Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
A |
T |
7: 120,140,463 (GRCm39) |
I1588F |
probably benign |
Het |
Abcc2 |
A |
T |
19: 43,795,683 (GRCm39) |
T480S |
probably benign |
Het |
Acnat1 |
A |
G |
4: 49,447,498 (GRCm39) |
I361T |
probably damaging |
Het |
Adamts10 |
A |
T |
17: 33,768,529 (GRCm39) |
H869L |
probably benign |
Het |
Agpat5 |
T |
C |
8: 18,929,629 (GRCm39) |
C253R |
probably benign |
Het |
Agtrap |
T |
A |
4: 148,168,434 (GRCm39) |
H15L |
probably damaging |
Het |
Ahnak |
T |
A |
19: 8,985,286 (GRCm39) |
V2190E |
probably damaging |
Het |
Alx4 |
A |
G |
2: 93,505,732 (GRCm39) |
E278G |
probably damaging |
Het |
Amz2 |
T |
C |
11: 109,319,697 (GRCm39) |
S28P |
probably damaging |
Het |
Atr |
T |
A |
9: 95,748,786 (GRCm39) |
Y444N |
probably benign |
Het |
Brdt |
T |
C |
5: 107,496,479 (GRCm39) |
I197T |
probably benign |
Het |
Ccser1 |
G |
T |
6: 62,356,878 (GRCm39) |
S772I |
probably damaging |
Het |
Cdh16 |
T |
C |
8: 105,343,100 (GRCm39) |
H657R |
probably benign |
Het |
Ceacam5 |
A |
T |
7: 17,493,502 (GRCm39) |
K842* |
probably null |
Het |
Cep120 |
G |
A |
18: 53,856,358 (GRCm39) |
T353I |
probably benign |
Het |
Chrnb1 |
T |
C |
11: 69,684,410 (GRCm39) |
N164S |
possibly damaging |
Het |
Cse1l |
T |
C |
2: 166,764,111 (GRCm39) |
F123L |
probably damaging |
Het |
Cul7 |
T |
A |
17: 46,974,116 (GRCm39) |
L1467H |
probably damaging |
Het |
Dcx |
G |
C |
X: 142,706,099 (GRCm39) |
L231V |
probably damaging |
Het |
Dnah12 |
T |
C |
14: 26,514,221 (GRCm39) |
|
probably null |
Het |
Dnah2 |
A |
T |
11: 69,355,756 (GRCm39) |
M2227K |
probably damaging |
Het |
Dnajc30 |
G |
A |
5: 135,093,186 (GRCm39) |
A28T |
probably benign |
Het |
Dnm1l |
T |
C |
16: 16,147,830 (GRCm39) |
T306A |
probably benign |
Het |
Elapor2 |
T |
G |
5: 9,316,275 (GRCm39) |
L2R |
probably damaging |
Het |
Enpp3 |
C |
A |
10: 24,652,669 (GRCm39) |
E763* |
probably null |
Het |
Esyt3 |
T |
C |
9: 99,202,364 (GRCm39) |
S516G |
probably benign |
Het |
Exoc3 |
T |
C |
13: 74,330,435 (GRCm39) |
Q498R |
probably damaging |
Het |
Fbn2 |
T |
A |
18: 58,194,814 (GRCm39) |
N1449I |
probably damaging |
Het |
Fgb |
T |
C |
3: 82,952,287 (GRCm39) |
D194G |
probably benign |
Het |
Fgd3 |
T |
C |
13: 49,417,324 (GRCm39) |
D713G |
possibly damaging |
Het |
Foxb1 |
T |
A |
9: 69,667,383 (GRCm39) |
Y49F |
possibly damaging |
Het |
Fpr3 |
A |
G |
17: 18,191,670 (GRCm39) |
I314V |
probably damaging |
Het |
Gfod1 |
A |
T |
13: 43,456,921 (GRCm39) |
I18N |
probably damaging |
Het |
Gm5407 |
T |
C |
16: 49,117,283 (GRCm39) |
|
noncoding transcript |
Het |
Gpr89 |
A |
G |
3: 96,782,949 (GRCm39) |
F334L |
possibly damaging |
Het |
Gucy2d |
G |
T |
7: 98,093,054 (GRCm39) |
V144F |
probably benign |
Het |
H2-M10.5 |
C |
A |
17: 37,085,660 (GRCm39) |
P273H |
probably damaging |
Het |
H2-T13 |
T |
A |
17: 36,391,908 (GRCm39) |
K237M |
probably damaging |
Het |
Hcn2 |
A |
G |
10: 79,566,777 (GRCm39) |
M485V |
probably benign |
Het |
Helz2 |
G |
T |
2: 180,875,543 (GRCm39) |
S1650R |
probably damaging |
Het |
Ifnar2 |
T |
C |
16: 91,201,058 (GRCm39) |
V433A |
probably benign |
Het |
Igsf21 |
T |
A |
4: 139,834,623 (GRCm39) |
Y83F |
probably benign |
Het |
Kcnk18 |
A |
G |
19: 59,223,490 (GRCm39) |
I212V |
possibly damaging |
Het |
Kcns2 |
T |
C |
15: 34,839,855 (GRCm39) |
I406T |
probably damaging |
Het |
Krt42 |
C |
T |
11: 100,158,075 (GRCm39) |
V166M |
possibly damaging |
Het |
Lama3 |
T |
C |
18: 12,628,336 (GRCm39) |
M1476T |
probably benign |
Het |
Lcor |
A |
G |
19: 41,546,913 (GRCm39) |
R166G |
probably benign |
Het |
Mapt |
C |
T |
11: 104,218,901 (GRCm39) |
P354L |
probably damaging |
Het |
Mep1b |
A |
T |
18: 21,226,286 (GRCm39) |
I383F |
probably benign |
Het |
Mpzl1 |
C |
A |
1: 165,429,374 (GRCm39) |
C222F |
probably benign |
Het |
Mug2 |
T |
C |
6: 122,047,829 (GRCm39) |
L780P |
probably damaging |
Het |
Naip2 |
C |
T |
13: 100,288,665 (GRCm39) |
|
probably null |
Het |
Ndufab1 |
T |
C |
7: 121,695,914 (GRCm39) |
D41G |
probably benign |
Het |
Ntn1 |
A |
G |
11: 68,104,011 (GRCm39) |
C546R |
probably damaging |
Het |
Or2a5 |
T |
A |
6: 42,873,687 (GRCm39) |
F101I |
probably damaging |
Het |
Pakap |
A |
G |
4: 57,892,963 (GRCm39) |
E880G |
probably damaging |
Het |
Pde6b |
A |
G |
5: 108,575,056 (GRCm39) |
E639G |
probably benign |
Het |
Phf10 |
T |
C |
17: 15,177,071 (GRCm39) |
T83A |
probably benign |
Het |
Phkb |
T |
A |
8: 86,628,549 (GRCm39) |
I186N |
possibly damaging |
Het |
Plxnd1 |
C |
A |
6: 115,954,978 (GRCm39) |
A595S |
possibly damaging |
Het |
Ppara |
T |
A |
15: 85,685,300 (GRCm39) |
H416Q |
probably damaging |
Het |
Prodh |
T |
A |
16: 17,898,891 (GRCm39) |
D188V |
probably damaging |
Het |
Psmd14 |
A |
T |
2: 61,615,800 (GRCm39) |
K223M |
possibly damaging |
Het |
Ptpn5 |
A |
G |
7: 46,728,616 (GRCm39) |
M528T |
possibly damaging |
Het |
Rassf9 |
G |
A |
10: 102,380,800 (GRCm39) |
E59K |
probably benign |
Het |
Rnf2 |
A |
T |
1: 151,351,936 (GRCm39) |
L140H |
probably damaging |
Het |
Scai |
A |
G |
2: 38,970,093 (GRCm39) |
F557S |
probably damaging |
Het |
Sdk2 |
A |
G |
11: 113,747,552 (GRCm39) |
S653P |
possibly damaging |
Het |
Sec24c |
A |
G |
14: 20,739,179 (GRCm39) |
D534G |
probably benign |
Het |
Semp2l2a |
T |
A |
8: 13,887,143 (GRCm39) |
Q316L |
probably benign |
Het |
Septin4 |
T |
C |
11: 87,457,838 (GRCm39) |
S71P |
probably benign |
Het |
Serinc1 |
A |
G |
10: 57,395,561 (GRCm39) |
V375A |
probably benign |
Het |
Serpinb9f |
C |
T |
13: 33,509,829 (GRCm39) |
A7V |
probably damaging |
Het |
Smco1 |
T |
C |
16: 32,092,700 (GRCm39) |
S124P |
probably damaging |
Het |
Smim23 |
C |
A |
11: 32,774,441 (GRCm39) |
C26F |
possibly damaging |
Het |
Sppl2c |
T |
A |
11: 104,078,715 (GRCm39) |
M505K |
probably benign |
Het |
Sprr1b |
C |
A |
3: 92,344,775 (GRCm39) |
V34F |
possibly damaging |
Het |
Sun1 |
G |
A |
5: 139,221,487 (GRCm39) |
|
probably null |
Het |
Supt16 |
A |
G |
14: 52,415,592 (GRCm39) |
L381P |
possibly damaging |
Het |
Syne2 |
A |
G |
12: 75,946,020 (GRCm39) |
D364G |
possibly damaging |
Het |
Tax1bp1 |
G |
T |
6: 52,742,937 (GRCm39) |
V775F |
probably damaging |
Het |
Tial1 |
T |
A |
7: 128,046,383 (GRCm39) |
I231F |
probably damaging |
Het |
Tiam1 |
C |
A |
16: 89,595,582 (GRCm39) |
V1300L |
probably damaging |
Het |
Tmem132e |
A |
G |
11: 82,334,243 (GRCm39) |
T585A |
probably damaging |
Het |
Tnni3k |
C |
T |
3: 154,684,836 (GRCm39) |
A165T |
probably benign |
Het |
Tomm40 |
A |
T |
7: 19,444,886 (GRCm39) |
I165N |
probably damaging |
Het |
Tomt |
T |
C |
7: 101,550,454 (GRCm39) |
E104G |
probably damaging |
Het |
Topaz1 |
T |
C |
9: 122,596,078 (GRCm39) |
S950P |
possibly damaging |
Het |
Traf3ip2 |
C |
G |
10: 39,501,936 (GRCm39) |
P28R |
probably benign |
Het |
Trim24 |
C |
T |
6: 37,934,750 (GRCm39) |
P822S |
probably damaging |
Het |
Upf3a |
T |
G |
8: 13,842,108 (GRCm39) |
Y175D |
probably damaging |
Het |
Vars2 |
G |
A |
17: 35,977,814 (GRCm39) |
P69S |
probably benign |
Het |
Veph1 |
T |
C |
3: 66,151,976 (GRCm39) |
Y151C |
probably damaging |
Het |
Vmn2r11 |
T |
A |
5: 109,202,654 (GRCm39) |
D141V |
probably benign |
Het |
Vwa5b1 |
G |
A |
4: 138,319,331 (GRCm39) |
Q442* |
probably null |
Het |
Wdr17 |
T |
A |
8: 55,140,761 (GRCm39) |
D197V |
probably damaging |
Het |
Wdr70 |
G |
T |
15: 7,913,891 (GRCm39) |
T586N |
possibly damaging |
Het |
Wfdc18 |
G |
A |
11: 83,600,754 (GRCm39) |
G52R |
probably benign |
Het |
Zc3h6 |
T |
C |
2: 128,858,540 (GRCm39) |
I857T |
probably damaging |
Het |
Zfp318 |
TGAAGAAGAAGAAGAAGAAGAAGAAGAAG |
TGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAG |
17: 46,723,440 (GRCm39) |
|
probably benign |
Het |
Zfp318 |
GAAGAA |
GAAGAACAAGAA |
17: 46,723,450 (GRCm39) |
|
probably benign |
Het |
Zfp647 |
C |
T |
15: 76,796,151 (GRCm39) |
V170I |
probably benign |
Het |
Zfp871 |
T |
C |
17: 32,994,891 (GRCm39) |
N76D |
possibly damaging |
Het |
Zpld2 |
A |
G |
4: 133,919,986 (GRCm39) |
|
probably null |
Het |
Zwilch |
A |
G |
9: 64,068,234 (GRCm39) |
Y194H |
probably damaging |
Het |
|
Other mutations in Pkhd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00157:Pkhd1
|
APN |
1 |
20,637,098 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL00687:Pkhd1
|
APN |
1 |
20,594,294 (GRCm39) |
missense |
probably benign |
0.19 |
IGL00824:Pkhd1
|
APN |
1 |
20,151,408 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00870:Pkhd1
|
APN |
1 |
20,641,614 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00911:Pkhd1
|
APN |
1 |
20,187,971 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01015:Pkhd1
|
APN |
1 |
20,593,482 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01025:Pkhd1
|
APN |
1 |
20,279,400 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01064:Pkhd1
|
APN |
1 |
20,604,754 (GRCm39) |
splice site |
probably benign |
|
IGL01313:Pkhd1
|
APN |
1 |
20,271,248 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01340:Pkhd1
|
APN |
1 |
20,593,201 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01352:Pkhd1
|
APN |
1 |
20,619,939 (GRCm39) |
missense |
probably benign |
0.34 |
IGL01456:Pkhd1
|
APN |
1 |
20,269,683 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01530:Pkhd1
|
APN |
1 |
20,629,643 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01557:Pkhd1
|
APN |
1 |
20,187,203 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL01655:Pkhd1
|
APN |
1 |
20,604,857 (GRCm39) |
nonsense |
probably null |
|
IGL01790:Pkhd1
|
APN |
1 |
20,628,895 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01862:Pkhd1
|
APN |
1 |
20,429,134 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01874:Pkhd1
|
APN |
1 |
20,173,459 (GRCm39) |
missense |
probably benign |
0.32 |
IGL01901:Pkhd1
|
APN |
1 |
20,290,307 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01903:Pkhd1
|
APN |
1 |
20,268,361 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01981:Pkhd1
|
APN |
1 |
20,593,791 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL02068:Pkhd1
|
APN |
1 |
20,592,971 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02083:Pkhd1
|
APN |
1 |
20,271,451 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02084:Pkhd1
|
APN |
1 |
20,447,623 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02126:Pkhd1
|
APN |
1 |
20,187,419 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02136:Pkhd1
|
APN |
1 |
20,345,839 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02255:Pkhd1
|
APN |
1 |
20,654,325 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02272:Pkhd1
|
APN |
1 |
20,279,484 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02308:Pkhd1
|
APN |
1 |
20,140,600 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02364:Pkhd1
|
APN |
1 |
20,271,007 (GRCm39) |
missense |
probably benign |
|
IGL02389:Pkhd1
|
APN |
1 |
20,187,944 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02394:Pkhd1
|
APN |
1 |
20,269,710 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL02403:Pkhd1
|
APN |
1 |
20,632,642 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02415:Pkhd1
|
APN |
1 |
20,484,645 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02415:Pkhd1
|
APN |
1 |
20,592,983 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02455:Pkhd1
|
APN |
1 |
20,434,425 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02502:Pkhd1
|
APN |
1 |
20,462,389 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02511:Pkhd1
|
APN |
1 |
20,143,731 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02530:Pkhd1
|
APN |
1 |
20,187,944 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02532:Pkhd1
|
APN |
1 |
20,187,944 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02534:Pkhd1
|
APN |
1 |
20,187,944 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02556:Pkhd1
|
APN |
1 |
20,380,934 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02570:Pkhd1
|
APN |
1 |
20,590,480 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02605:Pkhd1
|
APN |
1 |
20,621,126 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02641:Pkhd1
|
APN |
1 |
20,628,976 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02741:Pkhd1
|
APN |
1 |
20,290,253 (GRCm39) |
splice site |
probably benign |
|
IGL02752:Pkhd1
|
APN |
1 |
20,623,815 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL02890:Pkhd1
|
APN |
1 |
20,431,235 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02959:Pkhd1
|
APN |
1 |
20,678,640 (GRCm39) |
nonsense |
probably null |
|
IGL02960:Pkhd1
|
APN |
1 |
20,447,670 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02990:Pkhd1
|
APN |
1 |
20,593,187 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL03037:Pkhd1
|
APN |
1 |
20,592,923 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03082:Pkhd1
|
APN |
1 |
20,635,857 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03114:Pkhd1
|
APN |
1 |
20,268,395 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03288:Pkhd1
|
APN |
1 |
20,271,243 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03328:Pkhd1
|
APN |
1 |
20,151,524 (GRCm39) |
splice site |
probably benign |
|
IGL03375:Pkhd1
|
APN |
1 |
20,187,247 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03380:Pkhd1
|
APN |
1 |
20,270,894 (GRCm39) |
missense |
probably damaging |
1.00 |
0152:Pkhd1
|
UTSW |
1 |
20,593,118 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL03046:Pkhd1
|
UTSW |
1 |
20,607,589 (GRCm39) |
missense |
possibly damaging |
0.81 |
LCD18:Pkhd1
|
UTSW |
1 |
20,681,638 (GRCm39) |
intron |
probably benign |
|
P0035:Pkhd1
|
UTSW |
1 |
20,187,571 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4260001:Pkhd1
|
UTSW |
1 |
20,293,130 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0063:Pkhd1
|
UTSW |
1 |
20,282,174 (GRCm39) |
missense |
probably benign |
0.02 |
R0063:Pkhd1
|
UTSW |
1 |
20,282,174 (GRCm39) |
missense |
probably benign |
0.02 |
R0071:Pkhd1
|
UTSW |
1 |
20,271,568 (GRCm39) |
missense |
probably benign |
0.11 |
R0071:Pkhd1
|
UTSW |
1 |
20,271,568 (GRCm39) |
missense |
probably benign |
0.11 |
R0094:Pkhd1
|
UTSW |
1 |
20,279,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R0094:Pkhd1
|
UTSW |
1 |
20,279,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R0103:Pkhd1
|
UTSW |
1 |
20,593,583 (GRCm39) |
missense |
probably benign |
0.04 |
R0103:Pkhd1
|
UTSW |
1 |
20,593,583 (GRCm39) |
missense |
probably benign |
0.04 |
R0105:Pkhd1
|
UTSW |
1 |
20,593,956 (GRCm39) |
nonsense |
probably null |
|
R0105:Pkhd1
|
UTSW |
1 |
20,593,956 (GRCm39) |
nonsense |
probably null |
|
R0115:Pkhd1
|
UTSW |
1 |
20,420,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R0193:Pkhd1
|
UTSW |
1 |
20,429,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R0245:Pkhd1
|
UTSW |
1 |
20,610,624 (GRCm39) |
missense |
probably benign |
0.03 |
R0277:Pkhd1
|
UTSW |
1 |
20,345,762 (GRCm39) |
missense |
probably benign |
0.04 |
R0310:Pkhd1
|
UTSW |
1 |
20,620,046 (GRCm39) |
splice site |
probably null |
|
R0323:Pkhd1
|
UTSW |
1 |
20,345,762 (GRCm39) |
missense |
probably benign |
0.04 |
R0395:Pkhd1
|
UTSW |
1 |
20,451,771 (GRCm39) |
missense |
probably benign |
0.26 |
R0412:Pkhd1
|
UTSW |
1 |
20,188,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R0506:Pkhd1
|
UTSW |
1 |
20,629,693 (GRCm39) |
missense |
probably benign |
0.00 |
R0512:Pkhd1
|
UTSW |
1 |
20,380,738 (GRCm39) |
splice site |
probably benign |
|
R0550:Pkhd1
|
UTSW |
1 |
20,417,447 (GRCm39) |
missense |
probably null |
1.00 |
R0584:Pkhd1
|
UTSW |
1 |
20,309,660 (GRCm39) |
nonsense |
probably null |
|
R0586:Pkhd1
|
UTSW |
1 |
20,594,335 (GRCm39) |
missense |
probably benign |
0.04 |
R0598:Pkhd1
|
UTSW |
1 |
20,271,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R0603:Pkhd1
|
UTSW |
1 |
20,187,397 (GRCm39) |
missense |
probably benign |
0.05 |
R0634:Pkhd1
|
UTSW |
1 |
20,187,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R0677:Pkhd1
|
UTSW |
1 |
20,594,454 (GRCm39) |
missense |
probably benign |
0.01 |
R0746:Pkhd1
|
UTSW |
1 |
20,268,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R0781:Pkhd1
|
UTSW |
1 |
20,187,708 (GRCm39) |
missense |
probably benign |
0.01 |
R0840:Pkhd1
|
UTSW |
1 |
20,420,745 (GRCm39) |
missense |
probably damaging |
0.98 |
R0946:Pkhd1
|
UTSW |
1 |
20,269,605 (GRCm39) |
missense |
probably benign |
0.10 |
R1018:Pkhd1
|
UTSW |
1 |
20,271,483 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1028:Pkhd1
|
UTSW |
1 |
20,187,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R1136:Pkhd1
|
UTSW |
1 |
20,593,053 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1178:Pkhd1
|
UTSW |
1 |
20,655,381 (GRCm39) |
critical splice donor site |
probably null |
|
R1180:Pkhd1
|
UTSW |
1 |
20,655,381 (GRCm39) |
critical splice donor site |
probably null |
|
R1222:Pkhd1
|
UTSW |
1 |
20,637,680 (GRCm39) |
missense |
probably benign |
0.07 |
R1334:Pkhd1
|
UTSW |
1 |
20,604,129 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1335:Pkhd1
|
UTSW |
1 |
20,641,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R1387:Pkhd1
|
UTSW |
1 |
20,625,447 (GRCm39) |
splice site |
probably benign |
|
R1411:Pkhd1
|
UTSW |
1 |
20,444,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R1443:Pkhd1
|
UTSW |
1 |
20,604,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R1448:Pkhd1
|
UTSW |
1 |
20,655,381 (GRCm39) |
critical splice donor site |
probably null |
|
R1468:Pkhd1
|
UTSW |
1 |
20,593,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Pkhd1
|
UTSW |
1 |
20,593,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R1473:Pkhd1
|
UTSW |
1 |
20,593,207 (GRCm39) |
missense |
probably benign |
0.00 |
R1524:Pkhd1
|
UTSW |
1 |
20,188,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R1532:Pkhd1
|
UTSW |
1 |
20,187,625 (GRCm39) |
missense |
probably benign |
0.08 |
R1565:Pkhd1
|
UTSW |
1 |
20,417,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R1572:Pkhd1
|
UTSW |
1 |
20,417,664 (GRCm39) |
missense |
probably benign |
0.02 |
R1583:Pkhd1
|
UTSW |
1 |
20,188,049 (GRCm39) |
missense |
probably benign |
|
R1617:Pkhd1
|
UTSW |
1 |
20,268,274 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1631:Pkhd1
|
UTSW |
1 |
20,593,121 (GRCm39) |
missense |
probably benign |
0.06 |
R1655:Pkhd1
|
UTSW |
1 |
20,654,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R1707:Pkhd1
|
UTSW |
1 |
20,621,064 (GRCm39) |
splice site |
probably benign |
|
R1753:Pkhd1
|
UTSW |
1 |
20,604,129 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1782:Pkhd1
|
UTSW |
1 |
20,635,935 (GRCm39) |
missense |
probably damaging |
0.98 |
R1791:Pkhd1
|
UTSW |
1 |
20,655,376 (GRCm39) |
splice site |
probably benign |
|
R1822:Pkhd1
|
UTSW |
1 |
20,417,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R1823:Pkhd1
|
UTSW |
1 |
20,417,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R1824:Pkhd1
|
UTSW |
1 |
20,417,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R1836:Pkhd1
|
UTSW |
1 |
20,187,293 (GRCm39) |
missense |
probably benign |
0.01 |
R1862:Pkhd1
|
UTSW |
1 |
20,621,244 (GRCm39) |
missense |
probably benign |
0.00 |
R1863:Pkhd1
|
UTSW |
1 |
20,621,244 (GRCm39) |
missense |
probably benign |
0.00 |
R1869:Pkhd1
|
UTSW |
1 |
20,685,491 (GRCm39) |
critical splice donor site |
probably null |
|
R1928:Pkhd1
|
UTSW |
1 |
20,151,524 (GRCm39) |
splice site |
probably benign |
|
R1969:Pkhd1
|
UTSW |
1 |
20,451,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R1970:Pkhd1
|
UTSW |
1 |
20,451,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R1981:Pkhd1
|
UTSW |
1 |
20,187,284 (GRCm39) |
missense |
probably benign |
0.00 |
R2008:Pkhd1
|
UTSW |
1 |
20,269,683 (GRCm39) |
missense |
probably damaging |
0.99 |
R2034:Pkhd1
|
UTSW |
1 |
20,270,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R2061:Pkhd1
|
UTSW |
1 |
20,683,036 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2062:Pkhd1
|
UTSW |
1 |
20,271,559 (GRCm39) |
missense |
probably damaging |
0.97 |
R2108:Pkhd1
|
UTSW |
1 |
20,623,798 (GRCm39) |
nonsense |
probably null |
|
R2142:Pkhd1
|
UTSW |
1 |
20,594,119 (GRCm39) |
missense |
probably benign |
0.00 |
R2148:Pkhd1
|
UTSW |
1 |
20,484,444 (GRCm39) |
critical splice donor site |
probably null |
|
R2176:Pkhd1
|
UTSW |
1 |
20,623,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R2202:Pkhd1
|
UTSW |
1 |
20,607,584 (GRCm39) |
missense |
probably benign |
0.06 |
R2255:Pkhd1
|
UTSW |
1 |
20,635,863 (GRCm39) |
missense |
probably benign |
0.23 |
R2269:Pkhd1
|
UTSW |
1 |
20,604,759 (GRCm39) |
critical splice donor site |
probably null |
|
R2275:Pkhd1
|
UTSW |
1 |
20,271,073 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2340:Pkhd1
|
UTSW |
1 |
20,271,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R2431:Pkhd1
|
UTSW |
1 |
20,271,389 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2679:Pkhd1
|
UTSW |
1 |
20,279,406 (GRCm39) |
missense |
probably benign |
0.03 |
R2850:Pkhd1
|
UTSW |
1 |
20,579,300 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2851:Pkhd1
|
UTSW |
1 |
20,128,526 (GRCm39) |
missense |
probably benign |
0.16 |
R2853:Pkhd1
|
UTSW |
1 |
20,128,526 (GRCm39) |
missense |
probably benign |
0.16 |
R2984:Pkhd1
|
UTSW |
1 |
20,293,185 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2987:Pkhd1
|
UTSW |
1 |
20,174,823 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3692:Pkhd1
|
UTSW |
1 |
20,625,353 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3721:Pkhd1
|
UTSW |
1 |
20,655,879 (GRCm39) |
missense |
probably benign |
0.08 |
R3746:Pkhd1
|
UTSW |
1 |
20,128,524 (GRCm39) |
makesense |
probably null |
|
R3838:Pkhd1
|
UTSW |
1 |
20,604,853 (GRCm39) |
missense |
possibly damaging |
0.66 |
R3843:Pkhd1
|
UTSW |
1 |
20,628,947 (GRCm39) |
missense |
probably benign |
0.00 |
R3861:Pkhd1
|
UTSW |
1 |
20,271,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R3893:Pkhd1
|
UTSW |
1 |
20,382,362 (GRCm39) |
nonsense |
probably null |
|
R3926:Pkhd1
|
UTSW |
1 |
20,621,097 (GRCm39) |
missense |
probably benign |
0.00 |
R4183:Pkhd1
|
UTSW |
1 |
20,188,031 (GRCm39) |
missense |
probably benign |
0.03 |
R4184:Pkhd1
|
UTSW |
1 |
20,633,910 (GRCm39) |
missense |
probably benign |
0.06 |
R4184:Pkhd1
|
UTSW |
1 |
20,279,501 (GRCm39) |
missense |
probably benign |
0.03 |
R4255:Pkhd1
|
UTSW |
1 |
20,664,158 (GRCm39) |
missense |
probably damaging |
0.99 |
R4275:Pkhd1
|
UTSW |
1 |
20,128,608 (GRCm39) |
missense |
probably benign |
0.00 |
R4342:Pkhd1
|
UTSW |
1 |
20,128,841 (GRCm39) |
missense |
probably benign |
0.00 |
R4386:Pkhd1
|
UTSW |
1 |
20,484,516 (GRCm39) |
missense |
probably benign |
0.00 |
R4402:Pkhd1
|
UTSW |
1 |
20,309,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R4431:Pkhd1
|
UTSW |
1 |
20,593,538 (GRCm39) |
missense |
probably damaging |
0.99 |
R4560:Pkhd1
|
UTSW |
1 |
20,282,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R4561:Pkhd1
|
UTSW |
1 |
20,604,943 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4570:Pkhd1
|
UTSW |
1 |
20,451,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R4571:Pkhd1
|
UTSW |
1 |
20,683,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R4588:Pkhd1
|
UTSW |
1 |
20,271,092 (GRCm39) |
missense |
probably benign |
0.00 |
R4598:Pkhd1
|
UTSW |
1 |
20,573,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R4651:Pkhd1
|
UTSW |
1 |
20,451,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R4657:Pkhd1
|
UTSW |
1 |
20,434,391 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4718:Pkhd1
|
UTSW |
1 |
20,151,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R4740:Pkhd1
|
UTSW |
1 |
20,594,354 (GRCm39) |
missense |
probably benign |
|
R4750:Pkhd1
|
UTSW |
1 |
20,594,336 (GRCm39) |
missense |
possibly damaging |
0.57 |
R4816:Pkhd1
|
UTSW |
1 |
20,269,639 (GRCm39) |
missense |
probably damaging |
0.99 |
R4825:Pkhd1
|
UTSW |
1 |
20,607,625 (GRCm39) |
missense |
probably damaging |
0.96 |
R4885:Pkhd1
|
UTSW |
1 |
20,140,712 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4907:Pkhd1
|
UTSW |
1 |
20,279,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R4944:Pkhd1
|
UTSW |
1 |
20,358,429 (GRCm39) |
missense |
probably null |
0.01 |
R5062:Pkhd1
|
UTSW |
1 |
20,655,935 (GRCm39) |
missense |
probably benign |
0.00 |
R5090:Pkhd1
|
UTSW |
1 |
20,270,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R5104:Pkhd1
|
UTSW |
1 |
20,655,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R5187:Pkhd1
|
UTSW |
1 |
20,279,448 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5202:Pkhd1
|
UTSW |
1 |
20,617,565 (GRCm39) |
missense |
probably benign |
0.01 |
R5240:Pkhd1
|
UTSW |
1 |
20,345,865 (GRCm39) |
missense |
probably benign |
0.04 |
R5248:Pkhd1
|
UTSW |
1 |
20,604,769 (GRCm39) |
missense |
probably benign |
0.00 |
R5252:Pkhd1
|
UTSW |
1 |
20,420,635 (GRCm39) |
critical splice donor site |
probably null |
|
R5293:Pkhd1
|
UTSW |
1 |
20,579,300 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5311:Pkhd1
|
UTSW |
1 |
20,636,094 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5317:Pkhd1
|
UTSW |
1 |
20,520,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R5346:Pkhd1
|
UTSW |
1 |
20,593,658 (GRCm39) |
missense |
probably damaging |
0.96 |
R5346:Pkhd1
|
UTSW |
1 |
20,462,321 (GRCm39) |
missense |
probably benign |
|
R5431:Pkhd1
|
UTSW |
1 |
20,188,060 (GRCm39) |
missense |
probably benign |
0.25 |
R5447:Pkhd1
|
UTSW |
1 |
20,309,609 (GRCm39) |
missense |
probably benign |
0.00 |
R5478:Pkhd1
|
UTSW |
1 |
20,271,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R5497:Pkhd1
|
UTSW |
1 |
20,447,628 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5554:Pkhd1
|
UTSW |
1 |
20,151,476 (GRCm39) |
missense |
probably damaging |
0.99 |
R5579:Pkhd1
|
UTSW |
1 |
20,593,366 (GRCm39) |
missense |
probably damaging |
0.96 |
R5614:Pkhd1
|
UTSW |
1 |
20,143,750 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5648:Pkhd1
|
UTSW |
1 |
20,628,850 (GRCm39) |
missense |
probably benign |
0.04 |
R5651:Pkhd1
|
UTSW |
1 |
20,188,031 (GRCm39) |
missense |
probably benign |
0.03 |
R5665:Pkhd1
|
UTSW |
1 |
20,658,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R5681:Pkhd1
|
UTSW |
1 |
20,617,685 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5754:Pkhd1
|
UTSW |
1 |
20,593,875 (GRCm39) |
nonsense |
probably null |
|
R5760:Pkhd1
|
UTSW |
1 |
20,143,778 (GRCm39) |
missense |
probably benign |
0.02 |
R5776:Pkhd1
|
UTSW |
1 |
20,279,409 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5782:Pkhd1
|
UTSW |
1 |
20,128,824 (GRCm39) |
missense |
probably benign |
|
R5810:Pkhd1
|
UTSW |
1 |
20,270,897 (GRCm39) |
missense |
probably benign |
0.26 |
R5814:Pkhd1
|
UTSW |
1 |
20,269,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R5816:Pkhd1
|
UTSW |
1 |
20,128,902 (GRCm39) |
missense |
probably benign |
0.03 |
R5835:Pkhd1
|
UTSW |
1 |
20,271,307 (GRCm39) |
missense |
probably benign |
0.01 |
R5844:Pkhd1
|
UTSW |
1 |
20,451,685 (GRCm39) |
missense |
probably benign |
0.00 |
R5847:Pkhd1
|
UTSW |
1 |
20,444,960 (GRCm39) |
nonsense |
probably null |
|
R5852:Pkhd1
|
UTSW |
1 |
20,447,632 (GRCm39) |
missense |
probably benign |
0.22 |
R5863:Pkhd1
|
UTSW |
1 |
20,590,434 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6213:Pkhd1
|
UTSW |
1 |
20,593,994 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6351:Pkhd1
|
UTSW |
1 |
20,282,175 (GRCm39) |
missense |
probably benign |
0.00 |
R6386:Pkhd1
|
UTSW |
1 |
20,621,244 (GRCm39) |
missense |
probably damaging |
0.96 |
R6542:Pkhd1
|
UTSW |
1 |
20,655,927 (GRCm39) |
missense |
probably benign |
0.02 |
R6579:Pkhd1
|
UTSW |
1 |
20,271,047 (GRCm39) |
missense |
probably benign |
0.01 |
R6658:Pkhd1
|
UTSW |
1 |
20,682,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R6765:Pkhd1
|
UTSW |
1 |
20,128,563 (GRCm39) |
missense |
probably benign |
|
R6886:Pkhd1
|
UTSW |
1 |
20,417,504 (GRCm39) |
missense |
probably benign |
0.01 |
R6892:Pkhd1
|
UTSW |
1 |
20,593,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R6900:Pkhd1
|
UTSW |
1 |
20,604,925 (GRCm39) |
missense |
probably benign |
0.06 |
R6932:Pkhd1
|
UTSW |
1 |
20,632,675 (GRCm39) |
missense |
probably benign |
0.19 |
R7191:Pkhd1
|
UTSW |
1 |
20,628,943 (GRCm39) |
missense |
probably benign |
0.00 |
R7220:Pkhd1
|
UTSW |
1 |
20,593,350 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7329:Pkhd1
|
UTSW |
1 |
20,617,743 (GRCm39) |
missense |
probably damaging |
0.96 |
R7361:Pkhd1
|
UTSW |
1 |
20,664,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R7381:Pkhd1
|
UTSW |
1 |
20,271,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R7388:Pkhd1
|
UTSW |
1 |
20,309,528 (GRCm39) |
missense |
not run |
|
R7436:Pkhd1
|
UTSW |
1 |
20,270,925 (GRCm39) |
missense |
probably benign |
|
R7473:Pkhd1
|
UTSW |
1 |
20,619,980 (GRCm39) |
missense |
probably damaging |
0.99 |
R7578:Pkhd1
|
UTSW |
1 |
20,417,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R7751:Pkhd1
|
UTSW |
1 |
20,271,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R7755:Pkhd1
|
UTSW |
1 |
20,617,717 (GRCm39) |
missense |
probably damaging |
0.98 |
R7757:Pkhd1
|
UTSW |
1 |
20,632,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R7832:Pkhd1
|
UTSW |
1 |
20,573,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R7834:Pkhd1
|
UTSW |
1 |
20,382,273 (GRCm39) |
missense |
probably benign |
|
R7920:Pkhd1
|
UTSW |
1 |
20,345,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R8014:Pkhd1
|
UTSW |
1 |
20,579,115 (GRCm39) |
critical splice donor site |
probably null |
|
R8034:Pkhd1
|
UTSW |
1 |
20,451,662 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8085:Pkhd1
|
UTSW |
1 |
20,683,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R8087:Pkhd1
|
UTSW |
1 |
20,593,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R8103:Pkhd1
|
UTSW |
1 |
20,270,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R8122:Pkhd1
|
UTSW |
1 |
20,632,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R8273:Pkhd1
|
UTSW |
1 |
20,607,644 (GRCm39) |
splice site |
probably benign |
|
R8485:Pkhd1
|
UTSW |
1 |
20,593,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R8504:Pkhd1
|
UTSW |
1 |
20,590,432 (GRCm39) |
missense |
probably benign |
0.10 |
R8544:Pkhd1
|
UTSW |
1 |
20,593,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R8692:Pkhd1
|
UTSW |
1 |
20,462,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R8787:Pkhd1
|
UTSW |
1 |
20,358,461 (GRCm39) |
missense |
probably damaging |
0.99 |
R8853:Pkhd1
|
UTSW |
1 |
20,143,679 (GRCm39) |
critical splice donor site |
probably null |
|
R8907:Pkhd1
|
UTSW |
1 |
20,187,785 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8934:Pkhd1
|
UTSW |
1 |
20,462,234 (GRCm39) |
critical splice donor site |
probably null |
|
R8990:Pkhd1
|
UTSW |
1 |
20,417,529 (GRCm39) |
missense |
probably benign |
0.00 |
R8998:Pkhd1
|
UTSW |
1 |
20,434,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R9024:Pkhd1
|
UTSW |
1 |
20,592,975 (GRCm39) |
missense |
probably benign |
0.24 |
R9035:Pkhd1
|
UTSW |
1 |
20,573,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R9092:Pkhd1
|
UTSW |
1 |
20,632,586 (GRCm39) |
missense |
probably benign |
0.00 |
R9238:Pkhd1
|
UTSW |
1 |
20,604,799 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9258:Pkhd1
|
UTSW |
1 |
20,444,174 (GRCm39) |
missense |
probably damaging |
0.99 |
R9262:Pkhd1
|
UTSW |
1 |
20,618,351 (GRCm39) |
missense |
probably benign |
0.01 |
R9297:Pkhd1
|
UTSW |
1 |
20,293,118 (GRCm39) |
missense |
probably benign |
0.06 |
R9452:Pkhd1
|
UTSW |
1 |
20,682,953 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9515:Pkhd1
|
UTSW |
1 |
20,637,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R9540:Pkhd1
|
UTSW |
1 |
20,269,570 (GRCm39) |
missense |
probably benign |
0.00 |
R9542:Pkhd1
|
UTSW |
1 |
20,188,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R9629:Pkhd1
|
UTSW |
1 |
20,462,437 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9644:Pkhd1
|
UTSW |
1 |
20,617,690 (GRCm39) |
missense |
probably benign |
0.04 |
R9739:Pkhd1
|
UTSW |
1 |
20,420,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R9767:Pkhd1
|
UTSW |
1 |
20,484,636 (GRCm39) |
missense |
probably benign |
|
R9781:Pkhd1
|
UTSW |
1 |
20,187,665 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9803:Pkhd1
|
UTSW |
1 |
20,637,073 (GRCm39) |
missense |
probably damaging |
1.00 |
X0012:Pkhd1
|
UTSW |
1 |
20,444,150 (GRCm39) |
missense |
probably damaging |
1.00 |
X0067:Pkhd1
|
UTSW |
1 |
20,590,450 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Pkhd1
|
UTSW |
1 |
20,593,971 (GRCm39) |
missense |
possibly damaging |
0.81 |
Z1177:Pkhd1
|
UTSW |
1 |
20,593,845 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Pkhd1
|
UTSW |
1 |
20,380,818 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Pkhd1
|
UTSW |
1 |
20,188,107 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Pkhd1
|
UTSW |
1 |
20,621,243 (GRCm39) |
missense |
probably benign |
|
Z1177:Pkhd1
|
UTSW |
1 |
20,594,162 (GRCm39) |
missense |
probably damaging |
1.00 |
|