Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2410004B18Rik |
C |
T |
3: 145,643,976 (GRCm39) |
P55S |
probably damaging |
Het |
Adgre4 |
T |
C |
17: 56,098,497 (GRCm39) |
S136P |
probably benign |
Het |
Aoc1l1 |
C |
T |
6: 48,952,687 (GRCm39) |
T204I |
probably damaging |
Het |
Arap1 |
C |
A |
7: 101,022,222 (GRCm39) |
A8E |
probably damaging |
Het |
Arid1a |
A |
T |
4: 133,480,401 (GRCm39) |
H174Q |
possibly damaging |
Het |
Btbd2 |
A |
G |
10: 80,480,539 (GRCm39) |
I358T |
probably benign |
Het |
Camkk2 |
G |
A |
5: 122,875,575 (GRCm39) |
R492* |
probably null |
Het |
Capn3 |
T |
C |
2: 120,294,421 (GRCm39) |
V23A |
probably benign |
Het |
Carm1 |
T |
G |
9: 21,491,606 (GRCm39) |
V225G |
probably benign |
Het |
Ccdc113 |
T |
A |
8: 96,267,459 (GRCm39) |
N141K |
probably benign |
Het |
Ccdc60 |
C |
A |
5: 116,284,243 (GRCm39) |
M298I |
probably benign |
Het |
Celsr3 |
C |
T |
9: 108,723,016 (GRCm39) |
P2801L |
probably benign |
Het |
Clec4n |
T |
A |
6: 123,207,505 (GRCm39) |
V23E |
probably damaging |
Het |
Cmtr2 |
T |
G |
8: 110,948,382 (GRCm39) |
L231V |
probably damaging |
Het |
Csrnp3 |
T |
G |
2: 65,853,363 (GRCm39) |
V585G |
probably null |
Het |
Ctnnd2 |
T |
C |
15: 30,647,257 (GRCm39) |
S318P |
probably damaging |
Het |
Cubn |
A |
T |
2: 13,344,828 (GRCm39) |
|
probably null |
Het |
Dgkd |
C |
A |
1: 87,857,549 (GRCm39) |
P754T |
possibly damaging |
Het |
Dnah7a |
A |
G |
1: 53,724,142 (GRCm39) |
S108P |
probably benign |
Het |
Dnajc24 |
A |
G |
2: 105,832,268 (GRCm39) |
|
probably benign |
Het |
Dner |
A |
T |
1: 84,423,177 (GRCm39) |
S475R |
probably damaging |
Het |
Dtnb |
T |
C |
12: 3,831,190 (GRCm39) |
L630P |
probably benign |
Het |
Fbh1 |
G |
A |
2: 11,762,339 (GRCm39) |
A566V |
probably damaging |
Het |
Fbxw19 |
G |
T |
9: 109,315,004 (GRCm39) |
T186K |
probably benign |
Het |
Flacc1 |
A |
T |
1: 58,698,437 (GRCm39) |
V327D |
possibly damaging |
Het |
Gm4825 |
A |
G |
15: 85,395,245 (GRCm39) |
|
noncoding transcript |
Het |
Grhl2 |
T |
A |
15: 37,336,558 (GRCm39) |
V54D |
probably damaging |
Het |
Hmcn1 |
T |
C |
1: 150,551,742 (GRCm39) |
I2621V |
probably benign |
Het |
Hmcn1 |
T |
A |
1: 150,553,127 (GRCm39) |
E2521V |
possibly damaging |
Het |
Kcng1 |
A |
G |
2: 168,104,904 (GRCm39) |
V314A |
probably benign |
Het |
Kif13a |
G |
A |
13: 47,018,314 (GRCm39) |
|
probably benign |
Het |
Kif21a |
G |
A |
15: 90,855,051 (GRCm39) |
A703V |
probably damaging |
Het |
Kifc1 |
A |
G |
17: 34,103,561 (GRCm39) |
|
probably null |
Het |
Klk13 |
T |
A |
7: 43,370,431 (GRCm39) |
N31K |
possibly damaging |
Het |
Klri1 |
T |
A |
6: 129,674,347 (GRCm39) |
H221L |
probably benign |
Het |
Ltbp4 |
G |
A |
7: 27,028,443 (GRCm39) |
P273L |
unknown |
Het |
Med16 |
T |
C |
10: 79,742,929 (GRCm39) |
H14R |
possibly damaging |
Het |
Mpeg1 |
G |
A |
19: 12,440,275 (GRCm39) |
V578M |
probably damaging |
Het |
Mrgpra2a |
T |
A |
7: 47,076,983 (GRCm39) |
I92F |
probably benign |
Het |
Muc5b |
T |
C |
7: 141,416,374 (GRCm39) |
C3107R |
possibly damaging |
Het |
Myo5a |
T |
A |
9: 75,055,139 (GRCm39) |
F441I |
probably damaging |
Het |
Ndst4 |
T |
A |
3: 125,232,331 (GRCm39) |
L300* |
probably null |
Het |
Nlgn2 |
G |
T |
11: 69,718,136 (GRCm39) |
D356E |
probably damaging |
Het |
Nlrp2 |
T |
C |
7: 5,330,737 (GRCm39) |
E553G |
probably damaging |
Het |
Oas1f |
G |
A |
5: 120,994,502 (GRCm39) |
C341Y |
possibly damaging |
Het |
Olfm5 |
A |
T |
7: 103,809,619 (GRCm39) |
C111S |
possibly damaging |
Het |
Oplah |
G |
A |
15: 76,181,664 (GRCm39) |
T1119I |
probably damaging |
Het |
Or2ag15 |
T |
C |
7: 106,340,601 (GRCm39) |
E180G |
probably damaging |
Het |
Or5d46 |
T |
C |
2: 88,170,545 (GRCm39) |
L212P |
probably damaging |
Het |
Or6c74 |
C |
T |
10: 129,870,187 (GRCm39) |
Q231* |
probably null |
Het |
Or6f2 |
A |
T |
7: 139,756,596 (GRCm39) |
I188L |
probably benign |
Het |
Or8b12c |
A |
G |
9: 37,715,242 (GRCm39) |
I12V |
probably benign |
Het |
Or8g51 |
T |
A |
9: 38,609,500 (GRCm39) |
H58L |
probably benign |
Het |
Pde10a |
T |
C |
17: 9,161,750 (GRCm39) |
I477T |
possibly damaging |
Het |
Pde4b |
A |
G |
4: 102,454,657 (GRCm39) |
E108G |
probably damaging |
Het |
Pdgfrb |
A |
T |
18: 61,198,855 (GRCm39) |
T338S |
probably benign |
Het |
Pgghg |
A |
G |
7: 140,523,260 (GRCm39) |
M180V |
probably benign |
Het |
Phactr4 |
G |
A |
4: 132,104,559 (GRCm39) |
T256I |
probably benign |
Het |
Pot1b |
A |
T |
17: 55,969,531 (GRCm39) |
Y546N |
probably damaging |
Het |
Rangap1 |
T |
C |
15: 81,590,704 (GRCm39) |
T463A |
probably benign |
Het |
Rap1gds1 |
T |
C |
3: 138,756,317 (GRCm39) |
I13V |
probably null |
Het |
Rbak |
A |
T |
5: 143,160,437 (GRCm39) |
Y205* |
probably null |
Het |
Reg3b |
A |
T |
6: 78,348,797 (GRCm39) |
K31M |
probably damaging |
Het |
Rfpl4 |
A |
T |
7: 5,118,533 (GRCm39) |
Y12* |
probably null |
Het |
Rnase6 |
A |
G |
14: 51,367,889 (GRCm39) |
N94D |
possibly damaging |
Het |
Rtn4 |
T |
C |
11: 29,686,464 (GRCm39) |
L273P |
probably damaging |
Het |
Ryr3 |
A |
C |
2: 112,624,812 (GRCm39) |
F2203V |
probably damaging |
Het |
Sae1 |
A |
T |
7: 16,102,490 (GRCm39) |
D161E |
possibly damaging |
Het |
Sema5a |
T |
C |
15: 32,562,877 (GRCm39) |
F296S |
possibly damaging |
Het |
Sh3rf1 |
C |
A |
8: 61,837,897 (GRCm39) |
P814Q |
probably damaging |
Het |
Slc22a29 |
C |
A |
19: 8,146,557 (GRCm39) |
R415M |
probably benign |
Het |
Slc25a25 |
C |
T |
2: 32,310,663 (GRCm39) |
|
probably null |
Het |
Slco4c1 |
T |
A |
1: 96,795,654 (GRCm39) |
M135L |
probably benign |
Het |
Slfn1 |
A |
G |
11: 83,012,579 (GRCm39) |
I232V |
possibly damaging |
Het |
Slitrk1 |
T |
A |
14: 109,149,622 (GRCm39) |
N363I |
probably damaging |
Het |
Srr |
A |
G |
11: 74,799,542 (GRCm39) |
V311A |
probably damaging |
Het |
Tasor |
T |
C |
14: 27,160,621 (GRCm39) |
S128P |
probably damaging |
Het |
Tasor |
C |
T |
14: 27,201,746 (GRCm39) |
H1419Y |
possibly damaging |
Het |
Tenm1 |
T |
C |
X: 41,916,078 (GRCm39) |
D402G |
probably benign |
Het |
Topors |
T |
C |
4: 40,261,044 (GRCm39) |
R747G |
unknown |
Het |
Trank1 |
A |
T |
9: 111,220,696 (GRCm39) |
I2478F |
probably damaging |
Het |
Trim69 |
A |
G |
2: 121,998,165 (GRCm39) |
N46D |
probably benign |
Het |
Trpm1 |
T |
A |
7: 63,879,978 (GRCm39) |
L661Q |
probably damaging |
Het |
Ttbk1 |
A |
C |
17: 46,791,150 (GRCm39) |
F45V |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,644,649 (GRCm39) |
K4708R |
probably damaging |
Het |
Unkl |
A |
G |
17: 25,428,619 (GRCm39) |
|
probably benign |
Het |
Uros |
A |
T |
7: 133,288,735 (GRCm39) |
N257K |
probably benign |
Het |
Usp25 |
A |
G |
16: 76,873,259 (GRCm39) |
Y439C |
probably damaging |
Het |
Vgf |
A |
G |
5: 137,061,029 (GRCm39) |
|
probably benign |
Het |
Vmn2r8 |
A |
T |
5: 108,947,152 (GRCm39) |
D533E |
probably damaging |
Het |
Vps13a |
A |
T |
19: 16,702,995 (GRCm39) |
Y653N |
probably damaging |
Het |
Zfp358 |
T |
C |
8: 3,545,742 (GRCm39) |
V135A |
possibly damaging |
Het |
|
Other mutations in Dysf |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00309:Dysf
|
APN |
6 |
84,085,081 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00340:Dysf
|
APN |
6 |
84,118,933 (GRCm39) |
missense |
probably benign |
0.02 |
IGL00429:Dysf
|
APN |
6 |
84,166,826 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00465:Dysf
|
APN |
6 |
84,176,830 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00800:Dysf
|
APN |
6 |
84,126,980 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01069:Dysf
|
APN |
6 |
84,176,767 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01094:Dysf
|
APN |
6 |
84,171,368 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01420:Dysf
|
APN |
6 |
84,126,741 (GRCm39) |
nonsense |
probably null |
|
IGL01649:Dysf
|
APN |
6 |
84,176,821 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01923:Dysf
|
APN |
6 |
84,187,811 (GRCm39) |
makesense |
probably null |
|
IGL01991:Dysf
|
APN |
6 |
84,090,600 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01999:Dysf
|
APN |
6 |
84,090,600 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02002:Dysf
|
APN |
6 |
84,187,769 (GRCm39) |
splice site |
probably benign |
|
IGL02136:Dysf
|
APN |
6 |
84,085,149 (GRCm39) |
missense |
probably benign |
0.43 |
IGL02318:Dysf
|
APN |
6 |
84,163,446 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02378:Dysf
|
APN |
6 |
84,088,887 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02404:Dysf
|
APN |
6 |
84,093,043 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02416:Dysf
|
APN |
6 |
84,169,896 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02535:Dysf
|
APN |
6 |
84,126,679 (GRCm39) |
missense |
possibly damaging |
0.45 |
IGL02553:Dysf
|
APN |
6 |
84,107,109 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02559:Dysf
|
APN |
6 |
84,044,428 (GRCm39) |
splice site |
probably benign |
|
IGL02563:Dysf
|
APN |
6 |
84,163,498 (GRCm39) |
splice site |
probably benign |
|
IGL02647:Dysf
|
APN |
6 |
84,114,355 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02820:Dysf
|
APN |
6 |
84,077,187 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02858:Dysf
|
APN |
6 |
84,076,471 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02860:Dysf
|
APN |
6 |
84,167,880 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02861:Dysf
|
APN |
6 |
84,016,519 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03008:Dysf
|
APN |
6 |
84,050,876 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03023:Dysf
|
APN |
6 |
84,169,989 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03074:Dysf
|
APN |
6 |
84,165,208 (GRCm39) |
missense |
probably benign |
0.25 |
IGL03342:Dysf
|
APN |
6 |
84,167,854 (GRCm39) |
missense |
probably benign |
|
PIT4305001:Dysf
|
UTSW |
6 |
84,077,216 (GRCm39) |
nonsense |
probably null |
|
R0067:Dysf
|
UTSW |
6 |
84,040,313 (GRCm39) |
missense |
possibly damaging |
0.58 |
R0106:Dysf
|
UTSW |
6 |
84,090,318 (GRCm39) |
missense |
probably benign |
0.07 |
R0106:Dysf
|
UTSW |
6 |
84,090,318 (GRCm39) |
missense |
probably benign |
0.07 |
R0124:Dysf
|
UTSW |
6 |
84,042,084 (GRCm39) |
splice site |
probably benign |
|
R0219:Dysf
|
UTSW |
6 |
84,106,443 (GRCm39) |
splice site |
probably benign |
|
R0238:Dysf
|
UTSW |
6 |
84,041,461 (GRCm39) |
nonsense |
probably null |
|
R0238:Dysf
|
UTSW |
6 |
84,041,461 (GRCm39) |
nonsense |
probably null |
|
R0239:Dysf
|
UTSW |
6 |
84,041,461 (GRCm39) |
nonsense |
probably null |
|
R0239:Dysf
|
UTSW |
6 |
84,041,461 (GRCm39) |
nonsense |
probably null |
|
R0426:Dysf
|
UTSW |
6 |
84,126,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R0455:Dysf
|
UTSW |
6 |
84,117,649 (GRCm39) |
missense |
probably benign |
0.29 |
R0482:Dysf
|
UTSW |
6 |
84,129,387 (GRCm39) |
missense |
probably benign |
0.03 |
R0545:Dysf
|
UTSW |
6 |
84,076,443 (GRCm39) |
missense |
probably damaging |
0.99 |
R0625:Dysf
|
UTSW |
6 |
84,088,969 (GRCm39) |
splice site |
probably null |
|
R0676:Dysf
|
UTSW |
6 |
84,090,318 (GRCm39) |
missense |
probably benign |
0.07 |
R0699:Dysf
|
UTSW |
6 |
84,167,828 (GRCm39) |
missense |
probably benign |
0.00 |
R1165:Dysf
|
UTSW |
6 |
84,044,051 (GRCm39) |
missense |
probably damaging |
0.98 |
R1455:Dysf
|
UTSW |
6 |
84,090,368 (GRCm39) |
missense |
probably benign |
0.01 |
R1582:Dysf
|
UTSW |
6 |
84,074,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R1584:Dysf
|
UTSW |
6 |
84,044,029 (GRCm39) |
missense |
probably benign |
0.04 |
R1605:Dysf
|
UTSW |
6 |
84,083,923 (GRCm39) |
missense |
probably damaging |
0.96 |
R1674:Dysf
|
UTSW |
6 |
84,156,697 (GRCm39) |
missense |
probably benign |
0.01 |
R1739:Dysf
|
UTSW |
6 |
84,089,217 (GRCm39) |
critical splice donor site |
probably null |
|
R1765:Dysf
|
UTSW |
6 |
84,167,884 (GRCm39) |
splice site |
probably null |
|
R1813:Dysf
|
UTSW |
6 |
84,128,906 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1900:Dysf
|
UTSW |
6 |
84,016,549 (GRCm39) |
missense |
probably damaging |
0.97 |
R2216:Dysf
|
UTSW |
6 |
84,184,227 (GRCm39) |
splice site |
probably null |
|
R2242:Dysf
|
UTSW |
6 |
84,163,491 (GRCm39) |
critical splice donor site |
probably null |
|
R2243:Dysf
|
UTSW |
6 |
84,163,491 (GRCm39) |
critical splice donor site |
probably null |
|
R2245:Dysf
|
UTSW |
6 |
84,163,491 (GRCm39) |
critical splice donor site |
probably null |
|
R2246:Dysf
|
UTSW |
6 |
84,163,491 (GRCm39) |
critical splice donor site |
probably null |
|
R2280:Dysf
|
UTSW |
6 |
84,041,476 (GRCm39) |
missense |
probably damaging |
0.99 |
R2374:Dysf
|
UTSW |
6 |
84,074,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R2403:Dysf
|
UTSW |
6 |
84,016,549 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2763:Dysf
|
UTSW |
6 |
84,083,914 (GRCm39) |
missense |
probably benign |
0.00 |
R2895:Dysf
|
UTSW |
6 |
84,163,491 (GRCm39) |
critical splice donor site |
probably null |
|
R2916:Dysf
|
UTSW |
6 |
84,163,491 (GRCm39) |
critical splice donor site |
probably null |
|
R2918:Dysf
|
UTSW |
6 |
84,163,491 (GRCm39) |
critical splice donor site |
probably null |
|
R3402:Dysf
|
UTSW |
6 |
84,163,491 (GRCm39) |
critical splice donor site |
probably null |
|
R3403:Dysf
|
UTSW |
6 |
84,163,491 (GRCm39) |
critical splice donor site |
probably null |
|
R3434:Dysf
|
UTSW |
6 |
84,047,870 (GRCm39) |
missense |
probably benign |
0.00 |
R3772:Dysf
|
UTSW |
6 |
84,129,333 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3781:Dysf
|
UTSW |
6 |
84,163,491 (GRCm39) |
critical splice donor site |
probably null |
|
R3789:Dysf
|
UTSW |
6 |
84,163,491 (GRCm39) |
critical splice donor site |
probably null |
|
R3822:Dysf
|
UTSW |
6 |
84,184,070 (GRCm39) |
splice site |
probably benign |
|
R3918:Dysf
|
UTSW |
6 |
84,163,491 (GRCm39) |
critical splice donor site |
probably null |
|
R3919:Dysf
|
UTSW |
6 |
84,163,491 (GRCm39) |
critical splice donor site |
probably null |
|
R3939:Dysf
|
UTSW |
6 |
84,163,491 (GRCm39) |
critical splice donor site |
probably null |
|
R3942:Dysf
|
UTSW |
6 |
84,163,491 (GRCm39) |
critical splice donor site |
probably null |
|
R4177:Dysf
|
UTSW |
6 |
84,044,013 (GRCm39) |
nonsense |
probably null |
|
R4179:Dysf
|
UTSW |
6 |
84,163,491 (GRCm39) |
critical splice donor site |
probably null |
|
R4180:Dysf
|
UTSW |
6 |
84,163,491 (GRCm39) |
critical splice donor site |
probably null |
|
R4299:Dysf
|
UTSW |
6 |
84,045,059 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4419:Dysf
|
UTSW |
6 |
84,184,224 (GRCm39) |
critical splice donor site |
probably null |
|
R4446:Dysf
|
UTSW |
6 |
84,182,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R4577:Dysf
|
UTSW |
6 |
84,114,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R4680:Dysf
|
UTSW |
6 |
84,074,697 (GRCm39) |
missense |
probably damaging |
0.99 |
R4708:Dysf
|
UTSW |
6 |
84,074,697 (GRCm39) |
missense |
probably damaging |
0.99 |
R4709:Dysf
|
UTSW |
6 |
84,074,697 (GRCm39) |
missense |
probably damaging |
0.99 |
R4710:Dysf
|
UTSW |
6 |
84,074,697 (GRCm39) |
missense |
probably damaging |
0.99 |
R4725:Dysf
|
UTSW |
6 |
84,074,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R4742:Dysf
|
UTSW |
6 |
84,074,697 (GRCm39) |
missense |
probably damaging |
0.99 |
R4743:Dysf
|
UTSW |
6 |
84,074,697 (GRCm39) |
missense |
probably damaging |
0.99 |
R4749:Dysf
|
UTSW |
6 |
84,043,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R4787:Dysf
|
UTSW |
6 |
84,180,310 (GRCm39) |
nonsense |
probably null |
|
R4850:Dysf
|
UTSW |
6 |
84,074,697 (GRCm39) |
missense |
probably damaging |
0.99 |
R4868:Dysf
|
UTSW |
6 |
84,156,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R4871:Dysf
|
UTSW |
6 |
84,044,005 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4951:Dysf
|
UTSW |
6 |
84,091,102 (GRCm39) |
critical splice donor site |
probably null |
|
R4952:Dysf
|
UTSW |
6 |
84,126,968 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5009:Dysf
|
UTSW |
6 |
84,128,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R5072:Dysf
|
UTSW |
6 |
84,114,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R5073:Dysf
|
UTSW |
6 |
84,114,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R5074:Dysf
|
UTSW |
6 |
84,114,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R5252:Dysf
|
UTSW |
6 |
84,163,450 (GRCm39) |
missense |
probably damaging |
0.98 |
R5260:Dysf
|
UTSW |
6 |
84,127,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R5447:Dysf
|
UTSW |
6 |
84,172,245 (GRCm39) |
missense |
probably damaging |
0.98 |
R5501:Dysf
|
UTSW |
6 |
84,064,800 (GRCm39) |
missense |
probably damaging |
0.99 |
R5533:Dysf
|
UTSW |
6 |
84,163,453 (GRCm39) |
missense |
probably damaging |
0.99 |
R5611:Dysf
|
UTSW |
6 |
84,041,860 (GRCm39) |
missense |
probably damaging |
0.98 |
R5618:Dysf
|
UTSW |
6 |
84,083,806 (GRCm39) |
missense |
probably benign |
0.03 |
R5884:Dysf
|
UTSW |
6 |
84,163,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R5927:Dysf
|
UTSW |
6 |
84,184,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R6045:Dysf
|
UTSW |
6 |
84,091,054 (GRCm39) |
missense |
probably damaging |
0.99 |
R6056:Dysf
|
UTSW |
6 |
84,083,844 (GRCm39) |
missense |
probably benign |
|
R6084:Dysf
|
UTSW |
6 |
83,996,586 (GRCm39) |
missense |
probably damaging |
0.98 |
R6084:Dysf
|
UTSW |
6 |
84,089,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R6146:Dysf
|
UTSW |
6 |
84,180,181 (GRCm39) |
missense |
probably damaging |
0.96 |
R6220:Dysf
|
UTSW |
6 |
84,126,727 (GRCm39) |
missense |
probably damaging |
0.97 |
R6232:Dysf
|
UTSW |
6 |
84,075,235 (GRCm39) |
missense |
probably benign |
0.26 |
R6247:Dysf
|
UTSW |
6 |
84,043,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R6298:Dysf
|
UTSW |
6 |
84,084,118 (GRCm39) |
splice site |
probably null |
|
R6306:Dysf
|
UTSW |
6 |
84,114,248 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6377:Dysf
|
UTSW |
6 |
83,985,945 (GRCm39) |
missense |
probably benign |
|
R6415:Dysf
|
UTSW |
6 |
84,117,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R6444:Dysf
|
UTSW |
6 |
84,167,822 (GRCm39) |
missense |
probably benign |
0.36 |
R6470:Dysf
|
UTSW |
6 |
84,043,926 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6504:Dysf
|
UTSW |
6 |
83,985,907 (GRCm39) |
missense |
probably benign |
0.03 |
R6557:Dysf
|
UTSW |
6 |
84,163,366 (GRCm39) |
missense |
probably damaging |
0.99 |
R6665:Dysf
|
UTSW |
6 |
84,107,098 (GRCm39) |
missense |
probably benign |
|
R6701:Dysf
|
UTSW |
6 |
84,089,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R6776:Dysf
|
UTSW |
6 |
84,041,876 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6909:Dysf
|
UTSW |
6 |
84,169,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R7007:Dysf
|
UTSW |
6 |
84,090,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R7013:Dysf
|
UTSW |
6 |
84,114,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R7035:Dysf
|
UTSW |
6 |
84,163,374 (GRCm39) |
missense |
probably benign |
0.02 |
R7094:Dysf
|
UTSW |
6 |
84,077,184 (GRCm39) |
missense |
probably benign |
0.43 |
R7124:Dysf
|
UTSW |
6 |
84,167,883 (GRCm39) |
splice site |
probably null |
|
R7156:Dysf
|
UTSW |
6 |
84,064,858 (GRCm39) |
critical splice donor site |
probably null |
|
R7261:Dysf
|
UTSW |
6 |
84,169,992 (GRCm39) |
missense |
probably damaging |
0.98 |
R7296:Dysf
|
UTSW |
6 |
84,083,880 (GRCm39) |
missense |
probably benign |
0.33 |
R7356:Dysf
|
UTSW |
6 |
84,044,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R7359:Dysf
|
UTSW |
6 |
84,172,306 (GRCm39) |
splice site |
probably null |
|
R7384:Dysf
|
UTSW |
6 |
84,091,087 (GRCm39) |
missense |
probably benign |
0.17 |
R7409:Dysf
|
UTSW |
6 |
84,126,664 (GRCm39) |
missense |
probably benign |
0.00 |
R7449:Dysf
|
UTSW |
6 |
84,114,362 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7476:Dysf
|
UTSW |
6 |
84,041,878 (GRCm39) |
missense |
probably benign |
0.08 |
R7496:Dysf
|
UTSW |
6 |
84,044,460 (GRCm39) |
missense |
probably benign |
0.43 |
R7573:Dysf
|
UTSW |
6 |
84,107,104 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7616:Dysf
|
UTSW |
6 |
84,078,945 (GRCm39) |
missense |
probably benign |
0.01 |
R7684:Dysf
|
UTSW |
6 |
84,077,117 (GRCm39) |
missense |
probably benign |
0.00 |
R7808:Dysf
|
UTSW |
6 |
84,047,911 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7836:Dysf
|
UTSW |
6 |
84,114,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R7868:Dysf
|
UTSW |
6 |
84,091,081 (GRCm39) |
missense |
probably benign |
0.00 |
R7873:Dysf
|
UTSW |
6 |
84,060,747 (GRCm39) |
missense |
probably benign |
|
R7956:Dysf
|
UTSW |
6 |
83,985,978 (GRCm39) |
missense |
probably benign |
0.01 |
R8130:Dysf
|
UTSW |
6 |
84,114,358 (GRCm39) |
missense |
probably damaging |
0.97 |
R8357:Dysf
|
UTSW |
6 |
84,165,227 (GRCm39) |
missense |
probably benign |
0.01 |
R8383:Dysf
|
UTSW |
6 |
83,996,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R8457:Dysf
|
UTSW |
6 |
84,165,227 (GRCm39) |
missense |
probably benign |
0.01 |
R8693:Dysf
|
UTSW |
6 |
84,088,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R8738:Dysf
|
UTSW |
6 |
84,171,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R8808:Dysf
|
UTSW |
6 |
83,996,466 (GRCm39) |
start gained |
probably benign |
|
R8836:Dysf
|
UTSW |
6 |
84,093,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R8915:Dysf
|
UTSW |
6 |
84,156,736 (GRCm39) |
missense |
probably benign |
|
R8959:Dysf
|
UTSW |
6 |
84,078,945 (GRCm39) |
missense |
probably benign |
0.01 |
R9091:Dysf
|
UTSW |
6 |
84,077,216 (GRCm39) |
nonsense |
probably null |
|
R9095:Dysf
|
UTSW |
6 |
84,156,666 (GRCm39) |
missense |
probably benign |
0.01 |
R9162:Dysf
|
UTSW |
6 |
84,089,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R9164:Dysf
|
UTSW |
6 |
84,180,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R9166:Dysf
|
UTSW |
6 |
84,126,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R9173:Dysf
|
UTSW |
6 |
84,171,379 (GRCm39) |
missense |
probably benign |
0.10 |
R9191:Dysf
|
UTSW |
6 |
84,045,048 (GRCm39) |
missense |
probably benign |
0.43 |
R9270:Dysf
|
UTSW |
6 |
84,077,216 (GRCm39) |
nonsense |
probably null |
|
R9328:Dysf
|
UTSW |
6 |
84,050,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R9470:Dysf
|
UTSW |
6 |
84,090,352 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9509:Dysf
|
UTSW |
6 |
84,187,779 (GRCm39) |
missense |
probably damaging |
0.98 |
R9511:Dysf
|
UTSW |
6 |
84,090,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R9526:Dysf
|
UTSW |
6 |
84,128,885 (GRCm39) |
missense |
probably damaging |
0.99 |
R9751:Dysf
|
UTSW |
6 |
84,163,450 (GRCm39) |
missense |
probably damaging |
0.98 |
X0063:Dysf
|
UTSW |
6 |
84,040,336 (GRCm39) |
missense |
probably damaging |
0.97 |
X0066:Dysf
|
UTSW |
6 |
84,091,084 (GRCm39) |
missense |
possibly damaging |
0.77 |
Z1176:Dysf
|
UTSW |
6 |
84,049,667 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Dysf
|
UTSW |
6 |
84,064,799 (GRCm39) |
missense |
probably benign |
0.39 |
Z1177:Dysf
|
UTSW |
6 |
84,041,505 (GRCm39) |
missense |
probably benign |
|
|