Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9030624J02Rik |
T |
A |
7: 118,791,448 (GRCm38) |
I455N |
probably damaging |
Het |
A2m |
T |
C |
6: 121,638,284 (GRCm38) |
M1T |
probably null |
Het |
Aatf |
T |
A |
11: 84,449,138 (GRCm38) |
D449V |
probably damaging |
Het |
Acbd3 |
T |
A |
1: 180,721,944 (GRCm38) |
|
probably benign |
Het |
BC005561 |
A |
G |
5: 104,522,240 (GRCm38) |
K1543E |
probably benign |
Het |
Bicc1 |
T |
A |
10: 70,953,484 (GRCm38) |
I366F |
possibly damaging |
Het |
Ccdc74a |
T |
C |
16: 17,649,749 (GRCm38) |
S184P |
possibly damaging |
Het |
Cntn4 |
T |
C |
6: 106,525,485 (GRCm38) |
V401A |
probably damaging |
Het |
Cux2 |
T |
C |
5: 121,873,753 (GRCm38) |
T540A |
probably damaging |
Het |
Disp2 |
G |
T |
2: 118,791,684 (GRCm38) |
E966* |
probably null |
Het |
Dpp7 |
A |
G |
2: 25,354,919 (GRCm38) |
Y209H |
probably benign |
Het |
Dstyk |
T |
A |
1: 132,449,487 (GRCm38) |
F277Y |
probably damaging |
Het |
Dtx1 |
A |
T |
5: 120,694,408 (GRCm38) |
|
probably null |
Het |
Ear-ps2 |
G |
A |
14: 44,047,060 (GRCm38) |
|
noncoding transcript |
Het |
Ednra |
T |
C |
8: 77,664,995 (GRCm38) |
H422R |
probably benign |
Het |
Erlec1 |
T |
A |
11: 30,952,640 (GRCm38) |
I67F |
probably benign |
Het |
Fam161b |
G |
A |
12: 84,348,558 (GRCm38) |
|
probably benign |
Het |
Gata5 |
A |
T |
2: 180,327,379 (GRCm38) |
C345* |
probably null |
Het |
Glmp |
T |
C |
3: 88,328,274 (GRCm38) |
V47A |
probably damaging |
Het |
Gm9762 |
T |
A |
3: 78,966,550 (GRCm38) |
|
noncoding transcript |
Het |
Gnas |
A |
T |
2: 174,298,080 (GRCm38) |
D14V |
probably damaging |
Het |
Gnl3 |
T |
C |
14: 31,017,329 (GRCm38) |
S53G |
probably damaging |
Het |
Grhl3 |
C |
T |
4: 135,548,466 (GRCm38) |
V527M |
probably damaging |
Het |
Hoxd10 |
T |
A |
2: 74,694,187 (GRCm38) |
L281* |
probably null |
Het |
Kif16b |
T |
G |
2: 142,690,694 (GRCm38) |
Y1175S |
probably benign |
Het |
Kif2b |
A |
G |
11: 91,576,846 (GRCm38) |
S204P |
probably benign |
Het |
Klhl40 |
T |
A |
9: 121,778,734 (GRCm38) |
I320N |
probably damaging |
Het |
Ksr2 |
G |
A |
5: 117,708,147 (GRCm38) |
R693Q |
probably damaging |
Het |
Mis12 |
A |
G |
11: 71,025,326 (GRCm38) |
K62E |
possibly damaging |
Het |
Mlc1 |
A |
G |
15: 88,974,777 (GRCm38) |
C102R |
probably damaging |
Het |
Muc5b |
T |
C |
7: 141,857,361 (GRCm38) |
I1348T |
unknown |
Het |
Myh7b |
A |
G |
2: 155,629,322 (GRCm38) |
E1130G |
probably damaging |
Het |
Nat8f4 |
T |
C |
6: 85,901,386 (GRCm38) |
T52A |
probably benign |
Het |
Nxpe2 |
C |
A |
9: 48,320,521 (GRCm38) |
V379L |
probably benign |
Het |
Olfr1231 |
C |
A |
2: 89,302,902 (GRCm38) |
S230I |
possibly damaging |
Het |
Olfr1231 |
T |
A |
2: 89,302,903 (GRCm38) |
S230C |
probably damaging |
Het |
Olfr1448 |
C |
T |
19: 12,919,934 (GRCm38) |
C125Y |
probably damaging |
Het |
Olfr1465 |
A |
T |
19: 13,313,717 (GRCm38) |
D189E |
probably benign |
Het |
Olfr288 |
G |
A |
15: 98,186,868 (GRCm38) |
R310W |
probably damaging |
Het |
Pcdhga7 |
A |
T |
18: 37,717,208 (GRCm38) |
Y756F |
probably damaging |
Het |
Pcsk6 |
T |
A |
7: 65,959,241 (GRCm38) |
Y284N |
probably damaging |
Het |
Pdcd11 |
T |
C |
19: 47,126,347 (GRCm38) |
V1367A |
possibly damaging |
Het |
Postn |
T |
A |
3: 54,375,071 (GRCm38) |
N484K |
probably damaging |
Het |
Prkd3 |
C |
T |
17: 78,961,171 (GRCm38) |
V572I |
probably benign |
Het |
Qser1 |
T |
C |
2: 104,787,183 (GRCm38) |
S1005G |
probably benign |
Het |
Radil |
G |
T |
5: 142,486,801 (GRCm38) |
D951E |
probably benign |
Het |
Ripk1 |
C |
T |
13: 34,027,942 (GRCm38) |
R352* |
probably null |
Het |
Sacs |
T |
C |
14: 61,212,747 (GRCm38) |
F4081L |
probably benign |
Het |
Sbf1 |
A |
G |
15: 89,315,085 (GRCm38) |
V11A |
possibly damaging |
Het |
Sgip1 |
T |
A |
4: 102,934,587 (GRCm38) |
F536I |
probably damaging |
Het |
Slc45a1 |
A |
G |
4: 150,638,284 (GRCm38) |
L381P |
probably damaging |
Het |
Smarcad1 |
C |
T |
6: 65,052,641 (GRCm38) |
P71L |
probably benign |
Het |
Spns1 |
T |
A |
7: 126,377,037 (GRCm38) |
D14V |
probably damaging |
Het |
Sv2c |
T |
A |
13: 95,986,018 (GRCm38) |
I417F |
possibly damaging |
Het |
Tas2r113 |
T |
A |
6: 132,893,516 (GRCm38) |
M169K |
probably benign |
Het |
Tgm1 |
A |
T |
14: 55,705,681 (GRCm38) |
N567K |
probably benign |
Het |
Trpm6 |
T |
C |
19: 18,853,791 (GRCm38) |
V1340A |
probably benign |
Het |
Tspan18 |
A |
T |
2: 93,312,030 (GRCm38) |
|
probably null |
Het |
Txndc11 |
C |
T |
16: 11,084,314 (GRCm38) |
V679I |
probably damaging |
Het |
Usf1 |
G |
T |
1: 171,416,964 (GRCm38) |
G144V |
possibly damaging |
Het |
Vmn1r59 |
T |
C |
7: 5,454,452 (GRCm38) |
Y103C |
probably damaging |
Het |
Vmn2r23 |
A |
T |
6: 123,741,826 (GRCm38) |
I713F |
probably damaging |
Het |
Vmn2r79 |
A |
T |
7: 87,037,960 (GRCm38) |
I850F |
probably damaging |
Het |
Wdr90 |
C |
T |
17: 25,855,363 (GRCm38) |
R676H |
probably benign |
Het |
Zfp867 |
G |
A |
11: 59,463,661 (GRCm38) |
R281W |
probably damaging |
Het |
Zfp939 |
T |
C |
7: 39,472,942 (GRCm38) |
|
noncoding transcript |
Het |
|
Other mutations in Tln2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00468:Tln2
|
APN |
9 |
67,344,187 (GRCm38) |
missense |
possibly damaging |
0.59 |
IGL01110:Tln2
|
APN |
9 |
67,250,582 (GRCm38) |
nonsense |
probably null |
|
IGL01112:Tln2
|
APN |
9 |
67,311,811 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01307:Tln2
|
APN |
9 |
67,395,467 (GRCm38) |
missense |
probably benign |
0.25 |
IGL01374:Tln2
|
APN |
9 |
67,261,923 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01625:Tln2
|
APN |
9 |
67,370,623 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01865:Tln2
|
APN |
9 |
67,250,614 (GRCm38) |
nonsense |
probably null |
|
IGL01999:Tln2
|
APN |
9 |
67,392,505 (GRCm38) |
missense |
possibly damaging |
0.81 |
IGL02002:Tln2
|
APN |
9 |
67,356,698 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL02005:Tln2
|
APN |
9 |
67,392,505 (GRCm38) |
missense |
possibly damaging |
0.81 |
IGL02015:Tln2
|
APN |
9 |
67,361,439 (GRCm38) |
splice site |
probably benign |
|
IGL02368:Tln2
|
APN |
9 |
67,240,810 (GRCm38) |
splice site |
probably benign |
|
IGL02444:Tln2
|
APN |
9 |
67,258,592 (GRCm38) |
splice site |
probably benign |
|
IGL02646:Tln2
|
APN |
9 |
67,255,996 (GRCm38) |
missense |
probably benign |
0.43 |
IGL02744:Tln2
|
APN |
9 |
67,229,376 (GRCm38) |
nonsense |
probably null |
|
IGL02869:Tln2
|
APN |
9 |
67,221,525 (GRCm38) |
splice site |
probably benign |
|
IGL02930:Tln2
|
APN |
9 |
67,393,662 (GRCm38) |
nonsense |
probably null |
|
IGL03100:Tln2
|
APN |
9 |
67,295,737 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03326:Tln2
|
APN |
9 |
67,334,257 (GRCm38) |
missense |
possibly damaging |
0.67 |
Harrier
|
UTSW |
9 |
67,330,552 (GRCm38) |
nonsense |
probably null |
|
Marsh
|
UTSW |
9 |
67,272,654 (GRCm38) |
missense |
probably benign |
0.19 |
BB008:Tln2
|
UTSW |
9 |
67,258,460 (GRCm38) |
critical splice donor site |
probably null |
|
BB018:Tln2
|
UTSW |
9 |
67,258,460 (GRCm38) |
critical splice donor site |
probably null |
|
R0047:Tln2
|
UTSW |
9 |
67,240,672 (GRCm38) |
splice site |
probably benign |
|
R0047:Tln2
|
UTSW |
9 |
67,240,672 (GRCm38) |
splice site |
probably benign |
|
R0107:Tln2
|
UTSW |
9 |
67,370,706 (GRCm38) |
missense |
probably damaging |
1.00 |
R0494:Tln2
|
UTSW |
9 |
67,355,197 (GRCm38) |
missense |
probably benign |
0.22 |
R0884:Tln2
|
UTSW |
9 |
67,370,733 (GRCm38) |
missense |
probably damaging |
1.00 |
R0947:Tln2
|
UTSW |
9 |
67,295,813 (GRCm38) |
missense |
probably benign |
0.08 |
R0989:Tln2
|
UTSW |
9 |
67,229,454 (GRCm38) |
missense |
probably damaging |
1.00 |
R1195:Tln2
|
UTSW |
9 |
67,258,566 (GRCm38) |
missense |
probably damaging |
0.96 |
R1195:Tln2
|
UTSW |
9 |
67,258,566 (GRCm38) |
missense |
probably damaging |
0.96 |
R1195:Tln2
|
UTSW |
9 |
67,258,566 (GRCm38) |
missense |
probably damaging |
0.96 |
R1486:Tln2
|
UTSW |
9 |
67,311,839 (GRCm38) |
missense |
probably damaging |
1.00 |
R1527:Tln2
|
UTSW |
9 |
67,272,668 (GRCm38) |
missense |
possibly damaging |
0.95 |
R1584:Tln2
|
UTSW |
9 |
67,296,414 (GRCm38) |
missense |
probably damaging |
1.00 |
R1636:Tln2
|
UTSW |
9 |
67,306,532 (GRCm38) |
missense |
probably damaging |
1.00 |
R1656:Tln2
|
UTSW |
9 |
67,227,107 (GRCm38) |
missense |
possibly damaging |
0.81 |
R1707:Tln2
|
UTSW |
9 |
67,375,807 (GRCm38) |
missense |
probably benign |
0.00 |
R1749:Tln2
|
UTSW |
9 |
67,286,514 (GRCm38) |
missense |
probably benign |
0.01 |
R1751:Tln2
|
UTSW |
9 |
67,286,514 (GRCm38) |
missense |
probably benign |
0.01 |
R1761:Tln2
|
UTSW |
9 |
67,286,514 (GRCm38) |
missense |
probably benign |
0.01 |
R1767:Tln2
|
UTSW |
9 |
67,286,514 (GRCm38) |
missense |
probably benign |
0.01 |
R1815:Tln2
|
UTSW |
9 |
67,229,423 (GRCm38) |
missense |
probably damaging |
1.00 |
R1840:Tln2
|
UTSW |
9 |
67,342,043 (GRCm38) |
missense |
probably damaging |
1.00 |
R1847:Tln2
|
UTSW |
9 |
67,362,687 (GRCm38) |
nonsense |
probably null |
|
R1964:Tln2
|
UTSW |
9 |
67,342,135 (GRCm38) |
missense |
probably benign |
0.00 |
R1968:Tln2
|
UTSW |
9 |
67,255,901 (GRCm38) |
missense |
probably damaging |
1.00 |
R2036:Tln2
|
UTSW |
9 |
67,272,704 (GRCm38) |
missense |
possibly damaging |
0.76 |
R2038:Tln2
|
UTSW |
9 |
67,397,653 (GRCm38) |
start codon destroyed |
probably benign |
0.01 |
R2152:Tln2
|
UTSW |
9 |
67,302,560 (GRCm38) |
missense |
probably damaging |
1.00 |
R2153:Tln2
|
UTSW |
9 |
67,302,560 (GRCm38) |
missense |
probably damaging |
1.00 |
R2154:Tln2
|
UTSW |
9 |
67,302,560 (GRCm38) |
missense |
probably damaging |
1.00 |
R2191:Tln2
|
UTSW |
9 |
67,355,221 (GRCm38) |
missense |
probably damaging |
1.00 |
R2192:Tln2
|
UTSW |
9 |
67,355,221 (GRCm38) |
missense |
probably damaging |
1.00 |
R2201:Tln2
|
UTSW |
9 |
67,375,757 (GRCm38) |
missense |
probably damaging |
1.00 |
R3116:Tln2
|
UTSW |
9 |
67,355,139 (GRCm38) |
missense |
probably benign |
0.10 |
R3151:Tln2
|
UTSW |
9 |
67,330,547 (GRCm38) |
critical splice donor site |
probably null |
|
R3795:Tln2
|
UTSW |
9 |
67,255,915 (GRCm38) |
missense |
probably damaging |
0.97 |
R3953:Tln2
|
UTSW |
9 |
67,370,629 (GRCm38) |
missense |
probably damaging |
1.00 |
R4450:Tln2
|
UTSW |
9 |
67,344,065 (GRCm38) |
critical splice donor site |
probably null |
|
R4685:Tln2
|
UTSW |
9 |
67,302,572 (GRCm38) |
missense |
probably damaging |
1.00 |
R4688:Tln2
|
UTSW |
9 |
67,397,653 (GRCm38) |
start codon destroyed |
probably benign |
0.01 |
R4696:Tln2
|
UTSW |
9 |
67,395,461 (GRCm38) |
missense |
probably damaging |
1.00 |
R4700:Tln2
|
UTSW |
9 |
67,346,527 (GRCm38) |
missense |
probably benign |
0.03 |
R4701:Tln2
|
UTSW |
9 |
67,346,527 (GRCm38) |
missense |
probably benign |
0.03 |
R4741:Tln2
|
UTSW |
9 |
67,386,555 (GRCm38) |
critical splice donor site |
probably null |
|
R4806:Tln2
|
UTSW |
9 |
67,331,733 (GRCm38) |
missense |
probably benign |
0.29 |
R4807:Tln2
|
UTSW |
9 |
67,331,733 (GRCm38) |
missense |
probably benign |
0.29 |
R4808:Tln2
|
UTSW |
9 |
67,331,733 (GRCm38) |
missense |
probably benign |
0.29 |
R4967:Tln2
|
UTSW |
9 |
67,355,125 (GRCm38) |
missense |
probably damaging |
0.97 |
R5061:Tln2
|
UTSW |
9 |
67,354,468 (GRCm38) |
missense |
probably benign |
|
R5092:Tln2
|
UTSW |
9 |
67,256,028 (GRCm38) |
missense |
probably benign |
0.13 |
R5093:Tln2
|
UTSW |
9 |
67,334,314 (GRCm38) |
missense |
probably benign |
0.44 |
R5126:Tln2
|
UTSW |
9 |
67,258,535 (GRCm38) |
missense |
probably damaging |
1.00 |
R5204:Tln2
|
UTSW |
9 |
67,354,482 (GRCm38) |
missense |
probably benign |
0.00 |
R5236:Tln2
|
UTSW |
9 |
67,365,923 (GRCm38) |
missense |
probably damaging |
0.99 |
R5287:Tln2
|
UTSW |
9 |
67,242,359 (GRCm38) |
missense |
probably damaging |
1.00 |
R5568:Tln2
|
UTSW |
9 |
67,311,865 (GRCm38) |
missense |
probably damaging |
1.00 |
R5571:Tln2
|
UTSW |
9 |
67,334,320 (GRCm38) |
missense |
possibly damaging |
0.88 |
R5642:Tln2
|
UTSW |
9 |
67,296,358 (GRCm38) |
missense |
probably benign |
0.01 |
R5711:Tln2
|
UTSW |
9 |
67,392,547 (GRCm38) |
missense |
probably benign |
0.00 |
R5776:Tln2
|
UTSW |
9 |
67,258,250 (GRCm38) |
missense |
probably damaging |
1.00 |
R5791:Tln2
|
UTSW |
9 |
67,386,605 (GRCm38) |
missense |
probably damaging |
0.98 |
R5866:Tln2
|
UTSW |
9 |
67,266,868 (GRCm38) |
missense |
probably damaging |
1.00 |
R5888:Tln2
|
UTSW |
9 |
67,229,403 (GRCm38) |
missense |
probably damaging |
1.00 |
R5902:Tln2
|
UTSW |
9 |
67,362,717 (GRCm38) |
missense |
probably benign |
0.02 |
R6106:Tln2
|
UTSW |
9 |
67,323,020 (GRCm38) |
missense |
probably damaging |
0.99 |
R6175:Tln2
|
UTSW |
9 |
67,224,081 (GRCm38) |
missense |
probably damaging |
1.00 |
R6385:Tln2
|
UTSW |
9 |
67,278,129 (GRCm38) |
missense |
probably benign |
0.45 |
R6430:Tln2
|
UTSW |
9 |
67,272,665 (GRCm38) |
missense |
probably damaging |
1.00 |
R6441:Tln2
|
UTSW |
9 |
67,272,689 (GRCm38) |
missense |
probably damaging |
1.00 |
R6738:Tln2
|
UTSW |
9 |
67,386,664 (GRCm38) |
missense |
possibly damaging |
0.91 |
R6776:Tln2
|
UTSW |
9 |
67,262,905 (GRCm38) |
missense |
probably damaging |
1.00 |
R6794:Tln2
|
UTSW |
9 |
67,286,558 (GRCm38) |
missense |
probably benign |
0.07 |
R6850:Tln2
|
UTSW |
9 |
67,258,535 (GRCm38) |
missense |
probably damaging |
1.00 |
R6907:Tln2
|
UTSW |
9 |
67,397,635 (GRCm38) |
missense |
probably damaging |
0.98 |
R6909:Tln2
|
UTSW |
9 |
67,392,532 (GRCm38) |
missense |
probably damaging |
0.97 |
R6951:Tln2
|
UTSW |
9 |
67,258,485 (GRCm38) |
missense |
probably damaging |
0.97 |
R7015:Tln2
|
UTSW |
9 |
67,362,647 (GRCm38) |
missense |
possibly damaging |
0.55 |
R7051:Tln2
|
UTSW |
9 |
67,346,417 (GRCm38) |
missense |
probably benign |
0.00 |
R7246:Tln2
|
UTSW |
9 |
67,262,979 (GRCm38) |
missense |
probably damaging |
1.00 |
R7292:Tln2
|
UTSW |
9 |
67,346,461 (GRCm38) |
missense |
probably benign |
|
R7753:Tln2
|
UTSW |
9 |
67,395,473 (GRCm38) |
missense |
probably damaging |
1.00 |
R7868:Tln2
|
UTSW |
9 |
67,348,226 (GRCm38) |
missense |
probably damaging |
1.00 |
R7931:Tln2
|
UTSW |
9 |
67,258,460 (GRCm38) |
critical splice donor site |
probably null |
|
R8023:Tln2
|
UTSW |
9 |
67,224,064 (GRCm38) |
missense |
probably damaging |
1.00 |
R8081:Tln2
|
UTSW |
9 |
67,356,747 (GRCm38) |
missense |
probably damaging |
1.00 |
R8164:Tln2
|
UTSW |
9 |
67,319,420 (GRCm38) |
missense |
probably benign |
0.31 |
R8192:Tln2
|
UTSW |
9 |
67,346,529 (GRCm38) |
nonsense |
probably null |
|
R8495:Tln2
|
UTSW |
9 |
67,354,467 (GRCm38) |
missense |
probably benign |
0.01 |
R8734:Tln2
|
UTSW |
9 |
67,272,654 (GRCm38) |
missense |
probably benign |
0.19 |
R8739:Tln2
|
UTSW |
9 |
67,258,273 (GRCm38) |
missense |
probably damaging |
1.00 |
R8757:Tln2
|
UTSW |
9 |
67,367,218 (GRCm38) |
missense |
probably damaging |
1.00 |
R8759:Tln2
|
UTSW |
9 |
67,367,218 (GRCm38) |
missense |
probably damaging |
1.00 |
R8770:Tln2
|
UTSW |
9 |
67,323,022 (GRCm38) |
missense |
probably benign |
|
R8781:Tln2
|
UTSW |
9 |
67,255,951 (GRCm38) |
missense |
probably damaging |
1.00 |
R8812:Tln2
|
UTSW |
9 |
67,221,411 (GRCm38) |
missense |
possibly damaging |
0.75 |
R8814:Tln2
|
UTSW |
9 |
67,221,411 (GRCm38) |
missense |
possibly damaging |
0.75 |
R8816:Tln2
|
UTSW |
9 |
67,221,517 (GRCm38) |
missense |
probably damaging |
1.00 |
R8816:Tln2
|
UTSW |
9 |
67,221,411 (GRCm38) |
missense |
possibly damaging |
0.75 |
R8833:Tln2
|
UTSW |
9 |
67,221,411 (GRCm38) |
missense |
possibly damaging |
0.75 |
R8835:Tln2
|
UTSW |
9 |
67,397,693 (GRCm38) |
splice site |
probably benign |
|
R8837:Tln2
|
UTSW |
9 |
67,250,584 (GRCm38) |
missense |
probably damaging |
0.99 |
R8843:Tln2
|
UTSW |
9 |
67,395,545 (GRCm38) |
missense |
probably damaging |
1.00 |
R8864:Tln2
|
UTSW |
9 |
67,330,552 (GRCm38) |
nonsense |
probably null |
|
R8867:Tln2
|
UTSW |
9 |
67,330,550 (GRCm38) |
missense |
probably damaging |
0.98 |
R8921:Tln2
|
UTSW |
9 |
67,266,823 (GRCm38) |
missense |
probably damaging |
0.99 |
R9080:Tln2
|
UTSW |
9 |
67,346,561 (GRCm38) |
missense |
probably damaging |
1.00 |
R9083:Tln2
|
UTSW |
9 |
67,362,645 (GRCm38) |
missense |
probably damaging |
0.96 |
R9150:Tln2
|
UTSW |
9 |
67,221,496 (GRCm38) |
missense |
probably damaging |
1.00 |
R9287:Tln2
|
UTSW |
9 |
67,370,698 (GRCm38) |
missense |
probably benign |
0.20 |
R9330:Tln2
|
UTSW |
9 |
67,321,931 (GRCm38) |
missense |
possibly damaging |
0.61 |
R9343:Tln2
|
UTSW |
9 |
67,323,071 (GRCm38) |
missense |
probably benign |
0.10 |
R9355:Tln2
|
UTSW |
9 |
67,355,247 (GRCm38) |
missense |
possibly damaging |
0.46 |
R9383:Tln2
|
UTSW |
9 |
67,370,761 (GRCm38) |
missense |
probably benign |
0.17 |
R9386:Tln2
|
UTSW |
9 |
67,365,967 (GRCm38) |
missense |
possibly damaging |
0.78 |
R9407:Tln2
|
UTSW |
9 |
67,229,450 (GRCm38) |
missense |
probably damaging |
1.00 |
R9483:Tln2
|
UTSW |
9 |
67,392,487 (GRCm38) |
missense |
probably damaging |
1.00 |
R9523:Tln2
|
UTSW |
9 |
67,258,484 (GRCm38) |
missense |
probably damaging |
0.99 |
R9642:Tln2
|
UTSW |
9 |
67,250,544 (GRCm38) |
missense |
probably benign |
0.02 |
R9703:Tln2
|
UTSW |
9 |
67,386,656 (GRCm38) |
missense |
probably damaging |
1.00 |
X0027:Tln2
|
UTSW |
9 |
67,376,853 (GRCm38) |
missense |
probably damaging |
1.00 |
X0064:Tln2
|
UTSW |
9 |
67,348,138 (GRCm38) |
missense |
probably damaging |
1.00 |
X0067:Tln2
|
UTSW |
9 |
67,370,691 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1176:Tln2
|
UTSW |
9 |
67,346,485 (GRCm38) |
missense |
possibly damaging |
0.46 |
|