Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700001J03Rik |
T |
G |
5: 146,185,219 (GRCm38) |
S18R |
probably benign |
Het |
2010315B03Rik |
A |
C |
9: 124,293,766 (GRCm38) |
V176G |
probably benign |
Het |
Abcb1a |
T |
A |
5: 8,715,732 (GRCm38) |
|
probably null |
Het |
Acad11 |
C |
A |
9: 104,075,877 (GRCm38) |
P102T |
probably damaging |
Het |
Aggf1 |
T |
A |
13: 95,364,713 (GRCm38) |
D387V |
probably damaging |
Het |
Akr1c13 |
G |
A |
13: 4,198,497 (GRCm38) |
V234I |
probably benign |
Het |
Alg5 |
A |
G |
3: 54,746,473 (GRCm38) |
Y210C |
possibly damaging |
Het |
Arl8a |
C |
A |
1: 135,147,099 (GRCm38) |
A41E |
probably benign |
Het |
Axin1 |
C |
A |
17: 26,173,756 (GRCm38) |
T337K |
possibly damaging |
Het |
Bdp1 |
A |
G |
13: 100,056,267 (GRCm38) |
L1353P |
probably damaging |
Het |
C9 |
A |
T |
15: 6,459,643 (GRCm38) |
E160D |
probably damaging |
Het |
Cbx6 |
T |
C |
15: 79,828,680 (GRCm38) |
D182G |
probably damaging |
Het |
Ccdc144b |
T |
G |
3: 36,010,660 (GRCm38) |
*521C |
probably null |
Het |
Cep57l1 |
T |
C |
10: 41,721,682 (GRCm38) |
R242G |
possibly damaging |
Het |
Chst8 |
T |
C |
7: 34,675,724 (GRCm38) |
D230G |
probably damaging |
Het |
Col3a1 |
A |
C |
1: 45,346,110 (GRCm38) |
D129A |
probably damaging |
Het |
Cst12 |
A |
G |
2: 148,789,473 (GRCm38) |
E38G |
possibly damaging |
Het |
Disp1 |
G |
T |
1: 183,088,096 (GRCm38) |
A920E |
probably damaging |
Het |
Dtna |
T |
G |
18: 23,535,149 (GRCm38) |
|
probably null |
Het |
Elp3 |
T |
A |
14: 65,582,929 (GRCm38) |
H97L |
probably damaging |
Het |
Exoc8 |
A |
G |
8: 124,897,575 (GRCm38) |
F18L |
possibly damaging |
Het |
Extl3 |
T |
C |
14: 65,077,320 (GRCm38) |
T138A |
probably benign |
Het |
Foxi2 |
G |
T |
7: 135,410,667 (GRCm38) |
G95C |
probably damaging |
Het |
Foxj2 |
G |
T |
6: 122,833,271 (GRCm38) |
Q196H |
probably benign |
Het |
Frem1 |
A |
T |
4: 82,989,189 (GRCm38) |
D811E |
probably damaging |
Het |
Frmd4a |
A |
T |
2: 4,603,448 (GRCm38) |
E709V |
probably damaging |
Het |
Fscn3 |
T |
A |
6: 28,436,201 (GRCm38) |
*499K |
probably null |
Het |
Galc |
C |
T |
12: 98,242,744 (GRCm38) |
G217D |
possibly damaging |
Het |
Gm5592 |
G |
T |
7: 41,216,118 (GRCm38) |
|
probably benign |
Het |
Hnrnpul1 |
A |
G |
7: 25,743,011 (GRCm38) |
S269P |
probably benign |
Het |
Hrh1 |
T |
C |
6: 114,480,535 (GRCm38) |
V259A |
probably benign |
Het |
Lef1 |
T |
C |
3: 131,184,733 (GRCm38) |
S167P |
probably benign |
Het |
Mtf2 |
T |
C |
5: 108,093,352 (GRCm38) |
I248T |
probably benign |
Het |
Muc2 |
C |
T |
7: 141,745,608 (GRCm38) |
T130M |
possibly damaging |
Het |
Myo16 |
T |
C |
8: 10,435,880 (GRCm38) |
F653S |
probably damaging |
Het |
Myo1e |
T |
C |
9: 70,343,135 (GRCm38) |
|
probably null |
Het |
Myo5a |
G |
T |
9: 75,116,336 (GRCm38) |
|
probably benign |
Het |
Nlrp1b |
T |
A |
11: 71,182,663 (GRCm38) |
D118V |
probably damaging |
Het |
Npat |
T |
C |
9: 53,572,620 (GRCm38) |
F1412S |
probably damaging |
Het |
Olfr1377 |
G |
A |
11: 50,984,775 (GRCm38) |
E25K |
probably benign |
Het |
Olfr884 |
T |
G |
9: 38,048,140 (GRCm38) |
L306R |
probably benign |
Het |
Onecut3 |
G |
T |
10: 80,495,707 (GRCm38) |
A234S |
unknown |
Het |
Osbpl6 |
T |
A |
2: 76,546,000 (GRCm38) |
I73K |
probably damaging |
Het |
Otog |
C |
T |
7: 46,288,519 (GRCm38) |
T1884I |
probably benign |
Het |
Pax6 |
C |
A |
2: 105,696,502 (GRCm38) |
P251Q |
probably benign |
Het |
Pias4 |
A |
G |
10: 81,164,034 (GRCm38) |
Y62H |
possibly damaging |
Het |
Pknox1 |
T |
A |
17: 31,590,713 (GRCm38) |
V97D |
possibly damaging |
Het |
Plekhf1 |
A |
G |
7: 38,221,598 (GRCm38) |
V182A |
probably damaging |
Het |
Plscr4 |
T |
C |
9: 92,484,780 (GRCm38) |
V149A |
probably damaging |
Het |
Polr2l |
A |
T |
7: 141,473,396 (GRCm38) |
L35Q |
probably damaging |
Het |
Ppp3ca |
T |
C |
3: 136,890,489 (GRCm38) |
I305T |
probably damaging |
Het |
Ptprg |
G |
A |
14: 12,122,068 (GRCm38) |
A311T |
probably benign |
Het |
Raet1e |
T |
G |
10: 22,181,332 (GRCm38) |
I185R |
probably damaging |
Het |
Rims1 |
A |
C |
1: 22,479,462 (GRCm38) |
V520G |
probably damaging |
Het |
Rp1 |
A |
T |
1: 4,345,878 (GRCm38) |
D1670E |
probably damaging |
Het |
Rps6ka1 |
A |
T |
4: 133,860,557 (GRCm38) |
I352N |
probably damaging |
Het |
Rtp3 |
T |
C |
9: 110,987,350 (GRCm38) |
|
probably benign |
Het |
Ryr3 |
T |
A |
2: 112,733,031 (GRCm38) |
|
probably null |
Het |
Sall3 |
A |
G |
18: 80,974,476 (GRCm38) |
V79A |
probably damaging |
Het |
Sdsl |
C |
T |
5: 120,462,054 (GRCm38) |
V93M |
probably damaging |
Het |
Slc7a13 |
A |
G |
4: 19,819,390 (GRCm38) |
N197D |
probably benign |
Het |
Slit1 |
T |
A |
19: 41,721,044 (GRCm38) |
R137* |
probably null |
Het |
Stxbp5 |
C |
A |
10: 9,770,623 (GRCm38) |
R115L |
probably damaging |
Het |
Tcea1 |
G |
A |
1: 4,894,944 (GRCm38) |
R290H |
probably damaging |
Het |
Tmem132e |
A |
T |
11: 82,434,512 (GRCm38) |
T113S |
probably damaging |
Het |
Tpp1 |
A |
T |
7: 105,749,251 (GRCm38) |
I286N |
probably damaging |
Het |
Trio |
G |
A |
15: 27,732,538 (GRCm38) |
R3086* |
probably null |
Het |
Usp22 |
T |
A |
11: 61,160,636 (GRCm38) |
N294Y |
probably damaging |
Het |
Usp44 |
T |
A |
10: 93,846,071 (GRCm38) |
S128T |
probably benign |
Het |
Zc3h7b |
T |
C |
15: 81,769,183 (GRCm38) |
|
probably null |
Het |
Zfhx2 |
T |
C |
14: 55,066,915 (GRCm38) |
Y1204C |
possibly damaging |
Het |
|
Other mutations in Bptf |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00553:Bptf
|
APN |
11 |
107,055,279 (GRCm38) |
missense |
possibly damaging |
0.88 |
IGL00664:Bptf
|
APN |
11 |
107,077,665 (GRCm38) |
missense |
possibly damaging |
0.78 |
IGL00705:Bptf
|
APN |
11 |
107,095,708 (GRCm38) |
splice site |
probably benign |
|
IGL00796:Bptf
|
APN |
11 |
107,054,550 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00834:Bptf
|
APN |
11 |
107,073,928 (GRCm38) |
missense |
possibly damaging |
0.59 |
IGL01155:Bptf
|
APN |
11 |
107,080,727 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01314:Bptf
|
APN |
11 |
107,054,853 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01371:Bptf
|
APN |
11 |
107,055,907 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01567:Bptf
|
APN |
11 |
107,058,774 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01794:Bptf
|
APN |
11 |
107,053,221 (GRCm38) |
critical splice donor site |
probably null |
|
IGL02108:Bptf
|
APN |
11 |
107,074,988 (GRCm38) |
missense |
probably benign |
0.45 |
IGL02367:Bptf
|
APN |
11 |
107,073,352 (GRCm38) |
missense |
probably benign |
|
IGL02437:Bptf
|
APN |
11 |
107,074,695 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02589:Bptf
|
APN |
11 |
107,111,531 (GRCm38) |
missense |
possibly damaging |
0.92 |
IGL02897:Bptf
|
APN |
11 |
107,047,121 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02935:Bptf
|
APN |
11 |
107,080,799 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02954:Bptf
|
APN |
11 |
107,054,749 (GRCm38) |
missense |
possibly damaging |
0.89 |
IGL02982:Bptf
|
APN |
11 |
107,076,674 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03109:Bptf
|
APN |
11 |
107,061,701 (GRCm38) |
missense |
possibly damaging |
0.53 |
IGL03265:Bptf
|
APN |
11 |
107,054,628 (GRCm38) |
missense |
probably benign |
0.00 |
IGL03403:Bptf
|
APN |
11 |
107,099,733 (GRCm38) |
missense |
possibly damaging |
0.51 |
Anodyne
|
UTSW |
11 |
107,043,631 (GRCm38) |
critical splice donor site |
probably null |
|
Arroyo
|
UTSW |
11 |
107,042,690 (GRCm38) |
missense |
probably benign |
0.32 |
mojado
|
UTSW |
11 |
107,044,640 (GRCm38) |
missense |
probably benign |
0.03 |
IGL03097:Bptf
|
UTSW |
11 |
107,077,680 (GRCm38) |
missense |
probably damaging |
1.00 |
PIT4486001:Bptf
|
UTSW |
11 |
107,054,788 (GRCm38) |
missense |
probably damaging |
0.98 |
R0066:Bptf
|
UTSW |
11 |
107,062,136 (GRCm38) |
missense |
possibly damaging |
0.90 |
R0157:Bptf
|
UTSW |
11 |
107,074,658 (GRCm38) |
missense |
possibly damaging |
0.89 |
R0320:Bptf
|
UTSW |
11 |
107,072,819 (GRCm38) |
missense |
probably damaging |
1.00 |
R0328:Bptf
|
UTSW |
11 |
107,047,127 (GRCm38) |
missense |
probably damaging |
1.00 |
R0402:Bptf
|
UTSW |
11 |
107,074,114 (GRCm38) |
missense |
probably damaging |
1.00 |
R0482:Bptf
|
UTSW |
11 |
107,081,262 (GRCm38) |
missense |
probably benign |
0.13 |
R0574:Bptf
|
UTSW |
11 |
107,076,527 (GRCm38) |
missense |
probably damaging |
1.00 |
R0598:Bptf
|
UTSW |
11 |
107,072,965 (GRCm38) |
missense |
probably damaging |
0.99 |
R0599:Bptf
|
UTSW |
11 |
107,068,382 (GRCm38) |
missense |
probably damaging |
1.00 |
R0601:Bptf
|
UTSW |
11 |
107,061,692 (GRCm38) |
missense |
probably benign |
0.04 |
R0744:Bptf
|
UTSW |
11 |
107,110,812 (GRCm38) |
critical splice donor site |
probably null |
|
R0836:Bptf
|
UTSW |
11 |
107,110,812 (GRCm38) |
critical splice donor site |
probably null |
|
R0885:Bptf
|
UTSW |
11 |
107,043,791 (GRCm38) |
missense |
probably damaging |
1.00 |
R1070:Bptf
|
UTSW |
11 |
107,055,055 (GRCm38) |
missense |
possibly damaging |
0.92 |
R1252:Bptf
|
UTSW |
11 |
107,073,251 (GRCm38) |
missense |
probably benign |
0.00 |
R1370:Bptf
|
UTSW |
11 |
107,047,094 (GRCm38) |
missense |
probably damaging |
0.99 |
R1428:Bptf
|
UTSW |
11 |
107,073,047 (GRCm38) |
missense |
probably damaging |
0.99 |
R1467:Bptf
|
UTSW |
11 |
107,055,055 (GRCm38) |
missense |
possibly damaging |
0.92 |
R1467:Bptf
|
UTSW |
11 |
107,055,055 (GRCm38) |
missense |
possibly damaging |
0.92 |
R1742:Bptf
|
UTSW |
11 |
107,110,951 (GRCm38) |
missense |
probably damaging |
1.00 |
R1816:Bptf
|
UTSW |
11 |
107,060,579 (GRCm38) |
missense |
probably damaging |
1.00 |
R1858:Bptf
|
UTSW |
11 |
107,073,301 (GRCm38) |
missense |
probably benign |
0.00 |
R1989:Bptf
|
UTSW |
11 |
107,074,826 (GRCm38) |
missense |
probably damaging |
1.00 |
R2253:Bptf
|
UTSW |
11 |
107,111,322 (GRCm38) |
missense |
probably damaging |
1.00 |
R2392:Bptf
|
UTSW |
11 |
107,072,747 (GRCm38) |
missense |
probably damaging |
1.00 |
R2431:Bptf
|
UTSW |
11 |
107,047,240 (GRCm38) |
missense |
possibly damaging |
0.48 |
R3022:Bptf
|
UTSW |
11 |
107,111,637 (GRCm38) |
critical splice acceptor site |
probably null |
|
R3161:Bptf
|
UTSW |
11 |
107,074,476 (GRCm38) |
missense |
probably damaging |
1.00 |
R3686:Bptf
|
UTSW |
11 |
107,074,198 (GRCm38) |
missense |
probably benign |
0.25 |
R3687:Bptf
|
UTSW |
11 |
107,074,198 (GRCm38) |
missense |
probably benign |
0.25 |
R3688:Bptf
|
UTSW |
11 |
107,074,198 (GRCm38) |
missense |
probably benign |
0.25 |
R3787:Bptf
|
UTSW |
11 |
107,073,827 (GRCm38) |
missense |
probably damaging |
1.00 |
R3834:Bptf
|
UTSW |
11 |
107,073,857 (GRCm38) |
missense |
probably benign |
0.05 |
R3885:Bptf
|
UTSW |
11 |
107,074,513 (GRCm38) |
missense |
probably damaging |
0.97 |
R4090:Bptf
|
UTSW |
11 |
107,081,523 (GRCm38) |
missense |
probably damaging |
0.99 |
R4398:Bptf
|
UTSW |
11 |
107,110,844 (GRCm38) |
missense |
probably damaging |
1.00 |
R4437:Bptf
|
UTSW |
11 |
107,074,474 (GRCm38) |
missense |
possibly damaging |
0.59 |
R4514:Bptf
|
UTSW |
11 |
107,077,692 (GRCm38) |
missense |
probably damaging |
1.00 |
R4565:Bptf
|
UTSW |
11 |
107,073,010 (GRCm38) |
missense |
probably damaging |
1.00 |
R4715:Bptf
|
UTSW |
11 |
107,047,181 (GRCm38) |
missense |
probably damaging |
1.00 |
R4748:Bptf
|
UTSW |
11 |
107,095,880 (GRCm38) |
missense |
probably damaging |
0.96 |
R4885:Bptf
|
UTSW |
11 |
107,074,648 (GRCm38) |
missense |
probably benign |
0.39 |
R4901:Bptf
|
UTSW |
11 |
107,110,860 (GRCm38) |
nonsense |
probably null |
|
R4995:Bptf
|
UTSW |
11 |
107,054,565 (GRCm38) |
missense |
probably damaging |
0.98 |
R5057:Bptf
|
UTSW |
11 |
107,082,528 (GRCm38) |
missense |
probably damaging |
0.98 |
R5120:Bptf
|
UTSW |
11 |
107,073,385 (GRCm38) |
missense |
probably damaging |
0.99 |
R5320:Bptf
|
UTSW |
11 |
107,081,367 (GRCm38) |
nonsense |
probably null |
|
R5329:Bptf
|
UTSW |
11 |
107,073,295 (GRCm38) |
missense |
probably benign |
0.06 |
R5418:Bptf
|
UTSW |
11 |
107,111,294 (GRCm38) |
missense |
probably damaging |
1.00 |
R5461:Bptf
|
UTSW |
11 |
107,061,764 (GRCm38) |
missense |
probably damaging |
1.00 |
R5664:Bptf
|
UTSW |
11 |
107,073,699 (GRCm38) |
missense |
probably benign |
0.01 |
R5718:Bptf
|
UTSW |
11 |
107,111,434 (GRCm38) |
missense |
probably damaging |
1.00 |
R5774:Bptf
|
UTSW |
11 |
107,111,137 (GRCm38) |
missense |
probably damaging |
1.00 |
R5851:Bptf
|
UTSW |
11 |
107,110,862 (GRCm38) |
missense |
probably damaging |
1.00 |
R5930:Bptf
|
UTSW |
11 |
107,073,196 (GRCm38) |
missense |
probably damaging |
1.00 |
R5949:Bptf
|
UTSW |
11 |
107,111,089 (GRCm38) |
missense |
probably damaging |
0.99 |
R5975:Bptf
|
UTSW |
11 |
107,035,864 (GRCm38) |
utr 3 prime |
probably benign |
|
R6027:Bptf
|
UTSW |
11 |
107,074,945 (GRCm38) |
missense |
probably damaging |
1.00 |
R6128:Bptf
|
UTSW |
11 |
107,074,690 (GRCm38) |
missense |
possibly damaging |
0.87 |
R6337:Bptf
|
UTSW |
11 |
107,058,779 (GRCm38) |
missense |
possibly damaging |
0.89 |
R6407:Bptf
|
UTSW |
11 |
107,111,126 (GRCm38) |
missense |
probably damaging |
1.00 |
R6470:Bptf
|
UTSW |
11 |
107,072,767 (GRCm38) |
missense |
probably damaging |
1.00 |
R6487:Bptf
|
UTSW |
11 |
107,077,726 (GRCm38) |
missense |
probably damaging |
0.99 |
R6501:Bptf
|
UTSW |
11 |
107,077,683 (GRCm38) |
missense |
probably null |
1.00 |
R6755:Bptf
|
UTSW |
11 |
107,047,256 (GRCm38) |
missense |
probably benign |
0.27 |
R6861:Bptf
|
UTSW |
11 |
107,062,565 (GRCm38) |
missense |
probably damaging |
1.00 |
R6866:Bptf
|
UTSW |
11 |
107,073,580 (GRCm38) |
missense |
probably damaging |
1.00 |
R6879:Bptf
|
UTSW |
11 |
107,042,690 (GRCm38) |
missense |
probably benign |
0.32 |
R6927:Bptf
|
UTSW |
11 |
107,054,595 (GRCm38) |
missense |
probably damaging |
1.00 |
R6944:Bptf
|
UTSW |
11 |
107,080,823 (GRCm38) |
missense |
probably damaging |
1.00 |
R7082:Bptf
|
UTSW |
11 |
107,086,747 (GRCm38) |
missense |
probably benign |
0.00 |
R7136:Bptf
|
UTSW |
11 |
107,099,715 (GRCm38) |
missense |
probably damaging |
1.00 |
R7162:Bptf
|
UTSW |
11 |
107,043,631 (GRCm38) |
critical splice donor site |
probably null |
|
R7171:Bptf
|
UTSW |
11 |
107,131,407 (GRCm38) |
missense |
unknown |
|
R7193:Bptf
|
UTSW |
11 |
107,054,809 (GRCm38) |
nonsense |
probably null |
|
R7210:Bptf
|
UTSW |
11 |
107,054,464 (GRCm38) |
nonsense |
probably null |
|
R7221:Bptf
|
UTSW |
11 |
107,054,832 (GRCm38) |
missense |
probably damaging |
1.00 |
R7316:Bptf
|
UTSW |
11 |
107,110,914 (GRCm38) |
nonsense |
probably null |
|
R7316:Bptf
|
UTSW |
11 |
107,073,109 (GRCm38) |
missense |
probably damaging |
1.00 |
R7422:Bptf
|
UTSW |
11 |
107,060,558 (GRCm38) |
missense |
probably damaging |
1.00 |
R7454:Bptf
|
UTSW |
11 |
107,044,640 (GRCm38) |
missense |
probably benign |
0.03 |
R7657:Bptf
|
UTSW |
11 |
107,074,729 (GRCm38) |
missense |
probably damaging |
1.00 |
R7718:Bptf
|
UTSW |
11 |
107,081,456 (GRCm38) |
missense |
possibly damaging |
0.65 |
R7827:Bptf
|
UTSW |
11 |
107,047,187 (GRCm38) |
missense |
probably benign |
0.01 |
R7844:Bptf
|
UTSW |
11 |
107,074,061 (GRCm38) |
missense |
probably damaging |
0.97 |
R7992:Bptf
|
UTSW |
11 |
107,110,883 (GRCm38) |
missense |
probably benign |
0.00 |
R8001:Bptf
|
UTSW |
11 |
107,047,340 (GRCm38) |
nonsense |
probably null |
|
R8037:Bptf
|
UTSW |
11 |
107,055,950 (GRCm38) |
missense |
probably damaging |
1.00 |
R8122:Bptf
|
UTSW |
11 |
107,036,591 (GRCm38) |
critical splice acceptor site |
probably null |
|
R8235:Bptf
|
UTSW |
11 |
107,076,632 (GRCm38) |
missense |
probably benign |
0.04 |
R8308:Bptf
|
UTSW |
11 |
107,052,989 (GRCm38) |
missense |
probably damaging |
0.99 |
R8409:Bptf
|
UTSW |
11 |
107,062,669 (GRCm38) |
missense |
probably damaging |
1.00 |
R8464:Bptf
|
UTSW |
11 |
107,131,342 (GRCm38) |
missense |
probably benign |
0.01 |
R8477:Bptf
|
UTSW |
11 |
107,052,853 (GRCm38) |
missense |
probably damaging |
0.98 |
R8482:Bptf
|
UTSW |
11 |
107,043,698 (GRCm38) |
missense |
probably benign |
0.19 |
R8515:Bptf
|
UTSW |
11 |
107,055,238 (GRCm38) |
missense |
possibly damaging |
0.85 |
R8519:Bptf
|
UTSW |
11 |
107,061,764 (GRCm38) |
missense |
probably damaging |
1.00 |
R8708:Bptf
|
UTSW |
11 |
107,073,314 (GRCm38) |
missense |
probably damaging |
1.00 |
R8708:Bptf
|
UTSW |
11 |
107,073,313 (GRCm38) |
missense |
probably damaging |
0.99 |
R8722:Bptf
|
UTSW |
11 |
107,131,469 (GRCm38) |
missense |
unknown |
|
R8732:Bptf
|
UTSW |
11 |
107,040,380 (GRCm38) |
missense |
probably damaging |
1.00 |
R8783:Bptf
|
UTSW |
11 |
107,131,531 (GRCm38) |
missense |
unknown |
|
R8828:Bptf
|
UTSW |
11 |
107,055,010 (GRCm38) |
missense |
probably damaging |
0.98 |
R9004:Bptf
|
UTSW |
11 |
107,054,887 (GRCm38) |
missense |
probably damaging |
1.00 |
R9010:Bptf
|
UTSW |
11 |
107,073,750 (GRCm38) |
missense |
probably damaging |
1.00 |
R9035:Bptf
|
UTSW |
11 |
107,073,016 (GRCm38) |
missense |
probably damaging |
1.00 |
R9083:Bptf
|
UTSW |
11 |
107,068,350 (GRCm38) |
missense |
probably damaging |
1.00 |
R9211:Bptf
|
UTSW |
11 |
107,055,298 (GRCm38) |
missense |
probably damaging |
1.00 |
R9345:Bptf
|
UTSW |
11 |
107,080,762 (GRCm38) |
missense |
possibly damaging |
0.77 |
R9393:Bptf
|
UTSW |
11 |
107,074,308 (GRCm38) |
missense |
probably benign |
0.00 |
R9451:Bptf
|
UTSW |
11 |
107,044,585 (GRCm38) |
missense |
probably damaging |
1.00 |
R9561:Bptf
|
UTSW |
11 |
107,074,128 (GRCm38) |
nonsense |
probably null |
|
R9632:Bptf
|
UTSW |
11 |
107,061,719 (GRCm38) |
missense |
probably damaging |
1.00 |
R9648:Bptf
|
UTSW |
11 |
107,052,894 (GRCm38) |
missense |
probably damaging |
0.99 |
R9650:Bptf
|
UTSW |
11 |
107,044,586 (GRCm38) |
missense |
probably benign |
0.15 |
R9658:Bptf
|
UTSW |
11 |
107,111,344 (GRCm38) |
missense |
probably damaging |
1.00 |
R9775:Bptf
|
UTSW |
11 |
107,043,676 (GRCm38) |
missense |
probably benign |
0.04 |
R9776:Bptf
|
UTSW |
11 |
107,078,570 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1088:Bptf
|
UTSW |
11 |
107,074,582 (GRCm38) |
missense |
probably benign |
0.00 |
Z1176:Bptf
|
UTSW |
11 |
107,058,684 (GRCm38) |
missense |
probably damaging |
1.00 |
|