NM_000208.4(INSR):c.707A>G (p.His236Arg)
|
rs121913145
|
0.00002
|
NM_000208.4(INSR):c.1195C>T (p.Arg399Ter)
|
rs121913151
|
0.00001
|
NM_000208.4(INSR):c.1246C>T (p.Arg416Ter)
|
rs778989302
|
0.00001
|
NM_000208.4(INSR):c.1459A>G (p.Lys487Glu)
|
rs121913136
|
0.00001
|
NM_000208.4(INSR):c.1466A>G (p.Asn489Ser)
|
rs121913147
|
0.00001
|
NM_000208.4(INSR):c.1610+2T>C
|
rs797045624
|
0.00001
|
NM_000208.4(INSR):c.3059G>A (p.Arg1020Gln)
|
rs121913148
|
0.00001
|
NM_000208.4(INSR):c.3079C>T (p.Arg1027Ter)
|
rs121913144
|
0.00001
|
NM_000208.4(INSR):c.3572G>A (p.Arg1191Gln)
|
rs121913150
|
0.00001
|
INSR, EX17, ALU
|
|
|
NG_008852.1:g.[135909G>T;8170_32961del24792]
|
|
|
NM_000208.2:c.[1465A>G;3160G>A]
|
|
|
NM_000208.2:c.[2504G>T;2525C>T]
|
|
|
NM_000208.2:c.[766C>T;2997T>G]
|
|
|
NM_000208.3(INSR):c.2683-542_2842+544del
|
|
|
NM_000208.4(INSR):c.1124-2A>G
|
rs587776819
|
|
NM_000208.4(INSR):c.1177G>A (p.Gly393Arg)
|
rs267607184
|
|
NM_000208.4(INSR):c.1225T>G (p.Phe409Val)
|
rs121913142
|
|
NM_000208.4(INSR):c.126C>A (p.Asn42Lys)
|
rs121913143
|
|
NM_000208.4(INSR):c.1316G>C (p.Trp439Ser)
|
rs121913158
|
|
NM_000208.4(INSR):c.1348C>T (p.Gln450Ter)
|
rs2144950571
|
|
NM_000208.4(INSR):c.1372A>G (p.Asn458Asp)
|
rs121913160
|
|
NM_000208.4(INSR):c.164T>C (p.Val55Ala)
|
rs121913152
|
|
NM_000208.4(INSR):c.172G>A (p.Gly58Arg)
|
rs52836744
|
|
NM_000208.4(INSR):c.2030_2267+1del
|
|
|
NM_000208.4(INSR):c.2095C>T (p.Gln699Ter)
|
rs121913137
|
|
NM_000208.4(INSR):c.2286G>T (p.Arg762Ser)
|
rs121913138
|
|
NM_000208.4(INSR):c.2480_2487del (p.Gln827fs)
|
rs587776820
|
|
NM_000208.4(INSR):c.25dup (p.Ala9fs)
|
|
|
NM_000208.4(INSR):c.2770C>T (p.Arg924Ter)
|
rs387906538
|
|
NM_000208.4(INSR):c.3104G>T (p.Gly1035Val)
|
rs121913135
|
|
NM_000208.4(INSR):c.338G>C (p.Arg113Pro)
|
rs121913153
|
|
NM_000208.4(INSR):c.3481G>A (p.Ala1161Thr)
|
rs121913139
|
|
NM_000208.4(INSR):c.3485C>A (p.Ala1162Glu)
|
rs121913154
|
|
NM_000208.4(INSR):c.350_353del (p.Asn117fs)
|
rs1347163319
|
|
NM_000208.4(INSR):c.3540G>A (p.Met1180Ile)
|
rs121913157
|
|
NM_000208.4(INSR):c.3601C>T (p.Arg1201Trp)
|
rs1568426700
|
|
NM_000208.4(INSR):c.3602G>A (p.Arg1201Gln)
|
rs121913156
|
|
NM_000208.4(INSR):c.3633_3634del (p.Val1212fs)
|
|
|
NM_000208.4(INSR):c.3680G>C (p.Trp1227Ser)
|
rs121913140
|
|
NM_000208.4(INSR):c.394G>A (p.Gly132Ser)
|
rs886037750
|
|
NM_000208.4(INSR):c.438C>G (p.Ile146Met)
|
rs121913159
|
|
NM_000208.4(INSR):c.442A>T (p.Lys148Ter)
|
rs121913155
|
|
NM_000208.4(INSR):c.479G>A (p.Trp160Ter)
|
rs121913146
|
|
NM_000208.4(INSR):c.509dup (p.Asn170fs)
|
|
|
NM_000208.4(INSR):c.632C>T (p.Thr211Ile)
|
rs1967766760
|
|
NM_000208.4(INSR):c.779T>C (p.Leu260Pro)
|
rs121913141
|
|