Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930433I11Rik |
T |
C |
7: 40,643,282 (GRCm39) |
I317T |
possibly damaging |
Het |
Acsl5 |
G |
A |
19: 55,257,260 (GRCm39) |
|
probably null |
Het |
Ahrr |
G |
A |
13: 74,378,035 (GRCm39) |
T136I |
probably damaging |
Het |
AI597479 |
G |
A |
1: 43,150,261 (GRCm39) |
D124N |
probably damaging |
Het |
Arap2 |
G |
T |
5: 62,761,914 (GRCm39) |
A1604D |
probably damaging |
Het |
Bcl6 |
G |
A |
16: 23,784,976 (GRCm39) |
R675* |
probably null |
Het |
Cadps2 |
T |
C |
6: 23,688,955 (GRCm39) |
N118S |
probably benign |
Het |
Caskin1 |
T |
A |
17: 24,719,657 (GRCm39) |
|
probably null |
Het |
Cc2d1a |
C |
T |
8: 84,862,389 (GRCm39) |
V684M |
possibly damaging |
Het |
Ccdc91 |
T |
C |
6: 147,435,676 (GRCm39) |
S87P |
possibly damaging |
Het |
Cdr2l |
A |
G |
11: 115,281,792 (GRCm39) |
Q99R |
probably benign |
Het |
Celsr3 |
T |
C |
9: 108,715,203 (GRCm39) |
L2066P |
possibly damaging |
Het |
Cep95 |
A |
C |
11: 106,700,050 (GRCm39) |
L313F |
possibly damaging |
Het |
Chst10 |
G |
A |
1: 38,913,088 (GRCm39) |
T63M |
probably damaging |
Het |
Clrn2 |
G |
A |
5: 45,611,258 (GRCm39) |
G36R |
probably damaging |
Het |
Cnn2 |
T |
G |
10: 79,830,349 (GRCm39) |
Y273* |
probably null |
Het |
Crtap |
T |
C |
9: 114,207,164 (GRCm39) |
T365A |
probably benign |
Het |
D630045J12Rik |
T |
C |
6: 38,171,964 (GRCm39) |
T735A |
possibly damaging |
Het |
Disp2 |
C |
T |
2: 118,622,292 (GRCm39) |
A1008V |
probably damaging |
Het |
Dmrt3 |
A |
G |
19: 25,588,317 (GRCm39) |
D52G |
probably damaging |
Het |
Dmrta1 |
T |
G |
4: 89,576,700 (GRCm39) |
L52R |
probably damaging |
Het |
Dmrta2 |
A |
G |
4: 109,839,185 (GRCm39) |
T311A |
probably damaging |
Het |
Dnm1 |
T |
A |
2: 32,230,479 (GRCm39) |
N112Y |
probably damaging |
Het |
Ep400 |
A |
G |
5: 110,833,229 (GRCm39) |
F2034L |
unknown |
Het |
F12 |
G |
A |
13: 55,566,310 (GRCm39) |
A494V |
probably damaging |
Het |
Fbp2 |
A |
T |
13: 62,989,675 (GRCm39) |
F210L |
probably benign |
Het |
Fbxo31 |
T |
A |
8: 122,281,060 (GRCm39) |
Q362L |
possibly damaging |
Het |
Fkbp4 |
C |
T |
6: 128,412,787 (GRCm39) |
A95T |
probably benign |
Het |
Frmd6 |
T |
G |
12: 70,923,983 (GRCm39) |
C80W |
probably damaging |
Het |
Fsip2 |
A |
G |
2: 82,813,085 (GRCm39) |
I3135V |
probably benign |
Het |
Garre1 |
G |
T |
7: 33,945,133 (GRCm39) |
N582K |
possibly damaging |
Het |
Guca2b |
T |
A |
4: 119,514,887 (GRCm39) |
E34V |
probably damaging |
Het |
Hdlbp |
G |
A |
1: 93,341,637 (GRCm39) |
T974I |
probably damaging |
Het |
Hsdl2 |
T |
A |
4: 59,617,653 (GRCm39) |
M460K |
possibly damaging |
Het |
Ift172 |
C |
T |
5: 31,429,419 (GRCm39) |
V581M |
probably damaging |
Het |
Ift74 |
A |
G |
4: 94,549,189 (GRCm39) |
K313R |
possibly damaging |
Het |
Ints4 |
T |
A |
7: 97,184,493 (GRCm39) |
|
probably null |
Het |
Iqca1l |
C |
T |
5: 24,757,648 (GRCm39) |
E150K |
probably benign |
Het |
Kif21b |
A |
C |
1: 136,075,562 (GRCm39) |
T230P |
probably damaging |
Het |
Kit |
A |
T |
5: 75,776,034 (GRCm39) |
Y272F |
probably benign |
Het |
Krt77 |
G |
A |
15: 101,773,931 (GRCm39) |
T241M |
probably benign |
Het |
Lce1j |
T |
A |
3: 92,696,491 (GRCm39) |
S96C |
unknown |
Het |
Marveld3 |
T |
A |
8: 110,674,820 (GRCm39) |
D332V |
probably damaging |
Het |
Matr3 |
G |
T |
18: 35,705,974 (GRCm39) |
V300F |
probably damaging |
Het |
Mical1 |
T |
A |
10: 41,361,253 (GRCm39) |
|
probably null |
Het |
Mslnl |
T |
A |
17: 25,962,184 (GRCm39) |
V194E |
probably benign |
Het |
Mug1 |
C |
A |
6: 121,857,864 (GRCm39) |
T1119K |
probably damaging |
Het |
Mug1 |
C |
T |
6: 121,861,302 (GRCm39) |
P1308S |
probably damaging |
Het |
Neb |
C |
A |
2: 52,195,295 (GRCm39) |
|
probably null |
Het |
Neo1 |
T |
A |
9: 58,810,206 (GRCm39) |
T1082S |
probably damaging |
Het |
Nkx6-2 |
C |
T |
7: 139,162,045 (GRCm39) |
|
probably null |
Het |
Or10g6 |
T |
C |
9: 39,934,526 (GRCm39) |
I279T |
probably benign |
Het |
Or8k27 |
T |
A |
2: 86,275,652 (GRCm39) |
I225L |
probably damaging |
Het |
Orc1 |
A |
T |
4: 108,452,656 (GRCm39) |
E177V |
probably benign |
Het |
Parp1 |
G |
A |
1: 180,426,629 (GRCm39) |
V924I |
possibly damaging |
Het |
Pax2 |
A |
T |
19: 44,777,298 (GRCm39) |
I165F |
probably benign |
Het |
Pnma2 |
C |
T |
14: 67,153,980 (GRCm39) |
P135S |
probably benign |
Het |
Ranbp17 |
A |
G |
11: 33,247,420 (GRCm39) |
I718T |
probably damaging |
Het |
Rbm25 |
T |
A |
12: 83,710,965 (GRCm39) |
D359E |
unknown |
Het |
Rgs3 |
T |
C |
4: 62,535,363 (GRCm39) |
L194P |
probably damaging |
Het |
Serpinb6b |
A |
G |
13: 33,155,598 (GRCm39) |
I104V |
probably benign |
Het |
Smg9 |
A |
G |
7: 24,120,286 (GRCm39) |
D420G |
probably benign |
Het |
Smpd1 |
C |
T |
7: 105,203,693 (GRCm39) |
|
probably benign |
Het |
Snx17 |
T |
A |
5: 31,354,692 (GRCm39) |
M318K |
probably damaging |
Het |
Spata31e5 |
A |
T |
1: 28,815,848 (GRCm39) |
M728K |
possibly damaging |
Het |
Stard10 |
G |
A |
7: 100,995,258 (GRCm39) |
D337N |
probably damaging |
Het |
Tex14 |
A |
G |
11: 87,375,545 (GRCm39) |
T103A |
probably damaging |
Het |
Tle1 |
A |
G |
4: 72,088,953 (GRCm39) |
S97P |
probably benign |
Het |
Tnfrsf8 |
T |
A |
4: 145,041,654 (GRCm39) |
M1L |
unknown |
Het |
Traf3ip2 |
T |
C |
10: 39,502,173 (GRCm39) |
L107P |
possibly damaging |
Het |
Trpc7 |
A |
T |
13: 56,937,579 (GRCm39) |
S626T |
possibly damaging |
Het |
Ubl7 |
T |
A |
9: 57,837,039 (GRCm39) |
I350N |
probably damaging |
Het |
Ubr3 |
T |
A |
2: 69,851,967 (GRCm39) |
I1878N |
probably damaging |
Het |
Usp24 |
G |
T |
4: 106,245,116 (GRCm39) |
|
probably null |
Het |
Vcan |
A |
T |
13: 89,837,229 (GRCm39) |
S2772T |
possibly damaging |
Het |
Vmn2r79 |
T |
C |
7: 86,686,851 (GRCm39) |
V744A |
probably damaging |
Het |
Wbp2nl |
T |
C |
15: 82,189,903 (GRCm39) |
S32P |
probably damaging |
Het |
Wwc1 |
A |
G |
11: 35,788,201 (GRCm39) |
|
probably null |
Het |
Zfp629 |
C |
T |
7: 127,211,463 (GRCm39) |
W115* |
probably null |
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 |
R1960:Dysf
|
UTSW |
6 |
84,050,885 (GRCm39) |
missense |
probably benign |
0.12 |
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 |
84,089,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R6084:Dysf
|
UTSW |
6 |
83,996,586 (GRCm39) |
missense |
probably damaging |
0.98 |
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 |
|
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 |
|
|