Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.48483805_48483809delinsCTTCTCA2175509335FBN1c.3838+9_3838+13delinsAGAAG (n.3838+9_3838+13delinsAGAAG)
n.2512+9_2512+13delinsAGAAG
c.637-9159_637-9155delinsAGAAG (n.637-9159_637-9155delinsAGAAG)
15g.48483806T>ACA051565FBN1c.3838+12A>T (n.3838+12A>T)
n.2512+12A>T
c.637-9156A>T (n.637-9156A>T)
dbSNP ExAC gnomAD v2 gnomAD v4
15g.48483806T=CA2175509336FBN1c.3838+12A= (n.3838+12A=)
n.2512+12A=
c.637-9156A= (n.637-9156A=)
15g.48483808_48483811delCA969555182FBN1c.3838+9_3838+12del (n.3838+9_3838+12del)
n.2512+9_2512+12del
c.637-9159_637-9156del (n.637-9159_637-9156del)
dbSNP gnomAD v3 gnomAD v4
15g.48483808_48483809delinsCTCA2175509340FBN1c.3838+9_3838+10delinsAG (n.3838+9_3838+10delinsAG)
n.2512+9_2512+10delinsAG
c.637-9159_637-9158delinsAG (n.637-9159_637-9158delinsAG)
15g.48483811delCA617835380FBN1c.3838+9del (n.3838+9del)
n.2512+9del
c.637-9159del (n.637-9159del)
dbSNP gnomAD v2 gnomAD v4
15g.48483811T>CCA2575717185FBN1c.3838+7A>G (n.3838+7A>G)
n.2512+7A>G
c.637-9161A>G (n.637-9161A>G)
15g.48483813C=CA2175509344FBN1c.3838+5G= (n.3838+5G=)
n.2512+5G=
c.637-9163G= (n.637-9163G=)
15g.48483813C>TCA2175509346FBN1c.3838+5G>A (n.3838+5G>A)
n.2512+5G>A
c.637-9163G>A (n.637-9163G>A)
dbSNP gnomAD v4
15g.48483815T>ACA658824434FBN1c.3838+3A>T (n.3838+3A>T)
n.2512+3A>T
c.637-9165A>T (n.637-9165A>T)
ClinVar dbSNP
15g.48483815T=CA2175509350FBN1c.3838+3A= (n.3838+3A=)
n.2512+3A=
c.637-9165A= (n.637-9165A=)
15g.48483816A>CCA392323508FBN1c.3838+2T>G (n.3838+2T>G)
n.2512+2T>G
c.637-9166T>G (n.637-9166T>G)
15g.48483816A>GCA392323511FBN1c.3838+2T>C (n.3838+2T>C)
n.2512+2T>C
c.637-9166T>C (n.637-9166T>C)
ClinVar
15g.48483816A>TCA392323514FBN1c.3838+2T>A (n.3838+2T>A)
n.2512+2T>A
c.637-9166T>A (n.637-9166T>A)
15g.48483817C>ACA392323517FBN1c.3838+1G>T (n.3838+1G>T)
n.2512+1G>T
c.637-9167G>T (n.637-9167G>T)
15g.48483817C>GCA392323519FBN1c.3838+1G>C (n.3838+1G>C)
n.2512+1G>C
c.637-9167G>C (n.637-9167G>C)
15g.48483817C>TCA392323521FBN1c.3838+1G>A (n.3838+1G>A)
n.2512+1G>A
c.637-9167G>A (n.637-9167G>A)
15g.48483818C>ACA392323524FBN1c.3838G>T (p.Asp1280Tyr)
n.2512G>T
c.637-9168G>T (n.637-9168G>T)
15g.48483818C=CA2175509357FBN1c.3838G= (p.Asp1280=)
n.2512G=
c.637-9168G= (n.637-9168G=)
15g.48483818C>GCA392323527FBN1c.3838G>C (p.Asp1280His)
n.2512G>C
c.637-9168G>C (n.637-9168G>C)
15g.48483818C>TCA014572FBN1c.3838G>A (p.Asp1280Asn)
n.2512G>A
c.637-9168G>A (n.637-9168G>A)
ClinVar dbSNP
15g.48483819_48483823delCA2695220657FBN1c.3834_3838del (p.Cys1278Ter)
n.2508_2512del
c.637-9172_637-9168del (n.637-9172_637-9168del)
15g.48483819T>ACA490016915FBN1c.3837A>T (p.Val1279=)
n.2511A>T
c.637-9169A>T (n.637-9169A>T)
15g.48483819T>CCA269525957FBN1c.3837A>G (p.Val1279=)
n.2511A>G
c.637-9169A>G (n.637-9169A>G)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.48483819T>GCA490016913FBN1c.3837A>C (p.Val1279=)
n.2511A>C
c.637-9169A>C (n.637-9169A>C)
15g.48483819T=CA2175509369FBN1c.3837A= (p.Val1279=)
n.2511A=
c.637-9169A= (n.637-9169A=)
15g.48483820A>CCA392323539FBN1c.3836T>G (p.Val1279Gly)
n.2510T>G
c.637-9170T>G (n.637-9170T>G)
15g.48483820A>GCA392323535FBN1c.3836T>C (p.Val1279Ala)
n.2510T>C
c.637-9170T>C (n.637-9170T>C)
gnomAD v4 COSMIC
15g.48483820A>TCA392323533FBN1c.3836T>A (p.Val1279Glu)
n.2510T>A
c.637-9170T>A (n.637-9170T>A)
15g.48483820dupCA2695220658FBN1c.3836dup (p.Asp1280ArgfsTer4)
n.2510dup
c.637-9170dup (n.637-9170dup)
15g.48483821delCA2695220659FBN1c.3835del (p.Val1279Ter)
n.2509del
c.637-9171del (n.637-9171del)
15g.48483821C>ACA392323541FBN1c.3835G>T (p.Val1279Leu)
n.2509G>T
c.637-9171G>T (n.637-9171G>T)
15g.48483821C>GCA392323542FBN1c.3835G>C (p.Val1279Leu)
n.2509G>C
c.637-9171G>C (n.637-9171G>C)
15g.48483821C>TCA392323545FBN1c.3835G>A (p.Val1279Ile)
n.2509G>A
c.637-9171G>A (n.637-9171G>A)
ClinVar dbSNP gnomAD v4
15g.48483822A=CA2175509380FBN1c.3834T= (p.Cys1278=)
n.2508T=
c.637-9172T= (n.637-9172T=)
15g.48483822A>CCA10588585FBN1c.3834T>G (p.Cys1278Trp)
n.2508T>G
c.637-9172T>G (n.637-9172T>G)
ClinVar dbSNP
15g.48483822A>GCA490016922FBN1c.3834T>C (p.Cys1278=)
n.2508T>C
c.637-9172T>C (n.637-9172T>C)
ClinVar dbSNP gnomAD v3 gnomAD v4
15g.48483822A>TCA392323549FBN1c.3834T>A (p.Cys1278Ter)
n.2508T>A
c.637-9172T>A (n.637-9172T>A)
15g.48483823C>ACA392323553FBN1c.3833G>T (p.Cys1278Phe)
n.2507G>T
c.637-9173G>T (n.637-9173G>T)
15g.48483823C>GCA392323555FBN1c.3833G>C (p.Cys1278Ser)
n.2507G>C
c.637-9173G>C (n.637-9173G>C)
ClinVar
15g.48483823C>TCA392323557FBN1c.3833G>A (p.Cys1278Tyr)
n.2507G>A
c.637-9173G>A (n.637-9173G>A)
ClinVar
15g.48483823dupCA2695220660FBN1c.3833dup (p.Cys1278TrpfsTer6)
n.2507dup
c.637-9173dup (n.637-9173dup)
15g.48483824A>CCA392323561FBN1c.3832T>G (p.Cys1278Gly)
n.2506T>G
c.637-9174T>G (n.637-9174T>G)
15g.48483824A>GCA392323563FBN1c.3832T>C (p.Cys1278Arg)
n.2506T>C
c.637-9174T>C (n.637-9174T>C)
15g.48483824A>TCA392323565FBN1c.3832T>A (p.Cys1278Ser)
n.2506T>A
c.637-9174T>A (n.637-9174T>A)
15g.48483825A>CCA490016927FBN1c.3831T>G (p.Thr1277=)
n.2505T>G
c.637-9175T>G (n.637-9175T>G)
15g.48483825A>GCA490016929FBN1c.3831T>C (p.Thr1277=)
n.2505T>C
c.637-9175T>C (n.637-9175T>C)
15g.48483825A>TCA490016930FBN1c.3831T>A (p.Thr1277=)
n.2505T>A
c.637-9175T>A (n.637-9175T>A)
15g.48483826G>ACA392323566FBN1c.3830C>T (p.Thr1277Ile)
n.2504C>T
c.637-9176C>T (n.637-9176C>T)
gnomAD v4
15g.48483826G>CCA392323568FBN1c.3830C>G (p.Thr1277Ser)
n.2504C>G
c.637-9176C>G (n.637-9176C>G)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.48483826G=CA2175509390FBN1c.3830C= (p.Thr1277=)
n.2504C=
c.637-9176C= (n.637-9176C=)
15g.48483826G>TCA392323570FBN1c.3830C>A (p.Thr1277Asn)
n.2504C>A
c.637-9176C>A (n.637-9176C>A)
15g.48483833_48483840delCA2580089557FBN1c.3823_3830del (p.Met1275LeufsTer6)
n.2497_2504del
c.637-9183_637-9176del (n.637-9183_637-9176del)
ClinVar
15g.48483827T>ACA392323574FBN1c.3829A>T (p.Thr1277Ser)
n.2503A>T
c.637-9177A>T (n.637-9177A>T)
15g.48483827T>CCA392323576FBN1c.3829A>G (p.Thr1277Ala)
n.2503A>G
c.637-9177A>G (n.637-9177A>G)
15g.48483827T>GCA392323572FBN1c.3829A>C (p.Thr1277Pro)
n.2503A>C
c.637-9177A>C (n.637-9177A>C)
15g.48483828C>ACA392323579FBN1c.3828G>T (p.Lys1276Asn)
n.2502G>T
c.637-9178G>T (n.637-9178G>T)
15g.48483828C>GCA392323581FBN1c.3828G>C (p.Lys1276Asn)
n.2502G>C
c.637-9178G>C (n.637-9178G>C)
15g.48483828C>TCA490016935FBN1c.3828G>A (p.Lys1276=)
n.2502G>A
c.637-9178G>A (n.637-9178G>A)
15g.48483829T>ACA392323583FBN1c.3827A>T (p.Lys1276Met)
n.2501A>T
c.637-9179A>T (n.637-9179A>T)
15g.48483829T>CCA392323586FBN1c.3827A>G (p.Lys1276Arg)
n.2501A>G
c.637-9179A>G (n.637-9179A>G)
15g.48483829T>GCA392323588FBN1c.3827A>C (p.Lys1276Thr)
n.2501A>C
c.637-9179A>C (n.637-9179A>C)
15g.48483830T>ACA392323595FBN1c.3826A>T (p.Lys1276Ter)
n.2500A>T
c.637-9180A>T (n.637-9180A>T)
15g.48483830T>CCA392323593FBN1c.3826A>G (p.Lys1276Glu)
n.2500A>G
c.637-9180A>G (n.637-9180A>G)
15g.48483830T>GCA392323591FBN1c.3826A>C (p.Lys1276Gln)
n.2500A>C
c.637-9180A>C (n.637-9180A>C)
15g.48483831C>ACA392323599FBN1c.3825G>T (p.Met1275Ile)
n.2499G>T
c.637-9181G>T (n.637-9181G>T)
15g.48483831C>GCA392323601FBN1c.3825G>C (p.Met1275Ile)
n.2499G>C
c.637-9181G>C (n.637-9181G>C)
15g.48483831C>TCA392323604FBN1c.3825G>A (p.Met1275Ile)
n.2499G>A
c.637-9181G>A (n.637-9181G>A)
15g.48483832A>CCA392323606FBN1c.3824T>G (p.Met1275Arg)
n.2498T>G
c.637-9182T>G (n.637-9182T>G)
15g.48483832A>GCA392323608FBN1c.3824T>C (p.Met1275Thr)
n.2498T>C
c.637-9182T>C (n.637-9182T>C)
15g.48483832A>TCA392323616FBN1c.3824T>A (p.Met1275Lys)
n.2498T>A
c.637-9182T>A (n.637-9182T>A)
15g.48483833T>ACA392323618FBN1c.3823A>T (p.Met1275Leu)
n.2497A>T
c.637-9183A>T (n.637-9183A>T)
15g.48483833T>CCA392323622FBN1c.3823A>G (p.Met1275Val)
n.2497A>G
c.637-9183A>G (n.637-9183A>G)
ClinVar dbSNP
15g.48483833T>GCA051554FBN1c.3823A>C (p.Met1275Leu)
n.2497A>C
c.637-9183A>C (n.637-9183A>C)
dbSNP ExAC gnomAD v2 gnomAD v4
15g.48483833T=CA2175509397FBN1c.3823A= (p.Met1275=)
n.2497A=
c.637-9183A= (n.637-9183A=)
15g.48483834G>ACA490016943FBN1c.3822C>T (p.Asp1274=)
n.2496C>T
c.637-9184C>T (n.637-9184C>T)
15g.48483834G>CCA392323624FBN1c.3822C>G (p.Asp1274Glu)
n.2496C>G
c.637-9184C>G (n.637-9184C>G)
15g.48483834G>TCA392323625FBN1c.3822C>A (p.Asp1274Glu)
n.2496C>A
c.637-9184C>A (n.637-9184C>A)
gnomAD v4
15g.48483835delCA2580089559FBN1c.3821del (p.Asp1274AlafsTer2)
n.2495del
c.637-9185del (n.637-9185del)
ClinVar
15g.48483835T>ACA392323628FBN1c.3821A>T (p.Asp1274Val)
n.2495A>T
c.637-9185A>T (n.637-9185A>T)
15g.48483835T>CCA392323630FBN1c.3821A>G (p.Asp1274Gly)
n.2495A>G
c.637-9185A>G (n.637-9185A>G)
gnomAD v4
15g.48483835T>GCA392323631FBN1c.3821A>C (p.Asp1274Ala)
n.2495A>C
c.637-9185A>C (n.637-9185A>C)
15g.48483836C>ACA392323632FBN1c.3820G>T (p.Asp1274Tyr)
n.2494G>T
c.637-9186G>T (n.637-9186G>T)
15g.48483836C>GCA392323633FBN1c.3820G>C (p.Asp1274His)
n.2494G>C
c.637-9186G>C (n.637-9186G>C)
15g.48483836C>TCA392323635FBN1c.3820G>A (p.Asp1274Asn)
n.2494G>A
c.637-9186G>A (n.637-9186G>A)
15g.48483837T>ACA392323637FBN1c.3819A>T (p.Glu1273Asp)
n.2493A>T
c.637-9187A>T (n.637-9187A>T)
15g.48483837T>CCA490016953FBN1c.3819A>G (p.Glu1273=)
n.2493A>G
c.637-9187A>G (n.637-9187A>G)
15g.48483837T>GCA392323639FBN1c.3819A>C (p.Glu1273Asp)
n.2493A>C
c.637-9187A>C (n.637-9187A>C)
15g.48483838T>ACA392323644FBN1c.3818A>T (p.Glu1273Val)
n.2492A>T
c.637-9188A>T (n.637-9188A>T)
15g.48483838T>CCA392323641FBN1c.3818A>G (p.Glu1273Gly)
n.2492A>G
c.637-9188A>G (n.637-9188A>G)
15g.48483838T>GCA392323642FBN1c.3818A>C (p.Glu1273Ala)
n.2492A>C
c.637-9188A>C (n.637-9188A>C)
15g.48483839C>ACA392323647FBN1c.3817G>T (p.Glu1273Ter)
n.2491G>T
c.637-9189G>T (n.637-9189G>T)
15g.48483839C>GCA392323658FBN1c.3817G>C (p.Glu1273Gln)
n.2491G>C
c.637-9189G>C (n.637-9189G>C)
15g.48483839C>TCA392323655FBN1c.3817G>A (p.Glu1273Lys)
n.2491G>A
c.637-9189G>A (n.637-9189G>A)
15g.48483840delCA2573150789FBN1c.3816del (p.Glu1273LysfsTer3)
n.2490del
c.637-9190del (n.637-9190del)
ClinVar dbSNP
15g.48483840A>CCA490016960FBN1c.3816T>G (p.Ser1272=)
n.2490T>G
c.637-9190T>G (n.637-9190T>G)
15g.48483840A>GCA490016961FBN1c.3816T>C (p.Ser1272=)
n.2490T>C
c.637-9190T>C (n.637-9190T>C)
15g.48483840A>TCA490016962FBN1c.3816T>A (p.Ser1272=)
n.2490T>A
c.637-9190T>A (n.637-9190T>A)
15g.48483840_48483841delinsAGCA2175509406FBN1c.3815_3816delinsCT (p.Ser1272=)
n.2489_2490delinsCT
c.637-9191_637-9190delinsCT (n.637-9191_637-9190delinsCT)
15g.48483841delCA658798366FBN1c.3815del (p.Ser1272LeufsTer4)
n.2489del
c.637-9191del (n.637-9191del)
ClinVar dbSNP
15g.48483841G>ACA392323661FBN1c.3815C>T (p.Ser1272Phe)
n.2489C>T
c.637-9191C>T (n.637-9191C>T)
15g.48483841G>CCA392323663FBN1c.3815C>G (p.Ser1272Cys)
n.2489C>G
c.637-9191C>G (n.637-9191C>G)
15g.48483841G=CA2175509415FBN1c.3815C= (p.Ser1272=)
n.2489C=
c.637-9191C= (n.637-9191C=)
15g.48483841G>TCA392323665FBN1c.3815C>A (p.Ser1272Tyr)
n.2489C>A
c.637-9191C>A (n.637-9191C>A)
ClinVar dbSNP
15g.48483842A>CCA392323668FBN1c.3814T>G (p.Ser1272Ala)
n.2488T>G
c.637-9192T>G (n.637-9192T>G)
15g.48483842A>GCA392323671FBN1c.3814T>C (p.Ser1272Pro)
n.2488T>C
c.637-9192T>C (n.637-9192T>C)
15g.48483842A>TCA392323673FBN1c.3814T>A (p.Ser1272Thr)
n.2488T>A
c.637-9192T>A (n.637-9192T>A)
15g.48483843T>ACA490016970FBN1c.3813A>T (p.Ala1271=)
n.2487A>T
c.637-9193A>T (n.637-9193A>T)
gnomAD v4
15g.48483843T>CCA490016973FBN1c.3813A>G (p.Ala1271=)
n.2487A>G
c.637-9193A>G (n.637-9193A>G)
15g.48483843T>GCA490016975FBN1c.3813A>C (p.Ala1271=)
n.2487A>C
c.637-9193A>C (n.637-9193A>C)
15g.48483844G>ACA392323680FBN1c.3812C>T (p.Ala1271Val)
n.2486C>T
c.637-9194C>T (n.637-9194C>T)
15g.48483844G>CCA392323678FBN1c.3812C>G (p.Ala1271Gly)
n.2486C>G
c.637-9194C>G (n.637-9194C>G)
15g.48483844G>TCA392323676FBN1c.3812C>A (p.Ala1271Glu)
n.2486C>A
c.637-9194C>A (n.637-9194C>A)
15g.48483845C>ACA392323683FBN1c.3811G>T (p.Ala1271Ser)
n.2485G>T
c.637-9195G>T (n.637-9195G>T)
gnomAD v4
15g.48483845C=CA2175509421FBN1c.3811G= (p.Ala1271=)
n.2485G=
c.637-9195G= (n.637-9195G=)
15g.48483845C>GCA392323685FBN1c.3811G>C (p.Ala1271Pro)
n.2485G>C
c.637-9195G>C (n.637-9195G>C)
15g.48483845C>TCA269525999FBN1c.3811G>A (p.Ala1271Thr)
n.2485G>A
c.637-9195G>A (n.637-9195G>A)
ClinVar dbSNP gnomAD v3 gnomAD v4
15g.48483846C>ACA392323690FBN1c.3810G>T (p.Met1270Ile)
n.2484G>T
c.637-9196G>T (n.637-9196G>T)
15g.48483846C>GCA392323692FBN1c.3810G>C (p.Met1270Ile)
n.2484G>C
c.637-9196G>C (n.637-9196G>C)
15g.48483846C>TCA392323694FBN1c.3810G>A (p.Met1270Ile)
n.2484G>A
c.637-9196G>A (n.637-9196G>A)
15g.48483847A>CCA392323698FBN1c.3809T>G (p.Met1270Arg)
n.2483T>G
c.637-9197T>G (n.637-9197T>G)
15g.48483847A>GCA392323702FBN1c.3809T>C (p.Met1270Thr)
n.2483T>C
c.637-9197T>C (n.637-9197T>C)
15g.48483847A>TCA392323700FBN1c.3809T>A (p.Met1270Lys)
n.2483T>A
c.637-9197T>A (n.637-9197T>A)
15g.48483848T>ACA392323705FBN1c.3808A>T (p.Met1270Leu)
n.2482A>T
c.637-9198A>T (n.637-9198A>T)
ClinVar gnomAD v4
15g.48483848T>CCA392323707FBN1c.3808A>G (p.Met1270Val)
n.2482A>G
c.637-9198A>G (n.637-9198A>G)
15g.48483848T>GCA392323709FBN1c.3808A>C (p.Met1270Leu)
n.2482A>C
c.637-9198A>C (n.637-9198A>C)
dbSNP gnomAD v2 gnomAD v4
15g.48483848T=CA2175509424FBN1c.3808A= (p.Met1270=)
n.2482A=
c.637-9198A= (n.637-9198A=)
15g.48483849G>ACA490016993FBN1c.3807C>T (p.Phe1269=)
n.2481C>T
c.637-9199C>T (n.637-9199C>T)
15g.48483849G>CCA392323713FBN1c.3807C>G (p.Phe1269Leu)
n.2481C>G
c.637-9199C>G (n.637-9199C>G)
15g.48483849G>TCA392323714FBN1c.3807C>A (p.Phe1269Leu)
n.2481C>A
c.637-9199C>A (n.637-9199C>A)
gnomAD v4
15g.48483850A>CCA392323717FBN1c.3806T>G (p.Phe1269Cys)
n.2480T>G
c.637-9200T>G (n.637-9200T>G)
15g.48483850A>GCA392323719FBN1c.3806T>C (p.Phe1269Ser)
n.2480T>C
c.637-9200T>C (n.637-9200T>C)
ClinVar gnomAD v4
15g.48483850A>TCA392323721FBN1c.3806T>A (p.Phe1269Tyr)
n.2480T>A
c.637-9200T>A (n.637-9200T>A)
15g.48483851A>CCA392323725FBN1c.3805T>G (p.Phe1269Val)
n.2479T>G
c.637-9201T>G (n.637-9201T>G)
15g.48483851A>GCA392323727FBN1c.3805T>C (p.Phe1269Leu)
n.2479T>C
c.637-9201T>C (n.637-9201T>C)
15g.48483851A>TCA392323729FBN1c.3805T>A (p.Phe1269Ile)
n.2479T>A
c.637-9201T>A (n.637-9201T>A)
15g.48483852delCA2573054038FBN1c.3804del (p.Phe1269SerfsTer7)
n.2478del
c.637-9202del (n.637-9202del)
ClinVar dbSNP
15g.48483852T>ACA490017004FBN1c.3804A>T (p.Gly1268=)
n.2478A>T
c.637-9202A>T (n.637-9202A>T)
15g.48483852T>CCA490017003FBN1c.3804A>G (p.Gly1268=)
n.2478A>G
c.637-9202A>G (n.637-9202A>G)
dbSNP gnomAD v3 gnomAD v4
15g.48483852T>GCA490017002FBN1c.3804A>C (p.Gly1268=)
n.2478A>C
c.637-9202A>C (n.637-9202A>C)
15g.48483852T=CA2175509426FBN1c.3804A= (p.Gly1268=)
n.2478A=
c.637-9202A= (n.637-9202A=)
15g.48483853C>ACA392323731FBN1c.3803G>T (p.Gly1268Val)
n.2477G>T
c.637-9203G>T (n.637-9203G>T)
15g.48483853C>GCA392323736FBN1c.3803G>C (p.Gly1268Ala)
n.2477G>C
c.637-9203G>C (n.637-9203G>C)
15g.48483853C>TCA392323734FBN1c.3803G>A (p.Gly1268Glu)
n.2477G>A
c.637-9203G>A (n.637-9203G>A)
15g.48483854C>ACA392323738FBN1c.3802G>T (p.Gly1268Ter)
n.2476G>T
c.637-9204G>T (n.637-9204G>T)
15g.48483854C>GCA392323740FBN1c.3802G>C (p.Gly1268Arg)
n.2476G>C
c.637-9204G>C (n.637-9204G>C)
15g.48483854C>TCA392323742FBN1c.3802G>A (p.Gly1268Arg)
n.2476G>A
c.637-9204G>A (n.637-9204G>A)
COSMIC
15g.48483855A=CA2175509429FBN1c.3801T= (p.Asp1267=)
n.2475T=
c.637-9205T= (n.637-9205T=)
15g.48483855A>CCA392323745FBN1c.3801T>G (p.Asp1267Glu)
n.2475T>G
c.637-9205T>G (n.637-9205T>G)
15g.48483855A>GCA051550FBN1c.3801T>C (p.Asp1267=)
n.2475T>C
c.637-9205T>C (n.637-9205T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.48483855A>TCA392323749FBN1c.3801T>A (p.Asp1267Glu)
n.2475T>A
c.637-9205T>A (n.637-9205T>A)
15g.48483856T>ACA392323752FBN1c.3800A>T (p.Asp1267Val)
n.2474A>T
c.637-9206A>T (n.637-9206A>T)
15g.48483856T>CCA392323755FBN1c.3800A>G (p.Asp1267Gly)
n.2474A>G
c.637-9206A>G (n.637-9206A>G)
ClinVar
15g.48483856T>GCA392323757FBN1c.3800A>C (p.Asp1267Ala)
n.2474A>C
c.637-9206A>C (n.637-9206A>C)
15g.48483856_48483863delinsTCATAACACA2175509433FBN1c.3793_3800delinsTGTTATGA (p.Cys1265=)
n.2467_2474delinsTGTTATGA
c.637-9213_637-9206delinsTGTTATGA (n.637-9213_637-9206delinsTGTTATGA)
15g.48483857C>ACA392323760FBN1c.3799G>T (p.Asp1267Tyr)
n.2473G>T
c.637-9207G>T (n.637-9207G>T)
15g.48483857C>GCA392323761FBN1c.3799G>C (p.Asp1267His)
n.2473G>C
c.637-9207G>C (n.637-9207G>C)
15g.48483857C>TCA392323763FBN1c.3799G>A (p.Asp1267Asn)
n.2473G>A
c.637-9207G>A (n.637-9207G>A)
15g.48483859_48483865delCA658798367FBN1c.3793_3799del (p.Cys1265MetfsTer9)
n.2467_2473del
c.637-9213_637-9207del (n.637-9213_637-9207del)
ClinVar dbSNP
15g.48483858A=CA2175509445FBN1c.3798T= (p.Tyr1266=)
n.2472T=
c.637-9208T= (n.637-9208T=)
15g.48483858A>CCA392323767FBN1c.3798T>G (p.Tyr1266Ter)
n.2472T>G
c.637-9208T>G (n.637-9208T>G)
15g.48483858A>GCA051539FBN1c.3798T>C (p.Tyr1266=)
n.2472T>C
c.637-9208T>C (n.637-9208T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.48483858A>TCA269526018FBN1c.3798T>A (p.Tyr1266Ter)
n.2472T>A
c.637-9208T>A (n.637-9208T>A)
dbSNP
15g.48483859T>ACA014562FBN1c.3797A>T (p.Tyr1266Phe)
n.2471A>T
c.637-9209A>T (n.637-9209A>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.48483859T>CCA392323772FBN1c.3797A>G (p.Tyr1266Cys)
n.2471A>G
c.637-9209A>G (n.637-9209A>G)
gnomAD v4
15g.48483859T>GCA392323774FBN1c.3797A>C (p.Tyr1266Ser)
n.2471A>C
c.637-9209A>C (n.637-9209A>C)
15g.48483859T=CA2175509452FBN1c.3797A= (p.Tyr1266=)
n.2471A=
c.637-9209A= (n.637-9209A=)
15g.48483859dupCA2695220661FBN1c.3797dup (p.Tyr1266Ter)
n.2471dup
c.637-9209dup (n.637-9209dup)
15g.48483860A>CCA392323776FBN1c.3796T>G (p.Tyr1266Asp)
n.2470T>G
c.637-9210T>G (n.637-9210T>G)
15g.48483860A>GCA392323778FBN1c.3796T>C (p.Tyr1266His)
n.2470T>C
c.637-9210T>C (n.637-9210T>C)
15g.48483860A>TCA392323780FBN1c.3796T>A (p.Tyr1266Asn)
n.2470T>A
c.637-9210T>A (n.637-9210T>A)
15g.48483862_48483866delCA2695220662FBN1c.3792_3796del (p.Cys1265Ter)
n.2466_2470del
c.637-9214_637-9210del (n.637-9214_637-9210del)
15g.48483861A=CA2175509463FBN1c.3795T= (p.Cys1265=)
n.2469T=
c.637-9211T= (n.637-9211T=)
15g.48483861A>CCA392323782FBN1c.3795T>G (p.Cys1265Trp)
n.2469T>G
c.637-9211T>G (n.637-9211T>G)
15g.48483861A>GCA490017019FBN1c.3795T>C (p.Cys1265=)
n.2469T>C
c.637-9211T>C (n.637-9211T>C)
15g.48483861A>TCA392323784FBN1c.3795T>A (p.Cys1265Ter)
n.2469T>A
c.637-9211T>A (n.637-9211T>A)
ClinVar dbSNP
15g.48483862C>ACA392323787FBN1c.3794G>T (p.Cys1265Phe)
n.2468G>T
c.637-9212G>T (n.637-9212G>T)
ClinVar dbSNP
15g.48483862C=CA2175509470FBN1c.3794G= (p.Cys1265=)
n.2468G=
c.637-9212G= (n.637-9212G=)
15g.48483862C>GCA392323789FBN1c.3794G>C (p.Cys1265Ser)
n.2468G>C
c.637-9212G>C (n.637-9212G>C)
ClinVar dbSNP
15g.48483862C>TCA392323791FBN1c.3794G>A (p.Cys1265Tyr)
n.2468G>A
c.637-9212G>A (n.637-9212G>A)
ClinVar
15g.48483863delCA2695220663FBN1c.3793del (p.Cys1265ValfsTer11)
n.2467del
c.637-9213del (n.637-9213del)
15g.48483863A=CA2175509481FBN1c.3793T= (p.Cys1265=)
n.2467T=
c.637-9213T= (n.637-9213T=)
15g.48483863A>CCA392323798FBN1c.3793T>G (p.Cys1265Gly)
n.2467T>G
c.637-9213T>G (n.637-9213T>G)
15g.48483863A>GCA014552FBN1c.3793T>C (p.Cys1265Arg)
n.2467T>C
c.637-9213T>C (n.637-9213T>C)
ClinVar dbSNP
15g.48483863A>TCA392323794FBN1c.3793T>A (p.Cys1265Ser)
n.2467T>A
c.637-9213T>A (n.637-9213T>A)
15g.48483864C>ACA392323803FBN1c.3792G>T (p.Leu1264Phe)
n.2466G>T
c.637-9214G>T (n.637-9214G>T)
15g.48483864C=CA2175509488FBN1c.3792G= (p.Leu1264=)
n.2466G=
c.637-9214G= (n.637-9214G=)
15g.48483864C>GCA392323801FBN1c.3792G>C (p.Leu1264Phe)
n.2466G>C
c.637-9214G>C (n.637-9214G>C)
15g.48483864C>TCA490017033FBN1c.3792G>A (p.Leu1264=)
n.2466G>A
c.637-9214G>A (n.637-9214G>A)
dbSNP gnomAD v4
15g.48483865A>CCA392323811FBN1c.3791T>G (p.Leu1264Trp)
n.2465T>G
c.637-9215T>G (n.637-9215T>G)
15g.48483865A>GCA392323806FBN1c.3791T>C (p.Leu1264Ser)
n.2465T>C
c.637-9215T>C (n.637-9215T>C)
15g.48483865A>TCA392323808FBN1c.3791T>A (p.Leu1264Ter)
n.2465T>A
c.637-9215T>A (n.637-9215T>A)
15g.48483866A>CCA392323814FBN1c.3790T>G (p.Leu1264Val)
n.2464T>G
c.637-9216T>G (n.637-9216T>G)
15g.48483866A>GCA490017037FBN1c.3790T>C (p.Leu1264=)
n.2464T>C
c.637-9216T>C (n.637-9216T>C)
15g.48483866A>TCA392323816FBN1c.3790T>A (p.Leu1264Met)
n.2464T>A
c.637-9216T>A (n.637-9216T>A)
15g.48483867G>ACA490017038FBN1c.3789C>T (p.Cys1263=)
n.2463C>T
c.637-9217C>T (n.637-9217C>T)
15g.48483867G>CCA16042964FBN1c.3789C>G (p.Cys1263Trp)
n.2463C>G
c.637-9217C>G (n.637-9217C>G)
ClinVar dbSNP
15g.48483867G=CA2175509494FBN1c.3789C= (p.Cys1263=)
n.2463C=
c.637-9217C= (n.637-9217C=)
15g.48483867G>TCA392323823FBN1c.3789C>A (p.Cys1263Ter)
n.2463C>A
c.637-9217C>A (n.637-9217C>A)
15g.48483868C>ACA392323827FBN1c.3788G>T (p.Cys1263Phe)
n.2462G>T
c.637-9218G>T (n.637-9218G>T)
ClinVar gnomAD v4
15g.48483868C>GCA392323829FBN1c.3788G>C (p.Cys1263Ser)
n.2462G>C
c.637-9218G>C (n.637-9218G>C)
15g.48483868C>TCA392323831FBN1c.3788G>A (p.Cys1263Tyr)
n.2462G>A
c.637-9218G>A (n.637-9218G>A)
15g.48483869_48483870dupCA2695220664FBN1c.3787_3788dup (p.Leu1264AlafsTer13)
n.2461_2462dup
c.637-9219_637-9218dup (n.637-9219_637-9218dup)
15g.48483869A>CCA392323834FBN1c.3787T>G (p.Cys1263Gly)
n.2461T>G
c.637-9219T>G (n.637-9219T>G)
15g.48483869A>GCA392323836FBN1c.3787T>C (p.Cys1263Arg)
n.2461T>C
c.637-9219T>C (n.637-9219T>C)
15g.48483869A>TCA392323838FBN1c.3787T>A (p.Cys1263Ser)
n.2461T>A
c.637-9219T>A (n.637-9219T>A)
15g.48483870C>ACA392323843FBN1c.3786G>T (p.Arg1262Ser)
n.2460G>T
c.637-9220G>T (n.637-9220G>T)
ClinVar dbSNP
15g.48483870C=CA2175509507FBN1c.3786G= (p.Arg1262=)
n.2460G=
c.637-9220G= (n.637-9220G=)
15g.48483870C>GCA392323840FBN1c.3786G>C (p.Arg1262Ser)
n.2460G>C
c.637-9220G>C (n.637-9220G>C)
15g.48483870C>TCA490017055FBN1c.3786G>A (p.Arg1262=)
n.2460G>A
c.637-9220G>A (n.637-9220G>A)
ClinVar dbSNP
15g.48483871C>ACA392323845FBN1c.3785G>T (p.Arg1262Met)
n.2459G>T
c.637-9221G>T (n.637-9221G>T)
15g.48483871C=CA2175509516FBN1c.3785G= (p.Arg1262=)
n.2459G=
c.637-9221G= (n.637-9221G=)
15g.48483871C>GCA392323848FBN1c.3785G>C (p.Arg1262Thr)
n.2459G>C
c.637-9221G>C (n.637-9221G>C)
15g.48483871C>TCA051513FBN1c.3785G>A (p.Arg1262Lys)
n.2459G>A
c.637-9221G>A (n.637-9221G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.48483872T>ACA392323851FBN1c.3784A>T (p.Arg1262Trp)
n.2458A>T
c.637-9222A>T (n.637-9222A>T)
15g.48483872T>CCA392323853FBN1c.3784A>G (p.Arg1262Gly)
n.2458A>G
c.637-9222A>G (n.637-9222A>G)
15g.48483872T>GCA490017061FBN1c.3784A>C (p.Arg1262=)
n.2458A>C
c.637-9222A>C (n.637-9222A>C)
15g.48483872_48483873delinsTGCA2175509523FBN1c.3783_3784delinsCA (p.Tyr1261=)
n.2457_2458delinsCA
c.637-9223_637-9222delinsCA (n.637-9223_637-9222delinsCA)
15g.48483873delCA658824435FBN1c.3783del (p.Tyr1261Ter)
n.2457del
c.637-9223del (n.637-9223del)
ClinVar dbSNP
15g.48483873G>ACA490017063FBN1c.3783C>T (p.Tyr1261=)
n.2457C>T
c.637-9223C>T (n.637-9223C>T)
gnomAD v4
15g.48483873G>CCA392323856FBN1c.3783C>G (p.Tyr1261Ter)
n.2457C>G
c.637-9223C>G (n.637-9223C>G)
15g.48483873G>TCA392323858FBN1c.3783C>A (p.Tyr1261Ter)
n.2457C>A
c.637-9223C>A (n.637-9223C>A)
15g.48483874T>ACA392323861FBN1c.3782A>T (p.Tyr1261Phe)
n.2456A>T
c.637-9224A>T (n.637-9224A>T)
15g.48483874T>CCA392323863FBN1c.3782A>G (p.Tyr1261Cys)
n.2456A>G
c.637-9224A>G (n.637-9224A>G)
15g.48483874T>GCA392323864FBN1c.3782A>C (p.Tyr1261Ser)
n.2456A>C
c.637-9224A>C (n.637-9224A>C)
15g.48483875A>CCA392323867FBN1c.3781T>G (p.Tyr1261Asp)
n.2455T>G
c.637-9225T>G (n.637-9225T>G)
15g.48483875A>GCA392323868FBN1c.3781T>C (p.Tyr1261His)
n.2455T>C
c.637-9225T>C (n.637-9225T>C)
15g.48483875A>TCA392323872FBN1c.3781T>A (p.Tyr1261Asn)
n.2455T>A
c.637-9225T>A (n.637-9225T>A)
15g.48483876C>ACA392323875FBN1c.3780G>T (p.Glu1260Asp)
n.2454G>T
c.637-9226G>T (n.637-9226G>T)
15g.48483876C=CA2175509537FBN1c.3780G= (p.Glu1260=)
n.2454G=
c.637-9226G= (n.637-9226G=)
15g.48483876C>GCA392323877FBN1c.3780G>C (p.Glu1260Asp)
n.2454G>C
c.637-9226G>C (n.637-9226G>C)
15g.48483876C>TCA490017068FBN1c.3780G>A (p.Glu1260=)
n.2454G>A
c.637-9226G>A (n.637-9226G>A)
ClinVar dbSNP gnomAD v2 gnomAD v4
15g.48483877T>ACA392323880FBN1c.3779A>T (p.Glu1260Val)
n.2453A>T
c.637-9227A>T (n.637-9227A>T)
15g.48483877T>CCA392323882FBN1c.3779A>G (p.Glu1260Gly)
n.2453A>G
c.637-9227A>G (n.637-9227A>G)
dbSNP
15g.48483877T>GCA392323884FBN1c.3779A>C (p.Glu1260Ala)
n.2453A>C
c.637-9227A>C (n.637-9227A>C)
15g.48483877T=CA2175509543FBN1c.3779A= (p.Glu1260=)
n.2453A=
c.637-9227A= (n.637-9227A=)
15g.48483878C>ACA392323887FBN1c.3778G>T (p.Glu1260Ter)
n.2452G>T
c.637-9228G>T (n.637-9228G>T)
ClinVar dbSNP
15g.48483878C=CA2175509549FBN1c.3778G= (p.Glu1260=)
n.2452G=
c.637-9228G= (n.637-9228G=)
15g.48483878C>GCA392323889FBN1c.3778G>C (p.Glu1260Gln)
n.2452G>C
c.637-9228G>C (n.637-9228G>C)
15g.48483878C>TCA392323891FBN1c.3778G>A (p.Glu1260Lys)
n.2452G>A
c.637-9228G>A (n.637-9228G>A)
15g.48483879T>ACA490017075FBN1c.3777A>T (p.Gly1259=)
n.2451A>T
c.637-9229A>T (n.637-9229A>T)
15g.48483879T>CCA490017076FBN1c.3777A>G (p.Gly1259=)
n.2451A>G
c.637-9229A>G (n.637-9229A>G)
gnomAD v4
15g.48483879T>GCA490017079FBN1c.3777A>C (p.Gly1259=)
n.2451A>C
c.637-9229A>C (n.637-9229A>C)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
15g.48483879T=CA2175509553FBN1c.3777A= (p.Gly1259=)
n.2451A=
c.637-9229A= (n.637-9229A=)
15g.48483880C>ACA392323893FBN1c.3776G>T (p.Gly1259Val)
n.2450G>T
c.637-9230G>T (n.637-9230G>T)
15g.48483880C>GCA392323896FBN1c.3776G>C (p.Gly1259Ala)
n.2450G>C
c.637-9230G>C (n.637-9230G>C)
15g.48483880C>TCA392323898FBN1c.3776G>A (p.Gly1259Glu)
n.2450G>A
c.637-9230G>A (n.637-9230G>A)
15g.48483881C>ACA392323901FBN1c.3775G>T (p.Gly1259Ter)
n.2449G>T
c.637-9231G>T (n.637-9231G>T)
15g.48483881C>GCA392323904FBN1c.3775G>C (p.Gly1259Arg)
n.2449G>C
c.637-9231G>C (n.637-9231G>C)
15g.48483881C>TCA392323906FBN1c.3775G>A (p.Gly1259Arg)
n.2449G>A
c.637-9231G>A (n.637-9231G>A)
15g.48483882A>CCA490017087FBN1c.3774T>G (p.Pro1258=)
n.2448T>G
c.637-9232T>G (n.637-9232T>G)
15g.48483882A>GCA490017095FBN1c.3774T>C (p.Pro1258=)
n.2448T>C
c.637-9232T>C (n.637-9232T>C)
15g.48483882A>TCA490017099FBN1c.3774T>A (p.Pro1258=)
n.2448T>A
c.637-9232T>A (n.637-9232T>A)
15g.48483882_48483883delinsAGCA2175509556FBN1c.3773_3774delinsCT (p.Pro1258=)
n.2447_2448delinsCT
c.637-9233_637-9232delinsCT (n.637-9233_637-9232delinsCT)
15g.48483883G>ACA392323916FBN1c.3773C>T (p.Pro1258Leu)
n.2447C>T
c.637-9233C>T (n.637-9233C>T)
15g.48483883G>CCA392323914FBN1c.3773C>G (p.Pro1258Arg)
n.2447C>G
c.637-9233C>G (n.637-9233C>G)
dbSNP gnomAD v4
15g.48483883G=CA2175509566FBN1c.3773C= (p.Pro1258=)
n.2447C=
c.637-9233C= (n.637-9233C=)
15g.48483883G>TCA392323910FBN1c.3773C>A (p.Pro1258His)
n.2447C>A
c.637-9233C>A (n.637-9233C>A)
gnomAD v4 COSMIC
15g.48483885delCA014534FBN1c.3773del (p.Pro1258LeufsTer18)
n.2447del
c.637-9233del (n.637-9233del)
ClinVar dbSNP
15g.48483884G>ACA014524FBN1c.3772C>T (p.Pro1258Ser)
n.2446C>T
c.637-9234C>T (n.637-9234C>T)
ClinVar dbSNP COSMIC
15g.48483884G>CCA392323920FBN1c.3772C>G (p.Pro1258Ala)
n.2446C>G
c.637-9234C>G (n.637-9234C>G)
15g.48483884G=CA2175509581FBN1c.3772C= (p.Pro1258=)
n.2446C=
c.637-9234C= (n.637-9234C=)
15g.48483884G>TCA392323922FBN1c.3772C>A (p.Pro1258Thr)
n.2446C>A
c.637-9234C>A (n.637-9234C>A)
15g.48483885G>ACA490017105FBN1c.3771C>T (p.Ile1257=)
n.2445C>T
c.637-9235C>T (n.637-9235C>T)
ClinVar dbSNP
15g.48483885G>CCA392323925FBN1c.3771C>G (p.Ile1257Met)
n.2445C>G
c.637-9235C>G (n.637-9235C>G)
15g.48483885G=CA2175509591FBN1c.3771C= (p.Ile1257=)
n.2445C=
c.637-9235C= (n.637-9235C=)
15g.48483885G>TCA490017106FBN1c.3771C>A (p.Ile1257=)
n.2445C>A
c.637-9235C>A (n.637-9235C>A)
15g.48483886A=CA2175509594FBN1c.3770T= (p.Ile1257=)
n.2444T=
c.637-9236T= (n.637-9236T=)
15g.48483886A>CCA392323929FBN1c.3770T>G (p.Ile1257Ser)
n.2444T>G
c.637-9236T>G (n.637-9236T>G)
15g.48483886A>GCA392323931FBN1c.3770T>C (p.Ile1257Thr)
n.2444T>C
c.637-9236T>C (n.637-9236T>C)
15g.48483886A>TCA392323933FBN1c.3770T>A (p.Ile1257Asn)
n.2444T>A
c.637-9236T>A (n.637-9236T>A)
dbSNP gnomAD v2 gnomAD v4
15g.48483887T>ACA392323936FBN1c.3769A>T (p.Ile1257Phe)
n.2443A>T
c.637-9237A>T (n.637-9237A>T)
15g.48483887T>CCA392323938FBN1c.3769A>G (p.Ile1257Val)
n.2443A>G
c.637-9237A>G (n.637-9237A>G)
gnomAD v4
15g.48483887T>GCA392323940FBN1c.3769A>C (p.Ile1257Leu)
n.2443A>C
c.637-9237A>C (n.637-9237A>C)
15g.48483888A>CCA392323943FBN1c.3768T>G (p.Asn1256Lys)
n.2442T>G
c.637-9238T>G (n.637-9238T>G)
15g.48483888A>GCA490017119FBN1c.3768T>C (p.Asn1256=)
n.2442T>C
c.637-9238T>C (n.637-9238T>C)
15g.48483888A>TCA392323945FBN1c.3768T>A (p.Asn1256Lys)
n.2442T>A
c.637-9238T>A (n.637-9238T>A)
COSMIC
15g.48483888_48483891delinsATTTCA2175509598FBN1c.3765_3768delinsAAAT (p.Thr1255=)
n.2439_2442delinsAAAT
c.637-9241_637-9238delinsAAAT (n.637-9241_637-9238delinsAAAT)
15g.48483889T>ACA392323951FBN1c.3767A>T (p.Asn1256Ile)
n.2441A>T
c.637-9239A>T (n.637-9239A>T)
15g.48483889T>CCA392323953FBN1c.3767A>G (p.Asn1256Ser)
n.2441A>G
c.637-9239A>G (n.637-9239A>G)
15g.48483889T>GCA392323955FBN1c.3767A>C (p.Asn1256Thr)
n.2441A>C
c.637-9239A>C (n.637-9239A>C)
15g.48483889_48483891delinsGTACAGCA10587831FBN1c.3765_3767delinsCTGTAC (p.Asn1256delinsCysThr)
n.2439_2441delinsCTGTAC
c.637-9241_637-9239delinsCTGTAC (n.637-9241_637-9239delinsCTGTAC)
ClinVar dbSNP
15g.48483891delCA269526025FBN1c.3767del (p.Asn1256IlefsTer20)
n.2441del
c.637-9239del (n.637-9239del)
dbSNP
15g.48483890T>ACA392323959FBN1c.3766A>T (p.Asn1256Tyr)
n.2440A>T
c.637-9240A>T (n.637-9240A>T)
15g.48483890T>CCA051509FBN1c.3766A>G (p.Asn1256Asp)
n.2440A>G
c.637-9240A>G (n.637-9240A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.48483890T>GCA392323963FBN1c.3766A>C (p.Asn1256His)
n.2440A>C
c.637-9240A>C (n.637-9240A>C)
ClinVar dbSNP
15g.48483890T=CA2175509613FBN1c.3766A= (p.Asn1256=)
n.2440A=
c.637-9240A= (n.637-9240A=)
15g.48483891T>ACA490017127FBN1c.3765A>T (p.Thr1255=)
n.2439A>T
c.637-9241A>T (n.637-9241A>T)
15g.48483891T>CCA490017128FBN1c.3765A>G (p.Thr1255=)
n.2439A>G
c.637-9241A>G (n.637-9241A>G)
15g.48483891T>GCA490017129FBN1c.3765A>C (p.Thr1255=)
n.2439A>C
c.637-9241A>C (n.637-9241A>C)
15g.48483892G>ACA392323966FBN1c.3764C>T (p.Thr1255Ile)
n.2438C>T
c.637-9242C>T (n.637-9242C>T)
15g.48483892G>CCA392323968FBN1c.3764C>G (p.Thr1255Arg)
n.2438C>G
c.637-9242C>G (n.637-9242C>G)
gnomAD v4
15g.48483892G>TCA392323967FBN1c.3764C>A (p.Thr1255Lys)
n.2438C>A
c.637-9242C>A (n.637-9242C>A)
15g.48483892_48483896dupCA2695220665FBN1c.3760_3764dup (p.Asn1256AlafsTer22)
n.2434_2438dup
c.637-9246_637-9242dup (n.637-9246_637-9242dup)
15g.48483893T>ACA392323971FBN1c.3763A>T (p.Thr1255Ser)
n.2437A>T
c.637-9243A>T (n.637-9243A>T)
15g.48483893T>CCA392323973FBN1c.3763A>G (p.Thr1255Ala)
n.2437A>G
c.637-9243A>G (n.637-9243A>G)
15g.48483893T>GCA392323975FBN1c.3763A>C (p.Thr1255Pro)
n.2437A>C
c.637-9243A>C (n.637-9243A>C)
15g.48483894G>ACA490017133FBN1c.3762C>T (p.Cys1254=)
n.2436C>T
c.637-9244C>T (n.637-9244C>T)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
15g.48483894G>CCA392323978FBN1c.3762C>G (p.Cys1254Trp)
n.2436C>G
c.637-9244C>G (n.637-9244C>G)
15g.48483894G=CA2175509620FBN1c.3762C= (p.Cys1254=)
n.2436C=
c.637-9244C= (n.637-9244C=)
15g.48483894G>TCA392323981FBN1c.3762C>A (p.Cys1254Ter)
n.2436C>A
c.637-9244C>A (n.637-9244C>A)
15g.48483895C>ACA392323984FBN1c.3761G>T (p.Cys1254Phe)
n.2435G>T
c.637-9245G>T (n.637-9245G>T)
15g.48483895C=CA2175509628FBN1c.3761G= (p.Cys1254=)
n.2435G=
c.637-9245G= (n.637-9245G=)
15g.48483895C>GCA392323985FBN1c.3761G>C (p.Cys1254Ser)
n.2435G>C
c.637-9245G>C (n.637-9245G>C)
15g.48483895C>TCA392323988FBN1c.3761G>A (p.Cys1254Tyr)
n.2435G>A
c.637-9245G>A (n.637-9245G>A)
ClinVar dbSNP
15g.48483895_48483899delinsCACTGCA2175509629FBN1c.3757_3761delinsCAGTG (p.Gln1253=)
n.2431_2435delinsCAGTG
c.637-9249_637-9245delinsCAGTG (n.637-9249_637-9245delinsCAGTG)
15g.48483896A>CCA392323990FBN1c.3760T>G (p.Cys1254Gly)
n.2434T>G
c.637-9246T>G (n.637-9246T>G)
15g.48483896A>GCA392323991FBN1c.3760T>C (p.Cys1254Arg)
n.2434T>C
c.637-9246T>C (n.637-9246T>C)
15g.48483896A>TCA392323992FBN1c.3760T>A (p.Cys1254Ser)
n.2434T>A
c.637-9246T>A (n.637-9246T>A)
15g.48483896_48483897delinsACCA2175509636FBN1c.3759_3760delinsGT (p.Gln1253=)
n.2433_2434delinsGT
c.637-9247_637-9246delinsGT (n.637-9247_637-9246delinsGT)
15g.48483898_48483901delCA1139663894FBN1c.3757_3760del (p.Gln1253AlafsTer22)
n.2431_2434del
c.637-9249_637-9246del (n.637-9249_637-9246del)
ClinVar dbSNP
15g.48483897delCA658824436FBN1c.3759del (p.Gln1253HisfsTer23)
n.2433del
c.637-9247del (n.637-9247del)
ClinVar dbSNP
15g.48483897C>ACA392323993FBN1c.3759G>T (p.Gln1253His)
n.2433G>T
c.637-9247G>T (n.637-9247G>T)
15g.48483897C>GCA392323994FBN1c.3759G>C (p.Gln1253His)
n.2433G>C
c.637-9247G>C (n.637-9247G>C)
ClinVar dbSNP
15g.48483897C>TCA490017143FBN1c.3759G>A (p.Gln1253=)
n.2433G>A
c.637-9247G>A (n.637-9247G>A)
15g.48483898T>ACA392323998FBN1c.3758A>T (p.Gln1253Leu)
n.2432A>T
c.637-9248A>T (n.637-9248A>T)
15g.48483898T>CCA392324000FBN1c.3758A>G (p.Gln1253Arg)
n.2432A>G
c.637-9248A>G (n.637-9248A>G)
15g.48483898T>GCA392323999FBN1c.3758A>C (p.Gln1253Pro)
n.2432A>C
c.637-9248A>C (n.637-9248A>C)
ClinVar
15g.48483899G>ACA392324001FBN1c.3757C>T (p.Gln1253Ter)
n.2431C>T
c.637-9249C>T (n.637-9249C>T)
ClinVar dbSNP
15g.48483899G>CCA392324002FBN1c.3757C>G (p.Gln1253Glu)
n.2431C>G
c.637-9249C>G (n.637-9249C>G)
15g.48483899G=CA2175509654FBN1c.3757C= (p.Gln1253=)
n.2431C=
c.637-9249C= (n.637-9249C=)
15g.48483899G>TCA392324003FBN1c.3757C>A (p.Gln1253Lys)
n.2431C>A
c.637-9249C>A (n.637-9249C>A)
15g.48483900A>CCA490017151FBN1c.3756T>G (p.Gly1252=)
n.2430T>G
c.637-9250T>G (n.637-9250T>G)
gnomAD v4
15g.48483900A>GCA490017152FBN1c.3756T>C (p.Gly1252=)
n.2430T>C
c.637-9250T>C (n.637-9250T>C)
gnomAD v4
15g.48483900A>TCA490017153FBN1c.3756T>A (p.Gly1252=)
n.2430T>A
c.637-9250T>A (n.637-9250T>A)
15g.48483901C>ACA392324007FBN1c.3755G>T (p.Gly1252Val)
n.2429G>T
c.637-9251G>T (n.637-9251G>T)
15g.48483901C>GCA392324009FBN1c.3755G>C (p.Gly1252Ala)
n.2429G>C
c.637-9251G>C (n.637-9251G>C)
15g.48483901C>TCA392324011FBN1c.3755G>A (p.Gly1252Asp)
n.2429G>A
c.637-9251G>A (n.637-9251G>A)
15g.48483902C>ACA392324014FBN1c.3754G>T (p.Gly1252Cys)
n.2428G>T
c.637-9252G>T (n.637-9252G>T)
15g.48483902C>GCA392324016FBN1c.3754G>C (p.Gly1252Arg)
n.2428G>C
c.637-9252G>C (n.637-9252G>C)
15g.48483902C>TCA392324018FBN1c.3754G>A (p.Gly1252Ser)
n.2428G>A
c.637-9252G>A (n.637-9252G>A)
15g.48483903A>CCA490017161FBN1c.3753T>G (p.Gly1251=)
n.2427T>G
c.637-9253T>G (n.637-9253T>G)
15g.48483903A>GCA490017162FBN1c.3753T>C (p.Gly1251=)
n.2427T>C
c.637-9253T>C (n.637-9253T>C)
15g.48483903A>TCA490017163FBN1c.3753T>A (p.Gly1251=)
n.2427T>A
c.637-9253T>A (n.637-9253T>A)
15g.48483904C>ACA392324022FBN1c.3752G>T (p.Gly1251Val)
n.2426G>T
c.637-9254G>T (n.637-9254G>T)
gnomAD v4
15g.48483904C>GCA392324021FBN1c.3752G>C (p.Gly1251Ala)
n.2426G>C
c.637-9254G>C (n.637-9254G>C)
15g.48483904C>TCA392324020FBN1c.3752G>A (p.Gly1251Asp)
n.2426G>A
c.637-9254G>A (n.637-9254G>A)
15g.48483905C>ACA392324024FBN1c.3751G>T (p.Gly1251Cys)
n.2425G>T
c.637-9255G>T (n.637-9255G>T)
ClinVar
15g.48483905C>GCA392324026FBN1c.3751G>C (p.Gly1251Arg)
n.2425G>C
c.637-9255G>C (n.637-9255G>C)
15g.48483905C>TCA392324028FBN1c.3751G>A (p.Gly1251Ser)
n.2425G>A
c.637-9255G>A (n.637-9255G>A)
15g.48483906A>CCA392324031FBN1c.3750T>G (p.Asp1250Glu)
n.2424T>G
c.637-9256T>G (n.637-9256T>G)
ClinVar
15g.48483906A>GCA490017168FBN1c.3750T>C (p.Asp1250=)
n.2424T>C
c.637-9256T>C (n.637-9256T>C)
15g.48483906A>TCA392324032FBN1c.3750T>A (p.Asp1250Glu)
n.2424T>A
c.637-9256T>A (n.637-9256T>A)

Number of alleles fetched