Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010I14Rik |
C |
T |
17: 9,211,324 (GRCm39) |
H158Y |
probably damaging |
Het |
1810009J06Rik |
T |
A |
6: 40,945,141 (GRCm39) |
C207S |
probably damaging |
Het |
Aadac |
T |
A |
3: 59,944,759 (GRCm39) |
|
probably null |
Het |
Abca6 |
T |
A |
11: 110,075,502 (GRCm39) |
I1330F |
probably damaging |
Het |
Adar |
A |
T |
3: 89,653,202 (GRCm39) |
S263C |
probably benign |
Het |
Adra2b |
T |
C |
2: 127,205,734 (GRCm39) |
Y84H |
probably damaging |
Het |
Arnt2 |
A |
T |
7: 83,992,997 (GRCm39) |
V181E |
possibly damaging |
Het |
Atg7 |
T |
C |
6: 114,683,191 (GRCm39) |
L418P |
probably damaging |
Het |
Atp2c1 |
A |
G |
9: 105,323,322 (GRCm39) |
L181P |
probably damaging |
Het |
Awat2 |
G |
A |
X: 99,448,165 (GRCm39) |
P148S |
probably damaging |
Het |
Birc6 |
A |
G |
17: 74,941,880 (GRCm39) |
M2737V |
possibly damaging |
Het |
Ccdc81 |
A |
G |
7: 89,535,361 (GRCm39) |
C292R |
probably benign |
Het |
Cd14 |
T |
A |
18: 36,859,392 (GRCm39) |
E21V |
probably damaging |
Het |
Cdc14b |
A |
C |
13: 64,363,351 (GRCm39) |
C303W |
probably damaging |
Het |
Cdh23 |
T |
C |
10: 60,221,001 (GRCm39) |
I1248V |
probably benign |
Het |
Ceacam1 |
T |
C |
7: 25,174,133 (GRCm39) |
D174G |
probably benign |
Het |
Cgas |
T |
G |
9: 78,344,737 (GRCm39) |
Y228S |
probably damaging |
Het |
Chd7 |
A |
G |
4: 8,865,978 (GRCm39) |
M717V |
probably damaging |
Het |
Cib1 |
T |
C |
7: 79,882,120 (GRCm39) |
T20A |
possibly damaging |
Het |
Clec4d |
A |
G |
6: 123,239,319 (GRCm39) |
K9R |
probably benign |
Het |
Cntnap1 |
C |
A |
11: 101,068,850 (GRCm39) |
S131* |
probably null |
Het |
Crybg1 |
T |
C |
10: 43,834,326 (GRCm39) |
K1581R |
probably damaging |
Het |
Csf2 |
T |
G |
11: 54,139,284 (GRCm39) |
T100P |
probably benign |
Het |
Csrp2 |
T |
A |
10: 110,767,894 (GRCm39) |
D26E |
probably benign |
Het |
Cul1 |
T |
C |
6: 47,479,505 (GRCm39) |
V257A |
probably damaging |
Het |
Cul4a |
G |
A |
8: 13,186,406 (GRCm39) |
M505I |
possibly damaging |
Het |
Cul4a |
T |
C |
8: 13,186,854 (GRCm39) |
M530T |
probably benign |
Het |
Dcp2 |
T |
C |
18: 44,529,038 (GRCm39) |
M51T |
possibly damaging |
Het |
Ddx60 |
T |
A |
8: 62,401,903 (GRCm39) |
C260S |
probably benign |
Het |
Dennd2c |
G |
A |
3: 103,073,807 (GRCm39) |
R851H |
probably damaging |
Het |
Dnah11 |
T |
C |
12: 118,106,027 (GRCm39) |
E625G |
possibly damaging |
Het |
Edem1 |
T |
C |
6: 108,821,908 (GRCm39) |
W322R |
probably benign |
Het |
Egflam |
T |
C |
15: 7,276,586 (GRCm39) |
T527A |
probably damaging |
Het |
Ephb1 |
T |
A |
9: 101,848,322 (GRCm39) |
M659L |
possibly damaging |
Het |
Fbxl2 |
A |
G |
9: 113,818,237 (GRCm39) |
I203T |
probably benign |
Het |
Gabbr1 |
G |
A |
17: 37,359,351 (GRCm39) |
G109R |
probably damaging |
Het |
Gabra2 |
T |
C |
5: 71,171,793 (GRCm39) |
I148V |
possibly damaging |
Het |
Golga1 |
A |
G |
2: 38,937,099 (GRCm39) |
V161A |
probably benign |
Het |
Gps2 |
T |
G |
11: 69,807,246 (GRCm39) |
S301A |
probably benign |
Het |
H2-D1 |
T |
C |
17: 35,482,595 (GRCm39) |
L105P |
probably benign |
Het |
Igdcc4 |
T |
C |
9: 65,030,051 (GRCm39) |
V367A |
probably benign |
Het |
Igkv4-69 |
T |
G |
6: 69,260,782 (GRCm39) |
Y115S |
probably benign |
Het |
Itga5 |
A |
G |
15: 103,262,741 (GRCm39) |
L309P |
probably damaging |
Het |
Itih1 |
A |
G |
14: 30,651,580 (GRCm39) |
Y871H |
probably damaging |
Het |
Itpr2 |
T |
A |
6: 146,013,191 (GRCm39) |
N2662I |
probably damaging |
Het |
Kctd19 |
T |
A |
8: 106,115,102 (GRCm39) |
E486D |
probably damaging |
Het |
Kif5b |
C |
T |
18: 6,209,059 (GRCm39) |
R901Q |
possibly damaging |
Het |
Kmt2a |
G |
A |
9: 44,731,941 (GRCm39) |
S2792F |
probably benign |
Het |
Magi3 |
A |
G |
3: 103,927,718 (GRCm39) |
V1023A |
probably damaging |
Het |
Mapk9 |
C |
A |
11: 49,745,160 (GRCm39) |
R25S |
probably null |
Het |
Memo1 |
T |
C |
17: 74,552,003 (GRCm39) |
T98A |
possibly damaging |
Het |
Mill2 |
A |
G |
7: 18,590,529 (GRCm39) |
K203R |
probably damaging |
Het |
Mios |
T |
A |
6: 8,215,798 (GRCm39) |
H331Q |
probably damaging |
Het |
Muc6 |
G |
T |
7: 141,226,329 (GRCm39) |
S1566* |
probably null |
Het |
Muc6 |
A |
G |
7: 141,226,330 (GRCm39) |
|
probably benign |
Het |
Napsa |
T |
C |
7: 44,231,109 (GRCm39) |
F113L |
probably benign |
Het |
Or5ac16 |
T |
A |
16: 59,022,271 (GRCm39) |
I173F |
possibly damaging |
Het |
Or9m1 |
A |
G |
2: 87,734,011 (GRCm39) |
V3A |
probably benign |
Het |
Oscp1 |
T |
G |
4: 125,977,415 (GRCm39) |
V226G |
possibly damaging |
Het |
Osgin2 |
G |
T |
4: 15,998,358 (GRCm39) |
S421R |
probably damaging |
Het |
Pclaf |
A |
G |
9: 65,800,677 (GRCm39) |
N50D |
probably damaging |
Het |
Pdgfc |
A |
T |
3: 81,082,292 (GRCm39) |
I162F |
probably benign |
Het |
Plag1 |
T |
C |
4: 3,903,956 (GRCm39) |
T412A |
probably benign |
Het |
Pogz |
A |
T |
3: 94,785,504 (GRCm39) |
T820S |
probably benign |
Het |
Ptpn9 |
T |
A |
9: 56,967,196 (GRCm39) |
V473D |
probably damaging |
Het |
Qdpr |
A |
T |
5: 45,596,660 (GRCm39) |
M66K |
possibly damaging |
Het |
Qrich1 |
A |
G |
9: 108,411,621 (GRCm39) |
N382S |
possibly damaging |
Het |
Rbbp8 |
T |
C |
18: 11,875,736 (GRCm39) |
V883A |
possibly damaging |
Het |
Rgl1 |
T |
A |
1: 152,424,855 (GRCm39) |
I375F |
probably damaging |
Het |
Rif1 |
C |
T |
2: 51,988,421 (GRCm39) |
T720I |
probably benign |
Het |
Rilp |
A |
T |
11: 75,401,328 (GRCm39) |
Q95L |
probably benign |
Het |
Rnf169 |
T |
A |
7: 99,574,732 (GRCm39) |
N621I |
probably damaging |
Het |
Rps27a |
T |
C |
11: 29,497,229 (GRCm39) |
K27R |
probably null |
Het |
Sar1a |
T |
C |
10: 61,520,947 (GRCm39) |
V54A |
probably benign |
Het |
Sash1 |
T |
A |
10: 8,605,477 (GRCm39) |
H971L |
probably benign |
Het |
Sdk2 |
G |
A |
11: 113,671,843 (GRCm39) |
Q2102* |
probably null |
Het |
Serpina1e |
T |
A |
12: 103,917,466 (GRCm39) |
I68F |
probably damaging |
Het |
Serpinb9e |
A |
C |
13: 33,437,474 (GRCm39) |
Q119P |
probably benign |
Het |
Sh3tc2 |
A |
T |
18: 62,124,226 (GRCm39) |
K965* |
probably null |
Het |
Slc16a1 |
A |
T |
3: 104,556,782 (GRCm39) |
S56C |
probably damaging |
Het |
Slc26a11 |
T |
A |
11: 119,271,020 (GRCm39) |
L563Q |
possibly damaging |
Het |
Smarca2 |
G |
T |
19: 26,650,124 (GRCm39) |
E24* |
probably null |
Het |
Smgc |
G |
A |
15: 91,744,468 (GRCm39) |
G239D |
probably damaging |
Het |
Sos2 |
A |
T |
12: 69,663,636 (GRCm39) |
M616K |
possibly damaging |
Het |
Tet1 |
T |
A |
10: 62,648,726 (GRCm39) |
D1902V |
possibly damaging |
Het |
Thap2 |
C |
T |
10: 115,220,152 (GRCm39) |
C10Y |
probably damaging |
Het |
Tor2a |
G |
A |
2: 32,648,716 (GRCm39) |
G62D |
probably damaging |
Het |
Ubqln5 |
A |
T |
7: 103,778,095 (GRCm39) |
V243E |
possibly damaging |
Het |
Utrn |
A |
T |
10: 12,560,181 (GRCm39) |
D1369E |
probably damaging |
Het |
Vcan |
A |
G |
13: 89,840,861 (GRCm39) |
V1561A |
probably benign |
Het |
Vmn1r70 |
T |
C |
7: 10,367,737 (GRCm39) |
F56S |
possibly damaging |
Het |
Vmn2r25 |
A |
G |
6: 123,800,254 (GRCm39) |
L696S |
possibly damaging |
Het |
Washc2 |
A |
G |
6: 116,185,948 (GRCm39) |
T53A |
probably damaging |
Het |
Wnk1 |
T |
A |
6: 119,911,343 (GRCm39) |
T2417S |
possibly damaging |
Het |
Zbtb49 |
A |
T |
5: 38,361,105 (GRCm39) |
C12* |
probably null |
Het |
Zfp472 |
C |
A |
17: 33,196,848 (GRCm39) |
P308T |
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 |
|
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 |
|