Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg4 |
T |
C |
9: 44,198,627 (GRCm39) |
N42D |
probably damaging |
Het |
Adamdec1 |
G |
A |
14: 68,807,562 (GRCm39) |
T366I |
probably damaging |
Het |
Adamts7 |
C |
A |
9: 90,075,383 (GRCm39) |
H1038Q |
probably benign |
Het |
Aff3 |
T |
C |
1: 38,666,209 (GRCm39) |
D5G |
possibly damaging |
Het |
Amhr2 |
A |
T |
15: 102,362,688 (GRCm39) |
D485V |
probably damaging |
Het |
Arhgap35 |
A |
T |
7: 16,298,663 (GRCm39) |
F134Y |
probably damaging |
Het |
Asxl3 |
A |
G |
18: 22,649,534 (GRCm39) |
T508A |
probably benign |
Het |
Atp10a |
TGGCGGCGGC |
TGGCGGC |
7: 58,308,248 (GRCm39) |
|
probably benign |
Het |
Atp4a |
G |
A |
7: 30,419,650 (GRCm39) |
R671Q |
probably benign |
Het |
Atp9a |
A |
G |
2: 168,479,592 (GRCm39) |
F928L |
possibly damaging |
Het |
BC034090 |
A |
T |
1: 155,108,221 (GRCm39) |
D13E |
probably damaging |
Het |
Bco1 |
A |
G |
8: 117,855,980 (GRCm39) |
E425G |
probably benign |
Het |
Brsk1 |
T |
C |
7: 4,710,298 (GRCm39) |
S436P |
possibly damaging |
Het |
C1s1 |
T |
C |
6: 124,513,449 (GRCm39) |
I193V |
probably benign |
Het |
Calb2 |
A |
G |
8: 110,894,709 (GRCm39) |
F21L |
probably benign |
Het |
Catsperz |
T |
G |
19: 6,902,171 (GRCm39) |
T108P |
probably benign |
Het |
Cep57l1 |
T |
A |
10: 41,595,767 (GRCm39) |
D329V |
possibly damaging |
Het |
Cfdp1 |
A |
G |
8: 112,557,577 (GRCm39) |
F188S |
probably benign |
Het |
Chrna2 |
G |
A |
14: 66,386,292 (GRCm39) |
G146D |
probably damaging |
Het |
Col6a1 |
A |
C |
10: 76,550,506 (GRCm39) |
F520V |
unknown |
Het |
Cyb5d2 |
C |
A |
11: 72,669,771 (GRCm39) |
V43L |
probably damaging |
Het |
Cyp2c40 |
T |
C |
19: 39,775,290 (GRCm39) |
T321A |
probably benign |
Het |
Dnajc16 |
A |
C |
4: 141,490,859 (GRCm39) |
Y764D |
probably damaging |
Het |
Dsg1a |
G |
A |
18: 20,473,590 (GRCm39) |
V888M |
probably damaging |
Het |
F5 |
A |
C |
1: 164,012,489 (GRCm39) |
T468P |
probably damaging |
Het |
Faap24 |
A |
G |
7: 35,094,509 (GRCm39) |
M97T |
probably benign |
Het |
Fam227b |
A |
T |
2: 125,849,230 (GRCm39) |
I334N |
probably damaging |
Het |
Frem2 |
G |
T |
3: 53,562,864 (GRCm39) |
P548T |
probably damaging |
Het |
Gfm1 |
A |
G |
3: 67,340,731 (GRCm39) |
E94G |
probably damaging |
Het |
Gm17606 |
A |
T |
14: 54,885,696 (GRCm39) |
|
probably benign |
Het |
Gnb2 |
A |
T |
5: 137,528,515 (GRCm39) |
M1K |
probably null |
Het |
Gys1 |
G |
A |
7: 45,104,258 (GRCm39) |
A544T |
probably damaging |
Het |
Hdac5 |
T |
C |
11: 102,096,675 (GRCm39) |
Y230C |
probably damaging |
Het |
Hunk |
A |
T |
16: 90,244,196 (GRCm39) |
|
probably null |
Het |
Ifnl2 |
A |
G |
7: 28,209,635 (GRCm39) |
F51L |
probably damaging |
Het |
Itpr1 |
T |
C |
6: 108,387,892 (GRCm39) |
|
probably null |
Het |
Kcnj1 |
A |
G |
9: 32,307,918 (GRCm39) |
Y114C |
probably benign |
Het |
Kdm4b |
T |
A |
17: 56,706,459 (GRCm39) |
S322T |
probably damaging |
Het |
Kif27 |
T |
C |
13: 58,471,730 (GRCm39) |
E786G |
probably damaging |
Het |
Kif6 |
T |
C |
17: 50,060,909 (GRCm39) |
V414A |
probably benign |
Het |
L1td1 |
A |
G |
4: 98,621,861 (GRCm39) |
K141R |
possibly damaging |
Het |
Loxhd1 |
A |
G |
18: 77,490,581 (GRCm39) |
I1394V |
possibly damaging |
Het |
Lrfn5 |
A |
T |
12: 61,886,433 (GRCm39) |
M74L |
probably damaging |
Het |
Lrp6 |
C |
T |
6: 134,488,230 (GRCm39) |
D289N |
probably benign |
Het |
Mroh7 |
A |
G |
4: 106,548,710 (GRCm39) |
|
probably null |
Het |
Muc4 |
A |
C |
16: 32,589,651 (GRCm39) |
E2885A |
possibly damaging |
Het |
Myo18b |
G |
T |
5: 113,023,041 (GRCm39) |
|
probably benign |
Het |
Ncln |
G |
A |
10: 81,328,902 (GRCm39) |
A172V |
probably damaging |
Het |
Nek9 |
G |
A |
12: 85,367,666 (GRCm39) |
T335M |
possibly damaging |
Het |
Notch2 |
A |
G |
3: 98,042,829 (GRCm39) |
Y1398C |
probably damaging |
Het |
Or10g6 |
A |
T |
9: 39,933,823 (GRCm39) |
I45F |
probably damaging |
Het |
Or2d4 |
T |
A |
7: 106,544,074 (GRCm39) |
I45F |
probably damaging |
Het |
Or5p52 |
A |
T |
7: 107,502,188 (GRCm39) |
H88L |
probably benign |
Het |
Pax2 |
G |
A |
19: 44,749,376 (GRCm39) |
V40M |
probably damaging |
Het |
Pde6c |
A |
G |
19: 38,157,887 (GRCm39) |
Y637C |
probably damaging |
Het |
Plppr5 |
A |
G |
3: 117,414,618 (GRCm39) |
I80V |
probably damaging |
Het |
Pold1 |
G |
T |
7: 44,182,233 (GRCm39) |
P1100T |
probably damaging |
Het |
Rgl2 |
C |
T |
17: 34,152,200 (GRCm39) |
A329V |
possibly damaging |
Het |
Rilp |
T |
A |
11: 75,402,250 (GRCm39) |
Y250N |
probably damaging |
Het |
Rilpl1 |
A |
G |
5: 124,652,751 (GRCm39) |
V19A |
probably benign |
Het |
Rtp3 |
T |
C |
9: 110,815,519 (GRCm39) |
|
probably null |
Het |
Rufy4 |
A |
G |
1: 74,172,266 (GRCm39) |
K246E |
probably damaging |
Het |
Saraf |
C |
A |
8: 34,635,616 (GRCm39) |
A306E |
probably damaging |
Het |
Slc26a8 |
A |
T |
17: 28,857,658 (GRCm39) |
N828K |
probably benign |
Het |
Src |
C |
T |
2: 157,311,852 (GRCm39) |
P527S |
probably damaging |
Het |
Susd3 |
C |
T |
13: 49,384,778 (GRCm39) |
|
probably null |
Het |
Syngap1 |
T |
C |
17: 27,185,880 (GRCm39) |
L1270P |
probably damaging |
Het |
Taf1c |
G |
A |
8: 120,325,589 (GRCm39) |
P758S |
probably damaging |
Het |
Tenm2 |
A |
T |
11: 35,915,275 (GRCm39) |
N2087K |
probably damaging |
Het |
Tfrc |
A |
T |
16: 32,448,969 (GRCm39) |
I703F |
probably damaging |
Het |
Thap1 |
C |
G |
8: 26,650,874 (GRCm39) |
T48S |
probably benign |
Het |
Tspear |
T |
C |
10: 77,702,163 (GRCm39) |
F199L |
probably benign |
Het |
Usp17lc |
A |
T |
7: 103,067,797 (GRCm39) |
H364L |
probably benign |
Het |
Usp9x |
A |
G |
X: 12,989,747 (GRCm39) |
R776G |
possibly damaging |
Homo |
Vmn1r1 |
T |
C |
1: 181,984,789 (GRCm39) |
E292G |
possibly damaging |
Het |
Vmn1r125 |
T |
G |
7: 21,006,552 (GRCm39) |
V150G |
probably damaging |
Het |
Vmn1r167 |
A |
T |
7: 23,204,117 (GRCm39) |
L300I |
probably damaging |
Het |
Vmn2r106 |
A |
C |
17: 20,487,885 (GRCm39) |
I838S |
probably benign |
Het |
Wdr64 |
A |
T |
1: 175,554,060 (GRCm39) |
S197C |
probably damaging |
Het |
Zfp248 |
A |
T |
6: 118,410,268 (GRCm39) |
V47E |
possibly 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 |
|
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 |
17,098,522 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6573:Prune2
|
UTSW |
19 |
17,098,521 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
R7284:Prune2
|
UTSW |
19 |
17,097,250 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|