p.Gln648=)
Xg.108668323A>CCA413848339COL4A5c.3609A>C (p.Gln1203His)
c.3285A>C (p.Gln1095His)
c.1182A>C (p.Gln394His)
c.3624A>C (p.Gln1208His)
c.1944A>C (p.Gln648His)
Xg.108668323A>GCA10489155COL4A5c.3609A>G (p.Gln1203=)
c.3285A>G (p.Gln1095=)
c.1182A>G (p.Gln394=)
c.3624A>G (p.Gln1208=)
c.1944A>G (p.Gln648=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.108668323A>TCA413848342COL4A5c.3609A>T (p.Gln1203His)
c.3285A>T (p.Gln1095His)
c.1182A>T (p.Gln394His)
c.3624A>T (p.Gln1208His)
c.1944A>T (p.Gln648His)
Xg.108668324A>CCA413848349COL4A5c.3610A>C (p.Lys1204Gln)
c.3286A>C (p.Lys1096Gln)
c.1183A>C (p.Lys395Gln)
c.3625A>C (p.Lys1209Gln)
c.1945A>C (p.Lys649Gln)
Xg.108668324A>GCA413848346COL4A5c.3610A>G (p.Lys1204Glu)
c.3286A>G (p.Lys1096Glu)
c.1183A>G (p.Lys395Glu)
c.3625A>G (p.Lys1209Glu)
c.1945A>G (p.Lys649Glu)
Xg.108668324A>TCA413848344COL4A5c.3610A>T (p.Lys1204Ter)
c.3286A>T (p.Lys1096Ter)
c.1183A>T (p.Lys395Ter)
c.3625A>T (p.Lys1209Ter)
c.1945A>T (p.Lys649Ter)
Xg.108668325A>CCA413848350COL4A5c.3611A>C (p.Lys1204Thr)
c.3287A>C (p.Lys1096Thr)
c.1184A>C (p.Lys395Thr)
c.3626A>C (p.Lys1209Thr)
c.1946A>C (p.Lys649Thr)
Xg.108668325A>GCA413848353COL4A5c.3611A>G (p.Lys1204Arg)
c.3287A>G (p.Lys1096Arg)
c.1184A>G (p.Lys395Arg)
c.3626A>G (p.Lys1209Arg)
c.1946A>G (p.Lys649Arg)
COSMIC COSMIC
Xg.108668325A>TCA413848352COL4A5c.3611A>T (p.Lys1204Met)
c.3287A>T (p.Lys1096Met)
c.1184A>T (p.Lys395Met)
c.3626A>T (p.Lys1209Met)
c.1946A>T (p.Lys649Met)
Xg.108668326G>ACA517922547COL4A5c.3612G>A (p.Lys1204=)
c.3288G>A (p.Lys1096=)
c.1185G>A (p.Lys395=)
c.3627G>A (p.Lys1209=)
c.1947G>A (p.Lys649=)
Xg.108668326G>CCA413848354COL4A5c.3612G>C (p.Lys1204Asn)
c.3288G>C (p.Lys1096Asn)
c.1185G>C (p.Lys395Asn)
c.3627G>C (p.Lys1209Asn)
c.1947G>C (p.Lys649Asn)
Xg.108668326G>TCA413848356COL4A5c.3612G>T (p.Lys1204Asn)
c.3288G>T (p.Lys1096Asn)
c.1185G>T (p.Lys395Asn)
c.3627G>T (p.Lys1209Asn)
c.1947G>T (p.Lys649Asn)
Xg.108668328delCA2695235653COL4A5c.3614del (p.Gly1205ValfsTer?)
c.3290del (p.Gly1097ValfsTer?)
c.1187del (p.Gly396ValfsTer?)
c.3629del (p.Gly1210ValfsTer?)
c.1949del (p.Gly650ValfsTer?)
Xg.108668327G>ACA258909COL4A5c.3613G>A (p.Gly1205Ser)
c.3289G>A (p.Gly1097Ser)
c.1186G>A (p.Gly396Ser)
c.3628G>A (p.Gly1210Ser)
c.1948G>A (p.Gly650Ser)
ClinVar dbSNP
Xg.108668327G>CCA413848359COL4A5c.3613G>C (p.Gly1205Arg)
c.3289G>C (p.Gly1097Arg)
c.1186G>C (p.Gly396Arg)
c.3628G>C (p.Gly1210Arg)
c.1948G>C (p.Gly650Arg)
Xg.108668327G=CA2450712915COL4A5c.3613G= (p.Gly1205=)
c.3289G= (p.Gly1097=)
c.1186G= (p.Gly396=)
c.3628G= (p.Gly1210=)
c.1948G= (p.Gly650=)
Xg.108668327G>TCA258907COL4A5c.3613G>T (p.Gly1205Cys)
c.3289G>T (p.Gly1097Cys)
c.1186G>T (p.Gly396Cys)
c.3628G>T (p.Gly1210Cys)
c.1948G>T (p.Gly650Cys)
dbSNP
Xg.108668328G>ACA413848361COL4A5c.3614G>A (p.Gly1205Asp)
c.3290G>A (p.Gly1097Asp)
c.1187G>A (p.Gly396Asp)
c.3629G>A (p.Gly1210Asp)
c.1949G>A (p.Gly650Asp)
ClinVar dbSNP gnomAD v4
Xg.108668328G>CCA413848362COL4A5c.3614G>C (p.Gly1205Ala)
c.3290G>C (p.Gly1097Ala)
c.1187G>C (p.Gly396Ala)
c.3629G>C (p.Gly1210Ala)
c.1949G>C (p.Gly650Ala)
Xg.108668328G=CA2450712916COL4A5c.3614G= (p.Gly1205=)
c.3290G= (p.Gly1097=)
c.1187G= (p.Gly396=)
c.3629G= (p.Gly1210=)
c.1949G= (p.Gly650=)
Xg.108668328G>TCA413848363COL4A5c.3614G>T (p.Gly1205Val)
c.3290G>T (p.Gly1097Val)
c.1187G>T (p.Gly396Val)
c.3629G>T (p.Gly1210Val)
c.1949G>T (p.Gly650Val)
ClinVar dbSNP
Xg.108668329T>ACA517922550COL4A5c.3615T>A (p.Gly1205=)
c.3291T>A (p.Gly1097=)
c.1188T>A (p.Gly396=)
c.3630T>A (p.Gly1210=)
c.1950T>A (p.Gly650=)
Xg.108668329T>CCA517922548COL4A5c.3615T>C (p.Gly1205=)
c.3291T>C (p.Gly1097=)
c.1188T>C (p.Gly396=)
c.3630T>C (p.Gly1210=)
c.1950T>C (p.Gly650=)
Xg.108668329T>GCA517922549COL4A5c.3615T>G (p.Gly1205=)
c.3291T>G (p.Gly1097=)
c.1188T>G (p.Gly396=)
c.3630T>G (p.Gly1210=)
c.1950T>G (p.Gly650=)
Xg.108668329_108668333delinsTGATGCA2450712917COL4A5c.3615_3619delinsTGATG (p.Gly1205=)
c.3291_3295delinsTGATG (p.Gly1097=)
c.1188_1192delinsTGATG (p.Gly396=)
c.3630_3634delinsTGATG (p.Gly1210=)
c.1950_1954delinsTGATG (p.Gly650=)

Number of alleles fetched