Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adnp2 |
G |
T |
18: 80,174,036 (GRCm39) |
F124L |
probably benign |
Het |
Aicda |
A |
G |
6: 122,536,449 (GRCm39) |
K10E |
probably benign |
Het |
Als2 |
A |
G |
1: 59,226,575 (GRCm39) |
C910R |
probably benign |
Het |
Ankrd11 |
T |
A |
8: 123,619,156 (GRCm39) |
K1565N |
probably damaging |
Het |
Apol7b |
T |
C |
15: 77,308,909 (GRCm39) |
D63G |
probably damaging |
Het |
Arhgef4 |
T |
C |
1: 34,764,187 (GRCm39) |
C1148R |
possibly damaging |
Het |
Atg16l1 |
A |
G |
1: 87,694,629 (GRCm39) |
D102G |
probably damaging |
Het |
Babam2 |
T |
C |
5: 32,158,782 (GRCm39) |
V244A |
probably damaging |
Het |
Brd10 |
T |
G |
19: 29,720,990 (GRCm39) |
K622N |
probably damaging |
Het |
Cars1 |
G |
A |
7: 143,113,411 (GRCm39) |
A668V |
possibly damaging |
Het |
Ccdc168 |
T |
C |
1: 44,100,129 (GRCm39) |
D323G |
possibly damaging |
Het |
Ccdc185 |
T |
A |
1: 182,576,453 (GRCm39) |
S79C |
possibly damaging |
Het |
Ccdc88b |
G |
C |
19: 6,826,359 (GRCm39) |
R1119G |
probably damaging |
Het |
Cebpz |
A |
T |
17: 79,231,896 (GRCm39) |
V810E |
probably damaging |
Het |
Cep120 |
T |
C |
18: 53,871,654 (GRCm39) |
T73A |
probably damaging |
Het |
Chat |
C |
A |
14: 32,145,269 (GRCm39) |
C380F |
possibly damaging |
Het |
Cltc |
T |
C |
11: 86,648,087 (GRCm39) |
Q10R |
probably benign |
Het |
Cripto |
C |
T |
9: 110,769,781 (GRCm39) |
M169I |
probably benign |
Het |
Cst8 |
T |
C |
2: 148,646,622 (GRCm39) |
|
probably benign |
Het |
Cts3 |
C |
T |
13: 61,715,868 (GRCm39) |
|
probably null |
Het |
Cyp4a29 |
T |
A |
4: 115,105,707 (GRCm39) |
D136E |
probably benign |
Het |
Dmxl2 |
A |
C |
9: 54,286,297 (GRCm39) |
|
probably null |
Het |
Dsg4 |
T |
A |
18: 20,584,919 (GRCm39) |
V211E |
possibly damaging |
Het |
Efcab5 |
C |
T |
11: 77,008,656 (GRCm39) |
V957I |
probably damaging |
Het |
Eif4g2 |
A |
T |
7: 110,673,358 (GRCm39) |
L807Q |
possibly damaging |
Het |
Epha4 |
A |
G |
1: 77,366,731 (GRCm39) |
|
probably benign |
Het |
Epm2aip1 |
A |
T |
9: 111,101,458 (GRCm39) |
I144F |
probably benign |
Het |
Erbb4 |
C |
T |
1: 68,599,735 (GRCm39) |
R114H |
probably damaging |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Fam170a |
C |
T |
18: 50,415,038 (GRCm39) |
A228V |
probably damaging |
Het |
Foxred1 |
A |
T |
9: 35,117,571 (GRCm39) |
M254K |
possibly damaging |
Het |
Gm1527 |
T |
A |
3: 28,952,969 (GRCm39) |
C90S |
probably benign |
Het |
Gpr137b |
T |
C |
13: 13,533,947 (GRCm39) |
T370A |
probably benign |
Het |
Gtf2e2 |
A |
G |
8: 34,245,993 (GRCm39) |
|
probably benign |
Het |
Hgsnat |
A |
T |
8: 26,445,817 (GRCm39) |
L359* |
probably null |
Het |
Hhip |
A |
T |
8: 80,719,223 (GRCm39) |
C435S |
probably damaging |
Het |
Hoxa13 |
T |
C |
6: 52,236,107 (GRCm39) |
D310G |
possibly damaging |
Het |
Hspa14 |
T |
C |
2: 3,513,675 (GRCm39) |
Y18C |
probably damaging |
Het |
Ighg1 |
A |
G |
12: 113,293,270 (GRCm39) |
V140A |
probably damaging |
Het |
Ighv1-58 |
A |
T |
12: 115,275,930 (GRCm39) |
Y69* |
probably null |
Het |
Inpp5j |
A |
G |
11: 3,450,185 (GRCm39) |
F615L |
probably benign |
Het |
Kcna1 |
T |
A |
6: 126,619,873 (GRCm39) |
Y149F |
probably benign |
Het |
Kcnj6 |
A |
T |
16: 94,625,877 (GRCm39) |
|
probably null |
Het |
Krtap4-1 |
G |
T |
11: 99,518,637 (GRCm39) |
C124* |
probably null |
Het |
Lama1 |
T |
A |
17: 68,119,368 (GRCm39) |
L2615* |
probably null |
Het |
Lcp2 |
A |
T |
11: 34,018,439 (GRCm39) |
I72F |
probably damaging |
Het |
Med1 |
T |
A |
11: 98,062,532 (GRCm39) |
I189F |
possibly damaging |
Het |
Meioc |
C |
T |
11: 102,566,654 (GRCm39) |
R757C |
probably damaging |
Het |
Mtr |
T |
A |
13: 12,204,283 (GRCm39) |
H1171L |
probably damaging |
Het |
Mtr |
G |
C |
13: 12,204,284 (GRCm39) |
H1171D |
probably damaging |
Het |
Naa12 |
A |
G |
18: 80,255,339 (GRCm39) |
D211G |
probably benign |
Het |
Nlrc5 |
A |
G |
8: 95,202,620 (GRCm39) |
Y240C |
possibly damaging |
Het |
Nsun4 |
T |
A |
4: 115,908,259 (GRCm39) |
H767L |
possibly damaging |
Het |
Pcdha1 |
T |
A |
18: 37,064,189 (GRCm39) |
N284K |
probably benign |
Het |
Pcdhgb8 |
A |
C |
18: 37,896,414 (GRCm39) |
S495R |
probably benign |
Het |
Pramel1 |
T |
A |
4: 143,123,260 (GRCm39) |
I79N |
possibly damaging |
Het |
Prdm6 |
A |
T |
18: 53,673,390 (GRCm39) |
E183D |
possibly damaging |
Het |
Prkg2 |
T |
C |
5: 99,127,674 (GRCm39) |
I346V |
possibly damaging |
Het |
Ptprz1 |
A |
G |
6: 23,002,584 (GRCm39) |
D1558G |
probably damaging |
Het |
Pttg1ip2 |
A |
C |
5: 5,528,955 (GRCm39) |
L20R |
probably damaging |
Het |
Qng1 |
T |
A |
13: 58,529,800 (GRCm39) |
K271* |
probably null |
Het |
Rab11fip3 |
GCTCGTCT |
GCT |
17: 26,287,002 (GRCm39) |
|
probably null |
Het |
Rin2 |
C |
T |
2: 145,702,366 (GRCm39) |
T354I |
probably benign |
Het |
S100a6 |
A |
G |
3: 90,521,508 (GRCm39) |
D50G |
probably damaging |
Het |
Shroom3 |
T |
A |
5: 93,096,342 (GRCm39) |
|
probably benign |
Het |
Sipa1l1 |
G |
A |
12: 82,388,556 (GRCm39) |
V261M |
possibly damaging |
Het |
Slc5a4b |
T |
A |
10: 75,910,826 (GRCm39) |
I337F |
probably damaging |
Het |
Smarcc1 |
A |
G |
9: 109,961,273 (GRCm39) |
Y30C |
possibly damaging |
Het |
Swap70 |
A |
G |
7: 109,880,512 (GRCm39) |
K576E |
possibly damaging |
Het |
Syt6 |
A |
G |
3: 103,532,809 (GRCm39) |
|
probably benign |
Het |
Szt2 |
T |
C |
4: 118,241,097 (GRCm39) |
I1726V |
probably benign |
Het |
Thoc1 |
A |
G |
18: 9,987,651 (GRCm39) |
K453E |
possibly damaging |
Het |
Tmem38b |
A |
G |
4: 53,854,409 (GRCm39) |
I214V |
probably benign |
Het |
Tonsl |
A |
T |
15: 76,521,244 (GRCm39) |
I354N |
probably damaging |
Het |
Trappc9 |
T |
C |
15: 72,903,472 (GRCm39) |
I303V |
possibly damaging |
Het |
Trim66 |
A |
G |
7: 109,057,338 (GRCm39) |
S1032P |
probably damaging |
Het |
Tsc22d4 |
T |
C |
5: 137,756,590 (GRCm39) |
V6A |
probably benign |
Het |
Ubtd2 |
A |
G |
11: 32,449,260 (GRCm39) |
K36E |
probably benign |
Het |
Zkscan2 |
T |
C |
7: 123,097,883 (GRCm39) |
E171G |
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 |
R4030:Prex2
|
UTSW |
1 |
11,278,792 (GRCm39) |
missense |
probably benign |
0.06 |
R4214:Prex2
|
UTSW |
1 |
11,355,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R4214:Prex2
|
UTSW |
1 |
11,171,383 (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 |
R4900:Prex2
|
UTSW |
1 |
11,220,129 (GRCm39) |
splice site |
probably benign |
|
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 |
|
|