Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700093K21Rik |
A |
T |
11: 23,467,357 (GRCm39) |
M92K |
probably benign |
Het |
4931406C07Rik |
T |
C |
9: 15,212,660 (GRCm39) |
|
probably null |
Het |
A430005L14Rik |
G |
A |
4: 154,045,357 (GRCm39) |
V129M |
probably damaging |
Het |
Actg2 |
T |
C |
6: 83,499,801 (GRCm39) |
T150A |
possibly damaging |
Het |
Actn1 |
A |
T |
12: 80,306,806 (GRCm39) |
D20E |
probably benign |
Het |
Alcam |
C |
T |
16: 52,091,136 (GRCm39) |
E461K |
probably damaging |
Het |
Anapc1 |
G |
A |
2: 128,518,128 (GRCm39) |
P242L |
probably benign |
Het |
Ankrd49 |
A |
T |
9: 14,692,674 (GRCm39) |
D163E |
probably benign |
Het |
Atp8b5 |
G |
A |
4: 43,372,903 (GRCm39) |
R1149Q |
possibly damaging |
Het |
Cacnb3 |
G |
T |
15: 98,540,455 (GRCm39) |
V328F |
probably damaging |
Het |
Camk4 |
T |
C |
18: 33,309,275 (GRCm39) |
I226T |
probably damaging |
Het |
Ccdc148 |
T |
C |
2: 58,892,176 (GRCm39) |
D172G |
probably damaging |
Het |
Cdh12 |
A |
G |
15: 21,520,491 (GRCm39) |
I319V |
probably damaging |
Het |
Cenpc1 |
T |
C |
5: 86,209,857 (GRCm39) |
|
probably benign |
Het |
Cfap69 |
A |
C |
5: 5,632,457 (GRCm39) |
N15K |
probably damaging |
Het |
Ckap2l |
A |
C |
2: 129,127,087 (GRCm39) |
S364A |
possibly damaging |
Het |
Clic6 |
G |
A |
16: 92,324,972 (GRCm39) |
G36R |
probably damaging |
Het |
Col6a3 |
T |
C |
1: 90,749,583 (GRCm39) |
Y417C |
probably benign |
Het |
Cstf3 |
T |
A |
2: 104,494,623 (GRCm39) |
|
probably benign |
Het |
Cyp4f39 |
G |
A |
17: 32,711,304 (GRCm39) |
A484T |
probably benign |
Het |
Dntt |
C |
A |
19: 41,017,923 (GRCm39) |
P16T |
probably benign |
Het |
Dym |
T |
A |
18: 75,258,583 (GRCm39) |
I447N |
probably damaging |
Het |
Elmo1 |
T |
C |
13: 20,773,841 (GRCm39) |
V617A |
probably benign |
Het |
Elovl7 |
G |
A |
13: 108,419,160 (GRCm39) |
G264D |
probably damaging |
Het |
Epha7 |
T |
A |
4: 28,947,571 (GRCm39) |
Y610* |
probably null |
Het |
Fn1 |
T |
C |
1: 71,636,814 (GRCm39) |
I178V |
probably benign |
Het |
Fndc9 |
T |
C |
11: 46,129,152 (GRCm39) |
Y224H |
probably benign |
Het |
Gad1 |
T |
C |
2: 70,404,521 (GRCm39) |
V137A |
probably damaging |
Het |
Gapvd1 |
A |
G |
2: 34,590,773 (GRCm39) |
|
probably null |
Het |
Gbp11 |
C |
T |
5: 105,475,277 (GRCm39) |
C357Y |
probably damaging |
Het |
Gcc1 |
G |
A |
6: 28,419,163 (GRCm39) |
A390V |
probably benign |
Het |
Gm6811 |
A |
G |
17: 21,314,185 (GRCm39) |
|
noncoding transcript |
Het |
Htt |
A |
T |
5: 34,985,918 (GRCm39) |
D1063V |
probably damaging |
Het |
Igfn1 |
C |
T |
1: 135,898,839 (GRCm39) |
A576T |
probably damaging |
Het |
Il12rb2 |
T |
C |
6: 67,280,485 (GRCm39) |
Y240C |
probably damaging |
Het |
Itga3 |
T |
C |
11: 94,946,585 (GRCm39) |
D747G |
probably damaging |
Het |
Kcnip2 |
A |
C |
19: 45,782,979 (GRCm39) |
D134E |
probably damaging |
Het |
Kif2b |
C |
A |
11: 91,466,798 (GRCm39) |
R495I |
probably damaging |
Het |
Lef1 |
T |
C |
3: 130,993,938 (GRCm39) |
|
probably benign |
Het |
Lias |
C |
T |
5: 65,548,981 (GRCm39) |
R4C |
probably damaging |
Het |
Lpcat2 |
T |
C |
8: 93,591,560 (GRCm39) |
V68A |
probably benign |
Het |
Lrrc37 |
A |
T |
11: 103,505,768 (GRCm39) |
S2067T |
probably benign |
Het |
Lrrc8e |
A |
T |
8: 4,284,190 (GRCm39) |
K138N |
probably damaging |
Het |
Map4k5 |
G |
A |
12: 69,852,082 (GRCm39) |
H767Y |
probably benign |
Het |
Mga |
C |
A |
2: 119,791,333 (GRCm39) |
T2406K |
possibly damaging |
Het |
Mtx1 |
A |
T |
3: 89,116,648 (GRCm39) |
S418T |
probably benign |
Het |
Myh7 |
C |
T |
14: 55,224,973 (GRCm39) |
M531I |
probably benign |
Het |
Myorg |
C |
T |
4: 41,497,947 (GRCm39) |
R561H |
probably benign |
Het |
Ncaph2 |
T |
A |
15: 89,255,427 (GRCm39) |
M555K |
probably damaging |
Het |
Nckap1 |
C |
T |
2: 80,348,286 (GRCm39) |
S889N |
probably benign |
Het |
Ncoa6 |
T |
C |
2: 155,244,584 (GRCm39) |
|
probably benign |
Het |
Nrp2 |
A |
G |
1: 62,822,479 (GRCm39) |
S691G |
probably benign |
Het |
Odad2 |
T |
C |
18: 7,222,554 (GRCm39) |
T572A |
probably benign |
Het |
Odf2l |
A |
T |
3: 144,845,543 (GRCm39) |
|
probably null |
Het |
Or5aq6 |
T |
A |
2: 86,923,081 (GRCm39) |
H220L |
probably benign |
Het |
Pcdh20 |
A |
G |
14: 88,705,410 (GRCm39) |
V630A |
probably damaging |
Het |
Pebp4 |
T |
C |
14: 70,285,923 (GRCm39) |
|
probably null |
Het |
Ppfia3 |
T |
A |
7: 45,006,090 (GRCm39) |
M301L |
probably benign |
Het |
Ppp1r21 |
C |
A |
17: 88,858,097 (GRCm39) |
Q203K |
probably benign |
Het |
Prr23a1 |
T |
C |
9: 98,725,406 (GRCm39) |
V256A |
probably benign |
Het |
Rbfox1 |
A |
G |
16: 7,110,091 (GRCm39) |
R150G |
possibly damaging |
Het |
Rnps1-ps |
A |
T |
6: 7,982,943 (GRCm39) |
|
noncoding transcript |
Het |
Robo3 |
T |
C |
9: 37,329,005 (GRCm39) |
R1238G |
possibly damaging |
Het |
Rp9 |
T |
G |
9: 22,365,097 (GRCm39) |
Q35P |
probably damaging |
Het |
Rsrc1 |
C |
A |
3: 67,262,808 (GRCm39) |
A254E |
probably damaging |
Het |
Shtn1 |
T |
A |
19: 58,998,222 (GRCm39) |
K390N |
probably damaging |
Het |
Sidt2 |
C |
T |
9: 45,864,517 (GRCm39) |
V71I |
probably benign |
Het |
Sirt7 |
A |
G |
11: 120,515,365 (GRCm39) |
V97A |
possibly damaging |
Het |
Slc14a2 |
A |
G |
18: 78,206,419 (GRCm39) |
S466P |
probably benign |
Het |
Slc2a10 |
T |
A |
2: 165,357,361 (GRCm39) |
D340E |
probably benign |
Het |
Slc36a2 |
A |
C |
11: 55,075,735 (GRCm39) |
N17K |
probably benign |
Het |
Slc4a10 |
A |
C |
2: 62,155,071 (GRCm39) |
N1086T |
probably benign |
Het |
Sptb |
T |
C |
12: 76,676,423 (GRCm39) |
D177G |
probably damaging |
Het |
Srpk2 |
A |
T |
5: 23,730,748 (GRCm39) |
|
probably null |
Het |
Sucla2 |
T |
G |
14: 73,830,121 (GRCm39) |
V386G |
probably damaging |
Het |
Susd1 |
G |
T |
4: 59,424,089 (GRCm39) |
N45K |
possibly damaging |
Het |
Tbxas1 |
T |
C |
6: 38,994,822 (GRCm39) |
|
probably benign |
Het |
Topors |
C |
T |
4: 40,261,776 (GRCm39) |
E503K |
probably damaging |
Het |
Trpv5 |
T |
C |
6: 41,634,731 (GRCm39) |
R533G |
probably benign |
Het |
Tshr |
A |
G |
12: 91,504,115 (GRCm39) |
H351R |
possibly damaging |
Het |
Ube2f |
G |
A |
1: 91,203,037 (GRCm39) |
V94M |
probably damaging |
Het |
Ugdh |
A |
G |
5: 65,580,521 (GRCm39) |
S216P |
probably damaging |
Het |
Unc45b |
T |
A |
11: 82,802,531 (GRCm39) |
|
probably null |
Het |
Vmn1r226 |
A |
G |
17: 20,908,335 (GRCm39) |
E189G |
probably damaging |
Het |
Xrcc6 |
T |
G |
15: 81,913,900 (GRCm39) |
D75E |
probably benign |
Het |
Ypel1 |
A |
G |
16: 16,921,474 (GRCm39) |
L70P |
probably damaging |
Het |
Zcwpw1 |
A |
T |
5: 137,795,022 (GRCm39) |
R73W |
probably damaging |
Het |
Zfp219 |
T |
C |
14: 52,246,512 (GRCm39) |
E160G |
probably damaging |
Het |
Zfp804b |
G |
T |
5: 7,229,533 (GRCm39) |
|
probably benign |
Het |
Zscan22 |
C |
A |
7: 12,640,730 (GRCm39) |
P325T |
probably damaging |
Het |
|
Other mutations in Dnah3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00650:Dnah3
|
APN |
7 |
119,538,128 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01095:Dnah3
|
APN |
7 |
119,550,820 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01329:Dnah3
|
APN |
7 |
119,622,164 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01380:Dnah3
|
APN |
7 |
119,525,787 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01410:Dnah3
|
APN |
7 |
119,566,943 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01487:Dnah3
|
APN |
7 |
119,564,753 (GRCm39) |
nonsense |
probably null |
|
IGL01843:Dnah3
|
APN |
7 |
119,542,798 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01929:Dnah3
|
APN |
7 |
119,550,874 (GRCm39) |
nonsense |
probably null |
|
IGL01994:Dnah3
|
APN |
7 |
119,550,437 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL02115:Dnah3
|
APN |
7 |
119,628,277 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02273:Dnah3
|
APN |
7 |
119,550,494 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02299:Dnah3
|
APN |
7 |
119,566,802 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02421:Dnah3
|
APN |
7 |
119,550,215 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02514:Dnah3
|
APN |
7 |
119,565,470 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02596:Dnah3
|
APN |
7 |
119,538,137 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02716:Dnah3
|
APN |
7 |
119,536,246 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02738:Dnah3
|
APN |
7 |
119,564,720 (GRCm39) |
missense |
probably benign |
|
IGL03404:Dnah3
|
APN |
7 |
119,538,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R0964_Dnah3_480
|
UTSW |
7 |
119,551,962 (GRCm39) |
splice site |
probably benign |
|
R1778_Dnah3_238
|
UTSW |
7 |
119,677,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R4658_Dnah3_599
|
UTSW |
7 |
119,549,874 (GRCm39) |
missense |
probably damaging |
1.00 |
BB004:Dnah3
|
UTSW |
7 |
119,550,494 (GRCm39) |
missense |
probably damaging |
0.97 |
BB014:Dnah3
|
UTSW |
7 |
119,550,494 (GRCm39) |
missense |
probably damaging |
0.97 |
R0011:Dnah3
|
UTSW |
7 |
119,618,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R0195:Dnah3
|
UTSW |
7 |
119,676,998 (GRCm39) |
critical splice donor site |
probably null |
|
R0241:Dnah3
|
UTSW |
7 |
119,521,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R0241:Dnah3
|
UTSW |
7 |
119,521,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R0312:Dnah3
|
UTSW |
7 |
119,644,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R0316:Dnah3
|
UTSW |
7 |
119,564,882 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0370:Dnah3
|
UTSW |
7 |
119,685,943 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0426:Dnah3
|
UTSW |
7 |
119,542,795 (GRCm39) |
missense |
probably benign |
0.11 |
R0525:Dnah3
|
UTSW |
7 |
119,527,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R0625:Dnah3
|
UTSW |
7 |
119,671,110 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0627:Dnah3
|
UTSW |
7 |
119,620,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R0632:Dnah3
|
UTSW |
7 |
119,567,128 (GRCm39) |
missense |
probably benign |
0.11 |
R0928:Dnah3
|
UTSW |
7 |
119,629,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R0964:Dnah3
|
UTSW |
7 |
119,551,962 (GRCm39) |
splice site |
probably benign |
|
R0972:Dnah3
|
UTSW |
7 |
119,634,563 (GRCm39) |
splice site |
probably null |
|
R1066:Dnah3
|
UTSW |
7 |
119,660,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R1082:Dnah3
|
UTSW |
7 |
119,677,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R1127:Dnah3
|
UTSW |
7 |
119,522,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R1132:Dnah3
|
UTSW |
7 |
119,538,227 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1222:Dnah3
|
UTSW |
7 |
119,689,899 (GRCm39) |
missense |
probably benign |
0.28 |
R1420:Dnah3
|
UTSW |
7 |
119,551,202 (GRCm39) |
missense |
probably damaging |
0.99 |
R1456:Dnah3
|
UTSW |
7 |
119,646,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R1472:Dnah3
|
UTSW |
7 |
119,670,181 (GRCm39) |
missense |
probably benign |
0.12 |
R1617:Dnah3
|
UTSW |
7 |
119,689,169 (GRCm39) |
missense |
probably benign |
0.01 |
R1624:Dnah3
|
UTSW |
7 |
119,618,918 (GRCm39) |
missense |
probably damaging |
0.99 |
R1654:Dnah3
|
UTSW |
7 |
119,525,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R1673:Dnah3
|
UTSW |
7 |
119,570,402 (GRCm39) |
nonsense |
probably null |
|
R1687:Dnah3
|
UTSW |
7 |
119,645,009 (GRCm39) |
splice site |
probably null |
|
R1711:Dnah3
|
UTSW |
7 |
119,677,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R1738:Dnah3
|
UTSW |
7 |
119,634,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R1778:Dnah3
|
UTSW |
7 |
119,677,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R1866:Dnah3
|
UTSW |
7 |
119,528,079 (GRCm39) |
splice site |
probably null |
|
R1883:Dnah3
|
UTSW |
7 |
119,677,142 (GRCm39) |
missense |
probably benign |
0.06 |
R1894:Dnah3
|
UTSW |
7 |
119,685,557 (GRCm39) |
missense |
probably benign |
0.05 |
R1929:Dnah3
|
UTSW |
7 |
119,574,352 (GRCm39) |
missense |
probably benign |
0.10 |
R1988:Dnah3
|
UTSW |
7 |
119,567,182 (GRCm39) |
missense |
probably damaging |
0.99 |
R1988:Dnah3
|
UTSW |
7 |
119,566,793 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2010:Dnah3
|
UTSW |
7 |
119,694,400 (GRCm39) |
start codon destroyed |
probably benign |
0.00 |
R2022:Dnah3
|
UTSW |
7 |
119,550,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R2026:Dnah3
|
UTSW |
7 |
119,638,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R2063:Dnah3
|
UTSW |
7 |
119,551,132 (GRCm39) |
missense |
probably damaging |
0.96 |
R2131:Dnah3
|
UTSW |
7 |
119,566,982 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2152:Dnah3
|
UTSW |
7 |
119,551,236 (GRCm39) |
missense |
probably benign |
0.02 |
R2199:Dnah3
|
UTSW |
7 |
119,550,792 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2271:Dnah3
|
UTSW |
7 |
119,574,352 (GRCm39) |
missense |
probably benign |
0.10 |
R2350:Dnah3
|
UTSW |
7 |
119,645,011 (GRCm39) |
splice site |
probably null |
|
R2567:Dnah3
|
UTSW |
7 |
119,551,920 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2848:Dnah3
|
UTSW |
7 |
119,567,161 (GRCm39) |
missense |
probably benign |
0.01 |
R2902:Dnah3
|
UTSW |
7 |
119,550,722 (GRCm39) |
missense |
possibly damaging |
0.61 |
R2926:Dnah3
|
UTSW |
7 |
119,550,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R2944:Dnah3
|
UTSW |
7 |
119,550,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R3022:Dnah3
|
UTSW |
7 |
119,677,704 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3401:Dnah3
|
UTSW |
7 |
119,566,879 (GRCm39) |
missense |
probably benign |
0.00 |
R3402:Dnah3
|
UTSW |
7 |
119,566,879 (GRCm39) |
missense |
probably benign |
0.00 |
R3403:Dnah3
|
UTSW |
7 |
119,566,879 (GRCm39) |
missense |
probably benign |
0.00 |
R3919:Dnah3
|
UTSW |
7 |
119,550,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R3972:Dnah3
|
UTSW |
7 |
119,685,943 (GRCm39) |
missense |
probably damaging |
0.99 |
R4162:Dnah3
|
UTSW |
7 |
119,522,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R4184:Dnah3
|
UTSW |
7 |
119,682,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R4198:Dnah3
|
UTSW |
7 |
119,522,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R4199:Dnah3
|
UTSW |
7 |
119,522,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R4200:Dnah3
|
UTSW |
7 |
119,522,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R4239:Dnah3
|
UTSW |
7 |
119,628,248 (GRCm39) |
nonsense |
probably null |
|
R4478:Dnah3
|
UTSW |
7 |
119,671,086 (GRCm39) |
missense |
probably benign |
0.00 |
R4579:Dnah3
|
UTSW |
7 |
119,608,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R4600:Dnah3
|
UTSW |
7 |
119,689,169 (GRCm39) |
missense |
probably benign |
|
R4649:Dnah3
|
UTSW |
7 |
119,646,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R4658:Dnah3
|
UTSW |
7 |
119,549,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R4728:Dnah3
|
UTSW |
7 |
119,658,589 (GRCm39) |
missense |
probably damaging |
0.99 |
R4739:Dnah3
|
UTSW |
7 |
119,677,169 (GRCm39) |
missense |
possibly damaging |
0.54 |
R4758:Dnah3
|
UTSW |
7 |
119,678,629 (GRCm39) |
missense |
probably benign |
0.00 |
R4785:Dnah3
|
UTSW |
7 |
119,567,047 (GRCm39) |
missense |
probably benign |
0.29 |
R4789:Dnah3
|
UTSW |
7 |
119,610,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R4930:Dnah3
|
UTSW |
7 |
119,550,904 (GRCm39) |
nonsense |
probably null |
|
R4935:Dnah3
|
UTSW |
7 |
119,615,700 (GRCm39) |
nonsense |
probably null |
|
R4946:Dnah3
|
UTSW |
7 |
119,530,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R4981:Dnah3
|
UTSW |
7 |
119,555,424 (GRCm39) |
missense |
probably benign |
0.03 |
R4984:Dnah3
|
UTSW |
7 |
119,528,002 (GRCm39) |
missense |
probably benign |
0.04 |
R5025:Dnah3
|
UTSW |
7 |
119,671,128 (GRCm39) |
missense |
probably benign |
0.02 |
R5046:Dnah3
|
UTSW |
7 |
119,550,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R5056:Dnah3
|
UTSW |
7 |
119,620,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R5068:Dnah3
|
UTSW |
7 |
119,632,013 (GRCm39) |
missense |
probably benign |
|
R5069:Dnah3
|
UTSW |
7 |
119,632,013 (GRCm39) |
missense |
probably benign |
|
R5154:Dnah3
|
UTSW |
7 |
119,551,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R5208:Dnah3
|
UTSW |
7 |
119,631,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R5323:Dnah3
|
UTSW |
7 |
119,620,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R5330:Dnah3
|
UTSW |
7 |
119,542,871 (GRCm39) |
missense |
probably benign |
0.00 |
R5385:Dnah3
|
UTSW |
7 |
119,524,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R5391:Dnah3
|
UTSW |
7 |
119,689,299 (GRCm39) |
missense |
probably benign |
0.02 |
R5564:Dnah3
|
UTSW |
7 |
119,570,689 (GRCm39) |
critical splice donor site |
probably null |
|
R5594:Dnah3
|
UTSW |
7 |
119,570,844 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5610:Dnah3
|
UTSW |
7 |
119,538,288 (GRCm39) |
splice site |
probably null |
|
R5673:Dnah3
|
UTSW |
7 |
119,550,812 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5678:Dnah3
|
UTSW |
7 |
119,677,074 (GRCm39) |
missense |
probably benign |
0.00 |
R5737:Dnah3
|
UTSW |
7 |
119,658,421 (GRCm39) |
missense |
probably benign |
0.03 |
R5766:Dnah3
|
UTSW |
7 |
119,577,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R5769:Dnah3
|
UTSW |
7 |
119,689,175 (GRCm39) |
nonsense |
probably null |
|
R5789:Dnah3
|
UTSW |
7 |
119,542,822 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5791:Dnah3
|
UTSW |
7 |
119,530,696 (GRCm39) |
missense |
probably benign |
0.00 |
R5841:Dnah3
|
UTSW |
7 |
119,550,244 (GRCm39) |
utr 3 prime |
probably benign |
|
R5843:Dnah3
|
UTSW |
7 |
119,550,244 (GRCm39) |
utr 3 prime |
probably benign |
|
R5844:Dnah3
|
UTSW |
7 |
119,550,244 (GRCm39) |
utr 3 prime |
probably benign |
|
R5846:Dnah3
|
UTSW |
7 |
119,550,244 (GRCm39) |
utr 3 prime |
probably benign |
|
R5851:Dnah3
|
UTSW |
7 |
119,638,585 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5853:Dnah3
|
UTSW |
7 |
119,538,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R5857:Dnah3
|
UTSW |
7 |
119,550,244 (GRCm39) |
utr 3 prime |
probably benign |
|
R5865:Dnah3
|
UTSW |
7 |
119,574,331 (GRCm39) |
missense |
probably benign |
0.00 |
R5885:Dnah3
|
UTSW |
7 |
119,668,927 (GRCm39) |
missense |
probably benign |
0.10 |
R5898:Dnah3
|
UTSW |
7 |
119,677,724 (GRCm39) |
missense |
probably benign |
0.37 |
R5917:Dnah3
|
UTSW |
7 |
119,615,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R5964:Dnah3
|
UTSW |
7 |
119,522,103 (GRCm39) |
missense |
probably benign |
0.00 |
R5990:Dnah3
|
UTSW |
7 |
119,672,764 (GRCm39) |
missense |
probably benign |
|
R6004:Dnah3
|
UTSW |
7 |
119,685,520 (GRCm39) |
missense |
probably benign |
0.10 |
R6033:Dnah3
|
UTSW |
7 |
119,670,870 (GRCm39) |
missense |
probably benign |
0.00 |
R6033:Dnah3
|
UTSW |
7 |
119,670,870 (GRCm39) |
missense |
probably benign |
0.00 |
R6045:Dnah3
|
UTSW |
7 |
119,566,745 (GRCm39) |
missense |
probably damaging |
0.99 |
R6056:Dnah3
|
UTSW |
7 |
119,629,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R6133:Dnah3
|
UTSW |
7 |
119,685,469 (GRCm39) |
missense |
probably benign |
0.10 |
R6229:Dnah3
|
UTSW |
7 |
119,564,711 (GRCm39) |
missense |
probably benign |
0.11 |
R6237:Dnah3
|
UTSW |
7 |
119,608,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R6333:Dnah3
|
UTSW |
7 |
119,653,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R6408:Dnah3
|
UTSW |
7 |
119,522,191 (GRCm39) |
splice site |
probably null |
|
R6447:Dnah3
|
UTSW |
7 |
119,522,277 (GRCm39) |
missense |
probably benign |
0.12 |
R6606:Dnah3
|
UTSW |
7 |
119,660,179 (GRCm39) |
missense |
probably benign |
0.02 |
R6666:Dnah3
|
UTSW |
7 |
119,670,172 (GRCm39) |
missense |
probably benign |
0.16 |
R6733:Dnah3
|
UTSW |
7 |
119,522,197 (GRCm39) |
missense |
probably benign |
0.22 |
R6815:Dnah3
|
UTSW |
7 |
119,570,950 (GRCm39) |
missense |
probably benign |
|
R6882:Dnah3
|
UTSW |
7 |
119,570,407 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6934:Dnah3
|
UTSW |
7 |
119,653,824 (GRCm39) |
critical splice donor site |
probably null |
|
R6966:Dnah3
|
UTSW |
7 |
119,631,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R7025:Dnah3
|
UTSW |
7 |
119,629,233 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7207:Dnah3
|
UTSW |
7 |
119,570,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R7214:Dnah3
|
UTSW |
7 |
119,521,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R7222:Dnah3
|
UTSW |
7 |
119,670,746 (GRCm39) |
missense |
probably benign |
0.00 |
R7235:Dnah3
|
UTSW |
7 |
119,631,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R7241:Dnah3
|
UTSW |
7 |
119,542,856 (GRCm39) |
missense |
probably benign |
0.03 |
R7313:Dnah3
|
UTSW |
7 |
119,580,567 (GRCm39) |
missense |
probably benign |
0.39 |
R7342:Dnah3
|
UTSW |
7 |
119,629,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R7368:Dnah3
|
UTSW |
7 |
119,628,239 (GRCm39) |
missense |
probably benign |
|
R7375:Dnah3
|
UTSW |
7 |
119,550,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R7395:Dnah3
|
UTSW |
7 |
119,660,183 (GRCm39) |
missense |
probably benign |
0.00 |
R7395:Dnah3
|
UTSW |
7 |
119,565,474 (GRCm39) |
missense |
|
|
R7431:Dnah3
|
UTSW |
7 |
119,650,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R7499:Dnah3
|
UTSW |
7 |
119,660,135 (GRCm39) |
missense |
probably damaging |
0.99 |
R7515:Dnah3
|
UTSW |
7 |
119,672,815 (GRCm39) |
missense |
probably benign |
0.21 |
R7564:Dnah3
|
UTSW |
7 |
119,570,817 (GRCm39) |
missense |
probably benign |
|
R7618:Dnah3
|
UTSW |
7 |
119,577,601 (GRCm39) |
missense |
probably damaging |
0.97 |
R7697:Dnah3
|
UTSW |
7 |
119,566,657 (GRCm39) |
missense |
|
|
R7728:Dnah3
|
UTSW |
7 |
119,538,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R7757:Dnah3
|
UTSW |
7 |
119,570,438 (GRCm39) |
splice site |
probably null |
|
R7757:Dnah3
|
UTSW |
7 |
119,670,793 (GRCm39) |
missense |
probably benign |
|
R7774:Dnah3
|
UTSW |
7 |
119,550,975 (GRCm39) |
nonsense |
probably null |
|
R7804:Dnah3
|
UTSW |
7 |
119,610,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R7804:Dnah3
|
UTSW |
7 |
119,551,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R7857:Dnah3
|
UTSW |
7 |
119,550,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R7871:Dnah3
|
UTSW |
7 |
119,566,775 (GRCm39) |
missense |
|
|
R7903:Dnah3
|
UTSW |
7 |
119,641,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R7927:Dnah3
|
UTSW |
7 |
119,550,494 (GRCm39) |
missense |
probably damaging |
0.97 |
R7989:Dnah3
|
UTSW |
7 |
119,677,012 (GRCm39) |
missense |
probably benign |
|
R8142:Dnah3
|
UTSW |
7 |
119,660,189 (GRCm39) |
missense |
probably benign |
0.00 |
R8164:Dnah3
|
UTSW |
7 |
119,566,837 (GRCm39) |
missense |
probably damaging |
1.00 |
R8237:Dnah3
|
UTSW |
7 |
119,525,636 (GRCm39) |
missense |
probably benign |
0.01 |
R8313:Dnah3
|
UTSW |
7 |
119,550,375 (GRCm39) |
missense |
probably benign |
0.38 |
R8338:Dnah3
|
UTSW |
7 |
119,671,104 (GRCm39) |
missense |
probably benign |
0.01 |
R8355:Dnah3
|
UTSW |
7 |
119,551,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R8408:Dnah3
|
UTSW |
7 |
119,551,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R8411:Dnah3
|
UTSW |
7 |
119,610,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R8455:Dnah3
|
UTSW |
7 |
119,551,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R8483:Dnah3
|
UTSW |
7 |
119,536,253 (GRCm39) |
missense |
probably benign |
0.00 |
R8531:Dnah3
|
UTSW |
7 |
119,550,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R8885:Dnah3
|
UTSW |
7 |
119,561,375 (GRCm39) |
missense |
|
|
R8912:Dnah3
|
UTSW |
7 |
119,689,869 (GRCm39) |
missense |
probably benign |
0.06 |
R8966:Dnah3
|
UTSW |
7 |
119,549,881 (GRCm39) |
nonsense |
probably null |
|
R8982:Dnah3
|
UTSW |
7 |
119,536,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R9043:Dnah3
|
UTSW |
7 |
119,551,272 (GRCm39) |
missense |
probably benign |
|
R9053:Dnah3
|
UTSW |
7 |
119,618,987 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9059:Dnah3
|
UTSW |
7 |
119,684,368 (GRCm39) |
missense |
probably benign |
0.01 |
R9182:Dnah3
|
UTSW |
7 |
119,684,351 (GRCm39) |
missense |
probably damaging |
0.98 |
R9365:Dnah3
|
UTSW |
7 |
119,566,859 (GRCm39) |
missense |
|
|
R9383:Dnah3
|
UTSW |
7 |
119,646,819 (GRCm39) |
missense |
probably benign |
0.23 |
R9430:Dnah3
|
UTSW |
7 |
119,628,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R9449:Dnah3
|
UTSW |
7 |
119,551,473 (GRCm39) |
missense |
probably benign |
0.12 |
R9462:Dnah3
|
UTSW |
7 |
119,551,523 (GRCm39) |
missense |
probably benign |
0.05 |
R9505:Dnah3
|
UTSW |
7 |
119,644,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R9559:Dnah3
|
UTSW |
7 |
119,650,951 (GRCm39) |
missense |
probably benign |
0.07 |
R9562:Dnah3
|
UTSW |
7 |
119,610,114 (GRCm39) |
missense |
probably benign |
0.05 |
R9565:Dnah3
|
UTSW |
7 |
119,610,114 (GRCm39) |
missense |
probably benign |
0.05 |
R9609:Dnah3
|
UTSW |
7 |
119,670,236 (GRCm39) |
missense |
probably damaging |
0.98 |
R9622:Dnah3
|
UTSW |
7 |
119,561,356 (GRCm39) |
missense |
|
|
R9633:Dnah3
|
UTSW |
7 |
119,550,216 (GRCm39) |
missense |
probably benign |
|
R9654:Dnah3
|
UTSW |
7 |
119,641,396 (GRCm39) |
nonsense |
probably null |
|
R9665:Dnah3
|
UTSW |
7 |
119,644,981 (GRCm39) |
missense |
probably benign |
0.01 |
R9681:Dnah3
|
UTSW |
7 |
119,677,611 (GRCm39) |
missense |
probably benign |
0.04 |
R9717:Dnah3
|
UTSW |
7 |
119,574,299 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Dnah3
|
UTSW |
7 |
119,610,096 (GRCm39) |
missense |
probably null |
1.00 |
Z1088:Dnah3
|
UTSW |
7 |
119,685,520 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Dnah3
|
UTSW |
7 |
119,567,026 (GRCm39) |
missense |
|
|
Z1177:Dnah3
|
UTSW |
7 |
119,607,085 (GRCm39) |
missense |
probably benign |
|
Z1177:Dnah3
|
UTSW |
7 |
119,567,124 (GRCm39) |
missense |
probably damaging |
0.99 |
|