Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310034C09Rik |
A |
G |
16: 88,555,902 (GRCm39) |
T39A |
probably damaging |
Het |
Abca3 |
G |
A |
17: 24,596,681 (GRCm39) |
G378D |
probably damaging |
Het |
Abtb2 |
T |
C |
2: 103,397,565 (GRCm39) |
V165A |
possibly damaging |
Het |
Ache |
A |
G |
5: 137,288,504 (GRCm39) |
E70G |
probably damaging |
Het |
Adamtsl4 |
T |
C |
3: 95,588,119 (GRCm39) |
T623A |
probably benign |
Het |
Ahdc1 |
G |
A |
4: 132,791,935 (GRCm39) |
V1059I |
probably benign |
Het |
Ajuba |
G |
A |
14: 54,810,915 (GRCm39) |
Q357* |
probably null |
Het |
Ano7 |
A |
T |
1: 93,330,700 (GRCm39) |
D54V |
|
Het |
Apob |
A |
T |
12: 8,055,072 (GRCm39) |
D1357V |
probably damaging |
Het |
Atad2b |
T |
A |
12: 5,067,992 (GRCm39) |
Y997N |
probably damaging |
Het |
Bhlhe22 |
C |
A |
3: 18,110,006 (GRCm39) |
T352K |
probably damaging |
Het |
Bsn |
T |
C |
9: 107,992,533 (GRCm39) |
E1073G |
probably damaging |
Het |
Bzw2 |
G |
A |
12: 36,180,054 (GRCm39) |
R58* |
probably null |
Het |
C7 |
G |
T |
15: 5,023,725 (GRCm39) |
S694R |
probably benign |
Het |
Cbr2 |
T |
A |
11: 120,621,087 (GRCm39) |
H170L |
probably benign |
Het |
Cdcp3 |
G |
A |
7: 130,837,641 (GRCm39) |
W512* |
probably null |
Het |
Cgas |
C |
A |
9: 78,340,315 (GRCm39) |
K472N |
probably benign |
Het |
Ckap2l |
T |
C |
2: 129,126,975 (GRCm39) |
N401S |
probably benign |
Het |
Cldn1 |
A |
G |
16: 26,190,346 (GRCm39) |
F11L |
probably benign |
Het |
Cmtr1 |
A |
G |
17: 29,895,174 (GRCm39) |
T118A |
probably benign |
Het |
Cog6 |
T |
C |
3: 52,890,610 (GRCm39) |
E610G |
probably benign |
Het |
Col3a1 |
G |
T |
1: 45,371,301 (GRCm39) |
A451S |
probably null |
Het |
Cr1l |
T |
A |
1: 194,799,878 (GRCm39) |
R265S |
probably benign |
Het |
Dapk1 |
T |
C |
13: 60,902,024 (GRCm39) |
I951T |
probably benign |
Het |
Dnah9 |
T |
C |
11: 66,009,770 (GRCm39) |
N706D |
probably benign |
Het |
Dpysl5 |
A |
T |
5: 30,940,539 (GRCm39) |
T239S |
probably benign |
Het |
Ect2l |
T |
A |
10: 18,004,894 (GRCm39) |
Y913F |
probably benign |
Het |
Elf5 |
C |
A |
2: 103,269,641 (GRCm39) |
A74D |
possibly damaging |
Het |
Erap1 |
T |
C |
13: 74,814,258 (GRCm39) |
V399A |
probably benign |
Het |
Ercc4 |
A |
G |
16: 12,965,657 (GRCm39) |
D763G |
probably damaging |
Het |
Fam222b |
T |
A |
11: 78,045,683 (GRCm39) |
C415S |
possibly damaging |
Het |
Fat4 |
A |
C |
3: 39,031,511 (GRCm39) |
N2432T |
probably damaging |
Het |
Fbn2 |
G |
T |
18: 58,186,833 (GRCm39) |
C1689* |
probably null |
Het |
Frrs1l |
T |
A |
4: 56,972,282 (GRCm39) |
T140S |
probably damaging |
Het |
Gm5141 |
A |
T |
13: 62,924,877 (GRCm39) |
H10Q |
possibly damaging |
Het |
Inafm1 |
A |
T |
7: 16,007,079 (GRCm39) |
L46Q |
probably damaging |
Het |
Irak2 |
T |
C |
6: 113,650,045 (GRCm39) |
L260P |
probably damaging |
Het |
Kat2b |
T |
C |
17: 53,977,706 (GRCm39) |
L751P |
probably damaging |
Het |
Kcnh1 |
T |
A |
1: 192,019,913 (GRCm39) |
I413N |
probably benign |
Het |
Kirrel1 |
T |
C |
3: 86,990,695 (GRCm39) |
D709G |
probably benign |
Het |
Lama4 |
T |
C |
10: 38,956,536 (GRCm39) |
V1153A |
possibly damaging |
Het |
Lipg |
A |
T |
18: 75,088,655 (GRCm39) |
F98L |
probably benign |
Het |
Lman1 |
T |
C |
18: 66,127,936 (GRCm39) |
E236G |
probably damaging |
Het |
Lrp1 |
T |
A |
10: 127,409,325 (GRCm39) |
D1598V |
probably damaging |
Het |
Lrrc71 |
T |
A |
3: 87,650,384 (GRCm39) |
N230Y |
probably damaging |
Het |
Maneal |
T |
C |
4: 124,750,983 (GRCm39) |
S258G |
possibly damaging |
Het |
Marchf10 |
T |
A |
11: 105,281,532 (GRCm39) |
E251V |
probably damaging |
Het |
Mpdz |
A |
G |
4: 81,215,570 (GRCm39) |
I1484T |
probably damaging |
Het |
Mtcl1 |
T |
A |
17: 66,647,534 (GRCm39) |
N1882I |
probably benign |
Het |
Neb |
G |
A |
2: 52,110,212 (GRCm39) |
A212V |
probably benign |
Het |
Obscn |
G |
A |
11: 58,903,672 (GRCm39) |
S7434L |
probably benign |
Het |
Or14j8 |
A |
C |
17: 38,263,048 (GRCm39) |
I289S |
probably damaging |
Het |
Or1ad8 |
T |
A |
11: 50,898,223 (GRCm39) |
C141* |
probably null |
Het |
Or1j12 |
A |
T |
2: 36,342,872 (GRCm39) |
I92F |
probably damaging |
Het |
Or4k47 |
T |
C |
2: 111,451,538 (GRCm39) |
M294V |
probably benign |
Het |
Or8g2b |
A |
G |
9: 39,750,753 (GRCm39) |
M8V |
probably benign |
Het |
Orc6 |
T |
C |
8: 86,029,590 (GRCm39) |
|
probably null |
Het |
Otogl |
T |
G |
10: 107,710,394 (GRCm39) |
E565A |
possibly damaging |
Het |
Papss1 |
A |
G |
3: 131,290,899 (GRCm39) |
Q214R |
probably benign |
Het |
Pck2 |
G |
A |
14: 55,786,169 (GRCm39) |
V653M |
probably benign |
Het |
Plxna4 |
G |
A |
6: 32,192,113 (GRCm39) |
Q826* |
probably null |
Het |
Pms1 |
T |
A |
1: 53,295,889 (GRCm39) |
T161S |
probably benign |
Het |
Prkar2a |
C |
A |
9: 108,617,669 (GRCm39) |
N242K |
probably damaging |
Het |
Prss1 |
T |
A |
6: 41,439,690 (GRCm39) |
I141N |
probably damaging |
Het |
Puf60 |
A |
G |
15: 75,943,717 (GRCm39) |
V235A |
probably damaging |
Het |
Rapgef6 |
T |
A |
11: 54,437,252 (GRCm39) |
F65Y |
probably benign |
Het |
Rasgef1b |
T |
C |
5: 99,447,898 (GRCm39) |
E104G |
unknown |
Het |
Rcn3 |
T |
C |
7: 44,734,333 (GRCm39) |
Y225C |
probably damaging |
Het |
Rhot1 |
G |
C |
11: 80,137,560 (GRCm39) |
W354S |
probably damaging |
Het |
Scaper |
T |
A |
9: 55,745,460 (GRCm39) |
K603* |
probably null |
Het |
Selenbp1 |
G |
A |
3: 94,851,745 (GRCm39) |
V429I |
possibly damaging |
Het |
Setd5 |
T |
G |
6: 113,098,099 (GRCm39) |
S713A |
probably benign |
Het |
Shank1 |
T |
C |
7: 44,002,564 (GRCm39) |
Y1428H |
possibly damaging |
Het |
Slc11a1 |
G |
T |
1: 74,422,830 (GRCm39) |
W361L |
possibly damaging |
Het |
Spta1 |
A |
T |
1: 174,050,837 (GRCm39) |
D1772V |
possibly damaging |
Het |
St8sia6 |
T |
C |
2: 13,661,721 (GRCm39) |
H370R |
probably damaging |
Het |
Stkld1 |
A |
T |
2: 26,842,726 (GRCm39) |
D566V |
probably damaging |
Het |
Tango6 |
T |
C |
8: 107,415,791 (GRCm39) |
V204A |
probably benign |
Het |
Tdrd5 |
G |
A |
1: 156,129,293 (GRCm39) |
A139V |
probably damaging |
Het |
Tenm2 |
A |
T |
11: 36,062,263 (GRCm39) |
V534E |
probably damaging |
Het |
Tfip11 |
A |
T |
5: 112,479,044 (GRCm39) |
Q204L |
probably benign |
Het |
Tlr4 |
A |
T |
4: 66,759,430 (GRCm39) |
Q741L |
probably damaging |
Het |
Tmem18 |
A |
G |
12: 30,638,654 (GRCm39) |
M111V |
probably benign |
Het |
Togaram1 |
A |
G |
12: 65,042,292 (GRCm39) |
N1167S |
probably benign |
Het |
Trappc3 |
C |
T |
4: 126,168,945 (GRCm39) |
A145V |
possibly damaging |
Het |
Trbj2-3 |
T |
C |
6: 41,520,176 (GRCm39) |
F7S |
probably damaging |
Het |
Vinac1 |
A |
G |
2: 128,880,238 (GRCm39) |
S563P |
|
Het |
Vmn1r212 |
T |
A |
13: 23,067,731 (GRCm39) |
M201L |
probably benign |
Het |
Xaf1 |
C |
A |
11: 72,194,201 (GRCm39) |
C27* |
probably null |
Het |
Zeb1 |
T |
C |
18: 5,767,703 (GRCm39) |
V738A |
probably benign |
Het |
Zfp524 |
A |
T |
7: 5,020,883 (GRCm39) |
H137L |
probably damaging |
Het |
Zfyve19 |
A |
T |
2: 119,047,118 (GRCm39) |
H367L |
probably damaging |
Het |
Zim1 |
G |
A |
7: 6,680,872 (GRCm39) |
Q264* |
probably null |
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 |
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 |
R8309:Rp1
|
UTSW |
1 |
4,417,312 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
|