Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4833420G17Rik |
C |
T |
13: 119,610,573 (GRCm39) |
|
probably benign |
Het |
Abca9 |
A |
T |
11: 110,032,358 (GRCm39) |
L753Q |
probably damaging |
Het |
Acvrl1 |
A |
G |
15: 101,032,628 (GRCm39) |
|
probably null |
Het |
Adgrv1 |
A |
T |
13: 81,740,704 (GRCm39) |
N141K |
probably damaging |
Het |
Aftph |
C |
T |
11: 20,659,619 (GRCm39) |
|
probably null |
Het |
Aifm1 |
C |
T |
X: 47,571,637 (GRCm39) |
G371S |
probably benign |
Het |
Aldh3b2 |
A |
G |
19: 4,029,433 (GRCm39) |
M269V |
probably benign |
Het |
Ankrd44 |
T |
C |
1: 54,802,877 (GRCm39) |
Y207C |
probably damaging |
Het |
Arhgap15 |
G |
T |
2: 44,212,767 (GRCm39) |
M412I |
probably damaging |
Het |
Auts2 |
A |
C |
5: 131,468,296 (GRCm39) |
L783R |
probably damaging |
Het |
Baiap2l1 |
A |
T |
5: 144,215,363 (GRCm39) |
Y381N |
probably damaging |
Het |
Baiap3 |
T |
C |
17: 25,469,243 (GRCm39) |
D180G |
probably damaging |
Het |
Cant1 |
T |
C |
11: 118,302,038 (GRCm39) |
Y93C |
probably damaging |
Het |
Catsperg2 |
T |
C |
7: 29,416,423 (GRCm39) |
S330G |
probably benign |
Het |
Ccdc73 |
A |
T |
2: 104,848,111 (GRCm39) |
|
probably benign |
Het |
Cdc5l |
A |
T |
17: 45,703,967 (GRCm39) |
F752L |
possibly damaging |
Het |
Celsr2 |
G |
T |
3: 108,320,689 (GRCm39) |
H708N |
possibly damaging |
Het |
Cep170 |
T |
A |
1: 176,596,896 (GRCm39) |
K487M |
possibly damaging |
Het |
Cerkl |
A |
T |
2: 79,163,867 (GRCm39) |
N66K |
probably damaging |
Het |
Cilk1 |
G |
A |
9: 78,047,303 (GRCm39) |
V68I |
probably benign |
Het |
Clec11a |
C |
T |
7: 43,954,150 (GRCm39) |
A268T |
probably damaging |
Het |
Ctnna2 |
C |
A |
6: 77,091,912 (GRCm39) |
|
probably null |
Het |
Diaph3 |
C |
A |
14: 87,222,236 (GRCm39) |
R416L |
probably damaging |
Het |
Dnmbp |
T |
A |
19: 43,838,315 (GRCm39) |
N1170I |
probably damaging |
Het |
Erbb2 |
G |
T |
11: 98,318,279 (GRCm39) |
C505F |
probably damaging |
Het |
Ercc6 |
T |
A |
14: 32,289,479 (GRCm39) |
F904L |
probably damaging |
Het |
Exo5 |
C |
T |
4: 120,779,514 (GRCm39) |
G117D |
probably damaging |
Het |
F2 |
CAGAAAG |
CAG |
2: 91,465,302 (GRCm39) |
|
probably benign |
Het |
Fbxl5 |
A |
G |
5: 43,930,896 (GRCm39) |
Y64H |
probably damaging |
Het |
Gabra4 |
T |
A |
5: 71,798,207 (GRCm39) |
M207L |
probably damaging |
Het |
Galnt15 |
T |
C |
14: 31,771,786 (GRCm39) |
L277P |
probably damaging |
Het |
Gclm |
T |
C |
3: 122,049,261 (GRCm39) |
|
probably null |
Het |
Gm5493 |
T |
A |
17: 22,966,201 (GRCm39) |
C29S |
possibly damaging |
Het |
Grik3 |
A |
G |
4: 125,564,382 (GRCm39) |
T455A |
probably benign |
Het |
Grm3 |
A |
G |
5: 9,639,766 (GRCm39) |
V93A |
probably benign |
Het |
Hdgfl2 |
C |
T |
17: 56,406,217 (GRCm39) |
A535V |
possibly damaging |
Het |
Hfm1 |
A |
T |
5: 107,049,597 (GRCm39) |
S455T |
probably damaging |
Het |
Hmcn1 |
T |
A |
1: 150,613,007 (GRCm39) |
D1424V |
probably benign |
Het |
Hsd3b6 |
C |
T |
3: 98,715,120 (GRCm39) |
V91I |
probably benign |
Het |
Igdcc4 |
G |
A |
9: 65,030,039 (GRCm39) |
S363N |
possibly damaging |
Het |
Intu |
T |
C |
3: 40,647,347 (GRCm39) |
V740A |
probably benign |
Het |
Itga2 |
C |
T |
13: 114,992,717 (GRCm39) |
V838I |
probably benign |
Het |
Kif9 |
A |
G |
9: 110,318,965 (GRCm39) |
E143G |
probably damaging |
Het |
Kmt2c |
T |
A |
5: 25,614,205 (GRCm39) |
I172F |
probably benign |
Het |
Kmt2d |
G |
A |
15: 98,754,043 (GRCm39) |
R21W |
probably damaging |
Het |
Mdh1b |
A |
T |
1: 63,750,620 (GRCm39) |
D449E |
probably benign |
Het |
Meis1 |
T |
C |
11: 18,831,785 (GRCm39) |
I418V |
probably benign |
Het |
Nags |
T |
A |
11: 102,037,395 (GRCm39) |
M162K |
probably damaging |
Het |
Nufip1 |
A |
G |
14: 76,348,413 (GRCm39) |
D14G |
probably benign |
Het |
Or2l13 |
T |
A |
16: 19,306,227 (GRCm39) |
I213N |
probably damaging |
Het |
Or2n1c |
A |
C |
17: 38,519,208 (GRCm39) |
E24A |
possibly damaging |
Het |
Or7g28 |
T |
G |
9: 19,272,274 (GRCm39) |
I126L |
probably damaging |
Het |
Osmr |
A |
C |
15: 6,850,560 (GRCm39) |
V681G |
probably damaging |
Het |
Paxip1 |
G |
T |
5: 27,971,282 (GRCm39) |
Q356K |
unknown |
Het |
Pcdhac1 |
T |
A |
18: 37,223,595 (GRCm39) |
F136Y |
probably damaging |
Het |
Pla2g6 |
A |
G |
15: 79,171,328 (GRCm39) |
V699A |
probably benign |
Het |
Plcb3 |
A |
T |
19: 6,943,578 (GRCm39) |
V107E |
probably damaging |
Het |
Plch1 |
T |
A |
3: 63,681,136 (GRCm39) |
I164F |
probably damaging |
Het |
Plpp3 |
A |
T |
4: 105,052,077 (GRCm39) |
I73F |
probably damaging |
Het |
Plscr5 |
G |
A |
9: 92,080,574 (GRCm39) |
R20Q |
probably benign |
Het |
Prdm10 |
G |
A |
9: 31,252,779 (GRCm39) |
R504Q |
probably damaging |
Het |
Prss58 |
T |
C |
6: 40,874,751 (GRCm39) |
Y30C |
probably damaging |
Het |
Psg19 |
T |
A |
7: 18,530,894 (GRCm39) |
T87S |
probably benign |
Het |
Ptpn22 |
T |
G |
3: 103,789,418 (GRCm39) |
M294R |
probably benign |
Het |
Rai1 |
T |
A |
11: 60,079,482 (GRCm39) |
M1182K |
probably benign |
Het |
Sez6 |
T |
A |
11: 77,867,388 (GRCm39) |
V795D |
possibly damaging |
Het |
Shcbp1 |
A |
G |
8: 4,789,214 (GRCm39) |
V535A |
possibly damaging |
Het |
Skint9 |
A |
G |
4: 112,246,447 (GRCm39) |
Y222H |
probably benign |
Het |
Slc13a3 |
T |
A |
2: 165,253,816 (GRCm39) |
I446F |
probably damaging |
Het |
Slc2a3 |
C |
T |
6: 122,714,196 (GRCm39) |
R57H |
probably damaging |
Het |
Slc44a4 |
A |
G |
17: 35,140,219 (GRCm39) |
D208G |
probably benign |
Het |
Spata31d1b |
A |
T |
13: 59,863,838 (GRCm39) |
N329Y |
possibly damaging |
Het |
Strbp |
C |
T |
2: 37,517,499 (GRCm39) |
R192K |
probably damaging |
Het |
Tctn3 |
A |
T |
19: 40,600,548 (GRCm39) |
L14Q |
probably damaging |
Het |
Tenm2 |
T |
A |
11: 36,834,989 (GRCm39) |
D2V |
probably damaging |
Het |
Tmem63b |
T |
C |
17: 45,971,800 (GRCm39) |
E805G |
probably damaging |
Het |
Trhr |
A |
T |
15: 44,060,980 (GRCm39) |
N167Y |
probably damaging |
Het |
Trpc2 |
A |
G |
7: 101,744,390 (GRCm39) |
R721G |
probably benign |
Het |
Ttn |
C |
A |
2: 76,701,267 (GRCm39) |
|
probably benign |
Het |
Wdr91 |
A |
G |
6: 34,869,288 (GRCm39) |
I412T |
probably damaging |
Het |
Zcchc4 |
T |
A |
5: 52,953,952 (GRCm39) |
S211T |
probably benign |
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 |
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 |
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 |
|