Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930402F06Rik |
C |
A |
2: 35,265,884 (GRCm39) |
C262F |
probably damaging |
Het |
Acss1 |
T |
C |
2: 150,509,801 (GRCm39) |
|
probably null |
Het |
Adamtsl1 |
T |
C |
4: 86,260,492 (GRCm39) |
V909A |
possibly damaging |
Het |
Adprh |
G |
A |
16: 38,270,694 (GRCm39) |
T37M |
probably benign |
Het |
Ak9 |
T |
A |
10: 41,213,588 (GRCm39) |
Y264* |
probably null |
Het |
Aox3 |
G |
T |
1: 58,198,074 (GRCm39) |
A629S |
probably benign |
Het |
Apcs |
G |
A |
1: 172,721,900 (GRCm39) |
P149S |
probably damaging |
Het |
Arnt |
T |
A |
3: 95,377,294 (GRCm39) |
|
probably null |
Het |
Asb13 |
G |
A |
13: 3,692,065 (GRCm39) |
G15D |
probably damaging |
Het |
Bltp1 |
T |
G |
3: 37,000,657 (GRCm39) |
|
probably null |
Het |
Cacnb1 |
T |
G |
11: 97,894,146 (GRCm39) |
T459P |
probably benign |
Het |
Chrnb2 |
T |
C |
3: 89,654,630 (GRCm39) |
T718A |
unknown |
Het |
Cttn |
T |
A |
7: 144,014,999 (GRCm39) |
K70* |
probably null |
Het |
Cyp2f2 |
G |
A |
7: 26,828,678 (GRCm39) |
V183I |
probably benign |
Het |
Cyp39a1 |
T |
C |
17: 44,036,517 (GRCm39) |
V349A |
probably benign |
Het |
Ebf2 |
C |
A |
14: 67,649,386 (GRCm39) |
Y430* |
probably null |
Het |
Eef2 |
T |
C |
10: 81,017,182 (GRCm39) |
Y730H |
probably damaging |
Het |
Eif2ak2 |
G |
A |
17: 79,165,961 (GRCm39) |
T412I |
probably benign |
Het |
Fryl |
G |
A |
5: 73,207,682 (GRCm39) |
A2496V |
probably benign |
Het |
Galnt6 |
A |
G |
15: 100,614,088 (GRCm39) |
L71P |
probably damaging |
Het |
Gm7579 |
C |
T |
7: 141,766,163 (GRCm39) |
Q190* |
probably null |
Het |
H2-T3 |
T |
A |
17: 36,498,384 (GRCm39) |
R220S |
probably benign |
Het |
Hmcn1 |
A |
G |
1: 150,734,957 (GRCm39) |
V185A |
probably benign |
Het |
Ifi208 |
T |
A |
1: 173,510,242 (GRCm39) |
D132E |
possibly damaging |
Het |
Itgb4 |
G |
A |
11: 115,884,255 (GRCm39) |
V981I |
probably damaging |
Het |
Itsn2 |
A |
G |
12: 4,683,003 (GRCm39) |
T310A |
unknown |
Het |
Kat5 |
A |
G |
19: 5,657,577 (GRCm39) |
|
probably null |
Het |
Kif22 |
A |
T |
7: 126,632,397 (GRCm39) |
D304E |
probably damaging |
Het |
Mapre3 |
A |
T |
5: 31,020,719 (GRCm39) |
N147Y |
possibly damaging |
Het |
Morc2a |
T |
C |
11: 3,628,537 (GRCm39) |
V330A |
probably benign |
Het |
Mylk |
G |
A |
16: 34,734,525 (GRCm39) |
V709M |
possibly damaging |
Het |
Myo3a |
T |
G |
2: 22,287,476 (GRCm39) |
|
probably null |
Het |
N4bp2l2 |
A |
T |
5: 150,585,670 (GRCm39) |
D103E |
probably benign |
Het |
Nckap1 |
T |
C |
2: 80,336,530 (GRCm39) |
K1062R |
possibly damaging |
Het |
Nol9 |
T |
C |
4: 152,125,559 (GRCm39) |
V170A |
possibly damaging |
Het |
Numa1 |
A |
G |
7: 101,648,891 (GRCm39) |
Q874R |
possibly damaging |
Het |
Olig3 |
T |
G |
10: 19,232,732 (GRCm39) |
V119G |
probably damaging |
Het |
Or7g34 |
A |
G |
9: 19,478,587 (GRCm39) |
V31A |
probably benign |
Het |
Osbpl9 |
A |
G |
4: 108,922,906 (GRCm39) |
S485P |
probably benign |
Het |
Otogl |
A |
G |
10: 107,642,527 (GRCm39) |
F1301S |
probably damaging |
Het |
Pank3 |
A |
G |
11: 35,667,036 (GRCm39) |
Y51C |
probably damaging |
Het |
Pex5l |
T |
C |
3: 33,136,658 (GRCm39) |
|
probably benign |
Het |
Pgm1 |
G |
A |
4: 99,824,415 (GRCm39) |
|
probably null |
Het |
Psmd9 |
T |
G |
5: 123,366,479 (GRCm39) |
I37S |
probably damaging |
Het |
Qtrt2 |
A |
G |
16: 43,692,117 (GRCm39) |
S135P |
probably damaging |
Het |
Rexo5 |
T |
A |
7: 119,433,484 (GRCm39) |
|
probably null |
Het |
Rsrp1 |
T |
A |
4: 134,654,319 (GRCm39) |
D286E |
probably benign |
Het |
Scara3 |
C |
T |
14: 66,169,269 (GRCm39) |
C116Y |
probably damaging |
Het |
Serpina3b |
A |
T |
12: 104,096,793 (GRCm39) |
T25S |
probably benign |
Het |
Sh3pxd2a |
G |
A |
19: 47,257,138 (GRCm39) |
P555S |
probably damaging |
Het |
Slc1a2 |
T |
A |
2: 102,568,230 (GRCm39) |
L89Q |
probably damaging |
Het |
Tgm6 |
T |
A |
2: 129,983,763 (GRCm39) |
N307K |
probably damaging |
Het |
Tmem86b |
G |
T |
7: 4,631,484 (GRCm39) |
D189E |
probably damaging |
Het |
Trim65 |
G |
A |
11: 116,017,287 (GRCm39) |
R392C |
probably benign |
Het |
Trpc7 |
T |
C |
13: 56,930,362 (GRCm39) |
T769A |
probably benign |
Het |
Trrap |
T |
A |
5: 144,772,707 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
C |
2: 76,693,677 (GRCm39) |
E397G |
possibly damaging |
Het |
Vcl |
A |
T |
14: 21,037,112 (GRCm39) |
M237L |
possibly damaging |
Het |
Vmn1r36 |
G |
A |
6: 66,693,036 (GRCm39) |
Q280* |
probably null |
Het |
Vmn2r23 |
A |
T |
6: 123,718,312 (GRCm39) |
D555V |
probably damaging |
Het |
Wnk4 |
A |
G |
11: 101,153,625 (GRCm39) |
N229S |
probably damaging |
Het |
Zfp784 |
A |
C |
7: 5,038,910 (GRCm39) |
V216G |
possibly 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 |
R2197:Flnc
|
UTSW |
6 |
29,459,134 (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 |
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 |
|