Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930590J08Rik |
T |
C |
6: 91,895,091 (GRCm39) |
V262A |
probably benign |
Het |
Abtb2 |
A |
G |
2: 103,397,349 (GRCm39) |
E93G |
possibly damaging |
Het |
Adam5 |
A |
C |
8: 25,232,172 (GRCm39) |
|
probably null |
Het |
Adam5 |
G |
A |
8: 25,271,619 (GRCm39) |
T596I |
probably damaging |
Het |
Adgrb2 |
T |
A |
4: 129,907,668 (GRCm39) |
Y1001N |
probably damaging |
Het |
Aox1 |
T |
G |
1: 58,344,544 (GRCm39) |
S546A |
probably benign |
Het |
Asic2 |
T |
C |
11: 81,464,280 (GRCm39) |
|
probably benign |
Het |
Bcl11b |
T |
A |
12: 107,955,957 (GRCm39) |
N64I |
probably damaging |
Het |
Cacna1g |
A |
G |
11: 94,350,177 (GRCm39) |
F556S |
possibly damaging |
Het |
Cbl |
A |
G |
9: 44,064,166 (GRCm39) |
V790A |
probably benign |
Het |
Cd300c2 |
A |
T |
11: 114,891,807 (GRCm39) |
C22* |
probably null |
Het |
Cdh11 |
C |
T |
8: 103,374,090 (GRCm39) |
|
probably null |
Het |
Ces2g |
C |
T |
8: 105,693,989 (GRCm39) |
Q442* |
probably null |
Het |
Cps1 |
A |
T |
1: 67,200,063 (GRCm39) |
T404S |
probably damaging |
Het |
Csf2rb2 |
A |
T |
15: 78,170,174 (GRCm39) |
|
probably null |
Het |
Csmd2 |
A |
G |
4: 128,346,318 (GRCm39) |
Y1526C |
probably benign |
Het |
Cyp2a12 |
C |
T |
7: 26,730,640 (GRCm39) |
Q202* |
probably null |
Het |
Cyp2c39 |
G |
A |
19: 39,502,020 (GRCm39) |
M136I |
probably benign |
Het |
Cyp2j13 |
G |
A |
4: 95,947,280 (GRCm39) |
T257I |
probably damaging |
Het |
Dnah8 |
T |
A |
17: 30,965,949 (GRCm39) |
L2427Q |
probably damaging |
Het |
Dop1b |
G |
T |
16: 93,560,318 (GRCm39) |
|
probably null |
Het |
Entrep1 |
A |
G |
19: 23,952,790 (GRCm39) |
S507P |
possibly damaging |
Het |
Epcam |
T |
C |
17: 87,951,049 (GRCm39) |
V212A |
possibly damaging |
Het |
Flt1 |
C |
A |
5: 147,620,749 (GRCm39) |
A132S |
probably benign |
Het |
Flvcr2 |
T |
A |
12: 85,829,756 (GRCm39) |
V255D |
probably damaging |
Het |
Galc |
G |
T |
12: 98,197,731 (GRCm39) |
T326K |
probably damaging |
Het |
Gas2l3 |
CACTCGTCATACT |
CACT |
10: 89,266,820 (GRCm39) |
|
probably benign |
Het |
Gen1 |
A |
T |
12: 11,291,561 (GRCm39) |
Y808N |
probably benign |
Het |
Glis1 |
C |
T |
4: 107,476,761 (GRCm39) |
A306V |
probably damaging |
Het |
Gm10638 |
A |
G |
8: 87,473,028 (GRCm39) |
|
probably benign |
Het |
Gm12789 |
G |
A |
4: 101,846,182 (GRCm39) |
|
probably benign |
Het |
Gm27048 |
C |
T |
8: 81,661,228 (GRCm39) |
|
noncoding transcript |
Het |
Gm4204 |
T |
C |
1: 135,160,556 (GRCm39) |
|
noncoding transcript |
Het |
Gm904 |
A |
T |
13: 50,799,325 (GRCm39) |
I95F |
possibly damaging |
Het |
Gvin3 |
T |
G |
7: 106,197,793 (GRCm39) |
|
noncoding transcript |
Het |
Hjurp |
GT |
GTT |
1: 88,194,246 (GRCm39) |
|
probably null |
Het |
Ints11 |
G |
A |
4: 155,972,887 (GRCm39) |
D526N |
probably benign |
Het |
Itfg2 |
A |
G |
6: 128,393,279 (GRCm39) |
|
probably benign |
Het |
Jund |
T |
C |
8: 71,152,254 (GRCm39) |
V183A |
probably damaging |
Het |
Kcnj8 |
A |
G |
6: 142,512,221 (GRCm39) |
S129P |
probably damaging |
Het |
Kcnq3 |
A |
G |
15: 65,867,259 (GRCm39) |
S795P |
probably damaging |
Het |
Lhx8 |
G |
T |
3: 154,035,925 (GRCm39) |
A22E |
probably benign |
Het |
Lrp8 |
A |
G |
4: 107,664,006 (GRCm39) |
|
probably benign |
Het |
Lvrn |
G |
T |
18: 47,026,768 (GRCm39) |
A789S |
probably damaging |
Het |
Lvrn |
T |
C |
18: 47,014,479 (GRCm39) |
S526P |
probably damaging |
Het |
Mga |
T |
A |
2: 119,794,535 (GRCm39) |
C2622S |
possibly damaging |
Het |
Mroh8 |
T |
C |
2: 157,070,647 (GRCm39) |
E568G |
probably benign |
Het |
Ms4a4b |
C |
A |
19: 11,440,503 (GRCm39) |
|
probably benign |
Het |
Muc2 |
T |
C |
7: 141,303,280 (GRCm39) |
F99S |
probably benign |
Het |
Myo5c |
T |
A |
9: 75,180,825 (GRCm39) |
I738N |
probably damaging |
Het |
Naip6 |
A |
C |
13: 100,433,477 (GRCm39) |
V1120G |
probably damaging |
Het |
Ncl |
T |
C |
1: 86,283,901 (GRCm39) |
T307A |
probably benign |
Het |
Npr1 |
A |
T |
3: 90,363,272 (GRCm39) |
D869E |
possibly damaging |
Het |
Nup93 |
A |
G |
8: 95,013,231 (GRCm39) |
T36A |
probably benign |
Het |
Olfml2b |
C |
A |
1: 170,489,947 (GRCm39) |
T189N |
probably damaging |
Het |
Or4c12b |
A |
G |
2: 89,647,312 (GRCm39) |
N208S |
possibly damaging |
Het |
Or8b9 |
T |
C |
9: 37,766,608 (GRCm39) |
F165L |
probably benign |
Het |
P4htm |
A |
C |
9: 108,456,427 (GRCm39) |
W458G |
probably damaging |
Het |
Pdzrn4 |
G |
T |
15: 92,668,638 (GRCm39) |
R930L |
probably damaging |
Het |
Pgam5 |
G |
A |
5: 110,408,301 (GRCm39) |
A240V |
probably damaging |
Het |
Ptpru |
T |
G |
4: 131,515,693 (GRCm39) |
E897A |
probably damaging |
Het |
Rapgef2 |
A |
T |
3: 78,981,670 (GRCm39) |
N1256K |
probably benign |
Het |
Rhbdl3 |
A |
G |
11: 80,210,439 (GRCm39) |
E64G |
probably benign |
Het |
Sel1l3 |
A |
T |
5: 53,289,184 (GRCm39) |
L879Q |
probably damaging |
Het |
Siah1a |
G |
T |
8: 87,451,703 (GRCm39) |
D260E |
probably benign |
Het |
Skint6 |
T |
C |
4: 112,924,667 (GRCm39) |
I522V |
probably benign |
Het |
Slco4c1 |
G |
A |
1: 96,768,953 (GRCm39) |
P303L |
probably damaging |
Het |
Smok3c |
T |
C |
5: 138,062,813 (GRCm39) |
I100T |
probably damaging |
Het |
Snx24 |
C |
A |
18: 53,518,295 (GRCm39) |
Y141* |
probably null |
Het |
Tigit |
A |
G |
16: 43,469,594 (GRCm39) |
S166P |
probably damaging |
Het |
Tmem183a |
C |
T |
1: 134,275,904 (GRCm39) |
R324Q |
probably benign |
Het |
Tmie |
T |
C |
9: 110,696,001 (GRCm39) |
D130G |
possibly damaging |
Het |
Uggt1 |
G |
A |
1: 36,241,936 (GRCm39) |
R333* |
probably null |
Het |
Vmn2r111 |
T |
C |
17: 22,767,637 (GRCm39) |
N620S |
possibly damaging |
Het |
Vmn2r12 |
T |
A |
5: 109,240,852 (GRCm39) |
N87I |
probably damaging |
Het |
Vmn2r92 |
A |
G |
17: 18,404,605 (GRCm39) |
D583G |
probably benign |
Het |
Zdhhc17 |
T |
C |
10: 110,821,819 (GRCm39) |
D60G |
possibly damaging |
Het |
|
Other mutations in Prex2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00497:Prex2
|
APN |
1 |
11,256,876 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL00948:Prex2
|
APN |
1 |
11,240,838 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01087:Prex2
|
APN |
1 |
11,138,328 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01490:Prex2
|
APN |
1 |
11,254,769 (GRCm39) |
splice site |
probably null |
|
IGL01533:Prex2
|
APN |
1 |
11,256,965 (GRCm39) |
nonsense |
probably null |
|
IGL01661:Prex2
|
APN |
1 |
11,278,838 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01668:Prex2
|
APN |
1 |
11,223,869 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01674:Prex2
|
APN |
1 |
11,240,965 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01716:Prex2
|
APN |
1 |
11,336,278 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01867:Prex2
|
APN |
1 |
11,168,727 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01954:Prex2
|
APN |
1 |
11,210,235 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL01990:Prex2
|
APN |
1 |
11,193,457 (GRCm39) |
splice site |
probably benign |
|
IGL02022:Prex2
|
APN |
1 |
11,367,963 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02130:Prex2
|
APN |
1 |
11,230,386 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02130:Prex2
|
APN |
1 |
11,183,023 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02221:Prex2
|
APN |
1 |
11,131,569 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02369:Prex2
|
APN |
1 |
11,171,393 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02440:Prex2
|
APN |
1 |
11,223,881 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02477:Prex2
|
APN |
1 |
11,274,378 (GRCm39) |
missense |
probably benign |
|
IGL02492:Prex2
|
APN |
1 |
11,194,069 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03051:Prex2
|
APN |
1 |
11,212,889 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03154:Prex2
|
APN |
1 |
11,223,857 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL03158:Prex2
|
APN |
1 |
11,336,291 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03308:Prex2
|
APN |
1 |
11,255,399 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03338:Prex2
|
APN |
1 |
11,210,489 (GRCm39) |
missense |
probably benign |
0.01 |
R0042:Prex2
|
UTSW |
1 |
11,150,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R0052:Prex2
|
UTSW |
1 |
11,230,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R0052:Prex2
|
UTSW |
1 |
11,230,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R0138:Prex2
|
UTSW |
1 |
11,355,267 (GRCm39) |
splice site |
probably benign |
|
R0206:Prex2
|
UTSW |
1 |
11,355,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R0206:Prex2
|
UTSW |
1 |
11,355,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R0208:Prex2
|
UTSW |
1 |
11,355,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R0325:Prex2
|
UTSW |
1 |
11,270,281 (GRCm39) |
splice site |
probably null |
|
R0326:Prex2
|
UTSW |
1 |
11,355,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R0390:Prex2
|
UTSW |
1 |
11,159,930 (GRCm39) |
splice site |
probably null |
|
R0492:Prex2
|
UTSW |
1 |
11,256,857 (GRCm39) |
splice site |
probably benign |
|
R0512:Prex2
|
UTSW |
1 |
11,270,157 (GRCm39) |
missense |
probably benign |
|
R0515:Prex2
|
UTSW |
1 |
11,270,098 (GRCm39) |
missense |
probably damaging |
0.99 |
R0894:Prex2
|
UTSW |
1 |
11,252,122 (GRCm39) |
missense |
probably benign |
|
R1259:Prex2
|
UTSW |
1 |
11,359,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R1332:Prex2
|
UTSW |
1 |
11,274,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R1356:Prex2
|
UTSW |
1 |
11,150,316 (GRCm39) |
nonsense |
probably null |
|
R1451:Prex2
|
UTSW |
1 |
11,226,483 (GRCm39) |
missense |
probably benign |
0.01 |
R1488:Prex2
|
UTSW |
1 |
11,263,752 (GRCm39) |
missense |
probably benign |
0.05 |
R1512:Prex2
|
UTSW |
1 |
11,131,554 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1641:Prex2
|
UTSW |
1 |
11,301,996 (GRCm39) |
missense |
probably damaging |
0.99 |
R1667:Prex2
|
UTSW |
1 |
11,256,981 (GRCm39) |
missense |
probably benign |
|
R1678:Prex2
|
UTSW |
1 |
11,355,313 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1736:Prex2
|
UTSW |
1 |
11,160,108 (GRCm39) |
splice site |
probably benign |
|
R1781:Prex2
|
UTSW |
1 |
11,270,179 (GRCm39) |
missense |
probably benign |
0.17 |
R1804:Prex2
|
UTSW |
1 |
11,202,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R1836:Prex2
|
UTSW |
1 |
11,207,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R1899:Prex2
|
UTSW |
1 |
11,232,590 (GRCm39) |
nonsense |
probably null |
|
R1900:Prex2
|
UTSW |
1 |
11,232,590 (GRCm39) |
nonsense |
probably null |
|
R2020:Prex2
|
UTSW |
1 |
11,232,536 (GRCm39) |
missense |
probably damaging |
0.98 |
R2114:Prex2
|
UTSW |
1 |
11,256,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R2117:Prex2
|
UTSW |
1 |
11,256,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R2436:Prex2
|
UTSW |
1 |
11,336,376 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2902:Prex2
|
UTSW |
1 |
11,278,838 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2915:Prex2
|
UTSW |
1 |
11,240,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R2924:Prex2
|
UTSW |
1 |
11,168,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R2981:Prex2
|
UTSW |
1 |
11,252,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R3430:Prex2
|
UTSW |
1 |
11,220,078 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3832:Prex2
|
UTSW |
1 |
11,226,588 (GRCm39) |
splice site |
probably benign |
|
R3870:Prex2
|
UTSW |
1 |
11,230,416 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3963:Prex2
|
UTSW |
1 |
11,180,581 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4012:Prex2
|
UTSW |
1 |
11,254,740 (GRCm39) |
missense |
probably benign |
|
R4030:Prex2
|
UTSW |
1 |
11,278,792 (GRCm39) |
missense |
probably benign |
0.06 |
R4214:Prex2
|
UTSW |
1 |
11,171,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R4214:Prex2
|
UTSW |
1 |
11,355,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R4242:Prex2
|
UTSW |
1 |
11,226,528 (GRCm39) |
missense |
probably benign |
0.06 |
R4490:Prex2
|
UTSW |
1 |
11,232,487 (GRCm39) |
missense |
probably benign |
0.05 |
R4491:Prex2
|
UTSW |
1 |
11,232,487 (GRCm39) |
missense |
probably benign |
0.05 |
R4492:Prex2
|
UTSW |
1 |
11,232,487 (GRCm39) |
missense |
probably benign |
0.05 |
R4561:Prex2
|
UTSW |
1 |
11,254,769 (GRCm39) |
splice site |
probably null |
|
R4624:Prex2
|
UTSW |
1 |
11,359,489 (GRCm39) |
nonsense |
probably null |
|
R4647:Prex2
|
UTSW |
1 |
11,232,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R4657:Prex2
|
UTSW |
1 |
11,136,049 (GRCm39) |
missense |
probably benign |
0.00 |
R4706:Prex2
|
UTSW |
1 |
11,270,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R4806:Prex2
|
UTSW |
1 |
11,138,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R4922:Prex2
|
UTSW |
1 |
11,240,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R4961:Prex2
|
UTSW |
1 |
11,168,705 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5284:Prex2
|
UTSW |
1 |
11,336,314 (GRCm39) |
nonsense |
probably null |
|
R5305:Prex2
|
UTSW |
1 |
11,177,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R5307:Prex2
|
UTSW |
1 |
11,270,256 (GRCm39) |
missense |
probably damaging |
0.99 |
R5331:Prex2
|
UTSW |
1 |
11,210,235 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5385:Prex2
|
UTSW |
1 |
11,210,204 (GRCm39) |
missense |
probably damaging |
0.99 |
R5574:Prex2
|
UTSW |
1 |
11,210,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R5979:Prex2
|
UTSW |
1 |
11,202,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R6076:Prex2
|
UTSW |
1 |
11,256,174 (GRCm39) |
missense |
probably benign |
0.09 |
R6160:Prex2
|
UTSW |
1 |
11,064,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R6177:Prex2
|
UTSW |
1 |
11,207,001 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6221:Prex2
|
UTSW |
1 |
11,336,236 (GRCm39) |
missense |
probably benign |
0.01 |
R6293:Prex2
|
UTSW |
1 |
11,232,522 (GRCm39) |
missense |
probably benign |
|
R6335:Prex2
|
UTSW |
1 |
11,180,544 (GRCm39) |
missense |
probably benign |
0.13 |
R6401:Prex2
|
UTSW |
1 |
11,256,951 (GRCm39) |
missense |
probably benign |
0.00 |
R6427:Prex2
|
UTSW |
1 |
11,252,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R6467:Prex2
|
UTSW |
1 |
11,336,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R6564:Prex2
|
UTSW |
1 |
11,171,285 (GRCm39) |
splice site |
probably null |
|
R6734:Prex2
|
UTSW |
1 |
11,150,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R6753:Prex2
|
UTSW |
1 |
11,254,680 (GRCm39) |
missense |
probably damaging |
0.98 |
R6880:Prex2
|
UTSW |
1 |
11,202,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R6973:Prex2
|
UTSW |
1 |
11,182,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R6980:Prex2
|
UTSW |
1 |
11,232,487 (GRCm39) |
missense |
probably benign |
0.05 |
R6987:Prex2
|
UTSW |
1 |
11,240,976 (GRCm39) |
missense |
probably damaging |
0.99 |
R7085:Prex2
|
UTSW |
1 |
11,168,812 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7101:Prex2
|
UTSW |
1 |
11,223,833 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7106:Prex2
|
UTSW |
1 |
11,207,017 (GRCm39) |
missense |
probably benign |
0.33 |
R7319:Prex2
|
UTSW |
1 |
11,232,532 (GRCm39) |
missense |
probably benign |
0.10 |
R7342:Prex2
|
UTSW |
1 |
11,232,549 (GRCm39) |
missense |
probably benign |
0.00 |
R7469:Prex2
|
UTSW |
1 |
11,355,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R7528:Prex2
|
UTSW |
1 |
11,274,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R7592:Prex2
|
UTSW |
1 |
11,193,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R7650:Prex2
|
UTSW |
1 |
11,220,078 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7695:Prex2
|
UTSW |
1 |
11,232,497 (GRCm39) |
missense |
probably benign |
0.00 |
R7720:Prex2
|
UTSW |
1 |
11,252,161 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7733:Prex2
|
UTSW |
1 |
11,252,183 (GRCm39) |
missense |
probably benign |
0.31 |
R7859:Prex2
|
UTSW |
1 |
11,150,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R8247:Prex2
|
UTSW |
1 |
11,270,194 (GRCm39) |
missense |
probably benign |
|
R8300:Prex2
|
UTSW |
1 |
11,301,942 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8345:Prex2
|
UTSW |
1 |
11,270,118 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8352:Prex2
|
UTSW |
1 |
11,355,364 (GRCm39) |
missense |
probably benign |
|
R8352:Prex2
|
UTSW |
1 |
11,355,363 (GRCm39) |
missense |
probably benign |
|
R8410:Prex2
|
UTSW |
1 |
11,223,881 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8452:Prex2
|
UTSW |
1 |
11,355,364 (GRCm39) |
missense |
probably benign |
|
R8452:Prex2
|
UTSW |
1 |
11,355,363 (GRCm39) |
missense |
probably benign |
|
R8885:Prex2
|
UTSW |
1 |
11,240,799 (GRCm39) |
splice site |
probably benign |
|
R8926:Prex2
|
UTSW |
1 |
11,159,930 (GRCm39) |
splice site |
probably null |
|
R8968:Prex2
|
UTSW |
1 |
11,180,562 (GRCm39) |
nonsense |
probably null |
|
R9049:Prex2
|
UTSW |
1 |
11,256,130 (GRCm39) |
missense |
probably damaging |
0.98 |
R9398:Prex2
|
UTSW |
1 |
11,207,028 (GRCm39) |
missense |
probably benign |
0.00 |
R9452:Prex2
|
UTSW |
1 |
11,256,151 (GRCm39) |
missense |
probably benign |
0.01 |
R9549:Prex2
|
UTSW |
1 |
11,256,915 (GRCm39) |
missense |
probably damaging |
1.00 |
RF005:Prex2
|
UTSW |
1 |
11,255,390 (GRCm39) |
missense |
possibly damaging |
0.47 |
Z1177:Prex2
|
UTSW |
1 |
11,359,476 (GRCm39) |
critical splice acceptor site |
probably null |
|
|