Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
T |
A |
14: 32,382,908 (GRCm39) |
Y1019F |
probably benign |
Het |
4930455H04Rik |
T |
G |
3: 116,762,200 (GRCm39) |
|
probably benign |
Het |
9830107B12Rik |
A |
T |
17: 48,439,193 (GRCm39) |
|
probably benign |
Het |
Abcc8 |
A |
G |
7: 45,784,917 (GRCm39) |
V737A |
possibly damaging |
Het |
Adamts20 |
T |
A |
15: 94,229,329 (GRCm39) |
Y930F |
probably damaging |
Het |
Alkbh8 |
T |
A |
9: 3,369,825 (GRCm39) |
F365I |
probably damaging |
Het |
App |
G |
A |
16: 84,900,127 (GRCm39) |
H108Y |
probably damaging |
Het |
Bfsp1 |
T |
C |
2: 143,669,564 (GRCm39) |
|
probably benign |
Het |
Bltp3b |
T |
C |
10: 89,641,624 (GRCm39) |
S932P |
probably benign |
Het |
Cabin1 |
T |
C |
10: 75,578,263 (GRCm39) |
N478S |
probably damaging |
Het |
Camsap3 |
G |
A |
8: 3,654,795 (GRCm39) |
V796I |
probably damaging |
Het |
Carns1 |
A |
T |
19: 4,216,498 (GRCm39) |
|
probably null |
Het |
Ccdc121 |
A |
T |
5: 31,644,771 (GRCm39) |
I175L |
probably benign |
Het |
Clca3a1 |
C |
T |
3: 144,713,539 (GRCm39) |
M697I |
probably benign |
Het |
Cltc |
C |
T |
11: 86,593,074 (GRCm39) |
M1600I |
probably benign |
Het |
Cnot1 |
T |
A |
8: 96,467,637 (GRCm39) |
N1499Y |
probably damaging |
Het |
Crebbp |
T |
A |
16: 3,942,632 (GRCm39) |
I196L |
probably damaging |
Het |
Drc3 |
C |
A |
11: 60,249,475 (GRCm39) |
|
probably benign |
Het |
Fam161a |
T |
A |
11: 22,970,702 (GRCm39) |
Y234* |
probably null |
Het |
Il1r1 |
C |
A |
1: 40,352,330 (GRCm39) |
P500Q |
probably damaging |
Het |
Katnal1 |
G |
T |
5: 148,830,607 (GRCm39) |
|
probably benign |
Het |
Klhdc2 |
A |
G |
12: 69,343,827 (GRCm39) |
N20S |
probably benign |
Het |
Kmt2e |
A |
T |
5: 23,707,017 (GRCm39) |
T1527S |
possibly damaging |
Het |
Magi1 |
C |
T |
6: 93,724,205 (GRCm39) |
G270D |
probably damaging |
Het |
Mdn1 |
T |
A |
4: 32,715,922 (GRCm39) |
S2035T |
possibly damaging |
Het |
Mki67 |
A |
T |
7: 135,301,275 (GRCm39) |
M1253K |
probably benign |
Het |
Myh7 |
T |
C |
14: 55,226,336 (GRCm39) |
M435V |
possibly damaging |
Het |
Myh8 |
A |
G |
11: 67,183,505 (GRCm39) |
I739V |
probably benign |
Het |
Npnt |
T |
C |
3: 132,591,743 (GRCm39) |
K430R |
probably damaging |
Het |
Nrdc |
A |
G |
4: 108,904,857 (GRCm39) |
N696S |
probably benign |
Het |
Oit3 |
T |
C |
10: 59,261,306 (GRCm39) |
|
probably benign |
Het |
Or51a10 |
A |
G |
7: 103,699,376 (GRCm39) |
Y62H |
probably damaging |
Het |
Or51s1 |
A |
G |
7: 102,558,926 (GRCm39) |
I40T |
possibly damaging |
Het |
Or5bw2 |
A |
G |
7: 6,573,211 (GRCm39) |
T74A |
probably benign |
Het |
Or5p6 |
A |
T |
7: 107,631,328 (GRCm39) |
I74K |
possibly damaging |
Het |
Pkd1 |
G |
A |
17: 24,813,795 (GRCm39) |
|
probably null |
Het |
Plat |
A |
G |
8: 23,266,844 (GRCm39) |
M279V |
probably benign |
Het |
Prkd1 |
A |
T |
12: 50,439,693 (GRCm39) |
L378* |
probably null |
Het |
Rasgef1a |
C |
T |
6: 118,061,506 (GRCm39) |
T157I |
probably benign |
Het |
Rbm22 |
A |
G |
18: 60,693,929 (GRCm39) |
N11S |
probably damaging |
Het |
Ros1 |
T |
C |
10: 51,922,426 (GRCm39) |
|
probably benign |
Het |
Sema6d |
T |
A |
2: 124,495,562 (GRCm39) |
F3Y |
unknown |
Het |
Slit1 |
C |
A |
19: 41,599,483 (GRCm39) |
G1023C |
probably damaging |
Het |
Spata31h1 |
C |
A |
10: 82,120,568 (GRCm39) |
K4147N |
probably damaging |
Het |
Sptb |
T |
C |
12: 76,659,329 (GRCm39) |
|
probably benign |
Het |
Sspo |
T |
C |
6: 48,475,277 (GRCm39) |
I4881T |
probably benign |
Het |
Supt6 |
C |
A |
11: 78,111,969 (GRCm39) |
D1038Y |
probably damaging |
Het |
Tbc1d2b |
A |
T |
9: 90,087,144 (GRCm39) |
L945Q |
probably damaging |
Het |
Tgfbr3 |
G |
T |
5: 107,297,764 (GRCm39) |
A212E |
probably damaging |
Het |
Tipin |
A |
G |
9: 64,211,690 (GRCm39) |
T259A |
probably benign |
Het |
Traip |
T |
C |
9: 107,847,671 (GRCm39) |
S365P |
probably benign |
Het |
Tst |
T |
C |
15: 78,283,967 (GRCm39) |
T287A |
probably benign |
Het |
Tube1 |
C |
T |
10: 39,021,718 (GRCm39) |
|
probably benign |
Het |
Vmn1r37 |
T |
A |
6: 66,708,393 (GRCm39) |
N6K |
probably damaging |
Het |
Vmn2r111 |
C |
A |
17: 22,790,966 (GRCm39) |
E111* |
probably null |
Het |
Vmn2r17 |
C |
T |
5: 109,600,898 (GRCm39) |
T732I |
probably benign |
Het |
Vmn2r69 |
A |
T |
7: 85,055,836 (GRCm39) |
D767E |
possibly damaging |
Het |
|
Other mutations in Sis |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00582:Sis
|
APN |
3 |
72,853,969 (GRCm39) |
missense |
probably benign |
|
IGL00715:Sis
|
APN |
3 |
72,841,457 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00721:Sis
|
APN |
3 |
72,850,912 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00766:Sis
|
APN |
3 |
72,814,570 (GRCm39) |
splice site |
probably benign |
|
IGL00783:Sis
|
APN |
3 |
72,853,965 (GRCm39) |
missense |
probably benign |
|
IGL00805:Sis
|
APN |
3 |
72,841,532 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00932:Sis
|
APN |
3 |
72,848,289 (GRCm39) |
splice site |
probably benign |
|
IGL01020:Sis
|
APN |
3 |
72,874,171 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01024:Sis
|
APN |
3 |
72,819,209 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01286:Sis
|
APN |
3 |
72,848,358 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01514:Sis
|
APN |
3 |
72,843,253 (GRCm39) |
splice site |
probably benign |
|
IGL01986:Sis
|
APN |
3 |
72,852,545 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02110:Sis
|
APN |
3 |
72,836,032 (GRCm39) |
nonsense |
probably null |
|
IGL02132:Sis
|
APN |
3 |
72,854,804 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02152:Sis
|
APN |
3 |
72,796,319 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02200:Sis
|
APN |
3 |
72,850,937 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02244:Sis
|
APN |
3 |
72,863,523 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02307:Sis
|
APN |
3 |
72,819,167 (GRCm39) |
splice site |
probably benign |
|
IGL02374:Sis
|
APN |
3 |
72,832,789 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02437:Sis
|
APN |
3 |
72,826,947 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02571:Sis
|
APN |
3 |
72,863,637 (GRCm39) |
splice site |
probably benign |
|
IGL02601:Sis
|
APN |
3 |
72,820,543 (GRCm39) |
missense |
probably benign |
0.44 |
IGL03063:Sis
|
APN |
3 |
72,835,630 (GRCm39) |
missense |
probably benign |
|
IGL03382:Sis
|
APN |
3 |
72,836,052 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03397:Sis
|
APN |
3 |
72,843,212 (GRCm39) |
missense |
probably benign |
0.44 |
PIT1430001:Sis
|
UTSW |
3 |
72,830,162 (GRCm39) |
missense |
probably damaging |
0.97 |
R0013:Sis
|
UTSW |
3 |
72,817,809 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0013:Sis
|
UTSW |
3 |
72,817,809 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0046:Sis
|
UTSW |
3 |
72,839,427 (GRCm39) |
missense |
probably benign |
0.01 |
R0094:Sis
|
UTSW |
3 |
72,828,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R0096:Sis
|
UTSW |
3 |
72,835,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R0505:Sis
|
UTSW |
3 |
72,867,629 (GRCm39) |
missense |
probably benign |
0.29 |
R0544:Sis
|
UTSW |
3 |
72,858,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R0551:Sis
|
UTSW |
3 |
72,832,740 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0617:Sis
|
UTSW |
3 |
72,872,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R0698:Sis
|
UTSW |
3 |
72,817,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0701:Sis
|
UTSW |
3 |
72,848,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R0704:Sis
|
UTSW |
3 |
72,857,155 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0706:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0710:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0752:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0753:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0754:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0767:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0769:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0772:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0774:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0776:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0818:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0819:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0885:Sis
|
UTSW |
3 |
72,819,282 (GRCm39) |
nonsense |
probably null |
|
R1076:Sis
|
UTSW |
3 |
72,841,431 (GRCm39) |
missense |
probably damaging |
0.97 |
R1140:Sis
|
UTSW |
3 |
72,858,949 (GRCm39) |
missense |
probably damaging |
0.98 |
R1175:Sis
|
UTSW |
3 |
72,865,437 (GRCm39) |
splice site |
probably benign |
|
R1301:Sis
|
UTSW |
3 |
72,853,915 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1437:Sis
|
UTSW |
3 |
72,841,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Sis
|
UTSW |
3 |
72,839,393 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1466:Sis
|
UTSW |
3 |
72,839,393 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1472:Sis
|
UTSW |
3 |
72,796,360 (GRCm39) |
missense |
probably benign |
0.12 |
R1584:Sis
|
UTSW |
3 |
72,839,393 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1707:Sis
|
UTSW |
3 |
72,816,420 (GRCm39) |
splice site |
probably benign |
|
R1715:Sis
|
UTSW |
3 |
72,796,343 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1719:Sis
|
UTSW |
3 |
72,872,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1728:Sis
|
UTSW |
3 |
72,872,978 (GRCm39) |
nonsense |
probably null |
|
R1784:Sis
|
UTSW |
3 |
72,872,978 (GRCm39) |
nonsense |
probably null |
|
R1820:Sis
|
UTSW |
3 |
72,828,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R1972:Sis
|
UTSW |
3 |
72,828,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R1973:Sis
|
UTSW |
3 |
72,828,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R2054:Sis
|
UTSW |
3 |
72,820,570 (GRCm39) |
missense |
probably benign |
0.01 |
R2233:Sis
|
UTSW |
3 |
72,820,527 (GRCm39) |
missense |
probably benign |
0.03 |
R2235:Sis
|
UTSW |
3 |
72,820,527 (GRCm39) |
missense |
probably benign |
0.03 |
R2276:Sis
|
UTSW |
3 |
72,821,934 (GRCm39) |
nonsense |
probably null |
|
R2435:Sis
|
UTSW |
3 |
72,819,237 (GRCm39) |
missense |
probably benign |
0.01 |
R2885:Sis
|
UTSW |
3 |
72,816,506 (GRCm39) |
missense |
probably benign |
0.01 |
R2966:Sis
|
UTSW |
3 |
72,796,343 (GRCm39) |
missense |
probably benign |
0.30 |
R3708:Sis
|
UTSW |
3 |
72,850,856 (GRCm39) |
missense |
probably benign |
0.02 |
R3790:Sis
|
UTSW |
3 |
72,828,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R3807:Sis
|
UTSW |
3 |
72,832,929 (GRCm39) |
missense |
probably benign |
0.01 |
R3858:Sis
|
UTSW |
3 |
72,835,985 (GRCm39) |
missense |
probably damaging |
0.99 |
R3974:Sis
|
UTSW |
3 |
72,850,968 (GRCm39) |
missense |
probably damaging |
0.96 |
R3975:Sis
|
UTSW |
3 |
72,850,968 (GRCm39) |
missense |
probably damaging |
0.96 |
R4037:Sis
|
UTSW |
3 |
72,835,935 (GRCm39) |
missense |
probably benign |
|
R4080:Sis
|
UTSW |
3 |
72,828,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R4204:Sis
|
UTSW |
3 |
72,868,415 (GRCm39) |
missense |
probably benign |
|
R4394:Sis
|
UTSW |
3 |
72,863,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R4470:Sis
|
UTSW |
3 |
72,835,492 (GRCm39) |
splice site |
probably null |
|
R4573:Sis
|
UTSW |
3 |
72,835,570 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4868:Sis
|
UTSW |
3 |
72,850,881 (GRCm39) |
missense |
probably benign |
0.09 |
R5023:Sis
|
UTSW |
3 |
72,841,455 (GRCm39) |
missense |
probably benign |
0.05 |
R5264:Sis
|
UTSW |
3 |
72,857,089 (GRCm39) |
missense |
probably damaging |
0.98 |
R5414:Sis
|
UTSW |
3 |
72,859,826 (GRCm39) |
missense |
probably benign |
|
R5462:Sis
|
UTSW |
3 |
72,857,171 (GRCm39) |
missense |
probably damaging |
0.96 |
R5523:Sis
|
UTSW |
3 |
72,798,754 (GRCm39) |
missense |
probably benign |
0.00 |
R5584:Sis
|
UTSW |
3 |
72,817,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5587:Sis
|
UTSW |
3 |
72,821,909 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5725:Sis
|
UTSW |
3 |
72,872,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R5769:Sis
|
UTSW |
3 |
72,835,568 (GRCm39) |
missense |
probably damaging |
0.98 |
R5790:Sis
|
UTSW |
3 |
72,835,507 (GRCm39) |
missense |
probably benign |
|
R5864:Sis
|
UTSW |
3 |
72,857,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R5902:Sis
|
UTSW |
3 |
72,867,589 (GRCm39) |
critical splice donor site |
probably null |
|
R5925:Sis
|
UTSW |
3 |
72,828,713 (GRCm39) |
splice site |
probably null |
|
R6018:Sis
|
UTSW |
3 |
72,820,525 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6029:Sis
|
UTSW |
3 |
72,835,641 (GRCm39) |
missense |
probably benign |
0.30 |
R6124:Sis
|
UTSW |
3 |
72,860,544 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6171:Sis
|
UTSW |
3 |
72,868,360 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6182:Sis
|
UTSW |
3 |
72,811,626 (GRCm39) |
missense |
probably benign |
0.05 |
R6295:Sis
|
UTSW |
3 |
72,874,103 (GRCm39) |
missense |
probably damaging |
0.99 |
R6416:Sis
|
UTSW |
3 |
72,819,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R6431:Sis
|
UTSW |
3 |
72,865,507 (GRCm39) |
missense |
probably benign |
0.00 |
R6472:Sis
|
UTSW |
3 |
72,846,067 (GRCm39) |
nonsense |
probably null |
|
R6517:Sis
|
UTSW |
3 |
72,814,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R6701:Sis
|
UTSW |
3 |
72,856,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R6796:Sis
|
UTSW |
3 |
72,872,951 (GRCm39) |
missense |
probably benign |
0.06 |
R6853:Sis
|
UTSW |
3 |
72,798,759 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6906:Sis
|
UTSW |
3 |
72,826,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R7058:Sis
|
UTSW |
3 |
72,810,940 (GRCm39) |
missense |
probably damaging |
0.98 |
R7357:Sis
|
UTSW |
3 |
72,832,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R7381:Sis
|
UTSW |
3 |
72,820,625 (GRCm39) |
splice site |
probably null |
|
R7439:Sis
|
UTSW |
3 |
72,816,374 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7742:Sis
|
UTSW |
3 |
72,832,431 (GRCm39) |
missense |
probably benign |
0.19 |
R7813:Sis
|
UTSW |
3 |
72,832,801 (GRCm39) |
missense |
probably benign |
0.01 |
R7883:Sis
|
UTSW |
3 |
72,828,329 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7899:Sis
|
UTSW |
3 |
72,844,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R7915:Sis
|
UTSW |
3 |
72,828,471 (GRCm39) |
missense |
probably damaging |
0.99 |
R7985:Sis
|
UTSW |
3 |
72,844,294 (GRCm39) |
splice site |
probably null |
|
R8020:Sis
|
UTSW |
3 |
72,816,298 (GRCm39) |
critical splice donor site |
probably null |
|
R8023:Sis
|
UTSW |
3 |
72,859,813 (GRCm39) |
missense |
probably damaging |
0.97 |
R8029:Sis
|
UTSW |
3 |
72,828,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R8053:Sis
|
UTSW |
3 |
72,856,901 (GRCm39) |
nonsense |
probably null |
|
R8062:Sis
|
UTSW |
3 |
72,828,321 (GRCm39) |
nonsense |
probably null |
|
R8074:Sis
|
UTSW |
3 |
72,824,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R8085:Sis
|
UTSW |
3 |
72,814,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R8137:Sis
|
UTSW |
3 |
72,796,378 (GRCm39) |
missense |
probably benign |
0.22 |
R8349:Sis
|
UTSW |
3 |
72,810,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R8354:Sis
|
UTSW |
3 |
72,854,834 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8366:Sis
|
UTSW |
3 |
72,865,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R8449:Sis
|
UTSW |
3 |
72,810,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R8454:Sis
|
UTSW |
3 |
72,854,834 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8474:Sis
|
UTSW |
3 |
72,836,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R8515:Sis
|
UTSW |
3 |
72,836,742 (GRCm39) |
missense |
probably benign |
0.00 |
R8680:Sis
|
UTSW |
3 |
72,867,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R8703:Sis
|
UTSW |
3 |
72,867,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R9098:Sis
|
UTSW |
3 |
72,844,578 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9466:Sis
|
UTSW |
3 |
72,872,910 (GRCm39) |
critical splice donor site |
probably null |
|
R9574:Sis
|
UTSW |
3 |
72,828,490 (GRCm39) |
missense |
probably benign |
0.05 |
R9630:Sis
|
UTSW |
3 |
72,828,722 (GRCm39) |
missense |
probably benign |
0.11 |
R9680:Sis
|
UTSW |
3 |
72,863,621 (GRCm39) |
missense |
probably benign |
0.12 |
R9709:Sis
|
UTSW |
3 |
72,799,074 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9731:Sis
|
UTSW |
3 |
72,835,543 (GRCm39) |
missense |
probably benign |
0.01 |
X0009:Sis
|
UTSW |
3 |
72,796,355 (GRCm39) |
missense |
probably damaging |
0.99 |
X0024:Sis
|
UTSW |
3 |
72,836,003 (GRCm39) |
missense |
probably benign |
|
X0060:Sis
|
UTSW |
3 |
72,828,239 (GRCm39) |
intron |
probably benign |
|
Z1176:Sis
|
UTSW |
3 |
72,850,890 (GRCm39) |
missense |
probably benign |
0.25 |
Z1176:Sis
|
UTSW |
3 |
72,811,606 (GRCm39) |
missense |
probably benign |
0.05 |
Z1177:Sis
|
UTSW |
3 |
72,850,902 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sis
|
UTSW |
3 |
72,817,807 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sis
|
UTSW |
3 |
72,816,505 (GRCm39) |
missense |
possibly damaging |
0.88 |
|