Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930584F24Rik |
A |
T |
5: 26,684,776 (GRCm39) |
|
noncoding transcript |
Het |
Acvr1 |
A |
T |
2: 58,369,901 (GRCm39) |
V36E |
probably damaging |
Het |
Aldh4a1 |
A |
G |
4: 139,370,758 (GRCm39) |
I414V |
probably benign |
Het |
Alox5 |
C |
T |
6: 116,431,128 (GRCm39) |
C100Y |
probably damaging |
Het |
Ano5 |
T |
A |
7: 51,216,068 (GRCm39) |
D348E |
probably damaging |
Het |
Arhgap30 |
G |
A |
1: 171,230,839 (GRCm39) |
V199M |
probably damaging |
Het |
Arl13b |
T |
A |
16: 62,626,999 (GRCm39) |
Q234L |
probably benign |
Het |
Atxn1 |
C |
A |
13: 45,711,052 (GRCm39) |
E627* |
probably null |
Het |
Bend3 |
T |
C |
10: 43,386,197 (GRCm39) |
F197L |
probably benign |
Het |
Brca1 |
A |
T |
11: 101,420,638 (GRCm39) |
V190E |
possibly damaging |
Het |
Brpf1 |
T |
C |
6: 113,292,096 (GRCm39) |
W381R |
probably damaging |
Het |
Brwd1 |
A |
C |
16: 95,829,491 (GRCm39) |
|
probably null |
Het |
C1s2 |
T |
C |
6: 124,602,604 (GRCm39) |
I530V |
possibly damaging |
Het |
C2cd3 |
C |
T |
7: 100,089,397 (GRCm39) |
R1638W |
probably damaging |
Het |
Capns1 |
T |
A |
7: 29,893,511 (GRCm39) |
|
probably benign |
Het |
Cd109 |
CATTTATTTATTTATTTATTTATTTATTTATTTAT |
CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT |
9: 78,619,782 (GRCm39) |
|
probably benign |
Het |
Cep126 |
G |
A |
9: 8,100,554 (GRCm39) |
T660I |
possibly damaging |
Het |
Cep295 |
A |
C |
9: 15,246,080 (GRCm39) |
I744R |
probably damaging |
Het |
Chd3 |
T |
C |
11: 69,250,725 (GRCm39) |
E668G |
probably benign |
Het |
Chek2 |
A |
G |
5: 110,996,553 (GRCm39) |
T172A |
probably damaging |
Het |
Col6a4 |
A |
G |
9: 105,890,501 (GRCm39) |
|
probably null |
Het |
Coq3 |
G |
A |
4: 21,900,291 (GRCm39) |
V173I |
probably benign |
Het |
Cyp4x1 |
A |
T |
4: 114,970,098 (GRCm39) |
I343N |
probably damaging |
Het |
Dnah7b |
T |
A |
1: 46,176,703 (GRCm39) |
D774E |
probably benign |
Het |
Dnai3 |
T |
C |
3: 145,802,996 (GRCm39) |
D65G |
probably benign |
Het |
Ecm1 |
G |
A |
3: 95,643,275 (GRCm39) |
R342C |
probably damaging |
Het |
Esrra |
T |
C |
19: 6,890,197 (GRCm39) |
Y209C |
probably damaging |
Het |
Gpr149 |
A |
T |
3: 62,502,592 (GRCm39) |
D421E |
probably benign |
Het |
Gpr15 |
T |
C |
16: 58,538,937 (GRCm39) |
N51D |
probably damaging |
Het |
Gpr156 |
T |
C |
16: 37,812,558 (GRCm39) |
V298A |
probably damaging |
Het |
Hmcn2 |
G |
A |
2: 31,236,507 (GRCm39) |
G350D |
probably damaging |
Het |
Ifih1 |
A |
T |
2: 62,440,902 (GRCm39) |
N421K |
probably benign |
Het |
Ilvbl |
C |
A |
10: 78,412,564 (GRCm39) |
T95K |
probably damaging |
Het |
Itgb4 |
T |
A |
11: 115,890,625 (GRCm39) |
D1104E |
probably benign |
Het |
Katnip |
C |
A |
7: 125,415,743 (GRCm39) |
|
probably benign |
Het |
Lipf |
A |
T |
19: 33,942,180 (GRCm39) |
M37L |
probably benign |
Het |
Lyst |
T |
A |
13: 13,852,775 (GRCm39) |
N2258K |
probably benign |
Het |
Moxd1 |
A |
G |
10: 24,099,758 (GRCm39) |
Y86C |
probably damaging |
Het |
Muc5ac |
T |
C |
7: 141,367,629 (GRCm39) |
|
probably null |
Het |
Myo16 |
G |
A |
8: 10,610,145 (GRCm39) |
R1162H |
probably damaging |
Het |
Myo5c |
A |
T |
9: 75,208,092 (GRCm39) |
N1609Y |
probably damaging |
Het |
Nbeal1 |
T |
C |
1: 60,240,098 (GRCm39) |
F155L |
probably damaging |
Het |
Nek4 |
A |
T |
14: 30,704,290 (GRCm39) |
M602L |
possibly damaging |
Het |
Nek9 |
A |
G |
12: 85,348,622 (GRCm39) |
S971P |
probably damaging |
Het |
Nfya |
A |
T |
17: 48,700,570 (GRCm39) |
|
probably benign |
Het |
Nrxn3 |
A |
T |
12: 89,221,547 (GRCm39) |
N442I |
probably damaging |
Het |
Nup42 |
A |
C |
5: 24,383,075 (GRCm39) |
K200N |
probably benign |
Het |
Or1e26 |
T |
A |
11: 73,480,187 (GRCm39) |
I126L |
possibly damaging |
Het |
Or4c111 |
G |
A |
2: 88,843,713 (GRCm39) |
R232* |
probably null |
Het |
Or7g32 |
G |
A |
9: 19,389,423 (GRCm39) |
T38I |
probably damaging |
Het |
Pcdh15 |
T |
A |
10: 74,126,833 (GRCm39) |
I304N |
probably damaging |
Het |
Pigo |
G |
C |
4: 43,024,779 (GRCm39) |
P107A |
probably damaging |
Het |
Plin2 |
C |
T |
4: 86,575,481 (GRCm39) |
R356H |
probably benign |
Het |
Ppp1r9a |
G |
T |
6: 5,113,712 (GRCm39) |
E739* |
probably null |
Het |
Ppp3cc |
G |
T |
14: 70,478,397 (GRCm39) |
N268K |
probably damaging |
Het |
Prkag3 |
T |
A |
1: 74,779,919 (GRCm39) |
D472V |
probably damaging |
Het |
Ptch2 |
A |
T |
4: 116,968,046 (GRCm39) |
D846V |
probably damaging |
Het |
Rhob |
A |
T |
12: 8,549,388 (GRCm39) |
M82K |
probably damaging |
Het |
Rps6kc1 |
T |
A |
1: 190,531,672 (GRCm39) |
R777W |
possibly damaging |
Het |
Sap130 |
T |
A |
18: 31,844,380 (GRCm39) |
V850E |
probably damaging |
Het |
Sema3a |
T |
G |
5: 13,523,407 (GRCm39) |
N125K |
probably damaging |
Het |
Sema5a |
A |
G |
15: 32,460,431 (GRCm39) |
D64G |
probably damaging |
Het |
Sgo2b |
T |
A |
8: 64,384,507 (GRCm39) |
D163V |
possibly damaging |
Het |
Slc15a1 |
A |
T |
14: 121,728,651 (GRCm39) |
Y31* |
probably null |
Het |
Smchd1 |
A |
T |
17: 71,685,252 (GRCm39) |
M1392K |
probably benign |
Het |
Sobp |
T |
A |
10: 43,036,827 (GRCm39) |
N37I |
probably damaging |
Het |
Spock3 |
G |
T |
8: 63,673,739 (GRCm39) |
C142F |
probably damaging |
Het |
Stx6 |
A |
C |
1: 155,053,650 (GRCm39) |
S86R |
probably benign |
Het |
Sult2a4 |
C |
A |
7: 13,643,726 (GRCm39) |
M280I |
probably benign |
Het |
Synm |
A |
T |
7: 67,386,080 (GRCm39) |
D527E |
probably damaging |
Het |
Tax1bp1 |
C |
T |
6: 52,710,305 (GRCm39) |
R195W |
probably damaging |
Het |
Themis2 |
A |
T |
4: 132,519,796 (GRCm39) |
N76K |
possibly damaging |
Het |
Tmem8b |
A |
G |
4: 43,690,234 (GRCm39) |
T890A |
probably benign |
Het |
Traf7 |
T |
A |
17: 24,730,785 (GRCm39) |
H366L |
possibly damaging |
Het |
Trim30c |
A |
T |
7: 104,032,459 (GRCm39) |
V289D |
probably benign |
Het |
Tsr1 |
T |
A |
11: 74,792,914 (GRCm39) |
D407E |
probably damaging |
Het |
Ubap2 |
G |
T |
4: 41,235,593 (GRCm39) |
A33E |
probably damaging |
Het |
Unc13d |
C |
A |
11: 115,964,701 (GRCm39) |
R255L |
possibly damaging |
Het |
Ush2a |
G |
T |
1: 188,542,534 (GRCm39) |
G3367* |
probably null |
Het |
Vmn1r229 |
T |
C |
17: 21,034,791 (GRCm39) |
L12P |
probably damaging |
Het |
Vmn2r27 |
C |
A |
6: 124,177,474 (GRCm39) |
G510V |
probably damaging |
Het |
Vps4b |
T |
C |
1: 106,707,712 (GRCm39) |
E257G |
probably damaging |
Het |
Vps72 |
T |
C |
3: 95,026,462 (GRCm39) |
S136P |
probably damaging |
Het |
Wdr36 |
T |
C |
18: 32,976,938 (GRCm39) |
I181T |
possibly damaging |
Het |
Wfikkn1 |
C |
T |
17: 26,096,765 (GRCm39) |
A520T |
probably benign |
Het |
|
Other mutations in Plce1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Plce1
|
APN |
19 |
38,734,232 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00336:Plce1
|
APN |
19 |
38,640,350 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00430:Plce1
|
APN |
19 |
38,713,461 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00466:Plce1
|
APN |
19 |
38,709,473 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00477:Plce1
|
APN |
19 |
38,513,576 (GRCm39) |
missense |
probably benign |
0.39 |
IGL00839:Plce1
|
APN |
19 |
38,687,006 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01292:Plce1
|
APN |
19 |
38,640,229 (GRCm39) |
splice site |
probably benign |
|
IGL01665:Plce1
|
APN |
19 |
38,513,331 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01826:Plce1
|
APN |
19 |
38,727,682 (GRCm39) |
splice site |
probably benign |
|
IGL01833:Plce1
|
APN |
19 |
38,709,425 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02201:Plce1
|
APN |
19 |
38,757,890 (GRCm39) |
splice site |
probably benign |
|
IGL02276:Plce1
|
APN |
19 |
38,513,201 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02477:Plce1
|
APN |
19 |
38,707,997 (GRCm39) |
splice site |
probably benign |
|
IGL02746:Plce1
|
APN |
19 |
38,686,916 (GRCm39) |
missense |
probably damaging |
1.00 |
Angel_food
|
UTSW |
19 |
38,715,457 (GRCm39) |
splice site |
probably benign |
|
Heavenly
|
UTSW |
19 |
38,766,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R0058:Plce1
|
UTSW |
19 |
38,513,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0058:Plce1
|
UTSW |
19 |
38,513,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0064:Plce1
|
UTSW |
19 |
38,769,228 (GRCm39) |
critical splice donor site |
probably null |
|
R0116:Plce1
|
UTSW |
19 |
38,710,265 (GRCm39) |
missense |
probably benign |
|
R0138:Plce1
|
UTSW |
19 |
38,512,863 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0240:Plce1
|
UTSW |
19 |
38,717,330 (GRCm39) |
missense |
probably damaging |
0.99 |
R0240:Plce1
|
UTSW |
19 |
38,717,330 (GRCm39) |
missense |
probably damaging |
0.99 |
R0504:Plce1
|
UTSW |
19 |
38,766,465 (GRCm39) |
splice site |
probably benign |
|
R0506:Plce1
|
UTSW |
19 |
38,748,582 (GRCm39) |
missense |
probably benign |
0.04 |
R0578:Plce1
|
UTSW |
19 |
38,766,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R0645:Plce1
|
UTSW |
19 |
38,766,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R0730:Plce1
|
UTSW |
19 |
38,705,135 (GRCm39) |
missense |
probably damaging |
0.98 |
R0920:Plce1
|
UTSW |
19 |
38,724,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R1223:Plce1
|
UTSW |
19 |
38,755,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R1223:Plce1
|
UTSW |
19 |
38,690,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R1488:Plce1
|
UTSW |
19 |
38,705,247 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1598:Plce1
|
UTSW |
19 |
38,709,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R1624:Plce1
|
UTSW |
19 |
38,713,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R1732:Plce1
|
UTSW |
19 |
38,705,282 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1778:Plce1
|
UTSW |
19 |
38,769,234 (GRCm39) |
splice site |
probably benign |
|
R1797:Plce1
|
UTSW |
19 |
38,747,392 (GRCm39) |
critical splice donor site |
probably null |
|
R1872:Plce1
|
UTSW |
19 |
38,748,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R1876:Plce1
|
UTSW |
19 |
38,769,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R1991:Plce1
|
UTSW |
19 |
38,766,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R2080:Plce1
|
UTSW |
19 |
38,715,457 (GRCm39) |
splice site |
probably benign |
|
R2103:Plce1
|
UTSW |
19 |
38,766,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R2376:Plce1
|
UTSW |
19 |
38,766,430 (GRCm39) |
missense |
probably benign |
0.02 |
R2471:Plce1
|
UTSW |
19 |
38,768,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R2511:Plce1
|
UTSW |
19 |
38,748,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R2842:Plce1
|
UTSW |
19 |
38,512,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R3037:Plce1
|
UTSW |
19 |
38,766,328 (GRCm39) |
missense |
probably damaging |
0.98 |
R3104:Plce1
|
UTSW |
19 |
38,608,963 (GRCm39) |
missense |
probably benign |
0.00 |
R3700:Plce1
|
UTSW |
19 |
38,693,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R3750:Plce1
|
UTSW |
19 |
38,766,343 (GRCm39) |
missense |
probably benign |
|
R3753:Plce1
|
UTSW |
19 |
38,640,278 (GRCm39) |
missense |
probably benign |
0.09 |
R4027:Plce1
|
UTSW |
19 |
38,512,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R4057:Plce1
|
UTSW |
19 |
38,748,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R4376:Plce1
|
UTSW |
19 |
38,693,891 (GRCm39) |
critical splice donor site |
probably null |
|
R4433:Plce1
|
UTSW |
19 |
38,755,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R4520:Plce1
|
UTSW |
19 |
38,512,763 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4521:Plce1
|
UTSW |
19 |
38,512,763 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4522:Plce1
|
UTSW |
19 |
38,512,763 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4524:Plce1
|
UTSW |
19 |
38,512,763 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4650:Plce1
|
UTSW |
19 |
38,513,088 (GRCm39) |
missense |
probably benign |
0.30 |
R4673:Plce1
|
UTSW |
19 |
38,737,840 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4701:Plce1
|
UTSW |
19 |
38,713,451 (GRCm39) |
missense |
probably benign |
0.33 |
R4828:Plce1
|
UTSW |
19 |
38,757,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R5103:Plce1
|
UTSW |
19 |
38,755,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R5112:Plce1
|
UTSW |
19 |
38,640,277 (GRCm39) |
missense |
probably benign |
0.00 |
R5236:Plce1
|
UTSW |
19 |
38,758,791 (GRCm39) |
missense |
probably benign |
0.11 |
R5268:Plce1
|
UTSW |
19 |
38,747,279 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5288:Plce1
|
UTSW |
19 |
38,748,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R5384:Plce1
|
UTSW |
19 |
38,748,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R5386:Plce1
|
UTSW |
19 |
38,748,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R5448:Plce1
|
UTSW |
19 |
38,768,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R5452:Plce1
|
UTSW |
19 |
38,608,926 (GRCm39) |
missense |
probably benign |
0.01 |
R6004:Plce1
|
UTSW |
19 |
38,710,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R6062:Plce1
|
UTSW |
19 |
38,513,195 (GRCm39) |
missense |
probably benign |
|
R6147:Plce1
|
UTSW |
19 |
38,690,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R6247:Plce1
|
UTSW |
19 |
38,734,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R6278:Plce1
|
UTSW |
19 |
38,713,495 (GRCm39) |
splice site |
probably null |
|
R6306:Plce1
|
UTSW |
19 |
38,757,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R6317:Plce1
|
UTSW |
19 |
38,512,974 (GRCm39) |
nonsense |
probably null |
|
R6437:Plce1
|
UTSW |
19 |
38,513,576 (GRCm39) |
missense |
probably benign |
0.39 |
R6522:Plce1
|
UTSW |
19 |
38,736,965 (GRCm39) |
splice site |
probably null |
|
R7034:Plce1
|
UTSW |
19 |
38,727,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R7036:Plce1
|
UTSW |
19 |
38,727,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R7037:Plce1
|
UTSW |
19 |
38,690,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R7069:Plce1
|
UTSW |
19 |
38,747,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R7180:Plce1
|
UTSW |
19 |
38,768,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R7189:Plce1
|
UTSW |
19 |
38,748,581 (GRCm39) |
missense |
probably damaging |
0.97 |
R7227:Plce1
|
UTSW |
19 |
38,715,346 (GRCm39) |
missense |
probably benign |
0.00 |
R7253:Plce1
|
UTSW |
19 |
38,686,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R7278:Plce1
|
UTSW |
19 |
38,768,340 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7287:Plce1
|
UTSW |
19 |
38,690,347 (GRCm39) |
missense |
probably benign |
0.02 |
R7422:Plce1
|
UTSW |
19 |
38,640,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R7557:Plce1
|
UTSW |
19 |
38,753,848 (GRCm39) |
missense |
probably benign |
0.30 |
R7607:Plce1
|
UTSW |
19 |
38,513,196 (GRCm39) |
missense |
probably benign |
|
R7615:Plce1
|
UTSW |
19 |
38,513,109 (GRCm39) |
missense |
probably benign |
0.18 |
R7653:Plce1
|
UTSW |
19 |
38,737,763 (GRCm39) |
missense |
probably benign |
0.20 |
R7685:Plce1
|
UTSW |
19 |
38,736,877 (GRCm39) |
missense |
probably benign |
0.00 |
R7716:Plce1
|
UTSW |
19 |
38,705,295 (GRCm39) |
missense |
probably benign |
|
R7744:Plce1
|
UTSW |
19 |
38,608,899 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7790:Plce1
|
UTSW |
19 |
38,769,140 (GRCm39) |
missense |
probably damaging |
0.97 |
R7921:Plce1
|
UTSW |
19 |
38,608,997 (GRCm39) |
missense |
probably benign |
0.03 |
R8070:Plce1
|
UTSW |
19 |
38,690,283 (GRCm39) |
missense |
probably damaging |
0.99 |
R8087:Plce1
|
UTSW |
19 |
38,724,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R8116:Plce1
|
UTSW |
19 |
38,513,262 (GRCm39) |
missense |
probably benign |
0.32 |
R8178:Plce1
|
UTSW |
19 |
38,761,423 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8321:Plce1
|
UTSW |
19 |
38,640,380 (GRCm39) |
missense |
probably benign |
0.00 |
R8416:Plce1
|
UTSW |
19 |
38,761,441 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8544:Plce1
|
UTSW |
19 |
38,512,903 (GRCm39) |
missense |
probably benign |
0.00 |
R8713:Plce1
|
UTSW |
19 |
38,513,345 (GRCm39) |
missense |
probably benign |
0.01 |
R8850:Plce1
|
UTSW |
19 |
38,512,811 (GRCm39) |
missense |
probably benign |
|
R9217:Plce1
|
UTSW |
19 |
38,748,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R9231:Plce1
|
UTSW |
19 |
38,705,040 (GRCm39) |
missense |
probably benign |
0.13 |
R9232:Plce1
|
UTSW |
19 |
38,705,423 (GRCm39) |
missense |
probably benign |
0.16 |
R9332:Plce1
|
UTSW |
19 |
38,726,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R9473:Plce1
|
UTSW |
19 |
38,766,337 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9474:Plce1
|
UTSW |
19 |
38,766,337 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9475:Plce1
|
UTSW |
19 |
38,766,337 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9476:Plce1
|
UTSW |
19 |
38,766,337 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9751:Plce1
|
UTSW |
19 |
38,717,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R9780:Plce1
|
UTSW |
19 |
38,609,134 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9781:Plce1
|
UTSW |
19 |
38,513,654 (GRCm39) |
missense |
probably damaging |
1.00 |
RF018:Plce1
|
UTSW |
19 |
38,705,651 (GRCm39) |
missense |
probably damaging |
0.99 |
X0022:Plce1
|
UTSW |
19 |
38,715,443 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Plce1
|
UTSW |
19 |
38,766,358 (GRCm39) |
missense |
possibly damaging |
0.48 |
Z1176:Plce1
|
UTSW |
19 |
38,757,904 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Plce1
|
UTSW |
19 |
38,713,424 (GRCm39) |
nonsense |
probably null |
|
Z1176:Plce1
|
UTSW |
19 |
38,690,338 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Plce1
|
UTSW |
19 |
38,640,286 (GRCm39) |
missense |
probably null |
0.48 |
|