Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700011L22Rik |
T |
C |
8: 79,955,996 (GRCm39) |
Y87C |
probably benign |
Het |
5530401A14Rik |
A |
G |
11: 81,784,694 (GRCm39) |
|
probably benign |
Het |
Adamts5 |
T |
C |
16: 85,696,188 (GRCm39) |
D323G |
probably damaging |
Het |
Albfm1 |
A |
T |
5: 90,732,848 (GRCm39) |
Q553L |
possibly damaging |
Het |
Bicc1 |
G |
A |
10: 70,792,911 (GRCm39) |
R248* |
probably null |
Het |
Bivm |
T |
G |
1: 44,158,233 (GRCm39) |
|
probably benign |
Het |
Btnl12 |
G |
T |
16: 37,676,384 (GRCm39) |
Q128K |
probably benign |
Het |
Ccdc8 |
A |
C |
7: 16,729,956 (GRCm39) |
T482P |
unknown |
Het |
Ccnb2 |
T |
C |
9: 70,326,375 (GRCm39) |
I21V |
probably benign |
Het |
Cfap73 |
A |
T |
5: 120,769,777 (GRCm39) |
I82N |
probably damaging |
Het |
Chd3 |
A |
C |
11: 69,242,944 (GRCm39) |
F1426V |
possibly damaging |
Het |
Clcn2 |
A |
T |
16: 20,530,438 (GRCm39) |
|
probably null |
Het |
Col6a5 |
T |
C |
9: 105,803,117 (GRCm39) |
N1283D |
unknown |
Het |
Cyp39a1 |
G |
T |
17: 44,042,882 (GRCm39) |
G411W |
probably damaging |
Het |
D130052B06Rik |
A |
T |
11: 33,574,008 (GRCm39) |
I202L |
unknown |
Het |
Defa38 |
A |
T |
8: 21,585,248 (GRCm39) |
C65S |
possibly damaging |
Het |
Dlgap1 |
T |
C |
17: 71,125,093 (GRCm39) |
L948P |
probably damaging |
Het |
Dnah3 |
C |
T |
7: 119,566,745 (GRCm39) |
V2494M |
probably damaging |
Het |
Eif2ak4 |
C |
A |
2: 118,219,296 (GRCm39) |
S36* |
probably null |
Het |
Elmod3 |
C |
T |
6: 72,545,851 (GRCm39) |
R297H |
probably benign |
Het |
Epas1 |
C |
A |
17: 87,116,827 (GRCm39) |
R166S |
probably damaging |
Het |
Erv3 |
A |
G |
2: 131,697,942 (GRCm39) |
L139P |
probably damaging |
Het |
Fryl |
A |
G |
5: 73,275,894 (GRCm39) |
V90A |
probably damaging |
Het |
Fxr2 |
A |
G |
11: 69,541,877 (GRCm39) |
R439G |
possibly damaging |
Het |
Gabrd |
A |
T |
4: 155,470,931 (GRCm39) |
V259D |
possibly damaging |
Het |
Galnt10 |
A |
G |
11: 57,674,619 (GRCm39) |
Y536C |
probably damaging |
Het |
Gbp10 |
A |
T |
5: 105,366,269 (GRCm39) |
L545Q |
probably damaging |
Het |
Gfpt1 |
A |
T |
6: 87,062,239 (GRCm39) |
I517F |
probably damaging |
Het |
Glb1 |
T |
C |
9: 114,267,010 (GRCm39) |
Y225H |
probably damaging |
Het |
Gm1110 |
C |
T |
9: 26,794,505 (GRCm39) |
|
probably null |
Het |
Gmps |
C |
T |
3: 63,887,558 (GRCm39) |
P10L |
probably benign |
Het |
Greb1l |
T |
A |
18: 10,547,068 (GRCm39) |
V1465D |
probably damaging |
Het |
Helz2 |
A |
G |
2: 180,882,106 (GRCm39) |
V229A |
probably benign |
Het |
Hipk1 |
A |
T |
3: 103,654,218 (GRCm39) |
L924Q |
probably benign |
Het |
Ifngr1 |
T |
G |
10: 19,484,909 (GRCm39) |
L303V |
possibly damaging |
Het |
Kif22 |
T |
C |
7: 126,630,250 (GRCm39) |
N429D |
probably benign |
Het |
Ktn1 |
T |
C |
14: 47,914,253 (GRCm39) |
Y401H |
probably damaging |
Het |
Lars2 |
T |
G |
9: 123,201,053 (GRCm39) |
I39S |
probably damaging |
Het |
Lipf |
C |
T |
19: 33,944,244 (GRCm39) |
A151V |
probably damaging |
Het |
Lrp1 |
A |
T |
10: 127,402,469 (GRCm39) |
M2234K |
probably damaging |
Het |
Lrp1b |
A |
G |
2: 40,591,825 (GRCm39) |
V56A |
unknown |
Het |
Lyar |
T |
A |
5: 38,391,352 (GRCm39) |
H350Q |
probably benign |
Het |
Mill2 |
A |
T |
7: 18,590,489 (GRCm39) |
M190L |
probably benign |
Het |
Morc3 |
A |
G |
16: 93,671,733 (GRCm39) |
D921G |
probably damaging |
Het |
Mpp2 |
G |
T |
11: 101,950,180 (GRCm39) |
T558K |
probably benign |
Het |
Myh4 |
A |
G |
11: 67,135,550 (GRCm39) |
D379G |
probably benign |
Het |
Neb |
A |
C |
2: 52,084,437 (GRCm39) |
|
probably null |
Het |
Nedd1 |
G |
A |
10: 92,530,962 (GRCm39) |
R376* |
probably null |
Het |
Nlrc4 |
T |
G |
17: 74,753,954 (GRCm39) |
D143A |
probably damaging |
Het |
Nol10 |
G |
T |
12: 17,398,479 (GRCm39) |
|
probably benign |
Het |
Opn1sw |
A |
G |
6: 29,379,869 (GRCm39) |
S122P |
probably damaging |
Het |
Or10j3b |
C |
T |
1: 173,044,067 (GRCm39) |
T283I |
possibly damaging |
Het |
Or4f14d |
T |
G |
2: 111,960,881 (GRCm39) |
I92L |
possibly damaging |
Het |
Or52h7 |
C |
T |
7: 104,213,974 (GRCm39) |
T182I |
probably benign |
Het |
Or5an9 |
C |
A |
19: 12,187,659 (GRCm39) |
A243D |
probably damaging |
Het |
Or5h27 |
T |
A |
16: 59,006,454 (GRCm39) |
T131S |
probably benign |
Het |
Orm1 |
T |
A |
4: 63,262,929 (GRCm39) |
I32N |
possibly damaging |
Het |
Pcdhb5 |
T |
A |
18: 37,454,628 (GRCm39) |
V336E |
probably damaging |
Het |
Poli |
C |
T |
18: 70,650,540 (GRCm39) |
R363K |
possibly damaging |
Het |
Rabgap1l |
T |
C |
1: 160,472,893 (GRCm39) |
E515G |
probably benign |
Het |
Rem2 |
C |
A |
14: 54,715,225 (GRCm39) |
T134N |
probably damaging |
Het |
Rfc1 |
A |
G |
5: 65,436,892 (GRCm39) |
I596T |
probably damaging |
Het |
Ruvbl2 |
A |
T |
7: 45,074,433 (GRCm39) |
I202N |
probably damaging |
Het |
S100a6 |
T |
A |
3: 90,521,186 (GRCm39) |
I38N |
probably damaging |
Het |
Scel |
T |
C |
14: 103,829,649 (GRCm39) |
C435R |
probably benign |
Het |
Slc6a13 |
T |
A |
6: 121,298,587 (GRCm39) |
W146R |
probably damaging |
Het |
Sorcs1 |
T |
A |
19: 50,178,555 (GRCm39) |
K856* |
probably null |
Het |
Speer4e1 |
T |
G |
5: 14,987,195 (GRCm39) |
K70T |
possibly damaging |
Het |
Sucla2 |
T |
A |
14: 73,806,404 (GRCm39) |
C158* |
probably null |
Het |
Tie1 |
G |
A |
4: 118,341,888 (GRCm39) |
S187L |
probably benign |
Het |
Tmem200a |
T |
C |
10: 25,868,905 (GRCm39) |
T455A |
probably damaging |
Het |
Tra2a |
A |
G |
6: 49,229,398 (GRCm39) |
|
probably benign |
Het |
Tsnaxip1 |
A |
C |
8: 106,570,819 (GRCm39) |
E615A |
probably benign |
Het |
Tuba3b |
T |
A |
6: 145,566,900 (GRCm39) |
N380K |
probably damaging |
Het |
Umod |
C |
T |
7: 119,076,046 (GRCm39) |
S240N |
probably benign |
Het |
Vmn2r92 |
G |
A |
17: 18,388,305 (GRCm39) |
|
probably null |
Het |
Vps13b |
A |
G |
15: 35,671,462 (GRCm39) |
E1655G |
probably damaging |
Het |
Vwde |
A |
T |
6: 13,219,935 (GRCm39) |
I72N |
probably damaging |
Het |
Wbp11 |
G |
A |
6: 136,798,533 (GRCm39) |
A172V |
probably damaging |
Het |
Zbtb41 |
T |
A |
1: 139,351,770 (GRCm39) |
N294K |
probably benign |
Het |
Zfhx4 |
T |
A |
3: 5,462,019 (GRCm39) |
H1206Q |
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 |
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 |
|
|