Other mutations in this stock |
Total: 145 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921517D22Rik |
T |
C |
13: 59,839,406 (GRCm39) |
D13G |
probably benign |
Het |
4930442H23Rik |
C |
T |
10: 81,018,978 (GRCm39) |
|
probably benign |
Het |
Adamts13 |
T |
A |
2: 26,873,054 (GRCm39) |
S341T |
probably damaging |
Het |
Adamts2 |
A |
G |
11: 50,683,549 (GRCm39) |
I944V |
probably benign |
Het |
Adcy3 |
A |
G |
12: 4,256,542 (GRCm39) |
T783A |
probably benign |
Het |
Ago3 |
A |
T |
4: 126,262,296 (GRCm39) |
M418K |
probably benign |
Het |
Alpk1 |
G |
T |
3: 127,481,241 (GRCm39) |
N175K |
possibly damaging |
Het |
Als2 |
A |
G |
1: 59,254,472 (GRCm39) |
V295A |
probably benign |
Het |
Anapc13 |
T |
C |
9: 102,507,020 (GRCm39) |
I11T |
probably benign |
Het |
Ankrd12 |
T |
A |
17: 66,289,994 (GRCm39) |
N1813I |
probably damaging |
Het |
Anks1b |
A |
T |
10: 90,750,612 (GRCm39) |
I176F |
probably null |
Het |
Ap3d1 |
TTCTCTCTCTCTCTCTCT |
TTCTCTCTCTCTCTCT |
10: 80,548,612 (GRCm39) |
|
probably null |
Het |
Arhgap32 |
T |
C |
9: 32,172,076 (GRCm39) |
C1619R |
probably damaging |
Het |
Arhgap32 |
A |
G |
9: 32,040,949 (GRCm39) |
D67G |
probably damaging |
Het |
Atp1a4 |
A |
T |
1: 172,081,677 (GRCm39) |
Y158* |
probably null |
Het |
Atp8b5 |
A |
T |
4: 43,356,980 (GRCm39) |
D576V |
probably damaging |
Het |
Atrnl1 |
A |
G |
19: 57,617,590 (GRCm39) |
I122V |
probably damaging |
Het |
B430203G13Rik |
A |
T |
12: 17,974,520 (GRCm39) |
|
noncoding transcript |
Het |
Baz1b |
T |
G |
5: 135,246,267 (GRCm39) |
L572R |
possibly damaging |
Het |
Ccn3 |
A |
T |
15: 54,615,603 (GRCm39) |
|
probably null |
Het |
Ccnd2 |
T |
C |
6: 127,125,761 (GRCm39) |
T92A |
possibly damaging |
Het |
Ccndbp1 |
A |
T |
2: 120,839,003 (GRCm39) |
T5S |
probably benign |
Het |
Ccr2 |
G |
A |
9: 123,906,409 (GRCm39) |
V230I |
probably benign |
Het |
Cct4 |
T |
A |
11: 22,952,866 (GRCm39) |
V514E |
probably damaging |
Het |
Cep152 |
A |
G |
2: 125,428,249 (GRCm39) |
|
probably null |
Het |
Cflar |
C |
T |
1: 58,791,726 (GRCm39) |
T343M |
probably benign |
Het |
Chrm5 |
A |
C |
2: 112,309,930 (GRCm39) |
N395K |
probably benign |
Het |
Chrna10 |
G |
A |
7: 101,762,426 (GRCm39) |
P255S |
possibly damaging |
Het |
Chrna6 |
T |
A |
8: 27,897,134 (GRCm39) |
I248F |
probably damaging |
Het |
Clip1 |
T |
C |
5: 123,717,356 (GRCm39) |
D1387G |
probably damaging |
Het |
Clstn3 |
T |
C |
6: 124,414,331 (GRCm39) |
|
probably null |
Het |
Cntnap5a |
C |
T |
1: 116,029,295 (GRCm39) |
R250W |
probably benign |
Het |
Col12a1 |
C |
A |
9: 79,585,776 (GRCm39) |
V1228F |
possibly damaging |
Het |
Cxcr5 |
T |
C |
9: 44,424,638 (GRCm39) |
T340A |
probably benign |
Het |
Cyp2a4 |
G |
A |
7: 26,012,300 (GRCm39) |
R361K |
probably damaging |
Het |
Dnah1 |
T |
A |
14: 30,985,436 (GRCm39) |
K3818N |
probably damaging |
Het |
Dpy19l1 |
A |
T |
9: 24,336,119 (GRCm39) |
L529Q |
probably damaging |
Het |
Eif4g2 |
C |
T |
7: 110,676,003 (GRCm39) |
R399H |
probably damaging |
Het |
Elapor1 |
A |
T |
3: 108,365,543 (GRCm39) |
|
probably benign |
Het |
Fam76a |
A |
T |
4: 132,629,428 (GRCm39) |
|
probably null |
Het |
Fam76a |
A |
G |
4: 132,643,501 (GRCm39) |
Y78H |
probably damaging |
Het |
Fbn1 |
A |
T |
2: 125,166,839 (GRCm39) |
C2026S |
probably damaging |
Het |
Fbxo4 |
T |
C |
15: 3,998,523 (GRCm39) |
T312A |
probably benign |
Het |
Fbxw26 |
A |
G |
9: 109,553,868 (GRCm39) |
V257A |
possibly damaging |
Het |
Fhip1a |
G |
T |
3: 85,595,877 (GRCm39) |
T115K |
probably damaging |
Het |
Flnb |
A |
T |
14: 7,905,701 (GRCm38) |
E1150D |
probably benign |
Het |
Fndc3c1 |
A |
T |
X: 105,481,308 (GRCm39) |
S661R |
possibly damaging |
Het |
Gba2 |
A |
C |
4: 43,568,315 (GRCm39) |
L684R |
probably damaging |
Het |
Gbf1 |
G |
T |
19: 46,256,834 (GRCm39) |
C812F |
possibly damaging |
Het |
Glt8d2 |
A |
T |
10: 82,496,583 (GRCm39) |
D158E |
probably damaging |
Het |
Golga2 |
T |
A |
2: 32,187,168 (GRCm39) |
N89K |
probably damaging |
Het |
Got1 |
A |
G |
19: 43,491,376 (GRCm39) |
I358T |
possibly damaging |
Het |
Gpx6 |
C |
T |
13: 21,496,434 (GRCm39) |
Q3* |
probably null |
Het |
Grin1 |
T |
A |
2: 25,182,393 (GRCm39) |
H956L |
possibly damaging |
Het |
Grin2d |
A |
G |
7: 45,506,205 (GRCm39) |
V562A |
probably damaging |
Het |
Grm6 |
A |
G |
11: 50,748,104 (GRCm39) |
I405V |
probably benign |
Het |
Hcar2 |
C |
G |
5: 124,002,513 (GRCm39) |
G330A |
probably benign |
Het |
Hcfc1 |
T |
C |
X: 73,009,552 (GRCm39) |
K20E |
probably damaging |
Het |
Iars1 |
T |
A |
13: 49,878,139 (GRCm39) |
Y888N |
probably damaging |
Het |
Ifi206 |
A |
T |
1: 173,308,432 (GRCm39) |
H521Q |
probably benign |
Het |
Impg1 |
A |
G |
9: 80,305,732 (GRCm39) |
S112P |
probably benign |
Het |
Incenp |
C |
A |
19: 9,855,054 (GRCm39) |
R619M |
unknown |
Het |
Incenp |
T |
A |
19: 9,855,055 (GRCm39) |
R619W |
unknown |
Het |
Kat2b |
A |
G |
17: 53,960,231 (GRCm39) |
E513G |
possibly damaging |
Het |
Kbtbd12 |
G |
T |
6: 88,595,003 (GRCm39) |
L276I |
probably damaging |
Het |
Kctd9 |
T |
A |
14: 67,971,613 (GRCm39) |
D229E |
probably damaging |
Het |
Kdm1b |
C |
T |
13: 47,216,553 (GRCm39) |
R308W |
probably damaging |
Het |
Kif2b |
G |
A |
11: 91,467,254 (GRCm39) |
P343L |
probably benign |
Het |
Kntc1 |
T |
G |
5: 123,954,825 (GRCm39) |
M2081R |
possibly damaging |
Het |
Lamc1 |
T |
C |
1: 153,107,486 (GRCm39) |
N1231S |
probably damaging |
Het |
Lclat1 |
T |
A |
17: 73,547,065 (GRCm39) |
Y327* |
probably null |
Het |
Lgals3bp |
G |
A |
11: 118,284,340 (GRCm39) |
T413I |
probably damaging |
Het |
Lin54 |
A |
G |
5: 100,607,597 (GRCm39) |
I250T |
probably damaging |
Het |
Lrp1 |
T |
C |
10: 127,394,002 (GRCm39) |
N2621S |
probably benign |
Het |
Lrrtm3 |
T |
A |
10: 63,923,781 (GRCm39) |
H462L |
probably benign |
Het |
Lysmd1 |
A |
G |
3: 95,042,297 (GRCm39) |
Y57C |
probably damaging |
Het |
Mccc1 |
C |
A |
3: 36,030,022 (GRCm39) |
M429I |
probably damaging |
Het |
Metrnl |
A |
G |
11: 121,598,750 (GRCm39) |
E40G |
probably benign |
Het |
Mios |
T |
A |
6: 8,222,464 (GRCm39) |
M466K |
probably benign |
Het |
Mrgpra1 |
A |
G |
7: 46,985,218 (GRCm39) |
S154P |
probably damaging |
Het |
Mrpl24 |
T |
C |
3: 87,829,357 (GRCm39) |
|
probably null |
Het |
Myo1f |
A |
G |
17: 33,817,165 (GRCm39) |
N736S |
possibly damaging |
Het |
Myo1h |
A |
G |
5: 114,498,660 (GRCm39) |
I919V |
possibly damaging |
Het |
Nampt |
T |
C |
12: 32,898,713 (GRCm39) |
L443P |
possibly damaging |
Het |
Ndufaf2 |
C |
G |
13: 108,189,314 (GRCm39) |
A145P |
probably damaging |
Het |
Nek10 |
A |
T |
14: 14,855,714 (GRCm38) |
T403S |
probably benign |
Het |
Nme8 |
C |
A |
13: 19,842,100 (GRCm39) |
V219L |
probably damaging |
Het |
Nps |
T |
A |
7: 134,870,517 (GRCm39) |
L13Q |
probably damaging |
Het |
Nutm1 |
G |
A |
2: 112,079,281 (GRCm39) |
A878V |
probably benign |
Het |
Ogdh |
T |
C |
11: 6,299,875 (GRCm39) |
F794L |
probably damaging |
Het |
Or14a259 |
C |
A |
7: 86,012,943 (GRCm39) |
G201C |
probably damaging |
Het |
Or14c39 |
T |
C |
7: 86,343,736 (GRCm39) |
L24P |
probably damaging |
Het |
Or2t35 |
A |
C |
14: 14,407,729 (GRCm38) |
Y167S |
possibly damaging |
Het |
Or4f56 |
A |
T |
2: 111,703,395 (GRCm39) |
D268E |
possibly damaging |
Het |
Or5a3 |
A |
T |
19: 12,400,341 (GRCm39) |
I223F |
probably damaging |
Het |
Or5g29 |
A |
G |
2: 85,421,282 (GRCm39) |
T133A |
probably benign |
Het |
Pik3cg |
T |
C |
12: 32,255,198 (GRCm39) |
E263G |
probably damaging |
Het |
Pikfyve |
A |
G |
1: 65,307,005 (GRCm39) |
T1798A |
probably benign |
Het |
Poldip3 |
T |
C |
15: 83,015,702 (GRCm39) |
Y305C |
probably damaging |
Het |
Prkdc |
T |
C |
16: 15,466,840 (GRCm39) |
I107T |
probably benign |
Het |
Prmt2 |
A |
G |
10: 76,062,055 (GRCm39) |
I50T |
probably damaging |
Het |
Ptprd |
T |
C |
4: 76,058,790 (GRCm39) |
T168A |
probably benign |
Het |
Pudp |
A |
G |
18: 50,701,136 (GRCm39) |
V199A |
probably damaging |
Het |
Rab3c |
T |
C |
13: 110,198,434 (GRCm39) |
E198G |
probably benign |
Het |
Rasl12 |
A |
G |
9: 65,320,730 (GRCm39) |
Y156C |
probably damaging |
Het |
Rbm12 |
T |
C |
2: 155,938,484 (GRCm39) |
D596G |
possibly damaging |
Het |
Rbm6 |
T |
C |
9: 107,664,551 (GRCm39) |
E694G |
probably benign |
Het |
Rif1 |
T |
C |
2: 52,002,759 (GRCm39) |
V2071A |
probably damaging |
Het |
Ripply2 |
A |
T |
9: 86,901,849 (GRCm39) |
N125I |
probably damaging |
Het |
Rps6kc1 |
A |
T |
1: 190,482,385 (GRCm39) |
H284Q |
probably benign |
Het |
Scara3 |
A |
T |
14: 66,190,950 (GRCm39) |
M1K |
probably null |
Het |
Sfswap |
A |
G |
5: 129,590,147 (GRCm39) |
T215A |
probably damaging |
Het |
Shroom2 |
A |
C |
X: 151,443,903 (GRCm39) |
F421V |
probably benign |
Het |
Sipa1l3 |
A |
G |
7: 29,077,066 (GRCm39) |
V902A |
probably damaging |
Het |
Slamf8 |
G |
T |
1: 172,411,781 (GRCm39) |
P238Q |
probably damaging |
Het |
Slc44a3 |
T |
C |
3: 121,320,723 (GRCm39) |
T93A |
possibly damaging |
Het |
Slc5a7 |
A |
T |
17: 54,585,728 (GRCm39) |
I363N |
probably damaging |
Het |
Slc66a1 |
G |
T |
4: 139,027,312 (GRCm39) |
H343Q |
probably benign |
Het |
Slc7a2 |
T |
A |
8: 41,364,095 (GRCm39) |
M436K |
probably benign |
Het |
Spindoc |
A |
G |
19: 7,351,456 (GRCm39) |
S223P |
probably benign |
Het |
Stk11ip |
T |
C |
1: 75,506,925 (GRCm39) |
F669L |
possibly damaging |
Het |
Sun3 |
G |
A |
11: 8,988,266 (GRCm39) |
L19F |
probably benign |
Het |
Sycp1 |
C |
A |
3: 102,760,805 (GRCm39) |
A703S |
possibly damaging |
Het |
Tas2r139 |
T |
G |
6: 42,118,218 (GRCm39) |
F117V |
probably damaging |
Het |
Tdrd6 |
T |
C |
17: 43,936,467 (GRCm39) |
Y1527C |
probably damaging |
Het |
Tenm4 |
A |
C |
7: 96,423,253 (GRCm39) |
K683Q |
probably damaging |
Het |
Tfeb |
T |
A |
17: 48,099,152 (GRCm39) |
|
probably null |
Het |
Tmco4 |
T |
C |
4: 138,725,350 (GRCm39) |
S121P |
probably damaging |
Het |
Tmprss11d |
C |
T |
5: 86,454,140 (GRCm39) |
V222M |
probably damaging |
Het |
Tnks1bp1 |
T |
C |
2: 84,893,378 (GRCm39) |
W440R |
probably damaging |
Het |
Trp53bp2 |
A |
G |
1: 182,276,562 (GRCm39) |
T848A |
probably benign |
Het |
Tssk1 |
G |
A |
16: 17,712,926 (GRCm39) |
R237H |
probably benign |
Het |
Ttll4 |
A |
T |
1: 74,718,166 (GRCm39) |
T6S |
possibly damaging |
Het |
Ttn |
G |
T |
2: 76,552,141 (GRCm39) |
Y29419* |
probably null |
Het |
Ttn |
A |
G |
2: 76,599,947 (GRCm39) |
Y19076H |
probably damaging |
Het |
Ubr3 |
T |
A |
2: 69,789,947 (GRCm39) |
V867D |
probably damaging |
Het |
Usp29 |
A |
G |
7: 6,964,390 (GRCm39) |
T78A |
probably damaging |
Het |
Utrn |
T |
G |
10: 12,530,489 (GRCm39) |
Q2108P |
probably benign |
Het |
Vcan |
T |
C |
13: 89,853,908 (GRCm39) |
N351D |
probably damaging |
Het |
Vmn1r61 |
A |
T |
7: 5,614,124 (GRCm39) |
Y63* |
probably null |
Het |
Vmn1r61 |
A |
T |
7: 5,614,126 (GRCm39) |
Y63N |
probably benign |
Het |
Vmn1r85 |
A |
T |
7: 12,818,788 (GRCm39) |
W119R |
probably damaging |
Het |
Zbtb21 |
A |
C |
16: 97,751,655 (GRCm39) |
V190G |
possibly damaging |
Het |
Zfp157 |
C |
A |
5: 138,443,051 (GRCm39) |
T14N |
probably damaging |
Het |
Zfp942 |
A |
T |
17: 22,148,400 (GRCm39) |
H76Q |
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 |
|
R1677:Dnah3
|
UTSW |
7 |
119,527,963 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|