Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930523C07Rik |
A |
T |
1: 159,898,372 (GRCm39) |
|
probably benign |
Het |
4931429P17Rik |
A |
G |
13: 48,114,481 (GRCm39) |
|
noncoding transcript |
Het |
Acox3 |
T |
A |
5: 35,758,908 (GRCm39) |
I373N |
possibly damaging |
Het |
Adgrb1 |
G |
T |
15: 74,401,192 (GRCm39) |
A63S |
probably damaging |
Het |
Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
Aplp2 |
A |
T |
9: 31,062,215 (GRCm39) |
H692Q |
probably damaging |
Het |
Arhgap24 |
T |
C |
5: 103,039,953 (GRCm39) |
S297P |
probably benign |
Het |
Arhgap9 |
C |
T |
10: 127,164,758 (GRCm39) |
P561S |
probably benign |
Het |
Arhgef10l |
T |
G |
4: 140,291,600 (GRCm39) |
D62A |
probably damaging |
Het |
Asb14 |
T |
G |
14: 26,623,079 (GRCm39) |
F150L |
probably benign |
Het |
Atp8b3 |
A |
T |
10: 80,357,635 (GRCm39) |
|
probably null |
Het |
Atrnl1 |
A |
G |
19: 57,675,169 (GRCm39) |
D686G |
probably benign |
Het |
Bmpr1a |
A |
T |
14: 34,147,098 (GRCm39) |
|
probably benign |
Het |
Cc2d2a |
T |
A |
5: 43,881,030 (GRCm39) |
|
probably null |
Het |
Ccin |
T |
A |
4: 43,983,947 (GRCm39) |
I118N |
probably benign |
Het |
Cd8b1 |
G |
A |
6: 71,303,168 (GRCm39) |
G81D |
probably damaging |
Het |
Cep126 |
G |
A |
9: 8,100,383 (GRCm39) |
S717L |
probably benign |
Het |
Cip2a |
A |
C |
16: 48,838,767 (GRCm39) |
Q861H |
probably damaging |
Het |
Colgalt2 |
C |
T |
1: 152,276,114 (GRCm39) |
R76W |
probably damaging |
Het |
Copg1 |
A |
T |
6: 87,882,192 (GRCm39) |
T596S |
probably benign |
Het |
Cpb1 |
G |
A |
3: 20,329,655 (GRCm39) |
R24W |
probably damaging |
Het |
Csad |
T |
A |
15: 102,088,407 (GRCm39) |
D134V |
probably damaging |
Het |
Dchs2 |
A |
G |
3: 83,034,912 (GRCm39) |
|
probably benign |
Het |
Ddb2 |
A |
G |
2: 91,064,554 (GRCm39) |
W119R |
probably damaging |
Het |
Dhx57 |
A |
T |
17: 80,582,655 (GRCm39) |
S317T |
probably damaging |
Het |
Dlc1 |
A |
G |
8: 37,404,763 (GRCm39) |
V342A |
probably benign |
Het |
Dpp4 |
G |
A |
2: 62,189,679 (GRCm39) |
|
probably benign |
Het |
Dst |
G |
T |
1: 34,206,727 (GRCm39) |
W1005L |
probably damaging |
Het |
Ehmt1 |
T |
C |
2: 24,695,150 (GRCm39) |
M989V |
probably benign |
Het |
Entr1 |
T |
A |
2: 26,277,618 (GRCm39) |
N69Y |
probably damaging |
Het |
Gm5422 |
G |
A |
10: 31,124,458 (GRCm39) |
|
noncoding transcript |
Het |
Gm9944 |
A |
G |
4: 144,179,833 (GRCm39) |
|
probably benign |
Het |
Gtf2ird2 |
T |
C |
5: 134,245,829 (GRCm39) |
Y696H |
probably damaging |
Het |
H2-M11 |
T |
G |
17: 36,859,658 (GRCm39) |
V217G |
probably damaging |
Het |
Hunk |
C |
T |
16: 90,183,295 (GRCm39) |
|
probably benign |
Het |
Impg1 |
T |
C |
9: 80,285,799 (GRCm39) |
|
probably null |
Het |
Ints11 |
T |
G |
4: 155,959,655 (GRCm39) |
D87E |
probably benign |
Het |
Intu |
T |
A |
3: 40,595,073 (GRCm39) |
S21T |
probably benign |
Het |
Intu |
C |
A |
3: 40,637,931 (GRCm39) |
D472E |
possibly damaging |
Het |
Kbtbd3 |
T |
A |
9: 4,316,985 (GRCm39) |
N45K |
probably benign |
Het |
Kif1c |
C |
T |
11: 70,619,223 (GRCm39) |
L953F |
probably damaging |
Het |
Klrg2 |
C |
G |
6: 38,613,729 (GRCm39) |
E91D |
possibly damaging |
Het |
Lamc3 |
T |
C |
2: 31,802,141 (GRCm39) |
|
probably null |
Het |
Magi2 |
T |
G |
5: 20,420,491 (GRCm39) |
M309R |
probably damaging |
Het |
Magohb |
G |
A |
6: 131,261,600 (GRCm39) |
P147S |
probably damaging |
Het |
Mdn1 |
A |
G |
4: 32,693,504 (GRCm39) |
D1043G |
probably damaging |
Het |
Mtmr3 |
T |
C |
11: 4,454,095 (GRCm39) |
D203G |
probably damaging |
Het |
Mvp |
C |
T |
7: 126,600,744 (GRCm39) |
V86I |
probably benign |
Het |
Naip5 |
A |
T |
13: 100,379,363 (GRCm39) |
F226I |
probably damaging |
Het |
Nasp |
T |
A |
4: 116,476,133 (GRCm39) |
Q51L |
probably damaging |
Het |
Nf1 |
T |
A |
11: 79,426,430 (GRCm39) |
F1594I |
probably damaging |
Het |
Nod2 |
A |
C |
8: 89,397,104 (GRCm39) |
E816A |
possibly damaging |
Het |
Nom1 |
G |
A |
5: 29,640,316 (GRCm39) |
S214N |
probably damaging |
Het |
Or2l13b |
T |
C |
16: 19,348,927 (GRCm39) |
T248A |
probably benign |
Het |
Or8c9 |
T |
A |
9: 38,241,197 (GRCm39) |
F105I |
probably damaging |
Het |
Parp14 |
A |
C |
16: 35,678,219 (GRCm39) |
L583R |
probably damaging |
Het |
Pclo |
T |
C |
5: 14,763,238 (GRCm39) |
S3904P |
unknown |
Het |
Pkhd1 |
T |
A |
1: 20,621,064 (GRCm39) |
|
probably benign |
Het |
Plaat1 |
A |
G |
16: 29,046,978 (GRCm39) |
K166E |
probably damaging |
Het |
Polr1e |
A |
C |
4: 45,027,469 (GRCm39) |
D233A |
probably damaging |
Het |
Prr29 |
T |
C |
11: 106,267,509 (GRCm39) |
V124A |
probably damaging |
Het |
Rasgrp1 |
A |
T |
2: 117,129,028 (GRCm39) |
V197E |
probably damaging |
Het |
Rgma |
A |
T |
7: 73,067,707 (GRCm39) |
T415S |
unknown |
Het |
Sacs |
G |
T |
14: 61,447,211 (GRCm39) |
V3086L |
probably benign |
Het |
Sash1 |
A |
G |
10: 8,606,141 (GRCm39) |
S750P |
probably benign |
Het |
Scpppq1 |
T |
A |
5: 104,222,099 (GRCm39) |
|
probably benign |
Het |
Sema6a |
A |
T |
18: 47,416,512 (GRCm39) |
S372T |
probably benign |
Het |
Sis |
A |
G |
3: 72,816,420 (GRCm39) |
|
probably benign |
Het |
Skint8 |
T |
A |
4: 111,796,769 (GRCm39) |
V291D |
probably damaging |
Het |
Slc12a8 |
A |
G |
16: 33,371,377 (GRCm39) |
N171S |
probably damaging |
Het |
Slc25a40 |
G |
A |
5: 8,490,793 (GRCm39) |
|
probably null |
Het |
Spag6l |
A |
T |
16: 16,598,492 (GRCm39) |
I333N |
probably benign |
Het |
Sspo |
T |
A |
6: 48,454,811 (GRCm39) |
F2999L |
probably damaging |
Het |
Stambpl1 |
A |
C |
19: 34,216,221 (GRCm39) |
T363P |
probably damaging |
Het |
Tenm4 |
A |
T |
7: 96,537,892 (GRCm39) |
N1785Y |
probably damaging |
Het |
Tmed3 |
G |
A |
9: 89,584,833 (GRCm39) |
L141F |
probably damaging |
Het |
Tmem30c |
G |
T |
16: 57,086,843 (GRCm39) |
T320K |
possibly damaging |
Het |
Tnn |
T |
C |
1: 159,972,714 (GRCm39) |
Y296C |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,620,430 (GRCm39) |
A15802T |
probably damaging |
Het |
Usp53 |
T |
C |
3: 122,741,049 (GRCm39) |
M734V |
probably benign |
Het |
Vmn1r24 |
A |
G |
6: 57,933,497 (GRCm39) |
I7T |
probably benign |
Het |
Vmn1r74 |
T |
A |
7: 11,581,504 (GRCm39) |
V268E |
probably damaging |
Het |
Xirp1 |
A |
T |
9: 119,847,841 (GRCm39) |
H347Q |
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 |
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 |
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 |
|