Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700006A11Rik |
T |
G |
3: 124,200,163 (GRCm39) |
L476F |
probably damaging |
Het |
4930432E11Rik |
A |
T |
7: 29,278,591 (GRCm39) |
|
noncoding transcript |
Het |
A930011G23Rik |
A |
T |
5: 99,370,897 (GRCm39) |
|
probably benign |
Het |
Abcd3 |
A |
G |
3: 121,575,612 (GRCm39) |
Y217H |
probably damaging |
Het |
Abraxas1 |
A |
T |
5: 100,965,822 (GRCm39) |
|
probably benign |
Het |
Acsbg1 |
T |
C |
9: 54,523,346 (GRCm39) |
Y427C |
probably damaging |
Het |
Acsbg3 |
T |
A |
17: 57,192,169 (GRCm39) |
Y577* |
probably null |
Het |
Adam10 |
T |
A |
9: 70,683,651 (GRCm39) |
|
probably benign |
Het |
Adam24 |
G |
A |
8: 41,134,004 (GRCm39) |
V491I |
possibly damaging |
Het |
Adamts2 |
T |
G |
11: 50,647,524 (GRCm39) |
V299G |
probably damaging |
Het |
Adh7 |
A |
G |
3: 137,929,752 (GRCm39) |
T143A |
probably damaging |
Het |
Ahcyl1 |
A |
G |
3: 107,581,419 (GRCm39) |
S81P |
probably benign |
Het |
Arhgap20 |
C |
A |
9: 51,761,215 (GRCm39) |
T986K |
probably benign |
Het |
Atp13a5 |
A |
T |
16: 29,133,478 (GRCm39) |
I391N |
possibly damaging |
Het |
Atp6v0a1 |
C |
A |
11: 100,917,511 (GRCm39) |
A143E |
probably benign |
Het |
Calcrl |
A |
G |
2: 84,181,629 (GRCm39) |
I173T |
probably damaging |
Het |
Casz1 |
A |
G |
4: 149,017,394 (GRCm39) |
T228A |
probably benign |
Het |
Cckar |
A |
G |
5: 53,857,321 (GRCm39) |
I292T |
probably damaging |
Het |
Ccn5 |
G |
A |
2: 163,670,906 (GRCm39) |
V138M |
probably damaging |
Het |
Cfhr2 |
T |
A |
1: 139,786,383 (GRCm39) |
|
probably null |
Het |
Chkb |
T |
C |
15: 89,313,260 (GRCm39) |
I109V |
possibly damaging |
Het |
Clec2i |
T |
C |
6: 128,865,069 (GRCm39) |
|
probably null |
Het |
Clec4a4 |
T |
A |
6: 123,000,934 (GRCm39) |
W216R |
probably damaging |
Het |
Cntnap1 |
A |
C |
11: 101,077,337 (GRCm39) |
I1000L |
probably damaging |
Het |
Cp |
C |
A |
3: 20,011,549 (GRCm39) |
D34E |
possibly damaging |
Het |
Cse1l |
T |
C |
2: 166,782,044 (GRCm39) |
|
probably null |
Het |
Dennd3 |
T |
C |
15: 73,394,357 (GRCm39) |
|
probably null |
Het |
Dnah7a |
A |
G |
1: 53,616,382 (GRCm39) |
V1193A |
probably benign |
Het |
Eaf2 |
A |
G |
16: 36,630,832 (GRCm39) |
|
probably null |
Het |
Efcab3 |
T |
A |
11: 104,611,765 (GRCm39) |
S536T |
probably benign |
Het |
Ephb2 |
T |
C |
4: 136,421,136 (GRCm39) |
T405A |
possibly damaging |
Het |
Fam117a |
G |
A |
11: 95,269,779 (GRCm39) |
V348M |
probably damaging |
Het |
Fh1 |
T |
C |
1: 175,428,990 (GRCm39) |
*167W |
probably null |
Het |
Fmo9 |
T |
A |
1: 166,490,868 (GRCm39) |
I486F |
probably benign |
Het |
Gabbr1 |
T |
A |
17: 37,365,771 (GRCm39) |
I150N |
probably damaging |
Het |
Gfpt1 |
T |
C |
6: 87,054,179 (GRCm39) |
V478A |
possibly damaging |
Het |
Gm2663 |
A |
T |
6: 40,974,894 (GRCm39) |
V59E |
probably damaging |
Het |
Gm4868 |
T |
A |
5: 125,925,176 (GRCm39) |
|
noncoding transcript |
Het |
Heatr4 |
T |
A |
12: 84,026,934 (GRCm39) |
T108S |
probably benign |
Het |
Hells |
G |
T |
19: 38,935,286 (GRCm39) |
A319S |
probably benign |
Het |
Helz2 |
A |
G |
2: 180,876,780 (GRCm39) |
V1238A |
probably benign |
Het |
Helz2 |
T |
A |
2: 180,880,252 (GRCm39) |
Q488L |
possibly damaging |
Het |
Hkdc1 |
A |
G |
10: 62,227,162 (GRCm39) |
F765S |
probably damaging |
Het |
Hspg2 |
T |
A |
4: 137,245,820 (GRCm39) |
W938R |
probably damaging |
Het |
Itpr2 |
G |
A |
6: 146,060,399 (GRCm39) |
R2473* |
probably null |
Het |
Kctd1 |
C |
T |
18: 15,194,839 (GRCm39) |
V595I |
probably benign |
Het |
Krt7 |
A |
G |
15: 101,321,290 (GRCm39) |
Y369C |
probably damaging |
Het |
Krt72 |
T |
C |
15: 101,689,364 (GRCm39) |
T323A |
probably benign |
Het |
Krt76 |
A |
G |
15: 101,801,122 (GRCm39) |
L58P |
unknown |
Het |
Liph |
C |
A |
16: 21,786,800 (GRCm39) |
R272L |
probably benign |
Het |
Lrrc9 |
A |
T |
12: 72,502,772 (GRCm39) |
K248* |
probably null |
Het |
Mei4 |
T |
A |
9: 81,809,195 (GRCm39) |
S93T |
probably damaging |
Het |
Mgll |
T |
A |
6: 88,790,930 (GRCm39) |
Y183* |
probably null |
Het |
Myo5b |
A |
G |
18: 74,875,218 (GRCm39) |
M1541V |
probably benign |
Het |
Napg |
A |
G |
18: 63,115,762 (GRCm39) |
E66G |
probably benign |
Het |
Npr3 |
T |
C |
15: 11,851,572 (GRCm39) |
D406G |
probably damaging |
Het |
Nr2c2 |
A |
G |
6: 92,136,224 (GRCm39) |
T355A |
possibly damaging |
Het |
Or13j1 |
G |
A |
4: 43,706,041 (GRCm39) |
H176Y |
probably damaging |
Het |
Or4a71 |
A |
T |
2: 89,357,989 (GRCm39) |
I255K |
probably benign |
Het |
Or51m1 |
G |
T |
7: 103,578,668 (GRCm39) |
V213L |
probably benign |
Het |
Or51v8 |
A |
G |
7: 103,319,845 (GRCm39) |
I131T |
probably benign |
Het |
Or52z13 |
A |
T |
7: 103,247,107 (GRCm39) |
I195F |
probably damaging |
Het |
Or5b107 |
T |
C |
19: 13,142,404 (GRCm39) |
Y9H |
probably benign |
Het |
Or8d1 |
A |
G |
9: 38,766,846 (GRCm39) |
M163V |
possibly damaging |
Het |
Orai2 |
T |
C |
5: 136,179,793 (GRCm39) |
E80G |
probably damaging |
Het |
Pcdhb14 |
T |
A |
18: 37,582,535 (GRCm39) |
V547E |
probably damaging |
Het |
Pcdhb15 |
T |
C |
18: 37,609,084 (GRCm39) |
I772T |
possibly damaging |
Het |
Pcnt |
T |
C |
10: 76,244,630 (GRCm39) |
Q1150R |
probably damaging |
Het |
Pdcd6 |
A |
G |
13: 74,453,700 (GRCm39) |
I146T |
probably damaging |
Het |
Phldb2 |
T |
A |
16: 45,621,988 (GRCm39) |
D664V |
probably damaging |
Het |
Pik3ap1 |
A |
T |
19: 41,320,673 (GRCm39) |
V182E |
probably damaging |
Het |
Pip4k2a |
A |
G |
2: 18,852,433 (GRCm39) |
V283A |
probably benign |
Het |
Pkdrej |
A |
G |
15: 85,705,372 (GRCm39) |
V188A |
possibly damaging |
Het |
Pnpla6 |
T |
C |
8: 3,591,404 (GRCm39) |
W1151R |
probably damaging |
Het |
Ppp1r14c |
A |
G |
10: 3,316,890 (GRCm39) |
Y75C |
probably damaging |
Het |
Prl2b1 |
C |
T |
13: 27,567,452 (GRCm39) |
D224N |
probably benign |
Het |
Ptgis |
A |
G |
2: 167,056,778 (GRCm39) |
S270P |
probably benign |
Het |
Rgs11 |
C |
A |
17: 26,429,640 (GRCm39) |
A446D |
probably damaging |
Het |
Rims2 |
A |
G |
15: 39,545,098 (GRCm39) |
T1531A |
probably damaging |
Het |
Sbno1 |
A |
T |
5: 124,526,580 (GRCm39) |
|
probably benign |
Het |
Scarb2 |
C |
G |
5: 92,596,416 (GRCm39) |
M409I |
probably benign |
Het |
Scube3 |
C |
T |
17: 28,387,353 (GRCm39) |
|
probably benign |
Het |
Slc44a4 |
T |
C |
17: 35,140,901 (GRCm39) |
I180T |
probably damaging |
Het |
Slc9a2 |
T |
C |
1: 40,781,803 (GRCm39) |
M344T |
probably damaging |
Het |
Smc3 |
A |
T |
19: 53,627,800 (GRCm39) |
T860S |
probably benign |
Het |
Snrpa |
A |
G |
7: 26,891,174 (GRCm39) |
I99T |
probably benign |
Het |
Sorcs1 |
A |
G |
19: 50,163,481 (GRCm39) |
|
probably benign |
Het |
Suds3 |
T |
C |
5: 117,243,309 (GRCm39) |
K143R |
probably benign |
Het |
Supt20 |
A |
T |
3: 54,622,164 (GRCm39) |
M424L |
probably benign |
Het |
Tgtp2 |
T |
C |
11: 48,949,751 (GRCm39) |
M274V |
probably benign |
Het |
Tmem158 |
T |
A |
9: 123,088,974 (GRCm39) |
M213L |
probably benign |
Het |
Tnks |
C |
A |
8: 35,324,672 (GRCm39) |
R639L |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Trmt10c |
A |
C |
16: 55,854,938 (GRCm39) |
N232K |
possibly damaging |
Het |
Trpm6 |
C |
T |
19: 18,833,581 (GRCm39) |
R1587W |
probably damaging |
Het |
Trrap |
G |
A |
5: 144,765,400 (GRCm39) |
V2539I |
probably benign |
Het |
Tsg101 |
A |
G |
7: 46,556,835 (GRCm39) |
S115P |
probably benign |
Het |
Ttll13 |
G |
T |
7: 79,910,256 (GRCm39) |
V800L |
probably benign |
Het |
Vmn1r57 |
A |
G |
7: 5,223,576 (GRCm39) |
T34A |
possibly damaging |
Het |
Vmn2r118 |
T |
A |
17: 55,918,530 (GRCm39) |
T121S |
probably benign |
Het |
Wdr35 |
A |
G |
12: 9,035,772 (GRCm39) |
I238M |
possibly damaging |
Het |
Zfp81 |
T |
A |
17: 33,554,080 (GRCm39) |
T245S |
probably benign |
Het |
Zfyve26 |
G |
T |
12: 79,325,237 (GRCm39) |
P824Q |
probably damaging |
Het |
|
Other mutations in Sorl1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Sorl1
|
APN |
9 |
41,885,390 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01303:Sorl1
|
APN |
9 |
41,935,774 (GRCm39) |
splice site |
probably benign |
|
IGL01545:Sorl1
|
APN |
9 |
41,955,252 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01629:Sorl1
|
APN |
9 |
41,968,565 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01670:Sorl1
|
APN |
9 |
41,912,788 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL01684:Sorl1
|
APN |
9 |
41,892,007 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02154:Sorl1
|
APN |
9 |
41,915,330 (GRCm39) |
missense |
probably benign |
|
IGL02215:Sorl1
|
APN |
9 |
41,929,478 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02427:Sorl1
|
APN |
9 |
41,952,986 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02590:Sorl1
|
APN |
9 |
41,957,857 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02794:Sorl1
|
APN |
9 |
41,975,070 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02797:Sorl1
|
APN |
9 |
41,948,355 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02987:Sorl1
|
APN |
9 |
41,952,349 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03005:Sorl1
|
APN |
9 |
41,968,621 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03069:Sorl1
|
APN |
9 |
41,902,722 (GRCm39) |
missense |
probably benign |
|
IGL03288:Sorl1
|
APN |
9 |
41,944,858 (GRCm39) |
splice site |
probably benign |
|
N/A - 287:Sorl1
|
UTSW |
9 |
41,952,892 (GRCm39) |
nonsense |
probably null |
|
PIT4151001:Sorl1
|
UTSW |
9 |
41,879,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R0117:Sorl1
|
UTSW |
9 |
41,944,873 (GRCm39) |
missense |
probably benign |
0.10 |
R0173:Sorl1
|
UTSW |
9 |
41,979,229 (GRCm39) |
missense |
probably damaging |
0.99 |
R0318:Sorl1
|
UTSW |
9 |
41,993,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R0385:Sorl1
|
UTSW |
9 |
41,943,205 (GRCm39) |
missense |
probably damaging |
0.99 |
R0448:Sorl1
|
UTSW |
9 |
41,915,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R0492:Sorl1
|
UTSW |
9 |
41,902,667 (GRCm39) |
missense |
probably null |
0.00 |
R0512:Sorl1
|
UTSW |
9 |
41,979,128 (GRCm39) |
missense |
probably benign |
0.01 |
R0587:Sorl1
|
UTSW |
9 |
41,895,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R0600:Sorl1
|
UTSW |
9 |
41,955,196 (GRCm39) |
splice site |
probably benign |
|
R0831:Sorl1
|
UTSW |
9 |
41,982,365 (GRCm39) |
splice site |
probably benign |
|
R0924:Sorl1
|
UTSW |
9 |
41,919,470 (GRCm39) |
splice site |
probably benign |
|
R1013:Sorl1
|
UTSW |
9 |
41,913,855 (GRCm39) |
missense |
probably benign |
0.00 |
R1053:Sorl1
|
UTSW |
9 |
41,902,752 (GRCm39) |
missense |
probably benign |
|
R1077:Sorl1
|
UTSW |
9 |
41,925,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R1326:Sorl1
|
UTSW |
9 |
41,943,092 (GRCm39) |
missense |
probably benign |
0.14 |
R1348:Sorl1
|
UTSW |
9 |
41,911,708 (GRCm39) |
splice site |
probably null |
|
R1498:Sorl1
|
UTSW |
9 |
41,952,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1671:Sorl1
|
UTSW |
9 |
41,885,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R1713:Sorl1
|
UTSW |
9 |
41,907,538 (GRCm39) |
missense |
probably benign |
0.06 |
R1738:Sorl1
|
UTSW |
9 |
42,001,261 (GRCm39) |
missense |
probably benign |
0.33 |
R1871:Sorl1
|
UTSW |
9 |
41,881,021 (GRCm39) |
nonsense |
probably null |
|
R1912:Sorl1
|
UTSW |
9 |
41,993,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R1952:Sorl1
|
UTSW |
9 |
41,957,920 (GRCm39) |
missense |
probably benign |
|
R2071:Sorl1
|
UTSW |
9 |
41,890,753 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2153:Sorl1
|
UTSW |
9 |
41,895,788 (GRCm39) |
missense |
probably benign |
0.01 |
R2417:Sorl1
|
UTSW |
9 |
41,892,007 (GRCm39) |
missense |
probably damaging |
0.96 |
R2429:Sorl1
|
UTSW |
9 |
41,948,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R2866:Sorl1
|
UTSW |
9 |
41,881,077 (GRCm39) |
missense |
probably benign |
|
R3815:Sorl1
|
UTSW |
9 |
41,975,345 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3816:Sorl1
|
UTSW |
9 |
41,975,345 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3817:Sorl1
|
UTSW |
9 |
41,975,345 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3819:Sorl1
|
UTSW |
9 |
41,975,345 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3890:Sorl1
|
UTSW |
9 |
41,915,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R3941:Sorl1
|
UTSW |
9 |
41,900,764 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4409:Sorl1
|
UTSW |
9 |
41,946,744 (GRCm39) |
missense |
probably damaging |
0.99 |
R4410:Sorl1
|
UTSW |
9 |
41,915,288 (GRCm39) |
nonsense |
probably null |
|
R4610:Sorl1
|
UTSW |
9 |
41,943,210 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4664:Sorl1
|
UTSW |
9 |
41,915,347 (GRCm39) |
missense |
probably damaging |
0.97 |
R4666:Sorl1
|
UTSW |
9 |
41,915,347 (GRCm39) |
missense |
probably damaging |
0.97 |
R4668:Sorl1
|
UTSW |
9 |
41,895,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R4823:Sorl1
|
UTSW |
9 |
41,903,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R4874:Sorl1
|
UTSW |
9 |
41,975,048 (GRCm39) |
missense |
probably damaging |
0.99 |
R4898:Sorl1
|
UTSW |
9 |
41,952,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R4922:Sorl1
|
UTSW |
9 |
41,925,746 (GRCm39) |
splice site |
probably null |
|
R4976:Sorl1
|
UTSW |
9 |
41,894,299 (GRCm39) |
missense |
probably benign |
0.00 |
R4984:Sorl1
|
UTSW |
9 |
41,902,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R5046:Sorl1
|
UTSW |
9 |
41,907,590 (GRCm39) |
missense |
probably benign |
|
R5070:Sorl1
|
UTSW |
9 |
41,943,114 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5084:Sorl1
|
UTSW |
9 |
41,887,673 (GRCm39) |
missense |
probably benign |
0.01 |
R5202:Sorl1
|
UTSW |
9 |
41,944,879 (GRCm39) |
missense |
probably benign |
0.00 |
R5265:Sorl1
|
UTSW |
9 |
42,017,812 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5275:Sorl1
|
UTSW |
9 |
41,942,198 (GRCm39) |
missense |
probably benign |
0.33 |
R5368:Sorl1
|
UTSW |
9 |
41,890,686 (GRCm39) |
missense |
probably benign |
0.00 |
R5385:Sorl1
|
UTSW |
9 |
41,968,580 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5386:Sorl1
|
UTSW |
9 |
41,968,580 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5416:Sorl1
|
UTSW |
9 |
41,913,932 (GRCm39) |
nonsense |
probably null |
|
R5518:Sorl1
|
UTSW |
9 |
41,948,508 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5545:Sorl1
|
UTSW |
9 |
41,902,921 (GRCm39) |
missense |
probably benign |
0.08 |
R5864:Sorl1
|
UTSW |
9 |
42,003,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R5865:Sorl1
|
UTSW |
9 |
41,894,330 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6339:Sorl1
|
UTSW |
9 |
41,881,038 (GRCm39) |
missense |
probably benign |
0.10 |
R6484:Sorl1
|
UTSW |
9 |
41,887,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R6505:Sorl1
|
UTSW |
9 |
41,982,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R6591:Sorl1
|
UTSW |
9 |
41,913,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R6596:Sorl1
|
UTSW |
9 |
41,912,899 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6654:Sorl1
|
UTSW |
9 |
41,891,941 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6691:Sorl1
|
UTSW |
9 |
41,913,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R6702:Sorl1
|
UTSW |
9 |
41,982,497 (GRCm39) |
missense |
probably damaging |
0.97 |
R6703:Sorl1
|
UTSW |
9 |
41,982,497 (GRCm39) |
missense |
probably damaging |
0.97 |
R6775:Sorl1
|
UTSW |
9 |
42,003,748 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6792:Sorl1
|
UTSW |
9 |
42,010,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R6852:Sorl1
|
UTSW |
9 |
41,935,694 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6860:Sorl1
|
UTSW |
9 |
41,933,688 (GRCm39) |
missense |
probably benign |
0.01 |
R6925:Sorl1
|
UTSW |
9 |
41,944,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R7022:Sorl1
|
UTSW |
9 |
41,881,047 (GRCm39) |
missense |
probably benign |
0.11 |
R7033:Sorl1
|
UTSW |
9 |
41,942,279 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7091:Sorl1
|
UTSW |
9 |
41,913,930 (GRCm39) |
missense |
probably benign |
0.00 |
R7267:Sorl1
|
UTSW |
9 |
42,035,375 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7269:Sorl1
|
UTSW |
9 |
41,948,499 (GRCm39) |
missense |
probably damaging |
0.99 |
R7272:Sorl1
|
UTSW |
9 |
41,975,006 (GRCm39) |
splice site |
probably null |
|
R7537:Sorl1
|
UTSW |
9 |
41,891,984 (GRCm39) |
missense |
probably benign |
0.01 |
R7615:Sorl1
|
UTSW |
9 |
41,888,878 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7636:Sorl1
|
UTSW |
9 |
42,003,630 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7727:Sorl1
|
UTSW |
9 |
41,895,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R7763:Sorl1
|
UTSW |
9 |
41,955,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R7831:Sorl1
|
UTSW |
9 |
42,001,257 (GRCm39) |
missense |
probably benign |
0.17 |
R7956:Sorl1
|
UTSW |
9 |
41,900,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R7964:Sorl1
|
UTSW |
9 |
41,902,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R7977:Sorl1
|
UTSW |
9 |
41,888,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R7987:Sorl1
|
UTSW |
9 |
41,888,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R8151:Sorl1
|
UTSW |
9 |
41,979,229 (GRCm39) |
missense |
probably damaging |
0.99 |
R8219:Sorl1
|
UTSW |
9 |
41,952,857 (GRCm39) |
splice site |
probably null |
|
R8261:Sorl1
|
UTSW |
9 |
41,925,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R8283:Sorl1
|
UTSW |
9 |
41,942,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R8308:Sorl1
|
UTSW |
9 |
41,929,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R8348:Sorl1
|
UTSW |
9 |
41,903,041 (GRCm39) |
missense |
probably benign |
0.35 |
R8448:Sorl1
|
UTSW |
9 |
41,903,041 (GRCm39) |
missense |
probably benign |
0.35 |
R8524:Sorl1
|
UTSW |
9 |
41,885,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R8869:Sorl1
|
UTSW |
9 |
41,933,722 (GRCm39) |
missense |
probably benign |
0.01 |
R8898:Sorl1
|
UTSW |
9 |
41,911,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R8972:Sorl1
|
UTSW |
9 |
41,957,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R9012:Sorl1
|
UTSW |
9 |
41,982,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R9094:Sorl1
|
UTSW |
9 |
41,975,050 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9241:Sorl1
|
UTSW |
9 |
41,885,420 (GRCm39) |
nonsense |
probably null |
|
R9278:Sorl1
|
UTSW |
9 |
41,957,857 (GRCm39) |
missense |
probably benign |
0.01 |
R9288:Sorl1
|
UTSW |
9 |
41,952,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R9303:Sorl1
|
UTSW |
9 |
41,900,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R9330:Sorl1
|
UTSW |
9 |
41,979,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R9332:Sorl1
|
UTSW |
9 |
41,912,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R9468:Sorl1
|
UTSW |
9 |
42,035,384 (GRCm39) |
missense |
probably benign |
0.20 |
R9528:Sorl1
|
UTSW |
9 |
41,933,631 (GRCm39) |
critical splice donor site |
probably null |
|
R9544:Sorl1
|
UTSW |
9 |
41,993,105 (GRCm39) |
nonsense |
probably null |
|
R9563:Sorl1
|
UTSW |
9 |
41,957,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Sorl1
|
UTSW |
9 |
41,957,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R9588:Sorl1
|
UTSW |
9 |
41,993,105 (GRCm39) |
nonsense |
probably null |
|
R9634:Sorl1
|
UTSW |
9 |
41,907,590 (GRCm39) |
missense |
probably benign |
|
R9671:Sorl1
|
UTSW |
9 |
41,943,077 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9701:Sorl1
|
UTSW |
9 |
42,003,766 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Sorl1
|
UTSW |
9 |
42,035,244 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Sorl1
|
UTSW |
9 |
42,010,499 (GRCm39) |
missense |
possibly damaging |
0.64 |
Z1177:Sorl1
|
UTSW |
9 |
42,017,837 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Sorl1
|
UTSW |
9 |
41,902,934 (GRCm39) |
missense |
possibly damaging |
0.92 |
Z1177:Sorl1
|
UTSW |
9 |
42,035,208 (GRCm39) |
missense |
probably damaging |
1.00 |
Z31818:Sorl1
|
UTSW |
9 |
41,952,892 (GRCm39) |
nonsense |
probably null |
|
|