Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam21 |
T |
C |
12: 81,605,657 (GRCm39) |
I702V |
probably benign |
Het |
Adgre5 |
T |
C |
8: 84,450,515 (GRCm39) |
E815G |
probably damaging |
Het |
Adgrl2 |
A |
G |
3: 148,523,330 (GRCm39) |
V298A |
|
Het |
Akp3 |
A |
G |
1: 87,053,201 (GRCm39) |
D91G |
probably damaging |
Het |
Ano8 |
A |
G |
8: 71,937,642 (GRCm39) |
|
probably null |
Het |
Blvra |
T |
C |
2: 126,929,243 (GRCm39) |
S136P |
unknown |
Het |
Cacul1 |
T |
A |
19: 60,568,868 (GRCm39) |
M97L |
probably benign |
Het |
Ccdc80 |
T |
C |
16: 44,946,542 (GRCm39) |
V827A |
probably damaging |
Het |
Cep68 |
T |
C |
11: 20,192,166 (GRCm39) |
E11G |
probably benign |
Het |
Cfap221 |
A |
T |
1: 119,851,322 (GRCm39) |
V813E |
possibly damaging |
Het |
Chd6 |
A |
G |
2: 160,791,923 (GRCm39) |
V2478A |
probably damaging |
Het |
Chmp6 |
T |
C |
11: 119,807,783 (GRCm39) |
F148S |
probably benign |
Het |
Clca3a2 |
T |
A |
3: 144,503,362 (GRCm39) |
I863F |
probably damaging |
Het |
Cnnm2 |
T |
C |
19: 46,750,513 (GRCm39) |
V101A |
possibly damaging |
Het |
Cpne8 |
A |
T |
15: 90,400,109 (GRCm39) |
|
probably null |
Het |
Dmbt1 |
T |
G |
7: 130,668,192 (GRCm39) |
C483G |
unknown |
Het |
Dnah7b |
G |
A |
1: 46,329,894 (GRCm39) |
G3246D |
probably damaging |
Het |
Dnajc3 |
C |
A |
14: 119,209,816 (GRCm39) |
T297K |
probably benign |
Het |
Dpm3 |
A |
G |
3: 89,174,034 (GRCm39) |
|
probably null |
Het |
Eef2k |
A |
G |
7: 120,457,793 (GRCm39) |
N51D |
probably benign |
Het |
Erc1 |
G |
A |
6: 119,571,907 (GRCm39) |
Q1022* |
probably null |
Het |
Ercc5 |
T |
A |
1: 44,187,224 (GRCm39) |
M1K |
probably null |
Het |
Fam114a2 |
C |
T |
11: 57,404,515 (GRCm39) |
G83D |
probably damaging |
Het |
Fat4 |
C |
A |
3: 39,011,576 (GRCm39) |
Y2225* |
probably null |
Het |
Frk |
G |
A |
10: 34,423,292 (GRCm39) |
W123* |
probably null |
Het |
Gm11568 |
T |
A |
11: 99,749,292 (GRCm39) |
C166S |
unknown |
Het |
Gpr153 |
A |
G |
4: 152,366,858 (GRCm39) |
D337G |
probably benign |
Het |
Gpt2 |
T |
C |
8: 86,252,235 (GRCm39) |
F517L |
probably damaging |
Het |
Gsg1 |
C |
T |
6: 135,214,427 (GRCm39) |
E361K |
probably benign |
Het |
Hsfy2 |
G |
A |
1: 56,676,130 (GRCm39) |
R136* |
probably null |
Het |
Insm1 |
G |
A |
2: 146,065,738 (GRCm39) |
R518H |
probably damaging |
Het |
Kank1 |
G |
A |
19: 25,388,193 (GRCm39) |
C622Y |
probably damaging |
Het |
Katnb1 |
T |
A |
8: 95,825,357 (GRCm39) |
S640R |
probably damaging |
Het |
Kcnmb4 |
A |
G |
10: 116,254,180 (GRCm39) |
V199A |
probably benign |
Het |
Lamb1 |
T |
G |
12: 31,337,441 (GRCm39) |
S391A |
probably benign |
Het |
Larp7-ps |
A |
T |
4: 92,079,506 (GRCm39) |
V105E |
probably benign |
Het |
Macf1 |
T |
G |
4: 123,303,374 (GRCm39) |
D376A |
probably benign |
Het |
Map7d1 |
C |
A |
4: 126,128,179 (GRCm39) |
R614L |
unknown |
Het |
Mcm8 |
C |
T |
2: 132,681,440 (GRCm39) |
R667W |
probably damaging |
Het |
Med13l |
C |
T |
5: 118,866,539 (GRCm39) |
T531I |
probably benign |
Het |
Mstn |
G |
T |
1: 53,103,128 (GRCm39) |
A155S |
probably damaging |
Het |
Mycbp2 |
C |
T |
14: 103,434,690 (GRCm39) |
R2251K |
probably damaging |
Het |
Myo19 |
T |
C |
11: 84,796,463 (GRCm39) |
S692P |
probably benign |
Het |
Nipbl |
A |
T |
15: 8,325,120 (GRCm39) |
N2514K |
probably benign |
Het |
Nkd2 |
T |
A |
13: 73,995,561 (GRCm39) |
|
probably benign |
Het |
Nox3 |
T |
A |
17: 3,720,219 (GRCm39) |
Y322F |
probably damaging |
Het |
Nt5dc1 |
A |
G |
10: 34,275,805 (GRCm39) |
Y135H |
probably benign |
Het |
Oog3 |
T |
A |
4: 143,884,742 (GRCm39) |
H398L |
probably benign |
Het |
Or10g9 |
T |
A |
9: 39,912,181 (GRCm39) |
Y114F |
probably benign |
Het |
Or12j4 |
C |
T |
7: 140,045,947 (GRCm39) |
|
probably benign |
Het |
Or1e29 |
T |
C |
11: 73,667,847 (GRCm39) |
Y102C |
probably damaging |
Het |
Otogl |
A |
G |
10: 107,657,849 (GRCm39) |
L1027P |
probably damaging |
Het |
Pcdh20 |
T |
A |
14: 88,706,050 (GRCm39) |
I417F |
possibly damaging |
Het |
Pcdha12 |
T |
A |
18: 37,154,610 (GRCm39) |
V443E |
probably damaging |
Het |
Pcdhga2 |
A |
G |
18: 37,803,461 (GRCm39) |
D435G |
probably benign |
Het |
Pgghg |
T |
A |
7: 140,522,393 (GRCm39) |
S57R |
probably benign |
Het |
Ppm1m |
T |
C |
9: 106,073,810 (GRCm39) |
D301G |
probably damaging |
Het |
Ppp6r1 |
A |
G |
7: 4,642,899 (GRCm39) |
V519A |
probably benign |
Het |
Prss41 |
ACAGCAGCAGCAGCAGCAGCA |
ACAGCAGCAGCAGCAGCA |
17: 24,063,072 (GRCm39) |
|
probably benign |
Het |
Rasa3 |
C |
T |
8: 13,640,201 (GRCm39) |
|
probably null |
Het |
Robo4 |
T |
C |
9: 37,316,870 (GRCm39) |
V395A |
probably damaging |
Het |
Scrib |
A |
G |
15: 75,929,499 (GRCm39) |
S1123P |
probably damaging |
Het |
Setd1b |
A |
G |
5: 123,301,655 (GRCm39) |
K45E |
probably benign |
Het |
Slc14a1 |
T |
C |
18: 78,154,739 (GRCm39) |
S216G |
probably benign |
Het |
Slc25a45 |
A |
G |
19: 5,934,997 (GRCm39) |
Y282C |
probably damaging |
Het |
Slc6a5 |
T |
C |
7: 49,567,078 (GRCm39) |
S255P |
possibly damaging |
Het |
Smc2 |
A |
T |
4: 52,462,861 (GRCm39) |
Q617L |
possibly damaging |
Het |
Spo11 |
G |
A |
2: 172,825,870 (GRCm39) |
D103N |
probably benign |
Het |
Tcf20 |
A |
T |
15: 82,737,935 (GRCm39) |
M1172K |
possibly damaging |
Het |
Tesc |
T |
A |
5: 118,184,382 (GRCm39) |
S21T |
probably benign |
Het |
Tie1 |
C |
A |
4: 118,337,101 (GRCm39) |
|
probably null |
Het |
Trim24 |
T |
G |
6: 37,934,774 (GRCm39) |
|
probably null |
Het |
Trpm7 |
A |
G |
2: 126,673,115 (GRCm39) |
|
probably null |
Het |
Unc13d |
T |
C |
11: 115,965,259 (GRCm39) |
D193G |
possibly damaging |
Het |
Upk3a |
A |
T |
15: 84,902,225 (GRCm39) |
|
probably null |
Het |
Vmn2r25 |
T |
C |
6: 123,800,101 (GRCm39) |
N747S |
probably damaging |
Het |
Wipf1 |
GCCTCCTCCTCCTCCTCCTCCTCC |
GCCTCCTCCTCCTCCTCCTCC |
2: 73,270,418 (GRCm39) |
|
probably benign |
Het |
Zbtb2 |
G |
A |
10: 4,319,025 (GRCm39) |
Q334* |
probably null |
Het |
Zfp653 |
T |
C |
9: 21,967,824 (GRCm39) |
N494D |
probably damaging |
Het |
Zfp865 |
A |
G |
7: 5,034,259 (GRCm39) |
D748G |
possibly damaging |
Het |
Zzef1 |
T |
C |
11: 72,755,612 (GRCm39) |
S1014P |
possibly 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 |
R0707:Pcnt
|
UTSW |
10 |
76,256,375 (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 |
76,254,270 (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 |
|