Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
T |
C |
11: 110,074,933 (GRCm39) |
T1377A |
probably damaging |
Het |
AI661453 |
G |
T |
17: 47,778,439 (GRCm39) |
E722* |
probably null |
Het |
Ap2b1 |
A |
T |
11: 83,258,733 (GRCm39) |
K735* |
probably null |
Het |
Aqp4 |
T |
C |
18: 15,533,033 (GRCm39) |
E20G |
probably benign |
Het |
Atp6v1b1 |
G |
T |
6: 83,729,440 (GRCm39) |
V117L |
probably benign |
Het |
C1rb |
A |
G |
6: 124,557,390 (GRCm39) |
N509S |
probably benign |
Het |
Cep44 |
A |
G |
8: 56,985,842 (GRCm39) |
V350A |
probably benign |
Het |
Cmya5 |
T |
C |
13: 93,234,680 (GRCm39) |
Q136R |
probably benign |
Het |
Cntrl |
T |
C |
2: 35,001,691 (GRCm39) |
S32P |
probably damaging |
Het |
Cyp2d12 |
A |
T |
15: 82,441,164 (GRCm39) |
E201V |
possibly damaging |
Het |
Cyp4a14 |
G |
T |
4: 115,350,861 (GRCm39) |
Q138K |
probably damaging |
Het |
Dapk1 |
T |
C |
13: 60,899,007 (GRCm39) |
Y826H |
possibly damaging |
Het |
Dbh |
A |
G |
2: 27,061,448 (GRCm39) |
D294G |
probably benign |
Het |
Ddx10 |
A |
T |
9: 53,136,904 (GRCm39) |
L336Q |
probably damaging |
Het |
Dop1a |
A |
G |
9: 86,371,755 (GRCm39) |
T149A |
possibly damaging |
Het |
Epg5 |
A |
G |
18: 77,991,560 (GRCm39) |
T86A |
possibly damaging |
Het |
Fam171a1 |
A |
T |
2: 3,179,354 (GRCm39) |
Q60L |
probably damaging |
Het |
Farsb |
T |
A |
1: 78,456,740 (GRCm39) |
E41D |
probably benign |
Het |
Frem1 |
T |
C |
4: 82,832,217 (GRCm39) |
D1956G |
probably benign |
Het |
Fzd4 |
T |
A |
7: 89,056,992 (GRCm39) |
Y346* |
probably null |
Het |
Fzd7 |
A |
T |
1: 59,522,641 (GRCm39) |
S175C |
probably benign |
Het |
Gdi2 |
A |
G |
13: 3,598,956 (GRCm39) |
T47A |
probably benign |
Het |
Gpr155 |
A |
T |
2: 73,212,550 (GRCm39) |
H24Q |
probably benign |
Het |
Hdac7 |
A |
T |
15: 97,698,642 (GRCm39) |
N638K |
possibly damaging |
Het |
Hdac7 |
G |
T |
15: 97,704,369 (GRCm39) |
N515K |
probably benign |
Het |
Hnrnpul2 |
T |
C |
19: 8,802,336 (GRCm39) |
V401A |
probably damaging |
Het |
Ifi27l2b |
T |
A |
12: 103,417,519 (GRCm39) |
R223* |
probably null |
Het |
Igkv4-91 |
T |
G |
6: 68,745,761 (GRCm39) |
S46R |
probably benign |
Het |
Itk |
T |
A |
11: 46,222,722 (GRCm39) |
L582F |
probably damaging |
Het |
Kcnab2 |
T |
C |
4: 152,481,218 (GRCm39) |
I181V |
probably benign |
Het |
Krtap5-2 |
GCCACAGCCTCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACCACAGCCTCC |
GCCACAGCCTCC |
7: 141,729,136 (GRCm39) |
|
probably benign |
Het |
Lce1m |
C |
A |
3: 92,925,815 (GRCm39) |
G41W |
unknown |
Het |
Mapk10 |
T |
A |
5: 103,186,419 (GRCm39) |
K98* |
probably null |
Het |
Mapk8ip2 |
A |
G |
15: 89,345,856 (GRCm39) |
E812G |
probably damaging |
Het |
Mlh1 |
C |
A |
9: 111,081,931 (GRCm39) |
|
probably null |
Het |
Mroh1 |
A |
G |
15: 76,317,475 (GRCm39) |
D784G |
possibly damaging |
Het |
Neo1 |
A |
T |
9: 58,863,288 (GRCm39) |
D426E |
probably benign |
Het |
Nol4 |
T |
A |
18: 23,171,659 (GRCm39) |
M1L |
probably benign |
Het |
Nr1h3 |
A |
G |
2: 91,015,370 (GRCm39) |
F338S |
probably damaging |
Het |
Oasl2 |
A |
G |
5: 115,043,118 (GRCm39) |
K297E |
probably benign |
Het |
Or10ag59 |
A |
G |
2: 87,406,141 (GRCm39) |
T238A |
probably benign |
Het |
Or10z1 |
C |
T |
1: 174,078,236 (GRCm39) |
V86I |
probably benign |
Het |
Or4f14 |
A |
G |
2: 111,742,927 (GRCm39) |
I116T |
probably benign |
Het |
Or56a5 |
T |
C |
7: 104,793,007 (GRCm39) |
I164M |
probably benign |
Het |
Or5m5 |
A |
G |
2: 85,815,060 (GRCm39) |
N292S |
possibly damaging |
Het |
Osbpl9 |
T |
C |
4: 108,990,970 (GRCm39) |
T97A |
possibly damaging |
Het |
P3h2 |
A |
T |
16: 25,789,687 (GRCm39) |
Y527N |
probably damaging |
Het |
Papss2 |
A |
T |
19: 32,597,579 (GRCm39) |
H9L |
probably benign |
Het |
Pcdha4 |
C |
A |
18: 37,086,354 (GRCm39) |
S179Y |
possibly damaging |
Het |
Ppt1 |
A |
T |
4: 122,730,131 (GRCm39) |
D28V |
possibly damaging |
Het |
Prkcz |
T |
A |
4: 155,357,425 (GRCm39) |
Q345L |
possibly damaging |
Het |
Prr14l |
G |
T |
5: 32,984,597 (GRCm39) |
L1633I |
probably damaging |
Het |
Prss51 |
T |
A |
14: 64,333,376 (GRCm39) |
V13D |
possibly damaging |
Het |
Qrich2 |
TTGCAACACACCAGGCTGAACTGGACCTTGCTG |
TTG |
11: 116,347,868 (GRCm39) |
|
probably benign |
Het |
Rictor |
C |
T |
15: 6,801,635 (GRCm39) |
S441L |
probably benign |
Het |
Slc2a7 |
T |
C |
4: 150,239,141 (GRCm39) |
I122T |
possibly damaging |
Het |
Spata31e4 |
A |
T |
13: 50,855,817 (GRCm39) |
D485V |
probably damaging |
Het |
Sprr3 |
G |
A |
3: 92,364,415 (GRCm39) |
P143L |
probably benign |
Het |
Sugct |
A |
T |
13: 17,752,104 (GRCm39) |
S181T |
possibly damaging |
Het |
Syne2 |
G |
A |
12: 76,085,697 (GRCm39) |
R141Q |
probably benign |
Het |
Taok1 |
T |
C |
11: 77,428,725 (GRCm39) |
I992V |
probably benign |
Het |
Tbc1d21 |
A |
C |
9: 58,269,306 (GRCm39) |
|
probably null |
Het |
Thada |
T |
C |
17: 84,559,818 (GRCm39) |
D1453G |
probably damaging |
Het |
Thoc5 |
T |
C |
11: 4,852,156 (GRCm39) |
L104S |
probably damaging |
Het |
Tmem98 |
A |
G |
11: 80,705,137 (GRCm39) |
E75G |
probably damaging |
Het |
Tox3 |
A |
G |
8: 90,975,560 (GRCm39) |
L357P |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,197,603 (GRCm39) |
V4492A |
unknown |
Het |
Ulk4 |
A |
G |
9: 121,095,578 (GRCm39) |
|
probably null |
Het |
Ush2a |
A |
G |
1: 188,175,603 (GRCm39) |
T1234A |
probably benign |
Het |
Usp53 |
G |
A |
3: 122,742,887 (GRCm39) |
T683I |
probably damaging |
Het |
Vcan |
T |
A |
13: 89,837,442 (GRCm39) |
I2701F |
probably damaging |
Het |
Vmn2r72 |
G |
A |
7: 85,399,834 (GRCm39) |
A405V |
probably damaging |
Het |
Vmn2r96 |
A |
T |
17: 18,806,663 (GRCm39) |
T537S |
possibly damaging |
Het |
Vstm2a |
G |
T |
11: 16,213,040 (GRCm39) |
A142S |
probably damaging |
Het |
Zbtb41 |
A |
G |
1: 139,374,895 (GRCm39) |
D785G |
probably benign |
Het |
Zfp397 |
A |
T |
18: 24,090,129 (GRCm39) |
Q144H |
probably benign |
Het |
Zfp518a |
A |
T |
19: 40,904,249 (GRCm39) |
T1393S |
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 |
|
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 |
R8812:Tln2
|
UTSW |
9 |
67,128,693 (GRCm39) |
missense |
possibly damaging |
0.75 |
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 |
|