Other mutations in this stock |
Total: 192 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700128F08Rik |
T |
A |
9: 8,222,174 (GRCm39) |
|
noncoding transcript |
Het |
4933409G03Rik |
A |
G |
2: 68,445,065 (GRCm39) |
|
probably benign |
Het |
Acan |
T |
C |
7: 78,748,357 (GRCm39) |
S1043P |
probably damaging |
Het |
Ackr2 |
A |
G |
9: 121,738,249 (GRCm39) |
Y208C |
probably damaging |
Het |
Actg1 |
C |
T |
11: 120,238,305 (GRCm39) |
|
probably benign |
Het |
Actmap |
T |
A |
7: 26,900,468 (GRCm39) |
M149K |
probably damaging |
Het |
Adam1a |
T |
A |
5: 121,657,497 (GRCm39) |
T599S |
probably benign |
Het |
Adamts12 |
A |
T |
15: 11,270,748 (GRCm39) |
S668C |
probably damaging |
Het |
Adcy8 |
A |
G |
15: 64,626,711 (GRCm39) |
V709A |
possibly damaging |
Het |
Adgrf2 |
A |
C |
17: 43,021,645 (GRCm39) |
I393S |
probably damaging |
Het |
Ahnak |
G |
T |
19: 8,984,665 (GRCm39) |
G1983V |
probably damaging |
Het |
Aim2 |
T |
A |
1: 173,291,442 (GRCm39) |
D282E |
possibly damaging |
Het |
Ak8 |
A |
G |
2: 28,650,083 (GRCm39) |
Y370C |
probably damaging |
Het |
Akap9 |
A |
G |
5: 4,063,901 (GRCm39) |
D1750G |
probably damaging |
Het |
Als2cl |
T |
A |
9: 110,718,204 (GRCm39) |
V315E |
probably damaging |
Het |
Ankrd28 |
A |
C |
14: 31,477,698 (GRCm39) |
C115G |
probably benign |
Het |
Ap3b2 |
C |
T |
7: 81,121,680 (GRCm39) |
A519T |
probably damaging |
Het |
Apool |
C |
T |
X: 111,281,897 (GRCm39) |
T166I |
probably damaging |
Het |
Arhgef2 |
A |
T |
3: 88,539,247 (GRCm39) |
K65* |
probably null |
Het |
Arhgef38 |
G |
T |
3: 132,838,030 (GRCm39) |
Y633* |
probably null |
Het |
Asah2 |
T |
C |
19: 31,972,758 (GRCm39) |
N659S |
probably benign |
Het |
Atf7ip2 |
A |
G |
16: 10,059,750 (GRCm39) |
D430G |
possibly damaging |
Het |
Atp8a1 |
G |
A |
5: 67,970,463 (GRCm39) |
S92L |
probably benign |
Het |
Bag4 |
C |
T |
8: 26,259,516 (GRCm39) |
A228T |
probably benign |
Het |
C130073F10Rik |
C |
A |
4: 101,747,907 (GRCm39) |
S89I |
probably benign |
Het |
Cacna1g |
T |
C |
11: 94,334,041 (GRCm39) |
T867A |
probably damaging |
Het |
Ccdc88a |
T |
G |
11: 29,435,906 (GRCm39) |
N1276K |
probably benign |
Het |
Cdc42bpg |
T |
A |
19: 6,361,221 (GRCm39) |
V282E |
probably damaging |
Het |
Cdipt |
T |
A |
7: 126,577,530 (GRCm39) |
L92H |
probably damaging |
Het |
Celsr2 |
T |
A |
3: 108,306,268 (GRCm39) |
D2012V |
probably damaging |
Het |
Cenpt |
A |
G |
8: 106,573,768 (GRCm39) |
V254A |
probably benign |
Het |
Cep104 |
T |
A |
4: 154,072,883 (GRCm39) |
D380E |
probably damaging |
Het |
Cers5 |
C |
T |
15: 99,639,518 (GRCm39) |
R123Q |
probably benign |
Het |
Ces2h |
A |
G |
8: 105,741,236 (GRCm39) |
E76G |
probably damaging |
Het |
Cfap77 |
T |
A |
2: 28,874,400 (GRCm39) |
E143D |
probably benign |
Het |
Chmp7 |
C |
A |
14: 69,969,745 (GRCm39) |
R65L |
probably damaging |
Het |
Cldnd2 |
T |
A |
7: 43,091,613 (GRCm39) |
C65S |
possibly damaging |
Het |
Clec2g |
C |
A |
6: 128,958,842 (GRCm39) |
Y142* |
probably null |
Het |
Coch |
A |
T |
12: 51,651,802 (GRCm39) |
E549V |
probably benign |
Het |
Cog7 |
T |
C |
7: 121,563,467 (GRCm39) |
D215G |
probably benign |
Het |
Col4a2 |
T |
C |
8: 11,464,779 (GRCm39) |
V348A |
probably benign |
Het |
Col4a2 |
A |
G |
8: 11,496,197 (GRCm39) |
H1606R |
probably benign |
Het |
Cpd |
T |
C |
11: 76,702,620 (GRCm39) |
N583D |
probably damaging |
Het |
Cyp2d11 |
T |
A |
15: 82,273,428 (GRCm39) |
Y481F |
probably benign |
Het |
D130043K22Rik |
T |
C |
13: 25,083,648 (GRCm39) |
S1038P |
probably damaging |
Het |
Deptor |
C |
A |
15: 55,044,406 (GRCm39) |
H191N |
probably benign |
Het |
Dgkz |
A |
T |
2: 91,768,684 (GRCm39) |
I699N |
probably damaging |
Het |
Dnah12 |
C |
T |
14: 26,503,741 (GRCm39) |
T1653I |
probably damaging |
Het |
Dnah7c |
T |
A |
1: 46,809,333 (GRCm39) |
N3550K |
probably damaging |
Het |
Dnah8 |
A |
G |
17: 30,994,035 (GRCm39) |
K3384R |
probably null |
Het |
Dnajc11 |
A |
G |
4: 152,055,424 (GRCm39) |
|
probably benign |
Het |
Dnajc13 |
CT |
C |
9: 104,064,004 (GRCm39) |
|
probably benign |
Het |
Dnhd1 |
C |
A |
7: 105,323,056 (GRCm39) |
N521K |
probably benign |
Het |
Drg2 |
T |
C |
11: 60,352,222 (GRCm39) |
|
probably null |
Het |
Dync1h1 |
C |
T |
12: 110,615,941 (GRCm39) |
Q3030* |
probably null |
Het |
Efhb |
G |
A |
17: 53,733,272 (GRCm39) |
T533I |
probably damaging |
Het |
Eif2d |
T |
C |
1: 131,092,464 (GRCm39) |
V374A |
probably damaging |
Het |
Etfb |
T |
C |
7: 43,093,624 (GRCm39) |
V17A |
probably damaging |
Het |
Fcho1 |
T |
C |
8: 72,169,439 (GRCm39) |
T156A |
probably benign |
Het |
Fn1 |
A |
T |
1: 71,641,671 (GRCm39) |
|
probably null |
Het |
Fnip2 |
A |
T |
3: 79,388,959 (GRCm39) |
S561T |
probably damaging |
Het |
Frs2 |
T |
A |
10: 116,909,998 (GRCm39) |
T455S |
probably benign |
Het |
Fry |
G |
A |
5: 150,309,472 (GRCm39) |
E639K |
|
Het |
Fto |
T |
A |
8: 92,136,342 (GRCm39) |
D205E |
probably damaging |
Het |
Galnt2l |
A |
G |
8: 122,997,013 (GRCm39) |
|
probably benign |
Het |
Galntl6 |
G |
A |
8: 58,880,847 (GRCm39) |
P147L |
probably damaging |
Het |
Gigyf1 |
T |
A |
5: 137,523,032 (GRCm39) |
D844E |
probably benign |
Het |
Gle1 |
T |
C |
2: 29,830,244 (GRCm39) |
S267P |
probably damaging |
Het |
Glg1 |
G |
A |
8: 111,914,387 (GRCm39) |
R466W |
probably damaging |
Het |
Gm10277 |
T |
C |
11: 77,676,923 (GRCm39) |
|
probably benign |
Het |
Gm6871 |
T |
C |
7: 41,196,173 (GRCm39) |
I39V |
probably benign |
Het |
Gm9970 |
A |
G |
5: 31,398,410 (GRCm39) |
|
probably benign |
Het |
Gpr35 |
T |
G |
1: 92,911,107 (GRCm39) |
I57S |
probably damaging |
Het |
Gprin1 |
C |
T |
13: 54,887,770 (GRCm39) |
G168E |
possibly damaging |
Het |
Gtdc1 |
A |
G |
2: 44,679,067 (GRCm39) |
|
probably benign |
Het |
Gtf3c2 |
G |
T |
5: 31,317,401 (GRCm39) |
P586T |
probably damaging |
Het |
Gucy1a2 |
A |
T |
9: 3,759,424 (GRCm39) |
H410L |
probably benign |
Het |
Gucy2c |
A |
G |
6: 136,744,150 (GRCm39) |
S150P |
probably damaging |
Het |
Ifi214 |
T |
C |
1: 173,354,157 (GRCm39) |
Q171R |
probably benign |
Het |
Ifit1bl1 |
T |
C |
19: 34,571,721 (GRCm39) |
I245M |
probably benign |
Het |
Igkv4-50 |
T |
C |
6: 69,677,984 (GRCm39) |
K40R |
probably benign |
Het |
Igkv8-18 |
T |
A |
6: 70,333,280 (GRCm39) |
I74N |
probably damaging |
Het |
Il2ra |
T |
A |
2: 11,681,731 (GRCm39) |
M112K |
probably benign |
Het |
Itpr2 |
A |
G |
6: 146,274,671 (GRCm39) |
F837S |
probably damaging |
Het |
Kbtbd7 |
T |
C |
14: 79,666,240 (GRCm39) |
*691Q |
probably null |
Het |
Kcnn2 |
T |
A |
18: 45,693,416 (GRCm39) |
S331T |
possibly damaging |
Het |
Khnyn |
T |
A |
14: 56,123,946 (GRCm39) |
|
probably null |
Het |
Kif26a |
G |
A |
12: 112,142,007 (GRCm39) |
A754T |
probably benign |
Het |
Klra3 |
T |
A |
6: 130,304,095 (GRCm39) |
Y199F |
possibly damaging |
Het |
Lhx2 |
A |
G |
2: 38,250,003 (GRCm39) |
K274R |
probably damaging |
Het |
Lrp2 |
T |
C |
2: 69,363,899 (GRCm39) |
I313V |
probably benign |
Het |
Lrrfip1 |
A |
T |
1: 91,043,369 (GRCm39) |
E591D |
probably benign |
Het |
Lrrk2 |
G |
A |
15: 91,649,950 (GRCm39) |
E1696K |
probably damaging |
Het |
Lrrk2 |
A |
C |
15: 91,573,052 (GRCm39) |
E200A |
probably damaging |
Het |
Mast4 |
A |
T |
13: 102,909,080 (GRCm39) |
M465K |
probably damaging |
Het |
Moxd2 |
T |
G |
6: 40,855,793 (GRCm39) |
I599L |
probably benign |
Het |
Mug2 |
T |
C |
6: 122,048,831 (GRCm39) |
S866P |
probably damaging |
Het |
Ncam2 |
A |
G |
16: 81,231,772 (GRCm39) |
T79A |
possibly damaging |
Het |
Ncoa6 |
C |
A |
2: 155,263,221 (GRCm39) |
Q404H |
probably damaging |
Het |
Neb |
A |
G |
2: 52,169,091 (GRCm39) |
Y1815H |
probably damaging |
Het |
Nell1 |
A |
G |
7: 50,505,965 (GRCm39) |
D724G |
probably damaging |
Het |
Nkx3-2 |
A |
G |
5: 41,919,487 (GRCm39) |
V167A |
probably benign |
Het |
Nsun3 |
C |
A |
16: 62,555,482 (GRCm39) |
C348F |
possibly damaging |
Het |
Obox6 |
A |
T |
7: 15,568,697 (GRCm39) |
S60T |
possibly damaging |
Het |
Oog2 |
T |
A |
4: 143,920,511 (GRCm39) |
|
probably benign |
Het |
Or10g9b |
A |
T |
9: 39,917,564 (GRCm39) |
I227N |
probably damaging |
Het |
Or11g2 |
T |
A |
14: 50,856,026 (GRCm39) |
C116S |
probably benign |
Het |
Or1ad6 |
G |
A |
11: 50,860,093 (GRCm39) |
V83M |
possibly damaging |
Het |
Or1e16 |
T |
C |
11: 73,286,521 (GRCm39) |
D109G |
probably benign |
Het |
Or2i1 |
T |
C |
17: 37,507,915 (GRCm39) |
T315A |
probably damaging |
Het |
Or2n1e |
T |
A |
17: 38,586,438 (GRCm39) |
Y259N |
probably damaging |
Het |
Or9s18 |
T |
C |
13: 65,300,467 (GRCm39) |
V143A |
possibly damaging |
Het |
Pabpc1 |
A |
T |
15: 36,599,528 (GRCm39) |
V389E |
probably benign |
Het |
Pank4 |
A |
T |
4: 155,055,847 (GRCm39) |
M291L |
probably benign |
Het |
Pcf11 |
T |
C |
7: 92,308,041 (GRCm39) |
D709G |
probably benign |
Het |
Pcgf1 |
T |
A |
6: 83,056,938 (GRCm39) |
|
probably benign |
Het |
Pcnx1 |
A |
G |
12: 82,042,525 (GRCm39) |
I2256V |
probably benign |
Het |
Pex6 |
A |
G |
17: 47,033,214 (GRCm39) |
D579G |
probably benign |
Het |
Pex6 |
A |
G |
17: 47,035,633 (GRCm39) |
|
probably null |
Het |
Piezo2 |
C |
T |
18: 63,163,472 (GRCm39) |
A2149T |
probably damaging |
Het |
Pik3c2g |
A |
G |
6: 139,881,711 (GRCm39) |
E781G |
probably benign |
Het |
Pik3r4 |
G |
A |
9: 105,555,375 (GRCm39) |
V1111I |
possibly damaging |
Het |
Pkd1l2 |
T |
A |
8: 117,722,581 (GRCm39) |
|
probably null |
Het |
Plekhg1 |
T |
A |
10: 3,907,506 (GRCm39) |
S808T |
probably benign |
Het |
Pnkp |
T |
A |
7: 44,509,878 (GRCm39) |
|
probably benign |
Het |
Polr3c |
A |
T |
3: 96,630,977 (GRCm39) |
F148I |
probably damaging |
Het |
Ppard |
A |
T |
17: 28,505,417 (GRCm39) |
T35S |
probably benign |
Het |
Ptov1 |
T |
C |
7: 44,516,533 (GRCm39) |
D134G |
probably benign |
Het |
Ptprz1 |
T |
A |
6: 23,002,609 (GRCm39) |
S1566R |
probably benign |
Het |
Pum1 |
T |
C |
4: 130,445,504 (GRCm39) |
S158P |
probably benign |
Het |
Qki |
T |
C |
17: 10,435,217 (GRCm39) |
H269R |
probably damaging |
Het |
Qrsl1 |
T |
C |
10: 43,752,659 (GRCm39) |
Y388C |
probably damaging |
Het |
Rapgef1 |
T |
G |
2: 29,579,172 (GRCm39) |
I182S |
probably damaging |
Het |
Ret |
T |
C |
6: 118,140,154 (GRCm39) |
S1013G |
possibly damaging |
Het |
Rimbp3 |
A |
G |
16: 17,028,465 (GRCm39) |
R630G |
possibly damaging |
Het |
Rnmt |
A |
T |
18: 68,451,031 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
A |
T |
13: 11,592,795 (GRCm39) |
M4653K |
possibly damaging |
Het |
Sacm1l |
G |
A |
9: 123,419,895 (GRCm39) |
V553I |
probably benign |
Het |
Sec31b |
A |
T |
19: 44,521,116 (GRCm39) |
S110T |
probably damaging |
Het |
Serpina3k |
G |
A |
12: 104,307,119 (GRCm39) |
G117D |
probably damaging |
Het |
Sesn2 |
T |
C |
4: 132,221,902 (GRCm39) |
Y410C |
probably damaging |
Het |
Slc24a1 |
G |
A |
9: 64,856,836 (GRCm39) |
R24C |
probably benign |
Het |
Slc35g2 |
A |
C |
9: 100,434,555 (GRCm39) |
V372G |
probably benign |
Het |
Slc7a7 |
T |
C |
14: 54,646,190 (GRCm39) |
Y91C |
probably damaging |
Het |
Slc7a9 |
T |
A |
7: 35,152,988 (GRCm39) |
Y135* |
probably null |
Het |
Slco1a7 |
A |
T |
6: 141,668,905 (GRCm39) |
M509K |
probably benign |
Het |
Slco4a1 |
A |
G |
2: 180,115,408 (GRCm39) |
N662D |
probably damaging |
Het |
Slfn4 |
T |
A |
11: 83,080,108 (GRCm39) |
|
probably benign |
Het |
Slmap |
T |
C |
14: 26,189,690 (GRCm39) |
N156S |
probably damaging |
Het |
Smim29 |
A |
G |
17: 27,784,244 (GRCm39) |
|
probably benign |
Het |
Snx18 |
A |
G |
13: 113,754,310 (GRCm39) |
S208P |
probably benign |
Het |
Sorbs1 |
T |
A |
19: 40,303,133 (GRCm39) |
R485S |
probably benign |
Het |
Spib |
A |
G |
7: 44,178,309 (GRCm39) |
S154P |
probably damaging |
Het |
Spty2d1 |
T |
C |
7: 46,645,858 (GRCm39) |
D595G |
probably damaging |
Het |
St7 |
T |
A |
6: 17,906,515 (GRCm39) |
|
probably null |
Het |
Susd1 |
T |
C |
4: 59,428,029 (GRCm39) |
T52A |
possibly damaging |
Het |
Svs5 |
T |
A |
2: 164,079,043 (GRCm39) |
D288V |
possibly damaging |
Het |
Syt7 |
T |
A |
19: 10,420,288 (GRCm39) |
I355N |
probably damaging |
Het |
Tarm1 |
G |
A |
7: 3,545,416 (GRCm39) |
Q145* |
probably null |
Het |
Teddm2 |
T |
A |
1: 153,726,487 (GRCm39) |
E76V |
probably damaging |
Het |
Thsd7b |
T |
C |
1: 129,540,923 (GRCm39) |
S343P |
probably damaging |
Het |
Tigd2 |
T |
A |
6: 59,188,400 (GRCm39) |
H422Q |
probably benign |
Het |
Tle1 |
T |
C |
4: 72,043,256 (GRCm39) |
N538D |
possibly damaging |
Het |
Tmc2 |
A |
G |
2: 130,103,317 (GRCm39) |
|
probably null |
Het |
Tmtc1 |
A |
C |
6: 148,186,478 (GRCm39) |
|
probably null |
Het |
Tns3 |
C |
T |
11: 8,400,986 (GRCm39) |
R1104H |
probably benign |
Het |
Trim6 |
T |
C |
7: 103,881,855 (GRCm39) |
Y369H |
probably damaging |
Het |
Triobp |
G |
A |
15: 78,851,313 (GRCm39) |
R489K |
probably damaging |
Het |
Trpv4 |
T |
C |
5: 114,760,814 (GRCm39) |
D732G |
possibly damaging |
Het |
Trrap |
G |
A |
5: 144,753,380 (GRCm39) |
V1883I |
probably damaging |
Het |
Tsc2 |
C |
A |
17: 24,822,249 (GRCm39) |
V1141F |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,730,171 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
T |
2: 76,773,355 (GRCm39) |
M2395K |
unknown |
Het |
Tyrp1 |
A |
T |
4: 80,763,172 (GRCm39) |
D353V |
possibly damaging |
Het |
Ubd |
A |
C |
17: 37,506,593 (GRCm39) |
T160P |
probably benign |
Het |
Ugt2b36 |
G |
T |
5: 87,229,397 (GRCm39) |
Y156* |
probably null |
Het |
Ulk4 |
G |
A |
9: 121,092,704 (GRCm39) |
R178* |
probably null |
Het |
Unc13d |
A |
G |
11: 115,964,408 (GRCm39) |
V312A |
possibly damaging |
Het |
Urb2 |
G |
T |
8: 124,755,636 (GRCm39) |
A448S |
probably damaging |
Het |
Urod |
G |
A |
4: 116,848,870 (GRCm39) |
A92V |
possibly damaging |
Het |
Vmn1r33 |
T |
A |
6: 66,588,803 (GRCm39) |
R250S |
probably benign |
Het |
Vmn1r87 |
A |
T |
7: 12,866,254 (GRCm39) |
M11K |
possibly damaging |
Het |
Vmn2r77 |
C |
T |
7: 86,450,195 (GRCm39) |
T147I |
probably benign |
Het |
Vstm4 |
A |
G |
14: 32,639,859 (GRCm39) |
K96E |
possibly damaging |
Het |
Vxn |
T |
C |
1: 9,677,201 (GRCm39) |
S24P |
probably benign |
Het |
Washc4 |
A |
T |
10: 83,410,343 (GRCm39) |
M644L |
probably benign |
Het |
Wwp1 |
T |
C |
4: 19,661,990 (GRCm39) |
D172G |
probably benign |
Het |
Zbtb38 |
A |
T |
9: 96,569,737 (GRCm39) |
V449E |
probably damaging |
Het |
Zfhx4 |
T |
C |
3: 5,279,867 (GRCm39) |
|
probably benign |
Het |
Zfp229 |
C |
T |
17: 21,964,267 (GRCm39) |
H166Y |
possibly damaging |
Het |
Zfp512b |
A |
G |
2: 181,230,532 (GRCm39) |
S453P |
probably benign |
Het |
Zp2 |
C |
A |
7: 119,737,343 (GRCm39) |
V282L |
probably damaging |
Het |
|
Other mutations in F5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00840:F5
|
APN |
1 |
164,007,093 (GRCm39) |
missense |
probably benign |
0.15 |
IGL00843:F5
|
APN |
1 |
164,039,360 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00904:F5
|
APN |
1 |
164,021,578 (GRCm39) |
missense |
probably benign |
|
IGL00913:F5
|
APN |
1 |
164,032,465 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01099:F5
|
APN |
1 |
164,021,903 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01134:F5
|
APN |
1 |
164,019,548 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01313:F5
|
APN |
1 |
164,021,181 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01635:F5
|
APN |
1 |
164,035,427 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01697:F5
|
APN |
1 |
164,021,621 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01768:F5
|
APN |
1 |
164,003,914 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01795:F5
|
APN |
1 |
164,021,959 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01835:F5
|
APN |
1 |
164,021,937 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01843:F5
|
APN |
1 |
164,039,395 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01989:F5
|
APN |
1 |
164,003,876 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02036:F5
|
APN |
1 |
164,010,571 (GRCm39) |
splice site |
probably benign |
|
IGL02065:F5
|
APN |
1 |
164,017,695 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02077:F5
|
APN |
1 |
164,026,435 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02139:F5
|
APN |
1 |
164,020,243 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02210:F5
|
APN |
1 |
164,017,710 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02415:F5
|
APN |
1 |
164,019,498 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02440:F5
|
APN |
1 |
164,034,635 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02471:F5
|
APN |
1 |
164,001,860 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02535:F5
|
APN |
1 |
164,026,302 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02537:F5
|
APN |
1 |
164,020,686 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02628:F5
|
APN |
1 |
164,021,644 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02638:F5
|
APN |
1 |
164,012,177 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02824:F5
|
APN |
1 |
164,021,916 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02977:F5
|
APN |
1 |
164,021,590 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03028:F5
|
APN |
1 |
164,020,569 (GRCm39) |
nonsense |
probably null |
|
IGL03064:F5
|
APN |
1 |
164,023,163 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03127:F5
|
APN |
1 |
164,021,107 (GRCm39) |
missense |
probably benign |
0.45 |
IGL03131:F5
|
APN |
1 |
163,989,388 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL03348:F5
|
APN |
1 |
164,021,721 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL03387:F5
|
APN |
1 |
164,020,801 (GRCm39) |
missense |
probably damaging |
1.00 |
James_dean
|
UTSW |
1 |
164,032,389 (GRCm39) |
missense |
probably benign |
0.43 |
BB002:F5
|
UTSW |
1 |
164,003,935 (GRCm39) |
critical splice donor site |
probably null |
|
BB012:F5
|
UTSW |
1 |
164,003,935 (GRCm39) |
critical splice donor site |
probably null |
|
R0002:F5
|
UTSW |
1 |
164,029,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R0095:F5
|
UTSW |
1 |
164,019,537 (GRCm39) |
nonsense |
probably null |
|
R0116:F5
|
UTSW |
1 |
164,012,483 (GRCm39) |
missense |
probably benign |
0.01 |
R0359:F5
|
UTSW |
1 |
164,007,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R0426:F5
|
UTSW |
1 |
164,010,409 (GRCm39) |
missense |
probably damaging |
0.99 |
R0452:F5
|
UTSW |
1 |
164,012,676 (GRCm39) |
missense |
probably damaging |
0.99 |
R0457:F5
|
UTSW |
1 |
164,021,769 (GRCm39) |
missense |
probably benign |
0.00 |
R0520:F5
|
UTSW |
1 |
164,037,156 (GRCm39) |
missense |
probably benign |
0.15 |
R0522:F5
|
UTSW |
1 |
164,039,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R0554:F5
|
UTSW |
1 |
164,007,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R0575:F5
|
UTSW |
1 |
164,003,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R0734:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R0739:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1062:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1063:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1149:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1149:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1150:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1151:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1152:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1221:F5
|
UTSW |
1 |
163,989,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R1284:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1286:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1358:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1360:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1362:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1383:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1465:F5
|
UTSW |
1 |
164,026,402 (GRCm39) |
missense |
probably benign |
0.02 |
R1465:F5
|
UTSW |
1 |
164,026,402 (GRCm39) |
missense |
probably benign |
0.02 |
R1545:F5
|
UTSW |
1 |
164,036,529 (GRCm39) |
nonsense |
probably null |
|
R1561:F5
|
UTSW |
1 |
164,014,472 (GRCm39) |
nonsense |
probably null |
|
R1623:F5
|
UTSW |
1 |
164,023,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R1662:F5
|
UTSW |
1 |
164,035,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R1673:F5
|
UTSW |
1 |
164,007,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R1689:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1705:F5
|
UTSW |
1 |
164,045,059 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1732:F5
|
UTSW |
1 |
164,001,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R1763:F5
|
UTSW |
1 |
164,020,104 (GRCm39) |
missense |
probably benign |
0.04 |
R1774:F5
|
UTSW |
1 |
164,020,104 (GRCm39) |
missense |
probably benign |
0.04 |
R1799:F5
|
UTSW |
1 |
164,021,100 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1800:F5
|
UTSW |
1 |
164,010,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R1842:F5
|
UTSW |
1 |
164,012,129 (GRCm39) |
missense |
probably damaging |
0.99 |
R1915:F5
|
UTSW |
1 |
164,010,486 (GRCm39) |
missense |
probably damaging |
0.97 |
R1926:F5
|
UTSW |
1 |
164,007,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R2025:F5
|
UTSW |
1 |
164,037,044 (GRCm39) |
missense |
probably benign |
0.05 |
R2198:F5
|
UTSW |
1 |
164,034,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R2258:F5
|
UTSW |
1 |
164,019,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R2264:F5
|
UTSW |
1 |
164,021,971 (GRCm39) |
missense |
probably benign |
0.32 |
R2281:F5
|
UTSW |
1 |
164,023,289 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2407:F5
|
UTSW |
1 |
164,039,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R2445:F5
|
UTSW |
1 |
164,017,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R2860:F5
|
UTSW |
1 |
164,012,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R2861:F5
|
UTSW |
1 |
164,012,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R2862:F5
|
UTSW |
1 |
164,012,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R2899:F5
|
UTSW |
1 |
164,014,469 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2910:F5
|
UTSW |
1 |
164,032,389 (GRCm39) |
missense |
probably benign |
0.43 |
R2912:F5
|
UTSW |
1 |
164,021,488 (GRCm39) |
missense |
probably damaging |
0.98 |
R2996:F5
|
UTSW |
1 |
164,010,486 (GRCm39) |
missense |
probably damaging |
0.97 |
R3745:F5
|
UTSW |
1 |
164,014,348 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3901:F5
|
UTSW |
1 |
164,003,798 (GRCm39) |
missense |
probably benign |
0.08 |
R3902:F5
|
UTSW |
1 |
164,003,798 (GRCm39) |
missense |
probably benign |
0.08 |
R4365:F5
|
UTSW |
1 |
164,012,519 (GRCm39) |
missense |
probably damaging |
0.98 |
R4448:F5
|
UTSW |
1 |
164,026,468 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4490:F5
|
UTSW |
1 |
164,044,964 (GRCm39) |
missense |
probably benign |
0.40 |
R4514:F5
|
UTSW |
1 |
163,979,566 (GRCm39) |
unclassified |
probably benign |
|
R4598:F5
|
UTSW |
1 |
164,032,366 (GRCm39) |
missense |
probably benign |
0.05 |
R4608:F5
|
UTSW |
1 |
164,036,598 (GRCm39) |
missense |
probably benign |
0.12 |
R4661:F5
|
UTSW |
1 |
164,012,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R4667:F5
|
UTSW |
1 |
164,001,755 (GRCm39) |
missense |
probably benign |
0.00 |
R4689:F5
|
UTSW |
1 |
163,979,542 (GRCm39) |
unclassified |
probably benign |
|
R4716:F5
|
UTSW |
1 |
164,021,488 (GRCm39) |
missense |
probably damaging |
0.98 |
R4733:F5
|
UTSW |
1 |
164,009,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R4854:F5
|
UTSW |
1 |
164,019,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R4908:F5
|
UTSW |
1 |
164,039,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R4971:F5
|
UTSW |
1 |
164,021,755 (GRCm39) |
missense |
probably benign |
|
R5001:F5
|
UTSW |
1 |
164,023,139 (GRCm39) |
missense |
probably benign |
0.00 |
R5042:F5
|
UTSW |
1 |
164,047,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R5056:F5
|
UTSW |
1 |
164,019,601 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5061:F5
|
UTSW |
1 |
164,021,749 (GRCm39) |
missense |
probably benign |
0.00 |
R5143:F5
|
UTSW |
1 |
164,039,397 (GRCm39) |
missense |
probably damaging |
0.98 |
R5622:F5
|
UTSW |
1 |
164,020,134 (GRCm39) |
missense |
probably benign |
0.09 |
R5626:F5
|
UTSW |
1 |
164,036,604 (GRCm39) |
missense |
probably damaging |
0.98 |
R5658:F5
|
UTSW |
1 |
164,019,907 (GRCm39) |
missense |
probably damaging |
0.96 |
R5702:F5
|
UTSW |
1 |
164,022,116 (GRCm39) |
nonsense |
probably null |
|
R5795:F5
|
UTSW |
1 |
163,979,578 (GRCm39) |
missense |
probably benign |
0.09 |
R5884:F5
|
UTSW |
1 |
164,023,215 (GRCm39) |
missense |
probably benign |
0.01 |
R6036:F5
|
UTSW |
1 |
164,012,565 (GRCm39) |
missense |
probably damaging |
0.99 |
R6036:F5
|
UTSW |
1 |
164,012,565 (GRCm39) |
missense |
probably damaging |
0.99 |
R6151:F5
|
UTSW |
1 |
164,017,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R6151:F5
|
UTSW |
1 |
164,009,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R6345:F5
|
UTSW |
1 |
164,019,520 (GRCm39) |
missense |
probably benign |
0.13 |
R6391:F5
|
UTSW |
1 |
164,021,062 (GRCm39) |
missense |
probably damaging |
0.99 |
R6542:F5
|
UTSW |
1 |
164,022,037 (GRCm39) |
missense |
probably benign |
0.32 |
R6620:F5
|
UTSW |
1 |
164,014,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R6750:F5
|
UTSW |
1 |
164,021,076 (GRCm39) |
missense |
possibly damaging |
0.58 |
R6754:F5
|
UTSW |
1 |
164,021,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R6774:F5
|
UTSW |
1 |
164,014,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R6802:F5
|
UTSW |
1 |
164,006,925 (GRCm39) |
missense |
probably damaging |
0.98 |
R6810:F5
|
UTSW |
1 |
164,014,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R6983:F5
|
UTSW |
1 |
164,021,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R7000:F5
|
UTSW |
1 |
164,007,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R7151:F5
|
UTSW |
1 |
164,029,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R7193:F5
|
UTSW |
1 |
164,046,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R7230:F5
|
UTSW |
1 |
164,012,522 (GRCm39) |
missense |
probably benign |
|
R7324:F5
|
UTSW |
1 |
164,021,150 (GRCm39) |
small deletion |
probably benign |
|
R7350:F5
|
UTSW |
1 |
164,020,277 (GRCm39) |
missense |
probably benign |
0.08 |
R7466:F5
|
UTSW |
1 |
164,020,897 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7503:F5
|
UTSW |
1 |
164,019,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R7626:F5
|
UTSW |
1 |
164,014,481 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7742:F5
|
UTSW |
1 |
164,035,453 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7837:F5
|
UTSW |
1 |
164,014,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R7848:F5
|
UTSW |
1 |
163,989,446 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7925:F5
|
UTSW |
1 |
164,003,935 (GRCm39) |
critical splice donor site |
probably null |
|
R8053:F5
|
UTSW |
1 |
164,020,338 (GRCm39) |
missense |
probably benign |
0.26 |
R8094:F5
|
UTSW |
1 |
164,036,509 (GRCm39) |
missense |
probably benign |
0.06 |
R8175:F5
|
UTSW |
1 |
164,019,834 (GRCm39) |
nonsense |
probably null |
|
R8209:F5
|
UTSW |
1 |
164,021,959 (GRCm39) |
missense |
probably benign |
0.00 |
R8226:F5
|
UTSW |
1 |
164,021,959 (GRCm39) |
missense |
probably benign |
0.00 |
R8266:F5
|
UTSW |
1 |
164,012,693 (GRCm39) |
critical splice donor site |
probably null |
|
R8517:F5
|
UTSW |
1 |
164,003,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R8684:F5
|
UTSW |
1 |
164,045,111 (GRCm39) |
missense |
probably benign |
0.01 |
R8941:F5
|
UTSW |
1 |
164,026,440 (GRCm39) |
missense |
probably benign |
0.19 |
R9130:F5
|
UTSW |
1 |
164,001,830 (GRCm39) |
missense |
probably benign |
0.37 |
R9181:F5
|
UTSW |
1 |
164,019,895 (GRCm39) |
missense |
probably benign |
0.00 |
R9186:F5
|
UTSW |
1 |
164,021,470 (GRCm39) |
missense |
probably benign |
|
R9233:F5
|
UTSW |
1 |
164,047,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R9314:F5
|
UTSW |
1 |
164,029,146 (GRCm39) |
missense |
probably benign |
0.01 |
R9631:F5
|
UTSW |
1 |
164,014,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R9655:F5
|
UTSW |
1 |
164,021,730 (GRCm39) |
missense |
probably benign |
0.15 |
X0024:F5
|
UTSW |
1 |
164,020,557 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:F5
|
UTSW |
1 |
163,981,954 (GRCm39) |
missense |
probably benign |
0.04 |
Z1176:F5
|
UTSW |
1 |
164,012,085 (GRCm39) |
missense |
probably damaging |
0.97 |
|