Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700122O11Rik |
T |
G |
17: 48,347,723 (GRCm39) |
T194P |
possibly damaging |
Het |
4921504E06Rik |
T |
A |
2: 19,545,124 (GRCm39) |
M110L |
probably benign |
Het |
Acad9 |
T |
G |
3: 36,127,737 (GRCm39) |
I113R |
probably damaging |
Het |
Adam34l |
T |
C |
8: 44,079,442 (GRCm39) |
S261G |
possibly damaging |
Het |
Adamts6 |
A |
T |
13: 104,450,812 (GRCm39) |
I332F |
probably damaging |
Het |
Adcy8 |
C |
T |
15: 64,639,727 (GRCm39) |
G678S |
probably benign |
Het |
Afg3l2 |
C |
T |
18: 67,564,842 (GRCm39) |
V211I |
probably damaging |
Het |
Ahnak |
T |
C |
19: 8,991,937 (GRCm39) |
I4407T |
probably damaging |
Het |
Alpl |
G |
T |
4: 137,482,458 (GRCm39) |
H79N |
probably benign |
Het |
Apc |
A |
G |
18: 34,448,644 (GRCm39) |
I1813V |
probably damaging |
Het |
Ascc3 |
T |
C |
10: 50,525,908 (GRCm39) |
M540T |
probably damaging |
Het |
Blm |
T |
C |
7: 80,152,147 (GRCm39) |
E600G |
probably damaging |
Het |
Btbd8 |
T |
C |
5: 107,658,655 (GRCm39) |
W1742R |
probably damaging |
Het |
Cadps |
T |
A |
14: 12,522,337 (GRCm38) |
D609V |
probably damaging |
Het |
Ccdc69 |
C |
T |
11: 54,941,983 (GRCm39) |
M174I |
probably benign |
Het |
Cdk13 |
A |
T |
13: 17,913,748 (GRCm39) |
L877* |
probably null |
Het |
Cdk14 |
T |
C |
5: 5,143,047 (GRCm39) |
Y228C |
probably damaging |
Het |
Dip2c |
C |
T |
13: 9,617,882 (GRCm39) |
Q426* |
probably null |
Het |
Epyc |
T |
C |
10: 97,511,655 (GRCm39) |
I216T |
probably damaging |
Het |
Erbin |
A |
G |
13: 103,994,041 (GRCm39) |
S300P |
probably damaging |
Het |
Ercc3 |
A |
G |
18: 32,381,482 (GRCm39) |
T433A |
probably benign |
Het |
Exoc4 |
A |
G |
6: 33,243,026 (GRCm39) |
T80A |
probably damaging |
Het |
Foxm1 |
T |
A |
6: 128,352,465 (GRCm39) |
|
probably null |
Het |
Gaa |
A |
G |
11: 119,175,409 (GRCm39) |
|
probably null |
Het |
H2-Q4 |
A |
G |
17: 35,599,526 (GRCm39) |
E203G |
probably damaging |
Het |
Helt |
T |
C |
8: 46,745,355 (GRCm39) |
D214G |
probably damaging |
Het |
Hlcs |
A |
G |
16: 94,063,599 (GRCm39) |
V487A |
probably benign |
Het |
Hmmr |
A |
T |
11: 40,619,259 (GRCm39) |
S74T |
possibly damaging |
Het |
Hspa9 |
A |
T |
18: 35,079,701 (GRCm39) |
Y243N |
probably damaging |
Het |
Htt |
T |
G |
5: 35,010,215 (GRCm39) |
L1556R |
probably damaging |
Het |
Ift80 |
T |
C |
3: 68,898,117 (GRCm39) |
K73E |
possibly damaging |
Het |
Il6st |
G |
A |
13: 112,635,423 (GRCm39) |
A551T |
probably null |
Het |
Kdm5a |
T |
C |
6: 120,408,951 (GRCm39) |
S1545P |
probably benign |
Het |
Lef1 |
T |
A |
3: 130,905,236 (GRCm39) |
I39N |
probably damaging |
Het |
Lmo2 |
T |
C |
2: 103,811,407 (GRCm39) |
Y147H |
probably damaging |
Het |
Lrp6 |
A |
G |
6: 134,457,337 (GRCm39) |
|
probably null |
Het |
Macf1 |
T |
C |
4: 123,577,807 (GRCm39) |
D59G |
probably damaging |
Het |
Maged1 |
T |
C |
X: 93,580,523 (GRCm39) |
Y636C |
possibly damaging |
Het |
Mamdc4 |
T |
A |
2: 25,453,584 (GRCm39) |
D1195V |
probably damaging |
Het |
Mob3b |
A |
G |
4: 35,083,922 (GRCm39) |
V89A |
probably benign |
Het |
Mogs |
C |
T |
6: 83,094,631 (GRCm39) |
R483* |
probably null |
Het |
Mybphl |
A |
C |
3: 108,282,718 (GRCm39) |
T203P |
probably benign |
Het |
Myo15a |
A |
G |
11: 60,385,057 (GRCm39) |
T1720A |
probably damaging |
Het |
Myo16 |
T |
A |
8: 10,552,796 (GRCm39) |
F945I |
probably damaging |
Het |
Nbeal2 |
G |
A |
9: 110,463,139 (GRCm39) |
L1309F |
probably benign |
Het |
Nes |
A |
G |
3: 87,883,985 (GRCm39) |
Q748R |
possibly damaging |
Het |
Nhsl1 |
A |
T |
10: 18,387,340 (GRCm39) |
R205W |
probably damaging |
Het |
Nlrc3 |
A |
C |
16: 3,782,974 (GRCm39) |
L161R |
probably damaging |
Het |
Npy2r |
T |
A |
3: 82,448,487 (GRCm39) |
D96V |
probably damaging |
Het |
Or4d11 |
T |
A |
19: 12,013,518 (GRCm39) |
E196V |
probably damaging |
Het |
Or5w18 |
T |
G |
2: 87,632,847 (GRCm39) |
V38G |
probably damaging |
Het |
Pappa2 |
C |
T |
1: 158,662,498 (GRCm39) |
C1159Y |
probably damaging |
Het |
Phf21a |
T |
C |
2: 92,058,828 (GRCm39) |
|
probably null |
Het |
Pik3c2a |
T |
A |
7: 115,950,166 (GRCm39) |
|
probably null |
Het |
Psg22 |
A |
T |
7: 18,453,560 (GRCm39) |
Y85F |
possibly damaging |
Het |
Pttg1ip2 |
T |
A |
5: 5,505,964 (GRCm39) |
I106L |
probably benign |
Het |
Qtrt2 |
A |
G |
16: 43,689,455 (GRCm39) |
I181T |
probably damaging |
Het |
Sash1 |
A |
T |
10: 8,605,177 (GRCm39) |
V1071D |
probably benign |
Het |
Scn10a |
A |
T |
9: 119,442,802 (GRCm39) |
I1481N |
probably damaging |
Het |
Slc15a1 |
G |
A |
14: 121,713,399 (GRCm39) |
A376V |
possibly damaging |
Het |
Slc25a46 |
A |
T |
18: 31,742,778 (GRCm39) |
H29Q |
probably benign |
Het |
Slit2 |
T |
C |
5: 48,459,832 (GRCm39) |
C1354R |
probably damaging |
Het |
Ssu2 |
C |
T |
6: 112,360,902 (GRCm39) |
E52K |
possibly damaging |
Het |
Taar7e |
A |
T |
10: 23,913,732 (GRCm39) |
H74L |
possibly damaging |
Het |
Tcte1 |
A |
T |
17: 45,852,237 (GRCm39) |
N490I |
probably benign |
Het |
Tent4b |
T |
A |
8: 88,972,223 (GRCm39) |
|
probably null |
Het |
Tpst2 |
G |
T |
5: 112,455,880 (GRCm39) |
G140C |
probably damaging |
Het |
Trip11 |
A |
T |
12: 101,803,981 (GRCm39) |
F1634I |
probably damaging |
Het |
Trpm2 |
A |
G |
10: 77,761,600 (GRCm39) |
F1017L |
probably damaging |
Het |
Utp18 |
A |
G |
11: 93,766,948 (GRCm39) |
V253A |
possibly damaging |
Het |
Vmn2r102 |
A |
G |
17: 19,897,006 (GRCm39) |
T118A |
probably benign |
Het |
Vmn2r14 |
T |
C |
5: 109,369,109 (GRCm39) |
T155A |
probably benign |
Het |
Vmn2r19 |
T |
A |
6: 123,292,954 (GRCm39) |
M332K |
probably benign |
Het |
Vmn2r71 |
T |
A |
7: 85,269,845 (GRCm39) |
M452K |
probably benign |
Het |
Vmn2r79 |
T |
G |
7: 86,653,289 (GRCm39) |
L518R |
possibly damaging |
Het |
Vps13b |
T |
C |
15: 35,607,288 (GRCm39) |
S1074P |
probably damaging |
Het |
Vps13d |
A |
G |
4: 144,835,078 (GRCm39) |
S2757P |
probably damaging |
Het |
Wdr33 |
C |
A |
18: 32,022,029 (GRCm39) |
Q860K |
unknown |
Het |
Zfp423 |
T |
A |
8: 88,509,025 (GRCm39) |
I440F |
probably benign |
Het |
Zup1 |
A |
G |
10: 33,805,820 (GRCm39) |
V437A |
possibly damaging |
Het |
|
Other mutations in Dsp |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00502:Dsp
|
APN |
13 |
38,381,822 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01337:Dsp
|
APN |
13 |
38,376,663 (GRCm39) |
missense |
probably benign |
0.44 |
IGL01371:Dsp
|
APN |
13 |
38,377,593 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01473:Dsp
|
APN |
13 |
38,351,547 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01660:Dsp
|
APN |
13 |
38,360,471 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01723:Dsp
|
APN |
13 |
38,363,060 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01999:Dsp
|
APN |
13 |
38,365,162 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02313:Dsp
|
APN |
13 |
38,380,499 (GRCm39) |
nonsense |
probably null |
|
IGL02833:Dsp
|
APN |
13 |
38,376,897 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL03050:Dsp
|
APN |
13 |
38,372,421 (GRCm39) |
splice site |
probably benign |
|
IGL03353:Dsp
|
APN |
13 |
38,370,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R0052:Dsp
|
UTSW |
13 |
38,381,340 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0052:Dsp
|
UTSW |
13 |
38,381,340 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0078:Dsp
|
UTSW |
13 |
38,379,993 (GRCm39) |
missense |
probably benign |
0.22 |
R0230:Dsp
|
UTSW |
13 |
38,381,681 (GRCm39) |
missense |
probably benign |
0.03 |
R0234:Dsp
|
UTSW |
13 |
38,371,869 (GRCm39) |
missense |
probably benign |
0.13 |
R0234:Dsp
|
UTSW |
13 |
38,371,869 (GRCm39) |
missense |
probably benign |
0.13 |
R0285:Dsp
|
UTSW |
13 |
38,356,770 (GRCm39) |
missense |
probably benign |
|
R0326:Dsp
|
UTSW |
13 |
38,376,846 (GRCm39) |
nonsense |
probably null |
|
R0332:Dsp
|
UTSW |
13 |
38,366,204 (GRCm39) |
nonsense |
probably null |
|
R0471:Dsp
|
UTSW |
13 |
38,377,326 (GRCm39) |
nonsense |
probably null |
|
R0567:Dsp
|
UTSW |
13 |
38,376,414 (GRCm39) |
missense |
probably benign |
0.01 |
R0611:Dsp
|
UTSW |
13 |
38,371,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R0718:Dsp
|
UTSW |
13 |
38,380,740 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0926:Dsp
|
UTSW |
13 |
38,367,194 (GRCm39) |
missense |
probably damaging |
0.97 |
R1078:Dsp
|
UTSW |
13 |
38,367,082 (GRCm39) |
splice site |
probably benign |
|
R1183:Dsp
|
UTSW |
13 |
38,375,716 (GRCm39) |
nonsense |
probably null |
|
R1188:Dsp
|
UTSW |
13 |
38,378,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R1419:Dsp
|
UTSW |
13 |
38,370,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R1445:Dsp
|
UTSW |
13 |
38,375,907 (GRCm39) |
missense |
probably damaging |
0.98 |
R1467:Dsp
|
UTSW |
13 |
38,376,688 (GRCm39) |
missense |
probably benign |
0.00 |
R1467:Dsp
|
UTSW |
13 |
38,376,688 (GRCm39) |
missense |
probably benign |
0.00 |
R1478:Dsp
|
UTSW |
13 |
38,365,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R1568:Dsp
|
UTSW |
13 |
38,359,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R1572:Dsp
|
UTSW |
13 |
38,379,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R1676:Dsp
|
UTSW |
13 |
38,377,350 (GRCm39) |
nonsense |
probably null |
|
R1736:Dsp
|
UTSW |
13 |
38,376,966 (GRCm39) |
missense |
probably benign |
0.01 |
R1776:Dsp
|
UTSW |
13 |
38,380,593 (GRCm39) |
missense |
probably damaging |
0.99 |
R1829:Dsp
|
UTSW |
13 |
38,377,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R1878:Dsp
|
UTSW |
13 |
38,348,831 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2161:Dsp
|
UTSW |
13 |
38,380,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R2187:Dsp
|
UTSW |
13 |
38,360,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R2295:Dsp
|
UTSW |
13 |
38,381,022 (GRCm39) |
missense |
probably benign |
0.28 |
R2495:Dsp
|
UTSW |
13 |
38,377,453 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2566:Dsp
|
UTSW |
13 |
38,380,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R2888:Dsp
|
UTSW |
13 |
38,376,224 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3012:Dsp
|
UTSW |
13 |
38,377,318 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3614:Dsp
|
UTSW |
13 |
38,361,175 (GRCm39) |
missense |
probably damaging |
0.98 |
R3725:Dsp
|
UTSW |
13 |
38,381,594 (GRCm39) |
missense |
probably benign |
0.00 |
R3725:Dsp
|
UTSW |
13 |
38,378,665 (GRCm39) |
splice site |
probably null |
|
R3797:Dsp
|
UTSW |
13 |
38,361,260 (GRCm39) |
critical splice donor site |
probably null |
|
R3841:Dsp
|
UTSW |
13 |
38,381,681 (GRCm39) |
missense |
probably benign |
|
R4030:Dsp
|
UTSW |
13 |
38,375,404 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4124:Dsp
|
UTSW |
13 |
38,370,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R4279:Dsp
|
UTSW |
13 |
38,369,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R4334:Dsp
|
UTSW |
13 |
38,380,640 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4419:Dsp
|
UTSW |
13 |
38,379,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R4615:Dsp
|
UTSW |
13 |
38,375,608 (GRCm39) |
missense |
probably damaging |
0.98 |
R4627:Dsp
|
UTSW |
13 |
38,352,617 (GRCm39) |
missense |
probably benign |
0.01 |
R4639:Dsp
|
UTSW |
13 |
38,380,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R4687:Dsp
|
UTSW |
13 |
38,375,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R4735:Dsp
|
UTSW |
13 |
38,380,016 (GRCm39) |
missense |
probably damaging |
0.99 |
R4746:Dsp
|
UTSW |
13 |
38,379,080 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4772:Dsp
|
UTSW |
13 |
38,351,504 (GRCm39) |
nonsense |
probably null |
|
R4830:Dsp
|
UTSW |
13 |
38,376,840 (GRCm39) |
missense |
probably benign |
|
R4850:Dsp
|
UTSW |
13 |
38,376,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R4959:Dsp
|
UTSW |
13 |
38,375,686 (GRCm39) |
missense |
probably benign |
0.41 |
R4963:Dsp
|
UTSW |
13 |
38,381,846 (GRCm39) |
missense |
probably damaging |
0.99 |
R4969:Dsp
|
UTSW |
13 |
38,376,886 (GRCm39) |
missense |
probably benign |
0.00 |
R4978:Dsp
|
UTSW |
13 |
38,366,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R4989:Dsp
|
UTSW |
13 |
38,381,678 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5068:Dsp
|
UTSW |
13 |
38,381,099 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5069:Dsp
|
UTSW |
13 |
38,381,099 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5070:Dsp
|
UTSW |
13 |
38,381,099 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5133:Dsp
|
UTSW |
13 |
38,381,678 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5138:Dsp
|
UTSW |
13 |
38,379,821 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5138:Dsp
|
UTSW |
13 |
38,367,274 (GRCm39) |
missense |
probably benign |
0.37 |
R5153:Dsp
|
UTSW |
13 |
38,366,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R5199:Dsp
|
UTSW |
13 |
38,376,878 (GRCm39) |
nonsense |
probably null |
|
R5226:Dsp
|
UTSW |
13 |
38,370,746 (GRCm39) |
missense |
probably damaging |
0.99 |
R5265:Dsp
|
UTSW |
13 |
38,379,159 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5371:Dsp
|
UTSW |
13 |
38,378,865 (GRCm39) |
missense |
probably damaging |
0.97 |
R5484:Dsp
|
UTSW |
13 |
38,368,014 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5534:Dsp
|
UTSW |
13 |
38,379,818 (GRCm39) |
missense |
probably benign |
0.01 |
R5569:Dsp
|
UTSW |
13 |
38,376,628 (GRCm39) |
missense |
probably benign |
0.01 |
R5854:Dsp
|
UTSW |
13 |
38,351,477 (GRCm39) |
splice site |
probably null |
|
R5910:Dsp
|
UTSW |
13 |
38,376,445 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5929:Dsp
|
UTSW |
13 |
38,379,410 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5940:Dsp
|
UTSW |
13 |
38,380,002 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5948:Dsp
|
UTSW |
13 |
38,379,377 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5955:Dsp
|
UTSW |
13 |
38,378,934 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5970:Dsp
|
UTSW |
13 |
38,379,678 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6054:Dsp
|
UTSW |
13 |
38,351,585 (GRCm39) |
missense |
probably benign |
0.00 |
R6113:Dsp
|
UTSW |
13 |
38,376,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R6139:Dsp
|
UTSW |
13 |
38,376,382 (GRCm39) |
missense |
probably damaging |
0.97 |
R6328:Dsp
|
UTSW |
13 |
38,380,982 (GRCm39) |
nonsense |
probably null |
|
R6527:Dsp
|
UTSW |
13 |
38,379,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R6573:Dsp
|
UTSW |
13 |
38,380,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R6628:Dsp
|
UTSW |
13 |
38,351,598 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6738:Dsp
|
UTSW |
13 |
38,376,186 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6898:Dsp
|
UTSW |
13 |
38,376,193 (GRCm39) |
missense |
possibly damaging |
0.59 |
R6919:Dsp
|
UTSW |
13 |
38,351,631 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6951:Dsp
|
UTSW |
13 |
38,351,622 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7017:Dsp
|
UTSW |
13 |
38,370,683 (GRCm39) |
missense |
probably benign |
0.02 |
R7022:Dsp
|
UTSW |
13 |
38,375,716 (GRCm39) |
missense |
probably benign |
0.06 |
R7135:Dsp
|
UTSW |
13 |
38,363,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R7192:Dsp
|
UTSW |
13 |
38,379,569 (GRCm39) |
missense |
probably benign |
0.09 |
R7211:Dsp
|
UTSW |
13 |
38,372,511 (GRCm39) |
critical splice donor site |
probably null |
|
R7251:Dsp
|
UTSW |
13 |
38,377,524 (GRCm39) |
missense |
probably benign |
0.02 |
R7326:Dsp
|
UTSW |
13 |
38,376,859 (GRCm39) |
missense |
probably benign |
0.01 |
R7369:Dsp
|
UTSW |
13 |
38,381,501 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7376:Dsp
|
UTSW |
13 |
38,356,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R7406:Dsp
|
UTSW |
13 |
38,381,172 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7439:Dsp
|
UTSW |
13 |
38,379,425 (GRCm39) |
missense |
probably benign |
0.00 |
R7439:Dsp
|
UTSW |
13 |
38,360,478 (GRCm39) |
critical splice donor site |
probably null |
|
R7441:Dsp
|
UTSW |
13 |
38,379,425 (GRCm39) |
missense |
probably benign |
0.00 |
R7477:Dsp
|
UTSW |
13 |
38,356,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R7535:Dsp
|
UTSW |
13 |
38,376,765 (GRCm39) |
missense |
probably benign |
0.05 |
R7558:Dsp
|
UTSW |
13 |
38,352,742 (GRCm39) |
missense |
probably benign |
0.02 |
R7600:Dsp
|
UTSW |
13 |
38,375,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R7616:Dsp
|
UTSW |
13 |
38,375,458 (GRCm39) |
missense |
probably damaging |
0.98 |
R7702:Dsp
|
UTSW |
13 |
38,359,183 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7738:Dsp
|
UTSW |
13 |
38,369,151 (GRCm39) |
missense |
probably damaging |
0.97 |
R7815:Dsp
|
UTSW |
13 |
38,375,446 (GRCm39) |
missense |
probably benign |
0.31 |
R7882:Dsp
|
UTSW |
13 |
38,367,994 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7917:Dsp
|
UTSW |
13 |
38,351,615 (GRCm39) |
nonsense |
probably null |
|
R7971:Dsp
|
UTSW |
13 |
38,376,499 (GRCm39) |
missense |
probably damaging |
0.97 |
R8104:Dsp
|
UTSW |
13 |
38,352,600 (GRCm39) |
missense |
probably benign |
0.03 |
R8176:Dsp
|
UTSW |
13 |
38,376,786 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8303:Dsp
|
UTSW |
13 |
38,381,319 (GRCm39) |
missense |
probably benign |
|
R8323:Dsp
|
UTSW |
13 |
38,356,806 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8326:Dsp
|
UTSW |
13 |
38,375,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R8358:Dsp
|
UTSW |
13 |
38,376,457 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8410:Dsp
|
UTSW |
13 |
38,380,791 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8552:Dsp
|
UTSW |
13 |
38,369,117 (GRCm39) |
missense |
probably damaging |
0.98 |
R8713:Dsp
|
UTSW |
13 |
38,352,701 (GRCm39) |
missense |
probably damaging |
0.99 |
R8801:Dsp
|
UTSW |
13 |
38,381,502 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8900:Dsp
|
UTSW |
13 |
38,365,155 (GRCm39) |
missense |
probably damaging |
0.99 |
R8901:Dsp
|
UTSW |
13 |
38,365,155 (GRCm39) |
missense |
probably damaging |
0.99 |
R8968:Dsp
|
UTSW |
13 |
38,335,596 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9014:Dsp
|
UTSW |
13 |
38,376,700 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9021:Dsp
|
UTSW |
13 |
38,380,808 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9030:Dsp
|
UTSW |
13 |
38,352,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R9124:Dsp
|
UTSW |
13 |
38,377,276 (GRCm39) |
missense |
probably benign |
0.42 |
R9129:Dsp
|
UTSW |
13 |
38,377,126 (GRCm39) |
missense |
probably benign |
0.09 |
R9143:Dsp
|
UTSW |
13 |
38,377,337 (GRCm39) |
missense |
probably benign |
0.05 |
R9450:Dsp
|
UTSW |
13 |
38,376,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R9488:Dsp
|
UTSW |
13 |
38,377,218 (GRCm39) |
missense |
probably benign |
0.04 |
R9514:Dsp
|
UTSW |
13 |
38,371,781 (GRCm39) |
missense |
probably benign |
0.02 |
R9789:Dsp
|
UTSW |
13 |
38,367,937 (GRCm39) |
missense |
probably benign |
0.03 |
R9792:Dsp
|
UTSW |
13 |
38,379,494 (GRCm39) |
missense |
possibly damaging |
0.87 |
X0023:Dsp
|
UTSW |
13 |
38,381,660 (GRCm39) |
missense |
probably benign |
0.00 |
X0024:Dsp
|
UTSW |
13 |
38,377,231 (GRCm39) |
missense |
probably benign |
0.04 |
X0027:Dsp
|
UTSW |
13 |
38,370,622 (GRCm39) |
missense |
possibly damaging |
0.68 |
X0067:Dsp
|
UTSW |
13 |
38,366,288 (GRCm39) |
missense |
possibly damaging |
0.85 |
Z1176:Dsp
|
UTSW |
13 |
38,381,166 (GRCm39) |
missense |
possibly damaging |
0.81 |
Z1177:Dsp
|
UTSW |
13 |
38,376,830 (GRCm39) |
frame shift |
probably null |
|
Z1177:Dsp
|
UTSW |
13 |
38,335,665 (GRCm39) |
missense |
probably benign |
0.01 |
|