Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2410002F23Rik |
G |
T |
7: 43,900,435 (GRCm39) |
R113S |
probably benign |
Het |
Ackr2 |
A |
T |
9: 121,738,026 (GRCm39) |
I134F |
probably damaging |
Het |
Actr3b |
T |
A |
5: 26,036,709 (GRCm39) |
I174N |
possibly damaging |
Het |
Akap9 |
T |
A |
5: 4,094,847 (GRCm39) |
S2214T |
possibly damaging |
Het |
Arhgef12 |
C |
A |
9: 42,890,768 (GRCm39) |
R986L |
possibly damaging |
Het |
Brap |
G |
T |
5: 121,801,422 (GRCm39) |
S59I |
possibly damaging |
Het |
Btnl1 |
C |
T |
17: 34,598,578 (GRCm39) |
H65Y |
probably damaging |
Het |
C1s2 |
T |
C |
6: 124,612,004 (GRCm39) |
T121A |
probably damaging |
Het |
Capn1 |
T |
A |
19: 6,064,388 (GRCm39) |
Y37F |
probably benign |
Het |
Ccdc39 |
T |
C |
3: 33,869,650 (GRCm39) |
K726E |
probably damaging |
Het |
Cd300lb |
G |
A |
11: 114,816,865 (GRCm39) |
S195F |
probably damaging |
Het |
Chodl |
A |
C |
16: 78,738,251 (GRCm39) |
N73T |
possibly damaging |
Het |
Cimip2c |
G |
A |
5: 30,637,851 (GRCm39) |
G66E |
probably damaging |
Het |
Crnn |
A |
T |
3: 93,055,747 (GRCm39) |
M178L |
probably benign |
Het |
Cyp4a12b |
A |
G |
4: 115,290,110 (GRCm39) |
D221G |
probably damaging |
Het |
Dipk2a |
A |
T |
9: 94,406,498 (GRCm39) |
I303N |
probably damaging |
Het |
Dmxl2 |
A |
G |
9: 54,301,097 (GRCm39) |
V2338A |
probably benign |
Het |
Dnah9 |
G |
T |
11: 65,928,411 (GRCm39) |
P2086Q |
probably damaging |
Het |
Dsg2 |
A |
G |
18: 20,725,346 (GRCm39) |
I486V |
probably benign |
Het |
E2f8 |
A |
G |
7: 48,524,855 (GRCm39) |
S265P |
probably damaging |
Het |
Eif1b |
A |
G |
9: 120,323,296 (GRCm39) |
D52G |
probably benign |
Het |
Etl4 |
A |
T |
2: 20,790,153 (GRCm39) |
T602S |
probably benign |
Het |
Exoc3l2 |
A |
T |
7: 19,223,059 (GRCm39) |
|
probably benign |
Het |
Fbxl6 |
C |
A |
15: 76,421,173 (GRCm39) |
V297F |
probably damaging |
Het |
Fgr |
T |
A |
4: 132,725,786 (GRCm39) |
N398K |
probably benign |
Het |
G3bp1 |
A |
G |
11: 55,379,986 (GRCm39) |
R107G |
probably damaging |
Het |
Gp2 |
A |
T |
7: 119,052,155 (GRCm39) |
N186K |
probably benign |
Het |
Hbs1l |
T |
A |
10: 21,217,831 (GRCm39) |
L249* |
probably null |
Het |
Hmgcs2 |
T |
A |
3: 98,204,337 (GRCm39) |
L246* |
probably null |
Het |
Hsp90ab1 |
G |
T |
17: 45,880,254 (GRCm39) |
H96Q |
probably benign |
Het |
Ibtk |
C |
T |
9: 85,588,603 (GRCm39) |
V1078I |
probably benign |
Het |
Ltn1 |
T |
C |
16: 87,212,530 (GRCm39) |
D677G |
probably benign |
Het |
Lyst |
C |
T |
13: 13,887,405 (GRCm39) |
T3078I |
possibly damaging |
Het |
Mamdc4 |
A |
G |
2: 25,459,402 (GRCm39) |
F199S |
probably damaging |
Het |
Megf6 |
G |
T |
4: 154,261,578 (GRCm39) |
V68L |
probably benign |
Het |
Mki67 |
G |
A |
7: 135,299,592 (GRCm39) |
T1814I |
probably damaging |
Het |
Msantd5l |
T |
A |
11: 51,145,264 (GRCm39) |
I108F |
possibly damaging |
Het |
Mttp |
A |
T |
3: 137,800,763 (GRCm39) |
F766I |
probably benign |
Het |
Nbl1 |
T |
A |
4: 138,810,915 (GRCm39) |
|
probably null |
Het |
Nmrk1 |
T |
A |
19: 18,618,802 (GRCm39) |
L118Q |
probably damaging |
Het |
Nopchap1 |
C |
T |
10: 83,201,656 (GRCm39) |
S143L |
probably damaging |
Het |
Oog3 |
A |
T |
4: 143,886,082 (GRCm39) |
L172H |
probably damaging |
Het |
Or2y11 |
T |
G |
11: 49,443,260 (GRCm39) |
S229A |
probably damaging |
Het |
Osbpl1a |
T |
G |
18: 12,892,457 (GRCm39) |
Q332P |
probably damaging |
Het |
Pik3cg |
A |
G |
12: 32,243,709 (GRCm39) |
F921L |
possibly damaging |
Het |
Plch2 |
T |
C |
4: 155,069,054 (GRCm39) |
S1086G |
possibly damaging |
Het |
Plekha5 |
A |
G |
6: 140,369,942 (GRCm39) |
T18A |
possibly damaging |
Het |
Pogz |
T |
A |
3: 94,786,276 (GRCm39) |
S955T |
probably benign |
Het |
Pot1b |
A |
T |
17: 55,960,413 (GRCm39) |
I639N |
probably benign |
Het |
Prkdc |
T |
C |
16: 15,505,254 (GRCm39) |
I852T |
probably benign |
Het |
Prps1l1 |
A |
G |
12: 35,035,521 (GRCm39) |
K212R |
probably benign |
Het |
Ptpn5 |
A |
G |
7: 46,735,807 (GRCm39) |
Y304H |
probably damaging |
Het |
Ralgapa1 |
A |
G |
12: 55,822,973 (GRCm39) |
I281T |
possibly damaging |
Het |
Rgs22 |
A |
T |
15: 36,099,880 (GRCm39) |
Y278* |
probably null |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Rnf213 |
T |
A |
11: 119,333,489 (GRCm39) |
Y2899* |
probably null |
Het |
Rttn |
C |
T |
18: 89,004,197 (GRCm39) |
T397I |
possibly damaging |
Het |
Sacs |
G |
T |
14: 61,410,902 (GRCm39) |
|
probably null |
Het |
Sbf2 |
G |
T |
7: 110,060,419 (GRCm39) |
Q182K |
probably damaging |
Het |
Sec14l5 |
C |
T |
16: 4,984,968 (GRCm39) |
R105* |
probably null |
Het |
Sh2b1 |
A |
T |
7: 126,071,536 (GRCm39) |
D216E |
possibly damaging |
Het |
Sh3gl3 |
A |
G |
7: 81,920,008 (GRCm39) |
N72S |
possibly damaging |
Het |
Slc12a1 |
A |
T |
2: 125,015,619 (GRCm39) |
I391F |
probably damaging |
Het |
Slc36a2 |
G |
A |
11: 55,072,381 (GRCm39) |
A77V |
probably damaging |
Het |
Smc2 |
A |
T |
4: 52,474,987 (GRCm39) |
I888L |
probably benign |
Het |
Smoc1 |
C |
T |
12: 81,197,450 (GRCm39) |
T194M |
probably damaging |
Het |
Sorcs1 |
C |
T |
19: 50,666,630 (GRCm39) |
G93R |
probably benign |
Het |
Sox30 |
T |
G |
11: 45,882,595 (GRCm39) |
F542V |
probably damaging |
Het |
Svep1 |
A |
G |
4: 58,206,030 (GRCm39) |
V116A |
possibly damaging |
Het |
Synj2 |
A |
G |
17: 6,063,966 (GRCm39) |
D330G |
probably benign |
Het |
Tenm3 |
A |
C |
8: 48,796,384 (GRCm39) |
S202A |
possibly damaging |
Het |
Tg |
C |
T |
15: 66,601,443 (GRCm39) |
T151I |
probably benign |
Het |
Tnfaip2 |
A |
G |
12: 111,414,527 (GRCm39) |
E361G |
probably damaging |
Het |
Tnk1 |
A |
T |
11: 69,746,009 (GRCm39) |
D305E |
probably damaging |
Het |
Tpp1 |
A |
G |
7: 105,399,177 (GRCm39) |
L133P |
probably damaging |
Het |
Trappc1 |
T |
A |
11: 69,215,243 (GRCm39) |
M41K |
probably damaging |
Het |
Tsen54 |
A |
G |
11: 115,706,549 (GRCm39) |
D9G |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,804,598 (GRCm39) |
I225F |
probably damaging |
Het |
Ube4b |
T |
C |
4: 149,457,298 (GRCm39) |
K313R |
probably benign |
Het |
Vps50 |
T |
C |
6: 3,555,379 (GRCm39) |
V425A |
probably damaging |
Het |
Wbp2 |
A |
T |
11: 115,971,445 (GRCm39) |
Y153* |
probably null |
Het |
Xrn1 |
A |
G |
9: 95,861,273 (GRCm39) |
S478G |
probably benign |
Het |
Zfp354c |
T |
C |
11: 50,707,969 (GRCm39) |
E77G |
probably benign |
Het |
Zfp462 |
T |
C |
4: 55,008,496 (GRCm39) |
M154T |
probably benign |
Het |
Zfp704 |
A |
G |
3: 9,539,585 (GRCm39) |
V255A |
probably damaging |
Het |
Zfp763 |
G |
T |
17: 33,238,752 (GRCm39) |
A131E |
probably benign |
Het |
Zfp931 |
A |
T |
2: 177,711,651 (GRCm39) |
V32E |
probably null |
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 |
R0718:Cenpf
|
UTSW |
1 |
189,386,181 (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 |
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 |
|