NM_002335.4(LRP5):c.2220C>T (p.Asn740=)
|
rs2306862
|
0.11683
|
NM_002335.4(LRP5):c.1999G>A (p.Val667Met)
|
rs4988321
|
0.03472
|
NM_002335.4(LRP5):c.1330C>T (p.Arg444Cys)
|
rs80358308
|
0.00001
|
NM_002335.4(LRP5):c.1709G>A (p.Arg570Gln)
|
rs80358312
|
0.00001
|
NM_002335.4(LRP5):c.2202G>A (p.Trp734Ter)
|
rs121908667
|
0.00001
|
NM_002335.4(LRP5):c.4099G>A (p.Glu1367Lys)
|
rs28939709
|
0.00001
|
NM_002335.4(LRP5):c.4651G>A (p.Asp1551Asn)
|
rs724159827
|
0.00001
|
NM_002335.4(LRP5):c.731C>T (p.Thr244Met)
|
rs397514665
|
0.00001
|
NC_000011.8:g.(67967534_67967551)_(67974756_67974774)del
|
|
|
NM_002335.4(LRP5):c.1145C>T (p.Pro382Leu)
|
rs397514664
|
|
NM_002335.4(LRP5):c.1282C>T (p.Arg428Ter)
|
rs121908661
|
|
NM_002335.4(LRP5):c.1360G>A (p.Val454Met)
|
rs373910016
|
|
NM_002335.4(LRP5):c.1453G>T (p.Glu485Ter)
|
rs121908666
|
|
NM_002335.4(LRP5):c.1468del (p.Asp490fs)
|
rs1554967141
|
|
NM_002335.4(LRP5):c.1481G>A (p.Arg494Gln)
|
rs121908664
|
|
NM_002335.4(LRP5):c.1584+1G>A
|
rs1554967176
|
|
NM_002335.4(LRP5):c.1655C>T (p.Thr552Met)
|
rs397514663
|
|
NM_002335.4(LRP5):c.1708C>T (p.Arg570Trp)
|
rs121908665
|
|
NM_002335.4(LRP5):c.1828G>A (p.Gly610Arg)
|
rs80358313
|
|
NM_002335.4(LRP5):c.2151dup (p.Asp718Ter)
|
rs121908662
|
|
NM_002335.4(LRP5):c.2254C>G (p.Arg752Gly)
|
rs121908674
|
|
NM_002335.4(LRP5):c.2305del (p.Asp769fs)
|
rs1554971145
|
|
NM_002335.4(LRP5):c.2557C>T (p.Gln853Ter)
|
rs121908663
|
|
NM_002335.4(LRP5):c.29G>A (p.Trp10Ter)
|
rs121908660
|
|
NM_002335.4(LRP5):c.3562C>T (p.Arg1188Trp)
|
rs141178995
|
|
NM_002335.4(LRP5):c.3804del (p.Glu1270fs)
|
rs80358319
|
|
NM_002335.4(LRP5):c.4119dup (p.Lys1374fs)
|
rs80358321
|
|
NM_002335.4(LRP5):c.433C>T (p.Leu145Phe)
|
rs80358305
|
|
NM_002335.4(LRP5):c.4488+2T>G
|
rs80358322
|
|
NM_002335.4(LRP5):c.4587G>C (p.Arg1529Ser)
|
rs724159826
|
|
NM_002335.4(LRP5):c.4600C>T (p.Arg1534Ter)
|
rs149645175
|
|
NM_002335.4(LRP5):c.511G>C (p.Gly171Arg)
|
rs121908669
|
|
NM_002335.4(LRP5):c.512G>T (p.Gly171Val)
|
rs121908668
|
|
NM_002335.4(LRP5):c.640G>A (p.Ala214Thr)
|
rs121908671
|
|
NM_002335.4(LRP5):c.641C>T (p.Ala214Val)
|
rs121908672
|
|
NM_002335.4(LRP5):c.724G>A (p.Ala242Thr)
|
rs121908670
|
|
NM_002335.4(LRP5):c.758C>T (p.Thr253Ile)
|
rs121908673
|
|
NM_002335.4(LRP5):c.804_813del (p.Gly269fs)
|
rs80358307
|
|