Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930402F06Rik |
T |
A |
2: 35,279,599 (GRCm39) |
Y34F |
possibly damaging |
Het |
Abcb6 |
A |
T |
1: 75,149,588 (GRCm39) |
S664T |
probably benign |
Het |
Abcc4 |
C |
T |
14: 118,853,804 (GRCm39) |
V443M |
probably damaging |
Het |
Abhd2 |
G |
A |
7: 78,998,095 (GRCm39) |
G209D |
probably damaging |
Het |
Acte1 |
A |
G |
7: 143,437,680 (GRCm39) |
N126S |
possibly damaging |
Het |
Ampd2 |
C |
A |
3: 107,987,432 (GRCm39) |
V134L |
probably benign |
Het |
Apbb2 |
T |
A |
5: 66,520,179 (GRCm39) |
M449L |
probably benign |
Het |
Ccdc81 |
T |
A |
7: 89,526,786 (GRCm39) |
|
probably null |
Het |
Cd209b |
A |
T |
8: 3,976,559 (GRCm39) |
C42* |
probably null |
Het |
Cdhr18 |
G |
A |
14: 13,814,954 (GRCm38) |
Q860* |
probably null |
Het |
Clec18a |
A |
T |
8: 111,808,689 (GRCm39) |
M11K |
probably benign |
Het |
Clock |
A |
T |
5: 76,402,269 (GRCm39) |
S130R |
probably benign |
Het |
Col12a1 |
G |
A |
9: 79,512,465 (GRCm39) |
A2910V |
possibly damaging |
Het |
Col6a4 |
C |
T |
9: 105,952,414 (GRCm39) |
A495T |
probably benign |
Het |
Cyp4f37 |
A |
T |
17: 32,853,952 (GRCm39) |
N467I |
probably damaging |
Het |
Ddo |
G |
A |
10: 40,513,375 (GRCm39) |
V106M |
possibly damaging |
Het |
Dennd5a |
A |
G |
7: 109,500,332 (GRCm39) |
L931P |
probably damaging |
Het |
Dgcr6 |
A |
G |
16: 17,884,598 (GRCm39) |
D82G |
probably damaging |
Het |
Dnah7b |
T |
C |
1: 46,179,032 (GRCm39) |
S902P |
probably damaging |
Het |
Dnal4 |
T |
G |
15: 79,646,711 (GRCm39) |
I57L |
probably benign |
Het |
Dst |
T |
A |
1: 34,156,592 (GRCm39) |
I174N |
probably damaging |
Het |
Dync2i1 |
T |
C |
12: 116,219,705 (GRCm39) |
E79G |
probably damaging |
Het |
Dync2i2 |
A |
G |
2: 29,922,201 (GRCm39) |
L420P |
probably damaging |
Het |
Eeig2 |
G |
A |
3: 108,934,658 (GRCm39) |
|
probably benign |
Het |
Efhb |
T |
C |
17: 53,756,563 (GRCm39) |
T363A |
probably damaging |
Het |
Ehbp1l1 |
A |
G |
19: 5,767,103 (GRCm39) |
F1245S |
probably damaging |
Het |
Eif4g1 |
A |
G |
16: 20,507,578 (GRCm39) |
D1453G |
probably benign |
Het |
Fbp1 |
T |
C |
13: 63,016,831 (GRCm39) |
I224V |
probably benign |
Het |
Gm10782 |
T |
G |
13: 56,510,948 (GRCm39) |
F79V |
noncoding transcript |
Het |
Gpaa1 |
C |
G |
15: 76,216,160 (GRCm39) |
R47G |
possibly damaging |
Het |
Hs2st1 |
G |
A |
3: 144,143,365 (GRCm39) |
S226L |
possibly damaging |
Het |
Hydin |
A |
G |
8: 111,334,534 (GRCm39) |
Y4992C |
probably benign |
Het |
Ikbke |
A |
T |
1: 131,191,065 (GRCm39) |
C549* |
probably null |
Het |
Insrr |
G |
A |
3: 87,717,749 (GRCm39) |
G817S |
probably benign |
Het |
Itgb5 |
G |
A |
16: 33,685,923 (GRCm39) |
V88I |
probably benign |
Het |
Krt78 |
A |
G |
15: 101,854,922 (GRCm39) |
V963A |
probably benign |
Het |
Lars1 |
T |
C |
18: 42,376,093 (GRCm39) |
Y239C |
possibly damaging |
Het |
Map2k5 |
A |
G |
9: 63,246,361 (GRCm39) |
|
probably null |
Het |
Mfn2 |
A |
T |
4: 147,974,693 (GRCm39) |
W118R |
probably benign |
Het |
Mga |
T |
A |
2: 119,791,411 (GRCm39) |
I2550N |
probably damaging |
Het |
Mgam |
A |
G |
6: 40,722,111 (GRCm39) |
I401V |
possibly damaging |
Het |
Mrps18c |
A |
G |
5: 100,952,264 (GRCm39) |
Y141C |
probably damaging |
Het |
Myo1e |
A |
T |
9: 70,254,045 (GRCm39) |
I565L |
possibly damaging |
Het |
Nfatc4 |
G |
A |
14: 56,063,848 (GRCm39) |
E112K |
probably damaging |
Het |
Nubp1 |
A |
G |
16: 10,239,486 (GRCm39) |
M255V |
probably benign |
Het |
Or13n4 |
A |
C |
7: 106,423,620 (GRCm39) |
S38A |
probably benign |
Het |
Or52a33 |
A |
G |
7: 103,288,658 (GRCm39) |
S230P |
probably damaging |
Het |
Or8g33 |
C |
T |
9: 39,337,966 (GRCm39) |
V134I |
probably benign |
Het |
Pask |
A |
T |
1: 93,240,573 (GRCm39) |
C1264* |
probably null |
Het |
Pcgf2 |
T |
C |
11: 97,582,569 (GRCm39) |
T173A |
probably benign |
Het |
Plcg1 |
T |
C |
2: 160,595,853 (GRCm39) |
I574T |
probably benign |
Het |
Plin4 |
T |
C |
17: 56,411,437 (GRCm39) |
T865A |
probably damaging |
Het |
Pnpt1 |
T |
C |
11: 29,103,277 (GRCm39) |
V514A |
probably benign |
Het |
Ppp1r3a |
T |
A |
6: 14,719,700 (GRCm39) |
I405F |
probably benign |
Het |
Qpctl |
A |
G |
7: 18,882,398 (GRCm39) |
V86A |
probably benign |
Het |
Rab3gap1 |
G |
T |
1: 127,837,655 (GRCm39) |
W239L |
possibly damaging |
Het |
Ralgapa2 |
T |
A |
2: 146,246,786 (GRCm39) |
T939S |
possibly damaging |
Het |
Rapgef2 |
G |
T |
3: 78,990,509 (GRCm39) |
T923N |
possibly damaging |
Het |
Rit2 |
T |
A |
18: 31,286,898 (GRCm39) |
I96F |
probably damaging |
Het |
Rnase13 |
A |
T |
14: 52,159,893 (GRCm39) |
I82N |
probably damaging |
Het |
Serpinb9b |
G |
A |
13: 33,223,554 (GRCm39) |
E249K |
probably damaging |
Het |
Serpinb9c |
G |
T |
13: 33,334,094 (GRCm39) |
T344K |
possibly damaging |
Het |
Serpinh1 |
T |
C |
7: 98,998,151 (GRCm39) |
I160V |
possibly damaging |
Het |
Sipa1 |
A |
G |
19: 5,704,964 (GRCm39) |
S544P |
probably damaging |
Het |
Slc17a5 |
A |
T |
9: 78,478,311 (GRCm39) |
Y231* |
probably null |
Het |
Srcap |
T |
C |
7: 127,148,529 (GRCm39) |
V1959A |
probably damaging |
Het |
Srrm4 |
G |
A |
5: 116,729,626 (GRCm39) |
|
probably benign |
Het |
Stat1 |
T |
C |
1: 52,190,404 (GRCm39) |
I553T |
possibly damaging |
Het |
Stpg1 |
A |
G |
4: 135,256,903 (GRCm39) |
I231M |
probably benign |
Het |
Szt2 |
G |
GC |
4: 118,232,679 (GRCm39) |
|
probably null |
Het |
Trpv3 |
C |
T |
11: 73,170,747 (GRCm39) |
T209M |
probably damaging |
Het |
Tsc22d2 |
G |
T |
3: 58,324,544 (GRCm39) |
G479C |
unknown |
Het |
Ttc3 |
A |
G |
16: 94,267,838 (GRCm39) |
H1950R |
probably damaging |
Het |
Tusc3 |
A |
G |
8: 39,617,882 (GRCm39) |
*348W |
probably null |
Het |
Utp4 |
A |
T |
8: 107,642,853 (GRCm39) |
T504S |
probably benign |
Het |
Vmn1r15 |
A |
G |
6: 57,235,635 (GRCm39) |
M168V |
probably benign |
Het |
Wdsub1 |
C |
T |
2: 59,704,578 (GRCm39) |
|
probably benign |
Het |
Xrcc5 |
T |
A |
1: 72,358,286 (GRCm39) |
M207K |
possibly damaging |
Het |
Zc3h7a |
A |
T |
16: 10,964,417 (GRCm39) |
|
probably benign |
Het |
Zdbf2 |
T |
A |
1: 63,345,750 (GRCm39) |
N1376K |
possibly damaging |
Het |
Zfp558 |
A |
C |
9: 18,368,213 (GRCm39) |
S192A |
probably benign |
Het |
Zfp764l1 |
C |
T |
7: 126,992,496 (GRCm39) |
C38Y |
probably null |
Het |
Zfp964 |
A |
G |
8: 70,115,924 (GRCm39) |
T175A |
possibly damaging |
Het |
Zfp988 |
A |
G |
4: 147,416,765 (GRCm39) |
R400G |
probably damaging |
Het |
|
Other mutations in Rp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00323:Rp1
|
APN |
1 |
4,416,969 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00593:Rp1
|
APN |
1 |
4,415,626 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL00956:Rp1
|
APN |
1 |
4,422,435 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01070:Rp1
|
APN |
1 |
4,415,461 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01531:Rp1
|
APN |
1 |
4,419,168 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01668:Rp1
|
APN |
1 |
4,415,941 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01907:Rp1
|
APN |
1 |
4,418,730 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL02055:Rp1
|
APN |
1 |
4,422,745 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02071:Rp1
|
APN |
1 |
4,415,533 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02128:Rp1
|
APN |
1 |
4,417,608 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02244:Rp1
|
APN |
1 |
4,419,003 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02381:Rp1
|
APN |
1 |
4,422,613 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02499:Rp1
|
APN |
1 |
4,419,271 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02619:Rp1
|
APN |
1 |
4,418,673 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02832:Rp1
|
APN |
1 |
4,419,936 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02861:Rp1
|
APN |
1 |
4,416,375 (GRCm39) |
nonsense |
probably null |
|
IGL03288:Rp1
|
APN |
1 |
4,419,747 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03290:Rp1
|
APN |
1 |
4,420,264 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03303:Rp1
|
APN |
1 |
4,415,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R0041:Rp1
|
UTSW |
1 |
4,414,851 (GRCm39) |
missense |
probably benign |
0.36 |
R0111:Rp1
|
UTSW |
1 |
4,414,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R0363:Rp1
|
UTSW |
1 |
4,417,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R0440:Rp1
|
UTSW |
1 |
4,415,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R0442:Rp1
|
UTSW |
1 |
4,416,970 (GRCm39) |
missense |
probably benign |
0.09 |
R0528:Rp1
|
UTSW |
1 |
4,415,088 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0586:Rp1
|
UTSW |
1 |
4,418,060 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0639:Rp1
|
UTSW |
1 |
4,416,721 (GRCm39) |
missense |
probably benign |
0.00 |
R0856:Rp1
|
UTSW |
1 |
4,414,878 (GRCm39) |
missense |
probably benign |
0.05 |
R0908:Rp1
|
UTSW |
1 |
4,414,878 (GRCm39) |
missense |
probably benign |
0.05 |
R0968:Rp1
|
UTSW |
1 |
4,415,575 (GRCm39) |
missense |
probably benign |
0.00 |
R1099:Rp1
|
UTSW |
1 |
4,422,513 (GRCm39) |
missense |
possibly damaging |
0.45 |
R1242:Rp1
|
UTSW |
1 |
4,415,185 (GRCm39) |
missense |
probably benign |
0.03 |
R1301:Rp1
|
UTSW |
1 |
4,416,159 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1327:Rp1
|
UTSW |
1 |
4,418,193 (GRCm39) |
missense |
probably benign |
0.01 |
R1403:Rp1
|
UTSW |
1 |
4,416,520 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1403:Rp1
|
UTSW |
1 |
4,416,520 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1406:Rp1
|
UTSW |
1 |
4,422,144 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1406:Rp1
|
UTSW |
1 |
4,422,144 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1440:Rp1
|
UTSW |
1 |
4,417,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R1509:Rp1
|
UTSW |
1 |
4,418,760 (GRCm39) |
missense |
probably benign |
0.20 |
R1509:Rp1
|
UTSW |
1 |
4,417,917 (GRCm39) |
missense |
probably damaging |
0.98 |
R1538:Rp1
|
UTSW |
1 |
4,415,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R1609:Rp1
|
UTSW |
1 |
4,419,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R1666:Rp1
|
UTSW |
1 |
4,420,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R1703:Rp1
|
UTSW |
1 |
4,415,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R1782:Rp1
|
UTSW |
1 |
4,419,312 (GRCm39) |
missense |
probably benign |
0.00 |
R1799:Rp1
|
UTSW |
1 |
4,419,055 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1848:Rp1
|
UTSW |
1 |
4,417,455 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1908:Rp1
|
UTSW |
1 |
4,418,943 (GRCm39) |
missense |
probably damaging |
0.99 |
R1919:Rp1
|
UTSW |
1 |
4,422,894 (GRCm39) |
missense |
probably damaging |
0.99 |
R2087:Rp1
|
UTSW |
1 |
4,418,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R2211:Rp1
|
UTSW |
1 |
4,418,362 (GRCm39) |
missense |
probably damaging |
0.96 |
R2278:Rp1
|
UTSW |
1 |
4,418,250 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2287:Rp1
|
UTSW |
1 |
4,416,182 (GRCm39) |
nonsense |
probably null |
|
R2316:Rp1
|
UTSW |
1 |
4,415,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R2346:Rp1
|
UTSW |
1 |
4,418,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R2878:Rp1
|
UTSW |
1 |
4,418,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R3023:Rp1
|
UTSW |
1 |
4,422,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R3025:Rp1
|
UTSW |
1 |
4,422,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R3716:Rp1
|
UTSW |
1 |
4,419,988 (GRCm39) |
missense |
probably benign |
0.38 |
R3814:Rp1
|
UTSW |
1 |
4,419,931 (GRCm39) |
missense |
probably benign |
|
R3929:Rp1
|
UTSW |
1 |
4,422,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R4064:Rp1
|
UTSW |
1 |
4,415,623 (GRCm39) |
missense |
probably benign |
0.08 |
R4426:Rp1
|
UTSW |
1 |
4,418,147 (GRCm39) |
missense |
probably benign |
0.13 |
R4557:Rp1
|
UTSW |
1 |
4,414,886 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4764:Rp1
|
UTSW |
1 |
4,416,101 (GRCm39) |
missense |
probably damaging |
0.96 |
R4845:Rp1
|
UTSW |
1 |
4,419,451 (GRCm39) |
missense |
probably benign |
0.02 |
R4850:Rp1
|
UTSW |
1 |
4,418,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R4857:Rp1
|
UTSW |
1 |
4,422,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R4857:Rp1
|
UTSW |
1 |
4,422,539 (GRCm39) |
missense |
probably damaging |
0.99 |
R5159:Rp1
|
UTSW |
1 |
4,416,426 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5226:Rp1
|
UTSW |
1 |
4,418,256 (GRCm39) |
missense |
probably benign |
0.01 |
R5327:Rp1
|
UTSW |
1 |
4,419,583 (GRCm39) |
splice site |
probably null |
|
R5352:Rp1
|
UTSW |
1 |
4,417,321 (GRCm39) |
missense |
probably benign |
0.00 |
R5504:Rp1
|
UTSW |
1 |
4,420,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R5527:Rp1
|
UTSW |
1 |
4,416,616 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5529:Rp1
|
UTSW |
1 |
4,416,055 (GRCm39) |
missense |
probably benign |
0.42 |
R5569:Rp1
|
UTSW |
1 |
4,415,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R5622:Rp1
|
UTSW |
1 |
4,418,060 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5970:Rp1
|
UTSW |
1 |
4,418,685 (GRCm39) |
missense |
probably benign |
0.05 |
R5992:Rp1
|
UTSW |
1 |
4,218,926 (GRCm39) |
missense |
unknown |
|
R6004:Rp1
|
UTSW |
1 |
4,267,808 (GRCm39) |
missense |
unknown |
|
R6018:Rp1
|
UTSW |
1 |
4,423,059 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6074:Rp1
|
UTSW |
1 |
4,415,602 (GRCm39) |
missense |
probably benign |
0.02 |
R6127:Rp1
|
UTSW |
1 |
4,419,534 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6187:Rp1
|
UTSW |
1 |
4,420,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R6301:Rp1
|
UTSW |
1 |
4,417,477 (GRCm39) |
missense |
probably benign |
0.04 |
R6317:Rp1
|
UTSW |
1 |
4,112,212 (GRCm39) |
missense |
unknown |
|
R6405:Rp1
|
UTSW |
1 |
4,415,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R6445:Rp1
|
UTSW |
1 |
4,296,840 (GRCm39) |
missense |
unknown |
|
R6466:Rp1
|
UTSW |
1 |
4,418,109 (GRCm39) |
missense |
probably benign |
0.01 |
R6501:Rp1
|
UTSW |
1 |
4,381,503 (GRCm39) |
intron |
probably benign |
|
R6547:Rp1
|
UTSW |
1 |
4,240,528 (GRCm39) |
missense |
unknown |
|
R6604:Rp1
|
UTSW |
1 |
4,089,351 (GRCm39) |
missense |
unknown |
|
R6700:Rp1
|
UTSW |
1 |
4,420,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R6706:Rp1
|
UTSW |
1 |
4,212,887 (GRCm39) |
missense |
unknown |
|
R6831:Rp1
|
UTSW |
1 |
4,420,087 (GRCm39) |
splice site |
probably null |
|
R6918:Rp1
|
UTSW |
1 |
4,069,831 (GRCm39) |
missense |
unknown |
|
R6973:Rp1
|
UTSW |
1 |
4,422,217 (GRCm39) |
nonsense |
probably null |
|
R6981:Rp1
|
UTSW |
1 |
4,415,878 (GRCm39) |
missense |
probably benign |
0.06 |
R7009:Rp1
|
UTSW |
1 |
4,112,291 (GRCm39) |
missense |
unknown |
|
R7078:Rp1
|
UTSW |
1 |
4,277,014 (GRCm39) |
missense |
unknown |
|
R7112:Rp1
|
UTSW |
1 |
4,419,241 (GRCm39) |
missense |
probably benign |
0.43 |
R7135:Rp1
|
UTSW |
1 |
4,418,391 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7165:Rp1
|
UTSW |
1 |
4,420,140 (GRCm39) |
missense |
probably damaging |
0.99 |
R7199:Rp1
|
UTSW |
1 |
4,417,513 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7232:Rp1
|
UTSW |
1 |
4,298,824 (GRCm39) |
missense |
unknown |
|
R7367:Rp1
|
UTSW |
1 |
4,418,221 (GRCm39) |
missense |
probably benign |
0.42 |
R7484:Rp1
|
UTSW |
1 |
4,415,704 (GRCm39) |
missense |
probably benign |
0.10 |
R7500:Rp1
|
UTSW |
1 |
4,381,501 (GRCm39) |
missense |
unknown |
|
R7569:Rp1
|
UTSW |
1 |
4,355,063 (GRCm39) |
missense |
unknown |
|
R7642:Rp1
|
UTSW |
1 |
4,218,054 (GRCm39) |
missense |
unknown |
|
R7693:Rp1
|
UTSW |
1 |
4,417,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R7742:Rp1
|
UTSW |
1 |
4,240,457 (GRCm39) |
missense |
unknown |
|
R7759:Rp1
|
UTSW |
1 |
4,415,107 (GRCm39) |
missense |
probably benign |
|
R7784:Rp1
|
UTSW |
1 |
4,212,881 (GRCm39) |
missense |
unknown |
|
R7816:Rp1
|
UTSW |
1 |
4,417,926 (GRCm39) |
missense |
probably damaging |
0.98 |
R7866:Rp1
|
UTSW |
1 |
4,417,924 (GRCm39) |
missense |
probably benign |
0.02 |
R8215:Rp1
|
UTSW |
1 |
4,315,318 (GRCm39) |
missense |
unknown |
|
R8281:Rp1
|
UTSW |
1 |
4,418,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R8294:Rp1
|
UTSW |
1 |
4,416,220 (GRCm39) |
missense |
probably benign |
0.09 |
R8311:Rp1
|
UTSW |
1 |
4,418,572 (GRCm39) |
missense |
probably benign |
0.11 |
R8500:Rp1
|
UTSW |
1 |
4,416,813 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8559:Rp1
|
UTSW |
1 |
4,419,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R8672:Rp1
|
UTSW |
1 |
4,419,007 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8688:Rp1
|
UTSW |
1 |
4,416,628 (GRCm39) |
missense |
probably benign |
0.01 |
R8792:Rp1
|
UTSW |
1 |
4,095,091 (GRCm39) |
missense |
unknown |
|
R8859:Rp1
|
UTSW |
1 |
4,420,183 (GRCm39) |
missense |
probably benign |
0.07 |
R8945:Rp1
|
UTSW |
1 |
4,419,817 (GRCm39) |
missense |
probably benign |
0.42 |
R8959:Rp1
|
UTSW |
1 |
4,419,650 (GRCm39) |
intron |
probably benign |
|
R8979:Rp1
|
UTSW |
1 |
4,218,937 (GRCm39) |
missense |
unknown |
|
R9126:Rp1
|
UTSW |
1 |
4,417,136 (GRCm39) |
missense |
probably damaging |
0.99 |
R9156:Rp1
|
UTSW |
1 |
4,234,161 (GRCm39) |
missense |
unknown |
|
R9160:Rp1
|
UTSW |
1 |
4,416,720 (GRCm39) |
missense |
probably benign |
0.00 |
R9221:Rp1
|
UTSW |
1 |
4,315,266 (GRCm39) |
missense |
unknown |
|
R9263:Rp1
|
UTSW |
1 |
4,419,160 (GRCm39) |
missense |
probably benign |
0.02 |
R9263:Rp1
|
UTSW |
1 |
4,418,675 (GRCm39) |
missense |
probably benign |
0.25 |
R9302:Rp1
|
UTSW |
1 |
4,416,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R9318:Rp1
|
UTSW |
1 |
4,418,488 (GRCm39) |
missense |
probably benign |
0.09 |
R9414:Rp1
|
UTSW |
1 |
4,313,841 (GRCm39) |
missense |
unknown |
|
R9474:Rp1
|
UTSW |
1 |
4,162,838 (GRCm39) |
critical splice donor site |
probably null |
|
R9478:Rp1
|
UTSW |
1 |
4,417,545 (GRCm39) |
missense |
probably benign |
0.06 |
R9529:Rp1
|
UTSW |
1 |
4,416,447 (GRCm39) |
missense |
probably benign |
|
R9572:Rp1
|
UTSW |
1 |
4,418,662 (GRCm39) |
missense |
probably benign |
|
R9673:Rp1
|
UTSW |
1 |
4,337,792 (GRCm39) |
missense |
unknown |
|
R9709:Rp1
|
UTSW |
1 |
4,112,255 (GRCm39) |
missense |
unknown |
|
R9716:Rp1
|
UTSW |
1 |
4,212,833 (GRCm39) |
critical splice donor site |
probably null |
|
RF003:Rp1
|
UTSW |
1 |
4,414,917 (GRCm39) |
missense |
probably damaging |
0.99 |
V1662:Rp1
|
UTSW |
1 |
4,419,783 (GRCm39) |
missense |
probably damaging |
1.00 |
X0012:Rp1
|
UTSW |
1 |
4,417,918 (GRCm39) |
missense |
probably damaging |
0.96 |
|