Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310003L06Rik |
T |
A |
5: 88,119,504 (GRCm39) |
M87K |
possibly damaging |
Het |
Angel1 |
T |
C |
12: 86,770,153 (GRCm39) |
S36G |
possibly damaging |
Het |
Apol6 |
A |
G |
15: 76,935,697 (GRCm39) |
H322R |
unknown |
Het |
Arfgef2 |
G |
A |
2: 166,701,284 (GRCm39) |
R694Q |
probably damaging |
Het |
Bank1 |
A |
T |
3: 135,761,559 (GRCm39) |
N748K |
probably benign |
Het |
Bst1 |
T |
C |
5: 43,982,695 (GRCm39) |
I180T |
possibly damaging |
Het |
Cabin1 |
C |
A |
10: 75,570,892 (GRCm39) |
E795* |
probably null |
Het |
Ccdc168 |
A |
G |
1: 44,100,633 (GRCm39) |
V155A |
possibly damaging |
Het |
Cckar |
T |
A |
5: 53,857,163 (GRCm39) |
T416S |
probably damaging |
Het |
Ccng2 |
G |
T |
5: 93,416,616 (GRCm39) |
E46* |
probably null |
Het |
Ceacam9 |
T |
C |
7: 16,455,916 (GRCm39) |
S8P |
probably benign |
Het |
Cercam |
G |
A |
2: 29,766,071 (GRCm39) |
D317N |
possibly damaging |
Het |
Cfap54 |
T |
A |
10: 92,734,921 (GRCm39) |
M2377L |
unknown |
Het |
Cgnl1 |
A |
T |
9: 71,558,631 (GRCm39) |
L914H |
probably damaging |
Het |
Chst13 |
G |
A |
6: 90,286,506 (GRCm39) |
P152L |
probably damaging |
Het |
Clec2g |
T |
A |
6: 128,925,688 (GRCm39) |
F32L |
unknown |
Het |
Cntnap5c |
A |
T |
17: 58,671,159 (GRCm39) |
M1116L |
probably benign |
Het |
Col11a2 |
C |
A |
17: 34,283,760 (GRCm39) |
F1516L |
unknown |
Het |
Crb2 |
A |
G |
2: 37,680,698 (GRCm39) |
E542G |
probably benign |
Het |
Crisp1 |
A |
T |
17: 40,616,101 (GRCm39) |
|
probably benign |
Het |
Crybg3 |
G |
A |
16: 59,374,702 (GRCm39) |
T470M |
probably damaging |
Het |
Dusp9 |
TAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAG |
TAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAG |
X: 72,684,217 (GRCm39) |
|
probably benign |
Het |
Eif1ad |
T |
A |
19: 5,418,726 (GRCm39) |
V93D |
possibly damaging |
Het |
Entpd3 |
T |
C |
9: 120,384,825 (GRCm39) |
I134T |
probably benign |
Het |
Garre1 |
A |
T |
7: 33,938,491 (GRCm39) |
C1015S |
probably benign |
Het |
Gm19410 |
A |
G |
8: 36,282,011 (GRCm39) |
M1865V |
probably benign |
Het |
Gpat2 |
A |
G |
2: 127,277,146 (GRCm39) |
E728G |
probably benign |
Het |
Heatr5b |
C |
A |
17: 79,081,139 (GRCm39) |
S1371I |
probably damaging |
Het |
Ighv1-4 |
A |
T |
12: 114,450,949 (GRCm39) |
M53K |
possibly damaging |
Het |
Itch |
A |
T |
2: 155,020,991 (GRCm39) |
T169S |
probably benign |
Het |
Kifc2 |
A |
G |
15: 76,550,885 (GRCm39) |
N587S |
possibly damaging |
Het |
Klk1b16 |
A |
T |
7: 43,790,177 (GRCm39) |
D149V |
probably benign |
Het |
Kndc1 |
C |
T |
7: 139,507,708 (GRCm39) |
S1222F |
possibly damaging |
Het |
Lefty2 |
T |
A |
1: 180,722,172 (GRCm39) |
I170N |
probably damaging |
Het |
Lrrc14b |
A |
G |
13: 74,509,151 (GRCm39) |
F419L |
possibly damaging |
Het |
Mkrn2 |
T |
A |
6: 115,591,583 (GRCm39) |
V302E |
possibly damaging |
Het |
Msh4 |
T |
C |
3: 153,595,819 (GRCm39) |
K271R |
probably benign |
Het |
Muc6 |
T |
C |
7: 141,226,351 (GRCm39) |
T1559A |
unknown |
Het |
Naa16 |
T |
G |
14: 79,607,482 (GRCm39) |
R289S |
probably benign |
Het |
Nab1 |
T |
A |
1: 52,529,610 (GRCm39) |
I96F |
possibly damaging |
Het |
Ntn4 |
T |
C |
10: 93,480,506 (GRCm39) |
C77R |
|
Het |
Nusap1 |
A |
G |
2: 119,479,456 (GRCm39) |
T424A |
possibly damaging |
Het |
Or1p1 |
G |
T |
11: 74,180,305 (GRCm39) |
V278F |
probably damaging |
Het |
Or2w6 |
A |
G |
13: 21,842,681 (GRCm39) |
Y271H |
probably damaging |
Het |
Or4e2 |
T |
A |
14: 52,688,556 (GRCm39) |
S229T |
possibly damaging |
Het |
Otog |
A |
G |
7: 45,949,894 (GRCm39) |
D267G |
probably benign |
Het |
P2ry2 |
A |
C |
7: 100,647,358 (GRCm39) |
F316V |
probably benign |
Het |
Padi2 |
A |
G |
4: 140,663,924 (GRCm39) |
T426A |
probably damaging |
Het |
Pakap |
A |
T |
4: 57,883,192 (GRCm39) |
D845V |
probably damaging |
Het |
Plxna2 |
T |
C |
1: 194,471,217 (GRCm39) |
F996S |
possibly damaging |
Het |
Ppp4r3a |
T |
C |
12: 101,024,591 (GRCm39) |
M303V |
possibly damaging |
Het |
Prelid2 |
A |
T |
18: 42,065,781 (GRCm39) |
W85R |
probably damaging |
Het |
Rabep1 |
G |
A |
11: 70,810,034 (GRCm39) |
R532H |
probably damaging |
Het |
Rabgap1l |
G |
A |
1: 160,528,443 (GRCm39) |
R388W |
possibly damaging |
Het |
Rad51ap2 |
G |
T |
12: 11,508,675 (GRCm39) |
V866L |
probably benign |
Het |
Rassf3 |
C |
A |
10: 121,311,991 (GRCm39) |
E9* |
probably null |
Het |
Rbbp4 |
A |
C |
4: 129,216,180 (GRCm39) |
L189R |
probably benign |
Het |
Rims2 |
T |
A |
15: 39,315,786 (GRCm39) |
C597* |
probably null |
Het |
Rrp12 |
T |
A |
19: 41,871,929 (GRCm39) |
I452F |
probably benign |
Het |
Snx29 |
G |
A |
16: 11,449,391 (GRCm39) |
A279T |
probably benign |
Het |
Tdh |
C |
T |
14: 63,737,704 (GRCm39) |
S17N |
probably benign |
Het |
Tgm5 |
T |
C |
2: 120,879,371 (GRCm39) |
D555G |
possibly damaging |
Het |
Thbs1 |
A |
C |
2: 117,953,045 (GRCm39) |
D885A |
probably damaging |
Het |
Tmprss9 |
C |
A |
10: 80,733,701 (GRCm39) |
A921E |
unknown |
Het |
Trrap |
T |
A |
5: 144,783,226 (GRCm39) |
F3340I |
probably damaging |
Het |
Vmn1r72 |
A |
T |
7: 11,404,145 (GRCm39) |
M101K |
possibly damaging |
Het |
Vmn2r117 |
A |
G |
17: 23,679,445 (GRCm39) |
L593P |
probably benign |
Het |
Washc2 |
G |
A |
6: 116,198,823 (GRCm39) |
G295E |
probably damaging |
Het |
Zfp273 |
A |
T |
13: 67,974,177 (GRCm39) |
H435L |
probably damaging |
Het |
Zfp395 |
A |
G |
14: 65,623,948 (GRCm39) |
E139G |
possibly damaging |
Het |
Zfp512b |
G |
A |
2: 181,230,011 (GRCm39) |
A552V |
possibly damaging |
Het |
|
Other mutations in Bptf |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00553:Bptf
|
APN |
11 |
106,946,105 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00664:Bptf
|
APN |
11 |
106,968,491 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL00705:Bptf
|
APN |
11 |
106,986,534 (GRCm39) |
splice site |
probably benign |
|
IGL00796:Bptf
|
APN |
11 |
106,945,376 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00834:Bptf
|
APN |
11 |
106,964,754 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL01155:Bptf
|
APN |
11 |
106,971,553 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01314:Bptf
|
APN |
11 |
106,945,679 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01371:Bptf
|
APN |
11 |
106,946,733 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01567:Bptf
|
APN |
11 |
106,949,600 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01794:Bptf
|
APN |
11 |
106,944,047 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02108:Bptf
|
APN |
11 |
106,965,814 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02367:Bptf
|
APN |
11 |
106,964,178 (GRCm39) |
missense |
probably benign |
|
IGL02437:Bptf
|
APN |
11 |
106,965,521 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02589:Bptf
|
APN |
11 |
107,002,357 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02897:Bptf
|
APN |
11 |
106,937,947 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02935:Bptf
|
APN |
11 |
106,971,625 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02954:Bptf
|
APN |
11 |
106,945,575 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02982:Bptf
|
APN |
11 |
106,967,500 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03109:Bptf
|
APN |
11 |
106,952,527 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL03265:Bptf
|
APN |
11 |
106,945,454 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03403:Bptf
|
APN |
11 |
106,990,559 (GRCm39) |
missense |
possibly damaging |
0.51 |
Anodyne
|
UTSW |
11 |
106,934,457 (GRCm39) |
critical splice donor site |
probably null |
|
Arroyo
|
UTSW |
11 |
106,933,516 (GRCm39) |
missense |
probably benign |
0.32 |
mojado
|
UTSW |
11 |
106,935,466 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03097:Bptf
|
UTSW |
11 |
106,968,506 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4486001:Bptf
|
UTSW |
11 |
106,945,614 (GRCm39) |
missense |
probably damaging |
0.98 |
R0066:Bptf
|
UTSW |
11 |
106,952,962 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0157:Bptf
|
UTSW |
11 |
106,965,484 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0320:Bptf
|
UTSW |
11 |
106,963,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R0328:Bptf
|
UTSW |
11 |
106,937,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R0402:Bptf
|
UTSW |
11 |
106,964,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R0482:Bptf
|
UTSW |
11 |
106,972,088 (GRCm39) |
missense |
probably benign |
0.13 |
R0574:Bptf
|
UTSW |
11 |
106,967,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R0598:Bptf
|
UTSW |
11 |
106,963,791 (GRCm39) |
missense |
probably damaging |
0.99 |
R0599:Bptf
|
UTSW |
11 |
106,959,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R0601:Bptf
|
UTSW |
11 |
106,952,518 (GRCm39) |
missense |
probably benign |
0.04 |
R0744:Bptf
|
UTSW |
11 |
107,001,638 (GRCm39) |
critical splice donor site |
probably null |
|
R0836:Bptf
|
UTSW |
11 |
107,001,638 (GRCm39) |
critical splice donor site |
probably null |
|
R0885:Bptf
|
UTSW |
11 |
106,934,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R1070:Bptf
|
UTSW |
11 |
106,945,881 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1252:Bptf
|
UTSW |
11 |
106,964,077 (GRCm39) |
missense |
probably benign |
0.00 |
R1370:Bptf
|
UTSW |
11 |
106,937,920 (GRCm39) |
missense |
probably damaging |
0.99 |
R1428:Bptf
|
UTSW |
11 |
106,963,873 (GRCm39) |
missense |
probably damaging |
0.99 |
R1467:Bptf
|
UTSW |
11 |
106,945,881 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1467:Bptf
|
UTSW |
11 |
106,945,881 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1742:Bptf
|
UTSW |
11 |
107,001,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R1816:Bptf
|
UTSW |
11 |
106,951,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R1858:Bptf
|
UTSW |
11 |
106,964,127 (GRCm39) |
missense |
probably benign |
0.00 |
R1989:Bptf
|
UTSW |
11 |
106,965,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R2253:Bptf
|
UTSW |
11 |
107,002,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R2392:Bptf
|
UTSW |
11 |
106,963,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R2431:Bptf
|
UTSW |
11 |
106,938,066 (GRCm39) |
missense |
possibly damaging |
0.48 |
R3022:Bptf
|
UTSW |
11 |
107,002,463 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3161:Bptf
|
UTSW |
11 |
106,965,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R3686:Bptf
|
UTSW |
11 |
106,965,024 (GRCm39) |
missense |
probably benign |
0.25 |
R3687:Bptf
|
UTSW |
11 |
106,965,024 (GRCm39) |
missense |
probably benign |
0.25 |
R3688:Bptf
|
UTSW |
11 |
106,965,024 (GRCm39) |
missense |
probably benign |
0.25 |
R3787:Bptf
|
UTSW |
11 |
106,964,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R3834:Bptf
|
UTSW |
11 |
106,964,683 (GRCm39) |
missense |
probably benign |
0.05 |
R3885:Bptf
|
UTSW |
11 |
106,965,339 (GRCm39) |
missense |
probably damaging |
0.97 |
R4090:Bptf
|
UTSW |
11 |
106,972,349 (GRCm39) |
missense |
probably damaging |
0.99 |
R4398:Bptf
|
UTSW |
11 |
107,001,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R4437:Bptf
|
UTSW |
11 |
106,965,300 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4514:Bptf
|
UTSW |
11 |
106,968,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R4565:Bptf
|
UTSW |
11 |
106,963,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R4715:Bptf
|
UTSW |
11 |
106,938,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R4748:Bptf
|
UTSW |
11 |
106,986,706 (GRCm39) |
missense |
probably damaging |
0.96 |
R4764:Bptf
|
UTSW |
11 |
106,934,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R4885:Bptf
|
UTSW |
11 |
106,965,474 (GRCm39) |
missense |
probably benign |
0.39 |
R4901:Bptf
|
UTSW |
11 |
107,001,686 (GRCm39) |
nonsense |
probably null |
|
R4995:Bptf
|
UTSW |
11 |
106,945,391 (GRCm39) |
missense |
probably damaging |
0.98 |
R5057:Bptf
|
UTSW |
11 |
106,973,354 (GRCm39) |
missense |
probably damaging |
0.98 |
R5120:Bptf
|
UTSW |
11 |
106,964,211 (GRCm39) |
missense |
probably damaging |
0.99 |
R5320:Bptf
|
UTSW |
11 |
106,972,193 (GRCm39) |
nonsense |
probably null |
|
R5329:Bptf
|
UTSW |
11 |
106,964,121 (GRCm39) |
missense |
probably benign |
0.06 |
R5418:Bptf
|
UTSW |
11 |
107,002,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R5461:Bptf
|
UTSW |
11 |
106,952,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R5664:Bptf
|
UTSW |
11 |
106,964,525 (GRCm39) |
missense |
probably benign |
0.01 |
R5718:Bptf
|
UTSW |
11 |
107,002,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R5774:Bptf
|
UTSW |
11 |
107,001,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R5851:Bptf
|
UTSW |
11 |
107,001,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R5930:Bptf
|
UTSW |
11 |
106,964,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R5949:Bptf
|
UTSW |
11 |
107,001,915 (GRCm39) |
missense |
probably damaging |
0.99 |
R5975:Bptf
|
UTSW |
11 |
106,926,690 (GRCm39) |
utr 3 prime |
probably benign |
|
R6027:Bptf
|
UTSW |
11 |
106,965,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R6128:Bptf
|
UTSW |
11 |
106,965,516 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6337:Bptf
|
UTSW |
11 |
106,949,605 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6407:Bptf
|
UTSW |
11 |
107,001,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R6470:Bptf
|
UTSW |
11 |
106,963,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R6487:Bptf
|
UTSW |
11 |
106,968,552 (GRCm39) |
missense |
probably damaging |
0.99 |
R6501:Bptf
|
UTSW |
11 |
106,968,509 (GRCm39) |
missense |
probably null |
1.00 |
R6755:Bptf
|
UTSW |
11 |
106,938,082 (GRCm39) |
missense |
probably benign |
0.27 |
R6861:Bptf
|
UTSW |
11 |
106,953,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R6866:Bptf
|
UTSW |
11 |
106,964,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R6879:Bptf
|
UTSW |
11 |
106,933,516 (GRCm39) |
missense |
probably benign |
0.32 |
R6927:Bptf
|
UTSW |
11 |
106,945,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R6944:Bptf
|
UTSW |
11 |
106,971,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R7082:Bptf
|
UTSW |
11 |
106,977,573 (GRCm39) |
missense |
probably benign |
0.00 |
R7136:Bptf
|
UTSW |
11 |
106,990,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R7162:Bptf
|
UTSW |
11 |
106,934,457 (GRCm39) |
critical splice donor site |
probably null |
|
R7171:Bptf
|
UTSW |
11 |
107,022,233 (GRCm39) |
missense |
unknown |
|
R7193:Bptf
|
UTSW |
11 |
106,945,635 (GRCm39) |
nonsense |
probably null |
|
R7210:Bptf
|
UTSW |
11 |
106,945,290 (GRCm39) |
nonsense |
probably null |
|
R7221:Bptf
|
UTSW |
11 |
106,945,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R7316:Bptf
|
UTSW |
11 |
107,001,740 (GRCm39) |
nonsense |
probably null |
|
R7316:Bptf
|
UTSW |
11 |
106,963,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R7422:Bptf
|
UTSW |
11 |
106,951,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R7454:Bptf
|
UTSW |
11 |
106,935,466 (GRCm39) |
missense |
probably benign |
0.03 |
R7657:Bptf
|
UTSW |
11 |
106,965,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R7718:Bptf
|
UTSW |
11 |
106,972,282 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7827:Bptf
|
UTSW |
11 |
106,938,013 (GRCm39) |
missense |
probably benign |
0.01 |
R7844:Bptf
|
UTSW |
11 |
106,964,887 (GRCm39) |
missense |
probably damaging |
0.97 |
R7992:Bptf
|
UTSW |
11 |
107,001,709 (GRCm39) |
missense |
probably benign |
0.00 |
R8001:Bptf
|
UTSW |
11 |
106,938,166 (GRCm39) |
nonsense |
probably null |
|
R8037:Bptf
|
UTSW |
11 |
106,946,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R8122:Bptf
|
UTSW |
11 |
106,927,417 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8235:Bptf
|
UTSW |
11 |
106,967,458 (GRCm39) |
missense |
probably benign |
0.04 |
R8308:Bptf
|
UTSW |
11 |
106,943,815 (GRCm39) |
missense |
probably damaging |
0.99 |
R8409:Bptf
|
UTSW |
11 |
106,953,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R8464:Bptf
|
UTSW |
11 |
107,022,168 (GRCm39) |
missense |
probably benign |
0.01 |
R8477:Bptf
|
UTSW |
11 |
106,943,679 (GRCm39) |
missense |
probably damaging |
0.98 |
R8482:Bptf
|
UTSW |
11 |
106,934,524 (GRCm39) |
missense |
probably benign |
0.19 |
R8515:Bptf
|
UTSW |
11 |
106,946,064 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8519:Bptf
|
UTSW |
11 |
106,952,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R8708:Bptf
|
UTSW |
11 |
106,964,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R8708:Bptf
|
UTSW |
11 |
106,964,139 (GRCm39) |
missense |
probably damaging |
0.99 |
R8722:Bptf
|
UTSW |
11 |
107,022,295 (GRCm39) |
missense |
unknown |
|
R8732:Bptf
|
UTSW |
11 |
106,931,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R8783:Bptf
|
UTSW |
11 |
107,022,357 (GRCm39) |
missense |
unknown |
|
R8828:Bptf
|
UTSW |
11 |
106,945,836 (GRCm39) |
missense |
probably damaging |
0.98 |
R9004:Bptf
|
UTSW |
11 |
106,945,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R9035:Bptf
|
UTSW |
11 |
106,963,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R9083:Bptf
|
UTSW |
11 |
106,959,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R9211:Bptf
|
UTSW |
11 |
106,946,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R9345:Bptf
|
UTSW |
11 |
106,971,588 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9393:Bptf
|
UTSW |
11 |
106,965,134 (GRCm39) |
missense |
probably benign |
0.00 |
R9451:Bptf
|
UTSW |
11 |
106,935,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R9561:Bptf
|
UTSW |
11 |
106,964,954 (GRCm39) |
nonsense |
probably null |
|
R9632:Bptf
|
UTSW |
11 |
106,952,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R9648:Bptf
|
UTSW |
11 |
106,943,720 (GRCm39) |
missense |
probably damaging |
0.99 |
R9650:Bptf
|
UTSW |
11 |
106,935,412 (GRCm39) |
missense |
probably benign |
0.15 |
R9658:Bptf
|
UTSW |
11 |
107,002,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R9775:Bptf
|
UTSW |
11 |
106,934,502 (GRCm39) |
missense |
probably benign |
0.04 |
R9776:Bptf
|
UTSW |
11 |
106,969,396 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Bptf
|
UTSW |
11 |
106,965,408 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Bptf
|
UTSW |
11 |
106,949,510 (GRCm39) |
missense |
probably damaging |
1.00 |
|