Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610040J01Rik |
T |
A |
5: 64,055,561 (GRCm39) |
I99N |
probably damaging |
Het |
Ank3 |
G |
A |
10: 69,838,395 (GRCm39) |
R1566K |
possibly damaging |
Het |
Ankrd31 |
A |
G |
13: 96,988,181 (GRCm39) |
I1065V |
possibly damaging |
Het |
Aox1 |
A |
G |
1: 58,378,831 (GRCm39) |
T1027A |
probably benign |
Het |
Atm |
G |
A |
9: 53,399,222 (GRCm39) |
P1593L |
probably benign |
Het |
Atp13a5 |
T |
G |
16: 29,167,555 (GRCm39) |
I132L |
probably benign |
Het |
BC035044 |
A |
G |
6: 128,867,852 (GRCm39) |
|
probably benign |
Het |
Cadm3 |
CT |
C |
1: 173,176,691 (GRCm39) |
|
probably benign |
Homo |
Car3 |
C |
T |
3: 14,936,677 (GRCm39) |
P247S |
probably benign |
Het |
Ccdc7a |
T |
C |
8: 129,513,819 (GRCm39) |
Y160C |
probably damaging |
Het |
Cd1d1 |
A |
G |
3: 86,905,564 (GRCm39) |
V143A |
probably benign |
Het |
Cemip2 |
T |
A |
19: 21,779,369 (GRCm39) |
V393E |
probably damaging |
Het |
Cog6 |
A |
T |
3: 52,903,473 (GRCm39) |
F142I |
probably damaging |
Het |
Cracd |
A |
T |
5: 77,005,568 (GRCm39) |
D643V |
unknown |
Het |
Crhr1 |
T |
G |
11: 104,054,682 (GRCm39) |
N98K |
possibly damaging |
Het |
Csf1 |
A |
G |
3: 107,656,479 (GRCm39) |
V72A |
probably damaging |
Het |
Cwc15 |
T |
A |
9: 14,421,537 (GRCm39) |
I201K |
probably benign |
Het |
Dgka |
T |
C |
10: 128,559,515 (GRCm39) |
K482R |
probably benign |
Het |
Dnah7b |
T |
C |
1: 46,281,476 (GRCm39) |
S2846P |
possibly damaging |
Het |
Dst |
T |
A |
1: 34,314,347 (GRCm39) |
I4199N |
probably damaging |
Het |
Dusp7 |
A |
G |
9: 106,251,095 (GRCm39) |
T407A |
possibly damaging |
Het |
Eml2 |
G |
A |
7: 18,935,088 (GRCm39) |
V432I |
probably damaging |
Het |
Fem1a |
T |
C |
17: 56,564,083 (GRCm39) |
Y59H |
possibly damaging |
Het |
Fetub |
C |
T |
16: 22,751,081 (GRCm39) |
R143C |
probably damaging |
Het |
Filip1 |
A |
T |
9: 79,723,168 (GRCm39) |
D1150E |
probably benign |
Het |
Gabra1 |
A |
G |
11: 42,031,138 (GRCm39) |
V264A |
probably damaging |
Het |
Gm4131 |
T |
C |
14: 62,702,299 (GRCm39) |
E223G |
probably damaging |
Het |
Gon4l |
T |
C |
3: 88,763,156 (GRCm39) |
V333A |
probably damaging |
Het |
Gsk3b |
A |
G |
16: 38,028,408 (GRCm39) |
T289A |
probably benign |
Het |
Hmcn2 |
T |
C |
2: 31,301,846 (GRCm39) |
S2912P |
probably damaging |
Het |
Htr7 |
A |
T |
19: 36,018,969 (GRCm39) |
|
probably benign |
Het |
Ibsp |
A |
G |
5: 104,458,167 (GRCm39) |
T235A |
probably benign |
Het |
Ints13 |
A |
T |
6: 146,467,179 (GRCm39) |
D116E |
probably damaging |
Het |
Irag1 |
G |
T |
7: 110,470,790 (GRCm39) |
H848N |
probably benign |
Het |
Kctd19 |
T |
C |
8: 106,112,117 (GRCm39) |
N753S |
probably benign |
Het |
Mink1 |
A |
T |
11: 70,502,261 (GRCm39) |
K880* |
probably null |
Het |
Myo15b |
T |
A |
11: 115,753,625 (GRCm39) |
L824Q |
possibly damaging |
Het |
Napepld |
T |
C |
5: 21,870,320 (GRCm39) |
E366G |
probably benign |
Het |
Obscn |
T |
A |
11: 58,967,819 (GRCm39) |
T2662S |
possibly damaging |
Het |
Or2g7 |
T |
G |
17: 38,378,686 (GRCm39) |
L208R |
probably damaging |
Het |
Or2n1b |
T |
A |
17: 38,459,833 (GRCm39) |
M118K |
possibly damaging |
Het |
Or4k52 |
T |
C |
2: 111,611,567 (GRCm39) |
F301L |
probably benign |
Het |
Or52p1 |
A |
G |
7: 104,267,102 (GRCm39) |
D72G |
probably damaging |
Het |
Or5b12 |
A |
G |
19: 12,896,764 (GRCm39) |
V303A |
probably benign |
Het |
Or6d13 |
A |
G |
6: 116,518,277 (GRCm39) |
T288A |
possibly damaging |
Het |
Pah |
T |
C |
10: 87,412,077 (GRCm39) |
|
probably null |
Het |
Panx3 |
T |
G |
9: 37,578,725 (GRCm39) |
I85L |
probably benign |
Het |
Pate4 |
T |
C |
9: 35,519,086 (GRCm39) |
N94D |
probably benign |
Het |
Pde4d |
A |
G |
13: 110,086,755 (GRCm39) |
M610V |
possibly damaging |
Het |
Pik3c2b |
T |
C |
1: 132,994,449 (GRCm39) |
S138P |
probably benign |
Het |
Pkn1 |
T |
C |
8: 84,398,899 (GRCm39) |
N696S |
probably damaging |
Het |
Plppr2 |
A |
G |
9: 21,855,801 (GRCm39) |
E258G |
probably damaging |
Het |
Plxnd1 |
A |
T |
6: 115,955,453 (GRCm39) |
M538K |
probably damaging |
Het |
Prepl |
G |
T |
17: 85,390,696 (GRCm39) |
N87K |
probably benign |
Het |
Prkag2 |
C |
A |
5: 25,152,534 (GRCm39) |
R190L |
probably damaging |
Het |
Rara |
A |
G |
11: 98,861,048 (GRCm39) |
T179A |
probably benign |
Het |
Rfx7 |
A |
G |
9: 72,524,279 (GRCm39) |
K490E |
possibly damaging |
Het |
Rgsl1 |
C |
T |
1: 153,703,211 (GRCm39) |
V147M |
possibly damaging |
Het |
Rph3a |
A |
G |
5: 121,083,485 (GRCm39) |
I595T |
possibly damaging |
Het |
Rsf1 |
CG |
CGACGGCGGTG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Homo |
Slc35e2 |
C |
T |
4: 155,694,483 (GRCm39) |
P10L |
probably benign |
Het |
Slc8a2 |
T |
C |
7: 15,879,259 (GRCm39) |
F582L |
possibly damaging |
Het |
Sprr2e |
A |
G |
3: 92,260,171 (GRCm39) |
M1V |
probably null |
Het |
Steap1 |
T |
A |
5: 5,790,827 (GRCm39) |
R40S |
possibly damaging |
Het |
Tbc1d2 |
C |
T |
4: 46,629,912 (GRCm39) |
G252R |
probably benign |
Het |
Thsd7a |
A |
T |
6: 12,408,835 (GRCm39) |
V729E |
probably damaging |
Het |
Tmprss13 |
A |
G |
9: 45,256,630 (GRCm39) |
Y525C |
probably damaging |
Het |
Tnik |
A |
T |
3: 28,631,649 (GRCm39) |
H383L |
possibly damaging |
Het |
Vars1 |
T |
C |
17: 35,232,719 (GRCm39) |
L881S |
probably damaging |
Het |
Vmn1r201 |
A |
C |
13: 22,659,385 (GRCm39) |
S200R |
probably damaging |
Het |
Vmn2r130 |
A |
T |
17: 23,295,759 (GRCm39) |
H643L |
probably benign |
Het |
Vmn2r14 |
A |
T |
5: 109,369,133 (GRCm39) |
W147R |
probably benign |
Het |
Vps53 |
T |
C |
11: 75,992,844 (GRCm39) |
E367G |
probably benign |
Het |
Xab2 |
C |
T |
8: 3,661,822 (GRCm39) |
G544S |
probably damaging |
Het |
Ythdf3 |
T |
A |
3: 16,259,020 (GRCm39) |
V400E |
possibly damaging |
Het |
Zfand5 |
C |
T |
19: 21,257,060 (GRCm39) |
P147S |
probably benign |
Het |
Zfp768 |
A |
T |
7: 126,944,319 (GRCm39) |
|
probably null |
Het |
Zswim8 |
A |
G |
14: 20,763,521 (GRCm39) |
M423V |
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 |
R2104:Mdn1
|
UTSW |
4 |
32,743,843 (GRCm39) |
splice site |
probably null |
|
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 |
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 |
|