Other mutations in this stock |
Total: 101 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310002L09Rik |
A |
T |
4: 73,861,115 (GRCm39) |
W162R |
probably benign |
Het |
4930438A08Rik |
C |
A |
11: 58,184,464 (GRCm39) |
P394H |
probably damaging |
Het |
Aggf1 |
C |
T |
13: 95,508,123 (GRCm39) |
C81Y |
probably benign |
Het |
Agxt2 |
A |
T |
15: 10,378,963 (GRCm39) |
D188V |
probably damaging |
Het |
Angpt2 |
T |
C |
8: 18,748,132 (GRCm39) |
K376R |
probably benign |
Het |
Anxa5 |
A |
G |
3: 36,504,840 (GRCm39) |
S241P |
probably damaging |
Het |
Aox3 |
A |
T |
1: 58,209,018 (GRCm39) |
K850N |
probably damaging |
Het |
Arid5a |
T |
C |
1: 36,358,473 (GRCm39) |
M415T |
probably benign |
Het |
Aspa |
T |
A |
11: 73,199,578 (GRCm39) |
N233I |
probably damaging |
Het |
Atp4b |
C |
T |
8: 13,438,782 (GRCm39) |
R198Q |
probably damaging |
Het |
Atp8b2 |
A |
T |
3: 89,853,528 (GRCm39) |
V719E |
possibly damaging |
Het |
Bltp2 |
C |
A |
11: 78,162,210 (GRCm39) |
L691I |
possibly damaging |
Het |
Cacna1s |
T |
G |
1: 136,033,574 (GRCm39) |
V1017G |
probably damaging |
Het |
Chrna4 |
G |
T |
2: 180,671,235 (GRCm39) |
Q174K |
probably damaging |
Het |
Chrnb1 |
A |
T |
11: 69,677,765 (GRCm39) |
V329D |
probably damaging |
Het |
Chst14 |
T |
C |
2: 118,758,214 (GRCm39) |
L336P |
probably damaging |
Het |
Clec2e |
T |
C |
6: 129,077,772 (GRCm39) |
D22G |
probably benign |
Het |
Csrnp2 |
A |
C |
15: 100,380,263 (GRCm39) |
S343A |
probably benign |
Het |
Dapl1 |
C |
A |
2: 59,315,057 (GRCm39) |
A2E |
probably damaging |
Het |
Dlec1 |
G |
T |
9: 118,950,991 (GRCm39) |
R519L |
probably damaging |
Het |
Dmgdh |
T |
A |
13: 93,845,251 (GRCm39) |
F415I |
possibly damaging |
Het |
Dmgdh |
T |
C |
13: 93,888,834 (GRCm39) |
V824A |
probably damaging |
Het |
Dnah11 |
T |
G |
12: 117,892,191 (GRCm39) |
T3661P |
probably benign |
Het |
Dnah3 |
A |
G |
7: 119,629,254 (GRCm39) |
F1434L |
probably damaging |
Het |
Dnajc11 |
C |
A |
4: 152,062,583 (GRCm39) |
|
probably benign |
Het |
Dot1l |
A |
G |
10: 80,621,929 (GRCm39) |
E527G |
probably damaging |
Het |
Drc7 |
T |
C |
8: 95,801,679 (GRCm39) |
L680P |
probably damaging |
Het |
Ece1 |
A |
G |
4: 137,688,958 (GRCm39) |
Y665C |
probably damaging |
Het |
Emc1 |
A |
G |
4: 139,081,533 (GRCm39) |
K54E |
possibly damaging |
Het |
Enoph1 |
C |
T |
5: 100,215,760 (GRCm39) |
T247M |
probably damaging |
Het |
Exoc2 |
T |
C |
13: 31,084,812 (GRCm39) |
K383R |
probably benign |
Het |
Fam227b |
A |
T |
2: 125,962,972 (GRCm39) |
H181Q |
probably damaging |
Het |
Fsip2 |
A |
T |
2: 82,816,017 (GRCm39) |
M3917L |
probably benign |
Het |
Gtf3a |
T |
A |
5: 146,892,338 (GRCm39) |
|
probably benign |
Het |
Hgfac |
T |
A |
5: 35,198,973 (GRCm39) |
C11* |
probably null |
Het |
Hmcn1 |
C |
A |
1: 150,539,660 (GRCm39) |
A2944S |
probably damaging |
Het |
Hps5 |
T |
A |
7: 46,416,521 (GRCm39) |
Y947F |
probably benign |
Het |
Ighv2-5 |
A |
T |
12: 113,649,120 (GRCm39) |
I111K |
probably benign |
Het |
Inpp5e |
A |
T |
2: 26,297,860 (GRCm39) |
L247* |
probably null |
Het |
Kbtbd11 |
T |
C |
8: 15,077,577 (GRCm39) |
S59P |
probably benign |
Het |
Kctd19 |
G |
A |
8: 106,123,082 (GRCm39) |
H111Y |
probably damaging |
Het |
Kif1a |
T |
C |
1: 92,952,370 (GRCm39) |
D1303G |
probably damaging |
Het |
Kif7 |
A |
G |
7: 79,363,842 (GRCm39) |
V22A |
possibly damaging |
Het |
Lrit3 |
A |
T |
3: 129,583,004 (GRCm39) |
C328S |
probably damaging |
Het |
Lrrc37a |
G |
T |
11: 103,388,484 (GRCm39) |
Q2314K |
unknown |
Het |
LTO1 |
G |
T |
7: 144,469,023 (GRCm39) |
V17L |
possibly damaging |
Het |
Lurap1 |
G |
T |
4: 115,994,599 (GRCm39) |
P211T |
possibly damaging |
Het |
Mbd2 |
T |
A |
18: 70,713,874 (GRCm39) |
N5K |
possibly damaging |
Het |
Mbtps1 |
A |
C |
8: 120,242,341 (GRCm39) |
L894V |
probably benign |
Het |
Mefv |
G |
A |
16: 3,525,906 (GRCm39) |
S787F |
possibly damaging |
Het |
Miip |
T |
A |
4: 147,946,792 (GRCm39) |
I289F |
probably damaging |
Het |
Mogat2 |
T |
A |
7: 98,872,720 (GRCm39) |
I155F |
possibly damaging |
Het |
Mpp3 |
C |
A |
11: 101,902,515 (GRCm39) |
|
probably null |
Het |
Mrrf |
A |
G |
2: 36,067,233 (GRCm39) |
K220E |
probably damaging |
Het |
Mtmr6 |
C |
T |
14: 60,535,619 (GRCm39) |
P485L |
probably damaging |
Het |
Mtor |
G |
A |
4: 148,621,892 (GRCm39) |
R1896K |
probably benign |
Het |
Myh3 |
C |
T |
11: 66,978,371 (GRCm39) |
P453S |
probably benign |
Het |
Nebl |
A |
G |
2: 17,455,045 (GRCm39) |
V112A |
probably benign |
Het |
Nmnat2 |
G |
A |
1: 152,950,480 (GRCm39) |
W55* |
probably null |
Het |
Nprl3 |
A |
G |
11: 32,217,432 (GRCm39) |
S37P |
probably damaging |
Het |
Or4a73 |
T |
C |
2: 89,421,445 (GRCm39) |
N5D |
possibly damaging |
Het |
Pcdhga4 |
T |
G |
18: 37,819,383 (GRCm39) |
S311A |
probably benign |
Het |
Pcdhgb6 |
T |
C |
18: 37,876,165 (GRCm39) |
V291A |
probably benign |
Het |
Peg10 |
GAT |
GATCAT |
6: 4,756,449 (GRCm39) |
|
probably benign |
Het |
Peg3 |
T |
C |
7: 6,712,570 (GRCm39) |
E884G |
probably damaging |
Het |
Pgpep1 |
G |
A |
8: 71,105,101 (GRCm39) |
T53M |
probably damaging |
Het |
Phf12 |
A |
G |
11: 77,900,341 (GRCm39) |
T146A |
probably benign |
Het |
Polr3k |
C |
G |
2: 181,506,281 (GRCm39) |
N10K |
probably damaging |
Het |
Prickle4 |
C |
A |
17: 48,001,135 (GRCm39) |
G144C |
probably damaging |
Het |
Ptpn6 |
T |
C |
6: 124,709,398 (GRCm39) |
Y25C |
probably damaging |
Het |
Rad1 |
A |
G |
15: 10,488,160 (GRCm39) |
I95V |
probably damaging |
Het |
Rad23b |
A |
G |
4: 55,382,540 (GRCm39) |
T248A |
probably benign |
Het |
Rapgef3 |
T |
C |
15: 97,656,742 (GRCm39) |
D299G |
probably damaging |
Het |
Rcc2 |
T |
G |
4: 140,444,335 (GRCm39) |
V342G |
possibly damaging |
Het |
Rgs3 |
G |
T |
4: 62,544,143 (GRCm39) |
R136L |
probably damaging |
Het |
Scube2 |
A |
T |
7: 109,432,220 (GRCm39) |
C399* |
probably null |
Het |
Serpinb3d |
T |
C |
1: 107,007,452 (GRCm39) |
Y178C |
probably damaging |
Het |
Slc1a7 |
A |
G |
4: 107,869,458 (GRCm39) |
T508A |
probably benign |
Het |
Slc29a4 |
C |
T |
5: 142,705,832 (GRCm39) |
R439C |
probably damaging |
Het |
Sntg2 |
A |
G |
12: 30,362,560 (GRCm39) |
I62T |
probably benign |
Het |
Sowaha |
G |
A |
11: 53,369,914 (GRCm39) |
P274L |
probably damaging |
Het |
Sptan1 |
A |
G |
2: 29,886,794 (GRCm39) |
N869S |
probably benign |
Het |
Stx18 |
C |
A |
5: 38,263,908 (GRCm39) |
A64D |
probably damaging |
Het |
Stxbp5 |
A |
G |
10: 9,646,430 (GRCm39) |
V94A |
probably benign |
Het |
Sult1a1 |
T |
A |
7: 126,275,624 (GRCm39) |
|
probably null |
Het |
Susd1 |
G |
T |
4: 59,379,687 (GRCm39) |
H313Q |
possibly damaging |
Het |
Tdrd9 |
A |
T |
12: 111,951,475 (GRCm39) |
K88N |
probably damaging |
Het |
Tlr5 |
A |
C |
1: 182,801,603 (GRCm39) |
R302S |
possibly damaging |
Het |
Tnr |
C |
T |
1: 159,714,479 (GRCm39) |
T786I |
probably damaging |
Het |
Tprg1l |
A |
G |
4: 154,244,552 (GRCm39) |
S148P |
probably damaging |
Het |
Trpc4ap |
T |
A |
2: 155,512,994 (GRCm39) |
N127I |
probably damaging |
Het |
Tulp2 |
T |
A |
7: 45,139,797 (GRCm39) |
|
probably null |
Het |
Uggt2 |
C |
T |
14: 119,273,381 (GRCm39) |
|
probably null |
Het |
Ulk4 |
T |
A |
9: 121,102,021 (GRCm39) |
Y19F |
probably damaging |
Het |
Upf1 |
T |
C |
8: 70,785,687 (GRCm39) |
Y1053C |
probably damaging |
Het |
Vars2 |
A |
T |
17: 35,976,680 (GRCm39) |
H223Q |
probably benign |
Het |
Vmn2r106 |
T |
A |
17: 20,487,806 (GRCm39) |
|
probably null |
Het |
Ythdc2 |
T |
A |
18: 44,973,277 (GRCm39) |
F305I |
probably damaging |
Het |
Zfp281 |
T |
C |
1: 136,553,178 (GRCm39) |
F52S |
possibly damaging |
Het |
Zfp292 |
A |
T |
4: 34,809,784 (GRCm39) |
C1087S |
probably damaging |
Het |
Zfp335 |
A |
T |
2: 164,737,018 (GRCm39) |
|
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 |
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 |
|
|