Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930447C04Rik |
A |
T |
12: 72,956,502 (GRCm39) |
Y199* |
probably null |
Het |
Adhfe1 |
A |
T |
1: 9,637,029 (GRCm39) |
I394F |
probably benign |
Het |
Arhgap26 |
G |
T |
18: 39,379,893 (GRCm39) |
R485L |
probably damaging |
Het |
Atat1 |
T |
A |
17: 36,212,467 (GRCm39) |
N231I |
probably damaging |
Het |
B4galnt2 |
T |
C |
11: 95,760,100 (GRCm39) |
N309S |
probably benign |
Het |
Bank1 |
A |
T |
3: 135,772,134 (GRCm39) |
F499I |
probably damaging |
Het |
Bcl9l |
A |
G |
9: 44,416,365 (GRCm39) |
D146G |
possibly damaging |
Het |
Bglap3 |
A |
T |
3: 88,283,671 (GRCm39) |
|
probably benign |
Het |
Bscl2 |
C |
A |
19: 8,825,344 (GRCm39) |
T376K |
probably benign |
Het |
Cercam |
A |
T |
2: 29,761,033 (GRCm39) |
|
probably null |
Het |
Clec4f |
C |
T |
6: 83,633,012 (GRCm39) |
M1I |
probably null |
Het |
Clec4n |
A |
T |
6: 123,209,066 (GRCm39) |
I14F |
probably benign |
Het |
Cmya5 |
T |
C |
13: 93,227,093 (GRCm39) |
E2665G |
probably damaging |
Het |
Cog4 |
T |
A |
8: 111,578,915 (GRCm39) |
|
probably null |
Het |
Cubn |
A |
G |
2: 13,352,856 (GRCm39) |
F1961L |
probably benign |
Het |
Cyp4a29 |
A |
T |
4: 115,104,196 (GRCm39) |
H88L |
probably benign |
Het |
Dhdh |
A |
G |
7: 45,128,530 (GRCm39) |
L216P |
probably damaging |
Het |
Dpp6 |
T |
C |
5: 27,871,509 (GRCm39) |
F544S |
probably damaging |
Het |
Dthd1 |
C |
T |
5: 63,045,549 (GRCm39) |
T771I |
probably benign |
Het |
Emc10 |
A |
G |
7: 44,142,612 (GRCm39) |
|
probably null |
Het |
Fgg |
A |
T |
3: 82,920,072 (GRCm39) |
T284S |
probably benign |
Het |
Gask1a |
C |
T |
9: 121,794,784 (GRCm39) |
R313W |
probably damaging |
Het |
Gm3002 |
T |
A |
14: 3,824,737 (GRCm38) |
N24K |
probably damaging |
Het |
Gm8674 |
G |
A |
13: 50,056,034 (GRCm39) |
|
noncoding transcript |
Het |
Gpr63 |
G |
A |
4: 25,008,368 (GRCm39) |
W364* |
probably null |
Het |
Hcn4 |
C |
G |
9: 58,767,111 (GRCm39) |
P891A |
unknown |
Het |
Hcrtr1 |
A |
T |
4: 130,024,792 (GRCm39) |
F365I |
possibly damaging |
Het |
Hmcn2 |
A |
G |
2: 31,244,176 (GRCm39) |
|
probably null |
Het |
Hoxc5 |
T |
A |
15: 102,923,786 (GRCm39) |
L194H |
probably damaging |
Het |
Ifna11 |
A |
G |
4: 88,738,287 (GRCm39) |
N31S |
probably null |
Het |
Ikbke |
GCC |
G |
1: 131,203,004 (GRCm39) |
|
probably null |
Het |
Iqgap2 |
A |
T |
13: 95,766,514 (GRCm39) |
D1496E |
probably benign |
Het |
Kif28 |
G |
T |
1: 179,536,007 (GRCm39) |
Q556K |
probably damaging |
Het |
Klhl42 |
C |
T |
6: 147,009,502 (GRCm39) |
T447I |
possibly damaging |
Het |
Lrp1b |
A |
C |
2: 41,678,986 (GRCm39) |
D35E |
probably damaging |
Het |
Lsm14b |
A |
G |
2: 179,675,692 (GRCm39) |
|
probably benign |
Het |
Map3k1 |
T |
C |
13: 111,909,272 (GRCm39) |
E226G |
probably damaging |
Het |
Map3k14 |
T |
A |
11: 103,130,357 (GRCm39) |
N187Y |
probably benign |
Het |
Mcm6 |
A |
T |
1: 128,263,586 (GRCm39) |
V645E |
probably damaging |
Het |
Mdh1b |
G |
T |
1: 63,759,022 (GRCm39) |
P190Q |
probably damaging |
Het |
Meiob |
T |
G |
17: 25,037,353 (GRCm39) |
L77R |
probably damaging |
Het |
Mrgpra3 |
A |
T |
7: 47,239,267 (GRCm39) |
F220I |
probably benign |
Het |
Mrtfa |
C |
A |
15: 80,929,476 (GRCm39) |
|
probably benign |
Het |
Mtor |
T |
A |
4: 148,575,817 (GRCm39) |
S1324T |
possibly damaging |
Het |
Myot |
T |
A |
18: 44,487,995 (GRCm39) |
D437E |
possibly damaging |
Het |
Ncoa6 |
G |
T |
2: 155,263,252 (GRCm39) |
T394K |
possibly damaging |
Het |
Nf1 |
T |
A |
11: 79,456,379 (GRCm39) |
|
probably null |
Het |
Nup210 |
T |
A |
6: 91,013,451 (GRCm39) |
T1190S |
possibly damaging |
Het |
Odf1 |
T |
A |
15: 38,226,652 (GRCm39) |
I184N |
probably damaging |
Het |
Or10d1 |
C |
T |
9: 39,484,054 (GRCm39) |
C167Y |
probably damaging |
Het |
Or13d1 |
T |
C |
4: 52,970,960 (GRCm39) |
V113A |
possibly damaging |
Het |
Or1n1b |
A |
G |
2: 36,780,719 (GRCm39) |
I47T |
probably damaging |
Het |
Or5k15 |
G |
T |
16: 58,709,957 (GRCm39) |
Q209K |
possibly damaging |
Het |
Padi1 |
A |
G |
4: 140,572,901 (GRCm39) |
V21A |
probably benign |
Het |
Pdzrn3 |
C |
T |
6: 101,128,551 (GRCm39) |
R705H |
probably damaging |
Het |
Pik3cb |
T |
C |
9: 98,987,685 (GRCm39) |
I18V |
probably benign |
Het |
Pmpca |
T |
C |
2: 26,280,320 (GRCm39) |
S117P |
probably damaging |
Het |
Poteg |
T |
A |
8: 27,985,009 (GRCm39) |
|
probably benign |
Het |
Pramel32 |
T |
C |
4: 88,547,432 (GRCm39) |
T80A |
probably damaging |
Het |
Rab30 |
G |
A |
7: 92,478,771 (GRCm39) |
R72H |
probably damaging |
Het |
Ramp2 |
T |
A |
11: 101,138,383 (GRCm39) |
|
probably null |
Het |
Rbks |
G |
A |
5: 31,781,876 (GRCm39) |
T308I |
probably damaging |
Het |
Rnf112 |
A |
G |
11: 61,343,752 (GRCm39) |
|
probably benign |
Het |
Rnf38 |
G |
A |
4: 44,152,460 (GRCm39) |
P3S |
probably damaging |
Het |
Sec16a |
A |
G |
2: 26,302,883 (GRCm39) |
S2344P |
probably benign |
Het |
Slc16a8 |
C |
T |
15: 79,137,084 (GRCm39) |
V109M |
possibly damaging |
Het |
Slc28a1 |
A |
T |
7: 80,791,757 (GRCm39) |
T308S |
possibly damaging |
Het |
Slc39a3 |
T |
C |
10: 80,867,453 (GRCm39) |
T98A |
possibly damaging |
Het |
Smarcc2 |
T |
C |
10: 128,319,049 (GRCm39) |
F731L |
probably damaging |
Het |
Smc4 |
A |
G |
3: 68,925,572 (GRCm39) |
|
probably benign |
Het |
Sparcl1 |
T |
G |
5: 104,240,776 (GRCm39) |
D216A |
probably damaging |
Het |
Speg |
G |
A |
1: 75,364,513 (GRCm39) |
R192H |
probably damaging |
Het |
Sspo |
T |
C |
6: 48,441,539 (GRCm39) |
L1892P |
probably damaging |
Het |
Styxl2 |
A |
T |
1: 165,954,675 (GRCm39) |
V25E |
probably damaging |
Het |
Tacc2 |
A |
G |
7: 130,225,678 (GRCm39) |
N807D |
probably damaging |
Het |
Teddm1a |
A |
T |
1: 153,767,979 (GRCm39) |
K148* |
probably null |
Het |
Thbs1 |
A |
T |
2: 117,945,259 (GRCm39) |
E277D |
probably benign |
Het |
Ticrr |
G |
A |
7: 79,310,158 (GRCm39) |
R24Q |
probably damaging |
Het |
Tigd4 |
A |
G |
3: 84,502,460 (GRCm39) |
E459G |
probably benign |
Het |
Tln2 |
C |
A |
9: 67,262,407 (GRCm39) |
A615S |
probably damaging |
Het |
Tmprss5 |
T |
C |
9: 49,026,817 (GRCm39) |
V410A |
probably damaging |
Het |
Tnrc6a |
G |
T |
7: 122,789,095 (GRCm39) |
W1638L |
probably damaging |
Het |
Tpr |
A |
G |
1: 150,285,810 (GRCm39) |
D424G |
probably damaging |
Het |
Trim34a |
A |
T |
7: 103,910,271 (GRCm39) |
K358* |
probably null |
Het |
Tssk5 |
T |
A |
15: 76,258,856 (GRCm39) |
D10V |
possibly damaging |
Het |
Usp35 |
A |
C |
7: 96,962,782 (GRCm39) |
L470R |
probably damaging |
Het |
Usp42 |
T |
C |
5: 143,701,119 (GRCm39) |
D968G |
possibly damaging |
Het |
Utrn |
A |
G |
10: 12,331,164 (GRCm39) |
V2924A |
probably damaging |
Het |
Wdtc1 |
C |
A |
4: 133,021,654 (GRCm39) |
A627S |
probably damaging |
Het |
Xrra1 |
A |
G |
7: 99,555,730 (GRCm39) |
T366A |
probably damaging |
Het |
Zfp712 |
T |
A |
13: 67,188,773 (GRCm39) |
K585* |
probably null |
Het |
Zfp97 |
T |
A |
17: 17,365,393 (GRCm39) |
N297K |
probably damaging |
Het |
Zfp97 |
G |
T |
17: 17,364,938 (GRCm39) |
E146* |
probably null |
Het |
|
Other mutations in Tex15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00639:Tex15
|
APN |
8 |
34,065,339 (GRCm39) |
missense |
probably benign |
0.18 |
IGL00705:Tex15
|
APN |
8 |
34,071,620 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00820:Tex15
|
APN |
8 |
34,069,034 (GRCm39) |
splice site |
probably benign |
|
IGL01288:Tex15
|
APN |
8 |
34,061,412 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01328:Tex15
|
APN |
8 |
34,061,424 (GRCm39) |
nonsense |
probably null |
|
IGL01359:Tex15
|
APN |
8 |
34,071,926 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01603:Tex15
|
APN |
8 |
34,063,575 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01861:Tex15
|
APN |
8 |
34,060,717 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02052:Tex15
|
APN |
8 |
34,072,493 (GRCm39) |
missense |
probably benign |
0.28 |
IGL02560:Tex15
|
APN |
8 |
34,071,779 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02677:Tex15
|
APN |
8 |
34,061,108 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02739:Tex15
|
APN |
8 |
34,071,721 (GRCm39) |
missense |
possibly damaging |
0.68 |
Big_gulp
|
UTSW |
8 |
34,071,762 (GRCm39) |
missense |
probably damaging |
1.00 |
P0005:Tex15
|
UTSW |
8 |
34,060,896 (GRCm39) |
missense |
probably benign |
0.00 |
P0037:Tex15
|
UTSW |
8 |
34,071,608 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4377001:Tex15
|
UTSW |
8 |
34,061,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R0056:Tex15
|
UTSW |
8 |
34,072,055 (GRCm39) |
missense |
probably benign |
0.00 |
R0056:Tex15
|
UTSW |
8 |
34,072,055 (GRCm39) |
missense |
probably benign |
0.00 |
R0058:Tex15
|
UTSW |
8 |
34,071,530 (GRCm39) |
splice site |
probably benign |
|
R0058:Tex15
|
UTSW |
8 |
34,071,530 (GRCm39) |
splice site |
probably benign |
|
R0595:Tex15
|
UTSW |
8 |
34,062,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R0646:Tex15
|
UTSW |
8 |
34,072,354 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0688:Tex15
|
UTSW |
8 |
34,063,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R0842:Tex15
|
UTSW |
8 |
34,061,575 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0987:Tex15
|
UTSW |
8 |
34,066,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R1084:Tex15
|
UTSW |
8 |
34,067,032 (GRCm39) |
missense |
probably benign |
0.28 |
R1183:Tex15
|
UTSW |
8 |
34,064,893 (GRCm39) |
missense |
probably benign |
0.35 |
R1186:Tex15
|
UTSW |
8 |
34,061,661 (GRCm39) |
missense |
probably benign |
0.19 |
R1378:Tex15
|
UTSW |
8 |
34,065,244 (GRCm39) |
missense |
probably damaging |
0.99 |
R1500:Tex15
|
UTSW |
8 |
34,065,120 (GRCm39) |
missense |
probably damaging |
0.96 |
R1508:Tex15
|
UTSW |
8 |
34,066,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R1597:Tex15
|
UTSW |
8 |
34,061,511 (GRCm39) |
missense |
probably damaging |
0.96 |
R1636:Tex15
|
UTSW |
8 |
34,066,415 (GRCm39) |
nonsense |
probably null |
|
R1639:Tex15
|
UTSW |
8 |
34,060,845 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1809:Tex15
|
UTSW |
8 |
34,064,262 (GRCm39) |
missense |
probably benign |
|
R1843:Tex15
|
UTSW |
8 |
34,066,682 (GRCm39) |
missense |
probably benign |
0.27 |
R2029:Tex15
|
UTSW |
8 |
34,061,302 (GRCm39) |
missense |
probably damaging |
0.99 |
R2228:Tex15
|
UTSW |
8 |
34,061,265 (GRCm39) |
missense |
probably benign |
0.05 |
R2229:Tex15
|
UTSW |
8 |
34,061,265 (GRCm39) |
missense |
probably benign |
0.05 |
R2245:Tex15
|
UTSW |
8 |
34,061,524 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2246:Tex15
|
UTSW |
8 |
34,072,540 (GRCm39) |
missense |
possibly damaging |
0.49 |
R2880:Tex15
|
UTSW |
8 |
34,064,935 (GRCm39) |
nonsense |
probably null |
|
R2881:Tex15
|
UTSW |
8 |
34,064,935 (GRCm39) |
nonsense |
probably null |
|
R2882:Tex15
|
UTSW |
8 |
34,064,935 (GRCm39) |
nonsense |
probably null |
|
R3001:Tex15
|
UTSW |
8 |
34,064,556 (GRCm39) |
missense |
probably benign |
0.15 |
R3002:Tex15
|
UTSW |
8 |
34,064,556 (GRCm39) |
missense |
probably benign |
0.15 |
R3020:Tex15
|
UTSW |
8 |
34,066,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R3084:Tex15
|
UTSW |
8 |
34,064,913 (GRCm39) |
missense |
probably benign |
0.11 |
R3085:Tex15
|
UTSW |
8 |
34,064,913 (GRCm39) |
missense |
probably benign |
0.11 |
R3701:Tex15
|
UTSW |
8 |
34,064,194 (GRCm39) |
missense |
probably benign |
0.00 |
R3702:Tex15
|
UTSW |
8 |
34,064,194 (GRCm39) |
missense |
probably benign |
0.00 |
R3752:Tex15
|
UTSW |
8 |
34,061,443 (GRCm39) |
missense |
probably benign |
|
R4162:Tex15
|
UTSW |
8 |
34,071,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R4231:Tex15
|
UTSW |
8 |
34,062,165 (GRCm39) |
missense |
probably damaging |
0.99 |
R4589:Tex15
|
UTSW |
8 |
34,047,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R4707:Tex15
|
UTSW |
8 |
34,072,525 (GRCm39) |
missense |
probably benign |
0.00 |
R4773:Tex15
|
UTSW |
8 |
34,072,760 (GRCm39) |
missense |
probably benign |
0.42 |
R5063:Tex15
|
UTSW |
8 |
34,072,638 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5121:Tex15
|
UTSW |
8 |
34,061,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R5147:Tex15
|
UTSW |
8 |
34,062,340 (GRCm39) |
nonsense |
probably null |
|
R5166:Tex15
|
UTSW |
8 |
34,066,420 (GRCm39) |
missense |
probably benign |
0.07 |
R5173:Tex15
|
UTSW |
8 |
34,061,768 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5439:Tex15
|
UTSW |
8 |
34,064,199 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5537:Tex15
|
UTSW |
8 |
34,061,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R5580:Tex15
|
UTSW |
8 |
34,062,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R5588:Tex15
|
UTSW |
8 |
34,067,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R5696:Tex15
|
UTSW |
8 |
34,063,220 (GRCm39) |
missense |
probably benign |
0.01 |
R5734:Tex15
|
UTSW |
8 |
34,036,364 (GRCm39) |
missense |
probably benign |
0.01 |
R5756:Tex15
|
UTSW |
8 |
34,065,861 (GRCm39) |
missense |
probably benign |
0.17 |
R5823:Tex15
|
UTSW |
8 |
34,060,962 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6126:Tex15
|
UTSW |
8 |
34,063,591 (GRCm39) |
missense |
probably benign |
0.19 |
R6129:Tex15
|
UTSW |
8 |
34,064,158 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6276:Tex15
|
UTSW |
8 |
34,067,217 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6374:Tex15
|
UTSW |
8 |
34,065,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R6430:Tex15
|
UTSW |
8 |
34,061,329 (GRCm39) |
missense |
probably benign |
0.01 |
R6452:Tex15
|
UTSW |
8 |
34,062,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R6471:Tex15
|
UTSW |
8 |
34,071,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R6700:Tex15
|
UTSW |
8 |
34,064,917 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6918:Tex15
|
UTSW |
8 |
34,063,212 (GRCm39) |
missense |
probably benign |
0.27 |
R6958:Tex15
|
UTSW |
8 |
34,060,899 (GRCm39) |
missense |
probably benign |
0.01 |
R6970:Tex15
|
UTSW |
8 |
34,047,456 (GRCm39) |
missense |
probably benign |
0.03 |
R7059:Tex15
|
UTSW |
8 |
34,064,758 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7069:Tex15
|
UTSW |
8 |
34,060,748 (GRCm39) |
missense |
probably benign |
|
R7072:Tex15
|
UTSW |
8 |
34,065,459 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7212:Tex15
|
UTSW |
8 |
34,063,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R7212:Tex15
|
UTSW |
8 |
34,060,854 (GRCm39) |
nonsense |
probably null |
|
R7216:Tex15
|
UTSW |
8 |
34,063,014 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7219:Tex15
|
UTSW |
8 |
34,036,268 (GRCm39) |
missense |
probably benign |
0.40 |
R7313:Tex15
|
UTSW |
8 |
34,064,845 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7315:Tex15
|
UTSW |
8 |
34,071,544 (GRCm39) |
missense |
probably benign |
0.01 |
R7444:Tex15
|
UTSW |
8 |
34,066,590 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7455:Tex15
|
UTSW |
8 |
34,067,025 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7643:Tex15
|
UTSW |
8 |
34,065,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R7644:Tex15
|
UTSW |
8 |
34,064,445 (GRCm39) |
missense |
probably benign |
0.01 |
R7724:Tex15
|
UTSW |
8 |
34,036,291 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7779:Tex15
|
UTSW |
8 |
34,065,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R7798:Tex15
|
UTSW |
8 |
34,071,875 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7816:Tex15
|
UTSW |
8 |
34,071,683 (GRCm39) |
missense |
probably benign |
0.14 |
R7820:Tex15
|
UTSW |
8 |
34,065,090 (GRCm39) |
missense |
probably damaging |
0.98 |
R8041:Tex15
|
UTSW |
8 |
34,065,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R8150:Tex15
|
UTSW |
8 |
34,063,534 (GRCm39) |
missense |
probably benign |
0.06 |
R8152:Tex15
|
UTSW |
8 |
34,062,921 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8237:Tex15
|
UTSW |
8 |
34,067,427 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8250:Tex15
|
UTSW |
8 |
34,055,233 (GRCm39) |
missense |
probably null |
0.27 |
R8264:Tex15
|
UTSW |
8 |
34,072,390 (GRCm39) |
missense |
probably benign |
0.18 |
R8279:Tex15
|
UTSW |
8 |
34,061,765 (GRCm39) |
missense |
probably damaging |
0.96 |
R8353:Tex15
|
UTSW |
8 |
34,066,899 (GRCm39) |
nonsense |
probably null |
|
R8388:Tex15
|
UTSW |
8 |
34,065,237 (GRCm39) |
missense |
probably benign |
0.00 |
R8432:Tex15
|
UTSW |
8 |
34,066,572 (GRCm39) |
missense |
probably damaging |
0.99 |
R8453:Tex15
|
UTSW |
8 |
34,066,899 (GRCm39) |
nonsense |
probably null |
|
R8489:Tex15
|
UTSW |
8 |
34,067,574 (GRCm39) |
missense |
probably benign |
0.02 |
R8670:Tex15
|
UTSW |
8 |
34,064,746 (GRCm39) |
missense |
probably benign |
0.19 |
R8703:Tex15
|
UTSW |
8 |
34,062,724 (GRCm39) |
missense |
probably benign |
0.00 |
R8871:Tex15
|
UTSW |
8 |
34,066,992 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8945:Tex15
|
UTSW |
8 |
34,064,724 (GRCm39) |
missense |
probably benign |
0.00 |
R9104:Tex15
|
UTSW |
8 |
34,060,950 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9132:Tex15
|
UTSW |
8 |
34,067,554 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9207:Tex15
|
UTSW |
8 |
34,065,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R9210:Tex15
|
UTSW |
8 |
34,064,319 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9330:Tex15
|
UTSW |
8 |
34,065,143 (GRCm39) |
missense |
probably benign |
0.01 |
R9354:Tex15
|
UTSW |
8 |
34,063,344 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9365:Tex15
|
UTSW |
8 |
34,064,564 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9440:Tex15
|
UTSW |
8 |
34,072,273 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9534:Tex15
|
UTSW |
8 |
34,060,999 (GRCm39) |
missense |
probably benign |
0.45 |
R9570:Tex15
|
UTSW |
8 |
34,067,309 (GRCm39) |
missense |
probably damaging |
0.96 |
R9574:Tex15
|
UTSW |
8 |
34,064,509 (GRCm39) |
missense |
probably benign |
0.09 |
R9618:Tex15
|
UTSW |
8 |
34,062,397 (GRCm39) |
missense |
probably benign |
0.35 |
R9655:Tex15
|
UTSW |
8 |
34,066,784 (GRCm39) |
nonsense |
probably null |
|
R9786:Tex15
|
UTSW |
8 |
34,062,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R9798:Tex15
|
UTSW |
8 |
34,062,721 (GRCm39) |
missense |
probably damaging |
0.98 |
RF005:Tex15
|
UTSW |
8 |
34,066,705 (GRCm39) |
missense |
probably benign |
0.05 |
X0020:Tex15
|
UTSW |
8 |
34,066,607 (GRCm39) |
missense |
probably benign |
0.03 |
X0065:Tex15
|
UTSW |
8 |
34,065,545 (GRCm39) |
nonsense |
probably null |
|
Z1088:Tex15
|
UTSW |
8 |
34,061,343 (GRCm39) |
missense |
possibly damaging |
0.89 |
Z1088:Tex15
|
UTSW |
8 |
34,064,898 (GRCm39) |
missense |
probably benign |
|
Z1088:Tex15
|
UTSW |
8 |
34,061,838 (GRCm39) |
missense |
possibly damaging |
0.68 |
Z1176:Tex15
|
UTSW |
8 |
34,064,754 (GRCm39) |
missense |
possibly damaging |
0.84 |
|