Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adck2 |
T |
A |
6: 39,560,752 (GRCm39) |
V380E |
probably benign |
Het |
Anapc1 |
A |
T |
2: 128,470,549 (GRCm39) |
M1527K |
possibly damaging |
Het |
Arfgef3 |
T |
A |
10: 18,474,962 (GRCm39) |
I1575F |
probably damaging |
Het |
Atp4a |
G |
T |
7: 30,416,560 (GRCm39) |
G446C |
probably benign |
Het |
Bicra |
A |
T |
7: 15,709,070 (GRCm39) |
M1188K |
probably damaging |
Het |
Brd7 |
G |
A |
8: 89,072,478 (GRCm39) |
R331W |
probably benign |
Het |
Cactin |
A |
G |
10: 81,158,486 (GRCm39) |
T151A |
probably benign |
Het |
Cadps |
G |
A |
14: 12,376,675 (GRCm38) |
T1274M |
probably damaging |
Het |
Catsper3 |
T |
C |
13: 55,952,667 (GRCm39) |
M175T |
probably damaging |
Het |
Chd5 |
A |
G |
4: 152,450,589 (GRCm39) |
D605G |
probably damaging |
Het |
Chst12 |
G |
A |
5: 140,510,054 (GRCm39) |
R227H |
possibly damaging |
Het |
Cic |
T |
A |
7: 24,986,565 (GRCm39) |
S1299T |
probably damaging |
Het |
Cic |
C |
A |
7: 24,986,566 (GRCm39) |
S1299Y |
probably damaging |
Het |
Cimap1d |
C |
T |
10: 79,480,564 (GRCm39) |
|
probably null |
Het |
Cobl |
A |
T |
11: 12,204,524 (GRCm39) |
V644E |
probably benign |
Het |
Ddx31 |
A |
G |
2: 28,738,303 (GRCm39) |
T155A |
probably damaging |
Het |
Dnah8 |
T |
C |
17: 30,984,653 (GRCm39) |
I3117T |
probably damaging |
Het |
Doc2b |
A |
G |
11: 75,663,387 (GRCm39) |
V355A |
probably damaging |
Het |
Dock10 |
A |
T |
1: 80,556,340 (GRCm39) |
S578T |
probably benign |
Het |
Duox1 |
T |
C |
2: 122,163,878 (GRCm39) |
|
probably benign |
Het |
Epb41l5 |
T |
C |
1: 119,495,509 (GRCm39) |
|
probably null |
Het |
Fbp2 |
A |
T |
13: 63,001,862 (GRCm39) |
F118I |
probably damaging |
Het |
Fcer2a |
A |
G |
8: 3,738,796 (GRCm39) |
|
probably null |
Het |
Fmnl1 |
G |
A |
11: 103,072,996 (GRCm39) |
|
probably null |
Het |
Fry |
A |
T |
5: 150,183,811 (GRCm39) |
|
probably benign |
Het |
Git2 |
T |
C |
5: 114,871,290 (GRCm39) |
E208G |
probably damaging |
Het |
Hs6st3 |
T |
C |
14: 119,376,232 (GRCm39) |
F136L |
probably benign |
Het |
Hydin |
G |
A |
8: 111,124,655 (GRCm39) |
V555I |
probably benign |
Het |
Kcns1 |
A |
T |
2: 164,010,300 (GRCm39) |
I153N |
probably damaging |
Het |
Kmt2b |
A |
G |
7: 30,276,494 (GRCm39) |
L1726S |
probably damaging |
Het |
Loxl3 |
A |
G |
6: 83,027,114 (GRCm39) |
D615G |
probably damaging |
Het |
Negr1 |
T |
A |
3: 156,914,036 (GRCm39) |
|
probably benign |
Het |
Nfasc |
C |
A |
1: 132,564,731 (GRCm39) |
A70S |
probably benign |
Het |
Or4d1 |
T |
A |
11: 87,804,860 (GRCm39) |
N291Y |
probably damaging |
Het |
Or4p21 |
A |
T |
2: 88,276,889 (GRCm39) |
M131K |
possibly damaging |
Het |
Or52n4 |
A |
G |
7: 104,294,450 (GRCm39) |
M41T |
probably benign |
Het |
Or5g29 |
A |
G |
2: 85,421,154 (GRCm39) |
K90R |
probably benign |
Het |
Otud7a |
T |
C |
7: 63,346,992 (GRCm39) |
|
probably benign |
Het |
Pacs2 |
T |
C |
12: 113,032,890 (GRCm39) |
|
probably benign |
Het |
Pde7b |
A |
G |
10: 20,311,962 (GRCm39) |
C239R |
probably damaging |
Het |
Pdzd2 |
A |
T |
15: 12,368,027 (GRCm39) |
L2654Q |
probably damaging |
Het |
Pgap1 |
T |
C |
1: 54,575,110 (GRCm39) |
|
probably null |
Het |
Proz |
T |
A |
8: 13,115,356 (GRCm39) |
M124K |
probably benign |
Het |
Raet1d |
A |
G |
10: 22,247,328 (GRCm39) |
T135A |
probably benign |
Het |
Rapgef1 |
A |
G |
2: 29,592,682 (GRCm39) |
N558S |
possibly damaging |
Het |
Rpl7 |
C |
G |
1: 16,173,446 (GRCm39) |
G101A |
possibly damaging |
Het |
Sec14l1 |
G |
A |
11: 117,037,924 (GRCm39) |
|
probably benign |
Het |
Sfi1 |
CCTCTC |
CCTCTCTC |
11: 3,127,419 (GRCm39) |
|
probably benign |
Het |
Simc1 |
G |
T |
13: 54,698,338 (GRCm39) |
L1319F |
probably damaging |
Het |
Sspo |
A |
G |
6: 48,438,429 (GRCm39) |
E1499G |
possibly damaging |
Het |
Tango6 |
C |
T |
8: 107,473,993 (GRCm39) |
|
probably benign |
Het |
Tas2r118 |
T |
C |
6: 23,969,338 (GRCm39) |
Y241C |
probably damaging |
Het |
Tbck |
A |
G |
3: 132,430,636 (GRCm39) |
E344G |
probably benign |
Het |
Tcam1 |
G |
A |
11: 106,174,904 (GRCm39) |
E120K |
probably benign |
Het |
Thop1 |
T |
A |
10: 80,916,079 (GRCm39) |
|
probably benign |
Het |
Tmbim7 |
A |
T |
5: 3,716,866 (GRCm39) |
Y66F |
probably benign |
Het |
Tmc8 |
C |
T |
11: 117,677,207 (GRCm39) |
|
probably benign |
Het |
Tnfrsf19 |
A |
G |
14: 61,211,041 (GRCm39) |
S216P |
possibly damaging |
Het |
Trappc2l |
A |
G |
8: 123,341,132 (GRCm39) |
|
probably benign |
Het |
Trim67 |
A |
G |
8: 125,549,929 (GRCm39) |
R520G |
probably damaging |
Het |
Ubp1 |
T |
A |
9: 113,795,655 (GRCm39) |
|
probably null |
Het |
Vil1 |
T |
C |
1: 74,465,853 (GRCm39) |
L548P |
probably damaging |
Het |
Wdr3 |
A |
G |
3: 100,052,973 (GRCm39) |
V593A |
probably damaging |
Het |
Wdr5 |
A |
G |
2: 27,423,025 (GRCm39) |
Y243C |
probably damaging |
Het |
Zan |
T |
C |
5: 137,420,084 (GRCm39) |
T2858A |
unknown |
Het |
Zbtb37 |
A |
T |
1: 160,847,939 (GRCm39) |
V356E |
probably benign |
Het |
Zfp36 |
C |
T |
7: 28,077,759 (GRCm39) |
V50I |
probably damaging |
Het |
Zfp563 |
A |
T |
17: 33,323,659 (GRCm39) |
S85C |
possibly 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 |
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 |
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 |
|