Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.48445454A=CA2175492634FBN1c.5839T= (p.Cys1947=)
n.4513T=
c.838T= (p.Cys280=)
c.*1602T= (n.*1602T=)
c.1146T=
15g.48445454A>CCA392340093FBN1c.5839T>G (p.Cys1947Gly)
n.4513T>G
c.838T>G (p.Cys280Gly)
c.*1602T>G (n.*1602T>G)
c.1146T>G
ClinVar dbSNP
15g.48445454A>GCA392340092FBN1c.5839T>C (p.Cys1947Arg)
n.4513T>C
c.838T>C (p.Cys280Arg)
c.*1602T>C (n.*1602T>C)
c.1146T>C
ClinVar dbSNP
15g.48445454A>TCA392340091FBN1c.5839T>A (p.Cys1947Ser)
n.4513T>A
c.838T>A (p.Cys280Ser)
c.*1602T>A (n.*1602T>A)
c.1146T>A
ClinVar dbSNP
15g.48445455T>ACA392340094FBN1c.5838A>T (p.Gln1946His)
n.4512A>T
c.837A>T (p.Gln279His)
c.*1601A>T (n.*1601A>T)
c.1145A>T
15g.48445455T>CCA055736FBN1c.5838A>G (p.Gln1946=)
n.4512A>G
c.837A>G (p.Gln279=)
c.*1601A>G (n.*1601A>G)
c.1145A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.48445455T>GCA392340095FBN1c.5838A>C (p.Gln1946His)
n.4512A>C
c.837A>C (p.Gln279His)
c.*1601A>C (n.*1601A>C)
c.1145A>C
15g.48445455T=CA2175492644FBN1c.5838A= (p.Gln1946=)
n.4512A=
c.837A= (p.Gln279=)
c.*1601A= (n.*1601A=)
c.1145A=
15g.48445456T>ACA392340096FBN1c.5837A>T (p.Gln1946Leu)
n.4511A>T
c.836A>T (p.Gln279Leu)
c.*1600A>T (n.*1600A>T)
c.1144A>T
15g.48445456T>CCA392340097FBN1c.5837A>G (p.Gln1946Arg)
n.4511A>G
c.836A>G (p.Gln279Arg)
c.*1600A>G (n.*1600A>G)
c.1144A>G
dbSNP gnomAD v2 gnomAD v4
15g.48445456T>GCA392340098FBN1c.5837A>C (p.Gln1946Pro)
n.4511A>C
c.836A>C (p.Gln279Pro)
c.*1600A>C (n.*1600A>C)
c.1144A>C
15g.48445456T=CA2175492649FBN1c.5837A= (p.Gln1946=)
n.4511A=
c.836A= (p.Gln279=)
c.*1600A= (n.*1600A=)
c.1144A=
15g.48445457G>ACA392340099FBN1c.5836C>T (p.Gln1946Ter)
n.4510C>T
c.835C>T (p.Gln279Ter)
c.*1599C>T (n.*1599C>T)
c.1143C>T
ClinVar
15g.48445457G>CCA392340100FBN1c.5836C>G (p.Gln1946Glu)
n.4510C>G
c.835C>G (p.Gln279Glu)
c.*1599C>G (n.*1599C>G)
c.1143C>G
15g.48445457G>TCA392340101FBN1c.5836C>A (p.Gln1946Lys)
n.4510C>A
c.835C>A (p.Gln279Lys)
c.*1599C>A (n.*1599C>A)
c.1143C>A
15g.48445458delCA2573150957FBN1c.5836del (p.Gln1946AsnfsTer?)
n.4510del
c.835del (p.Gln279AsnfsTer?)
c.*1599del (n.*1599del)
c.1143del
ClinVar dbSNP
15g.48445458G>ACA490022591FBN1c.5835C>T (p.Gly1945=)
n.4509C>T
c.834C>T (p.Gly278=)
c.*1598C>T (n.*1598C>T)
c.1142C>T
15g.48445458G>CCA490022593FBN1c.5835C>G (p.Gly1945=)
n.4509C>G
c.834C>G (p.Gly278=)
c.*1598C>G (n.*1598C>G)
c.1142C>G
15g.48445458G>TCA490022596FBN1c.5835C>A (p.Gly1945=)
n.4509C>A
c.834C>A (p.Gly278=)
c.*1598C>A (n.*1598C>A)
c.1142C>A
gnomAD v4
15g.48445459C>ACA392340102FBN1c.5834G>T (p.Gly1945Val)
n.4508G>T
c.833G>T (p.Gly278Val)
c.*1597G>T (n.*1597G>T)
c.1141G>T
15g.48445459C=CA2175492654FBN1c.5834G= (p.Gly1945=)
n.4508G=
c.833G= (p.Gly278=)
c.*1597G= (n.*1597G=)
c.1141G=
15g.48445459C>GCA392340103FBN1c.5834G>C (p.Gly1945Ala)
n.4508G>C
c.833G>C (p.Gly278Ala)
c.*1597G>C (n.*1597G>C)
c.1141G>C
15g.48445459C>TCA392340104FBN1c.5834G>A (p.Gly1945Asp)
n.4508G>A
c.833G>A (p.Gly278Asp)
c.*1597G>A (n.*1597G>A)
c.1141G>A
ClinVar dbSNP
15g.48445460C>ACA392340106FBN1c.5833G>T (p.Gly1945Cys)
n.4507G>T
c.832G>T (p.Gly278Cys)
c.*1596G>T (n.*1596G>T)
c.1140G>T
15g.48445460C>GCA392340107FBN1c.5833G>C (p.Gly1945Arg)
n.4507G>C
c.832G>C (p.Gly278Arg)
c.*1596G>C (n.*1596G>C)
c.1140G>C
15g.48445460C>TCA392340105FBN1c.5833G>A (p.Gly1945Ser)
n.4507G>A
c.832G>A (p.Gly278Ser)
c.*1596G>A (n.*1596G>A)
c.1140G>A
15g.48445461A=CA2175492660FBN1c.5832T= (p.Asn1944=)
n.4506T=
c.831T= (p.Asn277=)
c.*1595T= (n.*1595T=)
c.1139T=
15g.48445461A>CCA392340108FBN1c.5832T>G (p.Asn1944Lys)
n.4506T>G
c.831T>G (p.Asn277Lys)
c.*1595T>G (n.*1595T>G)
c.1139T>G
15g.48445461A>GCA490022607FBN1c.5832T>C (p.Asn1944=)
n.4506T>C
c.831T>C (p.Asn277=)
c.*1595T>C (n.*1595T>C)
c.1139T>C
15g.48445461A>TCA392340109FBN1c.5832T>A (p.Asn1944Lys)
n.4506T>A
c.831T>A (p.Asn277Lys)
c.*1595T>A (n.*1595T>A)
c.1139T>A
15g.48445462T>ACA392340110FBN1c.5831A>T (p.Asn1944Ile)
n.4505A>T
c.830A>T (p.Asn277Ile)
c.*1594A>T (n.*1594A>T)
c.1138A>T
15g.48445462T>CCA392340111FBN1c.5831A>G (p.Asn1944Ser)
n.4505A>G
c.830A>G (p.Asn277Ser)
c.*1594A>G (n.*1594A>G)
c.1138A>G
15g.48445462T>GCA392340112FBN1c.5831A>C (p.Asn1944Thr)
n.4505A>C
c.830A>C (p.Asn277Thr)
c.*1594A>C (n.*1594A>C)
c.1138A>C
15g.48445463_48445464dupCA1139663931FBN1c.5830_5831dup (p.Asn1944LysfsTer?)
n.4504_4505dup
c.829_830dup (p.Asn277LysfsTer?)
c.*1593_*1594dup (n.*1593_*1594dup)
c.1137_1138dup
ClinVar dbSNP
15g.48445464delCA2580089691FBN1c.5831del (p.Asn1944MetfsTer?)
n.4505del
c.830del (p.Asn277MetfsTer?)
c.*1594del (n.*1594del)
c.1138del
ClinVar
15g.48445463T>ACA392340113FBN1c.5830A>T (p.Asn1944Tyr)
n.4504A>T
c.829A>T (p.Asn277Tyr)
c.*1593A>T (n.*1593A>T)
c.1137A>T
15g.48445463T>CCA392340114FBN1c.5830A>G (p.Asn1944Asp)
n.4504A>G
c.829A>G (p.Asn277Asp)
c.*1593A>G (n.*1593A>G)
c.1137A>G
15g.48445463T>GCA392340115FBN1c.5830A>C (p.Asn1944His)
n.4504A>C
c.829A>C (p.Asn277His)
c.*1593A>C (n.*1593A>C)
c.1137A>C
gnomAD v4
15g.48445464T>ACA392340116FBN1c.5829A>T (p.Arg1943Ser)
n.4503A>T
c.828A>T (p.Arg276Ser)
c.*1592A>T (n.*1592A>T)
c.1136A>T
15g.48445464T>CCA490022621FBN1c.5829A>G (p.Arg1943=)
n.4503A>G
c.828A>G (p.Arg276=)
c.*1592A>G (n.*1592A>G)
c.1136A>G
15g.48445464T>GCA392340117FBN1c.5829A>C (p.Arg1943Ser)
n.4503A>C
c.828A>C (p.Arg276Ser)
c.*1592A>C (n.*1592A>C)
c.1136A>C
15g.48445465C>ACA392340118FBN1c.5828G>T (p.Arg1943Ile)
n.4502G>T
c.827G>T (p.Arg276Ile)
c.*1591G>T (n.*1591G>T)
c.1135G>T
ClinVar dbSNP
15g.48445465C=CA2175492673FBN1c.5828G= (p.Arg1943=)
n.4502G=
c.827G= (p.Arg276=)
c.*1591G= (n.*1591G=)
c.1135G=
15g.48445465C>GCA392340119FBN1c.5828G>C (p.Arg1943Thr)
n.4502G>C
c.827G>C (p.Arg276Thr)
c.*1591G>C (n.*1591G>C)
c.1135G>C
15g.48445465C>TCA392340120FBN1c.5828G>A (p.Arg1943Lys)
n.4502G>A
c.827G>A (p.Arg276Lys)
c.*1591G>A (n.*1591G>A)
c.1135G>A
15g.48445466T>ACA392340122FBN1c.5827A>T (p.Arg1943Ter)
n.4501A>T
c.826A>T (p.Arg276Ter)
c.*1590A>T (n.*1590A>T)
c.1134A>T
15g.48445466T>CCA392340121FBN1c.5827A>G (p.Arg1943Gly)
n.4501A>G
c.826A>G (p.Arg276Gly)
c.*1590A>G (n.*1590A>G)
c.1134A>G
15g.48445466T>GCA490022629FBN1c.5827A>C (p.Arg1943=)
n.4501A>C
c.826A>C (p.Arg276=)
c.*1590A>C (n.*1590A>C)
c.1134A>C
15g.48445467G>ACA490022634FBN1c.5826C>T (p.Cys1942=)
n.4500C>T
c.825C>T (p.Cys275=)
c.*1589C>T (n.*1589C>T)
c.1133C>T
15g.48445467G>CCA392340123FBN1c.5826C>G (p.Cys1942Trp)
n.4500C>G
c.825C>G (p.Cys275Trp)
c.*1589C>G (n.*1589C>G)
c.1133C>G
15g.48445467G=CA2175492685FBN1c.5826C= (p.Cys1942=)
n.4500C=
c.825C= (p.Cys275=)
c.*1589C= (n.*1589C=)
c.1133C=
15g.48445467G>TCA269532860FBN1c.5826C>A (p.Cys1942Ter)
n.4500C>A
c.825C>A (p.Cys275Ter)
c.*1589C>A (n.*1589C>A)
c.1133C>A
ClinVar dbSNP
15g.48445468C>ACA016098FBN1c.5825G>T (p.Cys1942Phe)
n.4499G>T
c.824G>T (p.Cys275Phe)
c.*1588G>T (n.*1588G>T)
c.1132G>T
ClinVar dbSNP
15g.48445468C=CA2175492703FBN1c.5825G= (p.Cys1942=)
n.4499G=
c.824G= (p.Cys275=)
c.*1588G= (n.*1588G=)
c.1132G=
15g.48445468C>GCA10587808FBN1c.5825G>C (p.Cys1942Ser)
n.4499G>C
c.824G>C (p.Cys275Ser)
c.*1588G>C (n.*1588G>C)
c.1132G>C
ClinVar dbSNP
15g.48445468C>TCA392340124FBN1c.5825G>A (p.Cys1942Tyr)
n.4499G>A
c.824G>A (p.Cys275Tyr)
c.*1588G>A (n.*1588G>A)
c.1132G>A
ClinVar dbSNP
15g.48445468_48445470delinsCAACA2175492697FBN1c.5823_5825delinsTTG (p.Leu1941=)
n.4497_4499delinsTTG
c.822_824delinsTTG (p.Leu274=)
c.*1586_*1588delinsTTG (n.*1586_*1588delinsTTG)
c.1130_1132delinsTTG
15g.48445469A=CA2175492757FBN1c.5824T= (p.Cys1942=)
n.4498T=
c.823T= (p.Cys275=)
c.*1587T= (n.*1587T=)
c.1131T=
15g.48445469A>CCA392340125FBN1c.5824T>G (p.Cys1942Gly)
n.4498T>G
c.823T>G (p.Cys275Gly)
c.*1587T>G (n.*1587T>G)
c.1131T>G
ClinVar dbSNP
15g.48445469A>GCA392340126FBN1c.5824T>C (p.Cys1942Arg)
n.4498T>C
c.823T>C (p.Cys275Arg)
c.*1587T>C (n.*1587T>C)
c.1131T>C
ClinVar dbSNP
15g.48445469A>TCA392340127FBN1c.5824T>A (p.Cys1942Ser)
n.4498T>A
c.823T>A (p.Cys275Ser)
c.*1587T>A (n.*1587T>A)
c.1131T>A
ClinVar dbSNP
15g.48445470_48445471delCA16614638FBN1c.5823_5824del (p.Cys1942GlnfsTer7)
n.4497_4498del
c.822_823del (p.Cys275GlnfsTer7)
c.*1586_*1587del (n.*1586_*1587del)
c.1130_1131del
ClinVar dbSNP
15g.48445470A>CCA490022648FBN1c.5823T>G (p.Leu1941=)
n.4497T>G
c.822T>G (p.Leu274=)
c.*1586T>G (n.*1586T>G)
c.1130T>G
15g.48445470A>GCA490022650FBN1c.5823T>C (p.Leu1941=)
n.4497T>C
c.822T>C (p.Leu274=)
c.*1586T>C (n.*1586T>C)
c.1130T>C
15g.48445470A>TCA490022651FBN1c.5823T>A (p.Leu1941=)
n.4497T>A
c.822T>A (p.Leu274=)
c.*1586T>A (n.*1586T>A)
c.1130T>A
15g.48445471A>CCA392340130FBN1c.5822T>G (p.Leu1941Arg)
n.4496T>G
c.821T>G (p.Leu274Arg)
c.*1585T>G (n.*1585T>G)
c.1129T>G
15g.48445471A>GCA392340132FBN1c.5822T>C (p.Leu1941Pro)
n.4496T>C
c.821T>C (p.Leu274Pro)
c.*1585T>C (n.*1585T>C)
c.1129T>C
15g.48445471A>TCA392340133FBN1c.5822T>A (p.Leu1941His)
n.4496T>A
c.821T>A (p.Leu274His)
c.*1585T>A (n.*1585T>A)
c.1129T>A
15g.48445472G>ACA392340135FBN1c.5821C>T (p.Leu1941Phe)
n.4495C>T
c.820C>T (p.Leu274Phe)
c.*1584C>T (n.*1584C>T)
c.1128C>T
ClinVar dbSNP gnomAD v4
15g.48445472G>CCA392340136FBN1c.5821C>G (p.Leu1941Val)
n.4495C>G
c.820C>G (p.Leu274Val)
c.*1584C>G (n.*1584C>G)
c.1128C>G
15g.48445472G=CA2175492775FBN1c.5821C= (p.Leu1941=)
n.4495C=
c.820C= (p.Leu274=)
c.*1584C= (n.*1584C=)
c.1128C=
15g.48445472G>TCA392340138FBN1c.5821C>A (p.Leu1941Ile)
n.4495C>A
c.820C>A (p.Leu274Ile)
c.*1584C>A (n.*1584C>A)
c.1128C>A
COSMIC
15g.48445473A>CCA392340143FBN1c.5820T>G (p.Asn1940Lys)
n.4494T>G
c.819T>G (p.Asn273Lys)
c.*1583T>G (n.*1583T>G)
c.1127T>G
15g.48445473A>GCA490022669FBN1c.5820T>C (p.Asn1940=)
n.4494T>C
c.819T>C (p.Asn273=)
c.*1583T>C (n.*1583T>C)
c.1127T>C
15g.48445473A>TCA392340141FBN1c.5820T>A (p.Asn1940Lys)
n.4494T>A
c.819T>A (p.Asn273Lys)
c.*1583T>A (n.*1583T>A)
c.1127T>A
15g.48445474T>ACA392340145FBN1c.5819A>T (p.Asn1940Ile)
n.4493A>T
c.818A>T (p.Asn273Ile)
c.*1582A>T (n.*1582A>T)
c.1126A>T
15g.48445474T>CCA392340147FBN1c.5819A>G (p.Asn1940Ser)
n.4493A>G
c.818A>G (p.Asn273Ser)
c.*1582A>G (n.*1582A>G)
c.1126A>G
15g.48445474T>GCA392340148FBN1c.5819A>C (p.Asn1940Thr)
n.4493A>C
c.818A>C (p.Asn273Thr)
c.*1582A>C (n.*1582A>C)
c.1126A>C
15g.48445475T>ACA392340151FBN1c.5818A>T (p.Asn1940Tyr)
n.4492A>T
c.817A>T (p.Asn273Tyr)
c.*1581A>T (n.*1581A>T)
c.1125A>T
15g.48445475T>CCA392340153FBN1c.5818A>G (p.Asn1940Asp)
n.4492A>G
c.817A>G (p.Asn273Asp)
c.*1581A>G (n.*1581A>G)
c.1125A>G
15g.48445475T>GCA392340154FBN1c.5818A>C (p.Asn1940His)
n.4492A>C
c.817A>C (p.Asn273His)
c.*1581A>C (n.*1581A>C)
c.1125A>C
15g.48445475_48445476delinsTCCA2175492780FBN1c.5817_5818delinsGA (p.Gly1939=)
n.4491_4492delinsGA
c.816_817delinsGA (p.Gly272=)
c.*1580_*1581delinsGA (n.*1580_*1581delinsGA)
c.1124_1125delinsGA
15g.48445476C>ACA490022679FBN1c.5817G>T (p.Gly1939=)
n.4491G>T
c.816G>T (p.Gly272=)
c.*1580G>T (n.*1580G>T)
c.1124G>T
15g.48445476C=CA2175492792FBN1c.5817G= (p.Gly1939=)
n.4491G=
c.816G= (p.Gly272=)
c.*1580G= (n.*1580G=)
c.1124G=
15g.48445476C>GCA269532868FBN1c.5817G>C (p.Gly1939=)
n.4491G>C
c.816G>C (p.Gly272=)
c.*1580G>C (n.*1580G>C)
c.1124G>C
dbSNP gnomAD v4
15g.48445476C>TCA055731FBN1c.5817G>A (p.Gly1939=)
n.4491G>A
c.816G>A (p.Gly272=)
c.*1580G>A (n.*1580G>A)
c.1124G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.48445478delCA016091FBN1c.5817del (p.Asn1940IlefsTer?)
n.4491del
c.816del (p.Asn273IlefsTer?)
c.*1580del (n.*1580del)
c.1124del
ClinVar dbSNP
15g.48445477C>ACA392340160FBN1c.5816G>T (p.Gly1939Val)
n.4490G>T
c.815G>T (p.Gly272Val)
c.*1579G>T (n.*1579G>T)
c.1123G>T
15g.48445477C=CA2175492799FBN1c.5816G= (p.Gly1939=)
n.4490G=
c.815G= (p.Gly272=)
c.*1579G= (n.*1579G=)
c.1123G=
15g.48445477C>GCA392340163FBN1c.5816G>C (p.Gly1939Ala)
n.4490G>C
c.815G>C (p.Gly272Ala)
c.*1579G>C (n.*1579G>C)
c.1123G>C
dbSNP
15g.48445477C>TCA055723FBN1c.5816G>A (p.Gly1939Glu)
n.4490G>A
c.815G>A (p.Gly272Glu)
c.*1579G>A (n.*1579G>A)
c.1123G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.48445478C>ACA392340165FBN1c.5815G>T (p.Gly1939Trp)
n.4489G>T
c.814G>T (p.Gly272Trp)
c.*1578G>T (n.*1578G>T)
c.1122G>T
ClinVar
15g.48445478C>GCA392340166FBN1c.5815G>C (p.Gly1939Arg)
n.4489G>C
c.814G>C (p.Gly272Arg)
c.*1578G>C (n.*1578G>C)
c.1122G>C
COSMIC
15g.48445478C>TCA392340168FBN1c.5815G>A (p.Gly1939Arg)
n.4489G>A
c.814G>A (p.Gly272Arg)
c.*1578G>A (n.*1578G>A)
c.1122G>A
gnomAD v4
15g.48445479A>CCA392340171FBN1c.5814T>G (p.Asn1938Lys)
n.4488T>G
c.813T>G (p.Asn271Lys)
c.*1577T>G (n.*1577T>G)
c.1121T>G
15g.48445479A>GCA490022689FBN1c.5814T>C (p.Asn1938=)
n.4488T>C
c.813T>C (p.Asn271=)
c.*1577T>C (n.*1577T>C)
c.1121T>C
15g.48445479A>TCA392340172FBN1c.5814T>A (p.Asn1938Lys)
n.4488T>A
c.813T>A (p.Asn271Lys)
c.*1577T>A (n.*1577T>A)
c.1121T>A
15g.48445479_48445480delinsATCA2175492805FBN1c.5813_5814delinsAT (p.Asn1938=)
n.4487_4488delinsAT
c.812_813delinsAT (p.Asn271=)
c.*1576_*1577delinsAT (n.*1576_*1577delinsAT)
c.1120_1121delinsAT
15g.48445480T>ACA392340175FBN1c.5813A>T (p.Asn1938Ile)
n.4487A>T
c.812A>T (p.Asn271Ile)
c.*1576A>T (n.*1576A>T)
c.1120A>T
15g.48445480T>CCA392340180FBN1c.5813A>G (p.Asn1938Ser)
n.4487A>G
c.812A>G (p.Asn271Ser)
c.*1576A>G (n.*1576A>G)
c.1120A>G
15g.48445480T>GCA392340178FBN1c.5813A>C (p.Asn1938Thr)
n.4487A>C
c.812A>C (p.Asn271Thr)
c.*1576A>C (n.*1576A>C)
c.1120A>C
15g.48445482delCA055708FBN1c.5813del (p.Asn1938MetfsTer?)
n.4487del
c.812del (p.Asn271MetfsTer?)
c.*1576del (n.*1576del)
c.1120del
dbSNP ExAC gnomAD v2 gnomAD v4
15g.48445481T>ACA392340182FBN1c.5812A>T (p.Asn1938Tyr)
n.4486A>T
c.811A>T (p.Asn271Tyr)
c.*1575A>T (n.*1575A>T)
c.1119A>T
15g.48445481T>CCA392340184FBN1c.5812A>G (p.Asn1938Asp)
n.4486A>G
c.811A>G (p.Asn271Asp)
c.*1575A>G (n.*1575A>G)
c.1119A>G
15g.48445481T>GCA392340185FBN1c.5812A>C (p.Asn1938His)
n.4486A>C
c.811A>C (p.Asn271His)
c.*1575A>C (n.*1575A>C)
c.1119A>C
15g.48445482T>ACA490022713FBN1c.5811A>T (p.Gly1937=)
n.4485A>T
c.810A>T (p.Gly270=)
c.*1574A>T (n.*1574A>T)
c.1118A>T
15g.48445482T>CCA490022708FBN1c.5811A>G (p.Gly1937=)
n.4485A>G
c.810A>G (p.Gly270=)
c.*1574A>G (n.*1574A>G)
c.1118A>G
15g.48445482T>GCA490022706FBN1c.5811A>C (p.Gly1937=)
n.4485A>C
c.810A>C (p.Gly270=)
c.*1574A>C (n.*1574A>C)
c.1118A>C
15g.48445483C>ACA392340187FBN1c.5810G>T (p.Gly1937Val)
n.4484G>T
c.809G>T (p.Gly270Val)
c.*1573G>T (n.*1573G>T)
c.1117G>T
15g.48445483C=CA2175492811FBN1c.5810G= (p.Gly1937=)
n.4484G=
c.809G= (p.Gly270=)
c.*1573G= (n.*1573G=)
c.1117G=
15g.48445483C>GCA392340189FBN1c.5810G>C (p.Gly1937Ala)
n.4484G>C
c.809G>C (p.Gly270Ala)
c.*1573G>C (n.*1573G>C)
c.1117G>C
ClinVar dbSNP
15g.48445483C>TCA392340190FBN1c.5810G>A (p.Gly1937Glu)
n.4484G>A
c.809G>A (p.Gly270Glu)
c.*1573G>A (n.*1573G>A)
c.1117G>A
ClinVar dbSNP
15g.48445484C>ACA392340192FBN1c.5809G>T (p.Gly1937Ter)
n.4483G>T
c.808G>T (p.Gly270Ter)
c.*1572G>T (n.*1572G>T)
c.1116G>T
ClinVar dbSNP
15g.48445484C=CA2175492818FBN1c.5809G= (p.Gly1937=)
n.4483G=
c.808G= (p.Gly270=)
c.*1572G= (n.*1572G=)
c.1116G=
15g.48445484C>GCA392340193FBN1c.5809G>C (p.Gly1937Arg)
n.4483G>C
c.808G>C (p.Gly270Arg)
c.*1572G>C (n.*1572G>C)
c.1116G>C
15g.48445484C>TCA392340194FBN1c.5809G>A (p.Gly1937Arg)
n.4483G>A
c.808G>A (p.Gly270Arg)
c.*1572G>A (n.*1572G>A)
c.1116G>A
ClinVar gnomAD v4
15g.48445485A>CCA392340196FBN1c.5808T>G (p.Ser1936Arg)
n.4482T>G
c.807T>G (p.Ser269Arg)
c.*1571T>G (n.*1571T>G)
c.1115T>G
15g.48445485A>GCA490022725FBN1c.5808T>C (p.Ser1936=)
n.4482T>C
c.807T>C (p.Ser269=)
c.*1571T>C (n.*1571T>C)
c.1115T>C
15g.48445485A>TCA392340198FBN1c.5808T>A (p.Ser1936Arg)
n.4482T>A
c.807T>A (p.Ser269Arg)
c.*1571T>A (n.*1571T>A)
c.1115T>A
15g.48445486C>ACA392340200FBN1c.5807G>T (p.Ser1936Ile)
n.4481G>T
c.806G>T (p.Ser269Ile)
c.*1570G>T (n.*1570G>T)
c.1114G>T
15g.48445486C>GCA392340203FBN1c.5807G>C (p.Ser1936Thr)
n.4481G>C
c.806G>C (p.Ser269Thr)
c.*1570G>C (n.*1570G>C)
c.1114G>C
COSMIC
15g.48445486C>TCA392340201FBN1c.5807G>A (p.Ser1936Asn)
n.4481G>A
c.806G>A (p.Ser269Asn)
c.*1570G>A (n.*1570G>A)
c.1114G>A
gnomAD v4 COSMIC
15g.48445487T>ACA392340204FBN1c.5806A>T (p.Ser1936Cys)
n.4480A>T
c.805A>T (p.Ser269Cys)
c.*1569A>T (n.*1569A>T)
c.1113A>T
15g.48445487T>CCA353660FBN1c.5806A>G (p.Ser1936Gly)
n.4480A>G
c.805A>G (p.Ser269Gly)
c.*1569A>G (n.*1569A>G)
c.1113A>G
ClinVar dbSNP gnomAD v4
15g.48445487T>GCA392340206FBN1c.5806A>C (p.Ser1936Arg)
n.4480A>C
c.805A>C (p.Ser269Arg)
c.*1569A>C (n.*1569A>C)
c.1113A>C
15g.48445487T=CA2175492830FBN1c.5806A= (p.Ser1936=)
n.4480A=
c.805A= (p.Ser269=)
c.*1569A= (n.*1569A=)
c.1113A=
15g.48445488T>ACA490022739FBN1c.5805A>T (p.Ala1935=)
n.4479A>T
c.804A>T (p.Ala268=)
c.*1568A>T (n.*1568A>T)
c.1112A>T
15g.48445488T>CCA490022742FBN1c.5805A>G (p.Ala1935=)
n.4479A>G
c.804A>G (p.Ala268=)
c.*1568A>G (n.*1568A>G)
c.1112A>G
15g.48445488T>GCA055704FBN1c.5805A>C (p.Ala1935=)
n.4479A>C
c.804A>C (p.Ala268=)
c.*1568A>C (n.*1568A>C)
c.1112A>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.48445488T=CA2175492836FBN1c.5805A= (p.Ala1935=)
n.4479A=
c.804A= (p.Ala268=)
c.*1568A= (n.*1568A=)
c.1112A=
15g.48445489G>ACA392340209FBN1c.5804C>T (p.Ala1935Val)
n.4478C>T
c.803C>T (p.Ala268Val)
c.*1567C>T (n.*1567C>T)
c.1111C>T
15g.48445489G>CCA392340211FBN1c.5804C>G (p.Ala1935Gly)
n.4478C>G
c.803C>G (p.Ala268Gly)
c.*1567C>G (n.*1567C>G)
c.1111C>G
15g.48445489G>TCA392340212FBN1c.5804C>A (p.Ala1935Glu)
n.4478C>A
c.803C>A (p.Ala268Glu)
c.*1567C>A (n.*1567C>A)
c.1111C>A
15g.48445490C>ACA392340213FBN1c.5803G>T (p.Ala1935Ser)
n.4477G>T
c.802G>T (p.Ala268Ser)
c.*1566G>T (n.*1566G>T)
c.1110G>T
15g.48445490C>GCA392340214FBN1c.5803G>C (p.Ala1935Pro)
n.4477G>C
c.802G>C (p.Ala268Pro)
c.*1566G>C (n.*1566G>C)
c.1110G>C
15g.48445490C>TCA392340215FBN1c.5803G>A (p.Ala1935Thr)
n.4477G>A
c.802G>A (p.Ala268Thr)
c.*1566G>A (n.*1566G>A)
c.1110G>A
gnomAD v4
15g.48445491A>CCA392340217FBN1c.5802T>G (p.Cys1934Trp)
n.4476T>G
c.801T>G (p.Cys267Trp)
c.*1565T>G (n.*1565T>G)
c.1109T>G
ClinVar dbSNP
15g.48445491A>GCA490022755FBN1c.5802T>C (p.Cys1934=)
n.4476T>C
c.801T>C (p.Cys267=)
c.*1565T>C (n.*1565T>C)
c.1109T>C
15g.48445491A>TCA392340219FBN1c.5802T>A (p.Cys1934Ter)
n.4476T>A
c.801T>A (p.Cys267Ter)
c.*1565T>A (n.*1565T>A)
c.1109T>A
15g.48445492C>ACA392340222FBN1c.5801G>T (p.Cys1934Phe)
n.4475G>T
c.800G>T (p.Cys267Phe)
c.*1564G>T (n.*1564G>T)
c.1108G>T
15g.48445492C=CA2175492844FBN1c.5801G= (p.Cys1934=)
n.4475G=
c.800G= (p.Cys267=)
c.*1564G= (n.*1564G=)
c.1108G=
15g.48445492C>GCA392340225FBN1c.5801G>C (p.Cys1934Ser)
n.4475G>C
c.800G>C (p.Cys267Ser)
c.*1564G>C (n.*1564G>C)
c.1108G>C
ClinVar dbSNP
15g.48445492C>TCA016083FBN1c.5801G>A (p.Cys1934Tyr)
n.4475G>A
c.800G>A (p.Cys267Tyr)
c.*1564G>A (n.*1564G>A)
c.1108G>A
ClinVar dbSNP
15g.48445493A=CA2175492851FBN1c.5800T= (p.Cys1934=)
n.4474T=
c.799T= (p.Cys267=)
c.*1563T= (n.*1563T=)
c.1107T=
15g.48445493A>CCA392340227FBN1c.5800T>G (p.Cys1934Gly)
n.4474T>G
c.799T>G (p.Cys267Gly)
c.*1563T>G (n.*1563T>G)
c.1107T>G
15g.48445493A>GCA392340228FBN1c.5800T>C (p.Cys1934Arg)
n.4474T>C
c.799T>C (p.Cys267Arg)
c.*1563T>C (n.*1563T>C)
c.1107T>C
ClinVar dbSNP
15g.48445493A>TCA392340230FBN1c.5800T>A (p.Cys1934Ser)
n.4474T>A
c.799T>A (p.Cys267Ser)
c.*1563T>A (n.*1563T>A)
c.1107T>A
ClinVar dbSNP
15g.48445494T>ACA392340232FBN1c.5799A>T (p.Glu1933Asp)
n.4473A>T
c.798A>T (p.Glu266Asp)
c.*1562A>T (n.*1562A>T)
c.1106A>T
gnomAD v4
15g.48445494T>CCA490022773FBN1c.5799A>G (p.Glu1933=)
n.4473A>G
c.798A>G (p.Glu266=)
c.*1562A>G (n.*1562A>G)
c.1106A>G
dbSNP
15g.48445494T>GCA392340234FBN1c.5799A>C (p.Glu1933Asp)
n.4473A>C
c.798A>C (p.Glu266Asp)
c.*1562A>C (n.*1562A>C)
c.1106A>C
15g.48445494T=CA2175492856FBN1c.5799A= (p.Glu1933=)
n.4473A=
c.798A= (p.Glu266=)
c.*1562A= (n.*1562A=)
c.1106A=
15g.48445495T>ACA392340240FBN1c.5798A>T (p.Glu1933Val)
n.4472A>T
c.797A>T (p.Glu266Val)
c.*1561A>T (n.*1561A>T)
c.1105A>T
15g.48445495T>CCA392340236FBN1c.5798A>G (p.Glu1933Gly)
n.4472A>G
c.797A>G (p.Glu266Gly)
c.*1561A>G (n.*1561A>G)
c.1105A>G
15g.48445495T>GCA392340238FBN1c.5798A>C (p.Glu1933Ala)
n.4472A>C
c.797A>C (p.Glu266Ala)
c.*1561A>C (n.*1561A>C)
c.1105A>C
15g.48445498_48445500delCA2695220239FBN1c.5796_5798del (p.Asp1932del)
n.4470_4472del
c.795_797del (p.Asp265del)
c.*1559_*1561del (n.*1559_*1561del)
c.1103_1105del
15g.48445496delCA2695220241FBN1c.5797del (p.Glu1933AsnfsTer?)
n.4471del
c.796del (p.Glu266AsnfsTer?)
c.*1560del (n.*1560del)
c.1104del
15g.48445496C>ACA392340242FBN1c.5797G>T (p.Glu1933Ter)
n.4471G>T
c.796G>T (p.Glu266Ter)
c.*1560G>T (n.*1560G>T)
c.1104G>T
15g.48445496C>GCA392340244FBN1c.5797G>C (p.Glu1933Gln)
n.4471G>C
c.796G>C (p.Glu266Gln)
c.*1560G>C (n.*1560G>C)
c.1104G>C
15g.48445496C>TCA392340245FBN1c.5797G>A (p.Glu1933Lys)
n.4471G>A
c.796G>A (p.Glu266Lys)
c.*1560G>A (n.*1560G>A)
c.1104G>A
ClinVar dbSNP
15g.48445497A>CCA392340248FBN1c.5796T>G (p.Asp1932Glu)
n.4470T>G
c.795T>G (p.Asp265Glu)
c.*1559T>G (n.*1559T>G)
c.1103T>G
15g.48445497A>GCA490022778FBN1c.5796T>C (p.Asp1932=)
n.4470T>C
c.795T>C (p.Asp265=)
c.*1559T>C (n.*1559T>C)
c.1103T>C
15g.48445497A>TCA392340250FBN1c.5796T>A (p.Asp1932Glu)
n.4470T>A
c.795T>A (p.Asp265Glu)
c.*1559T>A (n.*1559T>A)
c.1103T>A
15g.48445498T>ACA392340251FBN1c.5795A>T (p.Asp1932Val)
n.4469A>T
c.794A>T (p.Asp265Val)
c.*1558A>T (n.*1558A>T)
c.1102A>T
15g.48445498T>CCA392340255FBN1c.5795A>G (p.Asp1932Gly)
n.4469A>G
c.794A>G (p.Asp265Gly)
c.*1558A>G (n.*1558A>G)
c.1102A>G
dbSNP
15g.48445498T>GCA392340253FBN1c.5795A>C (p.Asp1932Ala)
n.4469A>C
c.794A>C (p.Asp265Ala)
c.*1558A>C (n.*1558A>C)
c.1102A>C
ClinVar dbSNP
15g.48445498T=CA2175492868FBN1c.5795A= (p.Asp1932=)
n.4469A=
c.794A= (p.Asp265=)
c.*1558A= (n.*1558A=)
c.1102A=
15g.48445499C>ACA392340257FBN1c.5794G>T (p.Asp1932Tyr)
n.4468G>T
c.793G>T (p.Asp265Tyr)
c.*1557G>T (n.*1557G>T)
c.1101G>T
15g.48445499C>GCA392340261FBN1c.5794G>C (p.Asp1932His)
n.4468G>C
c.793G>C (p.Asp265His)
c.*1557G>C (n.*1557G>C)
c.1101G>C
15g.48445499C>TCA392340259FBN1c.5794G>A (p.Asp1932Asn)
n.4468G>A
c.793G>A (p.Asp265Asn)
c.*1557G>A (n.*1557G>A)
c.1101G>A
15g.48445501_48445503delCA2695220242FBN1c.5792_5794del (p.Val1931del)
n.4466_4468del
c.791_793del (p.Val264del)
c.*1555_*1557del (n.*1555_*1557del)
c.1099_1101del
15g.48445499_48445512delinsCAACATCTGCAGAACA2175492875FBN1c.5789-8_5794delinsTTCTGCAGATGTTG
n.4463-8_4468delinsTTCTGCAGATGTTG
c.788-8_793delinsTTCTGCAGATGTTG
c.*1552-8_*1557delinsTTCTGCAGATGTTG
c.1096-8_1101delinsTTCTGCAGATGTTG
15g.48445500A>CCA490022788FBN1c.5793T>G (p.Val1931=)
n.4467T>G
c.792T>G (p.Val264=)
c.*1556T>G (n.*1556T>G)
c.1100T>G
15g.48445500A>GCA490022790FBN1c.5793T>C (p.Val1931=)
n.4467T>C
c.792T>C (p.Val264=)
c.*1556T>C (n.*1556T>C)
c.1100T>C
15g.48445500A>TCA490022791FBN1c.5793T>A (p.Val1931=)
n.4467T>A
c.792T>A (p.Val264=)
c.*1556T>A (n.*1556T>A)
c.1100T>A
15g.48445502_48445514delCA16619949FBN1c.5789-8_5793del
n.4463-8_4467del
c.788-8_792del
c.*1552-8_*1556del
c.1096-8_1100del
ClinVar dbSNP
15g.48445501A>CCA392340263FBN1c.5792T>G (p.Val1931Gly)
n.4466T>G
c.791T>G (p.Val264Gly)
c.*1555T>G (n.*1555T>G)
c.1099T>G
15g.48445501A>GCA392340267FBN1c.5792T>C (p.Val1931Ala)
n.4466T>C
c.791T>C (p.Val264Ala)
c.*1555T>C (n.*1555T>C)
c.1099T>C
15g.48445501A>TCA392340265FBN1c.5792T>A (p.Val1931Asp)
n.4466T>A
c.791T>A (p.Val264Asp)
c.*1555T>A (n.*1555T>A)
c.1099T>A
15g.48445502C>ACA392340270FBN1c.5791G>T (p.Val1931Phe)
n.4465G>T
c.790G>T (p.Val264Phe)
c.*1554G>T (n.*1554G>T)
c.1098G>T
15g.48445502C=CA2175492890FBN1c.5791G= (p.Val1931=)
n.4465G=
c.790G= (p.Val264=)
c.*1554G= (n.*1554G=)
c.1098G=
15g.48445502C>GCA392340271FBN1c.5791G>C (p.Val1931Leu)
n.4465G>C
c.790G>C (p.Val264Leu)
c.*1554G>C (n.*1554G>C)
c.1098G>C
15g.48445502C>TCA392340272FBN1c.5791G>A (p.Val1931Ile)
n.4465G>A
c.790G>A (p.Val264Ile)
c.*1554G>A (n.*1554G>A)
c.1098G>A
ClinVar dbSNP gnomAD v4
15g.48445503A>CCA392340275FBN1c.5790T>G (p.Asp1930Glu)
n.4464T>G
c.789T>G (p.Asp263Glu)
c.*1553T>G (n.*1553T>G)
c.1097T>G
15g.48445503A>GCA490022801FBN1c.5790T>C (p.Asp1930=)
n.4464T>C
c.789T>C (p.Asp263=)
c.*1553T>C (n.*1553T>C)
c.1097T>C
15g.48445503A>TCA392340276FBN1c.5790T>A (p.Asp1930Glu)
n.4464T>A
c.789T>A (p.Asp263Glu)
c.*1553T>A (n.*1553T>A)
c.1097T>A
15g.48445504T>ACA392340278FBN1c.5789A>T (p.Asp1930Val)
n.4463A>T
c.788A>T (p.Asp263Val)
c.*1552A>T (n.*1552A>T)
c.1096A>T
15g.48445504T>CCA392340280FBN1c.5789A>G (p.Asp1930Gly)
n.4463A>G
c.788A>G (p.Asp263Gly)
c.*1552A>G (n.*1552A>G)
c.1096A>G
ClinVar
15g.48445504T>GCA392340283FBN1c.5789A>C (p.Asp1930Ala)
n.4463A>C
c.788A>C (p.Asp263Ala)
c.*1552A>C (n.*1552A>C)
c.1096A>C
15g.48445505C>ACA392340285FBN1c.5789-1G>T (n.5789-1G>T)
n.4463-1G>T
c.788-1G>T (n.788-1G>T)
c.*1552-1G>T (n.*1552-1G>T)
c.1096-1G>T
15g.48445505C=CA2175492902FBN1c.5789-1G= (n.5789-1G=)
n.4463-1G=
c.788-1G= (n.788-1G=)
c.*1552-1G= (n.*1552-1G=)
c.1096-1G=
15g.48445505C>GCA392340286FBN1c.5789-1G>C (n.5789-1G>C)
n.4463-1G>C
c.788-1G>C (n.788-1G>C)
c.*1552-1G>C (n.*1552-1G>C)
c.1096-1G>C
15g.48445505C>TCA392340288FBN1c.5789-1G>A (n.5789-1G>A)
n.4463-1G>A
c.788-1G>A (n.788-1G>A)
c.*1552-1G>A (n.*1552-1G>A)
c.1096-1G>A
ClinVar dbSNP
15g.48445506T>ACA392340293FBN1c.5789-2A>T (n.5789-2A>T)
n.4463-2A>T
c.788-2A>T (n.788-2A>T)
c.*1552-2A>T (n.*1552-2A>T)
c.1096-2A>T
15g.48445506T>CCA10587813FBN1c.5789-2A>G (n.5789-2A>G)
n.4463-2A>G
c.788-2A>G (n.788-2A>G)
c.*1552-2A>G (n.*1552-2A>G)
c.1096-2A>G
ClinVar dbSNP
15g.48445506T>GCA392340291FBN1c.5789-2A>C (n.5789-2A>C)
n.4463-2A>C
c.788-2A>C (n.788-2A>C)
c.*1552-2A>C (n.*1552-2A>C)
c.1096-2A>C
15g.48445506T=CA2175492907FBN1c.5789-2A= (n.5789-2A=)
n.4463-2A=
c.788-2A= (n.788-2A=)
c.*1552-2A= (n.*1552-2A=)
c.1096-2A=
15g.48445506_48445507insATACAGTCATTGTTGTGAGAAAGGATGAAACCATGATTCA2628347635FBN1c.5789-2_5789-1insATCATGGTTTCATCCTTTCTCACAACAATGACTGTATA (n.5789-2_5789-1insATCATGGTTTCATCCTTTCTCACAACAATGACTGTATA)
n.4463-2_4463-1insATCATGGTTTCATCCTTTCTCACAACAATGACTGTATA
c.788-2_788-1insATCATGGTTTCATCCTTTCTCACAACAATGACTGTATA (n.788-2_788-1insATCATGGTTTCATCCTTTCTCACAACAATGACTGTATA)
c.*1552-2_*1552-1insATCATGGTTTCATCCTTTCTCACAACAATGACTGTATA (n.*1552-2_*1552-1insATCATGGTTTCATCCTTTCTCACAACAATGACTGTATA)
c.1096-2_1096-1insATCATGGTTTCATCCTTTCTCACAACAATGACTGTATA
gnomAD v4
15g.48445506_48445507insATACACA2628347637FBN1c.5789-3_5789-2insTGTAT (n.5789-3_5789-2insTGTAT)
n.4463-3_4463-2insTGTAT
c.788-3_788-2insTGTAT (n.788-3_788-2insTGTAT)
c.*1552-3_*1552-2insTGTAT (n.*1552-3_*1552-2insTGTAT)
c.1096-3_1096-2insTGTAT
gnomAD v4
15g.48445506_48445507insATACAGTCATTGTTGTGAGAAAGGATGAAACCATGATTGCAGCGCA2628347638FBN1c.5789-3_5789-2insCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT (n.5789-3_5789-2insCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT)
n.4463-3_4463-2insCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT
c.788-3_788-2insCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT (n.788-3_788-2insCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT)
c.*1552-3_*1552-2insCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT (n.*1552-3_*1552-2insCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT)
c.1096-3_1096-2insCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT
gnomAD v4
15g.48445506_48445507insATACAGTCATTGTTGTGAGAAAGGATGAAACCATGATTGCAGCGGCAGTTGAAGGAACCAATTGTGTTCCGCA2628347636FBN1c.5789-3_5789-2insCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT (n.5789-3_5789-2insCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT)
n.4463-3_4463-2insCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT
c.788-3_788-2insCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT (n.788-3_788-2insCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT)
c.*1552-3_*1552-2insCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT (n.*1552-3_*1552-2insCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT)
c.1096-3_1096-2insCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT
gnomAD v4
15g.48445506_48445507insATACAGTCATTGTTGTGAGAAAGGATGAAACCATGATTGCAGCGGCAGTTGAAGGAACCAATTGTGTTCCGGCAAGTTCCATTCCCACAGCA617837075FBN1c.5789-3_5789-2insCTGTGGGAATGGAACTTGCCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT (n.5789-3_5789-2insCTGTGGGAATGGAACTTGCCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT)
n.4463-3_4463-2insCTGTGGGAATGGAACTTGCCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT
c.788-3_788-2insCTGTGGGAATGGAACTTGCCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT (n.788-3_788-2insCTGTGGGAATGGAACTTGCCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT)
c.*1552-3_*1552-2insCTGTGGGAATGGAACTTGCCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT (n.*1552-3_*1552-2insCTGTGGGAATGGAACTTGCCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT)
c.1096-3_1096-2insCTGTGGGAATGGAACTTGCCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGACTGTAT
gnomAD v2 gnomAD v4
15g.48445507G>ACA617837076FBN1c.5789-3C>T (n.5789-3C>T)
n.4463-3C>T
c.788-3C>T (n.788-3C>T)
c.*1552-3C>T (n.*1552-3C>T)
c.1096-3C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.48445507G=CA2175492911FBN1c.5789-3C= (n.5789-3C=)
n.4463-3C=
c.788-3C= (n.788-3C=)
c.*1552-3C= (n.*1552-3C=)
c.1096-3C=
15g.48445507G>TCA2695220244FBN1c.5789-3C>A (n.5789-3C>A)
n.4463-3C>A
c.788-3C>A (n.788-3C>A)
c.*1552-3C>A (n.*1552-3C>A)
c.1096-3C>A
15g.48445507_48445508insTCATTGTTGTGAGAAAGGATGAAACCATGATTGCAGCGGCAGTTGAAGGAACCAATTGTGTTCCGGCAAGTTCCATTCCCACA2628347639FBN1c.5789-4_5789-3insTGGGAATGGAACTTGCCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGA (n.5789-4_5789-3insTGGGAATGGAACTTGCCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGA)
n.4463-4_4463-3insTGGGAATGGAACTTGCCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGA
c.788-4_788-3insTGGGAATGGAACTTGCCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGA (n.788-4_788-3insTGGGAATGGAACTTGCCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGA)
c.*1552-4_*1552-3insTGGGAATGGAACTTGCCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGA (n.*1552-4_*1552-3insTGGGAATGGAACTTGCCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGA)
c.1096-4_1096-3insTGGGAATGGAACTTGCCGGAACACAATTGGTTCCTTCAACTGCCGCTGCAATCATGGTTTCATCCTTTCTCACAACAATGA
gnomAD v4
15g.48445508C>TCA2575716715FBN1c.5789-4G>A (n.5789-4G>A)
n.4463-4G>A
c.788-4G>A (n.788-4G>A)
c.*1552-4G>A (n.*1552-4G>A)
c.1096-4G>A
15g.48445510G>ACA2175492915FBN1c.5789-6C>T (n.5789-6C>T)
n.4463-6C>T
c.788-6C>T (n.788-6C>T)
c.*1552-6C>T (n.*1552-6C>T)
c.1096-6C>T
dbSNP
15g.48445510G=CA2175492914FBN1c.5789-6C= (n.5789-6C=)
n.4463-6C=
c.788-6C= (n.788-6C=)
c.*1552-6C= (n.*1552-6C=)
c.1096-6C=
15g.48445510_48445511insCGGCA2628347640FBN1c.5789-6_5789-5insCGC (n.5789-6_5789-5insCGC)
n.4463-6_4463-5insCGC
c.788-6_788-5insCGC (n.788-6_788-5insCGC)
c.*1552-6_*1552-5insCGC (n.*1552-6_*1552-5insCGC)
c.1096-6_1096-5insCGC
gnomAD v4
15g.48445511A>GCA2575716718FBN1c.5789-7T>C (n.5789-7T>C)
n.4463-7T>C
c.788-7T>C (n.788-7T>C)
c.*1552-7T>C (n.*1552-7T>C)
c.1096-7T>C
15g.48445513_48445519delinsTCA2695220245FBN1c.5789-15_5789-9delinsA (n.5789-15_5789-9delinsA)
n.4463-15_4463-9delinsA
c.788-15_788-9delinsA (n.788-15_788-9delinsA)
c.*1552-15_*1552-9delinsA (n.*1552-15_*1552-9delinsA)
c.1096-15_1096-9delinsA
15g.48445514A>TCA2573150958FBN1c.5789-10T>A (n.5789-10T>A)
n.4463-10T>A
c.788-10T>A (n.788-10T>A)
c.*1552-10T>A (n.*1552-10T>A)
c.1096-10T>A
ClinVar dbSNP
15g.48445515A>CCA2740096636FBN1c.5789-11T>G (n.5789-11T>G)
n.4463-11T>G
c.788-11T>G (n.788-11T>G)
c.*1552-11T>G (n.*1552-11T>G)
c.1096-11T>G
ClinVar
15g.48445517C>ACA055672FBN1c.5789-13G>T (n.5789-13G>T)
n.4463-13G>T
c.788-13G>T (n.788-13G>T)
c.*1552-13G>T (n.*1552-13G>T)
c.1096-13G>T
dbSNP ExAC gnomAD v2 gnomAD v4
15g.48445517C=CA2175492920FBN1c.5789-13G= (n.5789-13G=)
n.4463-13G=
c.788-13G= (n.788-13G=)
c.*1552-13G= (n.*1552-13G=)
c.1096-13G=
15g.48445517C>TCA055665FBN1c.5789-13G>A (n.5789-13G>A)
n.4463-13G>A
c.788-13G>A (n.788-13G>A)
c.*1552-13G>A (n.*1552-13G>A)
c.1096-13G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.48445518C>TCA2740096637FBN1c.5789-14G>A (n.5789-14G>A)
n.4463-14G>A
c.788-14G>A (n.788-14G>A)
c.*1552-14G>A (n.*1552-14G>A)
c.1096-14G>A
ClinVar
15g.48445519C>TCA2695220246FBN1c.5789-15G>A (n.5789-15G>A)
n.4463-15G>A
c.788-15G>A (n.788-15G>A)
c.*1552-15G>A (n.*1552-15G>A)
c.1096-15G>A
15g.48445521A=CA2175492927FBN1c.5789-17T= (n.5789-17T=)
n.4463-17T=
c.788-17T= (n.788-17T=)
c.*1552-17T= (n.*1552-17T=)
c.1096-17T=
15g.48445521A>GCA617837079FBN1c.5789-17T>C (n.5789-17T>C)
n.4463-17T>C
c.788-17T>C (n.788-17T>C)
c.*1552-17T>C (n.*1552-17T>C)
c.1096-17T>C
dbSNP gnomAD v2 gnomAD v4
15g.48445523C>ACA2628347641FBN1c.5789-19G>T (n.5789-19G>T)
n.4463-19G>T
c.788-19G>T (n.788-19G>T)
c.*1552-19G>T (n.*1552-19G>T)
c.1096-19G>T
gnomAD v4
15g.48445523C=CA2175492929FBN1c.5789-19G= (n.5789-19G=)
n.4463-19G=
c.788-19G= (n.788-19G=)
c.*1552-19G= (n.*1552-19G=)
c.1096-19G=
15g.48445523C>GCA617837081FBN1c.5789-19G>C (n.5789-19G>C)
n.4463-19G>C
c.788-19G>C (n.788-19G>C)
c.*1552-19G>C (n.*1552-19G>C)
c.1096-19G>C
dbSNP gnomAD v2 gnomAD v4
15g.48445526T>CCA2628347642FBN1c.5789-22A>G (n.5789-22A>G)
n.4463-22A>G
c.788-22A>G (n.788-22A>G)
c.*1552-22A>G (n.*1552-22A>G)
c.1096-22A>G
gnomAD v4
15g.48445528C>TCA2628347643FBN1c.5789-24G>A (n.5789-24G>A)
n.4463-24G>A
c.788-24G>A (n.788-24G>A)
c.*1552-24G>A (n.*1552-24G>A)
c.1096-24G>A
gnomAD v4
15g.48445529T>GCA2741427169FBN1c.5789-25A>C (n.5789-25A>C)
n.4463-25A>C
c.788-25A>C (n.788-25A>C)
c.*1552-25A>C (n.*1552-25A>C)
c.1096-25A>C
15g.48445529_48445531delCA2804070419FBN1c.5789-27_5789-25del (n.5789-27_5789-25del)
n.4463-27_4463-25del
c.788-27_788-25del (n.788-27_788-25del)
c.*1552-27_*1552-25del (n.*1552-27_*1552-25del)
c.1096-27_1096-25del
15g.48445531delCA2804070418FBN1c.5789-25del (n.5789-25del)
n.4463-25del
c.788-25del (n.788-25del)
c.*1552-25del (n.*1552-25del)
c.1096-25del
15g.48445533A>GCA2628347644FBN1c.5789-29T>C (n.5789-29T>C)
n.4463-29T>C
c.788-29T>C (n.788-29T>C)
c.*1552-29T>C (n.*1552-29T>C)
c.1096-29T>C
gnomAD v4
15g.48445534T>CCA2628347645FBN1c.5789-30A>G (n.5789-30A>G)
n.4463-30A>G
c.788-30A>G (n.788-30A>G)
c.*1552-30A>G (n.*1552-30A>G)
c.1096-30A>G
gnomAD v4
15g.48445535A=CA2175492935FBN1c.5789-31T= (n.5789-31T=)
n.4463-31T=
c.788-31T= (n.788-31T=)
c.*1552-31T= (n.*1552-31T=)
c.1096-31T=
15g.48445535A>GCA055679FBN1c.5789-31T>C (n.5789-31T>C)
n.4463-31T>C
c.788-31T>C (n.788-31T>C)
c.*1552-31T>C (n.*1552-31T>C)
c.1096-31T>C
dbSNP ExAC gnomAD v2 gnomAD v4
15g.48445536T>CCA2175492943FBN1c.5789-32A>G (n.5789-32A>G)
n.4463-32A>G
c.788-32A>G (n.788-32A>G)
c.*1552-32A>G (n.*1552-32A>G)
c.1096-32A>G
dbSNP gnomAD v4
15g.48445536T>GCA2628347646FBN1c.5789-32A>C (n.5789-32A>C)
n.4463-32A>C
c.788-32A>C (n.788-32A>C)
c.*1552-32A>C (n.*1552-32A>C)
c.1096-32A>C
gnomAD v4
15g.48445536T=CA2175492940FBN1c.5789-32A= (n.5789-32A=)
n.4463-32A=
c.788-32A= (n.788-32A=)
c.*1552-32A= (n.*1552-32A=)
c.1096-32A=
15g.48445538T>CCA2628347647FBN1c.5789-34A>G (n.5789-34A>G)
n.4463-34A>G
c.788-34A>G (n.788-34A>G)
c.*1552-34A>G (n.*1552-34A>G)
c.1096-34A>G
gnomAD v4
15g.48445541C>TCA2628347648FBN1c.5789-37G>A (n.5789-37G>A)
n.4463-37G>A
c.788-37G>A (n.788-37G>A)
c.*1552-37G>A (n.*1552-37G>A)
c.1096-37G>A
gnomAD v4
15g.48445542A=CA2175492945FBN1c.5789-38T= (n.5789-38T=)
n.4463-38T=
c.788-38T= (n.788-38T=)
c.*1552-38T= (n.*1552-38T=)
c.1096-38T=
15g.48445542A>CCA617837083FBN1c.5789-38T>G (n.5789-38T>G)
n.4463-38T>G
c.788-38T>G (n.788-38T>G)
c.*1552-38T>G (n.*1552-38T>G)
c.1096-38T>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.48445543A=CA2175492949FBN1c.5789-39T= (n.5789-39T=)
n.4463-39T=
c.788-39T= (n.788-39T=)
c.*1552-39T= (n.*1552-39T=)
c.1096-39T=
15g.48445543A>CCA617837084FBN1c.5789-39T>G (n.5789-39T>G)
n.4463-39T>G
c.788-39T>G (n.788-39T>G)
c.*1552-39T>G (n.*1552-39T>G)
c.1096-39T>G
dbSNP gnomAD v2 gnomAD v4
15g.48445543A>GCA055686FBN1c.5789-39T>C (n.5789-39T>C)
n.4463-39T>C
c.788-39T>C (n.788-39T>C)
c.*1552-39T>C (n.*1552-39T>C)
c.1096-39T>C
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.48445545G>ACA713394420FBN1c.5789-41C>T (n.5789-41C>T)
n.4463-41C>T
c.788-41C>T (n.788-41C>T)
c.*1552-41C>T (n.*1552-41C>T)
c.1096-41C>T
dbSNP
15g.48445545G=CA2175492956FBN1c.5789-41C= (n.5789-41C=)
n.4463-41C=
c.788-41C= (n.788-41C=)
c.*1552-41C= (n.*1552-41C=)
c.1096-41C=
15g.48445546A=CA2175492962FBN1c.5789-42T= (n.5789-42T=)
n.4463-42T=
c.788-42T= (n.788-42T=)
c.*1552-42T= (n.*1552-42T=)
c.1096-42T=
15g.48445546A>GCA617837085FBN1c.5789-42T>C (n.5789-42T>C)
n.4463-42T>C
c.788-42T>C (n.788-42T>C)
c.*1552-42T>C (n.*1552-42T>C)
c.1096-42T>C
dbSNP gnomAD v2
15g.48445546A>TCA2804070422FBN1c.5789-42T>A (n.5789-42T>A)
n.4463-42T>A
c.788-42T>A (n.788-42T>A)
c.*1552-42T>A (n.*1552-42T>A)
c.1096-42T>A
15g.48445548G>TCA2628347649FBN1c.5789-44C>A (n.5789-44C>A)
n.4463-44C>A
c.788-44C>A (n.788-44C>A)
c.*1552-44C>A (n.*1552-44C>A)
c.1096-44C>A
gnomAD v4
15g.48445549T>ACA055695FBN1c.5789-45A>T (n.5789-45A>T)
n.4463-45A>T
c.788-45A>T (n.788-45A>T)
c.*1552-45A>T (n.*1552-45A>T)
c.1096-45A>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.48445549T>CCA2628347650FBN1c.5789-45A>G (n.5789-45A>G)
n.4463-45A>G
c.788-45A>G (n.788-45A>G)
c.*1552-45A>G (n.*1552-45A>G)
c.1096-45A>G
gnomAD v4
15g.48445549T=CA2175492973FBN1c.5789-45A= (n.5789-45A=)
n.4463-45A=
c.788-45A= (n.788-45A=)
c.*1552-45A= (n.*1552-45A=)
c.1096-45A=
15g.48445550C>ACA2628347651FBN1c.5789-46G>T (n.5789-46G>T)
n.4463-46G>T
c.788-46G>T (n.788-46G>T)
c.*1552-46G>T (n.*1552-46G>T)
c.1096-46G>T
gnomAD v4
15g.48445554A>TCA2628347652FBN1c.5789-50T>A (n.5789-50T>A)
n.4463-50T>A
c.788-50T>A (n.788-50T>A)
c.*1552-50T>A (n.*1552-50T>A)
c.1096-50T>A
gnomAD v4

Number of alleles fetched