Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4833420G17Rik |
T |
C |
13: 119,610,757 (GRCm39) |
|
probably benign |
Het |
9030619P08Rik |
T |
A |
15: 75,303,267 (GRCm39) |
|
noncoding transcript |
Het |
A430033K04Rik |
G |
T |
5: 138,645,119 (GRCm39) |
E335* |
probably null |
Het |
Abcb1b |
A |
T |
5: 8,862,671 (GRCm39) |
T118S |
probably benign |
Het |
Abcb1b |
T |
A |
5: 8,911,602 (GRCm39) |
I133N |
probably damaging |
Het |
Acox3 |
A |
G |
5: 35,747,080 (GRCm39) |
N166D |
probably damaging |
Het |
Adam5 |
T |
C |
8: 25,276,248 (GRCm39) |
Y473C |
probably damaging |
Het |
Ankmy2 |
A |
G |
12: 36,236,917 (GRCm39) |
K242E |
possibly damaging |
Het |
Apc2 |
A |
C |
10: 80,149,841 (GRCm39) |
I1603L |
probably benign |
Het |
Arhgef25 |
T |
A |
10: 127,021,472 (GRCm39) |
I249F |
probably damaging |
Het |
Birc2 |
T |
C |
9: 7,860,553 (GRCm39) |
H255R |
probably benign |
Het |
Cables1 |
A |
T |
18: 12,074,334 (GRCm39) |
R486W |
possibly damaging |
Het |
Caskin1 |
A |
T |
17: 24,726,135 (GRCm39) |
D1414V |
probably damaging |
Het |
Ccdc175 |
A |
G |
12: 72,227,619 (GRCm39) |
S55P |
probably damaging |
Het |
Ccdc57 |
A |
T |
11: 120,751,978 (GRCm39) |
S868T |
probably benign |
Het |
Ccny |
A |
T |
18: 9,449,516 (GRCm39) |
|
probably null |
Het |
Cdc34b |
A |
T |
11: 94,633,087 (GRCm39) |
I96F |
probably damaging |
Het |
Ctnnd1 |
A |
G |
2: 84,452,417 (GRCm39) |
F69L |
possibly damaging |
Het |
Cul9 |
C |
T |
17: 46,849,451 (GRCm39) |
D565N |
probably damaging |
Het |
Cxcl16 |
A |
G |
11: 70,346,519 (GRCm39) |
V208A |
probably benign |
Het |
Cyb5rl |
A |
G |
4: 106,926,329 (GRCm39) |
|
probably benign |
Het |
Ddx18 |
T |
C |
1: 121,493,823 (GRCm39) |
K54E |
probably benign |
Het |
Ddx60 |
G |
A |
8: 62,432,372 (GRCm39) |
V885I |
probably damaging |
Het |
Dlg1 |
C |
T |
16: 31,573,626 (GRCm39) |
T9I |
probably benign |
Het |
Dnase1 |
T |
C |
16: 3,855,771 (GRCm39) |
|
probably benign |
Het |
Drd4 |
T |
C |
7: 140,873,690 (GRCm39) |
M114T |
probably damaging |
Het |
Egfr |
A |
T |
11: 16,858,949 (GRCm39) |
D976V |
probably damaging |
Het |
Eif2s1 |
T |
A |
12: 78,926,785 (GRCm39) |
N178K |
probably benign |
Het |
Exoc3l4 |
A |
G |
12: 111,395,155 (GRCm39) |
H591R |
probably benign |
Het |
Galntl6 |
T |
C |
8: 59,152,945 (GRCm39) |
|
probably benign |
Het |
Glipr1l2 |
T |
A |
10: 111,942,904 (GRCm39) |
I253K |
possibly damaging |
Het |
Gnat1 |
A |
T |
9: 107,554,433 (GRCm39) |
M115K |
probably benign |
Het |
Gtsf2 |
T |
C |
15: 103,352,755 (GRCm39) |
E88G |
possibly damaging |
Het |
Hormad1 |
T |
A |
3: 95,492,531 (GRCm39) |
|
probably null |
Het |
Hydin |
A |
T |
8: 111,217,305 (GRCm39) |
I1398F |
possibly damaging |
Het |
Ifnar1 |
T |
C |
16: 91,301,974 (GRCm39) |
V483A |
probably benign |
Het |
Ints11 |
T |
C |
4: 155,971,385 (GRCm39) |
F278L |
probably damaging |
Het |
Ints6 |
A |
G |
14: 62,939,911 (GRCm39) |
L593P |
probably damaging |
Het |
Krt7 |
C |
T |
15: 101,311,853 (GRCm39) |
R104C |
probably damaging |
Het |
Map4k1 |
A |
T |
7: 28,682,427 (GRCm39) |
H16L |
probably benign |
Het |
Mef2d |
T |
A |
3: 88,075,404 (GRCm39) |
I422N |
probably damaging |
Het |
Mipep |
G |
T |
14: 61,022,231 (GRCm39) |
R32L |
probably damaging |
Het |
Mon1a |
A |
G |
9: 107,779,850 (GRCm39) |
E473G |
probably damaging |
Het |
Mterf2 |
T |
A |
10: 84,955,979 (GRCm39) |
Q215L |
probably damaging |
Het |
Mybpc1 |
T |
A |
10: 88,391,525 (GRCm39) |
Y324F |
probably benign |
Het |
Myh11 |
T |
C |
16: 14,023,818 (GRCm39) |
E1512G |
probably damaging |
Het |
Myo1g |
A |
T |
11: 6,465,976 (GRCm39) |
F370I |
probably damaging |
Het |
Myo5c |
T |
A |
9: 75,204,791 (GRCm39) |
M1548K |
possibly damaging |
Het |
Myof |
T |
A |
19: 37,924,300 (GRCm39) |
I1306F |
probably damaging |
Het |
Nle1 |
A |
G |
11: 82,799,018 (GRCm39) |
F21S |
probably damaging |
Het |
Noc2l |
C |
G |
4: 156,330,368 (GRCm39) |
D513E |
probably damaging |
Het |
Or1e17 |
A |
T |
11: 73,832,028 (GRCm39) |
I319F |
probably benign |
Het |
Or2z2 |
A |
G |
11: 58,346,733 (GRCm39) |
V14A |
probably benign |
Het |
Orc1 |
T |
C |
4: 108,471,670 (GRCm39) |
*841R |
probably null |
Het |
Patz1 |
A |
G |
11: 3,257,720 (GRCm39) |
D573G |
probably damaging |
Het |
Pcdhga3 |
A |
G |
18: 37,809,154 (GRCm39) |
T536A |
probably benign |
Het |
Pde6h |
C |
T |
6: 136,938,201 (GRCm39) |
T58I |
possibly damaging |
Het |
Pip5k1a |
T |
C |
3: 94,978,094 (GRCm39) |
I275V |
probably benign |
Het |
Polr1e |
G |
A |
4: 45,029,429 (GRCm39) |
A297T |
probably damaging |
Het |
Polrmt |
A |
G |
10: 79,582,385 (GRCm39) |
M1T |
probably null |
Het |
Rbm34 |
T |
C |
8: 127,678,087 (GRCm39) |
D269G |
possibly damaging |
Het |
Rnf122 |
T |
A |
8: 31,602,177 (GRCm39) |
M1K |
probably null |
Het |
Rnf32 |
G |
A |
5: 29,403,576 (GRCm39) |
R7H |
probably benign |
Het |
Ryr2 |
T |
C |
13: 11,729,497 (GRCm39) |
E2375G |
possibly damaging |
Het |
Ryr2 |
T |
C |
13: 11,848,878 (GRCm39) |
T361A |
probably benign |
Het |
Serpina3m |
T |
C |
12: 104,355,360 (GRCm39) |
I9T |
probably benign |
Het |
Serpinb9 |
T |
A |
13: 33,192,847 (GRCm39) |
W135R |
probably damaging |
Het |
Sf3b1 |
T |
C |
1: 55,038,871 (GRCm39) |
N804S |
probably benign |
Het |
Shroom1 |
A |
G |
11: 53,355,999 (GRCm39) |
T350A |
probably benign |
Het |
Slc24a5 |
G |
A |
2: 124,910,188 (GRCm39) |
V30I |
probably benign |
Het |
Slc38a8 |
A |
T |
8: 120,209,423 (GRCm39) |
|
probably null |
Het |
Smarcd1 |
A |
G |
15: 99,605,862 (GRCm39) |
S378G |
possibly damaging |
Het |
Stx1b |
T |
C |
7: 127,407,093 (GRCm39) |
I55V |
probably damaging |
Het |
Sult2a8 |
A |
G |
7: 14,159,457 (GRCm39) |
V54A |
probably damaging |
Het |
Tacc2 |
T |
C |
7: 130,330,507 (GRCm39) |
S264P |
probably damaging |
Het |
Tbc1d4 |
A |
T |
14: 101,695,610 (GRCm39) |
Y943N |
probably damaging |
Het |
Tlr5 |
T |
C |
1: 182,801,038 (GRCm39) |
I114T |
probably benign |
Het |
Tmco6 |
T |
C |
18: 36,868,555 (GRCm39) |
|
probably null |
Het |
Treh |
T |
C |
9: 44,593,945 (GRCm39) |
L144P |
probably damaging |
Het |
Trmt2a |
T |
A |
16: 18,067,418 (GRCm39) |
C30* |
probably null |
Het |
Ttbk2 |
A |
T |
2: 120,603,758 (GRCm39) |
F258L |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,785,380 (GRCm39) |
D665G |
probably damaging |
Het |
Unc93b1 |
T |
C |
19: 3,992,023 (GRCm39) |
|
probably null |
Het |
Uroc1 |
T |
C |
6: 90,322,376 (GRCm39) |
L300P |
probably damaging |
Het |
Vps35l |
T |
C |
7: 118,379,491 (GRCm39) |
I426T |
possibly damaging |
Het |
Xbp1 |
A |
G |
11: 5,471,125 (GRCm39) |
E44G |
probably damaging |
Het |
Zfp451 |
A |
T |
1: 33,816,942 (GRCm39) |
V119D |
probably damaging |
Het |
Zfp457 |
T |
A |
13: 67,441,342 (GRCm39) |
H315L |
probably damaging |
Het |
Zfp518a |
T |
A |
19: 40,904,295 (GRCm39) |
V1408D |
possibly damaging |
Het |
Zfp52 |
T |
G |
17: 21,780,665 (GRCm39) |
L171R |
probably benign |
Het |
Zfp712 |
C |
T |
13: 67,188,676 (GRCm39) |
C617Y |
probably damaging |
Het |
Zfp770 |
T |
C |
2: 114,027,868 (GRCm39) |
N67S |
probably benign |
Het |
|
Other mutations in Pkd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00340:Pkd1
|
APN |
17 |
24,799,069 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00503:Pkd1
|
APN |
17 |
24,784,401 (GRCm39) |
missense |
probably benign |
|
IGL00549:Pkd1
|
APN |
17 |
24,791,735 (GRCm39) |
missense |
probably benign |
|
IGL00573:Pkd1
|
APN |
17 |
24,813,504 (GRCm39) |
nonsense |
probably null |
|
IGL00924:Pkd1
|
APN |
17 |
24,790,601 (GRCm39) |
nonsense |
probably null |
|
IGL01319:Pkd1
|
APN |
17 |
24,806,893 (GRCm39) |
unclassified |
probably benign |
|
IGL01326:Pkd1
|
APN |
17 |
24,795,148 (GRCm39) |
nonsense |
probably null |
|
IGL01457:Pkd1
|
APN |
17 |
24,813,795 (GRCm39) |
splice site |
probably null |
|
IGL01541:Pkd1
|
APN |
17 |
24,805,272 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01575:Pkd1
|
APN |
17 |
24,792,102 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01606:Pkd1
|
APN |
17 |
24,795,497 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01642:Pkd1
|
APN |
17 |
24,800,266 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01888:Pkd1
|
APN |
17 |
24,804,789 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01940:Pkd1
|
APN |
17 |
24,798,720 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL01958:Pkd1
|
APN |
17 |
24,799,298 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02005:Pkd1
|
APN |
17 |
24,804,978 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02121:Pkd1
|
APN |
17 |
24,794,901 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02148:Pkd1
|
APN |
17 |
24,798,810 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02409:Pkd1
|
APN |
17 |
24,792,597 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02442:Pkd1
|
APN |
17 |
24,784,200 (GRCm39) |
missense |
probably benign |
0.41 |
IGL02498:Pkd1
|
APN |
17 |
24,804,753 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02501:Pkd1
|
APN |
17 |
24,788,673 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02551:Pkd1
|
APN |
17 |
24,792,789 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02635:Pkd1
|
APN |
17 |
24,791,785 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02673:Pkd1
|
APN |
17 |
24,790,257 (GRCm39) |
missense |
probably benign |
0.40 |
IGL02808:Pkd1
|
APN |
17 |
24,812,478 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02816:Pkd1
|
APN |
17 |
24,813,489 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02863:Pkd1
|
APN |
17 |
24,788,726 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL02927:Pkd1
|
APN |
17 |
24,794,163 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02961:Pkd1
|
APN |
17 |
24,797,089 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL03003:Pkd1
|
APN |
17 |
24,812,577 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03066:Pkd1
|
APN |
17 |
24,805,208 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03182:Pkd1
|
APN |
17 |
24,792,792 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03384:Pkd1
|
APN |
17 |
24,784,871 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03404:Pkd1
|
APN |
17 |
24,783,380 (GRCm39) |
missense |
probably damaging |
0.97 |
PIT1430001:Pkd1
|
UTSW |
17 |
24,788,485 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4494001:Pkd1
|
UTSW |
17 |
24,796,775 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4677001:Pkd1
|
UTSW |
17 |
24,793,003 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0017:Pkd1
|
UTSW |
17 |
24,797,513 (GRCm39) |
critical splice donor site |
probably null |
|
R0017:Pkd1
|
UTSW |
17 |
24,797,513 (GRCm39) |
critical splice donor site |
probably null |
|
R0022:Pkd1
|
UTSW |
17 |
24,813,793 (GRCm39) |
missense |
probably damaging |
0.98 |
R0022:Pkd1
|
UTSW |
17 |
24,813,793 (GRCm39) |
missense |
probably damaging |
0.98 |
R0058:Pkd1
|
UTSW |
17 |
24,783,677 (GRCm39) |
missense |
probably benign |
0.06 |
R0058:Pkd1
|
UTSW |
17 |
24,783,677 (GRCm39) |
missense |
probably benign |
0.06 |
R0085:Pkd1
|
UTSW |
17 |
24,805,197 (GRCm39) |
missense |
probably damaging |
0.98 |
R0094:Pkd1
|
UTSW |
17 |
24,800,250 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0094:Pkd1
|
UTSW |
17 |
24,800,250 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0135:Pkd1
|
UTSW |
17 |
24,784,045 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0304:Pkd1
|
UTSW |
17 |
24,804,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R0427:Pkd1
|
UTSW |
17 |
24,812,476 (GRCm39) |
missense |
probably damaging |
0.98 |
R0502:Pkd1
|
UTSW |
17 |
24,793,766 (GRCm39) |
missense |
probably damaging |
0.99 |
R0518:Pkd1
|
UTSW |
17 |
24,814,193 (GRCm39) |
missense |
probably benign |
0.01 |
R0521:Pkd1
|
UTSW |
17 |
24,814,193 (GRCm39) |
missense |
probably benign |
0.01 |
R0544:Pkd1
|
UTSW |
17 |
24,804,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R0546:Pkd1
|
UTSW |
17 |
24,799,112 (GRCm39) |
missense |
probably benign |
0.44 |
R0626:Pkd1
|
UTSW |
17 |
24,794,549 (GRCm39) |
missense |
probably damaging |
0.96 |
R0648:Pkd1
|
UTSW |
17 |
24,813,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R1138:Pkd1
|
UTSW |
17 |
24,805,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R1302:Pkd1
|
UTSW |
17 |
24,787,210 (GRCm39) |
missense |
probably benign |
0.00 |
R1306:Pkd1
|
UTSW |
17 |
24,792,146 (GRCm39) |
missense |
probably damaging |
0.97 |
R1349:Pkd1
|
UTSW |
17 |
24,794,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R1372:Pkd1
|
UTSW |
17 |
24,794,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R1437:Pkd1
|
UTSW |
17 |
24,814,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R1515:Pkd1
|
UTSW |
17 |
24,813,827 (GRCm39) |
missense |
probably benign |
0.01 |
R1605:Pkd1
|
UTSW |
17 |
24,796,500 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1622:Pkd1
|
UTSW |
17 |
24,800,614 (GRCm39) |
missense |
probably benign |
|
R1623:Pkd1
|
UTSW |
17 |
24,797,243 (GRCm39) |
missense |
probably damaging |
0.99 |
R1726:Pkd1
|
UTSW |
17 |
24,783,150 (GRCm39) |
missense |
probably damaging |
0.96 |
R1756:Pkd1
|
UTSW |
17 |
24,813,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R1780:Pkd1
|
UTSW |
17 |
24,800,543 (GRCm39) |
missense |
probably benign |
|
R1785:Pkd1
|
UTSW |
17 |
24,810,073 (GRCm39) |
missense |
probably benign |
0.00 |
R1829:Pkd1
|
UTSW |
17 |
24,784,558 (GRCm39) |
missense |
probably benign |
|
R1869:Pkd1
|
UTSW |
17 |
24,813,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R1920:Pkd1
|
UTSW |
17 |
24,814,131 (GRCm39) |
missense |
probably damaging |
0.99 |
R1922:Pkd1
|
UTSW |
17 |
24,814,131 (GRCm39) |
missense |
probably damaging |
0.99 |
R1987:Pkd1
|
UTSW |
17 |
24,795,566 (GRCm39) |
splice site |
probably null |
|
R1988:Pkd1
|
UTSW |
17 |
24,795,566 (GRCm39) |
splice site |
probably null |
|
R1998:Pkd1
|
UTSW |
17 |
24,791,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R2007:Pkd1
|
UTSW |
17 |
24,798,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R2019:Pkd1
|
UTSW |
17 |
24,787,658 (GRCm39) |
nonsense |
probably null |
|
R2054:Pkd1
|
UTSW |
17 |
24,793,770 (GRCm39) |
missense |
probably benign |
0.00 |
R2061:Pkd1
|
UTSW |
17 |
24,788,888 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2196:Pkd1
|
UTSW |
17 |
24,799,046 (GRCm39) |
missense |
possibly damaging |
0.60 |
R2203:Pkd1
|
UTSW |
17 |
24,799,863 (GRCm39) |
missense |
probably benign |
0.01 |
R2301:Pkd1
|
UTSW |
17 |
24,793,586 (GRCm39) |
missense |
probably benign |
|
R2655:Pkd1
|
UTSW |
17 |
24,795,464 (GRCm39) |
missense |
probably damaging |
0.99 |
R2860:Pkd1
|
UTSW |
17 |
24,784,420 (GRCm39) |
missense |
probably benign |
0.43 |
R2861:Pkd1
|
UTSW |
17 |
24,784,420 (GRCm39) |
missense |
probably benign |
0.43 |
R3000:Pkd1
|
UTSW |
17 |
24,813,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R3150:Pkd1
|
UTSW |
17 |
24,798,765 (GRCm39) |
missense |
probably benign |
0.00 |
R3747:Pkd1
|
UTSW |
17 |
24,810,435 (GRCm39) |
missense |
possibly damaging |
0.67 |
R3812:Pkd1
|
UTSW |
17 |
24,784,615 (GRCm39) |
missense |
probably benign |
0.00 |
R3859:Pkd1
|
UTSW |
17 |
24,797,066 (GRCm39) |
splice site |
probably benign |
|
R3893:Pkd1
|
UTSW |
17 |
24,791,084 (GRCm39) |
critical splice donor site |
probably null |
|
R3947:Pkd1
|
UTSW |
17 |
24,797,011 (GRCm39) |
splice site |
probably benign |
|
R3949:Pkd1
|
UTSW |
17 |
24,797,011 (GRCm39) |
splice site |
probably benign |
|
R4176:Pkd1
|
UTSW |
17 |
24,806,971 (GRCm39) |
missense |
probably benign |
0.17 |
R4199:Pkd1
|
UTSW |
17 |
24,789,004 (GRCm39) |
missense |
probably benign |
0.41 |
R4225:Pkd1
|
UTSW |
17 |
24,812,497 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4439:Pkd1
|
UTSW |
17 |
24,804,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R4476:Pkd1
|
UTSW |
17 |
24,795,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R4716:Pkd1
|
UTSW |
17 |
24,795,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Pkd1
|
UTSW |
17 |
24,797,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R4802:Pkd1
|
UTSW |
17 |
24,797,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R4817:Pkd1
|
UTSW |
17 |
24,784,348 (GRCm39) |
splice site |
probably null |
|
R4903:Pkd1
|
UTSW |
17 |
24,790,976 (GRCm39) |
missense |
probably benign |
0.30 |
R4910:Pkd1
|
UTSW |
17 |
24,791,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R4966:Pkd1
|
UTSW |
17 |
24,805,042 (GRCm39) |
critical splice donor site |
probably null |
|
R5040:Pkd1
|
UTSW |
17 |
24,790,234 (GRCm39) |
missense |
probably benign |
0.02 |
R5042:Pkd1
|
UTSW |
17 |
24,788,861 (GRCm39) |
missense |
probably benign |
0.00 |
R5088:Pkd1
|
UTSW |
17 |
24,809,812 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5121:Pkd1
|
UTSW |
17 |
24,792,437 (GRCm39) |
missense |
probably benign |
|
R5296:Pkd1
|
UTSW |
17 |
24,795,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R5338:Pkd1
|
UTSW |
17 |
24,813,510 (GRCm39) |
missense |
probably benign |
|
R5356:Pkd1
|
UTSW |
17 |
24,812,551 (GRCm39) |
missense |
probably damaging |
0.97 |
R5357:Pkd1
|
UTSW |
17 |
24,784,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R5363:Pkd1
|
UTSW |
17 |
24,784,047 (GRCm39) |
missense |
probably benign |
|
R5383:Pkd1
|
UTSW |
17 |
24,793,349 (GRCm39) |
missense |
probably benign |
|
R5622:Pkd1
|
UTSW |
17 |
24,793,014 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5651:Pkd1
|
UTSW |
17 |
24,810,361 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5664:Pkd1
|
UTSW |
17 |
24,788,345 (GRCm39) |
missense |
probably damaging |
0.99 |
R5723:Pkd1
|
UTSW |
17 |
24,784,497 (GRCm39) |
missense |
probably benign |
0.01 |
R5797:Pkd1
|
UTSW |
17 |
24,811,615 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5838:Pkd1
|
UTSW |
17 |
24,799,186 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5866:Pkd1
|
UTSW |
17 |
24,799,935 (GRCm39) |
missense |
probably damaging |
0.99 |
R5873:Pkd1
|
UTSW |
17 |
24,788,804 (GRCm39) |
missense |
probably benign |
|
R5906:Pkd1
|
UTSW |
17 |
24,791,894 (GRCm39) |
missense |
probably benign |
0.16 |
R6047:Pkd1
|
UTSW |
17 |
24,814,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R6076:Pkd1
|
UTSW |
17 |
24,800,004 (GRCm39) |
missense |
probably benign |
0.14 |
R6151:Pkd1
|
UTSW |
17 |
24,794,580 (GRCm39) |
missense |
probably benign |
0.00 |
R6252:Pkd1
|
UTSW |
17 |
24,800,200 (GRCm39) |
missense |
probably damaging |
0.98 |
R6341:Pkd1
|
UTSW |
17 |
24,799,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R6540:Pkd1
|
UTSW |
17 |
24,794,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R6732:Pkd1
|
UTSW |
17 |
24,788,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R6836:Pkd1
|
UTSW |
17 |
24,800,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R6856:Pkd1
|
UTSW |
17 |
24,792,467 (GRCm39) |
missense |
probably benign |
0.05 |
R6865:Pkd1
|
UTSW |
17 |
24,795,461 (GRCm39) |
missense |
probably benign |
0.43 |
R6999:Pkd1
|
UTSW |
17 |
24,797,475 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7077:Pkd1
|
UTSW |
17 |
24,810,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R7123:Pkd1
|
UTSW |
17 |
24,813,742 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7134:Pkd1
|
UTSW |
17 |
24,813,086 (GRCm39) |
missense |
probably damaging |
0.99 |
R7210:Pkd1
|
UTSW |
17 |
24,794,840 (GRCm39) |
missense |
probably damaging |
0.98 |
R7323:Pkd1
|
UTSW |
17 |
24,794,025 (GRCm39) |
missense |
probably benign |
0.01 |
R7380:Pkd1
|
UTSW |
17 |
24,800,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R7407:Pkd1
|
UTSW |
17 |
24,813,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R7410:Pkd1
|
UTSW |
17 |
24,794,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R7492:Pkd1
|
UTSW |
17 |
24,788,715 (GRCm39) |
missense |
probably benign |
0.04 |
R7517:Pkd1
|
UTSW |
17 |
24,799,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R7543:Pkd1
|
UTSW |
17 |
24,814,227 (GRCm39) |
missense |
probably damaging |
0.99 |
R7560:Pkd1
|
UTSW |
17 |
24,792,605 (GRCm39) |
missense |
probably benign |
0.33 |
R7615:Pkd1
|
UTSW |
17 |
24,812,476 (GRCm39) |
missense |
probably damaging |
0.98 |
R7714:Pkd1
|
UTSW |
17 |
24,769,250 (GRCm39) |
missense |
unknown |
|
R7718:Pkd1
|
UTSW |
17 |
24,805,474 (GRCm39) |
missense |
probably benign |
0.15 |
R7731:Pkd1
|
UTSW |
17 |
24,792,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R7849:Pkd1
|
UTSW |
17 |
24,805,174 (GRCm39) |
missense |
probably damaging |
0.98 |
R7859:Pkd1
|
UTSW |
17 |
24,790,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R7866:Pkd1
|
UTSW |
17 |
24,809,881 (GRCm39) |
missense |
probably benign |
0.26 |
R7915:Pkd1
|
UTSW |
17 |
24,811,630 (GRCm39) |
nonsense |
probably null |
|
R7991:Pkd1
|
UTSW |
17 |
24,791,595 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8050:Pkd1
|
UTSW |
17 |
24,784,617 (GRCm39) |
missense |
probably benign |
0.26 |
R8086:Pkd1
|
UTSW |
17 |
24,800,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R8312:Pkd1
|
UTSW |
17 |
24,786,102 (GRCm39) |
missense |
probably benign |
0.02 |
R8385:Pkd1
|
UTSW |
17 |
24,794,702 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8393:Pkd1
|
UTSW |
17 |
24,791,621 (GRCm39) |
missense |
probably damaging |
0.99 |
R8552:Pkd1
|
UTSW |
17 |
24,810,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R8753:Pkd1
|
UTSW |
17 |
24,793,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R8822:Pkd1
|
UTSW |
17 |
24,784,615 (GRCm39) |
missense |
probably benign |
0.00 |
R8855:Pkd1
|
UTSW |
17 |
24,792,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R8866:Pkd1
|
UTSW |
17 |
24,792,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R8867:Pkd1
|
UTSW |
17 |
24,792,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R8960:Pkd1
|
UTSW |
17 |
24,795,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R8966:Pkd1
|
UTSW |
17 |
24,794,751 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9004:Pkd1
|
UTSW |
17 |
24,799,421 (GRCm39) |
missense |
probably benign |
|
R9015:Pkd1
|
UTSW |
17 |
24,784,636 (GRCm39) |
nonsense |
probably null |
|
R9069:Pkd1
|
UTSW |
17 |
24,791,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R9092:Pkd1
|
UTSW |
17 |
24,788,347 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9135:Pkd1
|
UTSW |
17 |
24,790,976 (GRCm39) |
missense |
|
|
R9307:Pkd1
|
UTSW |
17 |
24,769,451 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9312:Pkd1
|
UTSW |
17 |
24,797,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R9313:Pkd1
|
UTSW |
17 |
24,813,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R9380:Pkd1
|
UTSW |
17 |
24,769,262 (GRCm39) |
missense |
unknown |
|
R9383:Pkd1
|
UTSW |
17 |
24,794,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R9531:Pkd1
|
UTSW |
17 |
24,792,114 (GRCm39) |
missense |
probably damaging |
0.99 |
R9617:Pkd1
|
UTSW |
17 |
24,800,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R9691:Pkd1
|
UTSW |
17 |
24,796,812 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9792:Pkd1
|
UTSW |
17 |
24,800,172 (GRCm39) |
missense |
probably benign |
|
R9793:Pkd1
|
UTSW |
17 |
24,800,172 (GRCm39) |
missense |
probably benign |
|
X0024:Pkd1
|
UTSW |
17 |
24,810,366 (GRCm39) |
missense |
possibly damaging |
0.68 |
X0061:Pkd1
|
UTSW |
17 |
24,813,905 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Pkd1
|
UTSW |
17 |
24,805,138 (GRCm39) |
missense |
probably benign |
0.19 |
Z1088:Pkd1
|
UTSW |
17 |
24,784,579 (GRCm39) |
missense |
probably benign |
0.44 |
Z1177:Pkd1
|
UTSW |
17 |
24,794,465 (GRCm39) |
missense |
probably benign |
|
|