Other mutations in this stock |
Total: 120 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930470P17Rik |
C |
A |
2: 170,421,505 (GRCm39) |
G125V |
unknown |
Het |
Actr6 |
A |
T |
10: 89,561,717 (GRCm39) |
L143Q |
probably damaging |
Het |
Adamts18 |
A |
G |
8: 114,425,642 (GRCm39) |
Y1207H |
probably benign |
Het |
Adamts5 |
T |
A |
16: 85,696,466 (GRCm39) |
R230S |
probably benign |
Het |
Adat2 |
A |
T |
10: 13,432,650 (GRCm39) |
N51Y |
probably damaging |
Het |
Adgrv1 |
T |
C |
13: 81,567,546 (GRCm39) |
Y5209C |
possibly damaging |
Het |
Ahnak |
G |
T |
19: 8,991,008 (GRCm39) |
M4097I |
probably benign |
Het |
Akap13 |
A |
G |
7: 75,337,000 (GRCm39) |
T820A |
probably damaging |
Het |
Als2cl |
C |
T |
9: 110,719,887 (GRCm39) |
R492C |
probably damaging |
Het |
Aox3 |
G |
A |
1: 58,227,683 (GRCm39) |
|
probably null |
Het |
Arid4b |
G |
A |
13: 14,338,866 (GRCm39) |
V446M |
probably benign |
Het |
Armc2 |
A |
G |
10: 41,798,144 (GRCm39) |
L794P |
probably damaging |
Het |
Atp6v0a1 |
T |
A |
11: 100,911,341 (GRCm39) |
M80K |
probably benign |
Het |
Aup1 |
T |
C |
6: 83,032,115 (GRCm39) |
V94A |
probably damaging |
Het |
Bank1 |
A |
T |
3: 135,940,443 (GRCm39) |
I180K |
possibly damaging |
Het |
Becn1 |
A |
G |
11: 101,182,221 (GRCm39) |
L116P |
probably damaging |
Het |
Bsg |
A |
G |
10: 79,546,057 (GRCm39) |
|
probably benign |
Het |
Camk2a |
A |
T |
18: 61,076,208 (GRCm39) |
|
probably benign |
Het |
Ccdc180 |
A |
G |
4: 45,914,603 (GRCm39) |
E706G |
possibly damaging |
Het |
Cdk8 |
A |
T |
5: 146,220,437 (GRCm39) |
|
probably null |
Het |
Cpne4 |
A |
G |
9: 104,778,720 (GRCm39) |
|
probably null |
Het |
Cspp1 |
T |
A |
1: 10,196,688 (GRCm39) |
N900K |
probably damaging |
Het |
Cyp2c38 |
C |
A |
19: 39,449,065 (GRCm39) |
G96V |
probably damaging |
Het |
Dhx40 |
A |
G |
11: 86,667,462 (GRCm39) |
I261T |
probably damaging |
Het |
Dnah10 |
T |
C |
5: 124,856,322 (GRCm39) |
F2038L |
probably damaging |
Het |
Dnah7a |
A |
T |
1: 53,737,851 (GRCm39) |
D27E |
probably benign |
Het |
Dock10 |
A |
T |
1: 80,545,711 (GRCm39) |
|
probably null |
Het |
Dst |
A |
T |
1: 34,235,050 (GRCm39) |
K3710* |
probably null |
Het |
Dtl |
G |
T |
1: 191,273,618 (GRCm39) |
A430D |
probably damaging |
Het |
Ece2 |
T |
C |
16: 20,437,381 (GRCm39) |
L241P |
probably damaging |
Het |
Ecel1 |
T |
A |
1: 87,078,861 (GRCm39) |
Y526F |
probably benign |
Het |
Enpp2 |
T |
A |
15: 54,733,701 (GRCm39) |
R420* |
probably null |
Het |
Epb41 |
A |
C |
4: 131,664,747 (GRCm39) |
|
probably benign |
Het |
Eppin |
T |
C |
2: 164,431,371 (GRCm39) |
Y85C |
probably damaging |
Het |
Fam171a2 |
G |
A |
11: 102,329,559 (GRCm39) |
A400V |
probably damaging |
Het |
Fem1c |
A |
C |
18: 46,639,436 (GRCm39) |
C189G |
probably damaging |
Het |
Frmd4b |
A |
G |
6: 97,277,275 (GRCm39) |
V560A |
probably benign |
Het |
Fsip2 |
A |
T |
2: 82,818,535 (GRCm39) |
D4756V |
probably damaging |
Het |
Gabbr1 |
T |
C |
17: 37,359,330 (GRCm39) |
S102P |
probably damaging |
Het |
Garin3 |
G |
A |
11: 46,297,863 (GRCm39) |
G389D |
probably damaging |
Het |
Gm28042 |
G |
A |
2: 119,865,124 (GRCm39) |
A250T |
probably damaging |
Het |
Gm30275 |
T |
C |
14: 54,312,978 (GRCm39) |
|
probably benign |
Het |
Gm9762 |
A |
T |
3: 78,873,707 (GRCm39) |
|
noncoding transcript |
Het |
Gpr183 |
G |
T |
14: 122,192,275 (GRCm39) |
T82N |
possibly damaging |
Het |
Gps2 |
A |
G |
11: 69,805,617 (GRCm39) |
K45R |
probably benign |
Het |
Gramd2a |
A |
G |
9: 59,621,603 (GRCm39) |
|
probably benign |
Het |
Grap2 |
G |
A |
15: 80,530,345 (GRCm39) |
R155Q |
possibly damaging |
Het |
Hsdl1 |
T |
A |
8: 120,292,606 (GRCm39) |
Y203F |
possibly damaging |
Het |
Ifi204 |
A |
T |
1: 173,583,234 (GRCm39) |
I328N |
probably damaging |
Het |
Igsf3 |
T |
A |
3: 101,346,677 (GRCm39) |
|
probably null |
Het |
Il1rap |
T |
C |
16: 26,442,949 (GRCm39) |
I15T |
probably benign |
Het |
Il23r |
A |
T |
6: 67,443,300 (GRCm39) |
C268S |
probably damaging |
Het |
Irx4 |
A |
G |
13: 73,417,040 (GRCm39) |
T479A |
probably benign |
Het |
Kcnk7 |
G |
A |
19: 5,756,352 (GRCm39) |
V193I |
probably benign |
Het |
Kcnt1 |
G |
T |
2: 25,799,334 (GRCm39) |
|
probably benign |
Het |
Kif13b |
T |
G |
14: 64,994,902 (GRCm39) |
C885G |
probably benign |
Het |
Kif21b |
C |
A |
1: 136,090,838 (GRCm39) |
D1215E |
probably benign |
Het |
Klhdc2 |
A |
G |
12: 69,343,736 (GRCm39) |
|
probably benign |
Het |
Kmt2d |
G |
A |
15: 98,745,075 (GRCm39) |
|
probably benign |
Het |
Lama4 |
A |
G |
10: 38,924,050 (GRCm39) |
N486S |
probably benign |
Het |
Ldah |
G |
A |
12: 8,277,237 (GRCm39) |
A58T |
probably benign |
Het |
Lrrc24 |
T |
C |
15: 76,600,200 (GRCm39) |
Q313R |
probably benign |
Het |
Luzp1 |
A |
G |
4: 136,270,708 (GRCm39) |
D977G |
possibly damaging |
Het |
Meak7 |
A |
C |
8: 120,494,882 (GRCm39) |
L292R |
probably damaging |
Het |
Mrgpra4 |
A |
G |
7: 47,631,466 (GRCm39) |
L45P |
probably damaging |
Het |
Mrps28 |
C |
T |
3: 8,988,756 (GRCm39) |
G34D |
possibly damaging |
Het |
Myh8 |
A |
G |
11: 67,189,184 (GRCm39) |
E1120G |
probably damaging |
Het |
Myt1l |
A |
G |
12: 29,882,302 (GRCm39) |
E499G |
unknown |
Het |
Ncan |
C |
T |
8: 70,567,675 (GRCm39) |
E146K |
probably damaging |
Het |
Nlgn1 |
A |
T |
3: 25,487,958 (GRCm39) |
D763E |
probably damaging |
Het |
Or11g26 |
T |
C |
14: 50,752,966 (GRCm39) |
F102L |
probably benign |
Het |
Or13c7c |
G |
T |
4: 43,836,433 (GRCm39) |
A19D |
probably benign |
Het |
Or1e17 |
A |
T |
11: 73,831,378 (GRCm39) |
Y102F |
possibly damaging |
Het |
Or4c12 |
A |
T |
2: 89,774,147 (GRCm39) |
I104N |
possibly damaging |
Het |
Or5b118 |
C |
T |
19: 13,448,910 (GRCm39) |
T192I |
probably benign |
Het |
Or6c8b |
T |
A |
10: 128,882,711 (GRCm39) |
I74F |
possibly damaging |
Het |
Pak6 |
A |
T |
2: 118,525,029 (GRCm39) |
I552F |
probably damaging |
Het |
Pcbp1 |
G |
A |
6: 86,501,897 (GRCm39) |
A334V |
probably damaging |
Het |
Pclaf |
T |
C |
9: 65,798,062 (GRCm39) |
V32A |
probably benign |
Het |
Pga5 |
T |
A |
19: 10,654,053 (GRCm39) |
H50L |
probably benign |
Het |
Phyhipl |
A |
T |
10: 70,404,904 (GRCm39) |
D56E |
probably damaging |
Het |
Pik3ap1 |
C |
T |
19: 41,270,415 (GRCm39) |
R758H |
probably benign |
Het |
Plekha1 |
A |
G |
7: 130,507,094 (GRCm39) |
|
probably benign |
Het |
Plekhm1 |
A |
T |
11: 103,278,141 (GRCm39) |
N318K |
possibly damaging |
Het |
Ppargc1b |
G |
A |
18: 61,440,725 (GRCm39) |
A731V |
probably benign |
Het |
Pptc7 |
T |
C |
5: 122,451,844 (GRCm39) |
V100A |
possibly damaging |
Het |
Prl7a1 |
A |
T |
13: 27,817,564 (GRCm39) |
H233Q |
possibly damaging |
Het |
Prpf40a |
A |
G |
2: 53,034,861 (GRCm39) |
F776L |
probably damaging |
Het |
Prrc2c |
T |
C |
1: 162,533,009 (GRCm39) |
|
probably benign |
Het |
Psmb1 |
T |
C |
17: 15,718,524 (GRCm39) |
M1V |
probably null |
Het |
Ptpn3 |
A |
G |
4: 57,218,513 (GRCm39) |
F650S |
possibly damaging |
Het |
Ranbp17 |
A |
T |
11: 33,354,181 (GRCm39) |
*577R |
probably null |
Het |
Reln |
T |
A |
5: 22,176,868 (GRCm39) |
N1933Y |
probably benign |
Het |
Rgl2 |
T |
A |
17: 34,156,094 (GRCm39) |
H727Q |
probably benign |
Het |
Rhpn2 |
A |
G |
7: 35,070,549 (GRCm39) |
T160A |
probably damaging |
Het |
Rlf |
G |
A |
4: 121,004,652 (GRCm39) |
H1443Y |
probably damaging |
Het |
Rpgrip1l |
T |
C |
8: 92,007,444 (GRCm39) |
E382G |
probably damaging |
Het |
Rxrb |
T |
C |
17: 34,252,562 (GRCm39) |
S50P |
probably benign |
Het |
Scn4b |
A |
T |
9: 45,059,056 (GRCm39) |
E109V |
probably damaging |
Het |
Scrib |
C |
T |
15: 75,923,602 (GRCm39) |
|
probably null |
Het |
Slc22a29 |
A |
T |
19: 8,195,194 (GRCm39) |
V147D |
probably damaging |
Het |
Slc4a4 |
A |
T |
5: 89,102,721 (GRCm39) |
E53V |
probably null |
Het |
Slx4 |
A |
G |
16: 3,819,063 (GRCm39) |
S37P |
possibly damaging |
Het |
Spag9 |
G |
A |
11: 94,013,548 (GRCm39) |
G1127D |
probably damaging |
Het |
Srek1 |
T |
A |
13: 103,889,064 (GRCm39) |
|
probably benign |
Het |
Supt5 |
G |
T |
7: 28,015,795 (GRCm39) |
P849Q |
probably damaging |
Het |
Tex14 |
T |
C |
11: 87,324,639 (GRCm39) |
S2P |
probably damaging |
Het |
Them7 |
A |
G |
2: 105,209,153 (GRCm39) |
T158A |
probably benign |
Het |
Tll2 |
A |
G |
19: 41,118,948 (GRCm39) |
V260A |
possibly damaging |
Het |
Tlr6 |
A |
G |
5: 65,111,644 (GRCm39) |
V421A |
probably benign |
Het |
Tmc3 |
T |
G |
7: 83,264,218 (GRCm39) |
C649G |
probably damaging |
Het |
Tsc2 |
A |
C |
17: 24,822,254 (GRCm39) |
V1095G |
probably benign |
Het |
Vmn1r124 |
C |
T |
7: 20,994,172 (GRCm39) |
G124D |
probably damaging |
Het |
Vmn2r116 |
T |
C |
17: 23,606,138 (GRCm39) |
V350A |
probably benign |
Het |
Vps13d |
A |
G |
4: 144,832,468 (GRCm39) |
S2813P |
possibly damaging |
Het |
Wrap53 |
T |
A |
11: 69,454,758 (GRCm39) |
M204L |
possibly damaging |
Het |
Zfp277 |
A |
G |
12: 40,378,687 (GRCm39) |
V390A |
possibly damaging |
Het |
Zfp687 |
A |
T |
3: 94,918,987 (GRCm39) |
S262T |
probably benign |
Het |
Zfp831 |
T |
A |
2: 174,547,103 (GRCm39) |
S1429T |
probably benign |
Het |
Znfx1 |
G |
A |
2: 166,907,307 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Tnn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00095:Tnn
|
APN |
1 |
159,953,021 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL00433:Tnn
|
APN |
1 |
159,925,776 (GRCm39) |
splice site |
probably benign |
|
IGL00858:Tnn
|
APN |
1 |
159,915,962 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00939:Tnn
|
APN |
1 |
159,975,100 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01569:Tnn
|
APN |
1 |
159,948,124 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL01591:Tnn
|
APN |
1 |
159,953,144 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01628:Tnn
|
APN |
1 |
159,975,172 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01811:Tnn
|
APN |
1 |
159,934,705 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01813:Tnn
|
APN |
1 |
159,916,008 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02340:Tnn
|
APN |
1 |
159,972,775 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02488:Tnn
|
APN |
1 |
159,968,163 (GRCm39) |
missense |
probably benign |
0.21 |
IGL02535:Tnn
|
APN |
1 |
159,950,222 (GRCm39) |
splice site |
probably null |
|
IGL02563:Tnn
|
APN |
1 |
159,942,123 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02572:Tnn
|
APN |
1 |
159,913,677 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02740:Tnn
|
APN |
1 |
159,968,347 (GRCm39) |
splice site |
probably benign |
|
IGL02818:Tnn
|
APN |
1 |
159,943,848 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL03284:Tnn
|
APN |
1 |
159,953,022 (GRCm39) |
missense |
probably benign |
0.01 |
1mM(1):Tnn
|
UTSW |
1 |
159,924,911 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4305001:Tnn
|
UTSW |
1 |
159,913,647 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0023:Tnn
|
UTSW |
1 |
159,932,498 (GRCm39) |
missense |
probably benign |
0.00 |
R0234:Tnn
|
UTSW |
1 |
159,916,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R0234:Tnn
|
UTSW |
1 |
159,916,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R0316:Tnn
|
UTSW |
1 |
159,948,137 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0492:Tnn
|
UTSW |
1 |
159,948,327 (GRCm39) |
missense |
probably damaging |
0.99 |
R0547:Tnn
|
UTSW |
1 |
159,943,907 (GRCm39) |
intron |
probably benign |
|
R1067:Tnn
|
UTSW |
1 |
159,952,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R1563:Tnn
|
UTSW |
1 |
159,952,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R1565:Tnn
|
UTSW |
1 |
159,924,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R1615:Tnn
|
UTSW |
1 |
159,945,978 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1637:Tnn
|
UTSW |
1 |
159,975,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R1707:Tnn
|
UTSW |
1 |
159,972,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R1758:Tnn
|
UTSW |
1 |
159,975,154 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1797:Tnn
|
UTSW |
1 |
159,968,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R1847:Tnn
|
UTSW |
1 |
159,943,752 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1925:Tnn
|
UTSW |
1 |
159,924,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R2182:Tnn
|
UTSW |
1 |
159,968,170 (GRCm39) |
splice site |
probably null |
|
R2196:Tnn
|
UTSW |
1 |
159,924,798 (GRCm39) |
nonsense |
probably null |
|
R2225:Tnn
|
UTSW |
1 |
159,975,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R2227:Tnn
|
UTSW |
1 |
159,975,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R2286:Tnn
|
UTSW |
1 |
159,938,079 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2850:Tnn
|
UTSW |
1 |
159,966,857 (GRCm39) |
missense |
probably benign |
0.00 |
R3110:Tnn
|
UTSW |
1 |
159,943,856 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3111:Tnn
|
UTSW |
1 |
159,934,625 (GRCm39) |
missense |
probably damaging |
0.98 |
R3112:Tnn
|
UTSW |
1 |
159,943,856 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3729:Tnn
|
UTSW |
1 |
159,973,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R4183:Tnn
|
UTSW |
1 |
159,924,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R4439:Tnn
|
UTSW |
1 |
159,943,650 (GRCm39) |
missense |
probably benign |
|
R4441:Tnn
|
UTSW |
1 |
159,943,650 (GRCm39) |
missense |
probably benign |
|
R4588:Tnn
|
UTSW |
1 |
159,972,681 (GRCm39) |
missense |
probably benign |
0.25 |
R4646:Tnn
|
UTSW |
1 |
159,973,612 (GRCm39) |
missense |
probably benign |
|
R4647:Tnn
|
UTSW |
1 |
159,973,612 (GRCm39) |
missense |
probably benign |
|
R4648:Tnn
|
UTSW |
1 |
159,973,612 (GRCm39) |
missense |
probably benign |
|
R4701:Tnn
|
UTSW |
1 |
159,975,338 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4703:Tnn
|
UTSW |
1 |
159,943,815 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4737:Tnn
|
UTSW |
1 |
159,973,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Tnn
|
UTSW |
1 |
159,972,603 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4802:Tnn
|
UTSW |
1 |
159,972,603 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4868:Tnn
|
UTSW |
1 |
159,958,443 (GRCm39) |
missense |
possibly damaging |
0.64 |
R4977:Tnn
|
UTSW |
1 |
159,948,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R5011:Tnn
|
UTSW |
1 |
159,953,949 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5026:Tnn
|
UTSW |
1 |
159,973,707 (GRCm39) |
missense |
probably benign |
0.00 |
R5027:Tnn
|
UTSW |
1 |
159,972,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R5049:Tnn
|
UTSW |
1 |
159,968,308 (GRCm39) |
missense |
probably benign |
0.00 |
R5128:Tnn
|
UTSW |
1 |
159,950,464 (GRCm39) |
missense |
probably damaging |
0.98 |
R5234:Tnn
|
UTSW |
1 |
159,972,569 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5398:Tnn
|
UTSW |
1 |
159,975,092 (GRCm39) |
missense |
probably benign |
0.00 |
R5424:Tnn
|
UTSW |
1 |
159,950,272 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5452:Tnn
|
UTSW |
1 |
159,937,831 (GRCm39) |
missense |
probably benign |
0.13 |
R5466:Tnn
|
UTSW |
1 |
159,948,106 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6022:Tnn
|
UTSW |
1 |
159,937,928 (GRCm39) |
missense |
probably benign |
0.00 |
R6062:Tnn
|
UTSW |
1 |
159,925,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R6086:Tnn
|
UTSW |
1 |
159,913,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R6132:Tnn
|
UTSW |
1 |
159,973,641 (GRCm39) |
missense |
probably damaging |
0.96 |
R6324:Tnn
|
UTSW |
1 |
159,972,774 (GRCm39) |
missense |
probably damaging |
0.96 |
R6455:Tnn
|
UTSW |
1 |
159,942,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R6563:Tnn
|
UTSW |
1 |
159,915,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R6650:Tnn
|
UTSW |
1 |
159,942,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R6806:Tnn
|
UTSW |
1 |
159,948,278 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6810:Tnn
|
UTSW |
1 |
159,932,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R7157:Tnn
|
UTSW |
1 |
159,953,947 (GRCm39) |
nonsense |
probably null |
|
R7243:Tnn
|
UTSW |
1 |
159,934,687 (GRCm39) |
missense |
probably benign |
0.07 |
R7340:Tnn
|
UTSW |
1 |
159,973,592 (GRCm39) |
missense |
probably damaging |
0.98 |
R7472:Tnn
|
UTSW |
1 |
159,937,917 (GRCm39) |
missense |
probably benign |
0.12 |
R7502:Tnn
|
UTSW |
1 |
159,937,929 (GRCm39) |
missense |
probably benign |
0.00 |
R7527:Tnn
|
UTSW |
1 |
159,946,074 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7608:Tnn
|
UTSW |
1 |
159,915,984 (GRCm39) |
nonsense |
probably null |
|
R7746:Tnn
|
UTSW |
1 |
159,942,255 (GRCm39) |
missense |
probably damaging |
0.97 |
R8096:Tnn
|
UTSW |
1 |
159,950,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R8136:Tnn
|
UTSW |
1 |
159,934,630 (GRCm39) |
missense |
probably damaging |
0.96 |
R8191:Tnn
|
UTSW |
1 |
159,953,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R8334:Tnn
|
UTSW |
1 |
159,946,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R8335:Tnn
|
UTSW |
1 |
159,946,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R8337:Tnn
|
UTSW |
1 |
159,946,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R8338:Tnn
|
UTSW |
1 |
159,946,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R8427:Tnn
|
UTSW |
1 |
159,958,256 (GRCm39) |
missense |
probably damaging |
0.99 |
R8433:Tnn
|
UTSW |
1 |
159,924,790 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8479:Tnn
|
UTSW |
1 |
159,950,397 (GRCm39) |
missense |
probably benign |
0.06 |
R8505:Tnn
|
UTSW |
1 |
159,973,593 (GRCm39) |
missense |
probably damaging |
0.98 |
R8554:Tnn
|
UTSW |
1 |
159,937,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R8717:Tnn
|
UTSW |
1 |
159,943,846 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8850:Tnn
|
UTSW |
1 |
159,937,814 (GRCm39) |
critical splice donor site |
probably null |
|
R8928:Tnn
|
UTSW |
1 |
159,953,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R9209:Tnn
|
UTSW |
1 |
159,953,986 (GRCm39) |
missense |
probably benign |
0.02 |
X0019:Tnn
|
UTSW |
1 |
159,913,716 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Tnn
|
UTSW |
1 |
159,973,863 (GRCm39) |
missense |
probably benign |
|
Z1177:Tnn
|
UTSW |
1 |
159,954,097 (GRCm39) |
missense |
probably damaging |
0.98 |
|