Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot11 |
A |
G |
4: 106,617,329 (GRCm39) |
F259S |
probably damaging |
Het |
Aldh16a1 |
T |
A |
7: 44,793,931 (GRCm39) |
|
probably benign |
Het |
Ankrd24 |
A |
T |
10: 81,478,547 (GRCm39) |
|
probably benign |
Het |
Arhgap5 |
T |
C |
12: 52,564,951 (GRCm39) |
S641P |
probably damaging |
Het |
Arpp21 |
A |
C |
9: 111,986,824 (GRCm39) |
S242R |
probably benign |
Het |
Bpifb5 |
A |
G |
2: 154,070,820 (GRCm39) |
T204A |
probably benign |
Het |
Bud31 |
A |
G |
5: 145,083,265 (GRCm39) |
Y77C |
probably damaging |
Het |
Ccdc65 |
G |
A |
15: 98,607,095 (GRCm39) |
V101I |
possibly damaging |
Het |
Ccr7 |
T |
A |
11: 99,036,809 (GRCm39) |
T38S |
probably damaging |
Het |
Cdc14a |
T |
C |
3: 116,087,362 (GRCm39) |
|
probably benign |
Het |
Ces2f |
C |
T |
8: 105,677,618 (GRCm39) |
H208Y |
possibly damaging |
Het |
Chst1 |
C |
A |
2: 92,443,964 (GRCm39) |
N145K |
possibly damaging |
Het |
Clock |
A |
G |
5: 76,374,976 (GRCm39) |
V731A |
possibly damaging |
Het |
Cog6 |
C |
T |
3: 52,921,283 (GRCm39) |
V108I |
possibly damaging |
Het |
Cplane1 |
T |
A |
15: 8,287,805 (GRCm39) |
N2881K |
unknown |
Het |
Crtc2 |
T |
A |
3: 90,170,804 (GRCm39) |
F626I |
probably damaging |
Het |
Dicer1 |
A |
T |
12: 104,673,144 (GRCm39) |
F792I |
probably damaging |
Het |
Dnajc13 |
T |
C |
9: 104,049,781 (GRCm39) |
K1780R |
probably benign |
Het |
Dph5 |
A |
C |
3: 115,708,782 (GRCm39) |
N155H |
probably benign |
Het |
Dscam |
T |
C |
16: 96,626,982 (GRCm39) |
|
probably null |
Het |
Etl4 |
C |
A |
2: 20,810,382 (GRCm39) |
|
probably benign |
Het |
Flt3l |
T |
C |
7: 44,785,450 (GRCm39) |
S9G |
probably benign |
Het |
Fmnl2 |
A |
G |
2: 52,944,498 (GRCm39) |
E159G |
possibly damaging |
Het |
Fryl |
A |
G |
5: 73,240,715 (GRCm39) |
I1295T |
probably benign |
Het |
G530012D18Rik |
CAGAGAGA |
CAGAGAGAGA |
1: 85,504,945 (GRCm39) |
|
probably null |
Het |
Gatad2b |
T |
A |
3: 90,263,489 (GRCm39) |
S529T |
probably benign |
Het |
Herc6 |
G |
A |
6: 57,639,347 (GRCm39) |
G905E |
possibly damaging |
Het |
Hhip |
T |
A |
8: 80,724,884 (GRCm39) |
N296I |
probably damaging |
Het |
Hmgcr |
A |
T |
13: 96,787,151 (GRCm39) |
|
probably benign |
Het |
Kalrn |
T |
G |
16: 33,830,951 (GRCm39) |
N723H |
possibly damaging |
Het |
Mroh5 |
T |
A |
15: 73,662,588 (GRCm39) |
Y242F |
possibly damaging |
Het |
Msh3 |
T |
A |
13: 92,483,848 (GRCm39) |
K258* |
probably null |
Het |
Myo1a |
T |
C |
10: 127,555,732 (GRCm39) |
|
probably benign |
Het |
Nlrp4f |
C |
T |
13: 65,342,317 (GRCm39) |
E443K |
probably benign |
Het |
Nupr2 |
A |
G |
5: 129,937,533 (GRCm39) |
Y34C |
probably damaging |
Het |
Ociad1 |
T |
C |
5: 73,452,255 (GRCm39) |
|
probably benign |
Het |
Or1af1 |
A |
T |
2: 37,110,208 (GRCm39) |
K236* |
probably null |
Het |
Or5af2 |
T |
A |
11: 58,708,577 (GRCm39) |
L248M |
probably damaging |
Het |
Or5b3 |
A |
T |
19: 13,388,784 (GRCm39) |
M284L |
probably benign |
Het |
Or5p5 |
A |
G |
7: 107,414,331 (GRCm39) |
D182G |
probably damaging |
Het |
Or6ae1 |
T |
C |
7: 139,742,002 (GRCm39) |
N287S |
probably damaging |
Het |
P2ry12 |
C |
A |
3: 59,124,908 (GRCm39) |
V256F |
probably damaging |
Het |
Pcdhb22 |
T |
A |
18: 37,651,904 (GRCm39) |
I124N |
probably damaging |
Het |
Pfas |
A |
T |
11: 68,888,863 (GRCm39) |
N361K |
probably benign |
Het |
Plod2 |
T |
G |
9: 92,487,480 (GRCm39) |
L600V |
possibly damaging |
Het |
Pole |
T |
C |
5: 110,446,854 (GRCm39) |
Y631H |
probably damaging |
Het |
Proser1 |
T |
C |
3: 53,386,197 (GRCm39) |
L693P |
probably damaging |
Het |
Ptprd |
A |
G |
4: 75,875,476 (GRCm39) |
Y1195H |
probably damaging |
Het |
Rbm27 |
T |
A |
18: 42,459,091 (GRCm39) |
|
probably null |
Het |
Ric8a |
A |
G |
7: 140,437,886 (GRCm39) |
|
probably benign |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Rimkla |
C |
T |
4: 119,335,177 (GRCm39) |
V69M |
probably damaging |
Het |
Scfd1 |
A |
T |
12: 51,459,360 (GRCm39) |
K307M |
probably damaging |
Het |
Sh2b2 |
A |
G |
5: 136,261,117 (GRCm39) |
F33S |
probably damaging |
Het |
Smg7 |
T |
G |
1: 152,746,508 (GRCm39) |
|
probably null |
Het |
Srebf1 |
T |
C |
11: 60,094,942 (GRCm39) |
T486A |
probably benign |
Het |
Strn3 |
G |
A |
12: 51,657,187 (GRCm39) |
T642I |
probably damaging |
Het |
Syne2 |
T |
C |
12: 76,028,837 (GRCm39) |
|
probably null |
Het |
Syne3 |
A |
G |
12: 104,935,619 (GRCm39) |
L53P |
probably damaging |
Het |
Tcea1 |
T |
A |
1: 4,950,569 (GRCm39) |
|
probably benign |
Het |
Tmem30b |
T |
C |
12: 73,592,942 (GRCm39) |
N58D |
probably benign |
Het |
Tnpo1 |
A |
G |
13: 98,991,954 (GRCm39) |
Y641H |
probably damaging |
Het |
Trim25 |
A |
T |
11: 88,890,564 (GRCm39) |
T84S |
probably benign |
Het |
Trip4 |
A |
T |
9: 65,746,286 (GRCm39) |
F537I |
possibly damaging |
Het |
Uaca |
G |
A |
9: 60,755,900 (GRCm39) |
|
probably benign |
Het |
Ugt2b34 |
T |
A |
5: 87,040,758 (GRCm39) |
Y388F |
possibly damaging |
Het |
Vmn2r71 |
T |
C |
7: 85,268,640 (GRCm39) |
V281A |
probably benign |
Het |
Vps13d |
A |
T |
4: 144,882,502 (GRCm39) |
D1030E |
probably damaging |
Het |
Vps8 |
C |
A |
16: 21,261,107 (GRCm39) |
F82L |
probably damaging |
Het |
Zfp296 |
A |
G |
7: 19,313,661 (GRCm39) |
D172G |
probably benign |
Het |
Zfp977 |
C |
A |
7: 42,229,958 (GRCm39) |
C189F |
probably damaging |
Het |
|
Other mutations in Pcnt |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01075:Pcnt
|
APN |
10 |
76,258,738 (GRCm39) |
nonsense |
probably null |
|
IGL01307:Pcnt
|
APN |
10 |
76,247,422 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01549:Pcnt
|
APN |
10 |
76,203,320 (GRCm39) |
splice site |
probably null |
|
IGL01576:Pcnt
|
APN |
10 |
76,204,656 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01611:Pcnt
|
APN |
10 |
76,272,258 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01630:Pcnt
|
APN |
10 |
76,256,080 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01647:Pcnt
|
APN |
10 |
76,205,835 (GRCm39) |
nonsense |
probably null |
|
IGL01689:Pcnt
|
APN |
10 |
76,247,487 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01690:Pcnt
|
APN |
10 |
76,228,609 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01723:Pcnt
|
APN |
10 |
76,254,333 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL01920:Pcnt
|
APN |
10 |
76,240,362 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01958:Pcnt
|
APN |
10 |
76,269,513 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02210:Pcnt
|
APN |
10 |
76,225,053 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02225:Pcnt
|
APN |
10 |
76,225,308 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02228:Pcnt
|
APN |
10 |
76,225,308 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02237:Pcnt
|
APN |
10 |
76,188,818 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02279:Pcnt
|
APN |
10 |
76,239,599 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02303:Pcnt
|
APN |
10 |
76,278,393 (GRCm39) |
splice site |
probably benign |
|
IGL02355:Pcnt
|
APN |
10 |
76,210,996 (GRCm39) |
nonsense |
probably null |
|
IGL02362:Pcnt
|
APN |
10 |
76,210,996 (GRCm39) |
nonsense |
probably null |
|
IGL02428:Pcnt
|
APN |
10 |
76,265,090 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02536:Pcnt
|
APN |
10 |
76,216,063 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02715:Pcnt
|
APN |
10 |
76,204,556 (GRCm39) |
splice site |
probably benign |
|
IGL02800:Pcnt
|
APN |
10 |
76,248,417 (GRCm39) |
nonsense |
probably null |
|
IGL03395:Pcnt
|
APN |
10 |
76,272,325 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02799:Pcnt
|
UTSW |
10 |
76,248,417 (GRCm39) |
nonsense |
probably null |
|
PIT4520001:Pcnt
|
UTSW |
10 |
76,256,069 (GRCm39) |
missense |
probably damaging |
0.99 |
R0049:Pcnt
|
UTSW |
10 |
76,205,655 (GRCm39) |
unclassified |
probably benign |
|
R0049:Pcnt
|
UTSW |
10 |
76,205,655 (GRCm39) |
unclassified |
probably benign |
|
R0109:Pcnt
|
UTSW |
10 |
76,225,030 (GRCm39) |
missense |
probably benign |
0.00 |
R0117:Pcnt
|
UTSW |
10 |
76,244,561 (GRCm39) |
nonsense |
probably null |
|
R0254:Pcnt
|
UTSW |
10 |
76,228,414 (GRCm39) |
missense |
probably benign |
0.10 |
R0392:Pcnt
|
UTSW |
10 |
76,220,660 (GRCm39) |
missense |
probably benign |
|
R0511:Pcnt
|
UTSW |
10 |
76,240,429 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0570:Pcnt
|
UTSW |
10 |
76,247,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R0614:Pcnt
|
UTSW |
10 |
76,256,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R0635:Pcnt
|
UTSW |
10 |
76,240,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R0749:Pcnt
|
UTSW |
10 |
76,217,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R0969:Pcnt
|
UTSW |
10 |
76,263,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R1172:Pcnt
|
UTSW |
10 |
76,228,878 (GRCm39) |
splice site |
probably null |
|
R1174:Pcnt
|
UTSW |
10 |
76,228,878 (GRCm39) |
splice site |
probably null |
|
R1175:Pcnt
|
UTSW |
10 |
76,228,878 (GRCm39) |
splice site |
probably null |
|
R1512:Pcnt
|
UTSW |
10 |
76,240,496 (GRCm39) |
splice site |
probably null |
|
R1542:Pcnt
|
UTSW |
10 |
76,237,220 (GRCm39) |
missense |
probably benign |
0.02 |
R1542:Pcnt
|
UTSW |
10 |
76,225,221 (GRCm39) |
missense |
probably benign |
0.08 |
R1558:Pcnt
|
UTSW |
10 |
76,258,756 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1562:Pcnt
|
UTSW |
10 |
76,203,164 (GRCm39) |
missense |
probably benign |
0.02 |
R1762:Pcnt
|
UTSW |
10 |
76,190,971 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1779:Pcnt
|
UTSW |
10 |
76,244,630 (GRCm39) |
missense |
probably damaging |
0.99 |
R1869:Pcnt
|
UTSW |
10 |
76,215,740 (GRCm39) |
missense |
probably null |
0.94 |
R1911:Pcnt
|
UTSW |
10 |
76,204,650 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1985:Pcnt
|
UTSW |
10 |
76,216,171 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1995:Pcnt
|
UTSW |
10 |
76,228,633 (GRCm39) |
nonsense |
probably null |
|
R2073:Pcnt
|
UTSW |
10 |
76,216,214 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2111:Pcnt
|
UTSW |
10 |
76,256,360 (GRCm39) |
missense |
probably damaging |
0.99 |
R2112:Pcnt
|
UTSW |
10 |
76,256,360 (GRCm39) |
missense |
probably damaging |
0.99 |
R2309:Pcnt
|
UTSW |
10 |
76,278,460 (GRCm39) |
start gained |
probably benign |
|
R2902:Pcnt
|
UTSW |
10 |
76,211,064 (GRCm39) |
missense |
probably damaging |
0.98 |
R3623:Pcnt
|
UTSW |
10 |
76,269,584 (GRCm39) |
missense |
probably benign |
0.23 |
R4088:Pcnt
|
UTSW |
10 |
76,263,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R4300:Pcnt
|
UTSW |
10 |
76,203,225 (GRCm39) |
missense |
probably benign |
0.40 |
R4402:Pcnt
|
UTSW |
10 |
76,228,227 (GRCm39) |
missense |
probably benign |
0.00 |
R4407:Pcnt
|
UTSW |
10 |
76,210,704 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4483:Pcnt
|
UTSW |
10 |
76,237,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R4647:Pcnt
|
UTSW |
10 |
76,190,047 (GRCm39) |
missense |
probably benign |
0.01 |
R4734:Pcnt
|
UTSW |
10 |
76,273,040 (GRCm39) |
missense |
probably benign |
0.25 |
R4747:Pcnt
|
UTSW |
10 |
76,272,299 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4782:Pcnt
|
UTSW |
10 |
76,245,411 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4795:Pcnt
|
UTSW |
10 |
76,205,858 (GRCm39) |
missense |
probably benign |
0.21 |
R4831:Pcnt
|
UTSW |
10 |
76,248,335 (GRCm39) |
missense |
probably damaging |
0.96 |
R4873:Pcnt
|
UTSW |
10 |
76,205,688 (GRCm39) |
missense |
probably benign |
0.03 |
R4875:Pcnt
|
UTSW |
10 |
76,205,688 (GRCm39) |
missense |
probably benign |
0.03 |
R4946:Pcnt
|
UTSW |
10 |
76,192,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R5032:Pcnt
|
UTSW |
10 |
76,190,911 (GRCm39) |
missense |
probably benign |
0.00 |
R5033:Pcnt
|
UTSW |
10 |
76,235,779 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5106:Pcnt
|
UTSW |
10 |
76,237,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R5118:Pcnt
|
UTSW |
10 |
76,248,002 (GRCm39) |
missense |
probably damaging |
0.98 |
R5167:Pcnt
|
UTSW |
10 |
76,256,258 (GRCm39) |
missense |
probably damaging |
0.97 |
R5199:Pcnt
|
UTSW |
10 |
76,254,378 (GRCm39) |
missense |
probably benign |
0.09 |
R5223:Pcnt
|
UTSW |
10 |
76,216,106 (GRCm39) |
missense |
probably damaging |
0.99 |
R5241:Pcnt
|
UTSW |
10 |
76,269,451 (GRCm39) |
missense |
probably benign |
0.26 |
R5308:Pcnt
|
UTSW |
10 |
76,192,159 (GRCm39) |
nonsense |
probably null |
|
R5328:Pcnt
|
UTSW |
10 |
76,247,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R5454:Pcnt
|
UTSW |
10 |
76,225,381 (GRCm39) |
splice site |
probably null |
|
R5543:Pcnt
|
UTSW |
10 |
76,247,886 (GRCm39) |
missense |
probably benign |
0.01 |
R5588:Pcnt
|
UTSW |
10 |
76,278,445 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5647:Pcnt
|
UTSW |
10 |
76,221,675 (GRCm39) |
missense |
probably benign |
0.17 |
R5668:Pcnt
|
UTSW |
10 |
76,245,334 (GRCm39) |
missense |
probably benign |
0.16 |
R5712:Pcnt
|
UTSW |
10 |
76,265,105 (GRCm39) |
missense |
probably damaging |
0.96 |
R5714:Pcnt
|
UTSW |
10 |
76,256,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R5797:Pcnt
|
UTSW |
10 |
76,228,590 (GRCm39) |
missense |
probably benign |
0.00 |
R5946:Pcnt
|
UTSW |
10 |
76,217,897 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5955:Pcnt
|
UTSW |
10 |
76,247,456 (GRCm39) |
missense |
possibly damaging |
0.45 |
R6024:Pcnt
|
UTSW |
10 |
76,255,871 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6267:Pcnt
|
UTSW |
10 |
76,221,632 (GRCm39) |
missense |
probably benign |
0.02 |
R6485:Pcnt
|
UTSW |
10 |
76,225,164 (GRCm39) |
nonsense |
probably null |
|
R6605:Pcnt
|
UTSW |
10 |
76,265,032 (GRCm39) |
critical splice donor site |
probably null |
|
R6877:Pcnt
|
UTSW |
10 |
76,269,851 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6882:Pcnt
|
UTSW |
10 |
76,263,662 (GRCm39) |
missense |
probably benign |
0.00 |
R6919:Pcnt
|
UTSW |
10 |
76,221,632 (GRCm39) |
missense |
probably benign |
0.02 |
R7025:Pcnt
|
UTSW |
10 |
76,239,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R7098:Pcnt
|
UTSW |
10 |
76,220,673 (GRCm39) |
missense |
probably benign |
|
R7109:Pcnt
|
UTSW |
10 |
76,205,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R7121:Pcnt
|
UTSW |
10 |
76,263,761 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7143:Pcnt
|
UTSW |
10 |
76,224,894 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7152:Pcnt
|
UTSW |
10 |
76,247,194 (GRCm39) |
splice site |
probably null |
|
R7213:Pcnt
|
UTSW |
10 |
76,244,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R7368:Pcnt
|
UTSW |
10 |
76,235,835 (GRCm39) |
missense |
probably benign |
|
R7453:Pcnt
|
UTSW |
10 |
76,225,284 (GRCm39) |
missense |
probably benign |
|
R7486:Pcnt
|
UTSW |
10 |
76,254,271 (GRCm39) |
missense |
probably benign |
|
R7486:Pcnt
|
UTSW |
10 |
76,254,270 (GRCm39) |
missense |
probably benign |
0.03 |
R7538:Pcnt
|
UTSW |
10 |
76,235,773 (GRCm39) |
missense |
probably benign |
|
R7575:Pcnt
|
UTSW |
10 |
76,225,086 (GRCm39) |
missense |
probably benign |
0.32 |
R7662:Pcnt
|
UTSW |
10 |
76,223,356 (GRCm39) |
missense |
probably benign |
0.27 |
R7685:Pcnt
|
UTSW |
10 |
76,258,642 (GRCm39) |
missense |
probably benign |
0.14 |
R7764:Pcnt
|
UTSW |
10 |
76,190,082 (GRCm39) |
missense |
probably benign |
0.33 |
R7802:Pcnt
|
UTSW |
10 |
76,211,137 (GRCm39) |
splice site |
probably null |
|
R8432:Pcnt
|
UTSW |
10 |
76,256,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R8439:Pcnt
|
UTSW |
10 |
76,256,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R8493:Pcnt
|
UTSW |
10 |
76,239,457 (GRCm39) |
critical splice donor site |
probably null |
|
R8530:Pcnt
|
UTSW |
10 |
76,256,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R8535:Pcnt
|
UTSW |
10 |
76,256,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R8830:Pcnt
|
UTSW |
10 |
76,218,008 (GRCm39) |
missense |
probably benign |
0.03 |
R8878:Pcnt
|
UTSW |
10 |
76,244,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R8911:Pcnt
|
UTSW |
10 |
76,223,359 (GRCm39) |
missense |
probably damaging |
0.98 |
R8988:Pcnt
|
UTSW |
10 |
76,245,407 (GRCm39) |
nonsense |
probably null |
|
R9084:Pcnt
|
UTSW |
10 |
76,235,826 (GRCm39) |
missense |
probably benign |
0.09 |
R9169:Pcnt
|
UTSW |
10 |
76,221,572 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9372:Pcnt
|
UTSW |
10 |
76,258,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R9411:Pcnt
|
UTSW |
10 |
76,258,896 (GRCm39) |
missense |
probably damaging |
0.96 |
R9448:Pcnt
|
UTSW |
10 |
76,256,360 (GRCm39) |
missense |
probably damaging |
0.99 |
R9459:Pcnt
|
UTSW |
10 |
76,228,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R9479:Pcnt
|
UTSW |
10 |
76,217,963 (GRCm39) |
missense |
probably benign |
0.00 |
R9503:Pcnt
|
UTSW |
10 |
76,263,882 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9561:Pcnt
|
UTSW |
10 |
76,217,128 (GRCm39) |
nonsense |
probably null |
|
R9618:Pcnt
|
UTSW |
10 |
76,188,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R9648:Pcnt
|
UTSW |
10 |
76,190,089 (GRCm39) |
missense |
probably benign |
0.32 |
R9733:Pcnt
|
UTSW |
10 |
76,237,314 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Pcnt
|
UTSW |
10 |
76,217,991 (GRCm39) |
nonsense |
probably null |
|
Z1177:Pcnt
|
UTSW |
10 |
76,235,802 (GRCm39) |
missense |
probably benign |
0.00 |
|