Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamtsl4 |
A |
T |
3: 95,586,918 (GRCm39) |
Y811N |
possibly damaging |
Het |
Adrm1 |
T |
C |
2: 179,816,940 (GRCm39) |
|
probably benign |
Het |
Alms1 |
T |
A |
6: 85,598,803 (GRCm39) |
S1210T |
probably benign |
Het |
Ampd3 |
C |
T |
7: 110,377,015 (GRCm39) |
P11L |
probably damaging |
Het |
Arhgap5 |
A |
G |
12: 52,563,290 (GRCm39) |
E87G |
possibly damaging |
Het |
Armc5 |
C |
T |
7: 127,839,242 (GRCm39) |
|
probably benign |
Het |
Asic2 |
C |
G |
11: 80,862,282 (GRCm39) |
|
probably benign |
Het |
Asph |
A |
G |
4: 9,514,683 (GRCm39) |
|
probably benign |
Het |
Bicd2 |
T |
A |
13: 49,531,351 (GRCm39) |
|
probably null |
Het |
Brip1 |
A |
G |
11: 86,034,131 (GRCm39) |
L530P |
possibly damaging |
Het |
Bsn |
G |
T |
9: 107,988,559 (GRCm39) |
|
probably benign |
Het |
Btnl4 |
T |
A |
17: 34,688,608 (GRCm39) |
H390L |
probably benign |
Het |
Ccdc70 |
A |
C |
8: 22,463,324 (GRCm39) |
K38T |
probably damaging |
Het |
Ccni |
G |
A |
5: 93,350,175 (GRCm39) |
P35S |
probably benign |
Het |
Cdh17 |
A |
G |
4: 11,810,451 (GRCm39) |
D714G |
possibly damaging |
Het |
Cfap69 |
A |
T |
5: 5,671,924 (GRCm39) |
M328K |
probably damaging |
Het |
Cmah |
T |
G |
13: 24,601,193 (GRCm39) |
|
probably null |
Het |
Cog6 |
T |
C |
3: 52,918,050 (GRCm39) |
T163A |
probably benign |
Het |
Cyp2j8 |
G |
A |
4: 96,389,433 (GRCm39) |
S130F |
probably benign |
Het |
Dgki |
A |
G |
6: 36,989,831 (GRCm39) |
V636A |
probably damaging |
Het |
Dmkn |
T |
A |
7: 30,464,211 (GRCm39) |
|
probably benign |
Het |
Dnah6 |
A |
G |
6: 73,012,276 (GRCm39) |
I3679T |
possibly damaging |
Het |
Dsp |
A |
T |
13: 38,380,740 (GRCm39) |
Y2495F |
possibly damaging |
Het |
Exosc4 |
C |
T |
15: 76,213,689 (GRCm39) |
A171V |
probably benign |
Het |
Fbxw24 |
A |
G |
9: 109,452,577 (GRCm39) |
|
probably benign |
Het |
Flvcr1 |
A |
T |
1: 190,757,779 (GRCm39) |
L171Q |
probably damaging |
Het |
Fsd1 |
G |
T |
17: 56,303,445 (GRCm39) |
|
probably null |
Het |
Gm7732 |
A |
G |
17: 21,350,106 (GRCm39) |
|
noncoding transcript |
Het |
H2-K2 |
A |
C |
17: 34,194,597 (GRCm39) |
|
noncoding transcript |
Het |
Hgf |
A |
G |
5: 16,798,857 (GRCm39) |
N295S |
probably damaging |
Het |
Ift88 |
T |
A |
14: 57,754,870 (GRCm39) |
D811E |
probably benign |
Het |
Igsf9b |
T |
A |
9: 27,234,657 (GRCm39) |
|
probably null |
Het |
Immt |
T |
A |
6: 71,840,156 (GRCm39) |
V311E |
probably damaging |
Het |
Ipo11 |
T |
A |
13: 107,056,119 (GRCm39) |
N51I |
possibly damaging |
Het |
Isy1 |
T |
C |
6: 87,796,158 (GRCm39) |
K260E |
probably damaging |
Het |
Jchain |
T |
G |
5: 88,674,061 (GRCm39) |
I28L |
probably benign |
Het |
Jmjd1c |
T |
A |
10: 67,054,725 (GRCm39) |
|
probably null |
Het |
Kif13b |
T |
C |
14: 64,989,111 (GRCm39) |
|
probably benign |
Het |
Klhdc7b |
T |
C |
15: 89,272,372 (GRCm39) |
Y427H |
possibly damaging |
Het |
Klhl8 |
T |
C |
5: 104,024,159 (GRCm39) |
|
probably benign |
Het |
Lrp2 |
C |
T |
2: 69,341,292 (GRCm39) |
D963N |
probably damaging |
Het |
Ltbp3 |
G |
T |
19: 5,796,776 (GRCm39) |
|
probably benign |
Het |
Ltf |
C |
A |
9: 110,869,447 (GRCm39) |
Q41K |
probably benign |
Het |
Med4 |
T |
A |
14: 73,754,097 (GRCm39) |
I148N |
probably damaging |
Het |
Mlh3 |
T |
G |
12: 85,294,471 (GRCm39) |
S1242R |
possibly damaging |
Het |
Mllt6 |
T |
C |
11: 97,567,185 (GRCm39) |
|
probably benign |
Het |
Mpdz |
A |
G |
4: 81,210,710 (GRCm39) |
I1712T |
possibly damaging |
Het |
Mrgprb4 |
T |
A |
7: 47,848,301 (GRCm39) |
H209L |
probably benign |
Het |
Nkapl |
A |
T |
13: 21,652,610 (GRCm39) |
M1K |
probably null |
Het |
Nmur2 |
T |
A |
11: 55,920,324 (GRCm39) |
|
probably benign |
Het |
Nsun2 |
T |
A |
13: 69,691,816 (GRCm39) |
|
probably benign |
Het |
Or10ag60 |
A |
G |
2: 87,438,271 (GRCm39) |
I180V |
probably benign |
Het |
Or8k35 |
G |
A |
2: 86,424,425 (GRCm39) |
T249I |
probably benign |
Het |
Ovgp1 |
T |
C |
3: 105,882,146 (GRCm39) |
|
probably benign |
Het |
Pcdh8 |
A |
G |
14: 80,008,131 (GRCm39) |
V144A |
possibly damaging |
Het |
Pcnx3 |
G |
A |
19: 5,727,756 (GRCm39) |
|
probably benign |
Het |
Pla2r1 |
C |
A |
2: 60,309,874 (GRCm39) |
V570L |
possibly damaging |
Het |
Plxnd1 |
C |
A |
6: 115,943,599 (GRCm39) |
E1202D |
possibly damaging |
Het |
Ppp1r37 |
T |
C |
7: 19,266,179 (GRCm39) |
E529G |
probably benign |
Het |
Prdm15 |
A |
G |
16: 97,613,833 (GRCm39) |
F496L |
possibly damaging |
Het |
Prlhr |
G |
T |
19: 60,456,497 (GRCm39) |
S23* |
probably null |
Het |
Prlhr |
A |
T |
19: 60,456,443 (GRCm39) |
V41D |
probably benign |
Het |
Prpf4 |
C |
T |
4: 62,332,777 (GRCm39) |
|
probably benign |
Het |
Psg26 |
C |
T |
7: 18,209,160 (GRCm39) |
R416H |
probably benign |
Het |
Psg26 |
T |
C |
7: 18,212,212 (GRCm39) |
H381R |
probably benign |
Het |
Ralgds |
T |
G |
2: 28,439,128 (GRCm39) |
M717R |
probably benign |
Het |
Rbms1 |
T |
C |
2: 60,672,756 (GRCm39) |
N44D |
probably damaging |
Het |
Rpa1 |
T |
C |
11: 75,209,227 (GRCm39) |
|
probably benign |
Het |
Rprd2 |
T |
C |
3: 95,673,699 (GRCm39) |
N568S |
probably benign |
Het |
Rptor |
A |
G |
11: 119,763,202 (GRCm39) |
M929V |
probably benign |
Het |
Rspo1 |
T |
A |
4: 124,900,942 (GRCm39) |
C97S |
possibly damaging |
Het |
Scin |
C |
T |
12: 40,129,606 (GRCm39) |
G396S |
probably damaging |
Het |
Scn9a |
T |
C |
2: 66,377,456 (GRCm39) |
N409D |
probably damaging |
Het |
Sf3b1 |
A |
G |
1: 55,058,544 (GRCm39) |
I15T |
probably damaging |
Het |
Sh3bp2 |
T |
C |
5: 34,712,839 (GRCm39) |
V149A |
probably damaging |
Het |
Slc39a12 |
T |
A |
2: 14,412,237 (GRCm39) |
|
probably benign |
Het |
Sp9 |
G |
T |
2: 73,104,171 (GRCm39) |
A242S |
possibly damaging |
Het |
Srr |
A |
G |
11: 74,801,891 (GRCm39) |
V126A |
possibly damaging |
Het |
Tatdn3 |
G |
T |
1: 190,785,046 (GRCm39) |
|
probably benign |
Het |
Tex14 |
G |
A |
11: 87,390,439 (GRCm39) |
V379I |
probably benign |
Het |
Tmed6 |
T |
C |
8: 107,788,356 (GRCm39) |
N197S |
probably damaging |
Het |
Ttbk2 |
A |
T |
2: 120,575,641 (GRCm39) |
I1043N |
probably benign |
Het |
Ttbk2 |
G |
A |
2: 120,579,056 (GRCm39) |
L689F |
probably benign |
Het |
Ttn |
A |
G |
2: 76,641,040 (GRCm39) |
S5283P |
probably damaging |
Het |
Ube3b |
C |
A |
5: 114,540,616 (GRCm39) |
S441* |
probably null |
Het |
Ush2a |
G |
A |
1: 188,530,027 (GRCm39) |
C3272Y |
probably damaging |
Het |
Vac14 |
T |
A |
8: 111,359,109 (GRCm39) |
I95K |
probably damaging |
Het |
Vangl2 |
G |
A |
1: 171,833,784 (GRCm39) |
A433V |
probably damaging |
Het |
Vwa5b1 |
A |
T |
4: 138,336,135 (GRCm39) |
V153D |
probably damaging |
Het |
Zfhx3 |
T |
A |
8: 109,682,282 (GRCm39) |
D3240E |
unknown |
Het |
Zfp945 |
A |
G |
17: 23,070,004 (GRCm39) |
C632R |
probably damaging |
Het |
Zfyve26 |
G |
A |
12: 79,312,576 (GRCm39) |
|
probably benign |
Het |
Zyg11b |
A |
T |
4: 108,099,273 (GRCm39) |
I606N |
possibly damaging |
Het |
|
Other mutations in Cenpf |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00778:Cenpf
|
APN |
1 |
189,387,109 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01154:Cenpf
|
APN |
1 |
189,412,530 (GRCm39) |
missense |
probably benign |
0.19 |
IGL01434:Cenpf
|
APN |
1 |
189,390,065 (GRCm39) |
nonsense |
probably null |
|
IGL01461:Cenpf
|
APN |
1 |
189,389,293 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01615:Cenpf
|
APN |
1 |
189,385,381 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL01720:Cenpf
|
APN |
1 |
189,383,412 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01720:Cenpf
|
APN |
1 |
189,414,583 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01803:Cenpf
|
APN |
1 |
189,386,968 (GRCm39) |
nonsense |
probably null |
|
IGL02152:Cenpf
|
APN |
1 |
189,381,209 (GRCm39) |
missense |
probably benign |
|
IGL02222:Cenpf
|
APN |
1 |
189,386,641 (GRCm39) |
missense |
probably benign |
|
IGL02338:Cenpf
|
APN |
1 |
189,412,615 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02580:Cenpf
|
APN |
1 |
189,389,638 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02629:Cenpf
|
APN |
1 |
189,384,531 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02650:Cenpf
|
APN |
1 |
189,384,670 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02660:Cenpf
|
APN |
1 |
189,386,979 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02703:Cenpf
|
APN |
1 |
189,391,955 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02809:Cenpf
|
APN |
1 |
189,414,555 (GRCm39) |
splice site |
probably benign |
|
IGL02851:Cenpf
|
APN |
1 |
189,390,227 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02903:Cenpf
|
APN |
1 |
189,379,073 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03126:Cenpf
|
APN |
1 |
189,391,207 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03235:Cenpf
|
APN |
1 |
189,416,124 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03336:Cenpf
|
APN |
1 |
189,384,844 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03402:Cenpf
|
APN |
1 |
189,387,273 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02799:Cenpf
|
UTSW |
1 |
189,391,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R0011:Cenpf
|
UTSW |
1 |
189,382,903 (GRCm39) |
missense |
probably benign |
0.05 |
R0129:Cenpf
|
UTSW |
1 |
189,391,847 (GRCm39) |
missense |
probably benign |
0.26 |
R0157:Cenpf
|
UTSW |
1 |
189,384,556 (GRCm39) |
missense |
probably benign |
0.07 |
R0270:Cenpf
|
UTSW |
1 |
189,382,911 (GRCm39) |
missense |
probably benign |
0.01 |
R0607:Cenpf
|
UTSW |
1 |
189,414,660 (GRCm39) |
splice site |
probably null |
|
R0621:Cenpf
|
UTSW |
1 |
189,404,825 (GRCm39) |
missense |
probably benign |
|
R0639:Cenpf
|
UTSW |
1 |
189,390,259 (GRCm39) |
missense |
probably benign |
0.01 |
R0653:Cenpf
|
UTSW |
1 |
189,392,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R1157:Cenpf
|
UTSW |
1 |
189,390,650 (GRCm39) |
missense |
probably benign |
0.20 |
R1331:Cenpf
|
UTSW |
1 |
189,374,998 (GRCm39) |
missense |
probably damaging |
0.99 |
R1463:Cenpf
|
UTSW |
1 |
189,386,936 (GRCm39) |
missense |
probably damaging |
0.97 |
R1514:Cenpf
|
UTSW |
1 |
189,411,338 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1529:Cenpf
|
UTSW |
1 |
189,392,235 (GRCm39) |
missense |
probably benign |
0.00 |
R1574:Cenpf
|
UTSW |
1 |
189,384,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R1574:Cenpf
|
UTSW |
1 |
189,384,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R1662:Cenpf
|
UTSW |
1 |
189,389,968 (GRCm39) |
missense |
probably damaging |
0.99 |
R1671:Cenpf
|
UTSW |
1 |
189,411,341 (GRCm39) |
splice site |
probably null |
|
R1725:Cenpf
|
UTSW |
1 |
189,412,676 (GRCm39) |
missense |
probably damaging |
0.99 |
R1743:Cenpf
|
UTSW |
1 |
189,386,460 (GRCm39) |
missense |
probably benign |
0.19 |
R1874:Cenpf
|
UTSW |
1 |
189,416,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R1884:Cenpf
|
UTSW |
1 |
189,379,046 (GRCm39) |
missense |
probably benign |
|
R1980:Cenpf
|
UTSW |
1 |
189,386,112 (GRCm39) |
missense |
probably benign |
0.04 |
R2074:Cenpf
|
UTSW |
1 |
189,389,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R2096:Cenpf
|
UTSW |
1 |
189,385,656 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2109:Cenpf
|
UTSW |
1 |
189,411,264 (GRCm39) |
missense |
probably damaging |
0.99 |
R2113:Cenpf
|
UTSW |
1 |
189,411,299 (GRCm39) |
missense |
probably damaging |
0.96 |
R2134:Cenpf
|
UTSW |
1 |
189,390,839 (GRCm39) |
missense |
probably benign |
0.03 |
R2209:Cenpf
|
UTSW |
1 |
189,384,795 (GRCm39) |
missense |
probably benign |
0.04 |
R2875:Cenpf
|
UTSW |
1 |
189,390,841 (GRCm39) |
missense |
probably benign |
0.11 |
R2876:Cenpf
|
UTSW |
1 |
189,390,841 (GRCm39) |
missense |
probably benign |
0.11 |
R3433:Cenpf
|
UTSW |
1 |
189,392,146 (GRCm39) |
missense |
probably damaging |
0.99 |
R3709:Cenpf
|
UTSW |
1 |
189,381,009 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3786:Cenpf
|
UTSW |
1 |
189,390,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R4014:Cenpf
|
UTSW |
1 |
189,385,356 (GRCm39) |
missense |
probably benign |
0.01 |
R4108:Cenpf
|
UTSW |
1 |
189,416,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R4119:Cenpf
|
UTSW |
1 |
189,385,242 (GRCm39) |
missense |
probably benign |
0.01 |
R4177:Cenpf
|
UTSW |
1 |
189,400,816 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4422:Cenpf
|
UTSW |
1 |
189,390,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R4546:Cenpf
|
UTSW |
1 |
189,386,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R4592:Cenpf
|
UTSW |
1 |
189,411,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R4643:Cenpf
|
UTSW |
1 |
189,391,786 (GRCm39) |
missense |
probably benign |
0.00 |
R4650:Cenpf
|
UTSW |
1 |
189,392,235 (GRCm39) |
missense |
probably benign |
0.00 |
R4801:Cenpf
|
UTSW |
1 |
189,383,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R4802:Cenpf
|
UTSW |
1 |
189,383,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R4817:Cenpf
|
UTSW |
1 |
189,414,566 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4871:Cenpf
|
UTSW |
1 |
189,390,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R5037:Cenpf
|
UTSW |
1 |
189,416,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R5106:Cenpf
|
UTSW |
1 |
189,416,005 (GRCm39) |
missense |
probably benign |
0.00 |
R5208:Cenpf
|
UTSW |
1 |
189,403,243 (GRCm39) |
critical splice donor site |
probably null |
|
R5213:Cenpf
|
UTSW |
1 |
189,387,177 (GRCm39) |
missense |
probably benign |
0.04 |
R5237:Cenpf
|
UTSW |
1 |
189,391,730 (GRCm39) |
missense |
probably benign |
0.28 |
R5255:Cenpf
|
UTSW |
1 |
189,404,824 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5378:Cenpf
|
UTSW |
1 |
189,385,663 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5468:Cenpf
|
UTSW |
1 |
189,384,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R5510:Cenpf
|
UTSW |
1 |
189,415,100 (GRCm39) |
missense |
probably benign |
0.14 |
R5616:Cenpf
|
UTSW |
1 |
189,389,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R5652:Cenpf
|
UTSW |
1 |
189,389,279 (GRCm39) |
missense |
probably damaging |
0.99 |
R5735:Cenpf
|
UTSW |
1 |
189,386,560 (GRCm39) |
missense |
probably benign |
0.10 |
R5841:Cenpf
|
UTSW |
1 |
189,389,641 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5943:Cenpf
|
UTSW |
1 |
189,392,166 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6082:Cenpf
|
UTSW |
1 |
189,390,301 (GRCm39) |
missense |
probably benign |
0.11 |
R6108:Cenpf
|
UTSW |
1 |
189,394,210 (GRCm39) |
missense |
probably benign |
0.03 |
R6269:Cenpf
|
UTSW |
1 |
189,392,117 (GRCm39) |
missense |
probably benign |
0.37 |
R6284:Cenpf
|
UTSW |
1 |
189,384,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R6425:Cenpf
|
UTSW |
1 |
189,392,095 (GRCm39) |
missense |
probably benign |
0.09 |
R6587:Cenpf
|
UTSW |
1 |
189,390,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R6747:Cenpf
|
UTSW |
1 |
189,385,051 (GRCm39) |
missense |
probably benign |
0.15 |
R6811:Cenpf
|
UTSW |
1 |
189,386,739 (GRCm39) |
missense |
probably benign |
0.06 |
R6834:Cenpf
|
UTSW |
1 |
189,391,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R6951:Cenpf
|
UTSW |
1 |
189,385,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R7095:Cenpf
|
UTSW |
1 |
189,391,373 (GRCm39) |
missense |
probably benign |
0.01 |
R7128:Cenpf
|
UTSW |
1 |
189,417,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R7185:Cenpf
|
UTSW |
1 |
189,385,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R7292:Cenpf
|
UTSW |
1 |
189,382,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R7353:Cenpf
|
UTSW |
1 |
189,386,335 (GRCm39) |
nonsense |
probably null |
|
R7402:Cenpf
|
UTSW |
1 |
189,391,575 (GRCm39) |
nonsense |
probably null |
|
R7460:Cenpf
|
UTSW |
1 |
189,386,247 (GRCm39) |
missense |
probably damaging |
0.97 |
R7484:Cenpf
|
UTSW |
1 |
189,389,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R7574:Cenpf
|
UTSW |
1 |
189,390,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R7691:Cenpf
|
UTSW |
1 |
189,390,404 (GRCm39) |
nonsense |
probably null |
|
R7698:Cenpf
|
UTSW |
1 |
189,394,269 (GRCm39) |
missense |
probably benign |
0.01 |
R7901:Cenpf
|
UTSW |
1 |
189,389,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R7941:Cenpf
|
UTSW |
1 |
189,389,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R8007:Cenpf
|
UTSW |
1 |
189,379,144 (GRCm39) |
missense |
|
|
R8194:Cenpf
|
UTSW |
1 |
189,414,600 (GRCm39) |
missense |
probably benign |
0.06 |
R8420:Cenpf
|
UTSW |
1 |
189,404,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R8429:Cenpf
|
UTSW |
1 |
189,389,504 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8477:Cenpf
|
UTSW |
1 |
189,385,385 (GRCm39) |
missense |
probably benign |
|
R8492:Cenpf
|
UTSW |
1 |
189,390,926 (GRCm39) |
missense |
probably damaging |
0.99 |
R8510:Cenpf
|
UTSW |
1 |
189,382,903 (GRCm39) |
missense |
probably benign |
0.01 |
R8686:Cenpf
|
UTSW |
1 |
189,391,801 (GRCm39) |
missense |
probably benign |
0.00 |
R8696:Cenpf
|
UTSW |
1 |
189,390,194 (GRCm39) |
missense |
probably benign |
0.20 |
R8855:Cenpf
|
UTSW |
1 |
189,385,430 (GRCm39) |
missense |
probably benign |
0.11 |
R8901:Cenpf
|
UTSW |
1 |
189,394,248 (GRCm39) |
missense |
probably benign |
0.30 |
R8958:Cenpf
|
UTSW |
1 |
189,385,350 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9109:Cenpf
|
UTSW |
1 |
189,391,571 (GRCm39) |
missense |
probably benign |
0.06 |
R9135:Cenpf
|
UTSW |
1 |
189,404,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R9136:Cenpf
|
UTSW |
1 |
189,403,352 (GRCm39) |
missense |
probably benign |
0.02 |
R9198:Cenpf
|
UTSW |
1 |
189,388,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R9240:Cenpf
|
UTSW |
1 |
189,389,167 (GRCm39) |
missense |
probably benign |
0.01 |
R9303:Cenpf
|
UTSW |
1 |
189,392,271 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9305:Cenpf
|
UTSW |
1 |
189,392,271 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9354:Cenpf
|
UTSW |
1 |
189,379,114 (GRCm39) |
missense |
|
|
R9502:Cenpf
|
UTSW |
1 |
189,388,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R9619:Cenpf
|
UTSW |
1 |
189,385,965 (GRCm39) |
missense |
probably benign |
0.01 |
RF006:Cenpf
|
UTSW |
1 |
189,389,583 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Cenpf
|
UTSW |
1 |
189,386,071 (GRCm39) |
missense |
possibly damaging |
0.79 |
X0066:Cenpf
|
UTSW |
1 |
189,390,126 (GRCm39) |
missense |
probably benign |
0.23 |
Z1088:Cenpf
|
UTSW |
1 |
189,385,128 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Cenpf
|
UTSW |
1 |
189,391,669 (GRCm39) |
missense |
probably damaging |
1.00 |
|