Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017N19Rik |
T |
A |
10: 100,441,505 (GRCm39) |
F171L |
probably benign |
Het |
2410137M14Rik |
A |
T |
17: 37,288,909 (GRCm39) |
C152S |
unknown |
Het |
Alb |
T |
C |
5: 90,620,488 (GRCm39) |
F533L |
possibly damaging |
Het |
Alox12b |
T |
C |
11: 69,060,135 (GRCm39) |
M616T |
possibly damaging |
Het |
Atxn2l |
A |
G |
7: 126,091,924 (GRCm39) |
F968L |
probably benign |
Het |
Cadps2 |
G |
T |
6: 23,263,641 (GRCm39) |
H1227Q |
probably benign |
Het |
Cdh18 |
A |
T |
15: 23,474,413 (GRCm39) |
D761V |
possibly damaging |
Het |
Cdkl3 |
T |
C |
11: 51,909,284 (GRCm39) |
|
probably null |
Het |
Chrdl2 |
T |
C |
7: 99,659,249 (GRCm39) |
L9P |
unknown |
Het |
Ctr9 |
A |
G |
7: 110,651,618 (GRCm39) |
E946G |
unknown |
Het |
Cygb |
T |
A |
11: 116,540,116 (GRCm39) |
T178S |
probably benign |
Het |
Cyp2c67 |
A |
C |
19: 39,597,669 (GRCm39) |
M443R |
probably damaging |
Het |
Dnah12 |
A |
G |
14: 26,578,486 (GRCm39) |
T3082A |
probably benign |
Het |
Gm14496 |
A |
G |
2: 181,637,906 (GRCm39) |
I327V |
probably benign |
Het |
Gm29106 |
T |
A |
1: 118,126,885 (GRCm39) |
N192K |
possibly damaging |
Het |
H3f3a |
A |
T |
1: 180,639,490 (GRCm39) |
M1K |
probably null |
Het |
Htt |
T |
A |
5: 35,055,891 (GRCm39) |
W2601R |
possibly damaging |
Het |
Il18r1 |
T |
A |
1: 40,530,296 (GRCm39) |
I341K |
probably benign |
Het |
Kcnj1 |
G |
A |
9: 32,307,881 (GRCm39) |
V102I |
probably benign |
Het |
Lrp3 |
C |
A |
7: 34,910,922 (GRCm39) |
G41V |
probably damaging |
Het |
Lrrc9 |
G |
T |
12: 72,532,964 (GRCm39) |
K944N |
probably damaging |
Het |
Mettl21e |
T |
A |
1: 44,249,371 (GRCm39) |
E95V |
probably damaging |
Het |
Mib1 |
G |
A |
18: 10,798,446 (GRCm39) |
R769Q |
possibly damaging |
Het |
Myh7 |
C |
G |
14: 55,226,258 (GRCm39) |
D461H |
probably damaging |
Het |
Mymk |
A |
G |
2: 26,952,298 (GRCm39) |
S190P |
probably damaging |
Het |
Neb |
G |
A |
2: 52,215,761 (GRCm39) |
P182L |
probably damaging |
Het |
Nfil3 |
A |
G |
13: 53,122,449 (GRCm39) |
Y152H |
probably damaging |
Het |
Nisch |
A |
G |
14: 30,894,052 (GRCm39) |
Y1174H |
probably damaging |
Het |
Nyap1 |
G |
C |
5: 137,733,658 (GRCm39) |
Y458* |
probably null |
Het |
Or4d5 |
A |
C |
9: 40,011,973 (GRCm39) |
V271G |
possibly damaging |
Het |
Or52z13 |
T |
A |
7: 103,247,473 (GRCm39) |
C317S |
probably damaging |
Het |
Or5h17 |
G |
A |
16: 58,820,086 (GRCm39) |
V13I |
probably benign |
Het |
Pars2 |
T |
A |
4: 106,511,276 (GRCm39) |
Y353N |
probably damaging |
Het |
Patj |
G |
T |
4: 98,312,553 (GRCm39) |
G297V |
probably damaging |
Het |
Pcdh9 |
A |
T |
14: 94,124,693 (GRCm39) |
S492R |
probably damaging |
Het |
Pcyox1 |
G |
A |
6: 86,369,323 (GRCm39) |
R168C |
probably damaging |
Het |
Plbd1 |
A |
T |
6: 136,594,326 (GRCm39) |
Y308N |
possibly damaging |
Het |
Rax |
A |
G |
18: 66,071,284 (GRCm39) |
V117A |
probably benign |
Het |
Rdh9 |
C |
A |
10: 127,612,566 (GRCm39) |
N71K |
probably benign |
Het |
Sap130 |
A |
G |
18: 31,853,714 (GRCm39) |
N968S |
probably benign |
Het |
Sema5a |
A |
T |
15: 32,609,485 (GRCm39) |
I464F |
probably benign |
Het |
Sez6l |
T |
G |
5: 112,586,447 (GRCm39) |
D683A |
probably damaging |
Het |
Slit2 |
C |
A |
5: 48,459,649 (GRCm39) |
P1310T |
probably damaging |
Het |
Snap47 |
T |
C |
11: 59,328,904 (GRCm39) |
M133V |
probably benign |
Het |
Son |
TACCATGGACTCCCAGATGTTAGCCTCTAGCACCATGGACTCCCAGATGTTAGCCTCTAGCACCATGGACTCCCAGATGTTAGCAACTAGCACCATGGACTCCCAGATGTTAGC |
TACCATGGACTCCCAGATGTTAGCCTCTAGCACCATGGACTCCCAGATGTTAGCAACTAGCACCATGGACTCCCAGATGTTAGC |
16: 91,453,486 (GRCm39) |
|
probably benign |
Het |
Srcap |
G |
A |
7: 127,159,730 (GRCm39) |
S3202N |
unknown |
Het |
Ssh2 |
T |
C |
11: 77,344,441 (GRCm39) |
W809R |
probably benign |
Het |
Stau1 |
G |
T |
2: 166,792,870 (GRCm39) |
A365D |
possibly damaging |
Het |
Tfpi2 |
A |
G |
6: 3,968,281 (GRCm39) |
L15P |
probably damaging |
Het |
Thbs1 |
A |
T |
2: 117,945,508 (GRCm39) |
N329I |
possibly damaging |
Het |
Tmem65 |
A |
T |
15: 58,659,010 (GRCm39) |
D184E |
probably damaging |
Het |
Trpm6 |
G |
T |
19: 18,792,605 (GRCm39) |
E676D |
probably benign |
Het |
Vdr |
T |
G |
15: 97,782,771 (GRCm39) |
D17A |
possibly damaging |
Het |
Vmn1r123 |
C |
T |
7: 20,896,192 (GRCm39) |
T28I |
probably damaging |
Het |
Wdr90 |
A |
G |
17: 26,079,513 (GRCm39) |
L207P |
probably damaging |
Het |
Zfp354c |
TGTCACACTCG |
TG |
11: 50,706,065 (GRCm39) |
|
probably benign |
Het |
Zfp598 |
A |
G |
17: 24,898,304 (GRCm39) |
E402G |
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 |
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 |
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 |
|