Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm3 |
G |
A |
7: 119,383,527 (GRCm39) |
V563I |
probably benign |
Het |
Amer3 |
T |
C |
1: 34,627,759 (GRCm39) |
V666A |
probably benign |
Het |
Ankrd16 |
A |
G |
2: 11,784,711 (GRCm39) |
|
probably benign |
Het |
Ankub1 |
G |
T |
3: 57,580,296 (GRCm39) |
C120* |
probably null |
Het |
Arhgap31 |
T |
C |
16: 38,445,941 (GRCm39) |
I135V |
probably benign |
Het |
Atp2c2 |
G |
A |
8: 120,476,584 (GRCm39) |
G633D |
probably benign |
Het |
Camta1 |
T |
A |
4: 151,537,751 (GRCm39) |
Q143L |
probably damaging |
Het |
Casp8ap2 |
T |
C |
4: 32,644,727 (GRCm39) |
S1267P |
probably benign |
Het |
Ccn4 |
A |
G |
15: 66,791,176 (GRCm39) |
E326G |
probably benign |
Het |
Cdh1 |
T |
A |
8: 107,380,391 (GRCm39) |
|
probably benign |
Het |
Cdhr4 |
C |
A |
9: 107,873,460 (GRCm39) |
D397E |
probably damaging |
Het |
Cdk6 |
T |
G |
5: 3,394,387 (GRCm39) |
S7R |
probably benign |
Het |
Cert1 |
T |
A |
13: 96,771,394 (GRCm39) |
N550K |
probably damaging |
Het |
Cilp2 |
C |
A |
8: 70,335,442 (GRCm39) |
E519* |
probably null |
Het |
Clybl |
A |
G |
14: 122,548,718 (GRCm39) |
Y40C |
probably damaging |
Het |
Ctnnal1 |
T |
C |
4: 56,812,329 (GRCm39) |
*732W |
probably null |
Het |
Ctns |
A |
T |
11: 73,083,907 (GRCm39) |
S38R |
probably benign |
Het |
Cwh43 |
A |
T |
5: 73,578,873 (GRCm39) |
K293N |
possibly damaging |
Het |
Dcaf5 |
G |
T |
12: 80,385,635 (GRCm39) |
D830E |
probably benign |
Het |
Dmxl2 |
A |
G |
9: 54,322,848 (GRCm39) |
V1512A |
probably damaging |
Het |
Dnah9 |
A |
T |
11: 65,951,950 (GRCm39) |
C1850S |
probably damaging |
Het |
Dpp8 |
C |
T |
9: 64,981,849 (GRCm39) |
|
probably null |
Het |
Enam |
A |
T |
5: 88,649,646 (GRCm39) |
Q385L |
probably damaging |
Het |
Etv3 |
A |
G |
3: 87,443,369 (GRCm39) |
T318A |
possibly damaging |
Het |
Exd2 |
T |
G |
12: 80,543,575 (GRCm39) |
I586S |
probably benign |
Het |
Fat3 |
A |
G |
9: 15,909,813 (GRCm39) |
V2063A |
possibly damaging |
Het |
Fezf1 |
A |
G |
6: 23,247,331 (GRCm39) |
F248S |
possibly damaging |
Het |
Flnc |
T |
C |
6: 29,450,734 (GRCm39) |
|
probably null |
Het |
Foxc2 |
A |
G |
8: 121,844,819 (GRCm39) |
Y489C |
probably damaging |
Het |
Gfm2 |
A |
G |
13: 97,308,028 (GRCm39) |
E540G |
probably damaging |
Het |
Hrg |
T |
C |
16: 22,774,949 (GRCm39) |
I193T |
probably benign |
Het |
Ifih1 |
G |
A |
2: 62,440,889 (GRCm39) |
Q426* |
probably null |
Het |
Ifit1bl2 |
T |
A |
19: 34,596,920 (GRCm39) |
D232V |
probably benign |
Het |
Igf2bp1 |
A |
G |
11: 95,866,122 (GRCm39) |
V122A |
probably damaging |
Het |
Inpp1 |
T |
G |
1: 52,838,577 (GRCm39) |
Q24P |
probably damaging |
Het |
Kifc2 |
A |
G |
15: 76,545,454 (GRCm39) |
D67G |
probably damaging |
Het |
Lrrc43 |
G |
A |
5: 123,639,177 (GRCm39) |
G402D |
probably benign |
Het |
Lrrc8c |
C |
T |
5: 105,755,224 (GRCm39) |
T333M |
possibly damaging |
Het |
Mab21l3 |
G |
T |
3: 101,730,744 (GRCm39) |
A165D |
probably benign |
Het |
Mcub |
T |
A |
3: 129,712,337 (GRCm39) |
R179S |
probably benign |
Het |
Mdfi |
G |
C |
17: 48,135,562 (GRCm39) |
A56G |
possibly damaging |
Het |
Meox2 |
A |
G |
12: 37,217,476 (GRCm39) |
T226A |
probably damaging |
Het |
Mipol1 |
A |
G |
12: 57,352,842 (GRCm39) |
|
probably null |
Het |
Mms22l |
T |
G |
4: 24,591,084 (GRCm39) |
N1018K |
probably benign |
Het |
Mn1 |
T |
C |
5: 111,602,617 (GRCm39) |
I1285T |
possibly damaging |
Het |
Muc20 |
T |
G |
16: 32,614,547 (GRCm39) |
S277R |
probably damaging |
Het |
Muc6 |
C |
A |
7: 141,213,991 (GRCm39) |
V2845L |
probably benign |
Het |
Mup5 |
C |
A |
4: 61,751,962 (GRCm39) |
G96C |
probably damaging |
Het |
Neb |
T |
A |
2: 52,146,826 (GRCm39) |
M2813L |
probably benign |
Het |
Neb |
C |
A |
2: 52,161,570 (GRCm39) |
R2074L |
probably damaging |
Het |
Oasl2 |
A |
T |
5: 115,049,063 (GRCm39) |
K168* |
probably null |
Het |
Or6c5 |
T |
C |
10: 129,074,368 (GRCm39) |
S117P |
probably damaging |
Het |
P2rx2 |
C |
T |
5: 110,489,007 (GRCm39) |
D203N |
probably damaging |
Het |
Ptprg |
T |
C |
14: 11,952,897 (GRCm38) |
|
probably null |
Het |
Rims4 |
C |
T |
2: 163,706,785 (GRCm39) |
|
probably null |
Het |
Rtn4ip1 |
T |
A |
10: 43,808,402 (GRCm39) |
W60R |
probably benign |
Het |
Sccpdh |
T |
C |
1: 179,498,162 (GRCm39) |
S69P |
probably benign |
Het |
Serpina3b |
T |
A |
12: 104,105,069 (GRCm39) |
I415N |
probably benign |
Het |
Slc22a4 |
T |
C |
11: 53,874,436 (GRCm39) |
|
probably benign |
Het |
Slc4a5 |
G |
A |
6: 83,274,360 (GRCm39) |
A1076T |
probably benign |
Het |
Slit1 |
T |
C |
19: 41,590,686 (GRCm39) |
K1329E |
possibly damaging |
Het |
Synj2bp |
A |
C |
12: 81,548,826 (GRCm39) |
F138V |
probably benign |
Het |
Taar7a |
T |
C |
10: 23,868,959 (GRCm39) |
I141V |
probably damaging |
Het |
Tas1r3 |
T |
C |
4: 155,946,588 (GRCm39) |
E339G |
probably benign |
Het |
Tep1 |
A |
G |
14: 51,088,037 (GRCm39) |
|
probably benign |
Het |
Tgds |
A |
T |
14: 118,359,149 (GRCm39) |
Y146* |
probably null |
Het |
Tgm3 |
G |
A |
2: 129,879,403 (GRCm39) |
V332I |
probably benign |
Het |
Tnnt2 |
A |
G |
1: 135,771,547 (GRCm39) |
|
probably benign |
Het |
Top1 |
T |
A |
2: 160,546,739 (GRCm39) |
Y340N |
probably damaging |
Het |
Topbp1 |
T |
C |
9: 103,195,181 (GRCm39) |
|
probably benign |
Het |
Tpst1 |
A |
G |
5: 130,131,202 (GRCm39) |
N224S |
probably benign |
Het |
Traf4 |
A |
G |
11: 78,050,840 (GRCm39) |
F439L |
probably damaging |
Het |
Trim58 |
A |
G |
11: 58,533,964 (GRCm39) |
|
probably benign |
Het |
Tspan31 |
T |
C |
10: 126,904,004 (GRCm39) |
N205S |
probably damaging |
Het |
Ube3a |
T |
A |
7: 58,926,225 (GRCm39) |
N334K |
possibly damaging |
Het |
Ugt2a3 |
A |
T |
5: 87,477,541 (GRCm39) |
|
probably null |
Het |
Vwf |
G |
A |
6: 125,623,293 (GRCm39) |
V1797I |
probably benign |
Het |
Wdr81 |
G |
T |
11: 75,343,809 (GRCm39) |
P486Q |
probably damaging |
Het |
Whamm |
C |
T |
7: 81,241,519 (GRCm39) |
R277* |
probably null |
Het |
Yipf7 |
T |
A |
5: 69,678,462 (GRCm39) |
N56I |
possibly damaging |
Het |
Zfp523 |
A |
T |
17: 28,414,190 (GRCm39) |
T75S |
probably benign |
Het |
|
Other mutations in Mdn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Mdn1
|
APN |
4 |
32,723,651 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00426:Mdn1
|
APN |
4 |
32,719,214 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL00570:Mdn1
|
APN |
4 |
32,735,719 (GRCm39) |
missense |
probably benign |
|
IGL00573:Mdn1
|
APN |
4 |
32,666,619 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00983:Mdn1
|
APN |
4 |
32,735,525 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01288:Mdn1
|
APN |
4 |
32,730,864 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01359:Mdn1
|
APN |
4 |
32,743,686 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01457:Mdn1
|
APN |
4 |
32,715,922 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01530:Mdn1
|
APN |
4 |
32,711,938 (GRCm39) |
splice site |
probably benign |
|
IGL01684:Mdn1
|
APN |
4 |
32,726,857 (GRCm39) |
missense |
probably benign |
|
IGL01753:Mdn1
|
APN |
4 |
32,708,483 (GRCm39) |
missense |
probably benign |
|
IGL01901:Mdn1
|
APN |
4 |
32,669,591 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01952:Mdn1
|
APN |
4 |
32,723,657 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01960:Mdn1
|
APN |
4 |
32,758,393 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02019:Mdn1
|
APN |
4 |
32,749,948 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02100:Mdn1
|
APN |
4 |
32,715,708 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02117:Mdn1
|
APN |
4 |
32,709,364 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02154:Mdn1
|
APN |
4 |
32,740,395 (GRCm39) |
missense |
probably benign |
0.35 |
IGL02216:Mdn1
|
APN |
4 |
32,739,092 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02371:Mdn1
|
APN |
4 |
32,676,860 (GRCm39) |
splice site |
probably benign |
|
IGL02396:Mdn1
|
APN |
4 |
32,700,120 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02454:Mdn1
|
APN |
4 |
32,694,674 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02502:Mdn1
|
APN |
4 |
32,670,579 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02883:Mdn1
|
APN |
4 |
32,763,199 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02946:Mdn1
|
APN |
4 |
32,734,366 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02950:Mdn1
|
APN |
4 |
32,713,360 (GRCm39) |
splice site |
probably benign |
|
IGL03076:Mdn1
|
APN |
4 |
32,735,564 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03129:Mdn1
|
APN |
4 |
32,729,994 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL03234:Mdn1
|
APN |
4 |
32,732,842 (GRCm39) |
missense |
probably benign |
0.06 |
3-1:Mdn1
|
UTSW |
4 |
32,725,967 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03046:Mdn1
|
UTSW |
4 |
32,694,495 (GRCm39) |
missense |
possibly damaging |
0.73 |
P0035:Mdn1
|
UTSW |
4 |
32,749,934 (GRCm39) |
missense |
probably benign |
0.05 |
PIT4508001:Mdn1
|
UTSW |
4 |
32,719,223 (GRCm39) |
missense |
probably damaging |
0.97 |
PIT4618001:Mdn1
|
UTSW |
4 |
32,746,527 (GRCm39) |
missense |
probably benign |
0.20 |
R0008:Mdn1
|
UTSW |
4 |
32,718,317 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0110:Mdn1
|
UTSW |
4 |
32,738,619 (GRCm39) |
missense |
probably benign |
0.20 |
R0125:Mdn1
|
UTSW |
4 |
32,729,956 (GRCm39) |
missense |
probably damaging |
0.98 |
R0257:Mdn1
|
UTSW |
4 |
32,693,534 (GRCm39) |
missense |
probably damaging |
0.99 |
R0266:Mdn1
|
UTSW |
4 |
32,741,835 (GRCm39) |
missense |
probably damaging |
0.99 |
R0349:Mdn1
|
UTSW |
4 |
32,750,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R0362:Mdn1
|
UTSW |
4 |
32,746,439 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0421:Mdn1
|
UTSW |
4 |
32,684,707 (GRCm39) |
missense |
probably benign |
0.39 |
R0450:Mdn1
|
UTSW |
4 |
32,738,619 (GRCm39) |
missense |
probably benign |
0.20 |
R0465:Mdn1
|
UTSW |
4 |
32,699,204 (GRCm39) |
splice site |
probably benign |
|
R0469:Mdn1
|
UTSW |
4 |
32,738,619 (GRCm39) |
missense |
probably benign |
0.20 |
R0477:Mdn1
|
UTSW |
4 |
32,750,928 (GRCm39) |
missense |
probably benign |
0.02 |
R0481:Mdn1
|
UTSW |
4 |
32,767,182 (GRCm39) |
splice site |
probably benign |
|
R0504:Mdn1
|
UTSW |
4 |
32,698,916 (GRCm39) |
splice site |
probably benign |
|
R0522:Mdn1
|
UTSW |
4 |
32,672,837 (GRCm39) |
missense |
probably benign |
0.09 |
R0550:Mdn1
|
UTSW |
4 |
32,730,479 (GRCm39) |
missense |
probably benign |
0.13 |
R0607:Mdn1
|
UTSW |
4 |
32,732,829 (GRCm39) |
missense |
probably benign |
0.36 |
R0607:Mdn1
|
UTSW |
4 |
32,712,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R0664:Mdn1
|
UTSW |
4 |
32,768,011 (GRCm39) |
nonsense |
probably null |
|
R0701:Mdn1
|
UTSW |
4 |
32,699,263 (GRCm39) |
missense |
probably benign |
0.00 |
R0801:Mdn1
|
UTSW |
4 |
32,668,895 (GRCm39) |
missense |
probably benign |
0.04 |
R0841:Mdn1
|
UTSW |
4 |
32,752,032 (GRCm39) |
missense |
probably benign |
0.23 |
R0849:Mdn1
|
UTSW |
4 |
32,741,835 (GRCm39) |
missense |
probably damaging |
0.99 |
R0893:Mdn1
|
UTSW |
4 |
32,701,713 (GRCm39) |
missense |
probably benign |
0.01 |
R1114:Mdn1
|
UTSW |
4 |
32,746,568 (GRCm39) |
critical splice donor site |
probably null |
|
R1137:Mdn1
|
UTSW |
4 |
32,694,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R1185:Mdn1
|
UTSW |
4 |
32,735,576 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1185:Mdn1
|
UTSW |
4 |
32,735,576 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1185:Mdn1
|
UTSW |
4 |
32,735,576 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1257:Mdn1
|
UTSW |
4 |
32,667,089 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1356:Mdn1
|
UTSW |
4 |
32,700,334 (GRCm39) |
splice site |
probably benign |
|
R1466:Mdn1
|
UTSW |
4 |
32,730,788 (GRCm39) |
missense |
probably benign |
0.28 |
R1466:Mdn1
|
UTSW |
4 |
32,730,788 (GRCm39) |
missense |
probably benign |
0.28 |
R1518:Mdn1
|
UTSW |
4 |
32,739,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R1569:Mdn1
|
UTSW |
4 |
32,723,501 (GRCm39) |
missense |
probably null |
0.10 |
R1574:Mdn1
|
UTSW |
4 |
32,722,315 (GRCm39) |
missense |
probably benign |
|
R1574:Mdn1
|
UTSW |
4 |
32,722,315 (GRCm39) |
missense |
probably benign |
|
R1591:Mdn1
|
UTSW |
4 |
32,700,092 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1678:Mdn1
|
UTSW |
4 |
32,663,050 (GRCm39) |
missense |
probably damaging |
0.99 |
R1696:Mdn1
|
UTSW |
4 |
32,700,417 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1707:Mdn1
|
UTSW |
4 |
32,693,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R1749:Mdn1
|
UTSW |
4 |
32,773,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R1780:Mdn1
|
UTSW |
4 |
32,700,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R1833:Mdn1
|
UTSW |
4 |
32,720,761 (GRCm39) |
missense |
probably damaging |
0.97 |
R1858:Mdn1
|
UTSW |
4 |
32,730,881 (GRCm39) |
missense |
probably benign |
0.17 |
R1870:Mdn1
|
UTSW |
4 |
32,763,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R1887:Mdn1
|
UTSW |
4 |
32,742,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R1909:Mdn1
|
UTSW |
4 |
32,760,839 (GRCm39) |
small deletion |
probably benign |
|
R2075:Mdn1
|
UTSW |
4 |
32,716,058 (GRCm39) |
missense |
probably benign |
0.03 |
R2103:Mdn1
|
UTSW |
4 |
32,738,712 (GRCm39) |
missense |
possibly damaging |
0.75 |
R2110:Mdn1
|
UTSW |
4 |
32,700,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R2111:Mdn1
|
UTSW |
4 |
32,700,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R2206:Mdn1
|
UTSW |
4 |
32,716,271 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2221:Mdn1
|
UTSW |
4 |
32,763,306 (GRCm39) |
missense |
probably benign |
0.37 |
R2240:Mdn1
|
UTSW |
4 |
32,765,701 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2351:Mdn1
|
UTSW |
4 |
32,750,010 (GRCm39) |
missense |
probably benign |
0.21 |
R2421:Mdn1
|
UTSW |
4 |
32,723,621 (GRCm39) |
missense |
probably damaging |
0.96 |
R3036:Mdn1
|
UTSW |
4 |
32,750,013 (GRCm39) |
missense |
probably damaging |
0.99 |
R3434:Mdn1
|
UTSW |
4 |
32,733,726 (GRCm39) |
critical splice donor site |
probably null |
|
R3435:Mdn1
|
UTSW |
4 |
32,733,726 (GRCm39) |
critical splice donor site |
probably null |
|
R3783:Mdn1
|
UTSW |
4 |
32,720,818 (GRCm39) |
missense |
probably benign |
0.01 |
R3811:Mdn1
|
UTSW |
4 |
32,693,506 (GRCm39) |
nonsense |
probably null |
|
R3973:Mdn1
|
UTSW |
4 |
32,722,363 (GRCm39) |
missense |
probably benign |
0.00 |
R4154:Mdn1
|
UTSW |
4 |
32,707,475 (GRCm39) |
missense |
probably damaging |
0.96 |
R4372:Mdn1
|
UTSW |
4 |
32,743,809 (GRCm39) |
missense |
probably benign |
0.03 |
R4393:Mdn1
|
UTSW |
4 |
32,754,482 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4438:Mdn1
|
UTSW |
4 |
32,704,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R4471:Mdn1
|
UTSW |
4 |
32,668,860 (GRCm39) |
missense |
probably benign |
0.00 |
R4509:Mdn1
|
UTSW |
4 |
32,715,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R4538:Mdn1
|
UTSW |
4 |
32,722,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R4557:Mdn1
|
UTSW |
4 |
32,754,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R4570:Mdn1
|
UTSW |
4 |
32,741,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R4591:Mdn1
|
UTSW |
4 |
32,707,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R4658:Mdn1
|
UTSW |
4 |
32,730,749 (GRCm39) |
splice site |
probably null |
|
R4667:Mdn1
|
UTSW |
4 |
32,679,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R4684:Mdn1
|
UTSW |
4 |
32,666,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R4778:Mdn1
|
UTSW |
4 |
32,683,583 (GRCm39) |
nonsense |
probably null |
|
R4807:Mdn1
|
UTSW |
4 |
32,685,651 (GRCm39) |
splice site |
probably null |
|
R4923:Mdn1
|
UTSW |
4 |
32,671,608 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4951:Mdn1
|
UTSW |
4 |
32,707,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R4963:Mdn1
|
UTSW |
4 |
32,756,512 (GRCm39) |
missense |
probably benign |
0.00 |
R4971:Mdn1
|
UTSW |
4 |
32,739,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R4973:Mdn1
|
UTSW |
4 |
32,734,418 (GRCm39) |
missense |
probably benign |
0.01 |
R5122:Mdn1
|
UTSW |
4 |
32,670,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R5159:Mdn1
|
UTSW |
4 |
32,774,008 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5164:Mdn1
|
UTSW |
4 |
32,759,011 (GRCm39) |
splice site |
probably null |
|
R5215:Mdn1
|
UTSW |
4 |
32,741,418 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5217:Mdn1
|
UTSW |
4 |
32,723,690 (GRCm39) |
missense |
probably damaging |
0.98 |
R5219:Mdn1
|
UTSW |
4 |
32,723,690 (GRCm39) |
missense |
probably damaging |
0.98 |
R5365:Mdn1
|
UTSW |
4 |
32,723,690 (GRCm39) |
missense |
probably damaging |
0.98 |
R5366:Mdn1
|
UTSW |
4 |
32,723,690 (GRCm39) |
missense |
probably damaging |
0.98 |
R5368:Mdn1
|
UTSW |
4 |
32,723,690 (GRCm39) |
missense |
probably damaging |
0.98 |
R5445:Mdn1
|
UTSW |
4 |
32,723,690 (GRCm39) |
missense |
probably damaging |
0.98 |
R5462:Mdn1
|
UTSW |
4 |
32,720,897 (GRCm39) |
missense |
probably benign |
|
R5522:Mdn1
|
UTSW |
4 |
32,685,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R5525:Mdn1
|
UTSW |
4 |
32,767,961 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5578:Mdn1
|
UTSW |
4 |
32,728,167 (GRCm39) |
missense |
probably benign |
0.04 |
R5605:Mdn1
|
UTSW |
4 |
32,765,664 (GRCm39) |
missense |
probably benign |
|
R5621:Mdn1
|
UTSW |
4 |
32,716,371 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5636:Mdn1
|
UTSW |
4 |
32,695,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R5650:Mdn1
|
UTSW |
4 |
32,667,467 (GRCm39) |
splice site |
probably null |
|
R5780:Mdn1
|
UTSW |
4 |
32,722,950 (GRCm39) |
missense |
probably benign |
0.02 |
R5838:Mdn1
|
UTSW |
4 |
32,754,547 (GRCm39) |
missense |
probably damaging |
0.99 |
R5857:Mdn1
|
UTSW |
4 |
32,670,646 (GRCm39) |
missense |
probably benign |
0.09 |
R5895:Mdn1
|
UTSW |
4 |
32,695,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R5943:Mdn1
|
UTSW |
4 |
32,678,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R6008:Mdn1
|
UTSW |
4 |
32,741,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R6013:Mdn1
|
UTSW |
4 |
32,715,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R6075:Mdn1
|
UTSW |
4 |
32,689,581 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6151:Mdn1
|
UTSW |
4 |
32,684,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R6163:Mdn1
|
UTSW |
4 |
32,716,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R6181:Mdn1
|
UTSW |
4 |
32,715,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R6211:Mdn1
|
UTSW |
4 |
32,696,269 (GRCm39) |
missense |
probably benign |
0.12 |
R6249:Mdn1
|
UTSW |
4 |
32,708,484 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6251:Mdn1
|
UTSW |
4 |
32,748,590 (GRCm39) |
missense |
probably benign |
0.13 |
R6253:Mdn1
|
UTSW |
4 |
32,749,593 (GRCm39) |
missense |
probably benign |
0.25 |
R6273:Mdn1
|
UTSW |
4 |
32,715,979 (GRCm39) |
missense |
probably benign |
0.01 |
R6297:Mdn1
|
UTSW |
4 |
32,730,054 (GRCm39) |
nonsense |
probably null |
|
R6384:Mdn1
|
UTSW |
4 |
32,670,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R6463:Mdn1
|
UTSW |
4 |
32,773,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R6528:Mdn1
|
UTSW |
4 |
32,713,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R6688:Mdn1
|
UTSW |
4 |
32,774,041 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6762:Mdn1
|
UTSW |
4 |
32,676,786 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6794:Mdn1
|
UTSW |
4 |
32,741,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R6894:Mdn1
|
UTSW |
4 |
32,748,614 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6935:Mdn1
|
UTSW |
4 |
32,774,041 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6980:Mdn1
|
UTSW |
4 |
32,726,942 (GRCm39) |
critical splice donor site |
probably null |
|
R6995:Mdn1
|
UTSW |
4 |
32,733,374 (GRCm39) |
missense |
probably benign |
0.03 |
R7048:Mdn1
|
UTSW |
4 |
32,767,969 (GRCm39) |
missense |
probably benign |
0.00 |
R7082:Mdn1
|
UTSW |
4 |
32,762,341 (GRCm39) |
missense |
probably benign |
|
R7158:Mdn1
|
UTSW |
4 |
32,725,121 (GRCm39) |
missense |
probably benign |
0.09 |
R7166:Mdn1
|
UTSW |
4 |
32,746,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R7168:Mdn1
|
UTSW |
4 |
32,719,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R7175:Mdn1
|
UTSW |
4 |
32,694,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R7195:Mdn1
|
UTSW |
4 |
32,701,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R7250:Mdn1
|
UTSW |
4 |
32,695,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R7274:Mdn1
|
UTSW |
4 |
32,725,944 (GRCm39) |
missense |
probably benign |
0.12 |
R7330:Mdn1
|
UTSW |
4 |
32,723,685 (GRCm39) |
missense |
probably benign |
0.16 |
R7363:Mdn1
|
UTSW |
4 |
32,691,729 (GRCm39) |
missense |
probably damaging |
0.99 |
R7369:Mdn1
|
UTSW |
4 |
32,773,375 (GRCm39) |
missense |
probably damaging |
0.99 |
R7452:Mdn1
|
UTSW |
4 |
32,739,030 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7523:Mdn1
|
UTSW |
4 |
32,667,270 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7594:Mdn1
|
UTSW |
4 |
32,696,359 (GRCm39) |
missense |
probably benign |
0.27 |
R7605:Mdn1
|
UTSW |
4 |
32,694,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R7661:Mdn1
|
UTSW |
4 |
32,691,229 (GRCm39) |
missense |
probably benign |
0.08 |
R7689:Mdn1
|
UTSW |
4 |
32,739,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Mdn1
|
UTSW |
4 |
32,741,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R7700:Mdn1
|
UTSW |
4 |
32,741,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R7714:Mdn1
|
UTSW |
4 |
32,722,360 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7718:Mdn1
|
UTSW |
4 |
32,718,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R7762:Mdn1
|
UTSW |
4 |
32,734,421 (GRCm39) |
missense |
probably benign |
|
R7787:Mdn1
|
UTSW |
4 |
32,741,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R8111:Mdn1
|
UTSW |
4 |
32,674,003 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8222:Mdn1
|
UTSW |
4 |
32,707,477 (GRCm39) |
missense |
probably benign |
0.09 |
R8246:Mdn1
|
UTSW |
4 |
32,657,284 (GRCm39) |
missense |
probably benign |
0.06 |
R8267:Mdn1
|
UTSW |
4 |
32,742,485 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8286:Mdn1
|
UTSW |
4 |
32,731,960 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8305:Mdn1
|
UTSW |
4 |
32,725,107 (GRCm39) |
missense |
probably benign |
|
R8318:Mdn1
|
UTSW |
4 |
32,735,897 (GRCm39) |
critical splice donor site |
probably null |
|
R8379:Mdn1
|
UTSW |
4 |
32,756,453 (GRCm39) |
missense |
probably null |
1.00 |
R8384:Mdn1
|
UTSW |
4 |
32,765,680 (GRCm39) |
missense |
probably benign |
0.05 |
R8514:Mdn1
|
UTSW |
4 |
32,739,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R8560:Mdn1
|
UTSW |
4 |
32,743,830 (GRCm39) |
missense |
probably benign |
0.08 |
R8672:Mdn1
|
UTSW |
4 |
32,768,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R8708:Mdn1
|
UTSW |
4 |
32,725,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R8769:Mdn1
|
UTSW |
4 |
32,751,390 (GRCm39) |
missense |
probably damaging |
0.97 |
R8896:Mdn1
|
UTSW |
4 |
32,678,328 (GRCm39) |
missense |
probably benign |
0.28 |
R8918:Mdn1
|
UTSW |
4 |
32,744,579 (GRCm39) |
nonsense |
probably null |
|
R8920:Mdn1
|
UTSW |
4 |
32,719,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R8966:Mdn1
|
UTSW |
4 |
32,672,837 (GRCm39) |
nonsense |
probably null |
|
R8997:Mdn1
|
UTSW |
4 |
32,773,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R9120:Mdn1
|
UTSW |
4 |
32,701,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R9129:Mdn1
|
UTSW |
4 |
32,676,812 (GRCm39) |
missense |
probably benign |
0.24 |
R9131:Mdn1
|
UTSW |
4 |
32,762,275 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9200:Mdn1
|
UTSW |
4 |
32,760,791 (GRCm39) |
missense |
probably benign |
0.00 |
R9226:Mdn1
|
UTSW |
4 |
32,694,612 (GRCm39) |
missense |
probably benign |
0.25 |
R9235:Mdn1
|
UTSW |
4 |
32,739,122 (GRCm39) |
missense |
probably benign |
0.10 |
R9293:Mdn1
|
UTSW |
4 |
32,707,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R9315:Mdn1
|
UTSW |
4 |
32,760,911 (GRCm39) |
missense |
probably benign |
0.00 |
R9338:Mdn1
|
UTSW |
4 |
32,666,536 (GRCm39) |
missense |
probably benign |
0.00 |
R9353:Mdn1
|
UTSW |
4 |
32,693,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R9393:Mdn1
|
UTSW |
4 |
32,713,825 (GRCm39) |
missense |
|
|
R9420:Mdn1
|
UTSW |
4 |
32,678,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R9475:Mdn1
|
UTSW |
4 |
32,739,849 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9583:Mdn1
|
UTSW |
4 |
32,741,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R9600:Mdn1
|
UTSW |
4 |
32,684,723 (GRCm39) |
nonsense |
probably null |
|
R9640:Mdn1
|
UTSW |
4 |
32,754,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R9688:Mdn1
|
UTSW |
4 |
32,745,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R9744:Mdn1
|
UTSW |
4 |
32,715,711 (GRCm39) |
missense |
possibly damaging |
0.91 |
X0066:Mdn1
|
UTSW |
4 |
32,739,030 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Mdn1
|
UTSW |
4 |
32,696,244 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Mdn1
|
UTSW |
4 |
32,668,944 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Mdn1
|
UTSW |
4 |
32,667,102 (GRCm39) |
missense |
probably benign |
0.01 |
|