Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm5 |
A |
G |
4: 144,504,521 (GRCm39) |
L210P |
probably damaging |
Het |
Acacb |
G |
A |
5: 114,356,923 (GRCm39) |
V1285I |
probably damaging |
Het |
Acly |
A |
T |
11: 100,386,789 (GRCm39) |
I591N |
probably damaging |
Het |
Acr |
T |
A |
15: 89,457,427 (GRCm39) |
V225E |
probably damaging |
Het |
Actr8 |
A |
G |
14: 29,714,925 (GRCm39) |
D580G |
probably damaging |
Het |
Adamts12 |
C |
A |
15: 11,345,734 (GRCm39) |
Q1592K |
probably benign |
Het |
Aire |
T |
C |
10: 77,878,404 (GRCm39) |
E138G |
probably damaging |
Het |
Apob |
C |
T |
12: 8,056,884 (GRCm39) |
Q1789* |
probably null |
Het |
Cbx5 |
A |
C |
15: 103,114,256 (GRCm39) |
|
probably null |
Het |
Cd300lb |
A |
T |
11: 114,819,345 (GRCm39) |
W95R |
probably damaging |
Het |
Cdc16 |
A |
G |
8: 13,827,605 (GRCm39) |
T504A |
probably benign |
Het |
Ckap2l |
A |
G |
2: 129,114,455 (GRCm39) |
V596A |
possibly damaging |
Het |
Cntn1 |
T |
C |
15: 92,151,922 (GRCm39) |
W454R |
probably benign |
Het |
Crat |
C |
T |
2: 30,294,577 (GRCm39) |
R497Q |
probably benign |
Het |
Csf2rb |
A |
G |
15: 78,223,099 (GRCm39) |
T104A |
possibly damaging |
Het |
Cyp4a12b |
A |
G |
4: 115,289,760 (GRCm39) |
D209G |
possibly damaging |
Het |
Ddx23 |
T |
C |
15: 98,546,570 (GRCm39) |
E533G |
probably damaging |
Het |
Dscaml1 |
A |
G |
9: 45,660,744 (GRCm39) |
|
probably null |
Het |
Eif3l |
T |
G |
15: 78,968,336 (GRCm39) |
C202G |
probably benign |
Het |
Ephx4 |
T |
G |
5: 107,577,612 (GRCm39) |
M312R |
probably damaging |
Het |
Erich6 |
A |
T |
3: 58,534,112 (GRCm39) |
|
probably null |
Het |
Far2 |
G |
A |
6: 148,075,411 (GRCm39) |
D424N |
probably damaging |
Het |
Fat1 |
C |
A |
8: 45,489,221 (GRCm39) |
N3497K |
probably damaging |
Het |
Fstl3 |
G |
A |
10: 79,615,865 (GRCm39) |
C117Y |
probably damaging |
Het |
Fyb2 |
A |
T |
4: 104,870,499 (GRCm39) |
H700L |
probably benign |
Het |
Gm8356 |
T |
A |
14: 17,691,282 (GRCm39) |
M128L |
probably benign |
Het |
Golim4 |
G |
T |
3: 75,805,442 (GRCm39) |
|
probably null |
Het |
Grm1 |
T |
G |
10: 10,622,403 (GRCm39) |
D440A |
probably benign |
Het |
Gtf2a1 |
A |
G |
12: 91,529,747 (GRCm39) |
V322A |
probably benign |
Het |
Hid1 |
T |
C |
11: 115,243,407 (GRCm39) |
|
probably null |
Het |
Igfals |
G |
A |
17: 25,098,962 (GRCm39) |
V18M |
possibly damaging |
Het |
Klk1b24 |
G |
T |
7: 43,839,688 (GRCm39) |
|
probably null |
Het |
Lmbr1 |
T |
C |
5: 29,551,850 (GRCm39) |
|
probably benign |
Het |
Lrrc40 |
T |
C |
3: 157,746,194 (GRCm39) |
S90P |
probably benign |
Het |
Mapk9 |
T |
C |
11: 49,763,663 (GRCm39) |
Y185H |
probably damaging |
Het |
Marveld2 |
C |
T |
13: 100,748,068 (GRCm39) |
G337D |
probably damaging |
Het |
Mga |
G |
T |
2: 119,776,710 (GRCm39) |
R1539L |
probably damaging |
Het |
Mllt6 |
T |
A |
11: 97,563,442 (GRCm39) |
S342T |
probably benign |
Het |
Ms4a6c |
T |
C |
19: 11,449,893 (GRCm39) |
|
probably null |
Het |
Muc16 |
T |
A |
9: 18,558,064 (GRCm39) |
H2743L |
unknown |
Het |
Myl10 |
G |
C |
5: 136,726,825 (GRCm39) |
V70L |
probably benign |
Het |
Or10ag60 |
T |
C |
2: 87,438,281 (GRCm39) |
F183S |
probably damaging |
Het |
Or2l13 |
A |
G |
16: 19,305,753 (GRCm39) |
H55R |
possibly damaging |
Het |
Plcd3 |
T |
G |
11: 102,962,545 (GRCm39) |
K635N |
probably damaging |
Het |
Prkch |
T |
A |
12: 73,632,301 (GRCm39) |
|
probably null |
Het |
Rb1cc1 |
T |
C |
1: 6,344,441 (GRCm39) |
V1570A |
probably damaging |
Het |
Rp1 |
T |
C |
1: 4,415,704 (GRCm39) |
N1803D |
probably benign |
Het |
Rufy3 |
T |
A |
5: 88,746,331 (GRCm39) |
V72E |
probably benign |
Het |
Secisbp2l |
G |
A |
2: 125,613,452 (GRCm39) |
Q181* |
probably null |
Het |
Sgcb |
A |
G |
5: 73,797,188 (GRCm39) |
F191L |
possibly damaging |
Het |
Sgsh |
T |
A |
11: 119,237,183 (GRCm39) |
D477V |
probably damaging |
Het |
Shoc1 |
A |
T |
4: 59,062,286 (GRCm39) |
V924E |
probably damaging |
Het |
Slc22a28 |
C |
A |
19: 8,048,492 (GRCm39) |
S385I |
probably benign |
Het |
Slc26a3 |
T |
C |
12: 31,497,787 (GRCm39) |
V47A |
probably benign |
Het |
Slco2a1 |
A |
T |
9: 102,945,185 (GRCm39) |
I187F |
probably damaging |
Het |
Sltm |
T |
C |
9: 70,481,179 (GRCm39) |
S344P |
unknown |
Het |
Sort1 |
A |
G |
3: 108,246,141 (GRCm39) |
T373A |
probably damaging |
Het |
Stab1 |
A |
G |
14: 30,882,274 (GRCm39) |
F474L |
probably benign |
Het |
Tbc1d5 |
G |
T |
17: 51,224,573 (GRCm39) |
A326E |
possibly damaging |
Het |
Tcstv4 |
A |
T |
13: 120,770,017 (GRCm39) |
K112N |
probably damaging |
Het |
Vwa8 |
A |
C |
14: 79,219,674 (GRCm39) |
|
probably null |
Het |
Wdr70 |
G |
A |
15: 7,951,562 (GRCm39) |
T425I |
probably benign |
Het |
Zfp30 |
T |
C |
7: 29,492,231 (GRCm39) |
Y243H |
probably benign |
Het |
Zfp974 |
A |
T |
7: 27,611,559 (GRCm39) |
N55K |
possibly damaging |
Het |
Zftraf1 |
A |
G |
15: 76,530,435 (GRCm39) |
L295P |
probably 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 |
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 |
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 |
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 |
|