Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm2 |
A |
G |
3: 59,659,444 (GRCm39) |
E299G |
probably damaging |
Het |
Adamtsl4 |
C |
A |
3: 95,587,473 (GRCm39) |
R701L |
probably damaging |
Het |
Adgrf5 |
T |
C |
17: 43,761,890 (GRCm39) |
V1195A |
probably damaging |
Het |
Agpat5 |
A |
G |
8: 18,931,878 (GRCm39) |
T333A |
possibly damaging |
Het |
Aspm |
G |
T |
1: 139,392,033 (GRCm39) |
G795C |
probably damaging |
Het |
Car4 |
C |
A |
11: 84,856,626 (GRCm39) |
Q305K |
probably benign |
Het |
Catsperg1 |
T |
C |
7: 28,894,672 (GRCm39) |
N612S |
probably benign |
Het |
Cdc5l |
G |
A |
17: 45,726,511 (GRCm39) |
R354W |
probably damaging |
Het |
Cdh9 |
G |
A |
15: 16,851,099 (GRCm39) |
V623I |
probably benign |
Het |
Cfap65 |
A |
G |
1: 74,964,061 (GRCm39) |
V629A |
probably benign |
Het |
Chd1 |
G |
A |
17: 15,956,005 (GRCm39) |
V535I |
probably damaging |
Het |
Col12a1 |
A |
G |
9: 79,585,329 (GRCm39) |
V1316A |
probably damaging |
Het |
Col6a3 |
A |
T |
1: 90,712,965 (GRCm39) |
D1721E |
unknown |
Het |
Cop1 |
T |
A |
1: 159,154,734 (GRCm39) |
F647L |
probably damaging |
Het |
Corin |
A |
C |
5: 72,500,362 (GRCm39) |
S421A |
probably damaging |
Het |
Crb2 |
T |
C |
2: 37,680,833 (GRCm39) |
V587A |
probably damaging |
Het |
Ctc1 |
T |
A |
11: 68,920,636 (GRCm39) |
V646E |
possibly damaging |
Het |
Cyp2a12 |
A |
T |
7: 26,730,643 (GRCm39) |
M203L |
probably benign |
Het |
Dcdc2c |
T |
A |
12: 28,566,656 (GRCm39) |
K336M |
possibly damaging |
Het |
Ddx39a |
G |
A |
8: 84,448,950 (GRCm39) |
R275H |
probably benign |
Het |
Dennd2b |
A |
G |
7: 109,156,519 (GRCm39) |
L77P |
probably benign |
Het |
Des |
A |
G |
1: 75,339,572 (GRCm39) |
N310S |
possibly damaging |
Het |
Dlk1 |
C |
A |
12: 109,425,764 (GRCm39) |
S212R |
probably benign |
Het |
Dnajc5b |
A |
G |
3: 19,633,224 (GRCm39) |
E149G |
probably benign |
Het |
Dpep1 |
A |
T |
8: 123,920,828 (GRCm39) |
I3F |
probably benign |
Het |
Eml6 |
T |
A |
11: 29,753,108 (GRCm39) |
R934S |
probably benign |
Het |
Ercc6l2 |
T |
C |
13: 64,016,925 (GRCm39) |
L676P |
possibly damaging |
Het |
Fkbpl |
G |
A |
17: 34,864,303 (GRCm39) |
A24T |
probably benign |
Het |
Frem2 |
T |
A |
3: 53,560,575 (GRCm39) |
I1311F |
probably damaging |
Het |
Gldc |
T |
A |
19: 30,123,125 (GRCm39) |
M257L |
probably damaging |
Het |
Gm8674 |
T |
G |
13: 50,055,390 (GRCm39) |
|
noncoding transcript |
Het |
Gnai3 |
C |
T |
3: 108,030,857 (GRCm39) |
|
probably null |
Het |
Gtf3a |
A |
G |
5: 146,891,965 (GRCm39) |
D300G |
probably damaging |
Het |
Haus3 |
A |
T |
5: 34,323,449 (GRCm39) |
V387D |
probably damaging |
Het |
Hpf1 |
T |
A |
8: 61,346,768 (GRCm39) |
F28I |
possibly damaging |
Het |
Iars1 |
A |
G |
13: 49,843,967 (GRCm39) |
D147G |
probably damaging |
Het |
Ibtk |
A |
T |
9: 85,625,743 (GRCm39) |
D2E |
probably benign |
Het |
Ift140 |
T |
A |
17: 25,239,601 (GRCm39) |
I86K |
possibly damaging |
Het |
Igf2bp2 |
T |
A |
16: 21,898,241 (GRCm39) |
I235F |
probably damaging |
Het |
Ighv3-8 |
G |
T |
12: 114,286,252 (GRCm39) |
A30E |
probably benign |
Het |
Kcnq5 |
T |
A |
1: 21,575,949 (GRCm39) |
T252S |
probably damaging |
Het |
Lrrc4b |
A |
T |
7: 44,110,787 (GRCm39) |
N220Y |
probably damaging |
Het |
Ltbr |
G |
A |
6: 125,289,757 (GRCm39) |
R146W |
probably damaging |
Het |
Mamdc4 |
T |
C |
2: 25,454,702 (GRCm39) |
T1037A |
possibly damaging |
Het |
Mbd5 |
A |
T |
2: 49,162,106 (GRCm39) |
I863F |
possibly damaging |
Het |
Muc4 |
T |
A |
16: 32,570,484 (GRCm39) |
S515T |
possibly damaging |
Het |
Mylk4 |
T |
A |
13: 32,892,864 (GRCm39) |
|
probably null |
Het |
Neu4 |
G |
A |
1: 93,952,669 (GRCm39) |
R346H |
probably benign |
Het |
Nxpe5 |
T |
A |
5: 138,238,200 (GRCm39) |
Y253* |
probably null |
Het |
Olfml2b |
A |
T |
1: 170,477,330 (GRCm39) |
E155V |
probably damaging |
Het |
Or14a258 |
A |
G |
7: 86,034,867 (GRCm39) |
*334Q |
probably null |
Het |
Or6a2 |
T |
A |
7: 106,600,111 (GRCm39) |
N319Y |
probably benign |
Het |
Or8a1b |
T |
A |
9: 37,623,300 (GRCm39) |
I92F |
probably damaging |
Het |
Pamr1 |
G |
A |
2: 102,417,029 (GRCm39) |
A114T |
probably damaging |
Het |
Pglyrp4 |
C |
T |
3: 90,634,271 (GRCm39) |
L5F |
probably damaging |
Het |
Plce1 |
T |
A |
19: 38,747,279 (GRCm39) |
S1667T |
possibly damaging |
Het |
Qser1 |
A |
T |
2: 104,617,776 (GRCm39) |
V1012E |
possibly damaging |
Het |
R3hdm4 |
C |
T |
10: 79,748,292 (GRCm39) |
E162K |
possibly damaging |
Het |
Rcn3 |
A |
T |
7: 44,736,203 (GRCm39) |
D168E |
probably damaging |
Het |
Rdh1 |
T |
G |
10: 127,595,832 (GRCm39) |
V9G |
possibly damaging |
Het |
Rin2 |
A |
G |
2: 145,686,680 (GRCm39) |
T70A |
probably benign |
Het |
Rnf207 |
T |
C |
4: 152,398,346 (GRCm39) |
D276G |
probably damaging |
Het |
Rtel1 |
C |
T |
2: 180,982,354 (GRCm39) |
S368L |
probably benign |
Het |
Slc15a5 |
C |
A |
6: 138,056,751 (GRCm39) |
C55F |
probably damaging |
Het |
Slc36a4 |
T |
C |
9: 15,638,212 (GRCm39) |
F213L |
possibly damaging |
Het |
Snhg16 |
G |
T |
11: 116,562,582 (GRCm39) |
M18I |
probably benign |
Het |
Spata25 |
C |
T |
2: 164,669,954 (GRCm39) |
G19D |
probably damaging |
Het |
Tas2r102 |
A |
T |
6: 132,739,360 (GRCm39) |
L89F |
probably damaging |
Het |
Tbc1d1 |
A |
G |
5: 64,481,910 (GRCm39) |
K704E |
probably damaging |
Het |
Tert |
T |
G |
13: 73,775,473 (GRCm39) |
S75A |
probably damaging |
Het |
Tiparp |
T |
A |
3: 65,454,986 (GRCm39) |
L195Q |
possibly damaging |
Het |
Tmem205 |
A |
C |
9: 21,837,380 (GRCm39) |
Y57* |
probably null |
Het |
Tomm22 |
A |
G |
15: 79,555,428 (GRCm39) |
R5G |
probably benign |
Het |
Trav10 |
A |
T |
14: 53,743,515 (GRCm39) |
S39C |
probably benign |
Het |
Trav6-2 |
T |
A |
14: 52,905,205 (GRCm39) |
N75K |
probably benign |
Het |
Trio |
T |
C |
15: 27,748,372 (GRCm39) |
S2427G |
probably benign |
Het |
Ttc41 |
C |
A |
10: 86,580,342 (GRCm39) |
H763N |
possibly damaging |
Het |
Usp29 |
A |
T |
7: 6,964,583 (GRCm39) |
N142I |
probably damaging |
Het |
Vmn1r204 |
G |
T |
13: 22,740,912 (GRCm39) |
W181L |
probably damaging |
Het |
Vmn2r76 |
G |
A |
7: 85,875,267 (GRCm39) |
T570M |
probably damaging |
Het |
Wdr90 |
A |
G |
17: 26,069,819 (GRCm39) |
L1173P |
probably damaging |
Het |
Wnt9a |
T |
A |
11: 59,219,396 (GRCm39) |
C141S |
probably damaging |
Het |
Zfp462 |
A |
T |
4: 55,012,299 (GRCm39) |
I1422L |
probably benign |
Het |
|
Other mutations in Pdzd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00159:Pdzd2
|
APN |
15 |
12,458,069 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL00586:Pdzd2
|
APN |
15 |
12,365,853 (GRCm39) |
splice site |
probably null |
|
IGL00697:Pdzd2
|
APN |
15 |
12,373,733 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL00721:Pdzd2
|
APN |
15 |
12,374,498 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00971:Pdzd2
|
APN |
15 |
12,374,804 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01066:Pdzd2
|
APN |
15 |
12,402,718 (GRCm39) |
unclassified |
probably benign |
|
IGL01389:Pdzd2
|
APN |
15 |
12,374,712 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL01505:Pdzd2
|
APN |
15 |
12,458,293 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01527:Pdzd2
|
APN |
15 |
12,445,750 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01584:Pdzd2
|
APN |
15 |
12,592,569 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01763:Pdzd2
|
APN |
15 |
12,372,632 (GRCm39) |
missense |
probably benign |
|
IGL01915:Pdzd2
|
APN |
15 |
12,371,725 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01947:Pdzd2
|
APN |
15 |
12,592,440 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02058:Pdzd2
|
APN |
15 |
12,376,382 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02274:Pdzd2
|
APN |
15 |
12,445,735 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02408:Pdzd2
|
APN |
15 |
12,375,851 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02600:Pdzd2
|
APN |
15 |
12,411,105 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02637:Pdzd2
|
APN |
15 |
12,385,720 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02639:Pdzd2
|
APN |
15 |
12,592,329 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02712:Pdzd2
|
APN |
15 |
12,376,113 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02967:Pdzd2
|
APN |
15 |
12,374,427 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02992:Pdzd2
|
APN |
15 |
12,382,708 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL03005:Pdzd2
|
APN |
15 |
12,385,351 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03067:Pdzd2
|
APN |
15 |
12,388,628 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03335:Pdzd2
|
APN |
15 |
12,373,850 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4280001:Pdzd2
|
UTSW |
15 |
12,399,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R0022:Pdzd2
|
UTSW |
15 |
12,371,691 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0241:Pdzd2
|
UTSW |
15 |
12,368,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R0241:Pdzd2
|
UTSW |
15 |
12,368,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R0446:Pdzd2
|
UTSW |
15 |
12,375,110 (GRCm39) |
missense |
probably benign |
0.43 |
R0462:Pdzd2
|
UTSW |
15 |
12,592,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R0562:Pdzd2
|
UTSW |
15 |
12,592,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R0589:Pdzd2
|
UTSW |
15 |
12,376,385 (GRCm39) |
missense |
probably benign |
0.03 |
R0639:Pdzd2
|
UTSW |
15 |
12,458,144 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0925:Pdzd2
|
UTSW |
15 |
12,399,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R1015:Pdzd2
|
UTSW |
15 |
12,374,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R1054:Pdzd2
|
UTSW |
15 |
12,371,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R1070:Pdzd2
|
UTSW |
15 |
12,390,052 (GRCm39) |
critical splice donor site |
probably null |
|
R1099:Pdzd2
|
UTSW |
15 |
12,373,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R1122:Pdzd2
|
UTSW |
15 |
12,457,981 (GRCm39) |
missense |
probably benign |
0.25 |
R1126:Pdzd2
|
UTSW |
15 |
12,458,306 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1381:Pdzd2
|
UTSW |
15 |
12,385,525 (GRCm39) |
missense |
probably benign |
0.02 |
R1385:Pdzd2
|
UTSW |
15 |
12,411,108 (GRCm39) |
missense |
probably benign |
0.38 |
R1513:Pdzd2
|
UTSW |
15 |
12,373,915 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1538:Pdzd2
|
UTSW |
15 |
12,373,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R1750:Pdzd2
|
UTSW |
15 |
12,385,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R1775:Pdzd2
|
UTSW |
15 |
12,592,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R1801:Pdzd2
|
UTSW |
15 |
12,387,740 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1832:Pdzd2
|
UTSW |
15 |
12,390,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R1856:Pdzd2
|
UTSW |
15 |
12,373,941 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1870:Pdzd2
|
UTSW |
15 |
12,457,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R1879:Pdzd2
|
UTSW |
15 |
12,373,986 (GRCm39) |
missense |
possibly damaging |
0.61 |
R2072:Pdzd2
|
UTSW |
15 |
12,385,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R2073:Pdzd2
|
UTSW |
15 |
12,385,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R2075:Pdzd2
|
UTSW |
15 |
12,385,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R2125:Pdzd2
|
UTSW |
15 |
12,373,676 (GRCm39) |
missense |
probably benign |
0.37 |
R2142:Pdzd2
|
UTSW |
15 |
12,406,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R2155:Pdzd2
|
UTSW |
15 |
12,375,879 (GRCm39) |
missense |
probably benign |
0.43 |
R2282:Pdzd2
|
UTSW |
15 |
12,373,934 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2407:Pdzd2
|
UTSW |
15 |
12,373,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R3545:Pdzd2
|
UTSW |
15 |
12,375,557 (GRCm39) |
missense |
probably benign |
0.00 |
R3878:Pdzd2
|
UTSW |
15 |
12,376,262 (GRCm39) |
missense |
probably benign |
0.00 |
R3879:Pdzd2
|
UTSW |
15 |
12,375,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R4396:Pdzd2
|
UTSW |
15 |
12,387,732 (GRCm39) |
missense |
probably benign |
0.36 |
R4398:Pdzd2
|
UTSW |
15 |
12,376,061 (GRCm39) |
missense |
probably benign |
0.30 |
R4491:Pdzd2
|
UTSW |
15 |
12,385,723 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4492:Pdzd2
|
UTSW |
15 |
12,419,567 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4492:Pdzd2
|
UTSW |
15 |
12,385,723 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4656:Pdzd2
|
UTSW |
15 |
12,385,797 (GRCm39) |
missense |
probably benign |
0.00 |
R4715:Pdzd2
|
UTSW |
15 |
12,419,602 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4803:Pdzd2
|
UTSW |
15 |
12,374,681 (GRCm39) |
missense |
probably benign |
0.04 |
R4893:Pdzd2
|
UTSW |
15 |
12,385,429 (GRCm39) |
missense |
probably benign |
0.00 |
R4959:Pdzd2
|
UTSW |
15 |
12,375,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R4973:Pdzd2
|
UTSW |
15 |
12,375,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R5030:Pdzd2
|
UTSW |
15 |
12,592,494 (GRCm39) |
nonsense |
probably null |
|
R5174:Pdzd2
|
UTSW |
15 |
12,372,600 (GRCm39) |
missense |
probably benign |
0.01 |
R5230:Pdzd2
|
UTSW |
15 |
12,390,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R5256:Pdzd2
|
UTSW |
15 |
12,373,028 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5488:Pdzd2
|
UTSW |
15 |
12,382,762 (GRCm39) |
missense |
probably benign |
0.00 |
R5489:Pdzd2
|
UTSW |
15 |
12,382,762 (GRCm39) |
missense |
probably benign |
0.00 |
R5588:Pdzd2
|
UTSW |
15 |
12,374,367 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5605:Pdzd2
|
UTSW |
15 |
12,592,436 (GRCm39) |
nonsense |
probably null |
|
R5704:Pdzd2
|
UTSW |
15 |
12,385,761 (GRCm39) |
missense |
probably benign |
0.02 |
R5858:Pdzd2
|
UTSW |
15 |
12,442,675 (GRCm39) |
missense |
probably damaging |
0.97 |
R6048:Pdzd2
|
UTSW |
15 |
12,592,656 (GRCm39) |
splice site |
probably null |
|
R6222:Pdzd2
|
UTSW |
15 |
12,374,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R6311:Pdzd2
|
UTSW |
15 |
12,458,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R6734:Pdzd2
|
UTSW |
15 |
12,592,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R6897:Pdzd2
|
UTSW |
15 |
12,385,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R6900:Pdzd2
|
UTSW |
15 |
12,374,123 (GRCm39) |
missense |
probably benign |
|
R6955:Pdzd2
|
UTSW |
15 |
12,401,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R6959:Pdzd2
|
UTSW |
15 |
12,375,993 (GRCm39) |
missense |
probably benign |
0.17 |
R6992:Pdzd2
|
UTSW |
15 |
12,457,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R7014:Pdzd2
|
UTSW |
15 |
12,373,061 (GRCm39) |
missense |
probably benign |
0.14 |
R7014:Pdzd2
|
UTSW |
15 |
12,372,647 (GRCm39) |
missense |
probably benign |
0.13 |
R7110:Pdzd2
|
UTSW |
15 |
12,368,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R7180:Pdzd2
|
UTSW |
15 |
12,376,209 (GRCm39) |
missense |
probably damaging |
0.99 |
R7228:Pdzd2
|
UTSW |
15 |
12,458,231 (GRCm39) |
nonsense |
probably null |
|
R7228:Pdzd2
|
UTSW |
15 |
12,373,059 (GRCm39) |
missense |
probably benign |
0.01 |
R7317:Pdzd2
|
UTSW |
15 |
12,592,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R7322:Pdzd2
|
UTSW |
15 |
12,437,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R7349:Pdzd2
|
UTSW |
15 |
12,399,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R7600:Pdzd2
|
UTSW |
15 |
12,372,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R7663:Pdzd2
|
UTSW |
15 |
12,373,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R7712:Pdzd2
|
UTSW |
15 |
12,407,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R7716:Pdzd2
|
UTSW |
15 |
12,373,460 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7740:Pdzd2
|
UTSW |
15 |
12,374,102 (GRCm39) |
missense |
probably benign |
0.00 |
R7748:Pdzd2
|
UTSW |
15 |
12,385,872 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8017:Pdzd2
|
UTSW |
15 |
12,373,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R8019:Pdzd2
|
UTSW |
15 |
12,373,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R8108:Pdzd2
|
UTSW |
15 |
12,373,592 (GRCm39) |
missense |
probably benign |
0.01 |
R8109:Pdzd2
|
UTSW |
15 |
12,373,592 (GRCm39) |
missense |
probably benign |
0.01 |
R8110:Pdzd2
|
UTSW |
15 |
12,373,592 (GRCm39) |
missense |
probably benign |
0.01 |
R8111:Pdzd2
|
UTSW |
15 |
12,373,592 (GRCm39) |
missense |
probably benign |
0.01 |
R8145:Pdzd2
|
UTSW |
15 |
12,407,458 (GRCm39) |
missense |
probably benign |
0.37 |
R8220:Pdzd2
|
UTSW |
15 |
12,592,249 (GRCm39) |
missense |
probably damaging |
0.99 |
R8278:Pdzd2
|
UTSW |
15 |
12,375,995 (GRCm39) |
missense |
probably benign |
|
R8768:Pdzd2
|
UTSW |
15 |
12,437,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R8879:Pdzd2
|
UTSW |
15 |
12,402,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R9019:Pdzd2
|
UTSW |
15 |
12,375,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R9030:Pdzd2
|
UTSW |
15 |
12,374,385 (GRCm39) |
missense |
probably benign |
0.02 |
R9061:Pdzd2
|
UTSW |
15 |
12,374,753 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9302:Pdzd2
|
UTSW |
15 |
12,374,342 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9321:Pdzd2
|
UTSW |
15 |
12,386,023 (GRCm39) |
missense |
probably benign |
0.00 |
R9421:Pdzd2
|
UTSW |
15 |
12,375,114 (GRCm39) |
missense |
|
|
R9515:Pdzd2
|
UTSW |
15 |
12,374,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R9592:Pdzd2
|
UTSW |
15 |
12,458,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R9614:Pdzd2
|
UTSW |
15 |
12,375,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R9630:Pdzd2
|
UTSW |
15 |
12,374,443 (GRCm39) |
missense |
probably benign |
0.37 |
R9776:Pdzd2
|
UTSW |
15 |
12,457,909 (GRCm39) |
missense |
probably benign |
0.03 |
X0057:Pdzd2
|
UTSW |
15 |
12,411,113 (GRCm39) |
missense |
probably damaging |
1.00 |
X0063:Pdzd2
|
UTSW |
15 |
12,368,805 (GRCm39) |
missense |
possibly damaging |
0.77 |
X0066:Pdzd2
|
UTSW |
15 |
12,372,942 (GRCm39) |
missense |
probably benign |
0.00 |
|