NM_000883.4(IMPDH1):c.1142A>G (p.His381Arg)
|
rs61751223
|
0.00212
|
NM_000883.4(IMPDH1):c.*613T>C
|
rs11549800
|
0.00123
|
NM_000883.4(IMPDH1):c.1598A>G (p.Gln533Arg)
|
rs144498273
|
0.00088
|
NM_000883.4(IMPDH1):c.*102G>T
|
rs541712803
|
0.00043
|
NM_000883.4(IMPDH1):c.888C>T (p.Ile296=)
|
rs72624957
|
0.00031
|
NM_000883.4(IMPDH1):c.*642G>A
|
rs574318258
|
0.00025
|
NM_000883.4(IMPDH1):c.1714G>C (p.Glu572Gln)
|
rs150628823
|
0.00025
|
NM_000883.4(IMPDH1):c.*231C>G
|
rs1042267
|
0.00024
|
NM_000883.4(IMPDH1):c.1653C>T (p.His551=)
|
rs147882304
|
0.00019
|
NM_000883.4(IMPDH1):c.1226G>A (p.Gly409Asp)
|
rs375914533
|
0.00017
|
NM_000883.4(IMPDH1):c.841G>C (p.Glu281Gln)
|
rs145014241
|
0.00016
|
NM_000883.4(IMPDH1):c.675T>C (p.Ser225=)
|
rs373353058
|
0.00010
|
NM_000883.4(IMPDH1):c.443C>T (p.Thr148Met)
|
rs150278198
|
0.00006
|
NM_000883.4(IMPDH1):c.1280C>T (p.Pro427Leu)
|
rs763999626
|
0.00005
|
NM_000883.4(IMPDH1):c.1350C>T (p.Gly450=)
|
rs780213373
|
0.00005
|
NM_000883.4(IMPDH1):c.*259G>A
|
rs535964010
|
0.00004
|
NM_000883.4(IMPDH1):c.561C>T (p.Asn187=)
|
rs1042250
|
0.00004
|
NM_000883.4(IMPDH1):c.*321G>T
|
rs571536404
|
0.00003
|
NM_000883.4(IMPDH1):c.737G>A (p.Arg246Gln)
|
rs201071873
|
0.00003
|
NM_000883.4(IMPDH1):c.1589G>A (p.Gly530Asp)
|
rs756992593
|
0.00002
|
NM_000883.4(IMPDH1):c.*258C>T
|
rs886061981
|
0.00001
|
NM_000883.4(IMPDH1):c.*631C>T
|
rs760544024
|
0.00001
|
NM_000883.4(IMPDH1):c.1433C>T (p.Thr478Ile)
|
rs564132747
|
0.00001
|
NM_000883.4(IMPDH1):c.255-10C>T
|
rs1478038443
|
0.00001
|
NM_000883.4(IMPDH1):c.*105T>A
|
rs886061983
|
|
NM_000883.4(IMPDH1):c.*130A>G
|
rs1797626715
|
|
NM_000883.4(IMPDH1):c.*137G>C
|
rs72624973
|
|
NM_000883.4(IMPDH1):c.*168G>A
|
rs531478376
|
|
NM_000883.4(IMPDH1):c.*202C>T
|
rs886061982
|
|
NM_000883.4(IMPDH1):c.*223C>A
|
rs543042380
|
|
NM_000883.4(IMPDH1):c.*223C>T
|
rs543042380
|
|
NM_000883.4(IMPDH1):c.*256T>C
|
rs752294619
|
|
NM_000883.4(IMPDH1):c.*321G>A
|
rs571536404
|
|
NM_000883.4(IMPDH1):c.*410G>A
|
rs530960760
|
|
NM_000883.4(IMPDH1):c.1075-3C>T
|
rs1797968829
|
|
NM_000883.4(IMPDH1):c.1573G>T (p.Ala525Ser)
|
rs367951647
|
|
NM_000883.4(IMPDH1):c.1695-11C>T
|
rs1797754885
|
|
NM_000883.4(IMPDH1):c.1704G>A (p.Met568Ile)
|
rs886061984
|
|
NM_000883.4(IMPDH1):c.424C>T (p.Arg142Trp)
|
rs376769056
|
|
NM_000883.4(IMPDH1):c.694A>G (p.Thr232Ala)
|
rs979315605
|
|
NM_000883.4(IMPDH1):c.795G>A (p.Thr265=)
|
rs757423102
|
|