Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900092C05Rik |
G |
T |
7: 12,246,605 (GRCm39) |
E34* |
probably null |
Het |
4933421I07Rik |
C |
T |
7: 42,097,404 (GRCm39) |
R30H |
probably damaging |
Het |
AB124611 |
C |
A |
9: 21,450,400 (GRCm39) |
Q158K |
probably benign |
Het |
Abcc3 |
C |
T |
11: 94,247,873 (GRCm39) |
A1207T |
probably benign |
Het |
Abcc9 |
A |
T |
6: 142,628,643 (GRCm39) |
L367Q |
probably damaging |
Het |
Aftph |
T |
C |
11: 20,676,812 (GRCm39) |
K266E |
probably benign |
Het |
Akap9 |
T |
A |
5: 4,006,246 (GRCm39) |
D190E |
probably damaging |
Het |
Angel1 |
G |
T |
12: 86,767,298 (GRCm39) |
D359E |
probably damaging |
Het |
Ano6 |
T |
C |
15: 95,846,184 (GRCm39) |
I474T |
probably damaging |
Het |
Atp2c1 |
A |
T |
9: 105,398,008 (GRCm39) |
|
probably null |
Het |
Best1 |
T |
C |
19: 9,963,737 (GRCm39) |
|
probably null |
Het |
Bhlha9 |
A |
G |
11: 76,563,492 (GRCm39) |
S40G |
probably benign |
Het |
Cabin1 |
G |
A |
10: 75,530,668 (GRCm39) |
R178C |
|
Het |
Ccnb1ip1 |
A |
G |
14: 51,029,736 (GRCm39) |
Y109H |
probably damaging |
Het |
Col14a1 |
T |
C |
15: 55,381,715 (GRCm39) |
S1763P |
probably damaging |
Het |
Dars1 |
T |
C |
1: 128,300,004 (GRCm39) |
T327A |
probably benign |
Het |
Dhx8 |
T |
C |
11: 101,645,648 (GRCm39) |
Y889H |
probably damaging |
Het |
Dlg4 |
T |
A |
11: 69,932,908 (GRCm39) |
Y523* |
probably null |
Het |
Dnah10 |
A |
T |
5: 124,909,662 (GRCm39) |
D4484V |
probably benign |
Het |
Dnah9 |
A |
T |
11: 65,881,302 (GRCm39) |
M2591K |
probably damaging |
Het |
Dock2 |
T |
C |
11: 34,180,672 (GRCm39) |
E1715G |
probably benign |
Het |
Dym |
A |
G |
18: 75,252,242 (GRCm39) |
Y336C |
possibly damaging |
Het |
Ezh2 |
A |
G |
6: 47,521,453 (GRCm39) |
M439T |
probably benign |
Het |
Folr1 |
T |
G |
7: 101,508,677 (GRCm39) |
N83H |
possibly damaging |
Het |
Ganab |
T |
C |
19: 8,889,904 (GRCm39) |
L656P |
probably damaging |
Het |
Gmnc |
T |
C |
16: 26,779,542 (GRCm39) |
H161R |
probably benign |
Het |
Gria4 |
A |
G |
9: 4,472,017 (GRCm39) |
Y491H |
probably damaging |
Het |
Heatr3 |
T |
A |
8: 88,883,402 (GRCm39) |
C412S |
possibly damaging |
Het |
Hmgcr |
A |
C |
13: 96,789,173 (GRCm39) |
V716G |
probably damaging |
Het |
Igsf9 |
A |
G |
1: 172,324,479 (GRCm39) |
D799G |
probably damaging |
Het |
Ikbkb |
T |
C |
8: 23,158,976 (GRCm39) |
T501A |
probably benign |
Het |
Kbtbd3 |
C |
T |
9: 4,330,690 (GRCm39) |
R355* |
probably null |
Het |
Kcna7 |
T |
A |
7: 45,058,652 (GRCm39) |
I313N |
probably damaging |
Het |
Kirrel1 |
A |
C |
3: 86,990,694 (GRCm39) |
D709E |
probably benign |
Het |
Klb |
T |
A |
5: 65,540,821 (GRCm39) |
S971R |
probably benign |
Het |
Krtap4-13 |
A |
T |
11: 99,700,238 (GRCm39) |
C140* |
probably null |
Het |
Lacc1 |
A |
T |
14: 77,268,309 (GRCm39) |
L334Q |
probably damaging |
Het |
Map6d1 |
T |
A |
16: 20,059,775 (GRCm39) |
R97* |
probably null |
Het |
Mgat5b |
T |
C |
11: 116,835,746 (GRCm39) |
S129P |
probably damaging |
Het |
Mmp1a |
TG |
TGG |
9: 7,465,083 (GRCm38) |
|
probably null |
Het |
Myh9 |
G |
A |
15: 77,671,796 (GRCm39) |
R432C |
probably damaging |
Het |
Ncf4 |
A |
G |
15: 78,144,902 (GRCm39) |
T236A |
probably benign |
Het |
Neb |
T |
C |
2: 52,148,804 (GRCm39) |
D2581G |
probably damaging |
Het |
Nid1 |
T |
A |
13: 13,663,675 (GRCm39) |
M778K |
probably benign |
Het |
Npas2 |
A |
G |
1: 39,363,548 (GRCm39) |
D209G |
probably benign |
Het |
Nploc4 |
C |
T |
11: 120,307,196 (GRCm39) |
V181I |
possibly damaging |
Het |
Nrcam |
A |
T |
12: 44,610,817 (GRCm39) |
I506F |
probably damaging |
Het |
Or52w1 |
T |
A |
7: 105,017,752 (GRCm39) |
M73K |
probably damaging |
Het |
Or5h27 |
A |
G |
16: 59,006,331 (GRCm39) |
*172Q |
probably null |
Het |
Or6c3b |
T |
C |
10: 129,527,220 (GRCm39) |
N230S |
probably benign |
Het |
Pask |
T |
A |
1: 93,248,391 (GRCm39) |
Q970L |
probably benign |
Het |
Pfkfb4 |
T |
C |
9: 108,840,308 (GRCm39) |
I308T |
possibly damaging |
Het |
Pla2g4d |
A |
T |
2: 120,114,617 (GRCm39) |
L38Q |
probably damaging |
Het |
Pld1 |
A |
G |
3: 28,185,882 (GRCm39) |
T1036A |
possibly damaging |
Het |
Pom121l2 |
A |
G |
13: 22,166,775 (GRCm39) |
T349A |
probably damaging |
Het |
Ppp1r13b |
A |
G |
12: 111,801,400 (GRCm39) |
I551T |
possibly damaging |
Het |
Prps1l1 |
A |
G |
12: 35,035,317 (GRCm39) |
N144S |
possibly damaging |
Het |
Prss56 |
A |
G |
1: 87,113,123 (GRCm39) |
N179S |
probably null |
Het |
Ptprz1 |
C |
T |
6: 23,000,097 (GRCm39) |
T729I |
probably damaging |
Het |
Relch |
T |
A |
1: 105,662,308 (GRCm39) |
H942Q |
probably benign |
Het |
Rrp7a |
T |
C |
15: 83,006,071 (GRCm39) |
T60A |
probably damaging |
Het |
Snx27 |
A |
G |
3: 94,431,498 (GRCm39) |
Y299H |
probably damaging |
Het |
Spaca3 |
G |
T |
11: 80,754,847 (GRCm39) |
R96L |
possibly damaging |
Het |
Stat1 |
A |
G |
1: 52,188,081 (GRCm39) |
N495S |
probably benign |
Het |
Tas2r130 |
T |
C |
6: 131,607,270 (GRCm39) |
N175S |
probably benign |
Het |
Tcaf2 |
A |
G |
6: 42,606,472 (GRCm39) |
L494P |
probably damaging |
Het |
Tdrd12 |
C |
A |
7: 35,179,561 (GRCm39) |
|
probably null |
Het |
Thbs1 |
A |
G |
2: 117,949,837 (GRCm39) |
N604S |
probably damaging |
Het |
Togaram1 |
T |
C |
12: 65,055,454 (GRCm39) |
F1482L |
probably benign |
Het |
Trhr2 |
A |
T |
8: 123,087,114 (GRCm39) |
S109T |
probably damaging |
Het |
Trpc3 |
A |
T |
3: 36,678,562 (GRCm39) |
M841K |
probably damaging |
Het |
Tubgcp5 |
C |
T |
7: 55,473,315 (GRCm39) |
R798C |
probably benign |
Het |
Xirp2 |
T |
A |
2: 67,347,173 (GRCm39) |
M3138K |
probably benign |
Het |
Zdhhc4 |
G |
A |
5: 143,307,646 (GRCm39) |
T125I |
probably benign |
Het |
Zfp239 |
T |
A |
6: 117,848,716 (GRCm39) |
C151* |
probably null |
Het |
Zfp473 |
C |
T |
7: 44,382,627 (GRCm39) |
E569K |
not run |
Het |
Zzef1 |
T |
A |
11: 72,777,516 (GRCm39) |
D1782E |
probably damaging |
Het |
|
Other mutations in Prune2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00234:Prune2
|
APN |
19 |
17,145,708 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00848:Prune2
|
APN |
19 |
17,096,482 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00862:Prune2
|
APN |
19 |
17,096,713 (GRCm39) |
missense |
probably benign |
0.41 |
IGL00915:Prune2
|
APN |
19 |
16,993,617 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01084:Prune2
|
APN |
19 |
17,095,573 (GRCm39) |
missense |
probably benign |
0.19 |
IGL01109:Prune2
|
APN |
19 |
17,101,243 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01372:Prune2
|
APN |
19 |
17,102,433 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01650:Prune2
|
APN |
19 |
17,145,656 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01752:Prune2
|
APN |
19 |
17,101,267 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01812:Prune2
|
APN |
19 |
16,981,141 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01902:Prune2
|
APN |
19 |
17,096,002 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02195:Prune2
|
APN |
19 |
17,096,921 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02502:Prune2
|
APN |
19 |
17,101,245 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02569:Prune2
|
APN |
19 |
17,156,223 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02693:Prune2
|
APN |
19 |
17,101,855 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02737:Prune2
|
APN |
19 |
17,170,775 (GRCm39) |
nonsense |
probably null |
|
IGL02794:Prune2
|
APN |
19 |
17,096,725 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02985:Prune2
|
APN |
19 |
16,993,723 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03349:Prune2
|
APN |
19 |
17,100,710 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Prune2
|
UTSW |
19 |
17,102,646 (GRCm39) |
missense |
probably benign |
0.00 |
R0060:Prune2
|
UTSW |
19 |
16,981,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R0098:Prune2
|
UTSW |
19 |
17,101,267 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0098:Prune2
|
UTSW |
19 |
17,101,267 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0165:Prune2
|
UTSW |
19 |
17,099,974 (GRCm39) |
missense |
probably benign |
0.00 |
R0277:Prune2
|
UTSW |
19 |
17,098,753 (GRCm39) |
missense |
probably damaging |
0.99 |
R0321:Prune2
|
UTSW |
19 |
17,099,818 (GRCm39) |
missense |
probably benign |
0.39 |
R0321:Prune2
|
UTSW |
19 |
17,098,291 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0374:Prune2
|
UTSW |
19 |
17,098,274 (GRCm39) |
missense |
probably benign |
0.00 |
R0380:Prune2
|
UTSW |
19 |
17,101,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R0396:Prune2
|
UTSW |
19 |
17,100,444 (GRCm39) |
missense |
probably benign |
0.35 |
R0408:Prune2
|
UTSW |
19 |
17,099,674 (GRCm39) |
missense |
probably benign |
0.00 |
R0421:Prune2
|
UTSW |
19 |
17,100,675 (GRCm39) |
missense |
probably benign |
0.02 |
R0480:Prune2
|
UTSW |
19 |
16,984,156 (GRCm39) |
splice site |
probably benign |
|
R0531:Prune2
|
UTSW |
19 |
16,984,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R0546:Prune2
|
UTSW |
19 |
16,998,030 (GRCm39) |
splice site |
probably benign |
|
R0554:Prune2
|
UTSW |
19 |
17,102,582 (GRCm39) |
nonsense |
probably null |
|
R0659:Prune2
|
UTSW |
19 |
17,100,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R0699:Prune2
|
UTSW |
19 |
17,101,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R0781:Prune2
|
UTSW |
19 |
17,102,586 (GRCm39) |
missense |
probably benign |
|
R1110:Prune2
|
UTSW |
19 |
17,102,586 (GRCm39) |
missense |
probably benign |
|
R1178:Prune2
|
UTSW |
19 |
17,100,469 (GRCm39) |
missense |
probably benign |
0.22 |
R1181:Prune2
|
UTSW |
19 |
17,100,469 (GRCm39) |
missense |
probably benign |
0.22 |
R1337:Prune2
|
UTSW |
19 |
17,096,971 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1356:Prune2
|
UTSW |
19 |
17,189,681 (GRCm39) |
missense |
probably benign |
0.40 |
R1385:Prune2
|
UTSW |
19 |
17,102,312 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1659:Prune2
|
UTSW |
19 |
17,098,015 (GRCm39) |
missense |
possibly damaging |
0.59 |
R1738:Prune2
|
UTSW |
19 |
17,102,374 (GRCm39) |
missense |
probably benign |
0.01 |
R1756:Prune2
|
UTSW |
19 |
17,101,068 (GRCm39) |
missense |
probably benign |
0.01 |
R1765:Prune2
|
UTSW |
19 |
17,102,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R1782:Prune2
|
UTSW |
19 |
17,099,537 (GRCm39) |
missense |
probably benign |
0.00 |
R1817:Prune2
|
UTSW |
19 |
17,099,445 (GRCm39) |
missense |
probably benign |
0.00 |
R1838:Prune2
|
UTSW |
19 |
17,177,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R1851:Prune2
|
UTSW |
19 |
17,176,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R1852:Prune2
|
UTSW |
19 |
17,176,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R1866:Prune2
|
UTSW |
19 |
17,100,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R1911:Prune2
|
UTSW |
19 |
17,091,038 (GRCm39) |
missense |
probably benign |
0.02 |
R1983:Prune2
|
UTSW |
19 |
16,998,006 (GRCm39) |
missense |
probably damaging |
0.97 |
R2014:Prune2
|
UTSW |
19 |
17,097,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R2066:Prune2
|
UTSW |
19 |
17,098,042 (GRCm39) |
missense |
possibly damaging |
0.57 |
R2088:Prune2
|
UTSW |
19 |
17,097,109 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2111:Prune2
|
UTSW |
19 |
17,185,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R2128:Prune2
|
UTSW |
19 |
17,099,786 (GRCm39) |
missense |
probably benign |
0.00 |
R2165:Prune2
|
UTSW |
19 |
17,097,546 (GRCm39) |
missense |
probably benign |
0.19 |
R2241:Prune2
|
UTSW |
19 |
17,100,456 (GRCm39) |
missense |
probably damaging |
0.96 |
R2278:Prune2
|
UTSW |
19 |
17,095,919 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2504:Prune2
|
UTSW |
19 |
16,977,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R2508:Prune2
|
UTSW |
19 |
17,099,986 (GRCm39) |
missense |
probably benign |
0.43 |
R3055:Prune2
|
UTSW |
19 |
17,102,407 (GRCm39) |
missense |
probably damaging |
0.98 |
R3086:Prune2
|
UTSW |
19 |
17,098,777 (GRCm39) |
missense |
possibly damaging |
0.75 |
R3104:Prune2
|
UTSW |
19 |
17,096,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R3105:Prune2
|
UTSW |
19 |
17,096,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R3547:Prune2
|
UTSW |
19 |
17,101,712 (GRCm39) |
missense |
probably damaging |
0.96 |
R3702:Prune2
|
UTSW |
19 |
17,156,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R3753:Prune2
|
UTSW |
19 |
17,102,818 (GRCm39) |
missense |
probably benign |
0.38 |
R3933:Prune2
|
UTSW |
19 |
17,101,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R3935:Prune2
|
UTSW |
19 |
17,177,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R4022:Prune2
|
UTSW |
19 |
16,977,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R4042:Prune2
|
UTSW |
19 |
16,981,190 (GRCm39) |
critical splice donor site |
probably null |
|
R4164:Prune2
|
UTSW |
19 |
16,981,098 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4453:Prune2
|
UTSW |
19 |
17,099,274 (GRCm39) |
missense |
probably benign |
0.00 |
R4642:Prune2
|
UTSW |
19 |
16,998,019 (GRCm39) |
critical splice donor site |
probably null |
|
R4661:Prune2
|
UTSW |
19 |
16,977,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R4666:Prune2
|
UTSW |
19 |
17,097,552 (GRCm39) |
nonsense |
probably null |
|
R4823:Prune2
|
UTSW |
19 |
17,097,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R4897:Prune2
|
UTSW |
19 |
17,099,219 (GRCm39) |
missense |
probably benign |
0.03 |
R4922:Prune2
|
UTSW |
19 |
17,100,116 (GRCm39) |
missense |
probably benign |
0.00 |
R4962:Prune2
|
UTSW |
19 |
17,099,637 (GRCm39) |
missense |
probably benign |
0.11 |
R5026:Prune2
|
UTSW |
19 |
17,176,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R5042:Prune2
|
UTSW |
19 |
17,097,161 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5124:Prune2
|
UTSW |
19 |
17,177,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R5133:Prune2
|
UTSW |
19 |
16,980,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R5184:Prune2
|
UTSW |
19 |
17,193,721 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5234:Prune2
|
UTSW |
19 |
17,096,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R5339:Prune2
|
UTSW |
19 |
17,098,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R5363:Prune2
|
UTSW |
19 |
17,095,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R5382:Prune2
|
UTSW |
19 |
16,981,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R5436:Prune2
|
UTSW |
19 |
16,998,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R5480:Prune2
|
UTSW |
19 |
17,098,311 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5635:Prune2
|
UTSW |
19 |
17,095,573 (GRCm39) |
missense |
probably benign |
0.19 |
R5678:Prune2
|
UTSW |
19 |
17,096,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R5814:Prune2
|
UTSW |
19 |
16,993,725 (GRCm39) |
splice site |
probably null |
|
R5894:Prune2
|
UTSW |
19 |
17,098,755 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6011:Prune2
|
UTSW |
19 |
17,096,080 (GRCm39) |
missense |
probably benign |
0.35 |
R6207:Prune2
|
UTSW |
19 |
17,095,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R6218:Prune2
|
UTSW |
19 |
17,098,926 (GRCm39) |
missense |
probably benign |
0.00 |
R6573:Prune2
|
UTSW |
19 |
17,098,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R6573:Prune2
|
UTSW |
19 |
17,098,522 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6734:Prune2
|
UTSW |
19 |
16,981,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R6805:Prune2
|
UTSW |
19 |
17,097,954 (GRCm39) |
missense |
probably benign |
|
R6837:Prune2
|
UTSW |
19 |
17,156,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R6850:Prune2
|
UTSW |
19 |
17,099,552 (GRCm39) |
missense |
probably benign |
0.00 |
R6858:Prune2
|
UTSW |
19 |
17,095,470 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6874:Prune2
|
UTSW |
19 |
17,100,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R6954:Prune2
|
UTSW |
19 |
16,977,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R7098:Prune2
|
UTSW |
19 |
17,097,966 (GRCm39) |
missense |
probably benign |
0.39 |
R7102:Prune2
|
UTSW |
19 |
17,098,577 (GRCm39) |
missense |
probably benign |
0.24 |
R7246:Prune2
|
UTSW |
19 |
17,098,732 (GRCm39) |
missense |
probably damaging |
0.99 |
R7295:Prune2
|
UTSW |
19 |
17,097,261 (GRCm39) |
missense |
probably benign |
0.01 |
R7371:Prune2
|
UTSW |
19 |
17,096,734 (GRCm39) |
missense |
probably benign |
0.02 |
R7651:Prune2
|
UTSW |
19 |
17,097,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R7830:Prune2
|
UTSW |
19 |
17,100,038 (GRCm39) |
missense |
probably benign |
0.21 |
R7872:Prune2
|
UTSW |
19 |
17,096,798 (GRCm39) |
missense |
probably benign |
0.05 |
R7881:Prune2
|
UTSW |
19 |
17,100,393 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7966:Prune2
|
UTSW |
19 |
17,156,223 (GRCm39) |
missense |
probably damaging |
0.99 |
R7969:Prune2
|
UTSW |
19 |
17,179,034 (GRCm39) |
missense |
probably damaging |
0.98 |
R8092:Prune2
|
UTSW |
19 |
17,097,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R8110:Prune2
|
UTSW |
19 |
17,098,083 (GRCm39) |
missense |
probably benign |
0.22 |
R8115:Prune2
|
UTSW |
19 |
17,101,288 (GRCm39) |
missense |
probably benign |
0.02 |
R8129:Prune2
|
UTSW |
19 |
17,096,200 (GRCm39) |
missense |
probably benign |
0.01 |
R8169:Prune2
|
UTSW |
19 |
17,102,455 (GRCm39) |
missense |
probably benign |
0.10 |
R8171:Prune2
|
UTSW |
19 |
17,097,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R8176:Prune2
|
UTSW |
19 |
17,095,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R8200:Prune2
|
UTSW |
19 |
17,102,337 (GRCm39) |
missense |
probably benign |
0.01 |
R8217:Prune2
|
UTSW |
19 |
17,097,480 (GRCm39) |
missense |
probably benign |
0.01 |
R8258:Prune2
|
UTSW |
19 |
17,189,672 (GRCm39) |
missense |
unknown |
|
R8259:Prune2
|
UTSW |
19 |
17,189,672 (GRCm39) |
missense |
unknown |
|
R8289:Prune2
|
UTSW |
19 |
17,100,373 (GRCm39) |
missense |
probably benign |
0.43 |
R8329:Prune2
|
UTSW |
19 |
17,098,629 (GRCm39) |
missense |
probably benign |
0.02 |
R8342:Prune2
|
UTSW |
19 |
17,103,027 (GRCm39) |
missense |
probably benign |
0.01 |
R8558:Prune2
|
UTSW |
19 |
17,099,602 (GRCm39) |
missense |
probably damaging |
0.98 |
R8732:Prune2
|
UTSW |
19 |
17,097,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R8743:Prune2
|
UTSW |
19 |
17,096,920 (GRCm39) |
missense |
probably benign |
0.22 |
R8769:Prune2
|
UTSW |
19 |
17,100,442 (GRCm39) |
missense |
probably damaging |
0.96 |
R8862:Prune2
|
UTSW |
19 |
17,097,510 (GRCm39) |
missense |
probably benign |
0.04 |
R8936:Prune2
|
UTSW |
19 |
17,099,199 (GRCm39) |
missense |
probably benign |
0.24 |
R9040:Prune2
|
UTSW |
19 |
17,097,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R9084:Prune2
|
UTSW |
19 |
17,097,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R9224:Prune2
|
UTSW |
19 |
17,097,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R9273:Prune2
|
UTSW |
19 |
17,095,690 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9275:Prune2
|
UTSW |
19 |
17,101,144 (GRCm39) |
missense |
probably benign |
0.06 |
R9278:Prune2
|
UTSW |
19 |
17,101,144 (GRCm39) |
missense |
probably benign |
0.06 |
R9290:Prune2
|
UTSW |
19 |
17,145,691 (GRCm39) |
missense |
probably benign |
0.41 |
R9305:Prune2
|
UTSW |
19 |
17,097,625 (GRCm39) |
missense |
probably benign |
0.14 |
R9317:Prune2
|
UTSW |
19 |
17,099,034 (GRCm39) |
missense |
probably benign |
0.00 |
R9354:Prune2
|
UTSW |
19 |
17,099,986 (GRCm39) |
missense |
probably benign |
0.43 |
R9373:Prune2
|
UTSW |
19 |
17,099,502 (GRCm39) |
missense |
probably benign |
|
R9394:Prune2
|
UTSW |
19 |
16,981,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R9405:Prune2
|
UTSW |
19 |
17,193,708 (GRCm39) |
missense |
probably damaging |
0.99 |
R9476:Prune2
|
UTSW |
19 |
17,096,706 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9532:Prune2
|
UTSW |
19 |
17,099,794 (GRCm39) |
missense |
probably benign |
0.00 |
X0019:Prune2
|
UTSW |
19 |
17,098,881 (GRCm39) |
missense |
probably benign |
0.16 |
X0028:Prune2
|
UTSW |
19 |
17,100,249 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Prune2
|
UTSW |
19 |
17,099,739 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Prune2
|
UTSW |
19 |
17,096,154 (GRCm39) |
missense |
probably damaging |
1.00 |
|