Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm2 |
T |
A |
7: 119,190,321 (GRCm39) |
D70E |
probably damaging |
Het |
Adamts14 |
C |
T |
10: 61,057,674 (GRCm39) |
G561R |
probably damaging |
Het |
Alpk3 |
A |
T |
7: 80,728,401 (GRCm39) |
K510N |
probably damaging |
Het |
Ap3b1 |
A |
G |
13: 94,576,781 (GRCm39) |
N269D |
probably benign |
Het |
Ap3b1 |
T |
C |
13: 94,619,773 (GRCm39) |
S144P |
probably damaging |
Het |
Apba2 |
C |
A |
7: 64,395,464 (GRCm39) |
Q635K |
probably benign |
Het |
Aspg |
C |
T |
12: 112,079,519 (GRCm39) |
T99I |
probably benign |
Het |
Atp7b |
A |
G |
8: 22,487,512 (GRCm39) |
V1179A |
probably damaging |
Het |
Bbs12 |
T |
C |
3: 37,374,197 (GRCm39) |
V215A |
probably damaging |
Het |
Bcl2l11 |
C |
A |
2: 127,969,703 (GRCm39) |
|
probably benign |
Het |
Bglap3 |
T |
G |
3: 88,283,653 (GRCm39) |
|
probably benign |
Het |
Cchcr1 |
G |
A |
17: 35,835,890 (GRCm39) |
R284Q |
probably damaging |
Het |
Cdh26 |
C |
T |
2: 178,123,443 (GRCm39) |
Q662* |
probably null |
Het |
Cftr |
T |
A |
6: 18,313,645 (GRCm39) |
F1290I |
probably damaging |
Het |
Clip3 |
G |
A |
7: 29,991,731 (GRCm39) |
E36K |
probably damaging |
Het |
Cog2 |
A |
G |
8: 125,272,825 (GRCm39) |
I541V |
probably benign |
Het |
Cpt1b |
A |
T |
15: 89,309,417 (GRCm39) |
W39R |
probably damaging |
Het |
Csmd1 |
A |
G |
8: 15,982,471 (GRCm39) |
V2732A |
probably damaging |
Het |
Dlec1 |
A |
G |
9: 118,955,380 (GRCm39) |
D688G |
probably damaging |
Het |
Dnah12 |
A |
G |
14: 26,428,022 (GRCm39) |
E216G |
probably benign |
Het |
Dnah7b |
C |
A |
1: 46,226,450 (GRCm39) |
L1294I |
probably damaging |
Het |
Duox1 |
T |
A |
2: 122,174,637 (GRCm39) |
L1265Q |
probably damaging |
Het |
Fam91a1 |
T |
A |
15: 58,303,166 (GRCm39) |
D358E |
probably benign |
Het |
Fat3 |
A |
C |
9: 15,910,797 (GRCm39) |
I1735S |
probably benign |
Het |
Fkbpl |
G |
A |
17: 34,864,303 (GRCm39) |
A24T |
probably benign |
Het |
Gabrr1 |
T |
A |
4: 33,162,676 (GRCm39) |
M414K |
probably benign |
Het |
Gm21915 |
A |
C |
9: 40,581,995 (GRCm39) |
E29D |
possibly damaging |
Het |
Gm9955 |
G |
A |
18: 24,842,320 (GRCm39) |
|
probably benign |
Het |
Gpat2 |
C |
A |
2: 127,270,195 (GRCm39) |
D69E |
possibly damaging |
Het |
Grin2b |
T |
G |
6: 135,713,371 (GRCm39) |
I837L |
probably damaging |
Het |
Gucy2g |
T |
C |
19: 55,203,563 (GRCm39) |
D745G |
probably damaging |
Het |
H2-Q1 |
A |
G |
17: 35,540,332 (GRCm39) |
Y139C |
probably damaging |
Het |
Ints2 |
G |
C |
11: 86,141,798 (GRCm39) |
N216K |
probably benign |
Het |
Jmy |
G |
A |
13: 93,635,333 (GRCm39) |
P161L |
probably benign |
Het |
Kctd11 |
G |
A |
11: 69,770,799 (GRCm39) |
R80W |
possibly damaging |
Het |
Kif7 |
A |
G |
7: 79,360,880 (GRCm39) |
|
probably benign |
Het |
Kifc1 |
C |
T |
17: 34,102,059 (GRCm39) |
|
probably benign |
Het |
Lcor |
G |
A |
19: 41,574,839 (GRCm39) |
R1198Q |
probably damaging |
Het |
Mir412 |
C |
A |
12: 109,709,733 (GRCm39) |
|
noncoding transcript |
Het |
Mknk1 |
T |
A |
4: 115,733,834 (GRCm39) |
|
probably benign |
Het |
Mmp16 |
A |
G |
4: 18,054,354 (GRCm39) |
|
probably benign |
Het |
Mmp7 |
A |
G |
9: 7,697,646 (GRCm39) |
H227R |
probably damaging |
Het |
Myh4 |
A |
C |
11: 67,150,126 (GRCm39) |
D1861A |
probably damaging |
Het |
Nup205 |
T |
C |
6: 35,209,343 (GRCm39) |
L1550P |
probably damaging |
Het |
Or10g1 |
C |
T |
14: 52,647,525 (GRCm39) |
G268D |
probably benign |
Het |
Or2a56 |
G |
T |
6: 42,932,650 (GRCm39) |
A73S |
possibly damaging |
Het |
Or4c113 |
T |
A |
2: 88,884,963 (GRCm39) |
H269L |
probably benign |
Het |
Or4c58 |
T |
A |
2: 89,674,859 (GRCm39) |
I153F |
probably benign |
Het |
Or51af1 |
A |
G |
7: 103,141,927 (GRCm39) |
S53P |
possibly damaging |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Pafah1b2 |
A |
T |
9: 45,887,405 (GRCm39) |
C35* |
probably null |
Het |
Pappa |
T |
A |
4: 65,232,830 (GRCm39) |
F1323Y |
possibly damaging |
Het |
Phtf2 |
A |
T |
5: 20,979,071 (GRCm39) |
F519Y |
probably damaging |
Het |
Pigk |
T |
C |
3: 152,472,150 (GRCm39) |
I354T |
possibly damaging |
Het |
Plekha7 |
T |
C |
7: 115,724,040 (GRCm39) |
D1265G |
possibly damaging |
Het |
Prss12 |
A |
G |
3: 123,299,150 (GRCm39) |
R641G |
probably benign |
Het |
Prss28 |
A |
G |
17: 25,528,717 (GRCm39) |
Y53C |
probably damaging |
Het |
Rabgap1 |
G |
T |
2: 37,451,908 (GRCm39) |
C936F |
possibly damaging |
Het |
Rap1a |
T |
C |
3: 105,639,385 (GRCm39) |
I91M |
possibly damaging |
Het |
Rap1gap2 |
A |
T |
11: 74,283,063 (GRCm39) |
M679K |
probably damaging |
Het |
Rapgef5 |
T |
A |
12: 117,692,473 (GRCm39) |
L352I |
probably damaging |
Het |
Rhbdl3 |
G |
A |
11: 80,222,715 (GRCm39) |
V255M |
probably benign |
Het |
Rhot1 |
T |
C |
11: 80,141,996 (GRCm39) |
|
probably benign |
Het |
Rita1 |
A |
C |
5: 120,747,626 (GRCm39) |
V224G |
probably benign |
Het |
Scaf11 |
A |
C |
15: 96,318,189 (GRCm39) |
H458Q |
probably damaging |
Het |
Scamp4 |
T |
A |
10: 80,448,255 (GRCm39) |
S159T |
probably benign |
Het |
Setd5 |
T |
A |
6: 113,105,451 (GRCm39) |
Y828N |
probably damaging |
Het |
Sh3bp5 |
C |
A |
14: 31,099,452 (GRCm39) |
R265L |
probably benign |
Het |
Sipa1l2 |
A |
G |
8: 126,200,275 (GRCm39) |
S684P |
probably damaging |
Het |
Stard9 |
A |
T |
2: 120,544,039 (GRCm39) |
I4446F |
probably damaging |
Het |
Sult1c2 |
T |
C |
17: 54,138,926 (GRCm39) |
D217G |
probably benign |
Het |
Supt16 |
C |
A |
14: 52,419,653 (GRCm39) |
K148N |
probably benign |
Het |
Syne3 |
G |
A |
12: 104,913,251 (GRCm39) |
S570L |
probably benign |
Het |
Tcf3 |
G |
T |
10: 80,248,878 (GRCm39) |
D534E |
probably benign |
Het |
Tmed6 |
G |
T |
8: 107,790,786 (GRCm39) |
T87K |
probably damaging |
Het |
Trbv3 |
T |
C |
6: 41,025,335 (GRCm39) |
I3T |
probably benign |
Het |
Trbv4 |
T |
A |
6: 41,036,563 (GRCm39) |
Y29* |
probably null |
Het |
Ttl |
A |
G |
2: 128,917,904 (GRCm39) |
N122S |
probably benign |
Het |
Txndc11 |
T |
C |
16: 10,892,935 (GRCm39) |
T932A |
probably benign |
Het |
Ube2e2 |
G |
A |
14: 18,586,910 (GRCm38) |
A150V |
probably damaging |
Het |
Ube2ql1 |
T |
C |
13: 69,887,459 (GRCm39) |
M1V |
probably null |
Het |
Uqcrc1 |
A |
G |
9: 108,776,554 (GRCm39) |
|
probably benign |
Het |
Utrn |
T |
C |
10: 12,362,227 (GRCm39) |
D2702G |
probably damaging |
Het |
Vcan |
T |
A |
13: 89,840,810 (GRCm39) |
D618V |
probably damaging |
Het |
Vdac3-ps1 |
A |
G |
13: 18,205,787 (GRCm39) |
|
noncoding transcript |
Het |
Wee1 |
TCCCC |
TCCC |
7: 109,723,776 (GRCm39) |
|
probably null |
Het |
Zap70 |
G |
A |
1: 36,810,030 (GRCm39) |
V47M |
probably damaging |
Het |
Zfp770 |
A |
G |
2: 114,028,027 (GRCm39) |
M14T |
possibly damaging |
Het |
Zup1 |
C |
T |
10: 33,825,458 (GRCm39) |
G8D |
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 |
R4732: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 |
11,723,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Ryr2
|
UTSW |
13 |
11,702,818 (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 |
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 |
|