Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acan |
T |
C |
7: 78,749,452 (GRCm39) |
S1408P |
probably damaging |
Het |
Acap3 |
T |
C |
4: 155,990,169 (GRCm39) |
V783A |
probably damaging |
Het |
Akap8 |
T |
C |
17: 32,525,504 (GRCm39) |
N525S |
probably damaging |
Het |
Aqp1 |
C |
T |
6: 55,313,606 (GRCm39) |
T44M |
probably damaging |
Het |
Arap1 |
T |
C |
7: 101,053,585 (GRCm39) |
Y1305H |
probably damaging |
Het |
Atg2a |
T |
G |
19: 6,300,651 (GRCm39) |
S743A |
probably benign |
Het |
AW551984 |
G |
T |
9: 39,511,307 (GRCm39) |
L133I |
probably damaging |
Het |
Bahcc1 |
C |
A |
11: 120,164,587 (GRCm39) |
P802T |
possibly damaging |
Het |
Brd8 |
C |
A |
18: 34,743,002 (GRCm39) |
V288L |
probably benign |
Het |
Carmil2 |
T |
C |
8: 106,412,947 (GRCm39) |
|
probably null |
Het |
Catspere2 |
G |
A |
1: 177,905,048 (GRCm39) |
E153K |
possibly damaging |
Het |
Ccdc162 |
C |
T |
10: 41,542,737 (GRCm39) |
R379Q |
probably benign |
Het |
Cd200l1 |
T |
C |
16: 45,264,199 (GRCm39) |
T120A |
probably benign |
Het |
Cdh16 |
A |
G |
8: 105,341,136 (GRCm39) |
L116P |
probably damaging |
Het |
Cenpj |
A |
T |
14: 56,796,076 (GRCm39) |
H260Q |
possibly damaging |
Het |
Cenpq |
A |
G |
17: 41,244,027 (GRCm39) |
V17A |
possibly damaging |
Het |
Chil4 |
C |
A |
3: 106,109,121 (GRCm39) |
C394F |
probably damaging |
Het |
Chst9 |
T |
C |
18: 15,850,983 (GRCm39) |
I28V |
probably benign |
Het |
Clasp2 |
C |
A |
9: 113,728,649 (GRCm39) |
N873K |
probably damaging |
Het |
Clec4b2 |
T |
A |
6: 123,158,269 (GRCm39) |
M45K |
probably benign |
Het |
Cmya5 |
T |
A |
13: 93,200,048 (GRCm39) |
T3427S |
possibly damaging |
Het |
Cnih4 |
A |
G |
1: 180,989,777 (GRCm39) |
Y130C |
probably damaging |
Het |
Cpne9 |
T |
A |
6: 113,281,506 (GRCm39) |
M529K |
probably damaging |
Het |
Crppa |
A |
T |
12: 36,440,481 (GRCm39) |
N130Y |
probably damaging |
Het |
Ctsr |
T |
A |
13: 61,309,639 (GRCm39) |
Y190F |
probably damaging |
Het |
Cyp2j13 |
G |
A |
4: 95,945,153 (GRCm39) |
H351Y |
probably benign |
Het |
Dixdc1 |
T |
A |
9: 50,613,265 (GRCm39) |
Q230L |
probably damaging |
Het |
Dpep1 |
A |
T |
8: 123,926,764 (GRCm39) |
I226F |
probably benign |
Het |
Efcab3 |
A |
T |
11: 104,805,721 (GRCm39) |
N3076I |
unknown |
Het |
Ehd2 |
A |
G |
7: 15,691,603 (GRCm39) |
V243A |
probably benign |
Het |
Etnk2 |
T |
A |
1: 133,306,232 (GRCm39) |
Y353N |
probably benign |
Het |
Fgg |
G |
T |
3: 82,920,322 (GRCm39) |
G367V |
probably damaging |
Het |
Gm9772 |
T |
C |
17: 22,225,310 (GRCm39) |
*61Q |
probably null |
Het |
Grk5 |
T |
G |
19: 61,078,432 (GRCm39) |
D496E |
possibly damaging |
Het |
Hc |
T |
C |
2: 34,909,535 (GRCm39) |
N915S |
probably benign |
Het |
Iah1 |
G |
T |
12: 21,367,388 (GRCm39) |
Q31H |
probably benign |
Het |
Insr |
T |
C |
8: 3,219,714 (GRCm39) |
D936G |
probably benign |
Het |
Ints6 |
A |
C |
14: 62,939,902 (GRCm39) |
V596G |
probably benign |
Het |
Kcnj16 |
A |
G |
11: 110,915,677 (GRCm39) |
D113G |
possibly damaging |
Het |
Kdm4b |
A |
T |
17: 56,706,771 (GRCm39) |
I928F |
probably damaging |
Het |
Lrrc41 |
C |
T |
4: 115,932,488 (GRCm39) |
|
probably benign |
Het |
Lrrc8e |
G |
A |
8: 4,285,070 (GRCm39) |
V432I |
probably benign |
Het |
Mamdc4 |
T |
C |
2: 25,458,501 (GRCm39) |
E336G |
probably benign |
Het |
Maml2 |
C |
A |
9: 13,532,918 (GRCm39) |
Q711K |
|
Het |
Map3k14 |
T |
C |
11: 103,118,498 (GRCm39) |
T563A |
possibly damaging |
Het |
Mcu |
T |
A |
10: 59,303,535 (GRCm39) |
K101* |
probably null |
Het |
Mettl22 |
T |
A |
16: 8,303,792 (GRCm39) |
V286E |
probably damaging |
Het |
Mon2 |
A |
T |
10: 122,845,516 (GRCm39) |
N1396K |
possibly damaging |
Het |
Mprip |
T |
C |
11: 59,587,851 (GRCm39) |
|
probably benign |
Het |
Mrpl51 |
C |
T |
6: 125,170,344 (GRCm39) |
L117F |
probably damaging |
Het |
Myo1d |
C |
A |
11: 80,565,758 (GRCm39) |
V356F |
probably damaging |
Het |
Myo1d |
T |
A |
11: 80,567,758 (GRCm39) |
I241F |
probably benign |
Het |
Naalad2 |
A |
T |
9: 18,297,230 (GRCm39) |
|
probably benign |
Het |
Nacad |
T |
C |
11: 6,552,853 (GRCm39) |
T113A |
probably benign |
Het |
Nrap |
T |
A |
19: 56,352,843 (GRCm39) |
|
probably benign |
Het |
Or10b1 |
G |
A |
10: 78,356,284 (GRCm39) |
V281M |
possibly damaging |
Het |
Or2z2 |
T |
C |
11: 58,345,936 (GRCm39) |
T280A |
possibly damaging |
Het |
Or56b2 |
T |
A |
7: 104,337,387 (GRCm39) |
I55N |
probably damaging |
Het |
Or5ae1 |
T |
A |
7: 84,565,626 (GRCm39) |
I213N |
possibly damaging |
Het |
Or5w1 |
T |
C |
2: 87,486,591 (GRCm39) |
I225V |
possibly damaging |
Het |
Or6z3 |
T |
C |
7: 6,463,763 (GRCm39) |
L85P |
probably damaging |
Het |
Osbpl3 |
T |
C |
6: 50,328,852 (GRCm39) |
D117G |
probably damaging |
Het |
Parp9 |
C |
T |
16: 35,773,981 (GRCm39) |
R318* |
probably null |
Het |
Pcdhb18 |
A |
G |
18: 37,623,374 (GRCm39) |
I235V |
probably benign |
Het |
Pex16 |
T |
G |
2: 92,209,366 (GRCm39) |
|
probably benign |
Het |
Piezo2 |
T |
A |
18: 63,248,034 (GRCm39) |
M489L |
probably benign |
Het |
Pmepa1 |
C |
A |
2: 173,069,628 (GRCm39) |
G271V |
probably damaging |
Het |
Safb |
A |
G |
17: 56,910,579 (GRCm39) |
E659G |
unknown |
Het |
Scn9a |
T |
C |
2: 66,332,010 (GRCm39) |
T1289A |
probably damaging |
Het |
Secisbp2l |
T |
C |
2: 125,617,596 (GRCm39) |
D27G |
possibly damaging |
Het |
Serpina1f |
A |
G |
12: 103,660,240 (GRCm39) |
V14A |
probably benign |
Het |
Serpinb9b |
C |
A |
13: 33,213,452 (GRCm39) |
T3N |
possibly damaging |
Het |
Sfxn5 |
C |
T |
6: 85,206,182 (GRCm39) |
M315I |
probably benign |
Het |
Slc9b2 |
A |
G |
3: 135,035,530 (GRCm39) |
D333G |
probably benign |
Het |
Sostdc1 |
A |
G |
12: 36,367,229 (GRCm39) |
N135S |
possibly damaging |
Het |
Spg11 |
T |
G |
2: 121,901,425 (GRCm39) |
D1505A |
probably damaging |
Het |
Spmip8 |
A |
T |
8: 96,047,883 (GRCm39) |
|
probably benign |
Het |
Taar7a |
T |
C |
10: 23,869,279 (GRCm39) |
N34S |
probably benign |
Het |
Tcerg1l |
C |
A |
7: 137,811,526 (GRCm39) |
R556L |
possibly damaging |
Het |
Tcp11l1 |
T |
C |
2: 104,518,763 (GRCm39) |
K311R |
probably benign |
Het |
Trbv16 |
T |
G |
6: 41,128,972 (GRCm39) |
F52C |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,726,016 (GRCm39) |
R6073S |
unknown |
Het |
Uba1y |
T |
C |
Y: 828,818 (GRCm39) |
I542T |
possibly damaging |
Het |
Vmn1r214 |
T |
C |
13: 23,219,082 (GRCm39) |
I192T |
probably benign |
Het |
Vmn2r67 |
C |
T |
7: 84,786,346 (GRCm39) |
C553Y |
probably damaging |
Het |
Zdhhc17 |
G |
T |
10: 110,784,121 (GRCm39) |
H452N |
possibly damaging |
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 |
R1844:Cep350
|
UTSW |
1 |
155,724,374 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
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 |
|