Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A930011G23Rik |
A |
G |
5: 99,377,236 (GRCm39) |
S404P |
probably damaging |
Het |
A930011G23Rik |
G |
A |
5: 99,377,241 (GRCm39) |
P402L |
probably damaging |
Het |
Abca6 |
A |
G |
11: 110,109,832 (GRCm39) |
|
probably benign |
Het |
Adarb2 |
A |
T |
13: 8,619,756 (GRCm39) |
R81W |
probably damaging |
Het |
Adgrf4 |
T |
C |
17: 42,983,467 (GRCm39) |
I72V |
probably benign |
Het |
Banp |
A |
G |
8: 122,733,830 (GRCm39) |
I360V |
probably benign |
Het |
Bmp8a |
C |
A |
4: 123,210,220 (GRCm39) |
G289C |
possibly damaging |
Het |
Car3 |
A |
T |
3: 14,931,911 (GRCm39) |
H94L |
probably damaging |
Het |
Ccdc137 |
G |
A |
11: 120,350,927 (GRCm39) |
R108H |
possibly damaging |
Het |
Cdk14 |
T |
C |
5: 4,938,905 (GRCm39) |
N411S |
probably benign |
Het |
Col4a2 |
A |
G |
8: 11,483,800 (GRCm39) |
M907V |
probably benign |
Het |
Cyp4f17 |
T |
A |
17: 32,725,923 (GRCm39) |
W19R |
possibly damaging |
Het |
Eif2d |
T |
G |
1: 131,081,097 (GRCm39) |
|
probably benign |
Het |
Epx |
A |
G |
11: 87,762,144 (GRCm39) |
I369T |
possibly damaging |
Het |
Fcgbp |
A |
G |
7: 27,789,378 (GRCm39) |
E648G |
probably benign |
Het |
Fer1l4 |
G |
A |
2: 155,894,827 (GRCm39) |
P14L |
probably benign |
Het |
Folr1 |
A |
G |
7: 101,507,732 (GRCm39) |
F236S |
probably benign |
Het |
Foxj2 |
T |
G |
6: 122,819,732 (GRCm39) |
M540R |
possibly damaging |
Het |
Gtf2h1 |
A |
G |
7: 46,464,824 (GRCm39) |
T420A |
probably benign |
Het |
H2-T3 |
T |
A |
17: 36,498,248 (GRCm39) |
T222S |
probably damaging |
Het |
Ice1 |
A |
T |
13: 70,740,718 (GRCm39) |
M2163K |
probably damaging |
Het |
Inppl1 |
A |
G |
7: 101,481,450 (GRCm39) |
V244A |
probably benign |
Het |
Kansl3 |
A |
T |
1: 36,391,050 (GRCm39) |
V373D |
probably damaging |
Het |
Kdm3a |
A |
G |
6: 71,590,987 (GRCm39) |
|
probably benign |
Het |
Krtap1-3 |
A |
T |
11: 99,481,680 (GRCm39) |
C156S |
unknown |
Het |
Mab21l3 |
T |
C |
3: 101,726,045 (GRCm39) |
D317G |
probably damaging |
Het |
Nherf1 |
A |
G |
11: 115,054,539 (GRCm39) |
|
probably null |
Het |
Nox3 |
T |
C |
17: 3,733,191 (GRCm39) |
H240R |
probably damaging |
Het |
Nxn |
A |
T |
11: 76,164,858 (GRCm39) |
S218T |
probably benign |
Het |
Or5h22 |
A |
T |
16: 58,894,630 (GRCm39) |
I271K |
probably benign |
Het |
Or6c35 |
G |
A |
10: 129,169,397 (GRCm39) |
V216I |
probably benign |
Het |
Pcdhb13 |
T |
C |
18: 37,577,392 (GRCm39) |
V590A |
possibly damaging |
Het |
Pim3 |
T |
C |
15: 88,747,734 (GRCm39) |
V200A |
probably benign |
Het |
Plekha3 |
T |
C |
2: 76,510,524 (GRCm39) |
F20L |
probably damaging |
Het |
Pmp22 |
G |
T |
11: 63,049,118 (GRCm39) |
R120S |
possibly damaging |
Het |
Ppp1r9a |
A |
C |
6: 4,906,537 (GRCm39) |
D364A |
probably benign |
Het |
Psd |
A |
G |
19: 46,302,943 (GRCm39) |
F155L |
possibly damaging |
Het |
Rbm22 |
T |
C |
18: 60,704,891 (GRCm39) |
|
probably benign |
Het |
Ror2 |
C |
T |
13: 53,264,764 (GRCm39) |
S764N |
probably damaging |
Het |
Ryr2 |
A |
T |
13: 11,760,084 (GRCm39) |
F1556I |
probably damaging |
Het |
Scap |
G |
A |
9: 110,207,685 (GRCm39) |
A465T |
probably benign |
Het |
Sdf2 |
A |
G |
11: 78,141,844 (GRCm39) |
S60G |
probably damaging |
Het |
Sema3a |
T |
C |
5: 13,615,776 (GRCm39) |
I400T |
probably damaging |
Het |
Ski |
T |
C |
4: 155,244,191 (GRCm39) |
D478G |
probably damaging |
Het |
Slc12a7 |
A |
T |
13: 73,911,882 (GRCm39) |
|
probably benign |
Het |
Sned1 |
A |
G |
1: 93,211,322 (GRCm39) |
T1074A |
probably benign |
Het |
Srebf2 |
A |
G |
15: 82,059,298 (GRCm39) |
T239A |
probably damaging |
Het |
Stk4 |
C |
T |
2: 163,928,419 (GRCm39) |
H84Y |
probably benign |
Het |
Syne1 |
G |
T |
10: 5,318,295 (GRCm39) |
Q444K |
probably benign |
Het |
Tecpr1 |
T |
A |
5: 144,140,305 (GRCm39) |
I817F |
possibly damaging |
Het |
Tep1 |
G |
T |
14: 51,082,077 (GRCm39) |
Q1159K |
possibly damaging |
Het |
Tmem39b |
G |
A |
4: 129,572,442 (GRCm39) |
H387Y |
probably damaging |
Het |
Tpp1 |
T |
C |
7: 105,398,907 (GRCm39) |
H174R |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,535,617 (GRCm39) |
V35134I |
probably benign |
Het |
Usp34 |
A |
G |
11: 23,304,900 (GRCm39) |
I378V |
probably benign |
Het |
Vinac1 |
T |
C |
2: 128,889,968 (GRCm39) |
E42G |
probably benign |
Het |
Vmn2r1 |
T |
A |
3: 63,997,665 (GRCm39) |
H440Q |
probably benign |
Het |
Wdr38 |
A |
T |
2: 38,888,424 (GRCm39) |
N7I |
probably damaging |
Het |
Zcchc7 |
T |
A |
4: 44,931,244 (GRCm39) |
D144E |
possibly damaging |
Het |
Zic4 |
C |
A |
9: 91,266,228 (GRCm39) |
H284N |
probably damaging |
Het |
Zkscan6 |
A |
G |
11: 65,719,120 (GRCm39) |
H380R |
probably benign |
Het |
|
Other mutations in Dmxl2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Dmxl2
|
APN |
9 |
54,308,988 (GRCm39) |
missense |
probably benign |
|
IGL00226:Dmxl2
|
APN |
9 |
54,323,277 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00419:Dmxl2
|
APN |
9 |
54,313,951 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00551:Dmxl2
|
APN |
9 |
54,358,122 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00765:Dmxl2
|
APN |
9 |
54,322,706 (GRCm39) |
unclassified |
probably benign |
|
IGL00852:Dmxl2
|
APN |
9 |
54,330,597 (GRCm39) |
nonsense |
probably null |
|
IGL00857:Dmxl2
|
APN |
9 |
54,283,604 (GRCm39) |
missense |
probably benign |
0.32 |
IGL00952:Dmxl2
|
APN |
9 |
54,324,166 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01139:Dmxl2
|
APN |
9 |
54,366,248 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01346:Dmxl2
|
APN |
9 |
54,322,759 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01538:Dmxl2
|
APN |
9 |
54,352,660 (GRCm39) |
splice site |
probably benign |
|
IGL01645:Dmxl2
|
APN |
9 |
54,286,017 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02096:Dmxl2
|
APN |
9 |
54,308,349 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02104:Dmxl2
|
APN |
9 |
54,311,299 (GRCm39) |
nonsense |
probably null |
|
IGL02145:Dmxl2
|
APN |
9 |
54,281,981 (GRCm39) |
missense |
probably benign |
0.29 |
IGL02210:Dmxl2
|
APN |
9 |
54,311,333 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02238:Dmxl2
|
APN |
9 |
54,352,717 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02255:Dmxl2
|
APN |
9 |
54,301,052 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02364:Dmxl2
|
APN |
9 |
54,301,127 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02440:Dmxl2
|
APN |
9 |
54,313,899 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02546:Dmxl2
|
APN |
9 |
54,273,698 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02668:Dmxl2
|
APN |
9 |
54,324,229 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03229:Dmxl2
|
APN |
9 |
54,311,456 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03244:Dmxl2
|
APN |
9 |
54,323,655 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03277:Dmxl2
|
APN |
9 |
54,311,504 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03399:Dmxl2
|
APN |
9 |
54,353,956 (GRCm39) |
missense |
probably damaging |
1.00 |
BB003:Dmxl2
|
UTSW |
9 |
54,335,326 (GRCm39) |
missense |
probably benign |
0.01 |
BB013:Dmxl2
|
UTSW |
9 |
54,335,326 (GRCm39) |
missense |
probably benign |
0.01 |
I2288:Dmxl2
|
UTSW |
9 |
54,309,077 (GRCm39) |
missense |
probably damaging |
1.00 |
P0014:Dmxl2
|
UTSW |
9 |
54,309,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R0411:Dmxl2
|
UTSW |
9 |
54,286,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R0422:Dmxl2
|
UTSW |
9 |
54,307,224 (GRCm39) |
critical splice donor site |
probably null |
|
R0432:Dmxl2
|
UTSW |
9 |
54,324,235 (GRCm39) |
missense |
probably benign |
0.01 |
R0436:Dmxl2
|
UTSW |
9 |
54,291,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R0538:Dmxl2
|
UTSW |
9 |
54,301,120 (GRCm39) |
missense |
probably benign |
0.06 |
R0603:Dmxl2
|
UTSW |
9 |
54,313,190 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0605:Dmxl2
|
UTSW |
9 |
54,327,229 (GRCm39) |
missense |
probably benign |
0.01 |
R0625:Dmxl2
|
UTSW |
9 |
54,289,986 (GRCm39) |
missense |
probably benign |
|
R0626:Dmxl2
|
UTSW |
9 |
54,323,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R0736:Dmxl2
|
UTSW |
9 |
54,286,101 (GRCm39) |
missense |
probably damaging |
0.99 |
R0847:Dmxl2
|
UTSW |
9 |
54,313,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R0855:Dmxl2
|
UTSW |
9 |
54,273,724 (GRCm39) |
missense |
probably benign |
0.03 |
R0962:Dmxl2
|
UTSW |
9 |
54,353,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R1015:Dmxl2
|
UTSW |
9 |
54,275,049 (GRCm39) |
missense |
probably benign |
0.32 |
R1084:Dmxl2
|
UTSW |
9 |
54,323,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R1328:Dmxl2
|
UTSW |
9 |
54,303,533 (GRCm39) |
missense |
probably benign |
0.12 |
R1401:Dmxl2
|
UTSW |
9 |
54,322,712 (GRCm39) |
critical splice donor site |
probably null |
|
R1503:Dmxl2
|
UTSW |
9 |
54,354,272 (GRCm39) |
nonsense |
probably null |
|
R1609:Dmxl2
|
UTSW |
9 |
54,316,547 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1613:Dmxl2
|
UTSW |
9 |
54,289,311 (GRCm39) |
missense |
probably benign |
|
R1660:Dmxl2
|
UTSW |
9 |
54,358,314 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1712:Dmxl2
|
UTSW |
9 |
54,308,769 (GRCm39) |
missense |
probably benign |
0.00 |
R1772:Dmxl2
|
UTSW |
9 |
54,330,508 (GRCm39) |
splice site |
probably benign |
|
R1832:Dmxl2
|
UTSW |
9 |
54,368,233 (GRCm39) |
missense |
probably damaging |
0.97 |
R1922:Dmxl2
|
UTSW |
9 |
54,308,807 (GRCm39) |
missense |
probably benign |
|
R2104:Dmxl2
|
UTSW |
9 |
54,322,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R2109:Dmxl2
|
UTSW |
9 |
54,301,097 (GRCm39) |
missense |
probably benign |
0.06 |
R2145:Dmxl2
|
UTSW |
9 |
54,323,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R2199:Dmxl2
|
UTSW |
9 |
54,283,527 (GRCm39) |
missense |
probably benign |
0.35 |
R2352:Dmxl2
|
UTSW |
9 |
54,301,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R2516:Dmxl2
|
UTSW |
9 |
54,307,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R2981:Dmxl2
|
UTSW |
9 |
54,300,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R3430:Dmxl2
|
UTSW |
9 |
54,384,745 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3625:Dmxl2
|
UTSW |
9 |
54,300,927 (GRCm39) |
missense |
probably benign |
0.23 |
R3725:Dmxl2
|
UTSW |
9 |
54,301,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R3787:Dmxl2
|
UTSW |
9 |
54,277,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R4002:Dmxl2
|
UTSW |
9 |
54,381,116 (GRCm39) |
splice site |
probably benign |
|
R4004:Dmxl2
|
UTSW |
9 |
54,353,674 (GRCm39) |
missense |
probably benign |
0.04 |
R4005:Dmxl2
|
UTSW |
9 |
54,353,674 (GRCm39) |
missense |
probably benign |
0.04 |
R4012:Dmxl2
|
UTSW |
9 |
54,286,297 (GRCm39) |
splice site |
probably null |
|
R4014:Dmxl2
|
UTSW |
9 |
54,285,993 (GRCm39) |
splice site |
probably null |
|
R4115:Dmxl2
|
UTSW |
9 |
54,354,272 (GRCm39) |
nonsense |
probably null |
|
R4232:Dmxl2
|
UTSW |
9 |
54,327,193 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4388:Dmxl2
|
UTSW |
9 |
54,303,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R4513:Dmxl2
|
UTSW |
9 |
54,327,168 (GRCm39) |
missense |
probably null |
0.17 |
R4552:Dmxl2
|
UTSW |
9 |
54,359,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R4609:Dmxl2
|
UTSW |
9 |
54,353,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R4625:Dmxl2
|
UTSW |
9 |
54,311,404 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4694:Dmxl2
|
UTSW |
9 |
54,354,189 (GRCm39) |
missense |
probably benign |
0.04 |
R4711:Dmxl2
|
UTSW |
9 |
54,358,208 (GRCm39) |
missense |
probably benign |
0.37 |
R4715:Dmxl2
|
UTSW |
9 |
54,353,689 (GRCm39) |
splice site |
probably null |
|
R4746:Dmxl2
|
UTSW |
9 |
54,359,080 (GRCm39) |
missense |
probably benign |
0.04 |
R4789:Dmxl2
|
UTSW |
9 |
54,287,099 (GRCm39) |
missense |
probably benign |
0.30 |
R4825:Dmxl2
|
UTSW |
9 |
54,311,325 (GRCm39) |
missense |
probably benign |
0.01 |
R4911:Dmxl2
|
UTSW |
9 |
54,318,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R4995:Dmxl2
|
UTSW |
9 |
54,408,725 (GRCm39) |
utr 5 prime |
probably benign |
|
R5026:Dmxl2
|
UTSW |
9 |
54,323,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R5118:Dmxl2
|
UTSW |
9 |
54,368,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R5174:Dmxl2
|
UTSW |
9 |
54,352,768 (GRCm39) |
splice site |
probably null |
|
R5288:Dmxl2
|
UTSW |
9 |
54,286,041 (GRCm39) |
missense |
probably benign |
|
R5373:Dmxl2
|
UTSW |
9 |
54,276,473 (GRCm39) |
intron |
probably benign |
|
R5374:Dmxl2
|
UTSW |
9 |
54,276,473 (GRCm39) |
intron |
probably benign |
|
R5385:Dmxl2
|
UTSW |
9 |
54,286,041 (GRCm39) |
missense |
probably benign |
|
R5386:Dmxl2
|
UTSW |
9 |
54,286,041 (GRCm39) |
missense |
probably benign |
|
R5418:Dmxl2
|
UTSW |
9 |
54,281,935 (GRCm39) |
critical splice donor site |
probably null |
|
R5540:Dmxl2
|
UTSW |
9 |
54,301,141 (GRCm39) |
missense |
probably benign |
0.21 |
R5568:Dmxl2
|
UTSW |
9 |
54,330,643 (GRCm39) |
splice site |
probably null |
|
R5733:Dmxl2
|
UTSW |
9 |
54,283,550 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5758:Dmxl2
|
UTSW |
9 |
54,380,248 (GRCm39) |
missense |
probably benign |
0.28 |
R5759:Dmxl2
|
UTSW |
9 |
54,282,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R5893:Dmxl2
|
UTSW |
9 |
54,294,704 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6030:Dmxl2
|
UTSW |
9 |
54,300,957 (GRCm39) |
missense |
probably benign |
0.18 |
R6030:Dmxl2
|
UTSW |
9 |
54,300,957 (GRCm39) |
missense |
probably benign |
0.18 |
R6041:Dmxl2
|
UTSW |
9 |
54,324,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R6174:Dmxl2
|
UTSW |
9 |
54,301,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R6278:Dmxl2
|
UTSW |
9 |
54,323,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R6307:Dmxl2
|
UTSW |
9 |
54,289,990 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6349:Dmxl2
|
UTSW |
9 |
54,327,193 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6404:Dmxl2
|
UTSW |
9 |
54,282,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R6516:Dmxl2
|
UTSW |
9 |
54,323,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R6712:Dmxl2
|
UTSW |
9 |
54,318,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R6747:Dmxl2
|
UTSW |
9 |
54,323,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R6769:Dmxl2
|
UTSW |
9 |
54,323,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R6771:Dmxl2
|
UTSW |
9 |
54,323,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R6800:Dmxl2
|
UTSW |
9 |
54,316,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R6891:Dmxl2
|
UTSW |
9 |
54,387,664 (GRCm39) |
missense |
probably damaging |
0.99 |
R6920:Dmxl2
|
UTSW |
9 |
54,379,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R6979:Dmxl2
|
UTSW |
9 |
54,358,163 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7147:Dmxl2
|
UTSW |
9 |
54,324,013 (GRCm39) |
missense |
probably benign |
0.06 |
R7327:Dmxl2
|
UTSW |
9 |
54,308,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R7462:Dmxl2
|
UTSW |
9 |
54,273,916 (GRCm39) |
splice site |
probably null |
|
R7526:Dmxl2
|
UTSW |
9 |
54,308,241 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7569:Dmxl2
|
UTSW |
9 |
54,323,271 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7622:Dmxl2
|
UTSW |
9 |
54,379,502 (GRCm39) |
missense |
probably damaging |
0.99 |
R7638:Dmxl2
|
UTSW |
9 |
54,365,078 (GRCm39) |
missense |
unknown |
|
R7703:Dmxl2
|
UTSW |
9 |
54,368,370 (GRCm39) |
missense |
probably benign |
0.01 |
R7768:Dmxl2
|
UTSW |
9 |
54,288,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R7926:Dmxl2
|
UTSW |
9 |
54,335,326 (GRCm39) |
missense |
probably benign |
0.01 |
R7969:Dmxl2
|
UTSW |
9 |
54,354,165 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8007:Dmxl2
|
UTSW |
9 |
54,290,975 (GRCm39) |
nonsense |
probably null |
|
R8200:Dmxl2
|
UTSW |
9 |
54,387,630 (GRCm39) |
missense |
probably benign |
|
R8311:Dmxl2
|
UTSW |
9 |
54,354,217 (GRCm39) |
missense |
probably benign |
0.00 |
R8320:Dmxl2
|
UTSW |
9 |
54,291,043 (GRCm39) |
missense |
probably benign |
|
R8377:Dmxl2
|
UTSW |
9 |
54,286,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R8400:Dmxl2
|
UTSW |
9 |
54,291,037 (GRCm39) |
missense |
probably benign |
0.03 |
R8509:Dmxl2
|
UTSW |
9 |
54,335,341 (GRCm39) |
nonsense |
probably null |
|
R8698:Dmxl2
|
UTSW |
9 |
54,281,953 (GRCm39) |
missense |
probably benign |
0.10 |
R8768:Dmxl2
|
UTSW |
9 |
54,301,105 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8770:Dmxl2
|
UTSW |
9 |
54,311,298 (GRCm39) |
missense |
probably benign |
0.01 |
R8799:Dmxl2
|
UTSW |
9 |
54,327,027 (GRCm39) |
critical splice donor site |
probably null |
|
R8840:Dmxl2
|
UTSW |
9 |
54,309,139 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8898:Dmxl2
|
UTSW |
9 |
54,308,941 (GRCm39) |
missense |
probably benign |
0.01 |
R8954:Dmxl2
|
UTSW |
9 |
54,381,156 (GRCm39) |
missense |
probably benign |
0.04 |
R9083:Dmxl2
|
UTSW |
9 |
54,316,548 (GRCm39) |
missense |
probably benign |
0.29 |
R9114:Dmxl2
|
UTSW |
9 |
54,307,321 (GRCm39) |
missense |
|
|
R9115:Dmxl2
|
UTSW |
9 |
54,309,011 (GRCm39) |
missense |
probably benign |
|
R9263:Dmxl2
|
UTSW |
9 |
54,358,945 (GRCm39) |
missense |
probably benign |
0.01 |
R9272:Dmxl2
|
UTSW |
9 |
54,311,404 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9577:Dmxl2
|
UTSW |
9 |
54,323,664 (GRCm39) |
missense |
unknown |
|
R9673:Dmxl2
|
UTSW |
9 |
54,294,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R9722:Dmxl2
|
UTSW |
9 |
54,323,892 (GRCm39) |
missense |
probably benign |
0.00 |
R9726:Dmxl2
|
UTSW |
9 |
54,322,996 (GRCm39) |
missense |
probably benign |
0.09 |
R9797:Dmxl2
|
UTSW |
9 |
54,358,187 (GRCm39) |
missense |
probably benign |
0.00 |
X0064:Dmxl2
|
UTSW |
9 |
54,308,997 (GRCm39) |
missense |
probably benign |
|
Z1177:Dmxl2
|
UTSW |
9 |
54,289,318 (GRCm39) |
frame shift |
probably null |
|
|