NM_006269.2(RP1):c.2953A>T (p.Asn985Tyr)
|
rs2293869
|
0.33006
|
NM_006269.2(RP1):c.2615G>A (p.Arg872His)
|
rs444772
|
0.24558
|
NM_006269.2(RP1):c.4784G>A (p.Arg1595Gln)
|
rs35084330
|
0.03211
|
NM_006269.2(RP1):c.3699C>T (p.Ser1233=)
|
rs114557304
|
0.03129
|
NM_006269.2(RP1):c.1118C>T (p.Thr373Ile)
|
rs77775126
|
0.00985
|
NM_006269.2(RP1):c.*72G>A
|
rs73679499
|
0.00870
|
NM_006269.2(RP1):c.2255C>T (p.Thr752Met)
|
rs28399531
|
0.00832
|
NM_006269.2(RP1):c.2991T>C (p.Asn997=)
|
rs112667487
|
0.00829
|
NM_006269.2(RP1):c.2833G>T (p.Val945Leu)
|
rs16920621
|
0.00690
|
NM_006269.2(RP1):c.4565G>A (p.Gly1522Asp)
|
rs77860871
|
0.00580
|
NM_006269.2(RP1):c.885T>C (p.Val295=)
|
rs80043423
|
0.00468
|
NM_006269.2(RP1):c.616-6T>C
|
rs186571865
|
0.00458
|
NM_006269.2(RP1):c.382C>A (p.Leu128Ile)
|
rs147116231
|
0.00283
|
NM_006269.2(RP1):c.279G>T (p.Thr93=)
|
rs144293929
|
0.00184
|
NM_006269.2(RP1):c.4509T>C (p.Thr1503=)
|
rs144274712
|
0.00151
|
NM_006269.2(RP1):c.4512A>G (p.Leu1504=)
|
rs148722424
|
0.00150
|
NM_006269.2(RP1):c.6366T>C (p.Ile2122=)
|
rs114157620
|
0.00144
|
NM_006269.2(RP1):c.4511T>C (p.Leu1504Ser)
|
rs138106612
|
0.00127
|
NM_006269.2(RP1):c.2385C>T (p.Ile795=)
|
rs184739468
|
0.00105
|
NM_006269.2(RP1):c.487G>A (p.Asp163Asn)
|
rs370436803
|
0.00074
|
NM_006269.2(RP1):c.228C>T (p.Leu76=)
|
rs142600056
|
0.00073
|
NM_006269.2(RP1):c.618T>C (p.Val206=)
|
rs146337514
|
0.00051
|
NM_006269.2(RP1):c.*71C>T
|
rs185876566
|
0.00028
|
NM_006269.2(RP1):c.2116G>C (p.Gly706Arg)
|
rs199879316
|
0.00014
|
NM_006269.2(RP1):c.2938G>A (p.Gly980Ser)
|
rs202226256
|
0.00014
|
NM_006269.2(RP1):c.4299A>G (p.Ala1433=)
|
rs148918111
|
0.00013
|
NM_006269.2(RP1):c.441C>T (p.Pro147=)
|
rs547844896
|
0.00012
|
NM_006269.2(RP1):c.2894G>T (p.Ser965Ile)
|
rs201110322
|
0.00009
|
NM_006269.2(RP1):c.3024G>A (p.Gln1008=)
|
rs555160408
|
0.00009
|
NM_006269.2(RP1):c.3999C>T (p.Tyr1333=)
|
rs146602041
|
0.00008
|
NM_006269.2(RP1):c.4131C>T (p.Asp1377=)
|
rs538825686
|
0.00007
|
NM_006269.2(RP1):c.4735T>G (p.Leu1579Val)
|
rs200860068
|
0.00005
|
NM_001375654.1(RP1):c.1205A>T (p.Glu402Val)
|
|
|
NM_001375654.1(RP1):c.1459T>C (p.Tyr487His)
|
|
|
NM_006269.2(RP1):c.4876G>A (p.Gly1626Arg)
|
rs527236106
|
|
NM_006269.2(RP1):c.6098G>A (p.Cys2033Tyr)
|
rs61739567
|
|