Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acox1 |
A |
T |
11: 116,066,152 (GRCm39) |
S453T |
probably benign |
Het |
Ahnak2 |
A |
T |
12: 112,740,550 (GRCm39) |
V368D |
probably damaging |
Het |
Ankrd53 |
A |
T |
6: 83,745,134 (GRCm39) |
Y448F |
probably damaging |
Het |
Arhgef15 |
A |
T |
11: 68,840,751 (GRCm39) |
|
probably benign |
Het |
Atg2b |
T |
C |
12: 105,613,073 (GRCm39) |
N1166S |
probably benign |
Het |
Atl3 |
C |
T |
19: 7,486,910 (GRCm39) |
R77* |
probably null |
Het |
Bend6 |
T |
C |
1: 33,922,654 (GRCm39) |
|
probably benign |
Het |
Ccnt1 |
C |
A |
15: 98,465,444 (GRCm39) |
R25L |
probably damaging |
Het |
Cct4 |
A |
G |
11: 22,952,898 (GRCm39) |
T525A |
probably benign |
Het |
Cimap2 |
T |
A |
4: 106,467,724 (GRCm39) |
|
probably null |
Het |
Clcn1 |
G |
T |
6: 42,286,898 (GRCm39) |
V652L |
probably damaging |
Het |
Cntln |
T |
A |
4: 84,967,957 (GRCm39) |
Y725* |
probably null |
Het |
Cog5 |
T |
C |
12: 31,969,732 (GRCm39) |
F21L |
probably benign |
Het |
D6Ertd527e |
GGCAGCAGCAGCA |
GGCAGCAGCAGCAGCA |
6: 87,088,406 (GRCm39) |
|
probably benign |
Het |
Dnm2 |
A |
T |
9: 21,402,626 (GRCm39) |
|
probably benign |
Het |
Dnmt1 |
C |
T |
9: 20,819,854 (GRCm39) |
V1430I |
probably damaging |
Het |
Dpep1 |
A |
G |
8: 123,927,106 (GRCm39) |
D285G |
probably damaging |
Het |
Eef2kmt |
C |
T |
16: 5,066,867 (GRCm39) |
V129M |
probably damaging |
Het |
Epha3 |
A |
T |
16: 63,403,920 (GRCm39) |
M726K |
probably damaging |
Het |
Fat3 |
A |
G |
9: 16,289,019 (GRCm39) |
L168P |
probably damaging |
Het |
Frem3 |
T |
A |
8: 81,390,026 (GRCm39) |
F1759Y |
probably damaging |
Het |
Fubp3 |
T |
A |
2: 31,498,153 (GRCm39) |
S56R |
possibly damaging |
Het |
Gm1965 |
T |
C |
6: 89,122,392 (GRCm39) |
|
noncoding transcript |
Het |
Gm5592 |
C |
T |
7: 40,864,958 (GRCm39) |
|
probably benign |
Het |
H1f9 |
T |
A |
11: 94,858,843 (GRCm39) |
L46* |
probably null |
Het |
Irs1 |
TGGGGTGGACATCGAACTGAAGGAG |
TG |
1: 82,265,453 (GRCm39) |
913 |
probably null |
Het |
Isl1 |
A |
G |
13: 116,439,619 (GRCm39) |
M243T |
probably benign |
Het |
Itpr1 |
A |
T |
6: 108,366,498 (GRCm39) |
I142F |
probably damaging |
Het |
Jak1 |
T |
C |
4: 101,012,263 (GRCm39) |
T1069A |
probably damaging |
Het |
Jmjd1c |
T |
C |
10: 67,069,225 (GRCm39) |
V1848A |
probably benign |
Het |
Kdm5a |
T |
C |
6: 120,389,363 (GRCm39) |
V930A |
probably damaging |
Het |
Kdm5b |
C |
A |
1: 134,521,053 (GRCm39) |
|
probably null |
Het |
Lilra5 |
T |
C |
7: 4,241,713 (GRCm39) |
F171L |
possibly damaging |
Het |
Map1b |
A |
G |
13: 99,567,562 (GRCm39) |
S1720P |
unknown |
Het |
Mcpt1 |
A |
T |
14: 56,257,017 (GRCm39) |
Q185L |
probably damaging |
Het |
Mmp20 |
T |
A |
9: 7,644,027 (GRCm39) |
D238E |
possibly damaging |
Het |
Mov10l1 |
A |
T |
15: 88,904,472 (GRCm39) |
I784F |
possibly damaging |
Het |
Mroh2b |
C |
T |
15: 4,933,752 (GRCm39) |
P101S |
probably damaging |
Het |
Myh3 |
G |
T |
11: 66,987,765 (GRCm39) |
A1413S |
probably benign |
Het |
Naa80 |
A |
T |
9: 107,460,738 (GRCm39) |
Y211F |
probably damaging |
Het |
Npdc1 |
G |
A |
2: 25,298,957 (GRCm39) |
D284N |
probably damaging |
Het |
Or12j4 |
A |
G |
7: 140,046,989 (GRCm39) |
R292G |
probably damaging |
Het |
Or2t48 |
A |
C |
11: 58,420,308 (GRCm39) |
M168R |
probably damaging |
Het |
Or4a66 |
A |
G |
2: 88,531,544 (GRCm39) |
I43T |
probably damaging |
Het |
Or5g9 |
A |
G |
2: 85,551,793 (GRCm39) |
I15V |
probably benign |
Het |
Or8k22 |
A |
T |
2: 86,163,571 (GRCm39) |
M43K |
probably benign |
Het |
Or8k23 |
G |
A |
2: 86,186,094 (GRCm39) |
L211F |
probably benign |
Het |
Palld |
T |
A |
8: 62,140,415 (GRCm39) |
T531S |
probably benign |
Het |
Parp4 |
A |
G |
14: 56,823,195 (GRCm39) |
E105G |
probably benign |
Het |
Phf11a |
A |
T |
14: 59,525,028 (GRCm39) |
S59T |
probably damaging |
Het |
Ppp1r12b |
G |
T |
1: 134,883,471 (GRCm39) |
A17E |
probably benign |
Het |
Rad50 |
A |
T |
11: 53,541,480 (GRCm39) |
I1252N |
probably damaging |
Het |
Ramp3 |
A |
G |
11: 6,624,761 (GRCm39) |
|
probably null |
Het |
Rrbp1 |
G |
A |
2: 143,830,337 (GRCm39) |
T610I |
possibly damaging |
Het |
Scart2 |
T |
C |
7: 139,879,021 (GRCm39) |
I1051T |
probably benign |
Het |
Semp2l2a |
C |
T |
8: 13,888,007 (GRCm39) |
S28N |
probably benign |
Het |
Slc4a10 |
A |
G |
2: 62,098,531 (GRCm39) |
Y555C |
probably damaging |
Het |
Slc5a2 |
A |
G |
7: 127,866,677 (GRCm39) |
|
probably null |
Het |
Smoc1 |
T |
A |
12: 81,226,322 (GRCm39) |
D371E |
probably damaging |
Het |
Stmn1 |
T |
A |
4: 134,197,495 (GRCm39) |
|
probably benign |
Het |
Sulf1 |
C |
T |
1: 12,912,910 (GRCm39) |
L715F |
probably benign |
Het |
Surf1 |
T |
C |
2: 26,804,255 (GRCm39) |
T180A |
possibly damaging |
Het |
Syne2 |
A |
G |
12: 76,026,593 (GRCm39) |
I3474V |
probably damaging |
Het |
Tchh |
A |
T |
3: 93,352,455 (GRCm39) |
R632W |
unknown |
Het |
Tchh |
A |
T |
3: 93,354,895 (GRCm39) |
D1445V |
unknown |
Het |
Tctn1 |
A |
T |
5: 122,383,568 (GRCm39) |
M505K |
probably benign |
Het |
Tdrkh |
T |
A |
3: 94,332,897 (GRCm39) |
I150N |
probably damaging |
Het |
Tespa1 |
C |
T |
10: 130,198,028 (GRCm39) |
T350I |
probably benign |
Het |
Thbs1 |
A |
G |
2: 117,945,499 (GRCm39) |
Y326C |
possibly damaging |
Het |
Tmem208 |
C |
T |
8: 106,055,296 (GRCm39) |
S119F |
probably damaging |
Het |
Tmprss6 |
G |
C |
15: 78,329,588 (GRCm39) |
A91G |
probably damaging |
Het |
Trp53bp2 |
C |
T |
1: 182,259,147 (GRCm39) |
R67W |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,541,541 (GRCm39) |
I25488T |
possibly damaging |
Het |
Txnl4a |
A |
G |
18: 80,265,468 (GRCm39) |
E111G |
probably damaging |
Het |
Unc13b |
T |
G |
4: 43,237,137 (GRCm39) |
I3402M |
probably damaging |
Het |
Vmn1r188 |
A |
C |
13: 22,272,291 (GRCm39) |
I82L |
probably benign |
Het |
Zfp65 |
A |
G |
13: 67,856,994 (GRCm39) |
V95A |
probably benign |
Het |
Zfp985 |
T |
A |
4: 147,668,612 (GRCm39) |
S493R |
probably 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 |
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 |
|