Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2200002D01Rik |
CCTTCTCCTTCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
CCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
7: 28,947,048 (GRCm39) |
|
probably benign |
Het |
Aamdc |
A |
G |
7: 97,224,808 (GRCm39) |
V18A |
probably benign |
Het |
Adam12 |
T |
A |
7: 133,509,373 (GRCm39) |
I796F |
probably benign |
Het |
Adcy7 |
T |
A |
8: 89,037,646 (GRCm39) |
V238E |
possibly damaging |
Het |
Adgrv1 |
G |
A |
13: 81,691,497 (GRCm39) |
H1697Y |
probably damaging |
Het |
Adrb1 |
A |
G |
19: 56,711,825 (GRCm39) |
D341G |
probably benign |
Het |
Akap13 |
T |
C |
7: 75,354,275 (GRCm39) |
Y80H |
probably benign |
Het |
Akap9 |
C |
T |
5: 4,105,709 (GRCm39) |
L2927F |
probably damaging |
Het |
Alox8 |
T |
A |
11: 69,075,950 (GRCm39) |
D667V |
probably damaging |
Het |
Arhgap30 |
A |
G |
1: 171,236,002 (GRCm39) |
E792G |
probably benign |
Het |
Arhgef16 |
A |
G |
4: 154,365,432 (GRCm39) |
V561A |
possibly damaging |
Het |
Bcap29 |
A |
T |
12: 31,676,756 (GRCm39) |
Y105N |
probably damaging |
Het |
Best2 |
T |
A |
8: 85,740,147 (GRCm39) |
T6S |
|
Het |
Bfsp2 |
C |
A |
9: 103,357,251 (GRCm39) |
V59L |
possibly damaging |
Het |
Brd3 |
T |
A |
2: 27,349,815 (GRCm39) |
D246V |
|
Het |
Btnl1 |
T |
A |
17: 34,600,118 (GRCm39) |
V207E |
probably benign |
Het |
Ccdc122 |
T |
A |
14: 77,329,408 (GRCm39) |
Y154N |
|
Het |
Cfap43 |
A |
G |
19: 47,773,814 (GRCm39) |
Y656H |
probably damaging |
Het |
Clca3a2 |
A |
T |
3: 144,508,808 (GRCm39) |
Y670* |
probably null |
Het |
Coprs |
T |
C |
8: 13,935,081 (GRCm39) |
Y158C |
probably damaging |
Het |
Desi2 |
T |
G |
1: 178,084,170 (GRCm39) |
M106R |
unknown |
Het |
Dnaaf3 |
T |
C |
7: 4,531,100 (GRCm39) |
E111G |
probably damaging |
Het |
Epha10 |
T |
A |
4: 124,775,704 (GRCm39) |
F13I |
probably benign |
Het |
Fam193a |
T |
A |
5: 34,615,371 (GRCm39) |
F813L |
possibly damaging |
Het |
Fbn1 |
C |
A |
2: 125,207,551 (GRCm39) |
A981S |
probably benign |
Het |
Gga2 |
T |
A |
7: 121,611,448 (GRCm39) |
T37S |
probably damaging |
Het |
Glra3 |
T |
A |
8: 56,578,299 (GRCm39) |
F452Y |
probably damaging |
Het |
Gm10338 |
T |
A |
14: 19,280,438 (GRCm39) |
N96I |
probably damaging |
Het |
Gpd2 |
A |
T |
2: 57,195,866 (GRCm39) |
E149V |
possibly damaging |
Het |
Gpr137c |
T |
G |
14: 45,516,229 (GRCm39) |
L321* |
probably null |
Het |
Gsdmc2 |
T |
C |
15: 63,702,678 (GRCm39) |
I196M |
probably benign |
Het |
Habp2 |
A |
G |
19: 56,295,253 (GRCm39) |
D48G |
probably benign |
Het |
Hdc |
G |
T |
2: 126,458,149 (GRCm39) |
P58T |
probably damaging |
Het |
Heatr5a |
AGCACACTGCAGGAAGCTCACACAGCACAGCATACCTTCAGGAGTGCACACTGCAGGAAGCTCACACAGCACAGCATACCTTCAGGAGAGCACACTGCAGGAAGCTCA |
AGCACACTGCAGGAAGCTCACACAGCACAGCATACCTTCAGGAGAGCACACTGCAGGAAGCTCA |
12: 51,934,702 (GRCm39) |
|
probably benign |
Het |
Hnrnpr |
G |
T |
4: 136,063,615 (GRCm39) |
V342F |
probably damaging |
Het |
Hyal6 |
T |
A |
6: 24,734,929 (GRCm39) |
Y287* |
probably null |
Het |
Igsf8 |
T |
C |
1: 172,146,525 (GRCm39) |
Y571H |
|
Het |
Kalrn |
A |
G |
16: 33,854,864 (GRCm39) |
S1999P |
probably damaging |
Het |
Lama2 |
T |
A |
10: 26,877,170 (GRCm39) |
N2672I |
probably benign |
Het |
Lrrc7 |
T |
C |
3: 157,867,105 (GRCm39) |
R879G |
probably damaging |
Het |
Lrwd1 |
T |
G |
5: 136,160,413 (GRCm39) |
H307P |
probably benign |
Het |
Mau2 |
T |
C |
8: 70,480,153 (GRCm39) |
Y318C |
probably damaging |
Het |
Med13 |
T |
C |
11: 86,199,727 (GRCm39) |
Q660R |
probably benign |
Het |
Mepce |
G |
C |
5: 137,783,759 (GRCm39) |
P189R |
probably damaging |
Het |
Mical3 |
T |
A |
6: 121,001,758 (GRCm39) |
N578I |
probably damaging |
Het |
Mug1 |
T |
C |
6: 121,861,635 (GRCm39) |
S1366P |
probably damaging |
Het |
Nol11 |
A |
T |
11: 107,064,278 (GRCm39) |
D511E |
possibly damaging |
Het |
Obscn |
T |
A |
11: 58,994,340 (GRCm39) |
H1514L |
probably benign |
Het |
Onecut3 |
C |
A |
10: 80,331,887 (GRCm39) |
S349* |
probably null |
Het |
Or2l13b |
C |
T |
16: 19,349,026 (GRCm39) |
A215T |
probably benign |
Het |
Or4f57 |
A |
G |
2: 111,790,584 (GRCm39) |
V278A |
possibly damaging |
Het |
Or5ap2b-ps1 |
A |
T |
2: 85,693,922 (GRCm39) |
I56F |
probably damaging |
Het |
Or5b110-ps1 |
G |
A |
19: 13,259,558 (GRCm39) |
T288I |
unknown |
Het |
Or7e169 |
A |
G |
9: 19,757,816 (GRCm39) |
L33P |
possibly damaging |
Het |
Or7g34 |
T |
C |
9: 19,478,396 (GRCm39) |
I95V |
possibly damaging |
Het |
Or8g18 |
T |
C |
9: 39,149,625 (GRCm39) |
T32A |
probably benign |
Het |
Patl2 |
C |
T |
2: 121,955,374 (GRCm39) |
G297E |
probably benign |
Het |
Pdlim5 |
G |
A |
3: 142,010,111 (GRCm39) |
T168M |
probably damaging |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Pkd1l3 |
T |
C |
8: 110,395,849 (GRCm39) |
V2083A |
probably damaging |
Het |
Pkhd1 |
T |
A |
1: 20,637,741 (GRCm39) |
Y348F |
probably damaging |
Het |
Plekhg5 |
T |
A |
4: 152,198,826 (GRCm39) |
S1005T |
probably benign |
Het |
Ppp4r1 |
T |
A |
17: 66,142,073 (GRCm39) |
N709K |
probably null |
Het |
Pramel32 |
T |
A |
4: 88,546,219 (GRCm39) |
L374F |
possibly damaging |
Het |
Pramel40 |
G |
A |
5: 94,464,924 (GRCm39) |
V437I |
probably benign |
Het |
Reln |
T |
C |
5: 22,125,508 (GRCm39) |
D2725G |
possibly damaging |
Het |
Rnf41 |
T |
A |
10: 128,274,299 (GRCm39) |
I317K |
probably benign |
Het |
Rxfp2 |
T |
C |
5: 149,979,444 (GRCm39) |
V268A |
possibly damaging |
Het |
Sema5a |
A |
G |
15: 32,679,373 (GRCm39) |
H884R |
probably damaging |
Het |
Serpinh1 |
A |
T |
7: 98,996,484 (GRCm39) |
M236K |
probably damaging |
Het |
Sh3pxd2a |
A |
G |
19: 47,255,610 (GRCm39) |
L1064P |
probably damaging |
Het |
Skint6 |
T |
C |
4: 112,715,375 (GRCm39) |
H947R |
probably benign |
Het |
Slc12a3 |
T |
A |
8: 95,083,658 (GRCm39) |
M895K |
possibly damaging |
Het |
Slc22a3 |
C |
A |
17: 12,726,057 (GRCm39) |
R52L |
probably damaging |
Het |
Slc38a1 |
A |
G |
15: 96,487,965 (GRCm39) |
L180P |
probably damaging |
Het |
Slc4a3 |
T |
C |
1: 75,533,612 (GRCm39) |
V1078A |
probably damaging |
Het |
Snx30 |
T |
A |
4: 59,879,241 (GRCm39) |
V160E |
probably damaging |
Het |
Spata18 |
A |
T |
5: 73,829,840 (GRCm39) |
I332F |
|
Het |
Stard9 |
C |
G |
2: 120,534,564 (GRCm39) |
P3607R |
probably damaging |
Het |
Svep1 |
T |
A |
4: 58,084,144 (GRCm39) |
Y1876F |
possibly damaging |
Het |
Sytl1 |
A |
G |
4: 132,986,291 (GRCm39) |
|
probably null |
Het |
Tacc2 |
A |
C |
7: 130,366,041 (GRCm39) |
K567Q |
probably damaging |
Het |
Tfr2 |
A |
G |
5: 137,575,769 (GRCm39) |
D295G |
possibly damaging |
Het |
Tmem53 |
C |
A |
4: 117,125,122 (GRCm39) |
H78Q |
probably benign |
Het |
Tnnt2 |
G |
A |
1: 135,768,640 (GRCm39) |
E10K |
unknown |
Het |
Top2a |
T |
A |
11: 98,902,970 (GRCm39) |
I406F |
probably damaging |
Het |
Ttc1 |
C |
A |
11: 43,621,305 (GRCm39) |
R292I |
|
Het |
Ubr1 |
T |
G |
2: 120,703,627 (GRCm39) |
T1568P |
probably damaging |
Het |
Usp25 |
T |
G |
16: 76,852,076 (GRCm39) |
V197G |
probably damaging |
Het |
Usp9y |
A |
T |
Y: 1,432,188 (GRCm39) |
N432K |
probably benign |
Het |
Vmn2r26 |
T |
A |
6: 124,038,137 (GRCm39) |
Y571N |
probably damaging |
Het |
Zfp7 |
T |
C |
15: 76,775,484 (GRCm39) |
S509P |
probably damaging |
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 |
R5268:Pdzd2
|
UTSW |
15 |
12,592,263 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
|
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 |
|