Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm5 |
T |
A |
4: 144,507,191 (GRCm39) |
I65F |
possibly damaging |
Het |
Abca13 |
C |
A |
11: 9,283,257 (GRCm39) |
S3226R |
probably damaging |
Het |
Abhd14b |
A |
G |
9: 106,327,340 (GRCm39) |
I41V |
probably benign |
Het |
Acot2 |
T |
C |
12: 84,039,441 (GRCm39) |
S317P |
probably benign |
Het |
Acp7 |
T |
C |
7: 28,314,513 (GRCm39) |
E284G |
possibly damaging |
Het |
Adamts5 |
A |
G |
16: 85,696,714 (GRCm39) |
F148L |
probably benign |
Het |
Adcy10 |
C |
T |
1: 165,404,177 (GRCm39) |
P1611S |
unknown |
Het |
Agr2 |
A |
G |
12: 36,045,923 (GRCm39) |
T57A |
probably damaging |
Het |
Ankar |
T |
G |
1: 72,697,624 (GRCm39) |
I1060L |
probably benign |
Het |
Ano10 |
T |
A |
9: 122,005,409 (GRCm39) |
D77V |
unknown |
Het |
Anxa2r1 |
T |
A |
13: 120,496,797 (GRCm39) |
Q24L |
possibly damaging |
Het |
Apc2 |
G |
A |
10: 80,148,458 (GRCm39) |
V1171I |
probably damaging |
Het |
Apoa4 |
G |
A |
9: 46,152,772 (GRCm39) |
R19Q |
not run |
Het |
Arhgap33 |
A |
G |
7: 30,226,696 (GRCm39) |
S504P |
probably damaging |
Het |
Atg2a |
T |
C |
19: 6,311,707 (GRCm39) |
V1862A |
probably damaging |
Het |
Atp7b |
T |
C |
8: 22,512,331 (GRCm39) |
S511G |
probably benign |
Het |
Bcl10 |
A |
G |
3: 145,638,795 (GRCm39) |
K146E |
possibly damaging |
Het |
Bsg |
A |
T |
10: 79,545,631 (GRCm39) |
D181V |
probably damaging |
Het |
Btg4 |
T |
C |
9: 51,030,413 (GRCm39) |
V171A |
probably benign |
Het |
Cdh8 |
A |
C |
8: 99,957,138 (GRCm39) |
N188K |
probably benign |
Het |
Cflar |
C |
A |
1: 58,791,735 (GRCm39) |
T346K |
|
Het |
Chrna5 |
T |
C |
9: 54,912,117 (GRCm39) |
S306P |
probably damaging |
Het |
Cldn20 |
G |
A |
17: 3,582,886 (GRCm39) |
G20R |
probably damaging |
Het |
Clns1a |
G |
A |
7: 97,345,988 (GRCm39) |
A18T |
probably benign |
Het |
D130043K22Rik |
A |
G |
13: 25,066,588 (GRCm39) |
Y795C |
probably damaging |
Het |
Dync1li2 |
A |
C |
8: 105,169,175 (GRCm39) |
S38A |
probably benign |
Het |
Elapor1 |
A |
T |
3: 108,370,784 (GRCm39) |
|
probably null |
Het |
Eral1 |
A |
G |
11: 77,964,927 (GRCm39) |
I422T |
possibly damaging |
Het |
Exoc3 |
G |
A |
13: 74,320,275 (GRCm39) |
P729S |
probably benign |
Het |
Eya1 |
T |
A |
1: 14,299,736 (GRCm39) |
Y339F |
probably damaging |
Het |
Faah |
G |
T |
4: 115,862,364 (GRCm39) |
N206K |
probably damaging |
Het |
Fem1a |
A |
G |
17: 56,564,537 (GRCm39) |
E210G |
probably benign |
Het |
Gcc2 |
T |
A |
10: 58,105,786 (GRCm39) |
S341T |
probably damaging |
Het |
Gfpt2 |
A |
T |
11: 49,701,817 (GRCm39) |
I123F |
possibly damaging |
Het |
Gm3047 |
T |
A |
14: 4,558,271 (GRCm38) |
N164K |
probably damaging |
Het |
Gm3327 |
A |
G |
14: 44,362,334 (GRCm39) |
K78E |
|
Het |
Herpud1 |
A |
G |
8: 95,116,005 (GRCm39) |
I57V |
probably damaging |
Het |
Homer1 |
A |
T |
13: 93,529,547 (GRCm39) |
R285S |
possibly damaging |
Het |
Hps6 |
T |
A |
19: 45,992,456 (GRCm39) |
V131E |
possibly damaging |
Het |
Il1r1 |
T |
A |
1: 40,321,421 (GRCm39) |
I11N |
possibly damaging |
Het |
Jakmip1 |
T |
A |
5: 37,330,551 (GRCm39) |
D410E |
possibly damaging |
Het |
Kif3a |
T |
A |
11: 53,469,681 (GRCm39) |
F97L |
probably damaging |
Het |
Klf11 |
C |
T |
12: 24,703,742 (GRCm39) |
T76I |
probably damaging |
Het |
Ldlr |
A |
C |
9: 21,651,090 (GRCm39) |
T503P |
probably benign |
Het |
Mapk3 |
G |
C |
7: 126,363,463 (GRCm39) |
R279P |
|
Het |
Mb21d2 |
A |
T |
16: 28,647,664 (GRCm39) |
D103E |
probably benign |
Het |
Msh4 |
T |
A |
3: 153,594,385 (GRCm39) |
M333L |
probably benign |
Het |
Mycbp2 |
A |
G |
14: 103,513,829 (GRCm39) |
I836T |
probably damaging |
Het |
Myh1 |
A |
T |
11: 67,115,201 (GRCm39) |
E1912V |
possibly damaging |
Het |
Ncapd2 |
A |
G |
6: 125,150,364 (GRCm39) |
V887A |
probably benign |
Het |
Nlrp4a |
G |
A |
7: 26,148,963 (GRCm39) |
R190Q |
not run |
Het |
Nop53 |
T |
C |
7: 15,673,420 (GRCm39) |
T344A |
probably damaging |
Het |
Or2r3 |
A |
T |
6: 42,448,257 (GRCm39) |
L285Q |
possibly damaging |
Het |
Or5an11 |
T |
C |
19: 12,246,440 (GRCm39) |
V282A |
possibly damaging |
Het |
Or7h8 |
A |
G |
9: 20,124,041 (GRCm39) |
Y132C |
probably damaging |
Het |
Pcyox1l |
A |
C |
18: 61,831,461 (GRCm39) |
V266G |
probably damaging |
Het |
Pde5a |
A |
G |
3: 122,618,649 (GRCm39) |
Y654C |
probably damaging |
Het |
Polq |
T |
C |
16: 36,849,780 (GRCm39) |
S345P |
probably damaging |
Het |
Polr1f |
G |
T |
12: 33,483,631 (GRCm39) |
G128W |
probably damaging |
Het |
Prdm1 |
A |
T |
10: 44,334,503 (GRCm39) |
C8S |
probably benign |
Het |
Psg17 |
T |
A |
7: 18,552,585 (GRCm39) |
Q230L |
possibly damaging |
Het |
Rab11fip5 |
A |
T |
6: 85,325,312 (GRCm39) |
S332T |
possibly damaging |
Het |
Rac2 |
T |
A |
15: 78,446,131 (GRCm39) |
K186* |
probably null |
Het |
S100pbp |
T |
C |
4: 129,075,702 (GRCm39) |
N208D |
probably benign |
Het |
Scaf11 |
A |
T |
15: 96,318,268 (GRCm39) |
V432D |
possibly damaging |
Het |
Skic3 |
A |
C |
13: 76,298,854 (GRCm39) |
S1187R |
possibly damaging |
Het |
Slc34a1 |
G |
T |
13: 55,550,747 (GRCm39) |
C225F |
probably benign |
Het |
Slc35e2 |
A |
T |
4: 155,695,089 (GRCm39) |
M152L |
probably benign |
Het |
Slc49a3 |
A |
T |
5: 108,593,926 (GRCm39) |
I61K |
probably damaging |
Het |
Slc9a4 |
T |
A |
1: 40,651,411 (GRCm39) |
I563K |
probably benign |
Het |
Sppl3 |
T |
G |
5: 115,199,700 (GRCm39) |
|
probably null |
Het |
Stam |
T |
C |
2: 14,139,241 (GRCm39) |
F301L |
probably benign |
Het |
Supt16 |
G |
A |
14: 52,418,619 (GRCm39) |
R213W |
probably damaging |
Het |
Tbc1d8 |
A |
T |
1: 39,433,179 (GRCm39) |
D334E |
probably benign |
Het |
Tmem87a |
C |
T |
2: 120,202,004 (GRCm39) |
|
probably null |
Het |
Tnk1 |
T |
C |
11: 69,742,447 (GRCm39) |
Y661C |
probably damaging |
Het |
Tnpo2 |
G |
A |
8: 85,776,748 (GRCm39) |
R485H |
probably damaging |
Het |
Tnxb |
A |
G |
17: 34,937,492 (GRCm39) |
D2947G |
probably damaging |
Het |
Traf4 |
A |
G |
11: 78,051,617 (GRCm39) |
|
probably null |
Het |
Trappc10 |
A |
T |
10: 78,045,218 (GRCm39) |
M490K |
possibly damaging |
Het |
Trav12-1 |
A |
G |
14: 53,775,993 (GRCm39) |
T49A |
probably benign |
Het |
Ubap1l |
AGAGGAGGAGGAGGAGGA |
AGAGGAGGAGGAGGA |
9: 65,279,032 (GRCm39) |
|
probably benign |
Het |
Unc79 |
G |
T |
12: 103,137,837 (GRCm39) |
V2485L |
probably benign |
Het |
Ush2a |
T |
C |
1: 188,132,360 (GRCm39) |
S861P |
probably damaging |
Het |
Vcam1 |
A |
G |
3: 115,910,877 (GRCm39) |
V507A |
possibly damaging |
Het |
Vmn1r218 |
A |
G |
13: 23,320,895 (GRCm39) |
M81V |
probably benign |
Het |
Zfp652 |
G |
T |
11: 95,643,830 (GRCm39) |
V343L |
probably 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 |
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 |
|
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 |
|
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 |
|
|