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 |
F5 |
C |
T |
1: 164,009,226 (GRCm39) |
T332M |
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 |
A |
C |
15: 91,573,052 (GRCm39) |
E200A |
probably damaging |
Het |
Lrrk2 |
G |
A |
15: 91,649,950 (GRCm39) |
E1696K |
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: 47,035,633 (GRCm39) |
|
probably null |
Het |
Pex6 |
A |
G |
17: 47,033,214 (GRCm39) |
D579G |
probably benign |
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 |
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 Ryr2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00518:Ryr2
|
APN |
13 |
11,848,978 (GRCm39) |
splice site |
probably benign |
|
IGL00757:Ryr2
|
APN |
13 |
11,633,490 (GRCm39) |
splice site |
probably null |
|
IGL00838:Ryr2
|
APN |
13 |
11,583,389 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00849:Ryr2
|
APN |
13 |
11,600,364 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL00987:Ryr2
|
APN |
13 |
11,750,388 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01096:Ryr2
|
APN |
13 |
11,718,430 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01313:Ryr2
|
APN |
13 |
11,653,371 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01349:Ryr2
|
APN |
13 |
11,602,125 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01391:Ryr2
|
APN |
13 |
11,571,571 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL01401:Ryr2
|
APN |
13 |
11,606,238 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01412:Ryr2
|
APN |
13 |
11,756,922 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01419:Ryr2
|
APN |
13 |
11,814,723 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL01432:Ryr2
|
APN |
13 |
11,866,090 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL01533:Ryr2
|
APN |
13 |
11,736,676 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01571:Ryr2
|
APN |
13 |
11,736,647 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01584:Ryr2
|
APN |
13 |
11,616,644 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01611:Ryr2
|
APN |
13 |
11,606,202 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01632:Ryr2
|
APN |
13 |
11,609,854 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01643:Ryr2
|
APN |
13 |
11,707,563 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01647:Ryr2
|
APN |
13 |
11,600,366 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01730:Ryr2
|
APN |
13 |
11,616,728 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01834:Ryr2
|
APN |
13 |
11,610,311 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01921:Ryr2
|
APN |
13 |
11,569,436 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL01937:Ryr2
|
APN |
13 |
11,805,249 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01945:Ryr2
|
APN |
13 |
11,805,249 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02027:Ryr2
|
APN |
13 |
11,611,998 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02060:Ryr2
|
APN |
13 |
11,762,450 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02065:Ryr2
|
APN |
13 |
11,587,143 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02084:Ryr2
|
APN |
13 |
11,807,648 (GRCm39) |
nonsense |
probably null |
|
IGL02086:Ryr2
|
APN |
13 |
11,750,442 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02095:Ryr2
|
APN |
13 |
11,774,645 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02100:Ryr2
|
APN |
13 |
11,752,759 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02122:Ryr2
|
APN |
13 |
11,756,755 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02202:Ryr2
|
APN |
13 |
11,745,274 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02202:Ryr2
|
APN |
13 |
11,762,544 (GRCm39) |
splice site |
probably benign |
|
IGL02369:Ryr2
|
APN |
13 |
11,634,382 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02383:Ryr2
|
APN |
13 |
11,737,607 (GRCm39) |
splice site |
probably benign |
|
IGL02400:Ryr2
|
APN |
13 |
11,620,130 (GRCm39) |
splice site |
probably benign |
|
IGL02423:Ryr2
|
APN |
13 |
11,760,084 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02425:Ryr2
|
APN |
13 |
11,760,560 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02458:Ryr2
|
APN |
13 |
11,720,585 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02602:Ryr2
|
APN |
13 |
11,569,397 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02694:Ryr2
|
APN |
13 |
11,620,075 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02726:Ryr2
|
APN |
13 |
11,753,206 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02747:Ryr2
|
APN |
13 |
11,670,563 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02795:Ryr2
|
APN |
13 |
11,610,076 (GRCm39) |
missense |
probably benign |
0.21 |
IGL02876:Ryr2
|
APN |
13 |
11,722,679 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02878:Ryr2
|
APN |
13 |
11,933,205 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02887:Ryr2
|
APN |
13 |
11,606,155 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02926:Ryr2
|
APN |
13 |
11,774,721 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03030:Ryr2
|
APN |
13 |
11,699,365 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03064:Ryr2
|
APN |
13 |
11,658,788 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03102:Ryr2
|
APN |
13 |
11,650,468 (GRCm39) |
splice site |
probably benign |
|
IGL03152:Ryr2
|
APN |
13 |
11,868,036 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03176:Ryr2
|
APN |
13 |
11,756,909 (GRCm39) |
nonsense |
probably null |
|
IGL03180:Ryr2
|
APN |
13 |
11,583,449 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03213:Ryr2
|
APN |
13 |
11,739,273 (GRCm39) |
splice site |
probably benign |
|
IGL03390:Ryr2
|
APN |
13 |
11,787,302 (GRCm39) |
missense |
probably benign |
|
IGL03410:Ryr2
|
APN |
13 |
11,603,033 (GRCm39) |
missense |
probably damaging |
0.99 |
Arruda
|
UTSW |
13 |
11,658,781 (GRCm39) |
missense |
probably damaging |
1.00 |
Arruda2
|
UTSW |
13 |
11,894,382 (GRCm39) |
missense |
probably damaging |
1.00 |
Arruda3
|
UTSW |
13 |
11,570,334 (GRCm39) |
missense |
possibly damaging |
0.91 |
barricuda
|
UTSW |
13 |
11,609,900 (GRCm39) |
missense |
probably benign |
0.06 |
BB006:Ryr2
|
UTSW |
13 |
11,705,181 (GRCm39) |
nonsense |
probably null |
|
BB006:Ryr2
|
UTSW |
13 |
11,609,680 (GRCm39) |
missense |
probably damaging |
1.00 |
BB016:Ryr2
|
UTSW |
13 |
11,705,181 (GRCm39) |
nonsense |
probably null |
|
BB016:Ryr2
|
UTSW |
13 |
11,609,680 (GRCm39) |
missense |
probably damaging |
1.00 |
H8562:Ryr2
|
UTSW |
13 |
11,732,027 (GRCm39) |
splice site |
probably benign |
|
IGL02799:Ryr2
|
UTSW |
13 |
11,680,848 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02991:Ryr2
|
UTSW |
13 |
11,776,192 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4142001:Ryr2
|
UTSW |
13 |
11,722,682 (GRCm39) |
missense |
probably damaging |
0.97 |
PIT4260001:Ryr2
|
UTSW |
13 |
11,609,641 (GRCm39) |
missense |
possibly damaging |
0.93 |
PIT4458001:Ryr2
|
UTSW |
13 |
11,570,334 (GRCm39) |
missense |
probably benign |
0.29 |
R0003:Ryr2
|
UTSW |
13 |
11,839,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R0004:Ryr2
|
UTSW |
13 |
11,680,805 (GRCm39) |
missense |
probably benign |
|
R0018:Ryr2
|
UTSW |
13 |
11,610,109 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0048:Ryr2
|
UTSW |
13 |
11,610,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R0048:Ryr2
|
UTSW |
13 |
11,610,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R0056:Ryr2
|
UTSW |
13 |
11,683,924 (GRCm39) |
missense |
probably damaging |
0.97 |
R0062:Ryr2
|
UTSW |
13 |
11,884,002 (GRCm39) |
critical splice donor site |
probably null |
|
R0062:Ryr2
|
UTSW |
13 |
11,884,002 (GRCm39) |
critical splice donor site |
probably null |
|
R0080:Ryr2
|
UTSW |
13 |
11,583,361 (GRCm39) |
missense |
probably damaging |
0.98 |
R0116:Ryr2
|
UTSW |
13 |
11,724,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R0148:Ryr2
|
UTSW |
13 |
11,729,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R0206:Ryr2
|
UTSW |
13 |
11,691,137 (GRCm39) |
splice site |
probably benign |
|
R0226:Ryr2
|
UTSW |
13 |
11,787,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R0285:Ryr2
|
UTSW |
13 |
11,731,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R0365:Ryr2
|
UTSW |
13 |
11,683,725 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0401:Ryr2
|
UTSW |
13 |
11,720,570 (GRCm39) |
missense |
probably benign |
0.45 |
R0415:Ryr2
|
UTSW |
13 |
11,884,042 (GRCm39) |
missense |
probably damaging |
0.97 |
R0418:Ryr2
|
UTSW |
13 |
11,848,981 (GRCm39) |
splice site |
probably benign |
|
R0558:Ryr2
|
UTSW |
13 |
11,814,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R0558:Ryr2
|
UTSW |
13 |
11,653,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R0574:Ryr2
|
UTSW |
13 |
11,746,555 (GRCm39) |
missense |
probably benign |
0.02 |
R0586:Ryr2
|
UTSW |
13 |
11,650,445 (GRCm39) |
missense |
probably null |
|
R0601:Ryr2
|
UTSW |
13 |
11,720,519 (GRCm39) |
critical splice donor site |
probably null |
|
R0610:Ryr2
|
UTSW |
13 |
11,637,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R0648:Ryr2
|
UTSW |
13 |
11,739,219 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0727:Ryr2
|
UTSW |
13 |
11,581,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R0743:Ryr2
|
UTSW |
13 |
11,569,415 (GRCm39) |
missense |
probably damaging |
0.99 |
R0821:Ryr2
|
UTSW |
13 |
11,753,012 (GRCm39) |
missense |
probably benign |
0.35 |
R0884:Ryr2
|
UTSW |
13 |
11,569,415 (GRCm39) |
missense |
probably damaging |
0.99 |
R1104:Ryr2
|
UTSW |
13 |
11,684,855 (GRCm39) |
missense |
probably damaging |
0.99 |
R1114:Ryr2
|
UTSW |
13 |
11,960,867 (GRCm39) |
missense |
probably damaging |
0.98 |
R1167:Ryr2
|
UTSW |
13 |
11,674,999 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1238:Ryr2
|
UTSW |
13 |
11,774,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R1239:Ryr2
|
UTSW |
13 |
11,897,929 (GRCm39) |
critical splice donor site |
probably null |
|
R1296:Ryr2
|
UTSW |
13 |
11,702,765 (GRCm39) |
splice site |
probably benign |
|
R1400:Ryr2
|
UTSW |
13 |
11,609,962 (GRCm39) |
missense |
probably benign |
0.08 |
R1439:Ryr2
|
UTSW |
13 |
11,729,389 (GRCm39) |
splice site |
probably benign |
|
R1443:Ryr2
|
UTSW |
13 |
11,794,152 (GRCm39) |
missense |
probably benign |
0.19 |
R1446:Ryr2
|
UTSW |
13 |
11,753,035 (GRCm39) |
missense |
probably benign |
0.09 |
R1458:Ryr2
|
UTSW |
13 |
11,741,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R1497:Ryr2
|
UTSW |
13 |
11,616,727 (GRCm39) |
missense |
probably damaging |
0.99 |
R1505:Ryr2
|
UTSW |
13 |
11,569,478 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1548:Ryr2
|
UTSW |
13 |
11,569,435 (GRCm39) |
nonsense |
probably null |
|
R1551:Ryr2
|
UTSW |
13 |
11,800,029 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1567:Ryr2
|
UTSW |
13 |
11,774,563 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1581:Ryr2
|
UTSW |
13 |
11,809,449 (GRCm39) |
missense |
probably benign |
0.01 |
R1645:Ryr2
|
UTSW |
13 |
11,733,368 (GRCm39) |
nonsense |
probably null |
|
R1686:Ryr2
|
UTSW |
13 |
11,618,665 (GRCm39) |
splice site |
probably benign |
|
R1696:Ryr2
|
UTSW |
13 |
11,746,543 (GRCm39) |
missense |
probably benign |
0.02 |
R1708:Ryr2
|
UTSW |
13 |
11,602,328 (GRCm39) |
splice site |
probably null |
|
R1728:Ryr2
|
UTSW |
13 |
11,602,308 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1745:Ryr2
|
UTSW |
13 |
11,805,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R1771:Ryr2
|
UTSW |
13 |
11,760,062 (GRCm39) |
critical splice donor site |
probably null |
|
R1776:Ryr2
|
UTSW |
13 |
11,760,062 (GRCm39) |
critical splice donor site |
probably null |
|
R1783:Ryr2
|
UTSW |
13 |
11,715,257 (GRCm39) |
nonsense |
probably null |
|
R1801:Ryr2
|
UTSW |
13 |
11,610,167 (GRCm39) |
missense |
probably benign |
0.01 |
R1812:Ryr2
|
UTSW |
13 |
11,575,472 (GRCm39) |
missense |
probably damaging |
0.97 |
R1820:Ryr2
|
UTSW |
13 |
11,602,202 (GRCm39) |
missense |
probably damaging |
0.99 |
R1835:Ryr2
|
UTSW |
13 |
11,784,764 (GRCm39) |
missense |
probably benign |
0.06 |
R1868:Ryr2
|
UTSW |
13 |
11,746,586 (GRCm39) |
missense |
probably benign |
0.02 |
R1869:Ryr2
|
UTSW |
13 |
11,676,961 (GRCm39) |
missense |
probably damaging |
0.98 |
R1884:Ryr2
|
UTSW |
13 |
11,753,242 (GRCm39) |
missense |
probably damaging |
0.97 |
R1892:Ryr2
|
UTSW |
13 |
11,673,844 (GRCm39) |
nonsense |
probably null |
|
R1897:Ryr2
|
UTSW |
13 |
11,765,818 (GRCm39) |
missense |
probably benign |
0.09 |
R1899:Ryr2
|
UTSW |
13 |
11,606,222 (GRCm39) |
missense |
probably benign |
|
R1909:Ryr2
|
UTSW |
13 |
11,715,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R1918:Ryr2
|
UTSW |
13 |
11,571,584 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1937:Ryr2
|
UTSW |
13 |
11,683,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R1943:Ryr2
|
UTSW |
13 |
11,746,609 (GRCm39) |
missense |
probably benign |
0.10 |
R1956:Ryr2
|
UTSW |
13 |
11,695,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R1983:Ryr2
|
UTSW |
13 |
11,600,288 (GRCm39) |
splice site |
probably null |
|
R2018:Ryr2
|
UTSW |
13 |
11,866,074 (GRCm39) |
missense |
possibly damaging |
0.59 |
R2019:Ryr2
|
UTSW |
13 |
11,866,074 (GRCm39) |
missense |
possibly damaging |
0.59 |
R2060:Ryr2
|
UTSW |
13 |
11,610,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R2061:Ryr2
|
UTSW |
13 |
11,680,764 (GRCm39) |
splice site |
probably null |
|
R2088:Ryr2
|
UTSW |
13 |
11,677,115 (GRCm39) |
missense |
probably benign |
0.04 |
R2089:Ryr2
|
UTSW |
13 |
11,960,863 (GRCm39) |
missense |
probably benign |
0.23 |
R2091:Ryr2
|
UTSW |
13 |
11,960,863 (GRCm39) |
missense |
probably benign |
0.23 |
R2091:Ryr2
|
UTSW |
13 |
11,960,863 (GRCm39) |
missense |
probably benign |
0.23 |
R2127:Ryr2
|
UTSW |
13 |
11,727,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R2140:Ryr2
|
UTSW |
13 |
11,575,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R2153:Ryr2
|
UTSW |
13 |
11,592,759 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2179:Ryr2
|
UTSW |
13 |
11,720,679 (GRCm39) |
nonsense |
probably null |
|
R2207:Ryr2
|
UTSW |
13 |
11,825,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R2237:Ryr2
|
UTSW |
13 |
11,677,146 (GRCm39) |
missense |
probably benign |
0.18 |
R2258:Ryr2
|
UTSW |
13 |
11,753,102 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2312:Ryr2
|
UTSW |
13 |
11,753,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R2421:Ryr2
|
UTSW |
13 |
11,606,123 (GRCm39) |
missense |
probably damaging |
0.98 |
R2438:Ryr2
|
UTSW |
13 |
11,816,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R2483:Ryr2
|
UTSW |
13 |
11,774,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R2860:Ryr2
|
UTSW |
13 |
11,607,979 (GRCm39) |
missense |
probably damaging |
0.98 |
R2861:Ryr2
|
UTSW |
13 |
11,607,979 (GRCm39) |
missense |
probably damaging |
0.98 |
R2867:Ryr2
|
UTSW |
13 |
11,776,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R2867:Ryr2
|
UTSW |
13 |
11,776,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R3618:Ryr2
|
UTSW |
13 |
11,787,466 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3876:Ryr2
|
UTSW |
13 |
11,603,045 (GRCm39) |
missense |
probably damaging |
0.99 |
R3906:Ryr2
|
UTSW |
13 |
11,753,095 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3912:Ryr2
|
UTSW |
13 |
11,787,313 (GRCm39) |
missense |
probably damaging |
0.99 |
R4018:Ryr2
|
UTSW |
13 |
11,933,300 (GRCm39) |
missense |
probably damaging |
1.00 |
R4114:Ryr2
|
UTSW |
13 |
11,707,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R4119:Ryr2
|
UTSW |
13 |
11,794,153 (GRCm39) |
missense |
probably benign |
0.22 |
R4127:Ryr2
|
UTSW |
13 |
11,602,323 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4222:Ryr2
|
UTSW |
13 |
11,752,759 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4233:Ryr2
|
UTSW |
13 |
11,765,611 (GRCm39) |
missense |
probably benign |
0.20 |
R4355:Ryr2
|
UTSW |
13 |
11,664,698 (GRCm39) |
missense |
probably benign |
0.05 |
R4384:Ryr2
|
UTSW |
13 |
11,620,119 (GRCm39) |
missense |
probably damaging |
0.99 |
R4422:Ryr2
|
UTSW |
13 |
11,731,952 (GRCm39) |
nonsense |
probably null |
|
R4430:Ryr2
|
UTSW |
13 |
11,750,413 (GRCm39) |
missense |
probably damaging |
0.98 |
R4624:Ryr2
|
UTSW |
13 |
12,121,301 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4663:Ryr2
|
UTSW |
13 |
11,764,395 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4665:Ryr2
|
UTSW |
13 |
11,765,571 (GRCm39) |
splice site |
probably null |
|
R4668:Ryr2
|
UTSW |
13 |
11,608,003 (GRCm39) |
missense |
probably benign |
|
R4677:Ryr2
|
UTSW |
13 |
11,721,553 (GRCm39) |
missense |
probably damaging |
0.98 |
R4679:Ryr2
|
UTSW |
13 |
11,839,255 (GRCm39) |
missense |
probably benign |
0.34 |
R4680:Ryr2
|
UTSW |
13 |
11,610,119 (GRCm39) |
missense |
probably benign |
0.04 |
R4685:Ryr2
|
UTSW |
13 |
11,707,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R4709:Ryr2
|
UTSW |
13 |
11,731,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R4731:Ryr2
|
UTSW |
13 |
11,592,795 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4733:Ryr2
|
UTSW |
13 |
11,592,795 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4734:Ryr2
|
UTSW |
13 |
11,752,639 (GRCm39) |
missense |
probably damaging |
0.99 |
R4740:Ryr2
|
UTSW |
13 |
11,671,933 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4801:Ryr2
|
UTSW |
13 |
11,702,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Ryr2
|
UTSW |
13 |
11,723,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R4802:Ryr2
|
UTSW |
13 |
11,702,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R4802:Ryr2
|
UTSW |
13 |
11,723,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R4804:Ryr2
|
UTSW |
13 |
11,731,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R4811:Ryr2
|
UTSW |
13 |
11,670,584 (GRCm39) |
missense |
probably damaging |
0.97 |
R4850:Ryr2
|
UTSW |
13 |
11,760,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R4850:Ryr2
|
UTSW |
13 |
11,683,706 (GRCm39) |
missense |
probably damaging |
0.99 |
R4880:Ryr2
|
UTSW |
13 |
11,767,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R4917:Ryr2
|
UTSW |
13 |
11,609,872 (GRCm39) |
missense |
probably damaging |
0.96 |
R4918:Ryr2
|
UTSW |
13 |
11,609,872 (GRCm39) |
missense |
probably damaging |
0.96 |
R4922:Ryr2
|
UTSW |
13 |
11,724,849 (GRCm39) |
missense |
probably damaging |
0.99 |
R4933:Ryr2
|
UTSW |
13 |
11,960,831 (GRCm39) |
missense |
probably damaging |
0.96 |
R4950:Ryr2
|
UTSW |
13 |
11,756,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R4957:Ryr2
|
UTSW |
13 |
11,799,966 (GRCm39) |
missense |
probably damaging |
0.97 |
R4964:Ryr2
|
UTSW |
13 |
11,848,878 (GRCm39) |
missense |
probably benign |
0.00 |
R4964:Ryr2
|
UTSW |
13 |
11,729,497 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4966:Ryr2
|
UTSW |
13 |
11,729,497 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4966:Ryr2
|
UTSW |
13 |
11,848,878 (GRCm39) |
missense |
probably benign |
0.00 |
R4997:Ryr2
|
UTSW |
13 |
11,610,192 (GRCm39) |
missense |
probably benign |
0.09 |
R4998:Ryr2
|
UTSW |
13 |
11,658,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R5033:Ryr2
|
UTSW |
13 |
11,602,140 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5061:Ryr2
|
UTSW |
13 |
11,650,422 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5062:Ryr2
|
UTSW |
13 |
11,715,240 (GRCm39) |
missense |
probably damaging |
0.97 |
R5088:Ryr2
|
UTSW |
13 |
11,727,129 (GRCm39) |
nonsense |
probably null |
|
R5135:Ryr2
|
UTSW |
13 |
11,677,016 (GRCm39) |
missense |
probably benign |
0.05 |
R5138:Ryr2
|
UTSW |
13 |
11,675,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R5168:Ryr2
|
UTSW |
13 |
11,767,207 (GRCm39) |
missense |
probably benign |
|
R5187:Ryr2
|
UTSW |
13 |
11,787,338 (GRCm39) |
missense |
probably damaging |
0.99 |
R5197:Ryr2
|
UTSW |
13 |
11,653,316 (GRCm39) |
critical splice donor site |
probably null |
|
R5262:Ryr2
|
UTSW |
13 |
11,787,323 (GRCm39) |
missense |
probably damaging |
0.99 |
R5325:Ryr2
|
UTSW |
13 |
11,705,249 (GRCm39) |
missense |
probably damaging |
0.97 |
R5381:Ryr2
|
UTSW |
13 |
11,571,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R5437:Ryr2
|
UTSW |
13 |
11,670,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R5477:Ryr2
|
UTSW |
13 |
11,720,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R5497:Ryr2
|
UTSW |
13 |
11,720,587 (GRCm39) |
missense |
probably null |
0.15 |
R5509:Ryr2
|
UTSW |
13 |
11,760,487 (GRCm39) |
missense |
probably damaging |
0.98 |
R5518:Ryr2
|
UTSW |
13 |
11,702,795 (GRCm39) |
missense |
probably benign |
0.01 |
R5571:Ryr2
|
UTSW |
13 |
11,570,334 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5591:Ryr2
|
UTSW |
13 |
11,609,900 (GRCm39) |
missense |
probably benign |
0.06 |
R5619:Ryr2
|
UTSW |
13 |
11,723,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R5630:Ryr2
|
UTSW |
13 |
11,616,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R5644:Ryr2
|
UTSW |
13 |
11,610,468 (GRCm39) |
missense |
probably damaging |
0.99 |
R5667:Ryr2
|
UTSW |
13 |
11,774,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R5775:Ryr2
|
UTSW |
13 |
11,784,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R5836:Ryr2
|
UTSW |
13 |
11,618,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R5858:Ryr2
|
UTSW |
13 |
11,575,460 (GRCm39) |
missense |
probably damaging |
0.99 |
R5934:Ryr2
|
UTSW |
13 |
11,599,040 (GRCm39) |
missense |
probably damaging |
0.96 |
R5939:Ryr2
|
UTSW |
13 |
11,805,218 (GRCm39) |
missense |
probably damaging |
0.99 |
R5941:Ryr2
|
UTSW |
13 |
11,702,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R5945:Ryr2
|
UTSW |
13 |
11,675,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R5946:Ryr2
|
UTSW |
13 |
11,741,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R5966:Ryr2
|
UTSW |
13 |
11,677,124 (GRCm39) |
nonsense |
probably null |
|
R5974:Ryr2
|
UTSW |
13 |
11,729,397 (GRCm39) |
splice site |
probably null |
|
R6104:Ryr2
|
UTSW |
13 |
11,814,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R6118:Ryr2
|
UTSW |
13 |
11,807,575 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6149:Ryr2
|
UTSW |
13 |
11,683,903 (GRCm39) |
missense |
probably benign |
|
R6208:Ryr2
|
UTSW |
13 |
11,910,106 (GRCm39) |
missense |
probably benign |
0.04 |
R6217:Ryr2
|
UTSW |
13 |
11,848,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R6230:Ryr2
|
UTSW |
13 |
11,674,993 (GRCm39) |
missense |
probably damaging |
0.99 |
R6279:Ryr2
|
UTSW |
13 |
11,695,885 (GRCm39) |
missense |
probably damaging |
0.97 |
R6294:Ryr2
|
UTSW |
13 |
11,894,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R6300:Ryr2
|
UTSW |
13 |
11,695,885 (GRCm39) |
missense |
probably damaging |
0.97 |
R6350:Ryr2
|
UTSW |
13 |
11,776,282 (GRCm39) |
missense |
probably damaging |
0.98 |
R6484:Ryr2
|
UTSW |
13 |
11,677,269 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6489:Ryr2
|
UTSW |
13 |
11,848,893 (GRCm39) |
missense |
probably benign |
0.29 |
R6548:Ryr2
|
UTSW |
13 |
11,683,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R6591:Ryr2
|
UTSW |
13 |
11,609,609 (GRCm39) |
missense |
probably benign |
0.01 |
R6623:Ryr2
|
UTSW |
13 |
11,724,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R6649:Ryr2
|
UTSW |
13 |
11,610,529 (GRCm39) |
missense |
probably damaging |
0.99 |
R6691:Ryr2
|
UTSW |
13 |
11,609,609 (GRCm39) |
missense |
probably benign |
0.01 |
R6770:Ryr2
|
UTSW |
13 |
11,753,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R6802:Ryr2
|
UTSW |
13 |
11,701,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R6809:Ryr2
|
UTSW |
13 |
11,741,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R6893:Ryr2
|
UTSW |
13 |
11,844,540 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6911:Ryr2
|
UTSW |
13 |
11,842,445 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6915:Ryr2
|
UTSW |
13 |
11,760,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R6943:Ryr2
|
UTSW |
13 |
11,581,834 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6960:Ryr2
|
UTSW |
13 |
11,816,129 (GRCm39) |
missense |
probably benign |
0.28 |
R6997:Ryr2
|
UTSW |
13 |
11,669,266 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6998:Ryr2
|
UTSW |
13 |
11,727,052 (GRCm39) |
missense |
probably damaging |
0.99 |
R7001:Ryr2
|
UTSW |
13 |
11,809,491 (GRCm39) |
missense |
probably damaging |
0.98 |
R7047:Ryr2
|
UTSW |
13 |
11,839,286 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7089:Ryr2
|
UTSW |
13 |
11,664,662 (GRCm39) |
missense |
probably benign |
0.10 |
R7125:Ryr2
|
UTSW |
13 |
11,684,873 (GRCm39) |
missense |
probably damaging |
0.99 |
R7127:Ryr2
|
UTSW |
13 |
11,670,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R7131:Ryr2
|
UTSW |
13 |
11,683,697 (GRCm39) |
critical splice donor site |
probably null |
|
R7131:Ryr2
|
UTSW |
13 |
11,655,213 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7159:Ryr2
|
UTSW |
13 |
11,825,794 (GRCm39) |
missense |
probably damaging |
0.99 |
R7174:Ryr2
|
UTSW |
13 |
11,816,063 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7180:Ryr2
|
UTSW |
13 |
11,701,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R7182:Ryr2
|
UTSW |
13 |
11,774,643 (GRCm39) |
missense |
probably benign |
|
R7189:Ryr2
|
UTSW |
13 |
11,898,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R7241:Ryr2
|
UTSW |
13 |
11,680,799 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7244:Ryr2
|
UTSW |
13 |
11,612,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R7326:Ryr2
|
UTSW |
13 |
11,753,080 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7331:Ryr2
|
UTSW |
13 |
11,760,517 (GRCm39) |
missense |
probably benign |
|
R7365:Ryr2
|
UTSW |
13 |
11,655,161 (GRCm39) |
missense |
probably damaging |
0.99 |
R7372:Ryr2
|
UTSW |
13 |
11,695,885 (GRCm39) |
missense |
probably damaging |
0.97 |
R7395:Ryr2
|
UTSW |
13 |
11,799,997 (GRCm39) |
missense |
probably damaging |
0.98 |
R7404:Ryr2
|
UTSW |
13 |
11,750,506 (GRCm39) |
missense |
probably damaging |
0.97 |
R7417:Ryr2
|
UTSW |
13 |
11,571,634 (GRCm39) |
splice site |
probably null |
|
R7425:Ryr2
|
UTSW |
13 |
11,720,530 (GRCm39) |
missense |
probably benign |
0.20 |
R7444:Ryr2
|
UTSW |
13 |
11,570,349 (GRCm39) |
missense |
probably benign |
0.25 |
R7456:Ryr2
|
UTSW |
13 |
11,767,168 (GRCm39) |
missense |
probably benign |
|
R7460:Ryr2
|
UTSW |
13 |
11,720,596 (GRCm39) |
missense |
probably benign |
0.10 |
R7474:Ryr2
|
UTSW |
13 |
11,609,762 (GRCm39) |
missense |
probably benign |
0.04 |
R7543:Ryr2
|
UTSW |
13 |
11,653,317 (GRCm39) |
critical splice donor site |
probably null |
|
R7549:Ryr2
|
UTSW |
13 |
11,752,871 (GRCm39) |
missense |
probably benign |
0.15 |
R7558:Ryr2
|
UTSW |
13 |
11,814,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R7565:Ryr2
|
UTSW |
13 |
11,575,539 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7627:Ryr2
|
UTSW |
13 |
11,776,213 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7698:Ryr2
|
UTSW |
13 |
11,776,201 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7702:Ryr2
|
UTSW |
13 |
11,705,219 (GRCm39) |
missense |
probably damaging |
0.99 |
R7719:Ryr2
|
UTSW |
13 |
11,745,229 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7772:Ryr2
|
UTSW |
13 |
11,765,897 (GRCm39) |
missense |
probably benign |
|
R7797:Ryr2
|
UTSW |
13 |
11,816,066 (GRCm39) |
missense |
probably damaging |
0.99 |
R7829:Ryr2
|
UTSW |
13 |
11,842,493 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7855:Ryr2
|
UTSW |
13 |
11,721,509 (GRCm39) |
nonsense |
probably null |
|
R7872:Ryr2
|
UTSW |
13 |
11,610,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R7908:Ryr2
|
UTSW |
13 |
11,807,634 (GRCm39) |
missense |
probably benign |
0.01 |
R7929:Ryr2
|
UTSW |
13 |
11,609,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R7929:Ryr2
|
UTSW |
13 |
11,705,181 (GRCm39) |
nonsense |
probably null |
|
R7952:Ryr2
|
UTSW |
13 |
11,661,313 (GRCm39) |
splice site |
probably null |
|
R8008:Ryr2
|
UTSW |
13 |
11,671,980 (GRCm39) |
missense |
probably benign |
0.30 |
R8011:Ryr2
|
UTSW |
13 |
11,603,026 (GRCm39) |
critical splice donor site |
probably null |
|
R8097:Ryr2
|
UTSW |
13 |
11,960,881 (GRCm39) |
missense |
probably damaging |
0.98 |
R8133:Ryr2
|
UTSW |
13 |
11,618,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R8253:Ryr2
|
UTSW |
13 |
11,842,439 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8278:Ryr2
|
UTSW |
13 |
11,610,392 (GRCm39) |
nonsense |
probably null |
|
R8351:Ryr2
|
UTSW |
13 |
11,814,718 (GRCm39) |
missense |
probably damaging |
0.98 |
R8401:Ryr2
|
UTSW |
13 |
11,683,821 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8403:Ryr2
|
UTSW |
13 |
11,699,364 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8431:Ryr2
|
UTSW |
13 |
11,673,894 (GRCm39) |
missense |
probably benign |
0.00 |
R8509:Ryr2
|
UTSW |
13 |
11,592,664 (GRCm39) |
critical splice donor site |
probably null |
|
R8551:Ryr2
|
UTSW |
13 |
11,575,479 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8684:Ryr2
|
UTSW |
13 |
11,702,875 (GRCm39) |
missense |
probably damaging |
0.99 |
R8735:Ryr2
|
UTSW |
13 |
11,701,833 (GRCm39) |
missense |
probably damaging |
0.97 |
R8766:Ryr2
|
UTSW |
13 |
11,683,855 (GRCm39) |
missense |
probably damaging |
0.97 |
R8817:Ryr2
|
UTSW |
13 |
11,750,509 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8827:Ryr2
|
UTSW |
13 |
11,572,934 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8884:Ryr2
|
UTSW |
13 |
11,794,152 (GRCm39) |
missense |
probably benign |
0.19 |
R8889:Ryr2
|
UTSW |
13 |
11,799,990 (GRCm39) |
missense |
probably damaging |
0.99 |
R8891:Ryr2
|
UTSW |
13 |
11,814,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R8979:Ryr2
|
UTSW |
13 |
11,609,924 (GRCm39) |
missense |
probably benign |
0.00 |
R9013:Ryr2
|
UTSW |
13 |
11,618,618 (GRCm39) |
missense |
probably damaging |
0.98 |
R9040:Ryr2
|
UTSW |
13 |
11,609,672 (GRCm39) |
missense |
probably damaging |
0.97 |
R9044:Ryr2
|
UTSW |
13 |
11,752,989 (GRCm39) |
nonsense |
probably null |
|
R9056:Ryr2
|
UTSW |
13 |
11,610,817 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9084:Ryr2
|
UTSW |
13 |
11,616,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R9113:Ryr2
|
UTSW |
13 |
11,618,741 (GRCm39) |
intron |
probably benign |
|
R9116:Ryr2
|
UTSW |
13 |
11,587,185 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9125:Ryr2
|
UTSW |
13 |
11,669,292 (GRCm39) |
missense |
probably benign |
0.28 |
R9148:Ryr2
|
UTSW |
13 |
11,900,424 (GRCm39) |
missense |
probably benign |
0.02 |
R9210:Ryr2
|
UTSW |
13 |
11,844,560 (GRCm39) |
missense |
probably damaging |
0.99 |
R9212:Ryr2
|
UTSW |
13 |
11,844,560 (GRCm39) |
missense |
probably damaging |
0.99 |
R9233:Ryr2
|
UTSW |
13 |
11,610,772 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9254:Ryr2
|
UTSW |
13 |
11,898,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R9262:Ryr2
|
UTSW |
13 |
11,765,854 (GRCm39) |
missense |
probably damaging |
0.97 |
R9275:Ryr2
|
UTSW |
13 |
11,897,976 (GRCm39) |
missense |
probably benign |
0.10 |
R9278:Ryr2
|
UTSW |
13 |
11,897,976 (GRCm39) |
missense |
probably benign |
0.10 |
R9309:Ryr2
|
UTSW |
13 |
11,721,578 (GRCm39) |
missense |
probably damaging |
0.99 |
R9379:Ryr2
|
UTSW |
13 |
11,898,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R9409:Ryr2
|
UTSW |
13 |
11,695,973 (GRCm39) |
missense |
probably damaging |
0.99 |
R9429:Ryr2
|
UTSW |
13 |
11,809,459 (GRCm39) |
missense |
probably damaging |
0.97 |
R9445:Ryr2
|
UTSW |
13 |
11,787,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R9464:Ryr2
|
UTSW |
13 |
11,752,680 (GRCm39) |
missense |
probably benign |
0.00 |
R9467:Ryr2
|
UTSW |
13 |
11,571,490 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9546:Ryr2
|
UTSW |
13 |
11,602,101 (GRCm39) |
critical splice donor site |
probably null |
|
R9562:Ryr2
|
UTSW |
13 |
11,760,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R9609:Ryr2
|
UTSW |
13 |
11,683,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R9704:Ryr2
|
UTSW |
13 |
11,737,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R9764:Ryr2
|
UTSW |
13 |
11,701,935 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9772:Ryr2
|
UTSW |
13 |
11,609,785 (GRCm39) |
missense |
probably benign |
0.13 |
R9776:Ryr2
|
UTSW |
13 |
11,707,599 (GRCm39) |
missense |
probably damaging |
0.98 |
S24628:Ryr2
|
UTSW |
13 |
11,884,042 (GRCm39) |
missense |
probably damaging |
0.97 |
X0019:Ryr2
|
UTSW |
13 |
11,718,387 (GRCm39) |
missense |
probably benign |
0.04 |
Z1176:Ryr2
|
UTSW |
13 |
11,658,689 (GRCm39) |
critical splice donor site |
probably null |
|
Z1176:Ryr2
|
UTSW |
13 |
11,613,497 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1176:Ryr2
|
UTSW |
13 |
11,809,435 (GRCm39) |
nonsense |
probably null |
|
Z1177:Ryr2
|
UTSW |
13 |
11,765,759 (GRCm39) |
missense |
possibly damaging |
0.87 |
|