Other mutations in this stock |
Total: 126 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4833420G17Rik |
T |
C |
13: 119,606,496 (GRCm39) |
V246A |
probably benign |
Het |
Abcc10 |
T |
C |
17: 46,615,361 (GRCm39) |
S1343G |
possibly damaging |
Het |
Abcd3 |
C |
A |
3: 121,555,059 (GRCm39) |
|
probably null |
Het |
Actl6a |
T |
A |
3: 32,774,642 (GRCm39) |
M335K |
probably damaging |
Het |
Adamts9 |
A |
C |
6: 92,774,999 (GRCm39) |
C1090W |
probably damaging |
Het |
Ajuba |
T |
C |
14: 54,807,855 (GRCm39) |
Y459C |
probably damaging |
Het |
Aldh7a1 |
T |
A |
18: 56,667,325 (GRCm39) |
N316Y |
possibly damaging |
Het |
Ankhd1 |
A |
G |
18: 36,724,548 (GRCm39) |
E402G |
probably damaging |
Het |
Ankrd36 |
A |
G |
11: 5,639,340 (GRCm39) |
|
probably benign |
Het |
Apeh |
A |
T |
9: 107,963,662 (GRCm39) |
L551H |
probably damaging |
Het |
Avpr1a |
T |
A |
10: 122,285,274 (GRCm39) |
F189I |
probably damaging |
Het |
BC034090 |
T |
A |
1: 155,117,773 (GRCm39) |
H115L |
possibly damaging |
Het |
C4b |
A |
T |
17: 34,956,635 (GRCm39) |
D654E |
possibly damaging |
Het |
Carns1 |
T |
A |
19: 4,221,900 (GRCm39) |
|
probably null |
Het |
Ccdc146 |
T |
A |
5: 21,513,711 (GRCm39) |
E469V |
probably benign |
Het |
Cdc27 |
A |
G |
11: 104,397,966 (GRCm39) |
I804T |
probably benign |
Het |
Cdh23 |
G |
A |
10: 60,173,541 (GRCm39) |
T1651I |
probably damaging |
Het |
Cenpo |
G |
A |
12: 4,266,646 (GRCm39) |
P154L |
probably damaging |
Het |
Cenpu |
G |
A |
8: 47,015,534 (GRCm39) |
G150R |
probably benign |
Het |
Chrna10 |
C |
A |
7: 101,763,560 (GRCm39) |
L78F |
probably damaging |
Het |
Chrne |
A |
T |
11: 70,505,913 (GRCm39) |
N457K |
possibly damaging |
Het |
Cidea |
A |
T |
18: 67,493,236 (GRCm39) |
D85V |
probably damaging |
Het |
Cldn18 |
T |
C |
9: 99,591,911 (GRCm39) |
S31G |
possibly damaging |
Het |
Clpb |
T |
A |
7: 101,428,548 (GRCm39) |
I436N |
probably damaging |
Het |
Col11a2 |
T |
C |
17: 34,278,148 (GRCm39) |
|
probably null |
Het |
Cul7 |
T |
C |
17: 46,965,403 (GRCm39) |
V527A |
probably benign |
Het |
Dchs1 |
A |
C |
7: 105,407,236 (GRCm39) |
V2119G |
probably damaging |
Het |
Dchs1 |
T |
A |
7: 105,421,262 (GRCm39) |
D386V |
probably damaging |
Het |
Dcstamp |
A |
C |
15: 39,622,715 (GRCm39) |
Q345H |
probably damaging |
Het |
Dlgap3 |
A |
G |
4: 127,130,123 (GRCm39) |
I955V |
probably damaging |
Het |
Dvl1 |
A |
G |
4: 155,938,143 (GRCm39) |
D97G |
probably damaging |
Het |
Dync2h1 |
T |
C |
9: 7,016,791 (GRCm39) |
D3573G |
probably damaging |
Het |
Efr3b |
G |
T |
12: 4,033,419 (GRCm39) |
F129L |
probably benign |
Het |
Etaa1 |
G |
A |
11: 17,897,539 (GRCm39) |
L193F |
probably damaging |
Het |
Fam13c |
G |
A |
10: 70,388,899 (GRCm39) |
S474N |
probably benign |
Het |
Fam171a2 |
C |
A |
11: 102,328,693 (GRCm39) |
V689L |
possibly damaging |
Het |
Fastkd3 |
T |
C |
13: 68,732,704 (GRCm39) |
F342L |
probably benign |
Het |
Fat4 |
T |
C |
3: 39,050,095 (GRCm39) |
S3986P |
possibly damaging |
Het |
Fbxo38 |
A |
G |
18: 62,674,042 (GRCm39) |
M13T |
probably benign |
Het |
Fbxo48 |
G |
T |
11: 16,904,329 (GRCm39) |
L160F |
possibly damaging |
Het |
Fgr |
G |
A |
4: 132,713,664 (GRCm39) |
|
probably null |
Het |
Gbx2 |
T |
C |
1: 89,856,635 (GRCm39) |
T252A |
probably damaging |
Het |
Gm20671 |
A |
G |
5: 32,977,286 (GRCm39) |
S1823P |
probably damaging |
Het |
Gpatch8 |
A |
T |
11: 102,399,053 (GRCm39) |
|
probably null |
Het |
Gsdma |
A |
T |
11: 98,557,275 (GRCm39) |
|
probably null |
Het |
Gucy2g |
G |
A |
19: 55,203,548 (GRCm39) |
A750V |
probably damaging |
Het |
Hdac9 |
A |
G |
12: 34,479,557 (GRCm39) |
Y223H |
probably damaging |
Het |
Igsf5 |
C |
A |
16: 96,192,226 (GRCm39) |
T275N |
probably benign |
Het |
Il23r |
G |
A |
6: 67,463,275 (GRCm39) |
H73Y |
probably benign |
Het |
Ipo4 |
G |
T |
14: 55,863,653 (GRCm39) |
R1026S |
probably benign |
Het |
Jade1 |
T |
A |
3: 41,546,137 (GRCm39) |
I54N |
probably damaging |
Het |
Khdrbs1 |
G |
T |
4: 129,635,729 (GRCm39) |
D75E |
possibly damaging |
Het |
Lrwd1 |
A |
T |
5: 136,152,728 (GRCm39) |
D511E |
possibly damaging |
Het |
Ly75 |
A |
T |
2: 60,164,831 (GRCm39) |
C782* |
probably null |
Het |
Mmp3 |
C |
T |
9: 7,451,759 (GRCm39) |
R366* |
probably null |
Het |
Mrgpra6 |
A |
G |
7: 46,838,629 (GRCm39) |
C190R |
probably damaging |
Het |
Mtcl3 |
A |
G |
10: 29,072,766 (GRCm39) |
D686G |
probably benign |
Het |
Myh10 |
T |
A |
11: 68,692,434 (GRCm39) |
L1369Q |
probably damaging |
Het |
Myof |
C |
T |
19: 37,941,435 (GRCm39) |
A792T |
probably damaging |
Het |
Ncf1 |
A |
G |
5: 134,250,659 (GRCm39) |
L373P |
probably damaging |
Het |
Ncoa7 |
C |
A |
10: 30,598,813 (GRCm39) |
A37S |
probably benign |
Het |
Nfkb1 |
A |
G |
3: 135,318,303 (GRCm39) |
V310A |
possibly damaging |
Het |
Nmur2 |
T |
A |
11: 55,931,040 (GRCm39) |
I224F |
probably damaging |
Het |
Nr1d2 |
A |
T |
14: 18,211,922 (GRCm38) |
S394T |
probably benign |
Het |
Nudt12 |
A |
G |
17: 59,310,434 (GRCm39) |
W390R |
probably damaging |
Het |
Or11g24 |
T |
A |
14: 50,662,846 (GRCm39) |
V290E |
possibly damaging |
Het |
Or2m13 |
A |
G |
16: 19,226,547 (GRCm39) |
L73P |
probably damaging |
Het |
Or4a79 |
T |
A |
2: 89,551,649 (GRCm39) |
I269F |
possibly damaging |
Het |
Or4e1 |
T |
A |
14: 52,700,714 (GRCm39) |
T251S |
probably benign |
Het |
Or52a20 |
T |
C |
7: 103,366,562 (GRCm39) |
F254L |
probably benign |
Het |
Pate2 |
A |
G |
9: 35,581,837 (GRCm39) |
M44V |
probably damaging |
Het |
Pikfyve |
T |
C |
1: 65,283,568 (GRCm39) |
L735S |
probably damaging |
Het |
Plce1 |
C |
A |
19: 38,748,535 (GRCm39) |
N1755K |
probably damaging |
Het |
Pld1 |
C |
A |
3: 28,079,469 (GRCm39) |
R90S |
probably damaging |
Het |
Pnpla7 |
C |
A |
2: 24,931,031 (GRCm39) |
P882Q |
probably damaging |
Het |
Pold2 |
A |
G |
11: 5,826,760 (GRCm39) |
L58P |
probably damaging |
Het |
Ppm1d |
A |
G |
11: 85,202,609 (GRCm39) |
E104G |
probably damaging |
Het |
Ppm1e |
A |
T |
11: 87,249,377 (GRCm39) |
L118Q |
possibly damaging |
Het |
Ppp1r42 |
A |
G |
1: 10,069,660 (GRCm39) |
L134P |
probably damaging |
Het |
Prss36 |
C |
A |
7: 127,535,871 (GRCm39) |
R288L |
probably damaging |
Het |
Prss51 |
T |
A |
14: 64,334,543 (GRCm39) |
V108E |
probably damaging |
Het |
Psma3 |
G |
T |
12: 71,021,539 (GRCm39) |
G7W |
probably damaging |
Het |
Psmc3ip |
A |
T |
11: 100,983,430 (GRCm39) |
|
probably null |
Het |
Qser1 |
T |
C |
2: 104,616,987 (GRCm39) |
E1275G |
probably damaging |
Het |
Rai2 |
A |
G |
X: 160,561,636 (GRCm39) |
N363S |
probably benign |
Het |
Ranbp17 |
A |
T |
11: 33,169,241 (GRCm39) |
V991D |
possibly damaging |
Het |
Rcc2 |
A |
T |
4: 140,447,877 (GRCm39) |
K468* |
probably null |
Het |
S1pr2 |
T |
C |
9: 20,878,890 (GRCm39) |
T313A |
probably benign |
Het |
Sec1 |
C |
A |
7: 45,328,264 (GRCm39) |
R261L |
probably benign |
Het |
Sfi1 |
ACA |
ACATCTTCCCAAAGCCAGTCA |
11: 3,103,382 (GRCm39) |
|
probably benign |
Homo |
Sgip1 |
G |
A |
4: 102,791,763 (GRCm39) |
V362I |
possibly damaging |
Het |
Shroom4 |
T |
A |
X: 6,497,523 (GRCm39) |
C894* |
probably null |
Het |
Slc12a9 |
A |
T |
5: 137,329,276 (GRCm39) |
L126Q |
probably damaging |
Het |
Slx4 |
A |
G |
16: 3,808,669 (GRCm39) |
S424P |
probably damaging |
Het |
Smg5 |
T |
C |
3: 88,258,600 (GRCm39) |
S524P |
probably damaging |
Het |
Sncaip |
A |
G |
18: 53,018,113 (GRCm39) |
D418G |
probably damaging |
Het |
Spata31d1b |
C |
A |
13: 59,866,032 (GRCm39) |
T1060K |
possibly damaging |
Het |
Spink6 |
A |
G |
18: 44,215,347 (GRCm39) |
T66A |
probably damaging |
Het |
Sppl2c |
T |
A |
11: 104,078,127 (GRCm39) |
I309K |
possibly damaging |
Het |
Stk39 |
T |
A |
2: 68,240,383 (GRCm39) |
D116V |
probably damaging |
Het |
Supv3l1 |
A |
T |
10: 62,266,375 (GRCm39) |
N600K |
possibly damaging |
Het |
Svep1 |
T |
C |
4: 58,104,545 (GRCm39) |
K1226R |
possibly damaging |
Het |
Syne1 |
C |
T |
10: 4,991,494 (GRCm39) |
V557I |
probably benign |
Het |
Tas2r117 |
G |
T |
6: 132,780,117 (GRCm39) |
S85I |
probably benign |
Het |
Tcf20 |
T |
A |
15: 82,740,400 (GRCm39) |
Q350H |
probably damaging |
Het |
Tep1 |
A |
T |
14: 51,105,774 (GRCm39) |
L82Q |
probably damaging |
Het |
Tfb2m |
A |
C |
1: 179,373,437 (GRCm39) |
|
probably null |
Het |
Tm9sf1 |
C |
T |
14: 55,880,301 (GRCm39) |
G32D |
possibly damaging |
Het |
Tpd52 |
A |
T |
3: 8,996,255 (GRCm39) |
|
probably null |
Het |
Trappc8 |
A |
T |
18: 20,966,119 (GRCm39) |
|
probably null |
Het |
Trbv30 |
A |
G |
6: 41,258,854 (GRCm39) |
T88A |
probably benign |
Het |
Trim40 |
T |
A |
17: 37,199,757 (GRCm39) |
N107I |
probably damaging |
Het |
Trim80 |
A |
T |
11: 115,338,843 (GRCm39) |
T558S |
probably benign |
Het |
Ttn |
A |
G |
2: 76,708,692 (GRCm39) |
|
probably benign |
Het |
Vav3 |
A |
G |
3: 109,434,791 (GRCm39) |
M441V |
possibly damaging |
Het |
Vmn1r42 |
T |
A |
6: 89,822,366 (GRCm39) |
I68F |
probably damaging |
Het |
Vmn2r118 |
C |
T |
17: 55,918,565 (GRCm39) |
G109D |
probably benign |
Het |
Vmn2r5 |
T |
A |
3: 64,416,931 (GRCm39) |
M76L |
probably benign |
Het |
Vwa7 |
G |
T |
17: 35,243,902 (GRCm39) |
|
probably null |
Het |
Xndc1 |
T |
C |
7: 101,731,395 (GRCm39) |
V378A |
probably benign |
Het |
Zc3h12d |
A |
T |
10: 7,729,014 (GRCm39) |
D126V |
probably damaging |
Het |
Zc3h13 |
A |
G |
14: 75,581,059 (GRCm39) |
N1682S |
probably benign |
Het |
Zc3h15 |
T |
C |
2: 83,490,574 (GRCm39) |
I236T |
possibly damaging |
Het |
Zfp13 |
A |
T |
17: 23,800,156 (GRCm39) |
I34N |
probably damaging |
Het |
Zfp169 |
A |
T |
13: 48,643,751 (GRCm39) |
C459S |
possibly damaging |
Het |
Zfyve28 |
A |
G |
5: 34,374,311 (GRCm39) |
C568R |
probably damaging |
Het |
|
Other mutations in Prpf8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01375:Prpf8
|
APN |
11 |
75,385,121 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01376:Prpf8
|
APN |
11 |
75,385,121 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01393:Prpf8
|
APN |
11 |
75,385,121 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01395:Prpf8
|
APN |
11 |
75,385,121 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01554:Prpf8
|
APN |
11 |
75,386,472 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01560:Prpf8
|
APN |
11 |
75,381,232 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL01886:Prpf8
|
APN |
11 |
75,386,570 (GRCm39) |
missense |
probably benign |
0.32 |
IGL01946:Prpf8
|
APN |
11 |
75,390,818 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02022:Prpf8
|
APN |
11 |
75,392,660 (GRCm39) |
nonsense |
probably null |
|
IGL02077:Prpf8
|
APN |
11 |
75,386,635 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02141:Prpf8
|
APN |
11 |
75,381,498 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02455:Prpf8
|
APN |
11 |
75,400,084 (GRCm39) |
missense |
probably benign |
0.32 |
cutter
|
UTSW |
11 |
75,386,252 (GRCm39) |
splice site |
probably null |
|
BB009:Prpf8
|
UTSW |
11 |
75,383,423 (GRCm39) |
missense |
possibly damaging |
0.92 |
BB019:Prpf8
|
UTSW |
11 |
75,383,423 (GRCm39) |
missense |
possibly damaging |
0.92 |
PIT4514001:Prpf8
|
UTSW |
11 |
75,387,181 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0254:Prpf8
|
UTSW |
11 |
75,397,188 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0270:Prpf8
|
UTSW |
11 |
75,396,075 (GRCm39) |
missense |
probably damaging |
0.99 |
R0504:Prpf8
|
UTSW |
11 |
75,392,768 (GRCm39) |
splice site |
probably benign |
|
R0573:Prpf8
|
UTSW |
11 |
75,381,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R0613:Prpf8
|
UTSW |
11 |
75,394,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R0893:Prpf8
|
UTSW |
11 |
75,384,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R0967:Prpf8
|
UTSW |
11 |
75,385,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R0975:Prpf8
|
UTSW |
11 |
75,399,500 (GRCm39) |
unclassified |
probably benign |
|
R1123:Prpf8
|
UTSW |
11 |
75,386,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R1183:Prpf8
|
UTSW |
11 |
75,381,156 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1857:Prpf8
|
UTSW |
11 |
75,386,249 (GRCm39) |
critical splice donor site |
probably null |
|
R1901:Prpf8
|
UTSW |
11 |
75,395,570 (GRCm39) |
missense |
probably damaging |
0.99 |
R1950:Prpf8
|
UTSW |
11 |
75,387,337 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2116:Prpf8
|
UTSW |
11 |
75,378,547 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2147:Prpf8
|
UTSW |
11 |
75,381,357 (GRCm39) |
missense |
probably benign |
|
R2185:Prpf8
|
UTSW |
11 |
75,377,939 (GRCm39) |
nonsense |
probably null |
|
R2271:Prpf8
|
UTSW |
11 |
75,386,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R2272:Prpf8
|
UTSW |
11 |
75,386,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R2898:Prpf8
|
UTSW |
11 |
75,386,860 (GRCm39) |
missense |
probably benign |
0.00 |
R3744:Prpf8
|
UTSW |
11 |
75,397,547 (GRCm39) |
splice site |
probably null |
|
R3893:Prpf8
|
UTSW |
11 |
75,391,083 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4400:Prpf8
|
UTSW |
11 |
75,381,528 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4510:Prpf8
|
UTSW |
11 |
75,382,652 (GRCm39) |
missense |
probably damaging |
0.96 |
R4511:Prpf8
|
UTSW |
11 |
75,382,652 (GRCm39) |
missense |
probably damaging |
0.96 |
R4784:Prpf8
|
UTSW |
11 |
75,383,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R5089:Prpf8
|
UTSW |
11 |
75,400,054 (GRCm39) |
splice site |
probably null |
|
R5186:Prpf8
|
UTSW |
11 |
75,380,609 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5215:Prpf8
|
UTSW |
11 |
75,391,030 (GRCm39) |
missense |
probably benign |
0.02 |
R5288:Prpf8
|
UTSW |
11 |
75,386,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R5362:Prpf8
|
UTSW |
11 |
75,397,236 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5386:Prpf8
|
UTSW |
11 |
75,386,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R5423:Prpf8
|
UTSW |
11 |
75,399,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R5472:Prpf8
|
UTSW |
11 |
75,394,469 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5539:Prpf8
|
UTSW |
11 |
75,394,464 (GRCm39) |
missense |
probably benign |
0.20 |
R5620:Prpf8
|
UTSW |
11 |
75,395,927 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5669:Prpf8
|
UTSW |
11 |
75,395,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R5887:Prpf8
|
UTSW |
11 |
75,391,734 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5948:Prpf8
|
UTSW |
11 |
75,400,015 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6073:Prpf8
|
UTSW |
11 |
75,384,848 (GRCm39) |
critical splice donor site |
probably null |
|
R6250:Prpf8
|
UTSW |
11 |
75,384,334 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6358:Prpf8
|
UTSW |
11 |
75,382,321 (GRCm39) |
missense |
probably benign |
0.33 |
R6629:Prpf8
|
UTSW |
11 |
75,386,252 (GRCm39) |
splice site |
probably null |
|
R6804:Prpf8
|
UTSW |
11 |
75,390,635 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6922:Prpf8
|
UTSW |
11 |
75,381,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R7035:Prpf8
|
UTSW |
11 |
75,395,654 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7038:Prpf8
|
UTSW |
11 |
75,386,984 (GRCm39) |
missense |
probably benign |
0.02 |
R7089:Prpf8
|
UTSW |
11 |
75,399,374 (GRCm39) |
missense |
probably damaging |
0.99 |
R7101:Prpf8
|
UTSW |
11 |
75,381,226 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7114:Prpf8
|
UTSW |
11 |
75,394,181 (GRCm39) |
nonsense |
probably null |
|
R7182:Prpf8
|
UTSW |
11 |
75,381,553 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7290:Prpf8
|
UTSW |
11 |
75,384,783 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7323:Prpf8
|
UTSW |
11 |
75,382,610 (GRCm39) |
missense |
probably benign |
0.32 |
R7485:Prpf8
|
UTSW |
11 |
75,399,738 (GRCm39) |
nonsense |
probably null |
|
R7522:Prpf8
|
UTSW |
11 |
75,400,102 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7546:Prpf8
|
UTSW |
11 |
75,399,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R7596:Prpf8
|
UTSW |
11 |
75,382,330 (GRCm39) |
missense |
probably benign |
0.03 |
R7699:Prpf8
|
UTSW |
11 |
75,391,022 (GRCm39) |
missense |
probably benign |
0.02 |
R7731:Prpf8
|
UTSW |
11 |
75,399,732 (GRCm39) |
missense |
probably damaging |
0.97 |
R7821:Prpf8
|
UTSW |
11 |
75,385,300 (GRCm39) |
missense |
probably benign |
0.01 |
R7932:Prpf8
|
UTSW |
11 |
75,383,423 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8039:Prpf8
|
UTSW |
11 |
75,393,368 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8067:Prpf8
|
UTSW |
11 |
75,390,976 (GRCm39) |
missense |
probably damaging |
0.98 |
R8316:Prpf8
|
UTSW |
11 |
75,390,641 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8560:Prpf8
|
UTSW |
11 |
75,382,600 (GRCm39) |
nonsense |
probably null |
|
R8823:Prpf8
|
UTSW |
11 |
75,384,282 (GRCm39) |
missense |
probably benign |
0.05 |
R8977:Prpf8
|
UTSW |
11 |
75,386,870 (GRCm39) |
missense |
probably benign |
0.12 |
R9116:Prpf8
|
UTSW |
11 |
75,380,589 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9166:Prpf8
|
UTSW |
11 |
75,387,340 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9360:Prpf8
|
UTSW |
11 |
75,381,156 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9453:Prpf8
|
UTSW |
11 |
75,397,212 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9518:Prpf8
|
UTSW |
11 |
75,394,486 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9532:Prpf8
|
UTSW |
11 |
75,385,608 (GRCm39) |
missense |
probably benign |
0.01 |
R9626:Prpf8
|
UTSW |
11 |
75,385,681 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9760:Prpf8
|
UTSW |
11 |
75,394,257 (GRCm39) |
missense |
probably benign |
0.20 |
X0028:Prpf8
|
UTSW |
11 |
75,397,590 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Prpf8
|
UTSW |
11 |
75,394,160 (GRCm39) |
missense |
probably benign |
0.35 |
|