Other mutations in this stock |
Total: 150 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700016H13Rik |
T |
C |
5: 103,648,821 (GRCm38) |
*118W |
probably null |
Het |
1700061G19Rik |
A |
T |
17: 56,883,835 (GRCm38) |
N468Y |
probably benign |
Het |
4930595M18Rik |
G |
T |
X: 81,420,931 (GRCm38) |
T390N |
possibly damaging |
Het |
Abca13 |
C |
T |
11: 9,291,238 (GRCm38) |
Q1034* |
probably null |
Het |
Adgra3 |
T |
C |
5: 49,960,723 (GRCm38) |
H1161R |
probably damaging |
Het |
AF529169 |
T |
C |
9: 89,602,417 (GRCm38) |
H309R |
probably benign |
Het |
Aff1 |
T |
C |
5: 103,826,138 (GRCm38) |
|
probably benign |
Het |
Agap2 |
A |
G |
10: 127,091,702 (GRCm38) |
T1131A |
possibly damaging |
Het |
Ankrd12 |
A |
G |
17: 65,985,132 (GRCm38) |
V1102A |
probably benign |
Het |
Ankrd54 |
A |
T |
15: 79,062,731 (GRCm38) |
C23S |
probably damaging |
Het |
Anxa10 |
C |
T |
8: 62,077,967 (GRCm38) |
V70I |
probably benign |
Het |
Asap3 |
T |
C |
4: 136,234,325 (GRCm38) |
|
probably benign |
Het |
Asb13 |
T |
C |
13: 3,645,052 (GRCm38) |
|
probably null |
Het |
Atp6v1a |
A |
T |
16: 44,101,692 (GRCm38) |
|
probably benign |
Het |
Atp8b1 |
T |
G |
18: 64,564,541 (GRCm38) |
I411L |
probably benign |
Het |
Baiap3 |
T |
A |
17: 25,249,101 (GRCm38) |
N313I |
probably damaging |
Het |
Bok |
T |
C |
1: 93,686,487 (GRCm38) |
I14T |
probably benign |
Het |
Bri3bp |
T |
A |
5: 125,441,744 (GRCm38) |
|
probably null |
Het |
C2cd2l |
A |
G |
9: 44,316,202 (GRCm38) |
L186P |
probably damaging |
Het |
Cadm2 |
A |
T |
16: 66,882,814 (GRCm38) |
C44S |
probably damaging |
Het |
Capn11 |
T |
C |
17: 45,638,881 (GRCm38) |
|
probably benign |
Het |
Carm1 |
T |
A |
9: 21,569,591 (GRCm38) |
|
probably benign |
Het |
Ccdc189 |
T |
C |
7: 127,584,862 (GRCm38) |
E261G |
probably damaging |
Het |
Ccdc27 |
T |
C |
4: 154,036,484 (GRCm38) |
E285G |
unknown |
Het |
Cct3 |
T |
A |
3: 88,313,557 (GRCm38) |
D298E |
probably damaging |
Het |
Cd59b |
T |
A |
2: 104,080,986 (GRCm38) |
|
probably benign |
Het |
Cdh2 |
T |
C |
18: 16,629,576 (GRCm38) |
N437S |
probably benign |
Het |
Celsr3 |
T |
A |
9: 108,842,633 (GRCm38) |
I2470N |
probably damaging |
Het |
Cfap100 |
G |
A |
6: 90,415,906 (GRCm38) |
|
probably benign |
Het |
Cfap45 |
A |
T |
1: 172,532,189 (GRCm38) |
R98S |
possibly damaging |
Het |
Cfap54 |
T |
A |
10: 92,870,669 (GRCm38) |
H2757L |
unknown |
Het |
Chd1 |
C |
A |
17: 15,725,431 (GRCm38) |
N72K |
probably benign |
Het |
Cntn4 |
A |
T |
6: 106,667,540 (GRCm38) |
|
probably benign |
Het |
Cstf2t |
A |
T |
19: 31,084,626 (GRCm38) |
M521L |
probably benign |
Het |
Daam2 |
A |
T |
17: 49,498,883 (GRCm38) |
|
probably benign |
Het |
Ddias |
A |
T |
7: 92,859,337 (GRCm38) |
W457R |
probably benign |
Het |
Ddr2 |
C |
T |
1: 169,994,629 (GRCm38) |
V417I |
probably benign |
Het |
Dhx57 |
T |
C |
17: 80,270,371 (GRCm38) |
T570A |
probably damaging |
Het |
Dmp1 |
A |
G |
5: 104,207,630 (GRCm38) |
E32G |
possibly damaging |
Het |
Dtymk |
C |
T |
1: 93,801,788 (GRCm38) |
V14M |
possibly damaging |
Het |
Dync2li1 |
G |
A |
17: 84,649,271 (GRCm38) |
M286I |
probably benign |
Het |
Eea1 |
G |
A |
10: 96,021,667 (GRCm38) |
D664N |
possibly damaging |
Het |
Esp6 |
G |
T |
17: 40,565,396 (GRCm38) |
V112L |
probably benign |
Het |
Fam83h |
G |
T |
15: 76,006,169 (GRCm38) |
Q127K |
probably damaging |
Het |
Gabbr2 |
G |
A |
4: 46,677,474 (GRCm38) |
T802I |
probably benign |
Het |
Gart |
C |
A |
16: 91,623,403 (GRCm38) |
D851Y |
possibly damaging |
Het |
Gemin6 |
T |
A |
17: 80,228,095 (GRCm38) |
H161Q |
probably damaging |
Het |
Gm10912 |
T |
C |
2: 104,066,530 (GRCm38) |
S5P |
probably benign |
Het |
Gm4907 |
A |
T |
X: 23,907,051 (GRCm38) |
I264F |
probably benign |
Het |
Gm5941 |
G |
A |
X: 92,490,211 (GRCm38) |
A62T |
possibly damaging |
Het |
Gng2 |
G |
T |
14: 19,891,295 (GRCm38) |
D26E |
probably benign |
Het |
Gpr33 |
A |
G |
12: 52,023,635 (GRCm38) |
V207A |
probably benign |
Het |
Gstm3 |
T |
A |
3: 107,966,270 (GRCm38) |
|
probably benign |
Het |
Havcr1 |
T |
C |
11: 46,752,432 (GRCm38) |
C60R |
probably damaging |
Het |
Hspg2 |
T |
C |
4: 137,541,440 (GRCm38) |
S2157P |
probably benign |
Het |
Ift140 |
A |
G |
17: 25,090,933 (GRCm38) |
T1105A |
probably benign |
Het |
Igsf8 |
C |
A |
1: 172,316,259 (GRCm38) |
A56D |
possibly damaging |
Het |
Kat6a |
G |
T |
8: 22,862,214 (GRCm38) |
A5S |
probably damaging |
Het |
Kctd16 |
A |
G |
18: 40,530,775 (GRCm38) |
E319G |
probably damaging |
Het |
Kmo |
T |
C |
1: 175,647,140 (GRCm38) |
V157A |
possibly damaging |
Het |
Lrp5 |
T |
A |
19: 3,605,308 (GRCm38) |
I1071F |
probably damaging |
Het |
Lrrc17 |
A |
G |
5: 21,561,278 (GRCm38) |
T253A |
probably benign |
Het |
Mast2 |
T |
A |
4: 116,311,767 (GRCm38) |
H769L |
probably damaging |
Het |
Mast4 |
T |
C |
13: 102,853,900 (GRCm38) |
K50E |
probably damaging |
Het |
Mbd5 |
A |
G |
2: 49,256,689 (GRCm38) |
T304A |
possibly damaging |
Het |
Mbp |
T |
C |
18: 82,572,870 (GRCm38) |
S73P |
probably damaging |
Het |
Mc5r |
T |
A |
18: 68,339,092 (GRCm38) |
V174E |
probably damaging |
Het |
Med13 |
T |
A |
11: 86,307,038 (GRCm38) |
T736S |
probably benign |
Het |
Med13l |
T |
C |
5: 118,671,002 (GRCm38) |
|
probably benign |
Het |
Mlh3 |
C |
G |
12: 85,235,714 (GRCm38) |
A1382P |
possibly damaging |
Het |
Mpdz |
T |
C |
4: 81,359,991 (GRCm38) |
|
probably benign |
Het |
Muc5ac |
A |
G |
7: 141,796,265 (GRCm38) |
T582A |
possibly damaging |
Het |
Mum1l1 |
T |
A |
X: 139,235,695 (GRCm38) |
D327E |
probably damaging |
Het |
Nalcn |
A |
G |
14: 123,464,740 (GRCm38) |
F453S |
probably damaging |
Het |
Nrap |
T |
A |
19: 56,345,474 (GRCm38) |
M902L |
probably damaging |
Het |
Nup85 |
C |
T |
11: 115,568,370 (GRCm38) |
R100* |
probably null |
Het |
Nxf1 |
T |
G |
19: 8,764,591 (GRCm38) |
N296K |
probably damaging |
Het |
Ogg1 |
A |
G |
6: 113,328,420 (GRCm38) |
T65A |
probably damaging |
Het |
Ogt |
A |
G |
X: 101,644,199 (GRCm38) |
|
probably benign |
Het |
Olfr1258 |
A |
G |
2: 89,930,201 (GRCm38) |
T131A |
probably benign |
Het |
Olfr1298 |
C |
T |
2: 111,645,791 (GRCm38) |
V69I |
probably benign |
Het |
Olfr504 |
T |
A |
7: 108,565,276 (GRCm38) |
N173I |
probably benign |
Het |
Olfr558 |
T |
A |
7: 102,709,995 (GRCm38) |
H245Q |
probably damaging |
Het |
Ovol2 |
T |
C |
2: 144,331,790 (GRCm38) |
D24G |
probably damaging |
Het |
Pabpc1 |
A |
G |
15: 36,599,054 (GRCm38) |
|
probably benign |
Het |
Pak6 |
T |
C |
2: 118,693,687 (GRCm38) |
L441P |
probably damaging |
Het |
Pappa |
T |
A |
4: 65,189,315 (GRCm38) |
C654* |
probably null |
Het |
Paqr6 |
T |
A |
3: 88,365,991 (GRCm38) |
S97T |
probably damaging |
Het |
Parp14 |
T |
C |
16: 35,858,518 (GRCm38) |
N360S |
probably benign |
Het |
Pclo |
G |
T |
5: 14,677,859 (GRCm38) |
G2244* |
probably null |
Het |
Pdzrn3 |
A |
T |
6: 101,155,942 (GRCm38) |
|
probably null |
Het |
Pes1 |
T |
C |
11: 3,975,557 (GRCm38) |
M220T |
probably damaging |
Het |
Phip |
A |
T |
9: 82,876,221 (GRCm38) |
V1473E |
probably benign |
Het |
Pkd2l2 |
T |
A |
18: 34,430,268 (GRCm38) |
|
probably null |
Het |
Plch1 |
T |
C |
3: 63,753,256 (GRCm38) |
D302G |
probably damaging |
Het |
Plekhh2 |
A |
G |
17: 84,618,031 (GRCm38) |
T1419A |
probably benign |
Het |
Ppara |
A |
T |
15: 85,798,171 (GRCm38) |
E356V |
probably damaging |
Het |
Ppp1r37 |
G |
A |
7: 19,532,177 (GRCm38) |
P555S |
probably benign |
Het |
Ppp6r1 |
T |
C |
7: 4,639,710 (GRCm38) |
E545G |
possibly damaging |
Het |
Proser3 |
G |
A |
7: 30,540,699 (GRCm38) |
H327Y |
probably damaging |
Het |
Prss43 |
T |
A |
9: 110,829,508 (GRCm38) |
I292N |
probably damaging |
Het |
Pygl |
G |
C |
12: 70,206,404 (GRCm38) |
N271K |
probably damaging |
Het |
Rassf7 |
T |
A |
7: 141,216,990 (GRCm38) |
|
probably benign |
Het |
Rfx2 |
T |
C |
17: 56,803,722 (GRCm38) |
Y88C |
probably damaging |
Het |
Rpl6 |
T |
C |
5: 121,208,478 (GRCm38) |
V214A |
probably benign |
Het |
Rspo1 |
T |
A |
4: 124,991,432 (GRCm38) |
|
probably null |
Het |
Sav1 |
A |
C |
12: 69,966,205 (GRCm38) |
L366V |
probably benign |
Het |
Sema3b |
T |
G |
9: 107,604,156 (GRCm38) |
T52P |
possibly damaging |
Het |
Senp6 |
A |
G |
9: 80,116,559 (GRCm38) |
D40G |
probably damaging |
Het |
Sh3pxd2a |
A |
G |
19: 47,268,207 (GRCm38) |
S719P |
probably damaging |
Het |
Shank1 |
C |
T |
7: 44,352,294 (GRCm38) |
R1146W |
unknown |
Het |
Slc34a3 |
G |
T |
2: 25,231,233 (GRCm38) |
D307E |
probably benign |
Het |
Slc35b3 |
T |
C |
13: 38,937,275 (GRCm38) |
I330V |
probably benign |
Het |
Slc4a10 |
G |
A |
2: 62,243,398 (GRCm38) |
C268Y |
probably benign |
Het |
Slco6d1 |
A |
G |
1: 98,421,399 (GRCm38) |
E65G |
probably benign |
Het |
Slit2 |
A |
G |
5: 48,245,573 (GRCm38) |
|
probably benign |
Het |
Smcr8 |
T |
C |
11: 60,778,115 (GRCm38) |
Y30H |
probably damaging |
Het |
Snap47 |
A |
G |
11: 59,438,500 (GRCm38) |
|
probably benign |
Het |
Snrnp25 |
G |
A |
11: 32,206,960 (GRCm38) |
V15I |
probably damaging |
Het |
Spns2 |
T |
C |
11: 72,454,397 (GRCm38) |
Y449C |
probably damaging |
Het |
Stab2 |
T |
A |
10: 86,924,450 (GRCm38) |
|
probably benign |
Het |
Strip1 |
C |
A |
3: 107,614,613 (GRCm38) |
D750Y |
probably damaging |
Het |
Taf1c |
A |
T |
8: 119,599,983 (GRCm38) |
I438N |
probably damaging |
Het |
Tbc1d2 |
T |
A |
4: 46,609,003 (GRCm38) |
K745* |
probably null |
Het |
Tctn1 |
T |
C |
5: 122,264,144 (GRCm38) |
T76A |
probably damaging |
Het |
Tfpi |
T |
C |
2: 84,443,320 (GRCm38) |
|
probably benign |
Het |
Timm44 |
A |
T |
8: 4,266,592 (GRCm38) |
H317Q |
probably benign |
Het |
Tnfaip1 |
A |
T |
11: 78,530,014 (GRCm38) |
|
probably benign |
Het |
Tnpo3 |
A |
T |
6: 29,554,993 (GRCm38) |
|
probably benign |
Het |
Top3b |
T |
C |
16: 16,879,437 (GRCm38) |
|
probably benign |
Het |
Trak1 |
T |
A |
9: 121,453,285 (GRCm38) |
M410K |
possibly damaging |
Het |
Trpm3 |
C |
A |
19: 22,978,654 (GRCm38) |
P1160Q |
probably damaging |
Het |
Tyk2 |
T |
A |
9: 21,111,137 (GRCm38) |
T799S |
possibly damaging |
Het |
Ubfd1 |
G |
A |
7: 122,067,491 (GRCm38) |
|
probably benign |
Het |
Unc13a |
G |
A |
8: 71,642,173 (GRCm38) |
R1272* |
probably null |
Het |
Unc45b |
T |
A |
11: 82,940,205 (GRCm38) |
L797Q |
possibly damaging |
Het |
Urb2 |
C |
T |
8: 124,030,970 (GRCm38) |
Q1139* |
probably null |
Het |
Vmn2r66 |
A |
T |
7: 85,007,862 (GRCm38) |
S112T |
probably benign |
Het |
Vmn2r71 |
A |
T |
7: 85,623,634 (GRCm38) |
D552V |
probably benign |
Het |
Vmn2r76 |
A |
G |
7: 86,228,696 (GRCm38) |
Y498H |
probably benign |
Het |
Vmn2r84 |
A |
C |
10: 130,391,115 (GRCm38) |
W285G |
probably damaging |
Het |
Vps72 |
G |
T |
3: 95,122,583 (GRCm38) |
L304F |
probably damaging |
Het |
Wiz |
A |
T |
17: 32,356,441 (GRCm38) |
I907N |
probably damaging |
Het |
Yaf2 |
T |
C |
15: 93,285,536 (GRCm38) |
K131R |
probably damaging |
Het |
Zfp141 |
A |
T |
7: 42,476,056 (GRCm38) |
Y331N |
possibly damaging |
Het |
Zfp324 |
G |
T |
7: 12,971,024 (GRCm38) |
C380F |
probably damaging |
Het |
Zfp521 |
T |
C |
18: 13,845,062 (GRCm38) |
T765A |
probably benign |
Het |
Zfp616 |
A |
T |
11: 74,085,674 (GRCm38) |
H923L |
probably damaging |
Het |
Zfpm1 |
C |
T |
8: 122,335,846 (GRCm38) |
T548M |
probably damaging |
Het |
Zp2 |
A |
T |
7: 120,143,576 (GRCm38) |
|
probably benign |
Het |
|
Other mutations in 1110002E22Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0026:1110002E22Rik
|
UTSW |
3 |
138,066,805 (GRCm38) |
missense |
possibly damaging |
0.95 |
R0047:1110002E22Rik
|
UTSW |
3 |
138,066,264 (GRCm38) |
missense |
probably damaging |
0.97 |
R0047:1110002E22Rik
|
UTSW |
3 |
138,066,264 (GRCm38) |
missense |
probably damaging |
0.97 |
R0102:1110002E22Rik
|
UTSW |
3 |
138,068,113 (GRCm38) |
missense |
probably damaging |
1.00 |
R0102:1110002E22Rik
|
UTSW |
3 |
138,068,113 (GRCm38) |
missense |
probably damaging |
1.00 |
R0197:1110002E22Rik
|
UTSW |
3 |
138,069,871 (GRCm38) |
missense |
probably damaging |
1.00 |
R0239:1110002E22Rik
|
UTSW |
3 |
138,065,834 (GRCm38) |
small deletion |
probably benign |
|
R0394:1110002E22Rik
|
UTSW |
3 |
138,067,304 (GRCm38) |
missense |
probably damaging |
0.99 |
R0401:1110002E22Rik
|
UTSW |
3 |
138,070,306 (GRCm38) |
missense |
possibly damaging |
0.73 |
R0496:1110002E22Rik
|
UTSW |
3 |
138,068,244 (GRCm38) |
missense |
probably damaging |
1.00 |
R0591:1110002E22Rik
|
UTSW |
3 |
138,068,943 (GRCm38) |
nonsense |
probably null |
|
R0711:1110002E22Rik
|
UTSW |
3 |
138,068,225 (GRCm38) |
missense |
probably damaging |
0.99 |
R0908:1110002E22Rik
|
UTSW |
3 |
138,070,077 (GRCm38) |
missense |
probably damaging |
0.99 |
R0968:1110002E22Rik
|
UTSW |
3 |
138,067,206 (GRCm38) |
missense |
probably damaging |
0.99 |
R1023:1110002E22Rik
|
UTSW |
3 |
138,066,871 (GRCm38) |
missense |
probably damaging |
1.00 |
R1168:1110002E22Rik
|
UTSW |
3 |
138,067,900 (GRCm38) |
missense |
probably benign |
0.20 |
R1472:1110002E22Rik
|
UTSW |
3 |
138,067,552 (GRCm38) |
missense |
possibly damaging |
0.95 |
R1538:1110002E22Rik
|
UTSW |
3 |
138,065,401 (GRCm38) |
missense |
probably benign |
0.02 |
R1648:1110002E22Rik
|
UTSW |
3 |
138,069,420 (GRCm38) |
missense |
probably benign |
0.18 |
R1800:1110002E22Rik
|
UTSW |
3 |
138,066,718 (GRCm38) |
missense |
probably damaging |
1.00 |
R1919:1110002E22Rik
|
UTSW |
3 |
138,067,270 (GRCm38) |
missense |
probably damaging |
0.99 |
R1974:1110002E22Rik
|
UTSW |
3 |
138,067,267 (GRCm38) |
missense |
probably damaging |
1.00 |
R1990:1110002E22Rik
|
UTSW |
3 |
138,065,658 (GRCm38) |
nonsense |
probably null |
|
R1991:1110002E22Rik
|
UTSW |
3 |
138,065,658 (GRCm38) |
nonsense |
probably null |
|
R2102:1110002E22Rik
|
UTSW |
3 |
138,065,173 (GRCm38) |
missense |
probably damaging |
0.99 |
R2761:1110002E22Rik
|
UTSW |
3 |
138,067,780 (GRCm38) |
missense |
probably damaging |
0.99 |
R2899:1110002E22Rik
|
UTSW |
3 |
138,065,682 (GRCm38) |
missense |
probably benign |
0.00 |
R3618:1110002E22Rik
|
UTSW |
3 |
138,068,407 (GRCm38) |
missense |
probably damaging |
1.00 |
R3904:1110002E22Rik
|
UTSW |
3 |
138,066,639 (GRCm38) |
missense |
probably benign |
0.15 |
R3955:1110002E22Rik
|
UTSW |
3 |
138,068,073 (GRCm38) |
missense |
probably benign |
0.00 |
R4520:1110002E22Rik
|
UTSW |
3 |
138,070,266 (GRCm38) |
missense |
probably damaging |
0.99 |
R4619:1110002E22Rik
|
UTSW |
3 |
138,069,759 (GRCm38) |
missense |
probably damaging |
0.99 |
R4736:1110002E22Rik
|
UTSW |
3 |
138,068,485 (GRCm38) |
missense |
probably damaging |
0.99 |
R4752:1110002E22Rik
|
UTSW |
3 |
138,069,990 (GRCm38) |
missense |
possibly damaging |
0.91 |
R4777:1110002E22Rik
|
UTSW |
3 |
138,065,742 (GRCm38) |
missense |
probably benign |
0.09 |
R4780:1110002E22Rik
|
UTSW |
3 |
138,065,370 (GRCm38) |
missense |
probably benign |
0.02 |
R4824:1110002E22Rik
|
UTSW |
3 |
138,065,676 (GRCm38) |
missense |
probably benign |
0.00 |
R4829:1110002E22Rik
|
UTSW |
3 |
138,069,019 (GRCm38) |
missense |
probably damaging |
0.99 |
R4965:1110002E22Rik
|
UTSW |
3 |
138,069,672 (GRCm38) |
missense |
probably benign |
|
R5206:1110002E22Rik
|
UTSW |
3 |
138,066,511 (GRCm38) |
missense |
probably benign |
0.00 |
R5212:1110002E22Rik
|
UTSW |
3 |
138,065,850 (GRCm38) |
missense |
possibly damaging |
0.85 |
R5373:1110002E22Rik
|
UTSW |
3 |
138,067,635 (GRCm38) |
missense |
probably benign |
|
R5374:1110002E22Rik
|
UTSW |
3 |
138,067,635 (GRCm38) |
missense |
probably benign |
|
R5506:1110002E22Rik
|
UTSW |
3 |
138,067,947 (GRCm38) |
missense |
probably damaging |
1.00 |
R5528:1110002E22Rik
|
UTSW |
3 |
138,066,499 (GRCm38) |
missense |
probably benign |
|
R5536:1110002E22Rik
|
UTSW |
3 |
138,066,388 (GRCm38) |
missense |
possibly damaging |
0.89 |
R5587:1110002E22Rik
|
UTSW |
3 |
138,065,409 (GRCm38) |
missense |
probably benign |
|
R5759:1110002E22Rik
|
UTSW |
3 |
138,068,658 (GRCm38) |
missense |
probably benign |
|
R5933:1110002E22Rik
|
UTSW |
3 |
138,070,348 (GRCm38) |
missense |
probably damaging |
1.00 |
R5957:1110002E22Rik
|
UTSW |
3 |
138,070,161 (GRCm38) |
missense |
probably benign |
|
R6092:1110002E22Rik
|
UTSW |
3 |
138,068,940 (GRCm38) |
missense |
probably benign |
0.02 |
R6305:1110002E22Rik
|
UTSW |
3 |
138,067,980 (GRCm38) |
missense |
probably damaging |
1.00 |
R6457:1110002E22Rik
|
UTSW |
3 |
138,066,622 (GRCm38) |
missense |
probably damaging |
1.00 |
R6469:1110002E22Rik
|
UTSW |
3 |
138,066,975 (GRCm38) |
missense |
probably damaging |
0.97 |
R6499:1110002E22Rik
|
UTSW |
3 |
138,068,800 (GRCm38) |
missense |
probably damaging |
1.00 |
R6527:1110002E22Rik
|
UTSW |
3 |
138,067,527 (GRCm38) |
missense |
probably damaging |
0.99 |
R6580:1110002E22Rik
|
UTSW |
3 |
138,066,625 (GRCm38) |
missense |
probably benign |
0.00 |
R6693:1110002E22Rik
|
UTSW |
3 |
138,069,154 (GRCm38) |
missense |
probably benign |
0.00 |
R6751:1110002E22Rik
|
UTSW |
3 |
138,066,210 (GRCm38) |
missense |
probably damaging |
1.00 |
R6852:1110002E22Rik
|
UTSW |
3 |
138,065,169 (GRCm38) |
nonsense |
probably null |
|
R6920:1110002E22Rik
|
UTSW |
3 |
138,068,050 (GRCm38) |
missense |
probably damaging |
1.00 |
R7001:1110002E22Rik
|
UTSW |
3 |
138,065,511 (GRCm38) |
missense |
probably benign |
|
R7145:1110002E22Rik
|
UTSW |
3 |
138,070,059 (GRCm38) |
missense |
probably damaging |
1.00 |
R7238:1110002E22Rik
|
UTSW |
3 |
138,069,951 (GRCm38) |
missense |
probably damaging |
1.00 |
R7278:1110002E22Rik
|
UTSW |
3 |
138,065,476 (GRCm38) |
missense |
probably benign |
|
R7425:1110002E22Rik
|
UTSW |
3 |
138,065,695 (GRCm38) |
missense |
probably benign |
0.00 |
R7487:1110002E22Rik
|
UTSW |
3 |
138,066,868 (GRCm38) |
missense |
probably damaging |
1.00 |
R7557:1110002E22Rik
|
UTSW |
3 |
138,068,283 (GRCm38) |
nonsense |
probably null |
|
R7663:1110002E22Rik
|
UTSW |
3 |
138,066,126 (GRCm38) |
missense |
probably damaging |
0.98 |
R7743:1110002E22Rik
|
UTSW |
3 |
138,068,755 (GRCm38) |
missense |
probably damaging |
1.00 |
R7799:1110002E22Rik
|
UTSW |
3 |
138,069,601 (GRCm38) |
missense |
probably benign |
0.33 |
R8181:1110002E22Rik
|
UTSW |
3 |
138,068,395 (GRCm38) |
missense |
probably damaging |
0.99 |
R8264:1110002E22Rik
|
UTSW |
3 |
138,067,782 (GRCm38) |
missense |
probably damaging |
0.99 |
R8273:1110002E22Rik
|
UTSW |
3 |
138,066,450 (GRCm38) |
missense |
probably benign |
|
R8434:1110002E22Rik
|
UTSW |
3 |
138,067,260 (GRCm38) |
missense |
probably damaging |
0.97 |
R8530:1110002E22Rik
|
UTSW |
3 |
138,068,825 (GRCm38) |
missense |
probably damaging |
0.99 |
R8754:1110002E22Rik
|
UTSW |
3 |
138,066,037 (GRCm38) |
missense |
probably benign |
|
R8808:1110002E22Rik
|
UTSW |
3 |
138,070,113 (GRCm38) |
missense |
probably benign |
0.01 |
R8891:1110002E22Rik
|
UTSW |
3 |
138,066,759 (GRCm38) |
nonsense |
probably null |
|
R9026:1110002E22Rik
|
UTSW |
3 |
138,065,148 (GRCm38) |
missense |
possibly damaging |
0.53 |
R9177:1110002E22Rik
|
UTSW |
3 |
138,069,916 (GRCm38) |
missense |
probably damaging |
1.00 |
R9250:1110002E22Rik
|
UTSW |
3 |
138,066,628 (GRCm38) |
missense |
probably damaging |
1.00 |
R9291:1110002E22Rik
|
UTSW |
3 |
138,066,703 (GRCm38) |
missense |
probably benign |
0.02 |
R9293:1110002E22Rik
|
UTSW |
3 |
138,066,078 (GRCm38) |
missense |
possibly damaging |
0.93 |
R9307:1110002E22Rik
|
UTSW |
3 |
138,065,422 (GRCm38) |
missense |
probably benign |
0.04 |
R9439:1110002E22Rik
|
UTSW |
3 |
138,066,287 (GRCm38) |
missense |
probably benign |
0.00 |
R9509:1110002E22Rik
|
UTSW |
3 |
138,065,834 (GRCm38) |
small deletion |
probably benign |
|
R9582:1110002E22Rik
|
UTSW |
3 |
138,067,005 (GRCm38) |
missense |
probably damaging |
0.99 |
R9599:1110002E22Rik
|
UTSW |
3 |
138,068,506 (GRCm38) |
missense |
probably benign |
0.16 |
R9613:1110002E22Rik
|
UTSW |
3 |
138,065,365 (GRCm38) |
missense |
probably damaging |
0.98 |
R9670:1110002E22Rik
|
UTSW |
3 |
138,065,133 (GRCm38) |
missense |
probably benign |
|
X0003:1110002E22Rik
|
UTSW |
3 |
138,069,096 (GRCm38) |
missense |
probably damaging |
1.00 |
|