Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam11 |
A |
T |
11: 102,660,750 (GRCm39) |
I94F |
possibly damaging |
Het |
Ankrd50 |
A |
T |
3: 38,509,741 (GRCm39) |
D875E |
probably damaging |
Het |
Arf3 |
T |
C |
15: 98,639,285 (GRCm39) |
N60S |
probably benign |
Het |
Atxn2 |
T |
G |
5: 121,944,280 (GRCm39) |
|
probably null |
Het |
B3gnt8 |
A |
T |
7: 25,328,373 (GRCm39) |
I268F |
probably benign |
Het |
Bmp1 |
T |
A |
14: 70,723,712 (GRCm39) |
D708V |
possibly damaging |
Het |
C1s2 |
A |
G |
6: 124,609,069 (GRCm39) |
S163P |
probably damaging |
Het |
C3 |
A |
G |
17: 57,526,623 (GRCm39) |
I786T |
probably benign |
Het |
Cacna2d2 |
T |
A |
9: 107,404,602 (GRCm39) |
L1138Q |
probably damaging |
Het |
Cage1 |
T |
A |
13: 38,207,029 (GRCm39) |
Y272F |
probably damaging |
Het |
Cd300ld |
A |
T |
11: 114,875,058 (GRCm39) |
M192K |
possibly damaging |
Het |
Cdc5l |
A |
T |
17: 45,718,745 (GRCm39) |
F624I |
probably benign |
Het |
Cdh8 |
T |
A |
8: 99,922,897 (GRCm39) |
Q333L |
probably damaging |
Het |
Ciapin1 |
T |
A |
8: 95,555,787 (GRCm39) |
K128* |
probably null |
Het |
Col6a3 |
T |
A |
1: 90,731,467 (GRCm39) |
E988D |
probably benign |
Het |
Crip3 |
A |
G |
17: 46,740,338 (GRCm39) |
E46G |
probably damaging |
Het |
D5Ertd579e |
A |
G |
5: 36,772,137 (GRCm39) |
S753P |
possibly damaging |
Het |
Dock6 |
T |
A |
9: 21,744,177 (GRCm39) |
D126V |
probably damaging |
Het |
Duxf4 |
T |
A |
10: 58,072,158 (GRCm39) |
I19F |
possibly damaging |
Het |
Dvl3 |
A |
G |
16: 20,342,506 (GRCm39) |
E153G |
probably damaging |
Het |
Epas1 |
A |
T |
17: 87,136,471 (GRCm39) |
M748L |
probably benign |
Het |
Exoc8 |
A |
G |
8: 125,622,477 (GRCm39) |
L630P |
probably damaging |
Het |
Fam227a |
G |
A |
15: 79,507,668 (GRCm39) |
T454M |
probably damaging |
Het |
Galnt4 |
G |
A |
10: 98,944,509 (GRCm39) |
G78E |
probably damaging |
Het |
Ghr |
A |
T |
15: 3,362,956 (GRCm39) |
L172* |
probably null |
Het |
Gjb5 |
A |
T |
4: 127,250,063 (GRCm39) |
|
probably null |
Het |
Hdac5 |
T |
C |
11: 102,095,340 (GRCm39) |
D427G |
probably damaging |
Het |
Hsd17b4 |
G |
A |
18: 50,316,369 (GRCm39) |
|
probably null |
Het |
Kcnab1 |
T |
C |
3: 65,017,368 (GRCm39) |
I59T |
probably benign |
Het |
Kcnh7 |
A |
G |
2: 62,607,950 (GRCm39) |
Y544H |
probably damaging |
Het |
Kdm7a |
A |
G |
6: 39,123,870 (GRCm39) |
S765P |
probably damaging |
Het |
Lama1 |
A |
T |
17: 68,059,936 (GRCm39) |
H675L |
probably benign |
Het |
Lemd3 |
CCCTCCTCCTCCTCCTCCTCC |
CCCTCCTCCTCCTCCTCC |
10: 120,814,432 (GRCm39) |
|
probably benign |
Het |
Llgl1 |
T |
C |
11: 60,600,865 (GRCm39) |
S654P |
possibly damaging |
Het |
Lvrn |
G |
T |
18: 47,011,409 (GRCm39) |
M455I |
probably benign |
Het |
Mfsd12 |
T |
A |
10: 81,193,568 (GRCm39) |
L46Q |
probably damaging |
Het |
Mtcl1 |
A |
T |
17: 66,673,427 (GRCm39) |
M783K |
probably benign |
Het |
Mthfd1l |
A |
T |
10: 3,978,399 (GRCm39) |
T420S |
probably damaging |
Het |
Mybphl |
T |
A |
3: 108,284,635 (GRCm39) |
I294N |
probably damaging |
Het |
Or4c52 |
G |
A |
2: 89,845,768 (GRCm39) |
G165S |
probably damaging |
Het |
Or4f14b |
T |
C |
2: 111,775,658 (GRCm39) |
T48A |
possibly damaging |
Het |
Or52ab7 |
T |
A |
7: 102,977,831 (GRCm39) |
L46* |
probably null |
Het |
Oxa1l |
A |
T |
14: 54,598,924 (GRCm39) |
Q70L |
probably benign |
Het |
Pcdhac2 |
A |
T |
18: 37,279,185 (GRCm39) |
I722F |
probably damaging |
Het |
Pde4d |
A |
G |
13: 110,084,924 (GRCm39) |
D460G |
probably damaging |
Het |
Pth1r |
CGGG |
CGGGGGG |
9: 110,556,058 (GRCm39) |
|
probably benign |
Het |
Rab11fip3 |
A |
G |
17: 26,287,152 (GRCm39) |
S334P |
probably benign |
Het |
Ror2 |
C |
T |
13: 53,439,816 (GRCm39) |
|
probably null |
Het |
Scnn1g |
G |
C |
7: 121,366,519 (GRCm39) |
W572S |
probably damaging |
Het |
Skint5 |
G |
A |
4: 113,798,046 (GRCm39) |
S179L |
probably damaging |
Het |
Slc22a2 |
G |
T |
17: 12,817,949 (GRCm39) |
G175V |
probably damaging |
Het |
Spaca6 |
G |
A |
17: 18,056,416 (GRCm39) |
|
probably null |
Het |
Tbc1d30 |
C |
T |
10: 121,140,312 (GRCm39) |
R207H |
probably damaging |
Het |
Tdrd5 |
A |
G |
1: 156,087,435 (GRCm39) |
I829T |
probably benign |
Het |
Tmcc3 |
T |
C |
10: 94,414,780 (GRCm39) |
S161P |
probably damaging |
Het |
Tmem150b |
A |
G |
7: 4,719,353 (GRCm39) |
V189A |
probably benign |
Het |
Tmem248 |
A |
G |
5: 130,260,597 (GRCm39) |
D54G |
probably benign |
Het |
Trmt1 |
T |
A |
8: 85,417,487 (GRCm39) |
S121T |
probably damaging |
Het |
Tyk2 |
C |
T |
9: 21,026,503 (GRCm39) |
V698M |
probably damaging |
Het |
Usp17la |
A |
G |
7: 104,509,919 (GRCm39) |
R175G |
probably damaging |
Het |
Vav1 |
A |
G |
17: 57,610,140 (GRCm39) |
N464S |
probably benign |
Het |
Vmn2r57 |
T |
G |
7: 41,078,249 (GRCm39) |
|
probably null |
Het |
Vmn2r78 |
A |
G |
7: 86,570,535 (GRCm39) |
Y351C |
probably damaging |
Het |
|
Other mutations in Flnc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00952:Flnc
|
APN |
6 |
29,459,546 (GRCm39) |
nonsense |
probably null |
|
IGL01099:Flnc
|
APN |
6 |
29,433,617 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01656:Flnc
|
APN |
6 |
29,443,507 (GRCm39) |
splice site |
probably benign |
|
IGL01659:Flnc
|
APN |
6 |
29,448,670 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01780:Flnc
|
APN |
6 |
29,438,492 (GRCm39) |
nonsense |
probably null |
|
IGL01935:Flnc
|
APN |
6 |
29,454,279 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02039:Flnc
|
APN |
6 |
29,450,718 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02119:Flnc
|
APN |
6 |
29,447,511 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02122:Flnc
|
APN |
6 |
29,444,335 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02236:Flnc
|
APN |
6 |
29,454,375 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02350:Flnc
|
APN |
6 |
29,438,492 (GRCm39) |
nonsense |
probably null |
|
IGL02357:Flnc
|
APN |
6 |
29,438,492 (GRCm39) |
nonsense |
probably null |
|
IGL02428:Flnc
|
APN |
6 |
29,451,484 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02496:Flnc
|
APN |
6 |
29,440,684 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02516:Flnc
|
APN |
6 |
29,450,840 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02696:Flnc
|
APN |
6 |
29,446,697 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03165:Flnc
|
APN |
6 |
29,449,377 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03190:Flnc
|
APN |
6 |
29,445,636 (GRCm39) |
splice site |
probably benign |
|
I1329:Flnc
|
UTSW |
6 |
29,451,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R0111:Flnc
|
UTSW |
6 |
29,454,339 (GRCm39) |
missense |
probably damaging |
0.99 |
R0665:Flnc
|
UTSW |
6 |
29,455,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R0748:Flnc
|
UTSW |
6 |
29,446,343 (GRCm39) |
missense |
probably damaging |
0.99 |
R0960:Flnc
|
UTSW |
6 |
29,441,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R1328:Flnc
|
UTSW |
6 |
29,438,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R1502:Flnc
|
UTSW |
6 |
29,438,693 (GRCm39) |
missense |
probably benign |
0.45 |
R1544:Flnc
|
UTSW |
6 |
29,444,079 (GRCm39) |
missense |
probably benign |
0.00 |
R1565:Flnc
|
UTSW |
6 |
29,455,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R1640:Flnc
|
UTSW |
6 |
29,433,806 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1691:Flnc
|
UTSW |
6 |
29,441,213 (GRCm39) |
missense |
probably benign |
0.09 |
R1818:Flnc
|
UTSW |
6 |
29,457,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R1826:Flnc
|
UTSW |
6 |
29,455,184 (GRCm39) |
missense |
probably damaging |
0.99 |
R1851:Flnc
|
UTSW |
6 |
29,443,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R1898:Flnc
|
UTSW |
6 |
29,438,665 (GRCm39) |
nonsense |
probably null |
|
R1905:Flnc
|
UTSW |
6 |
29,459,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R1985:Flnc
|
UTSW |
6 |
29,444,415 (GRCm39) |
splice site |
probably benign |
|
R2016:Flnc
|
UTSW |
6 |
29,443,796 (GRCm39) |
critical splice donor site |
probably null |
|
R2017:Flnc
|
UTSW |
6 |
29,443,796 (GRCm39) |
critical splice donor site |
probably null |
|
R2020:Flnc
|
UTSW |
6 |
29,444,362 (GRCm39) |
missense |
probably damaging |
0.97 |
R2104:Flnc
|
UTSW |
6 |
29,450,734 (GRCm39) |
critical splice donor site |
probably null |
|
R2132:Flnc
|
UTSW |
6 |
29,443,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R2141:Flnc
|
UTSW |
6 |
29,448,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R2202:Flnc
|
UTSW |
6 |
29,459,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R2203:Flnc
|
UTSW |
6 |
29,459,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R2204:Flnc
|
UTSW |
6 |
29,459,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R2205:Flnc
|
UTSW |
6 |
29,459,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R2209:Flnc
|
UTSW |
6 |
29,455,844 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2248:Flnc
|
UTSW |
6 |
29,451,400 (GRCm39) |
missense |
probably damaging |
0.99 |
R2258:Flnc
|
UTSW |
6 |
29,438,665 (GRCm39) |
nonsense |
probably null |
|
R2259:Flnc
|
UTSW |
6 |
29,438,665 (GRCm39) |
nonsense |
probably null |
|
R2280:Flnc
|
UTSW |
6 |
29,438,665 (GRCm39) |
nonsense |
probably null |
|
R2281:Flnc
|
UTSW |
6 |
29,438,665 (GRCm39) |
nonsense |
probably null |
|
R2873:Flnc
|
UTSW |
6 |
29,447,542 (GRCm39) |
missense |
probably damaging |
0.96 |
R2900:Flnc
|
UTSW |
6 |
29,448,584 (GRCm39) |
missense |
probably damaging |
0.98 |
R3788:Flnc
|
UTSW |
6 |
29,454,056 (GRCm39) |
missense |
probably damaging |
0.99 |
R3799:Flnc
|
UTSW |
6 |
29,443,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R3801:Flnc
|
UTSW |
6 |
29,447,403 (GRCm39) |
missense |
probably damaging |
0.98 |
R3851:Flnc
|
UTSW |
6 |
29,453,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R3910:Flnc
|
UTSW |
6 |
29,459,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R3982:Flnc
|
UTSW |
6 |
29,442,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R3983:Flnc
|
UTSW |
6 |
29,442,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R4023:Flnc
|
UTSW |
6 |
29,451,634 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4676:Flnc
|
UTSW |
6 |
29,445,153 (GRCm39) |
splice site |
probably null |
|
R4694:Flnc
|
UTSW |
6 |
29,443,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R4695:Flnc
|
UTSW |
6 |
29,440,428 (GRCm39) |
missense |
probably damaging |
0.99 |
R4735:Flnc
|
UTSW |
6 |
29,455,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R4773:Flnc
|
UTSW |
6 |
29,445,038 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4828:Flnc
|
UTSW |
6 |
29,455,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R4856:Flnc
|
UTSW |
6 |
29,447,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R4879:Flnc
|
UTSW |
6 |
29,460,805 (GRCm39) |
missense |
probably damaging |
0.99 |
R4899:Flnc
|
UTSW |
6 |
29,446,842 (GRCm39) |
missense |
probably benign |
0.17 |
R4906:Flnc
|
UTSW |
6 |
29,447,524 (GRCm39) |
missense |
probably damaging |
0.99 |
R5089:Flnc
|
UTSW |
6 |
29,447,812 (GRCm39) |
missense |
probably damaging |
0.96 |
R5173:Flnc
|
UTSW |
6 |
29,455,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R5174:Flnc
|
UTSW |
6 |
29,448,893 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5290:Flnc
|
UTSW |
6 |
29,457,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R5338:Flnc
|
UTSW |
6 |
29,444,063 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5352:Flnc
|
UTSW |
6 |
29,449,317 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5397:Flnc
|
UTSW |
6 |
29,441,160 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5431:Flnc
|
UTSW |
6 |
29,456,383 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5481:Flnc
|
UTSW |
6 |
29,441,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R5511:Flnc
|
UTSW |
6 |
29,458,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R5539:Flnc
|
UTSW |
6 |
29,446,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R5549:Flnc
|
UTSW |
6 |
29,453,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R5567:Flnc
|
UTSW |
6 |
29,444,044 (GRCm39) |
nonsense |
probably null |
|
R5584:Flnc
|
UTSW |
6 |
29,446,627 (GRCm39) |
missense |
probably damaging |
0.98 |
R5689:Flnc
|
UTSW |
6 |
29,441,591 (GRCm39) |
missense |
probably benign |
0.03 |
R5753:Flnc
|
UTSW |
6 |
29,433,488 (GRCm39) |
missense |
probably benign |
|
R5786:Flnc
|
UTSW |
6 |
29,459,536 (GRCm39) |
nonsense |
probably null |
|
R5822:Flnc
|
UTSW |
6 |
29,459,429 (GRCm39) |
missense |
probably damaging |
0.98 |
R5823:Flnc
|
UTSW |
6 |
29,461,201 (GRCm39) |
missense |
probably damaging |
0.99 |
R5933:Flnc
|
UTSW |
6 |
29,441,105 (GRCm39) |
missense |
probably damaging |
0.99 |
R6043:Flnc
|
UTSW |
6 |
29,446,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R6320:Flnc
|
UTSW |
6 |
29,459,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R6337:Flnc
|
UTSW |
6 |
29,454,318 (GRCm39) |
missense |
probably damaging |
0.99 |
R6399:Flnc
|
UTSW |
6 |
29,458,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R6423:Flnc
|
UTSW |
6 |
29,445,155 (GRCm39) |
splice site |
probably null |
|
R6540:Flnc
|
UTSW |
6 |
29,446,376 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6547:Flnc
|
UTSW |
6 |
29,448,607 (GRCm39) |
missense |
probably damaging |
0.98 |
R6717:Flnc
|
UTSW |
6 |
29,450,901 (GRCm39) |
small deletion |
probably benign |
|
R6875:Flnc
|
UTSW |
6 |
29,445,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R7193:Flnc
|
UTSW |
6 |
29,450,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R7255:Flnc
|
UTSW |
6 |
29,445,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R7303:Flnc
|
UTSW |
6 |
29,460,849 (GRCm39) |
missense |
probably benign |
0.31 |
R7413:Flnc
|
UTSW |
6 |
29,452,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7422:Flnc
|
UTSW |
6 |
29,455,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R7559:Flnc
|
UTSW |
6 |
29,459,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R7632:Flnc
|
UTSW |
6 |
29,446,984 (GRCm39) |
missense |
probably damaging |
0.98 |
R7651:Flnc
|
UTSW |
6 |
29,444,049 (GRCm39) |
missense |
probably benign |
0.08 |
R7679:Flnc
|
UTSW |
6 |
29,456,789 (GRCm39) |
missense |
probably benign |
0.00 |
R7697:Flnc
|
UTSW |
6 |
29,456,516 (GRCm39) |
missense |
probably damaging |
0.98 |
R7788:Flnc
|
UTSW |
6 |
29,456,443 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7852:Flnc
|
UTSW |
6 |
29,440,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R7870:Flnc
|
UTSW |
6 |
29,454,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R7873:Flnc
|
UTSW |
6 |
29,456,990 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7921:Flnc
|
UTSW |
6 |
29,447,769 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7950:Flnc
|
UTSW |
6 |
29,456,381 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7953:Flnc
|
UTSW |
6 |
29,447,828 (GRCm39) |
missense |
probably damaging |
0.99 |
R7970:Flnc
|
UTSW |
6 |
29,447,525 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8071:Flnc
|
UTSW |
6 |
29,457,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R8143:Flnc
|
UTSW |
6 |
29,441,484 (GRCm39) |
missense |
probably benign |
0.20 |
R8166:Flnc
|
UTSW |
6 |
29,433,731 (GRCm39) |
missense |
probably damaging |
0.99 |
R8167:Flnc
|
UTSW |
6 |
29,455,921 (GRCm39) |
missense |
probably damaging |
0.98 |
R8306:Flnc
|
UTSW |
6 |
29,449,369 (GRCm39) |
missense |
probably benign |
0.05 |
R8428:Flnc
|
UTSW |
6 |
29,450,849 (GRCm39) |
missense |
probably benign |
0.36 |
R8466:Flnc
|
UTSW |
6 |
29,438,621 (GRCm39) |
missense |
probably damaging |
0.98 |
R8671:Flnc
|
UTSW |
6 |
29,443,501 (GRCm39) |
critical splice donor site |
probably null |
|
R8885:Flnc
|
UTSW |
6 |
29,455,410 (GRCm39) |
missense |
probably damaging |
0.96 |
R8922:Flnc
|
UTSW |
6 |
29,456,835 (GRCm39) |
missense |
probably damaging |
0.99 |
R8923:Flnc
|
UTSW |
6 |
29,452,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R8985:Flnc
|
UTSW |
6 |
29,440,499 (GRCm39) |
missense |
probably benign |
0.37 |
R9075:Flnc
|
UTSW |
6 |
29,447,646 (GRCm39) |
missense |
probably damaging |
0.96 |
R9098:Flnc
|
UTSW |
6 |
29,455,518 (GRCm39) |
nonsense |
probably null |
|
R9162:Flnc
|
UTSW |
6 |
29,455,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R9199:Flnc
|
UTSW |
6 |
29,441,490 (GRCm39) |
missense |
probably benign |
0.31 |
R9204:Flnc
|
UTSW |
6 |
29,452,353 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9273:Flnc
|
UTSW |
6 |
29,447,815 (GRCm39) |
missense |
probably benign |
0.08 |
R9411:Flnc
|
UTSW |
6 |
29,441,484 (GRCm39) |
missense |
probably benign |
|
R9412:Flnc
|
UTSW |
6 |
29,441,484 (GRCm39) |
missense |
probably benign |
|
R9413:Flnc
|
UTSW |
6 |
29,441,484 (GRCm39) |
missense |
probably benign |
|
R9451:Flnc
|
UTSW |
6 |
29,445,462 (GRCm39) |
missense |
probably damaging |
0.98 |
R9524:Flnc
|
UTSW |
6 |
29,461,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R9575:Flnc
|
UTSW |
6 |
29,454,399 (GRCm39) |
missense |
probably damaging |
0.98 |
R9582:Flnc
|
UTSW |
6 |
29,460,736 (GRCm39) |
missense |
probably damaging |
0.99 |
R9595:Flnc
|
UTSW |
6 |
29,433,720 (GRCm39) |
missense |
probably benign |
0.05 |
R9664:Flnc
|
UTSW |
6 |
29,457,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R9665:Flnc
|
UTSW |
6 |
29,455,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R9686:Flnc
|
UTSW |
6 |
29,456,434 (GRCm39) |
missense |
possibly damaging |
0.84 |
Z1088:Flnc
|
UTSW |
6 |
29,457,150 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Flnc
|
UTSW |
6 |
29,457,129 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Flnc
|
UTSW |
6 |
29,447,544 (GRCm39) |
missense |
probably damaging |
1.00 |
|