Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aco1 |
A |
G |
4: 40,197,566 (GRCm39) |
K857E |
probably benign |
Het |
Adam20 |
A |
G |
8: 41,249,080 (GRCm39) |
N397D |
probably benign |
Het |
Adgrf3 |
T |
G |
5: 30,404,211 (GRCm39) |
D347A |
probably damaging |
Het |
Ang6 |
C |
T |
14: 44,239,330 (GRCm39) |
E133K |
possibly damaging |
Het |
Arhgap23 |
T |
A |
11: 97,354,234 (GRCm39) |
W205R |
probably damaging |
Het |
Arhgef40 |
C |
A |
14: 52,235,080 (GRCm39) |
R1086S |
probably damaging |
Het |
Atr |
G |
T |
9: 95,787,870 (GRCm39) |
A1488S |
probably benign |
Het |
Cabin1 |
A |
T |
10: 75,579,184 (GRCm39) |
|
probably null |
Het |
Cby2 |
C |
T |
14: 75,820,850 (GRCm39) |
V292I |
probably benign |
Het |
Cdh22 |
A |
C |
2: 164,985,614 (GRCm39) |
F324C |
probably damaging |
Het |
Chd9 |
A |
T |
8: 91,683,323 (GRCm39) |
K588* |
probably null |
Het |
Clns1a |
A |
T |
7: 97,346,066 (GRCm39) |
I44F |
probably damaging |
Het |
Colgalt1 |
T |
C |
8: 72,063,995 (GRCm39) |
I51T |
possibly damaging |
Het |
Cpt2 |
C |
T |
4: 107,761,452 (GRCm39) |
E217K |
possibly damaging |
Het |
Ctss |
A |
G |
3: 95,454,105 (GRCm39) |
|
probably null |
Het |
Cyp1a1 |
A |
G |
9: 57,609,980 (GRCm39) |
T465A |
probably benign |
Het |
Dbn1 |
A |
G |
13: 55,629,160 (GRCm39) |
|
probably null |
Het |
Dennd1b |
A |
G |
1: 139,018,143 (GRCm39) |
|
probably null |
Het |
Dnajc1 |
A |
C |
2: 18,298,838 (GRCm39) |
Y49* |
probably null |
Het |
Dock10 |
T |
A |
1: 80,520,918 (GRCm39) |
I1188L |
probably damaging |
Het |
Dsg1c |
T |
G |
18: 20,416,096 (GRCm39) |
|
probably null |
Het |
Efcab6 |
G |
A |
15: 83,851,822 (GRCm39) |
T352I |
possibly damaging |
Het |
Eps8l3 |
T |
C |
3: 107,786,902 (GRCm39) |
L26P |
possibly damaging |
Het |
Fbxw26 |
A |
G |
9: 109,553,946 (GRCm39) |
V231A |
probably benign |
Het |
Fetub |
G |
A |
16: 22,754,419 (GRCm39) |
E209K |
possibly damaging |
Het |
Galc |
A |
T |
12: 98,212,556 (GRCm39) |
|
probably null |
Het |
Gm6871 |
A |
T |
7: 41,222,892 (GRCm39) |
N65K |
probably benign |
Het |
Gstp3 |
A |
G |
19: 4,107,540 (GRCm39) |
I208T |
probably benign |
Het |
Gtpbp3 |
A |
G |
8: 71,945,272 (GRCm39) |
Y448C |
probably benign |
Het |
Hdac7 |
G |
T |
15: 97,705,857 (GRCm39) |
Q385K |
probably damaging |
Het |
Hemgn |
C |
T |
4: 46,396,655 (GRCm39) |
V194M |
possibly damaging |
Het |
Idh2 |
G |
C |
7: 79,748,625 (GRCm39) |
T113R |
probably benign |
Het |
Jarid2 |
A |
C |
13: 45,056,219 (GRCm39) |
K336T |
possibly damaging |
Het |
Kcnj4 |
C |
T |
15: 79,369,216 (GRCm39) |
V255M |
probably damaging |
Het |
Ldhb |
C |
A |
6: 142,439,934 (GRCm39) |
W202L |
probably damaging |
Het |
Lmbrd2 |
T |
A |
15: 9,177,838 (GRCm39) |
Y512* |
probably null |
Het |
Lrp1 |
A |
G |
10: 127,431,152 (GRCm39) |
|
probably null |
Het |
Map3k12 |
G |
A |
15: 102,411,970 (GRCm39) |
P365S |
probably damaging |
Het |
Map3k5 |
G |
A |
10: 19,979,909 (GRCm39) |
D806N |
probably benign |
Het |
Matn3 |
A |
G |
12: 9,017,662 (GRCm39) |
E438G |
possibly damaging |
Het |
Mcmbp |
G |
A |
7: 128,325,698 (GRCm39) |
L97F |
probably damaging |
Het |
Mmp3 |
A |
T |
9: 7,453,662 (GRCm39) |
I428L |
probably benign |
Het |
Mphosph8 |
T |
C |
14: 56,934,616 (GRCm39) |
V855A |
probably damaging |
Het |
Mycbp2 |
T |
A |
14: 103,393,150 (GRCm39) |
H3027L |
possibly damaging |
Het |
Nbea |
C |
T |
3: 55,989,857 (GRCm39) |
R333H |
probably damaging |
Het |
Notch1 |
G |
T |
2: 26,350,446 (GRCm39) |
H2231Q |
probably benign |
Het |
Npas2 |
A |
T |
1: 39,364,456 (GRCm39) |
H266L |
probably damaging |
Het |
Oas3 |
A |
G |
5: 120,898,045 (GRCm39) |
S833P |
probably damaging |
Het |
Or1j15 |
T |
C |
2: 36,458,789 (GRCm39) |
Y60H |
probably damaging |
Het |
Or5ak24 |
T |
C |
2: 85,260,265 (GRCm39) |
T303A |
probably benign |
Het |
Or5w17 |
A |
C |
2: 87,584,334 (GRCm39) |
M1R |
probably null |
Het |
Or6c65 |
G |
A |
10: 129,603,725 (GRCm39) |
R120H |
probably benign |
Het |
Pak4 |
C |
T |
7: 28,264,690 (GRCm39) |
V71I |
possibly damaging |
Het |
Pitpnm1 |
T |
C |
19: 4,162,395 (GRCm39) |
V1075A |
probably damaging |
Het |
Pkp3 |
G |
A |
7: 140,668,415 (GRCm39) |
V555M |
probably damaging |
Het |
Plekhm2 |
T |
C |
4: 141,359,685 (GRCm39) |
T381A |
probably benign |
Het |
Plppr3 |
A |
G |
10: 79,702,244 (GRCm39) |
|
probably null |
Het |
Ppp2r5e |
A |
T |
12: 75,516,540 (GRCm39) |
F216I |
possibly damaging |
Het |
Ppp3ca |
T |
A |
3: 136,627,672 (GRCm39) |
V412D |
probably benign |
Het |
Prss50 |
A |
G |
9: 110,687,081 (GRCm39) |
|
probably benign |
Het |
Psph |
A |
C |
5: 129,843,532 (GRCm39) |
I174R |
probably damaging |
Het |
Ptov1 |
A |
G |
7: 44,514,991 (GRCm39) |
Y207H |
possibly damaging |
Het |
Ptprs |
A |
G |
17: 56,741,510 (GRCm39) |
S585P |
probably damaging |
Het |
Rnf146 |
A |
T |
10: 29,223,720 (GRCm39) |
H55Q |
probably damaging |
Het |
Rnf213 |
T |
A |
11: 119,332,009 (GRCm39) |
M2407K |
probably damaging |
Het |
Rnls |
A |
C |
19: 33,179,931 (GRCm39) |
L55R |
possibly damaging |
Het |
Rptor |
T |
C |
11: 119,647,146 (GRCm39) |
C246R |
probably damaging |
Het |
Rrp12 |
C |
T |
19: 41,866,222 (GRCm39) |
|
probably null |
Het |
Samd3 |
A |
G |
10: 26,127,672 (GRCm39) |
D223G |
probably damaging |
Het |
Sdad1 |
G |
A |
5: 92,453,155 (GRCm39) |
Q68* |
probably null |
Het |
Selenov |
G |
A |
7: 27,989,847 (GRCm39) |
T219M |
probably damaging |
Het |
Shd |
A |
G |
17: 56,278,554 (GRCm39) |
D39G |
possibly damaging |
Het |
Slc26a10 |
A |
T |
10: 127,014,279 (GRCm39) |
V245E |
probably damaging |
Het |
Slit1 |
A |
G |
19: 41,614,012 (GRCm39) |
L820P |
probably damaging |
Het |
Snap23 |
T |
C |
2: 120,421,163 (GRCm39) |
F96L |
probably benign |
Het |
Speer1k |
T |
C |
5: 10,998,994 (GRCm39) |
|
probably benign |
Het |
Spef1l |
A |
T |
7: 139,556,005 (GRCm39) |
I212N |
probably benign |
Het |
Stkld1 |
A |
G |
2: 26,840,115 (GRCm39) |
H395R |
probably damaging |
Het |
Syt13 |
G |
A |
2: 92,771,165 (GRCm39) |
G84D |
probably damaging |
Het |
Terb2 |
T |
A |
2: 122,016,990 (GRCm39) |
L37Q |
probably damaging |
Het |
Themis |
A |
G |
10: 28,657,753 (GRCm39) |
Y107C |
probably damaging |
Het |
Top2a |
T |
A |
11: 98,906,895 (GRCm39) |
T249S |
probably benign |
Het |
Tspo2 |
A |
T |
17: 48,756,148 (GRCm39) |
F71Y |
probably damaging |
Het |
Ttc21b |
T |
A |
2: 66,053,921 (GRCm39) |
K753* |
probably null |
Het |
Ttk |
A |
G |
9: 83,736,915 (GRCm39) |
Y458C |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,586,017 (GRCm39) |
R21905G |
probably damaging |
Het |
Ugt3a1 |
T |
A |
15: 9,351,254 (GRCm39) |
F88I |
probably benign |
Het |
Vmn1r119 |
A |
G |
7: 20,746,121 (GRCm39) |
L87P |
probably damaging |
Het |
Vmn1r36 |
A |
G |
6: 66,693,747 (GRCm39) |
F6L |
probably benign |
Het |
Vmn2r15 |
T |
A |
5: 109,434,860 (GRCm39) |
K615* |
probably null |
Het |
Wdr18 |
G |
A |
10: 79,802,561 (GRCm39) |
|
probably null |
Het |
Wdr6 |
A |
T |
9: 108,453,176 (GRCm39) |
W236R |
probably damaging |
Het |
Zbtb48 |
T |
C |
4: 152,110,955 (GRCm39) |
T187A |
probably benign |
Het |
|
Other mutations in Cep350 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00764:Cep350
|
APN |
1 |
155,816,492 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL00821:Cep350
|
APN |
1 |
155,737,950 (GRCm39) |
missense |
probably benign |
|
IGL00837:Cep350
|
APN |
1 |
155,829,137 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00977:Cep350
|
APN |
1 |
155,808,611 (GRCm39) |
missense |
probably null |
0.99 |
IGL01544:Cep350
|
APN |
1 |
155,828,933 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01616:Cep350
|
APN |
1 |
155,828,993 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01695:Cep350
|
APN |
1 |
155,819,904 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01902:Cep350
|
APN |
1 |
155,737,731 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01977:Cep350
|
APN |
1 |
155,787,714 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02388:Cep350
|
APN |
1 |
155,829,499 (GRCm39) |
missense |
probably benign |
0.28 |
IGL02475:Cep350
|
APN |
1 |
155,738,341 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02528:Cep350
|
APN |
1 |
155,770,361 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02598:Cep350
|
APN |
1 |
155,738,713 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02676:Cep350
|
APN |
1 |
155,737,977 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02728:Cep350
|
APN |
1 |
155,828,968 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02744:Cep350
|
APN |
1 |
155,807,279 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02817:Cep350
|
APN |
1 |
155,804,588 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02892:Cep350
|
APN |
1 |
155,744,552 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL03156:Cep350
|
APN |
1 |
155,733,788 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03166:Cep350
|
APN |
1 |
155,739,346 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL03216:Cep350
|
APN |
1 |
155,736,373 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03268:Cep350
|
APN |
1 |
155,829,295 (GRCm39) |
missense |
probably benign |
0.16 |
IGL03358:Cep350
|
APN |
1 |
155,804,285 (GRCm39) |
missense |
probably benign |
|
primed
|
UTSW |
1 |
155,829,334 (GRCm39) |
missense |
probably damaging |
0.98 |
stoked
|
UTSW |
1 |
155,791,321 (GRCm39) |
missense |
probably benign |
0.03 |
NA:Cep350
|
UTSW |
1 |
155,834,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R0060:Cep350
|
UTSW |
1 |
155,804,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R0060:Cep350
|
UTSW |
1 |
155,804,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R0066:Cep350
|
UTSW |
1 |
155,786,964 (GRCm39) |
missense |
probably damaging |
0.99 |
R0066:Cep350
|
UTSW |
1 |
155,786,964 (GRCm39) |
missense |
probably damaging |
0.99 |
R0172:Cep350
|
UTSW |
1 |
155,829,193 (GRCm39) |
missense |
probably benign |
0.00 |
R0365:Cep350
|
UTSW |
1 |
155,782,317 (GRCm39) |
missense |
probably benign |
0.00 |
R0472:Cep350
|
UTSW |
1 |
155,790,469 (GRCm39) |
missense |
probably damaging |
0.99 |
R0502:Cep350
|
UTSW |
1 |
155,776,629 (GRCm39) |
splice site |
probably null |
|
R0538:Cep350
|
UTSW |
1 |
155,724,366 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0547:Cep350
|
UTSW |
1 |
155,777,181 (GRCm39) |
splice site |
probably null |
|
R0565:Cep350
|
UTSW |
1 |
155,836,941 (GRCm39) |
splice site |
probably benign |
|
R0607:Cep350
|
UTSW |
1 |
155,747,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R0645:Cep350
|
UTSW |
1 |
155,816,458 (GRCm39) |
splice site |
probably null |
|
R0675:Cep350
|
UTSW |
1 |
155,835,499 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0828:Cep350
|
UTSW |
1 |
155,828,992 (GRCm39) |
missense |
probably benign |
0.00 |
R0863:Cep350
|
UTSW |
1 |
155,737,981 (GRCm39) |
missense |
probably benign |
0.00 |
R0969:Cep350
|
UTSW |
1 |
155,816,572 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1102:Cep350
|
UTSW |
1 |
155,807,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R1186:Cep350
|
UTSW |
1 |
155,751,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R1552:Cep350
|
UTSW |
1 |
155,786,484 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1560:Cep350
|
UTSW |
1 |
155,804,825 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1698:Cep350
|
UTSW |
1 |
155,829,104 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1729:Cep350
|
UTSW |
1 |
155,787,727 (GRCm39) |
missense |
probably benign |
0.17 |
R1735:Cep350
|
UTSW |
1 |
155,828,960 (GRCm39) |
missense |
probably damaging |
0.99 |
R1740:Cep350
|
UTSW |
1 |
155,804,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Cep350
|
UTSW |
1 |
155,804,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R1848:Cep350
|
UTSW |
1 |
155,829,397 (GRCm39) |
missense |
probably benign |
0.28 |
R1988:Cep350
|
UTSW |
1 |
155,808,850 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2008:Cep350
|
UTSW |
1 |
155,790,467 (GRCm39) |
missense |
probably benign |
0.16 |
R2241:Cep350
|
UTSW |
1 |
155,834,302 (GRCm39) |
splice site |
probably null |
|
R2245:Cep350
|
UTSW |
1 |
155,754,766 (GRCm39) |
missense |
probably benign |
0.10 |
R2402:Cep350
|
UTSW |
1 |
155,738,882 (GRCm39) |
missense |
probably benign |
|
R2566:Cep350
|
UTSW |
1 |
155,835,464 (GRCm39) |
critical splice donor site |
probably null |
|
R3160:Cep350
|
UTSW |
1 |
155,738,910 (GRCm39) |
missense |
probably benign |
0.00 |
R3162:Cep350
|
UTSW |
1 |
155,738,910 (GRCm39) |
missense |
probably benign |
0.00 |
R3769:Cep350
|
UTSW |
1 |
155,828,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R4035:Cep350
|
UTSW |
1 |
155,835,541 (GRCm39) |
missense |
probably benign |
0.06 |
R4158:Cep350
|
UTSW |
1 |
155,808,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R4160:Cep350
|
UTSW |
1 |
155,808,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R4213:Cep350
|
UTSW |
1 |
155,811,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R4483:Cep350
|
UTSW |
1 |
155,802,214 (GRCm39) |
missense |
probably benign |
0.01 |
R4648:Cep350
|
UTSW |
1 |
155,778,344 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4694:Cep350
|
UTSW |
1 |
155,804,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R4836:Cep350
|
UTSW |
1 |
155,804,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R4839:Cep350
|
UTSW |
1 |
155,804,240 (GRCm39) |
missense |
probably benign |
0.00 |
R4969:Cep350
|
UTSW |
1 |
155,736,025 (GRCm39) |
missense |
probably damaging |
0.99 |
R5014:Cep350
|
UTSW |
1 |
155,803,952 (GRCm39) |
missense |
probably benign |
0.00 |
R5027:Cep350
|
UTSW |
1 |
155,809,100 (GRCm39) |
missense |
probably benign |
0.01 |
R5144:Cep350
|
UTSW |
1 |
155,786,896 (GRCm39) |
missense |
probably damaging |
0.99 |
R5153:Cep350
|
UTSW |
1 |
155,811,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R5165:Cep350
|
UTSW |
1 |
155,804,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R5182:Cep350
|
UTSW |
1 |
155,733,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R5445:Cep350
|
UTSW |
1 |
155,770,469 (GRCm39) |
missense |
probably benign |
0.01 |
R5738:Cep350
|
UTSW |
1 |
155,741,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R5809:Cep350
|
UTSW |
1 |
155,809,087 (GRCm39) |
missense |
probably damaging |
0.98 |
R5855:Cep350
|
UTSW |
1 |
155,829,508 (GRCm39) |
missense |
probably benign |
0.00 |
R6103:Cep350
|
UTSW |
1 |
155,800,322 (GRCm39) |
missense |
probably benign |
0.05 |
R6139:Cep350
|
UTSW |
1 |
155,829,025 (GRCm39) |
missense |
probably benign |
0.03 |
R6285:Cep350
|
UTSW |
1 |
155,829,120 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6430:Cep350
|
UTSW |
1 |
155,770,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R6446:Cep350
|
UTSW |
1 |
155,737,900 (GRCm39) |
missense |
probably benign |
|
R6520:Cep350
|
UTSW |
1 |
155,809,082 (GRCm39) |
missense |
probably benign |
0.02 |
R6712:Cep350
|
UTSW |
1 |
155,733,852 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6940:Cep350
|
UTSW |
1 |
155,804,297 (GRCm39) |
missense |
probably benign |
0.01 |
R7020:Cep350
|
UTSW |
1 |
155,804,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R7056:Cep350
|
UTSW |
1 |
155,724,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R7141:Cep350
|
UTSW |
1 |
155,790,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R7215:Cep350
|
UTSW |
1 |
155,770,453 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7247:Cep350
|
UTSW |
1 |
155,786,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R7272:Cep350
|
UTSW |
1 |
155,829,334 (GRCm39) |
missense |
probably damaging |
0.98 |
R7336:Cep350
|
UTSW |
1 |
155,738,022 (GRCm39) |
missense |
probably benign |
0.17 |
R7361:Cep350
|
UTSW |
1 |
155,777,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R7390:Cep350
|
UTSW |
1 |
155,741,833 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7402:Cep350
|
UTSW |
1 |
155,803,961 (GRCm39) |
missense |
probably benign |
0.00 |
R7428:Cep350
|
UTSW |
1 |
155,770,365 (GRCm39) |
missense |
probably benign |
0.00 |
R7440:Cep350
|
UTSW |
1 |
155,816,518 (GRCm39) |
missense |
probably damaging |
0.98 |
R7520:Cep350
|
UTSW |
1 |
155,791,375 (GRCm39) |
missense |
probably benign |
0.05 |
R7529:Cep350
|
UTSW |
1 |
155,737,669 (GRCm39) |
missense |
probably benign |
0.08 |
R7635:Cep350
|
UTSW |
1 |
155,754,767 (GRCm39) |
nonsense |
probably null |
|
R7806:Cep350
|
UTSW |
1 |
155,737,809 (GRCm39) |
missense |
probably benign |
0.00 |
R8100:Cep350
|
UTSW |
1 |
155,829,148 (GRCm39) |
missense |
probably damaging |
0.97 |
R8192:Cep350
|
UTSW |
1 |
155,816,529 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8193:Cep350
|
UTSW |
1 |
155,737,825 (GRCm39) |
missense |
probably benign |
0.01 |
R8351:Cep350
|
UTSW |
1 |
155,747,780 (GRCm39) |
missense |
probably damaging |
0.99 |
R8406:Cep350
|
UTSW |
1 |
155,798,164 (GRCm39) |
missense |
probably benign |
0.00 |
R8451:Cep350
|
UTSW |
1 |
155,747,780 (GRCm39) |
missense |
probably damaging |
0.99 |
R8467:Cep350
|
UTSW |
1 |
155,791,321 (GRCm39) |
missense |
probably benign |
0.03 |
R8543:Cep350
|
UTSW |
1 |
155,738,122 (GRCm39) |
missense |
probably damaging |
0.98 |
R8714:Cep350
|
UTSW |
1 |
155,736,477 (GRCm39) |
missense |
probably damaging |
0.98 |
R8810:Cep350
|
UTSW |
1 |
155,803,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R8837:Cep350
|
UTSW |
1 |
155,737,518 (GRCm39) |
missense |
probably benign |
0.09 |
R8933:Cep350
|
UTSW |
1 |
155,739,161 (GRCm39) |
missense |
probably benign |
0.01 |
R9043:Cep350
|
UTSW |
1 |
155,773,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R9050:Cep350
|
UTSW |
1 |
155,738,687 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9067:Cep350
|
UTSW |
1 |
155,737,485 (GRCm39) |
missense |
probably benign |
0.00 |
R9105:Cep350
|
UTSW |
1 |
155,835,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R9295:Cep350
|
UTSW |
1 |
155,738,051 (GRCm39) |
nonsense |
probably null |
|
R9304:Cep350
|
UTSW |
1 |
155,829,464 (GRCm39) |
missense |
probably damaging |
0.98 |
R9456:Cep350
|
UTSW |
1 |
155,744,457 (GRCm39) |
missense |
probably benign |
0.00 |
R9575:Cep350
|
UTSW |
1 |
155,751,113 (GRCm39) |
missense |
probably benign |
0.03 |
R9715:Cep350
|
UTSW |
1 |
155,751,107 (GRCm39) |
missense |
probably benign |
0.00 |
R9749:Cep350
|
UTSW |
1 |
155,828,985 (GRCm39) |
missense |
probably benign |
0.02 |
R9758:Cep350
|
UTSW |
1 |
155,770,433 (GRCm39) |
missense |
probably damaging |
0.96 |
R9767:Cep350
|
UTSW |
1 |
155,739,018 (GRCm39) |
missense |
probably benign |
0.01 |
RF020:Cep350
|
UTSW |
1 |
155,791,224 (GRCm39) |
missense |
probably benign |
0.34 |
X0018:Cep350
|
UTSW |
1 |
155,829,032 (GRCm39) |
missense |
probably benign |
0.13 |
|