Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A230072I06Rik |
A |
G |
8: 12,329,556 (GRCm39) |
S4G |
unknown |
Het |
AA623943 |
T |
C |
11: 94,703,828 (GRCm39) |
|
noncoding transcript |
Het |
Abca13 |
T |
A |
11: 9,243,692 (GRCm39) |
S1852T |
probably damaging |
Het |
Ackr2 |
G |
A |
9: 121,738,540 (GRCm39) |
C305Y |
probably damaging |
Het |
Aebp1 |
T |
C |
11: 5,820,257 (GRCm39) |
V411A |
probably benign |
Het |
Akp3 |
G |
A |
1: 87,054,270 (GRCm39) |
R269H |
probably benign |
Het |
Alox15 |
C |
A |
11: 70,241,708 (GRCm39) |
G58W |
probably damaging |
Het |
Ankle2 |
A |
G |
5: 110,385,856 (GRCm39) |
N369S |
probably damaging |
Het |
Ankrd28 |
T |
A |
14: 31,465,311 (GRCm39) |
I289L |
probably benign |
Het |
Atp13a4 |
T |
A |
16: 29,252,805 (GRCm39) |
T714S |
possibly damaging |
Het |
Birc6 |
A |
C |
17: 74,977,369 (GRCm39) |
N4388T |
probably damaging |
Het |
Blm |
A |
T |
7: 80,114,592 (GRCm39) |
L1159Q |
probably damaging |
Het |
Caskin1 |
G |
A |
17: 24,723,521 (GRCm39) |
V770I |
probably benign |
Het |
Ccdc148 |
T |
A |
2: 58,713,657 (GRCm39) |
H498L |
probably damaging |
Het |
Cdh26 |
T |
A |
2: 178,101,919 (GRCm39) |
Y179* |
probably null |
Het |
Cela2a |
T |
A |
4: 141,552,864 (GRCm39) |
T38S |
probably benign |
Het |
Cep89 |
A |
G |
7: 35,117,151 (GRCm39) |
Y251C |
probably damaging |
Het |
Cluh |
T |
C |
11: 74,552,526 (GRCm39) |
S524P |
probably damaging |
Het |
Cpeb4 |
T |
C |
11: 31,822,801 (GRCm39) |
S172P |
probably damaging |
Het |
Ctnnd2 |
T |
C |
15: 30,847,523 (GRCm39) |
S705P |
probably damaging |
Het |
Dock2 |
T |
G |
11: 34,212,445 (GRCm39) |
D1232A |
probably benign |
Het |
Donson |
T |
C |
16: 91,484,738 (GRCm39) |
N9S |
possibly damaging |
Het |
Gdf9 |
T |
C |
11: 53,324,381 (GRCm39) |
L50P |
probably benign |
Het |
Gm10300 |
C |
T |
4: 131,802,458 (GRCm39) |
|
probably benign |
Het |
Gm8369 |
A |
G |
19: 11,482,248 (GRCm39) |
|
probably benign |
Het |
Gm8674 |
T |
A |
13: 50,055,924 (GRCm39) |
|
noncoding transcript |
Het |
Hepacam |
T |
A |
9: 37,296,101 (GRCm39) |
S417R |
possibly damaging |
Het |
Hibch |
T |
A |
1: 52,892,859 (GRCm39) |
L23Q |
probably benign |
Het |
Hmcn1 |
G |
A |
1: 150,525,358 (GRCm39) |
R3389C |
probably damaging |
Het |
Hsp90ab1 |
G |
T |
17: 45,881,575 (GRCm39) |
|
probably benign |
Het |
Hunk |
C |
A |
16: 90,272,791 (GRCm39) |
T365K |
probably damaging |
Het |
Il12a |
A |
T |
3: 68,602,595 (GRCm39) |
|
probably benign |
Het |
Ints13 |
A |
G |
6: 146,477,847 (GRCm39) |
V34A |
probably benign |
Het |
Intu |
A |
C |
3: 40,634,020 (GRCm39) |
M418L |
probably damaging |
Het |
Khdc4 |
A |
G |
3: 88,616,192 (GRCm39) |
R460G |
probably damaging |
Het |
Klra9 |
A |
G |
6: 130,156,036 (GRCm39) |
S240P |
probably damaging |
Het |
Mtpn |
C |
T |
6: 35,489,225 (GRCm39) |
D100N |
probably benign |
Het |
Ndrg1 |
A |
G |
15: 66,802,699 (GRCm39) |
|
probably benign |
Het |
Or11g24 |
T |
C |
14: 50,662,905 (GRCm39) |
*310Q |
probably null |
Het |
Or5k17 |
T |
C |
16: 58,746,860 (GRCm39) |
T25A |
probably benign |
Het |
Pate6 |
C |
T |
9: 35,700,297 (GRCm39) |
C96Y |
probably damaging |
Het |
Pax7 |
A |
G |
4: 139,557,682 (GRCm39) |
S30P |
probably damaging |
Het |
Pdcd11 |
A |
T |
19: 47,082,247 (GRCm39) |
T54S |
probably benign |
Het |
Pex19 |
T |
C |
1: 171,958,306 (GRCm39) |
V95A |
probably damaging |
Het |
Pkhd1l1 |
A |
G |
15: 44,383,103 (GRCm39) |
I1121V |
probably benign |
Het |
Pklr |
A |
T |
3: 89,049,091 (GRCm39) |
I146F |
probably benign |
Het |
Plcb1 |
T |
C |
2: 135,104,164 (GRCm39) |
Y278H |
possibly damaging |
Het |
Plcl1 |
T |
A |
1: 55,735,160 (GRCm39) |
I167N |
probably damaging |
Het |
Plekhh1 |
A |
T |
12: 79,125,461 (GRCm39) |
I1241F |
probably benign |
Het |
Plxnb2 |
G |
T |
15: 89,051,774 (GRCm39) |
D148E |
possibly damaging |
Het |
Pthlh |
T |
C |
6: 147,158,745 (GRCm39) |
I72V |
probably damaging |
Het |
Ptpru |
C |
T |
4: 131,513,067 (GRCm39) |
R880Q |
probably benign |
Het |
Rrp36 |
T |
C |
17: 46,978,932 (GRCm39) |
K209E |
probably damaging |
Het |
Scarb1 |
A |
G |
5: 125,381,286 (GRCm39) |
V86A |
probably damaging |
Het |
Sh2d7 |
A |
C |
9: 54,446,860 (GRCm39) |
S37R |
probably benign |
Het |
Slc13a2 |
A |
T |
11: 78,288,647 (GRCm39) |
V543E |
probably damaging |
Het |
Smarcal1 |
A |
G |
1: 72,630,296 (GRCm39) |
T117A |
probably benign |
Het |
Smok2a |
A |
G |
17: 13,445,865 (GRCm39) |
R481G |
possibly damaging |
Het |
Smr2 |
G |
A |
5: 88,256,699 (GRCm39) |
A126T |
probably benign |
Het |
Sspo |
G |
T |
6: 48,436,979 (GRCm39) |
W1304C |
possibly damaging |
Het |
Svep1 |
A |
G |
4: 58,116,524 (GRCm39) |
S909P |
possibly damaging |
Het |
Tchh |
A |
T |
3: 93,352,880 (GRCm39) |
K773N |
unknown |
Het |
Tmem156 |
T |
C |
5: 65,232,950 (GRCm39) |
N140S |
possibly damaging |
Het |
Tmem213 |
T |
C |
6: 38,092,589 (GRCm39) |
I107T |
possibly damaging |
Het |
Tpd52l2 |
A |
G |
2: 181,153,372 (GRCm39) |
Y161C |
probably damaging |
Het |
Trappc8 |
C |
T |
18: 20,951,139 (GRCm39) |
A1436T |
probably benign |
Het |
Ubr3 |
A |
G |
2: 69,795,855 (GRCm39) |
Y933C |
possibly damaging |
Het |
Ufm1 |
A |
T |
3: 53,765,303 (GRCm39) |
|
probably benign |
Het |
Wdr27 |
A |
T |
17: 15,103,931 (GRCm39) |
L725Q |
probably damaging |
Het |
Zdbf2 |
A |
G |
1: 63,345,035 (GRCm39) |
D1138G |
possibly damaging |
Het |
Zkscan16 |
G |
A |
4: 58,946,481 (GRCm39) |
V119M |
probably damaging |
Het |
Zmat5 |
A |
G |
11: 4,672,431 (GRCm39) |
D16G |
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 |
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 |
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 |
|