Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ap2a2 |
A |
G |
7: 141,211,236 (GRCm39) |
D924G |
probably benign |
Het |
Armh1 |
C |
A |
4: 117,070,938 (GRCm39) |
A396S |
probably benign |
Het |
Atrnl1 |
A |
G |
19: 57,618,738 (GRCm39) |
D152G |
probably damaging |
Het |
B3gnt8 |
A |
G |
7: 25,327,860 (GRCm39) |
I97V |
possibly damaging |
Het |
Bach1 |
A |
G |
16: 87,517,031 (GRCm39) |
D524G |
probably benign |
Het |
Caprin2 |
T |
C |
6: 148,784,954 (GRCm39) |
S107G |
probably damaging |
Het |
Ccnb1 |
A |
G |
13: 100,918,209 (GRCm39) |
I207T |
probably benign |
Het |
Cdh11 |
T |
C |
8: 103,400,515 (GRCm39) |
D151G |
probably damaging |
Het |
Cdh9 |
A |
G |
15: 16,851,115 (GRCm39) |
|
probably null |
Het |
Cep83 |
A |
T |
10: 94,586,502 (GRCm39) |
R433W |
probably damaging |
Het |
Cspg4b |
C |
A |
13: 113,457,420 (GRCm39) |
S1155R |
|
Het |
D3Ertd751e |
A |
G |
3: 41,708,163 (GRCm39) |
E100G |
probably benign |
Het |
Dchs2 |
C |
T |
3: 83,255,357 (GRCm39) |
A2351V |
probably benign |
Het |
Dhx40 |
T |
C |
11: 86,690,263 (GRCm39) |
T253A |
probably benign |
Het |
Dqx1 |
A |
G |
6: 83,036,680 (GRCm39) |
D228G |
probably benign |
Het |
Dync1h1 |
T |
C |
12: 110,627,327 (GRCm39) |
M4002T |
probably benign |
Het |
Flcn |
C |
T |
11: 59,686,625 (GRCm39) |
W376* |
probably null |
Het |
Fut11 |
T |
A |
14: 20,745,096 (GRCm39) |
V9E |
probably benign |
Het |
Fv1 |
T |
A |
4: 147,954,392 (GRCm39) |
N319K |
possibly damaging |
Het |
Ghrhr |
G |
T |
6: 55,361,727 (GRCm39) |
G298V |
probably benign |
Het |
Gm5800 |
T |
A |
14: 51,953,905 (GRCm39) |
|
probably null |
Het |
Grin2b |
A |
G |
6: 135,709,553 (GRCm39) |
M1331T |
probably benign |
Het |
Hyou1 |
A |
G |
9: 44,292,433 (GRCm39) |
|
probably null |
Het |
Igkv1-117 |
C |
A |
6: 68,098,792 (GRCm39) |
Q114K |
probably damaging |
Het |
Igkv4-68 |
A |
G |
6: 69,282,048 (GRCm39) |
V41A |
possibly damaging |
Het |
Inpp4b |
A |
G |
8: 82,772,968 (GRCm39) |
N754S |
probably damaging |
Het |
Isl2 |
G |
A |
9: 55,448,440 (GRCm39) |
|
probably null |
Het |
Kat2a |
G |
A |
11: 100,599,422 (GRCm39) |
Q523* |
probably null |
Het |
Lypd3 |
T |
C |
7: 24,337,865 (GRCm39) |
F77S |
possibly damaging |
Het |
Map4k2 |
T |
C |
19: 6,394,084 (GRCm39) |
L297P |
probably benign |
Het |
Naca |
T |
C |
10: 127,876,375 (GRCm39) |
V469A |
unknown |
Het |
Notch3 |
C |
T |
17: 32,377,480 (GRCm39) |
V199I |
probably benign |
Het |
Or4k44 |
T |
C |
2: 111,368,521 (GRCm39) |
I38V |
possibly damaging |
Het |
Or5b119 |
T |
C |
19: 13,456,795 (GRCm39) |
M256V |
possibly damaging |
Het |
Pabpc1 |
TGTACCTGTTGCATGGTA |
TGTA |
15: 36,598,212 (GRCm39) |
|
probably null |
Het |
Pcdhb8 |
A |
T |
18: 37,488,648 (GRCm39) |
I109L |
probably benign |
Het |
Pde2a |
A |
G |
7: 101,133,801 (GRCm39) |
D104G |
possibly damaging |
Het |
Phip |
A |
G |
9: 82,785,243 (GRCm39) |
V824A |
probably benign |
Het |
Plekhg4 |
T |
C |
8: 106,106,782 (GRCm39) |
Y853H |
probably damaging |
Het |
Plod1 |
T |
C |
4: 148,011,481 (GRCm39) |
K248R |
probably damaging |
Het |
Plxnd1 |
A |
T |
6: 115,953,600 (GRCm39) |
Y656N |
probably benign |
Het |
Pogz |
G |
A |
3: 94,763,517 (GRCm39) |
|
probably null |
Het |
Ppp1r3e |
T |
A |
14: 55,114,526 (GRCm39) |
S79C |
probably damaging |
Het |
Pprc1 |
T |
A |
19: 46,060,721 (GRCm39) |
D1595E |
probably damaging |
Het |
Ptprq |
A |
G |
10: 107,547,783 (GRCm39) |
V205A |
probably benign |
Het |
Rad51ap2 |
T |
C |
12: 11,507,116 (GRCm39) |
V346A |
possibly damaging |
Het |
Rgs12 |
T |
A |
5: 35,122,934 (GRCm39) |
L239H |
probably damaging |
Het |
Rrp8 |
T |
C |
7: 105,385,727 (GRCm39) |
|
probably benign |
Het |
Rsf1 |
GGCG |
GGCGACCGCCGCG |
7: 97,229,113 (GRCm39) |
|
probably benign |
Het |
Scaf1 |
A |
T |
7: 44,656,503 (GRCm39) |
V792D |
unknown |
Het |
Scrn2 |
G |
T |
11: 96,923,968 (GRCm39) |
R284L |
possibly damaging |
Het |
Sgsm1 |
T |
A |
5: 113,423,948 (GRCm39) |
Q461L |
possibly damaging |
Het |
Slc18b1 |
A |
G |
10: 23,702,080 (GRCm39) |
T434A |
probably benign |
Het |
Sltm |
C |
G |
9: 70,493,955 (GRCm39) |
P802R |
possibly damaging |
Het |
Smc4 |
CTA |
CTATA |
3: 68,925,400 (GRCm39) |
|
probably benign |
Het |
Snx33 |
A |
T |
9: 56,833,702 (GRCm39) |
D122E |
probably damaging |
Het |
Srebf2 |
G |
T |
15: 82,069,497 (GRCm39) |
V680L |
probably benign |
Het |
Sry |
GCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTG |
GCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTG |
Y: 2,662,638 (GRCm39) |
|
probably benign |
Het |
Tecpr1 |
C |
T |
5: 144,155,544 (GRCm39) |
V5M |
probably benign |
Het |
Tfg |
A |
G |
16: 56,532,997 (GRCm39) |
V54A |
possibly damaging |
Het |
Tmem237 |
C |
T |
1: 59,156,060 (GRCm39) |
C30Y |
probably benign |
Het |
Tmem245 |
T |
C |
4: 56,916,787 (GRCm39) |
K444R |
probably benign |
Het |
Trim25 |
T |
G |
11: 88,906,602 (GRCm39) |
L446R |
probably null |
Het |
Usp37 |
T |
C |
1: 74,507,533 (GRCm39) |
T495A |
probably benign |
Het |
Vmn1r94 |
T |
G |
7: 19,901,696 (GRCm39) |
T203P |
probably damaging |
Het |
Ywhah |
T |
A |
5: 33,184,010 (GRCm39) |
M71K |
probably benign |
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 |
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 |
|