Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
C |
A |
13: 77,480,471 (GRCm39) |
P1167Q |
probably damaging |
Het |
Abtb3 |
A |
G |
10: 85,463,113 (GRCm39) |
Q626R |
probably damaging |
Het |
Adcy10 |
A |
T |
1: 165,378,867 (GRCm39) |
Q885H |
probably damaging |
Het |
Alkal2 |
C |
T |
12: 30,940,055 (GRCm39) |
L139F |
probably damaging |
Het |
Ankrd17 |
A |
T |
5: 90,441,062 (GRCm39) |
M439K |
probably benign |
Het |
Arl11 |
C |
A |
14: 61,548,422 (GRCm39) |
Y77* |
probably null |
Het |
Bcas3 |
T |
C |
11: 85,449,973 (GRCm39) |
Y669H |
probably benign |
Het |
Bpifb3 |
C |
T |
2: 153,764,516 (GRCm39) |
A136V |
probably benign |
Het |
Ccne2 |
A |
G |
4: 11,202,279 (GRCm39) |
T345A |
probably benign |
Het |
Ciz1 |
T |
C |
2: 32,254,286 (GRCm39) |
S76P |
probably benign |
Het |
Clip4 |
A |
T |
17: 72,107,800 (GRCm39) |
K94* |
probably null |
Het |
Cthrc1 |
G |
A |
15: 38,947,866 (GRCm39) |
R195H |
probably damaging |
Het |
Ddx31 |
T |
C |
2: 28,730,816 (GRCm39) |
|
probably benign |
Het |
Elf2 |
T |
A |
3: 51,174,188 (GRCm39) |
D113V |
possibly damaging |
Het |
Esrrb |
A |
G |
12: 86,535,324 (GRCm39) |
N155S |
probably benign |
Het |
Flnb |
A |
G |
14: 7,887,624 (GRCm38) |
D478G |
probably benign |
Het |
Galm |
T |
A |
17: 80,435,215 (GRCm39) |
L24H |
probably damaging |
Het |
Gask1b |
T |
C |
3: 79,816,078 (GRCm39) |
S363P |
possibly damaging |
Het |
Gon4l |
G |
A |
3: 88,802,314 (GRCm39) |
G975D |
possibly damaging |
Het |
Hspbp1 |
T |
G |
7: 4,667,783 (GRCm39) |
M237L |
probably benign |
Het |
Ighv1-62-1 |
A |
T |
12: 115,350,367 (GRCm39) |
M100K |
probably damaging |
Het |
Ipo8 |
A |
T |
6: 148,676,575 (GRCm39) |
D971E |
possibly damaging |
Het |
Itgax |
C |
T |
7: 127,732,979 (GRCm39) |
A286V |
probably damaging |
Het |
Jpt2 |
T |
C |
17: 25,179,578 (GRCm39) |
Q3R |
probably benign |
Het |
Katnip |
A |
C |
7: 125,396,867 (GRCm39) |
R309S |
probably benign |
Het |
Klrg2 |
A |
C |
6: 38,613,838 (GRCm39) |
L55R |
probably damaging |
Het |
Lrp6 |
T |
A |
6: 134,433,141 (GRCm39) |
M1397L |
probably benign |
Het |
Lrrc31 |
T |
A |
3: 30,733,328 (GRCm39) |
Q462L |
probably benign |
Het |
Lyg2 |
T |
A |
1: 37,949,054 (GRCm39) |
I103F |
probably damaging |
Het |
Map10 |
T |
C |
8: 126,396,664 (GRCm39) |
V19A |
probably damaging |
Het |
Map1b |
T |
A |
13: 99,569,323 (GRCm39) |
M1133L |
unknown |
Het |
Mrgpra4 |
A |
G |
7: 47,631,481 (GRCm39) |
V40A |
probably benign |
Het |
Myh1 |
G |
A |
11: 67,099,967 (GRCm39) |
G626R |
probably benign |
Het |
Myo9a |
T |
C |
9: 59,687,030 (GRCm39) |
V45A |
probably benign |
Het |
Ncdn |
A |
G |
4: 126,638,905 (GRCm39) |
F638S |
possibly damaging |
Het |
Ncs1 |
T |
A |
2: 31,174,213 (GRCm39) |
M121K |
probably damaging |
Het |
Nf1 |
T |
C |
11: 79,437,180 (GRCm39) |
V16A |
probably damaging |
Het |
Nktr |
T |
A |
9: 121,579,317 (GRCm39) |
D1128E |
unknown |
Het |
Nup205 |
T |
G |
6: 35,191,269 (GRCm39) |
L1000R |
probably damaging |
Het |
Obscn |
T |
C |
11: 58,925,921 (GRCm39) |
E5604G |
probably damaging |
Het |
Or1p4-ps1 |
T |
A |
11: 74,208,534 (GRCm39) |
S228T |
unknown |
Het |
Or2p2 |
T |
C |
13: 21,257,220 (GRCm39) |
N84D |
probably damaging |
Het |
Or4a68 |
A |
G |
2: 89,270,209 (GRCm39) |
V138A |
probably benign |
Het |
Or4c35 |
G |
T |
2: 89,808,715 (GRCm39) |
A198S |
possibly damaging |
Het |
Or51ah3 |
G |
T |
7: 103,209,816 (GRCm39) |
C44F |
probably benign |
Het |
Or5b96 |
A |
T |
19: 12,867,560 (GRCm39) |
V127E |
probably damaging |
Het |
Or7g12 |
A |
G |
9: 18,899,812 (GRCm39) |
H176R |
possibly damaging |
Het |
Ovch2 |
T |
A |
7: 107,392,462 (GRCm39) |
I294F |
probably damaging |
Het |
Ovch2 |
A |
T |
7: 107,393,251 (GRCm39) |
C207* |
probably null |
Het |
P3h2 |
T |
A |
16: 25,801,467 (GRCm39) |
Y397F |
possibly damaging |
Het |
Pappa |
A |
T |
4: 65,123,166 (GRCm39) |
I834F |
possibly damaging |
Het |
Pcdha11 |
T |
C |
18: 37,140,716 (GRCm39) |
S782P |
probably benign |
Het |
Pex1 |
T |
C |
5: 3,681,614 (GRCm39) |
V980A |
probably benign |
Het |
Pik3c2a |
G |
T |
7: 115,951,112 (GRCm39) |
L1258I |
probably damaging |
Het |
Pmp22 |
T |
A |
11: 63,049,239 (GRCm39) |
*161R |
probably null |
Het |
Ppp1r26 |
T |
A |
2: 28,341,192 (GRCm39) |
M274K |
probably benign |
Het |
Ppp6r2 |
T |
C |
15: 89,167,275 (GRCm39) |
V830A |
probably benign |
Het |
Pramel34 |
T |
C |
5: 93,785,660 (GRCm39) |
T207A |
possibly damaging |
Het |
Prss1 |
T |
A |
6: 41,439,520 (GRCm39) |
N84K |
probably benign |
Het |
Rab3il1 |
G |
A |
19: 10,004,141 (GRCm39) |
A18T |
probably damaging |
Het |
Sbf2 |
A |
T |
7: 109,929,069 (GRCm39) |
S1471T |
probably damaging |
Het |
Setdb1 |
T |
A |
3: 95,263,371 (GRCm39) |
D45V |
probably damaging |
Het |
Sik3 |
G |
T |
9: 46,089,811 (GRCm39) |
V275L |
probably benign |
Het |
Skint6 |
C |
A |
4: 112,846,149 (GRCm39) |
M659I |
probably benign |
Het |
Slc24a1 |
T |
A |
9: 64,835,985 (GRCm39) |
D714V |
unknown |
Het |
Slc26a5 |
T |
A |
5: 22,018,880 (GRCm39) |
D653V |
probably damaging |
Het |
Snrnp27 |
A |
T |
6: 86,653,196 (GRCm39) |
C141S |
probably benign |
Het |
Stradb |
A |
G |
1: 59,033,478 (GRCm39) |
I380M |
probably benign |
Het |
Sult1e1 |
T |
C |
5: 87,735,501 (GRCm39) |
Y59C |
probably benign |
Het |
Tas2r122 |
C |
T |
6: 132,688,702 (GRCm39) |
A64T |
probably benign |
Het |
Tep1 |
C |
T |
14: 51,074,589 (GRCm39) |
C1812Y |
probably damaging |
Het |
Trio |
A |
T |
15: 27,905,311 (GRCm39) |
C152S |
unknown |
Het |
Tro |
G |
A |
X: 149,438,555 (GRCm39) |
S34L |
unknown |
Het |
Vmn1r15 |
A |
G |
6: 57,235,123 (GRCm39) |
|
probably benign |
Het |
Vmn1r19 |
A |
G |
6: 57,381,436 (GRCm39) |
|
probably benign |
Het |
Vmn1r75 |
A |
G |
7: 11,614,630 (GRCm39) |
T121A |
possibly damaging |
Het |
Vmn2r32 |
A |
G |
7: 7,477,669 (GRCm39) |
F241L |
probably damaging |
Het |
Vmn2r66 |
A |
G |
7: 84,654,893 (GRCm39) |
L472P |
probably damaging |
Het |
Ylpm1 |
G |
T |
12: 85,043,566 (GRCm39) |
W101C |
unknown |
Het |
Zdbf2 |
C |
A |
1: 63,347,272 (GRCm39) |
H1884N |
probably benign |
Het |
Zfp1005 |
T |
A |
2: 150,109,624 (GRCm39) |
C105S |
possibly damaging |
Het |
|
Other mutations in Tln2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00468:Tln2
|
APN |
9 |
67,251,469 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL01110:Tln2
|
APN |
9 |
67,157,864 (GRCm39) |
nonsense |
probably null |
|
IGL01112:Tln2
|
APN |
9 |
67,219,093 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01307:Tln2
|
APN |
9 |
67,302,749 (GRCm39) |
missense |
probably benign |
0.25 |
IGL01374:Tln2
|
APN |
9 |
67,169,205 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01625:Tln2
|
APN |
9 |
67,277,905 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01865:Tln2
|
APN |
9 |
67,157,896 (GRCm39) |
nonsense |
probably null |
|
IGL01999:Tln2
|
APN |
9 |
67,299,787 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02002:Tln2
|
APN |
9 |
67,263,980 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02005:Tln2
|
APN |
9 |
67,299,787 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02015:Tln2
|
APN |
9 |
67,268,721 (GRCm39) |
splice site |
probably benign |
|
IGL02368:Tln2
|
APN |
9 |
67,148,092 (GRCm39) |
splice site |
probably benign |
|
IGL02444:Tln2
|
APN |
9 |
67,165,874 (GRCm39) |
splice site |
probably benign |
|
IGL02646:Tln2
|
APN |
9 |
67,163,278 (GRCm39) |
missense |
probably benign |
0.43 |
IGL02744:Tln2
|
APN |
9 |
67,136,658 (GRCm39) |
nonsense |
probably null |
|
IGL02869:Tln2
|
APN |
9 |
67,128,807 (GRCm39) |
splice site |
probably benign |
|
IGL02930:Tln2
|
APN |
9 |
67,300,944 (GRCm39) |
nonsense |
probably null |
|
IGL03100:Tln2
|
APN |
9 |
67,203,019 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03326:Tln2
|
APN |
9 |
67,241,539 (GRCm39) |
missense |
possibly damaging |
0.67 |
Harrier
|
UTSW |
9 |
67,237,834 (GRCm39) |
nonsense |
probably null |
|
Marsh
|
UTSW |
9 |
67,179,936 (GRCm39) |
missense |
probably benign |
0.19 |
BB008:Tln2
|
UTSW |
9 |
67,165,742 (GRCm39) |
critical splice donor site |
probably null |
|
BB018:Tln2
|
UTSW |
9 |
67,165,742 (GRCm39) |
critical splice donor site |
probably null |
|
R0047:Tln2
|
UTSW |
9 |
67,147,954 (GRCm39) |
splice site |
probably benign |
|
R0047:Tln2
|
UTSW |
9 |
67,147,954 (GRCm39) |
splice site |
probably benign |
|
R0107:Tln2
|
UTSW |
9 |
67,277,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R0494:Tln2
|
UTSW |
9 |
67,262,479 (GRCm39) |
missense |
probably benign |
0.22 |
R0884:Tln2
|
UTSW |
9 |
67,278,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R0947:Tln2
|
UTSW |
9 |
67,203,095 (GRCm39) |
missense |
probably benign |
0.08 |
R0989:Tln2
|
UTSW |
9 |
67,136,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R1195:Tln2
|
UTSW |
9 |
67,165,848 (GRCm39) |
missense |
probably damaging |
0.96 |
R1195:Tln2
|
UTSW |
9 |
67,165,848 (GRCm39) |
missense |
probably damaging |
0.96 |
R1195:Tln2
|
UTSW |
9 |
67,165,848 (GRCm39) |
missense |
probably damaging |
0.96 |
R1486:Tln2
|
UTSW |
9 |
67,219,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R1527:Tln2
|
UTSW |
9 |
67,179,950 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1584:Tln2
|
UTSW |
9 |
67,203,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R1636:Tln2
|
UTSW |
9 |
67,213,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R1656:Tln2
|
UTSW |
9 |
67,134,389 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1707:Tln2
|
UTSW |
9 |
67,283,089 (GRCm39) |
missense |
probably benign |
0.00 |
R1749:Tln2
|
UTSW |
9 |
67,193,796 (GRCm39) |
missense |
probably benign |
0.01 |
R1751:Tln2
|
UTSW |
9 |
67,193,796 (GRCm39) |
missense |
probably benign |
0.01 |
R1761:Tln2
|
UTSW |
9 |
67,193,796 (GRCm39) |
missense |
probably benign |
0.01 |
R1767:Tln2
|
UTSW |
9 |
67,193,796 (GRCm39) |
missense |
probably benign |
0.01 |
R1815:Tln2
|
UTSW |
9 |
67,136,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R1840:Tln2
|
UTSW |
9 |
67,249,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R1847:Tln2
|
UTSW |
9 |
67,269,969 (GRCm39) |
nonsense |
probably null |
|
R1964:Tln2
|
UTSW |
9 |
67,249,417 (GRCm39) |
missense |
probably benign |
0.00 |
R1968:Tln2
|
UTSW |
9 |
67,163,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R2036:Tln2
|
UTSW |
9 |
67,179,986 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2038:Tln2
|
UTSW |
9 |
67,304,935 (GRCm39) |
start codon destroyed |
probably benign |
0.01 |
R2152:Tln2
|
UTSW |
9 |
67,209,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R2153:Tln2
|
UTSW |
9 |
67,209,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R2154:Tln2
|
UTSW |
9 |
67,209,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R2191:Tln2
|
UTSW |
9 |
67,262,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R2192:Tln2
|
UTSW |
9 |
67,262,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R2201:Tln2
|
UTSW |
9 |
67,283,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R3116:Tln2
|
UTSW |
9 |
67,262,421 (GRCm39) |
missense |
probably benign |
0.10 |
R3151:Tln2
|
UTSW |
9 |
67,237,829 (GRCm39) |
critical splice donor site |
probably null |
|
R3795:Tln2
|
UTSW |
9 |
67,163,197 (GRCm39) |
missense |
probably damaging |
0.97 |
R3953:Tln2
|
UTSW |
9 |
67,277,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R4450:Tln2
|
UTSW |
9 |
67,251,347 (GRCm39) |
critical splice donor site |
probably null |
|
R4685:Tln2
|
UTSW |
9 |
67,209,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R4688:Tln2
|
UTSW |
9 |
67,304,935 (GRCm39) |
start codon destroyed |
probably benign |
0.01 |
R4696:Tln2
|
UTSW |
9 |
67,302,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R4697:Tln2
|
UTSW |
9 |
67,302,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R4700:Tln2
|
UTSW |
9 |
67,253,809 (GRCm39) |
missense |
probably benign |
0.03 |
R4701:Tln2
|
UTSW |
9 |
67,253,809 (GRCm39) |
missense |
probably benign |
0.03 |
R4741:Tln2
|
UTSW |
9 |
67,293,837 (GRCm39) |
critical splice donor site |
probably null |
|
R4806:Tln2
|
UTSW |
9 |
67,239,015 (GRCm39) |
missense |
probably benign |
0.29 |
R4807:Tln2
|
UTSW |
9 |
67,239,015 (GRCm39) |
missense |
probably benign |
0.29 |
R4808:Tln2
|
UTSW |
9 |
67,239,015 (GRCm39) |
missense |
probably benign |
0.29 |
R4967:Tln2
|
UTSW |
9 |
67,262,407 (GRCm39) |
missense |
probably damaging |
0.97 |
R5061:Tln2
|
UTSW |
9 |
67,261,750 (GRCm39) |
missense |
probably benign |
|
R5092:Tln2
|
UTSW |
9 |
67,163,310 (GRCm39) |
missense |
probably benign |
0.13 |
R5093:Tln2
|
UTSW |
9 |
67,241,596 (GRCm39) |
missense |
probably benign |
0.44 |
R5126:Tln2
|
UTSW |
9 |
67,165,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R5204:Tln2
|
UTSW |
9 |
67,261,764 (GRCm39) |
missense |
probably benign |
0.00 |
R5236:Tln2
|
UTSW |
9 |
67,273,205 (GRCm39) |
missense |
probably damaging |
0.99 |
R5287:Tln2
|
UTSW |
9 |
67,149,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R5568:Tln2
|
UTSW |
9 |
67,219,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R5571:Tln2
|
UTSW |
9 |
67,241,602 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5642:Tln2
|
UTSW |
9 |
67,203,640 (GRCm39) |
missense |
probably benign |
0.01 |
R5711:Tln2
|
UTSW |
9 |
67,299,829 (GRCm39) |
missense |
probably benign |
0.00 |
R5776:Tln2
|
UTSW |
9 |
67,165,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R5791:Tln2
|
UTSW |
9 |
67,293,887 (GRCm39) |
missense |
probably damaging |
0.98 |
R5866:Tln2
|
UTSW |
9 |
67,174,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R5888:Tln2
|
UTSW |
9 |
67,136,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R5902:Tln2
|
UTSW |
9 |
67,269,999 (GRCm39) |
missense |
probably benign |
0.02 |
R6106:Tln2
|
UTSW |
9 |
67,230,302 (GRCm39) |
missense |
probably damaging |
0.99 |
R6175:Tln2
|
UTSW |
9 |
67,131,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R6385:Tln2
|
UTSW |
9 |
67,185,411 (GRCm39) |
missense |
probably benign |
0.45 |
R6430:Tln2
|
UTSW |
9 |
67,179,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R6441:Tln2
|
UTSW |
9 |
67,179,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R6738:Tln2
|
UTSW |
9 |
67,293,946 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6776:Tln2
|
UTSW |
9 |
67,170,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R6794:Tln2
|
UTSW |
9 |
67,193,840 (GRCm39) |
missense |
probably benign |
0.07 |
R6850:Tln2
|
UTSW |
9 |
67,165,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R6907:Tln2
|
UTSW |
9 |
67,304,917 (GRCm39) |
missense |
probably damaging |
0.98 |
R6909:Tln2
|
UTSW |
9 |
67,299,814 (GRCm39) |
missense |
probably damaging |
0.97 |
R6951:Tln2
|
UTSW |
9 |
67,165,767 (GRCm39) |
missense |
probably damaging |
0.97 |
R7015:Tln2
|
UTSW |
9 |
67,269,929 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7051:Tln2
|
UTSW |
9 |
67,253,699 (GRCm39) |
missense |
probably benign |
0.00 |
R7246:Tln2
|
UTSW |
9 |
67,170,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R7292:Tln2
|
UTSW |
9 |
67,253,743 (GRCm39) |
missense |
probably benign |
|
R7753:Tln2
|
UTSW |
9 |
67,302,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R7868:Tln2
|
UTSW |
9 |
67,255,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R7931:Tln2
|
UTSW |
9 |
67,165,742 (GRCm39) |
critical splice donor site |
probably null |
|
R8023:Tln2
|
UTSW |
9 |
67,131,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R8081:Tln2
|
UTSW |
9 |
67,264,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R8164:Tln2
|
UTSW |
9 |
67,226,702 (GRCm39) |
missense |
probably benign |
0.31 |
R8192:Tln2
|
UTSW |
9 |
67,253,811 (GRCm39) |
nonsense |
probably null |
|
R8495:Tln2
|
UTSW |
9 |
67,261,749 (GRCm39) |
missense |
probably benign |
0.01 |
R8734:Tln2
|
UTSW |
9 |
67,179,936 (GRCm39) |
missense |
probably benign |
0.19 |
R8739:Tln2
|
UTSW |
9 |
67,165,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R8757:Tln2
|
UTSW |
9 |
67,274,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R8759:Tln2
|
UTSW |
9 |
67,274,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R8770:Tln2
|
UTSW |
9 |
67,230,304 (GRCm39) |
missense |
probably benign |
|
R8781:Tln2
|
UTSW |
9 |
67,163,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R8814:Tln2
|
UTSW |
9 |
67,128,693 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8816:Tln2
|
UTSW |
9 |
67,128,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R8816:Tln2
|
UTSW |
9 |
67,128,693 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8833:Tln2
|
UTSW |
9 |
67,128,693 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8835:Tln2
|
UTSW |
9 |
67,304,975 (GRCm39) |
splice site |
probably benign |
|
R8837:Tln2
|
UTSW |
9 |
67,157,866 (GRCm39) |
missense |
probably damaging |
0.99 |
R8843:Tln2
|
UTSW |
9 |
67,302,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R8864:Tln2
|
UTSW |
9 |
67,237,834 (GRCm39) |
nonsense |
probably null |
|
R8867:Tln2
|
UTSW |
9 |
67,237,832 (GRCm39) |
missense |
probably damaging |
0.98 |
R8921:Tln2
|
UTSW |
9 |
67,174,105 (GRCm39) |
missense |
probably damaging |
0.99 |
R9080:Tln2
|
UTSW |
9 |
67,253,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R9083:Tln2
|
UTSW |
9 |
67,269,927 (GRCm39) |
missense |
probably damaging |
0.96 |
R9150:Tln2
|
UTSW |
9 |
67,128,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R9287:Tln2
|
UTSW |
9 |
67,277,980 (GRCm39) |
missense |
probably benign |
0.20 |
R9330:Tln2
|
UTSW |
9 |
67,229,213 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9343:Tln2
|
UTSW |
9 |
67,230,353 (GRCm39) |
missense |
probably benign |
0.10 |
R9355:Tln2
|
UTSW |
9 |
67,262,529 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9383:Tln2
|
UTSW |
9 |
67,278,043 (GRCm39) |
missense |
probably benign |
0.17 |
R9386:Tln2
|
UTSW |
9 |
67,273,249 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9407:Tln2
|
UTSW |
9 |
67,136,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R9483:Tln2
|
UTSW |
9 |
67,299,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R9523:Tln2
|
UTSW |
9 |
67,165,766 (GRCm39) |
missense |
probably damaging |
0.99 |
R9642:Tln2
|
UTSW |
9 |
67,157,826 (GRCm39) |
missense |
probably benign |
0.02 |
R9703:Tln2
|
UTSW |
9 |
67,293,938 (GRCm39) |
missense |
probably damaging |
1.00 |
X0027:Tln2
|
UTSW |
9 |
67,284,135 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Tln2
|
UTSW |
9 |
67,255,420 (GRCm39) |
missense |
probably damaging |
1.00 |
X0067:Tln2
|
UTSW |
9 |
67,277,973 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Tln2
|
UTSW |
9 |
67,253,767 (GRCm39) |
missense |
possibly damaging |
0.46 |
|