Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700056E22Rik |
C |
T |
1: 184,033,505 |
S119N |
probably benign |
Het |
4930503L19Rik |
T |
A |
18: 70,467,926 |
|
probably null |
Het |
5430419D17Rik |
T |
C |
7: 131,238,182 |
L611P |
probably damaging |
Het |
Adam18 |
T |
C |
8: 24,647,853 |
T324A |
probably benign |
Het |
Adamts20 |
T |
A |
15: 94,286,371 |
Q1517L |
probably benign |
Het |
AI429214 |
A |
G |
8: 36,994,319 |
Q207R |
probably benign |
Het |
Arhgef7 |
A |
G |
8: 11,819,659 |
T432A |
possibly damaging |
Het |
Atad2b |
A |
G |
12: 5,031,784 |
N1231S |
probably benign |
Het |
Atp13a1 |
T |
C |
8: 69,802,144 |
|
probably null |
Het |
Atp6v0a1 |
T |
A |
11: 101,055,491 |
L770* |
probably null |
Het |
Atp8b3 |
T |
C |
10: 80,534,198 |
N127S |
probably damaging |
Het |
B3gnt5 |
T |
A |
16: 19,770,010 |
D326E |
probably damaging |
Het |
Birc6 |
T |
A |
17: 74,565,861 |
S372T |
probably damaging |
Het |
Btbd9 |
T |
A |
17: 30,299,633 |
D451V |
probably damaging |
Het |
Cd46 |
T |
C |
1: 195,041,992 |
*366W |
probably null |
Het |
Cdh18 |
T |
A |
15: 23,473,995 |
D650E |
probably damaging |
Het |
Cenpc1 |
A |
T |
5: 86,037,908 |
V248E |
probably damaging |
Het |
Cep152 |
A |
G |
2: 125,594,899 |
S574P |
probably benign |
Het |
Chd2 |
A |
G |
7: 73,478,664 |
S858P |
probably damaging |
Het |
Cib4 |
T |
C |
5: 30,488,594 |
D110G |
probably damaging |
Het |
Col9a2 |
T |
A |
4: 121,039,788 |
|
probably null |
Het |
Csmd2 |
A |
T |
4: 128,496,188 |
I2239F |
possibly damaging |
Het |
Csmd3 |
C |
A |
15: 47,659,089 |
G2728V |
probably damaging |
Het |
Cxcl1 |
A |
T |
5: 90,891,767 |
K85* |
probably null |
Het |
Cyp2d11 |
A |
G |
15: 82,389,529 |
L416P |
possibly damaging |
Het |
Daam1 |
A |
C |
12: 71,915,784 |
K90T |
unknown |
Het |
Depdc5 |
T |
A |
5: 32,986,966 |
M1435K |
possibly damaging |
Het |
Diexf |
A |
T |
1: 193,114,703 |
N573K |
probably damaging |
Het |
Dip2c |
G |
A |
13: 9,576,908 |
A632T |
probably damaging |
Het |
Dld |
A |
T |
12: 31,334,054 |
I350N |
probably damaging |
Het |
Dmtf1 |
T |
A |
5: 9,127,987 |
I391F |
possibly damaging |
Het |
Efemp1 |
A |
G |
11: 28,854,538 |
E22G |
probably damaging |
Het |
Ephb6 |
A |
G |
6: 41,614,104 |
D65G |
probably damaging |
Het |
Fsip2 |
A |
T |
2: 82,977,092 |
T1252S |
probably benign |
Het |
Gm13084 |
T |
C |
4: 143,811,858 |
Y181C |
probably damaging |
Het |
Gm4847 |
A |
G |
1: 166,630,255 |
S510P |
probably benign |
Het |
Golga4 |
T |
C |
9: 118,537,273 |
I365T |
probably damaging |
Het |
Gp2 |
A |
T |
7: 119,454,543 |
L65Q |
probably damaging |
Het |
Ibtk |
T |
C |
9: 85,743,577 |
Y40C |
probably damaging |
Het |
Ice1 |
C |
A |
13: 70,602,427 |
V1847L |
probably benign |
Het |
Ift172 |
C |
T |
5: 31,265,355 |
R917H |
probably benign |
Het |
Itgae |
C |
T |
11: 73,138,509 |
Q1037* |
probably null |
Het |
Kbtbd7 |
A |
G |
14: 79,427,430 |
E234G |
possibly damaging |
Het |
Khsrp |
T |
C |
17: 57,025,576 |
T235A |
probably benign |
Het |
Klk13 |
T |
C |
7: 43,721,158 |
|
probably null |
Het |
Lrfn5 |
G |
A |
12: 61,843,437 |
G504D |
probably damaging |
Het |
Macf1 |
A |
G |
4: 123,476,000 |
V91A |
possibly damaging |
Het |
Map6 |
G |
A |
7: 99,336,743 |
G821D |
possibly damaging |
Het |
Mark1 |
A |
C |
1: 184,921,604 |
V167G |
probably damaging |
Het |
Mrgprf |
T |
A |
7: 145,308,256 |
L185Q |
probably damaging |
Het |
Mtor |
T |
A |
4: 148,550,188 |
V2422D |
probably damaging |
Het |
Myh13 |
T |
A |
11: 67,332,520 |
I222N |
probably damaging |
Het |
Myh7b |
G |
A |
2: 155,620,427 |
C350Y |
probably benign |
Het |
Nfix |
G |
A |
8: 84,726,526 |
R300C |
probably damaging |
Het |
Olfm3 |
C |
A |
3: 115,101,986 |
S172R |
probably benign |
Het |
Olfr1168 |
A |
T |
2: 88,184,978 |
T34S |
probably benign |
Het |
Olfr1231 |
A |
T |
2: 89,303,184 |
I136N |
probably damaging |
Het |
Olfr342 |
A |
G |
2: 36,528,008 |
I199V |
probably benign |
Het |
Olfr70 |
A |
G |
4: 43,696,706 |
S156P |
probably damaging |
Het |
Olfr912 |
T |
A |
9: 38,581,283 |
V2D |
possibly damaging |
Het |
Pacs1 |
A |
T |
19: 5,143,829 |
D557E |
probably damaging |
Het |
Pde1c |
A |
G |
6: 56,361,815 |
F11L |
probably benign |
Het |
Phactr2 |
T |
C |
10: 13,247,139 |
D343G |
possibly damaging |
Het |
Piezo2 |
T |
C |
18: 63,015,802 |
Y2659C |
probably damaging |
Het |
Pkd2l2 |
A |
G |
18: 34,428,252 |
T438A |
probably damaging |
Het |
Pld2 |
T |
C |
11: 70,557,081 |
W857R |
probably damaging |
Het |
Plxnb1 |
T |
C |
9: 109,102,142 |
V410A |
possibly damaging |
Het |
Ptger2 |
A |
G |
14: 44,989,500 |
Y179C |
probably damaging |
Het |
Ptpro |
T |
A |
6: 137,443,594 |
V1007D |
probably damaging |
Het |
Rcan1 |
A |
T |
16: 92,393,520 |
M177K |
probably benign |
Het |
Rilpl1 |
A |
G |
5: 124,501,871 |
S156P |
probably benign |
Het |
Rilpl1 |
A |
G |
5: 124,501,888 |
I122T |
possibly damaging |
Het |
Rims4 |
C |
T |
2: 163,863,929 |
V262M |
possibly damaging |
Het |
Rpa1 |
C |
T |
11: 75,312,973 |
|
probably null |
Het |
Saxo2 |
A |
G |
7: 82,634,870 |
V260A |
probably benign |
Het |
Sel1l |
T |
C |
12: 91,824,860 |
Y309C |
probably damaging |
Het |
Setd1b |
GCCCCCCC |
GCCCCCCCCCCCCC |
5: 123,160,703 |
|
probably benign |
Het |
Slc33a1 |
A |
G |
3: 63,943,304 |
F533S |
probably benign |
Het |
Slc38a4 |
C |
T |
15: 97,005,858 |
V421M |
probably benign |
Het |
Snx14 |
A |
G |
9: 88,400,721 |
|
probably null |
Het |
Spef2 |
A |
G |
15: 9,716,396 |
F368S |
probably damaging |
Het |
Sri |
A |
T |
5: 8,059,381 |
Q55L |
probably damaging |
Het |
Stat4 |
A |
G |
1: 52,096,820 |
I429M |
probably damaging |
Het |
Stkld1 |
A |
T |
2: 26,951,450 |
Q469L |
probably benign |
Het |
Tm9sf1 |
T |
C |
14: 55,642,935 |
T2A |
possibly damaging |
Het |
Tmco5 |
A |
G |
2: 116,883,218 |
T122A |
probably benign |
Het |
Tmem59l |
G |
A |
8: 70,486,060 |
P124S |
possibly damaging |
Het |
Tmem81 |
G |
A |
1: 132,507,924 |
R156Q |
probably damaging |
Het |
Trpv6 |
T |
A |
6: 41,625,188 |
T396S |
probably benign |
Het |
Usp24 |
T |
A |
4: 106,371,079 |
Y780* |
probably null |
Het |
Vmn1r120 |
A |
G |
7: 21,053,016 |
C257R |
probably damaging |
Het |
Vmn2r53 |
A |
G |
7: 12,601,392 |
F114L |
probably damaging |
Het |
Vwf |
A |
G |
6: 125,643,006 |
E1549G |
probably damaging |
Het |
Zfp626 |
G |
A |
7: 27,818,482 |
R296H |
probably damaging |
Het |
|
Other mutations in Dnah14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01086:Dnah14
|
APN |
1 |
181,752,046 (GRCm38) |
missense |
probably benign |
0.17 |
IGL01764:Dnah14
|
APN |
1 |
181,744,777 (GRCm38) |
missense |
probably benign |
0.00 |
IGL03218:Dnah14
|
APN |
1 |
181,755,269 (GRCm38) |
missense |
probably benign |
0.02 |
IGL03290:Dnah14
|
APN |
1 |
181,763,978 (GRCm38) |
splice site |
probably benign |
|
IGL03384:Dnah14
|
APN |
1 |
181,745,949 (GRCm38) |
missense |
probably benign |
0.03 |
R0009:Dnah14
|
UTSW |
1 |
181,769,407 (GRCm38) |
splice site |
probably benign |
|
R0125:Dnah14
|
UTSW |
1 |
181,752,063 (GRCm38) |
missense |
probably damaging |
0.99 |
R0579:Dnah14
|
UTSW |
1 |
181,744,747 (GRCm38) |
missense |
possibly damaging |
0.72 |
R0973:Dnah14
|
UTSW |
1 |
181,752,145 (GRCm38) |
missense |
probably damaging |
1.00 |
R0974:Dnah14
|
UTSW |
1 |
181,752,145 (GRCm38) |
missense |
probably damaging |
1.00 |
R1609:Dnah14
|
UTSW |
1 |
181,750,177 (GRCm38) |
missense |
probably damaging |
0.97 |
R1860:Dnah14
|
UTSW |
1 |
181,763,960 (GRCm38) |
missense |
probably damaging |
1.00 |
R2050:Dnah14
|
UTSW |
1 |
181,752,562 (GRCm38) |
missense |
probably damaging |
1.00 |
R2974:Dnah14
|
UTSW |
1 |
181,755,241 (GRCm38) |
critical splice acceptor site |
probably null |
|
R4715:Dnah14
|
UTSW |
1 |
181,757,223 (GRCm38) |
missense |
probably damaging |
1.00 |
R5076:Dnah14
|
UTSW |
1 |
181,757,234 (GRCm38) |
missense |
probably benign |
0.01 |
R5424:Dnah14
|
UTSW |
1 |
181,763,310 (GRCm38) |
missense |
possibly damaging |
0.95 |
R5808:Dnah14
|
UTSW |
1 |
181,741,159 (GRCm38) |
missense |
possibly damaging |
0.72 |
R5997:Dnah14
|
UTSW |
1 |
181,770,105 (GRCm38) |
missense |
probably benign |
0.00 |
R6052:Dnah14
|
UTSW |
1 |
181,666,487 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6061:Dnah14
|
UTSW |
1 |
181,709,051 (GRCm38) |
missense |
probably damaging |
1.00 |
R6089:Dnah14
|
UTSW |
1 |
181,750,154 (GRCm38) |
missense |
probably damaging |
1.00 |
R6092:Dnah14
|
UTSW |
1 |
181,621,833 (GRCm38) |
missense |
probably benign |
0.13 |
R6145:Dnah14
|
UTSW |
1 |
181,666,417 (GRCm38) |
missense |
probably benign |
0.00 |
R6163:Dnah14
|
UTSW |
1 |
181,666,361 (GRCm38) |
missense |
probably benign |
0.33 |
R6246:Dnah14
|
UTSW |
1 |
181,680,888 (GRCm38) |
missense |
probably benign |
0.00 |
R6302:Dnah14
|
UTSW |
1 |
181,601,206 (GRCm38) |
missense |
possibly damaging |
0.96 |
R6306:Dnah14
|
UTSW |
1 |
181,585,024 (GRCm38) |
frame shift |
probably null |
|
R6326:Dnah14
|
UTSW |
1 |
181,783,556 (GRCm38) |
missense |
probably damaging |
1.00 |
R6348:Dnah14
|
UTSW |
1 |
181,626,720 (GRCm38) |
missense |
possibly damaging |
0.83 |
R6367:Dnah14
|
UTSW |
1 |
181,755,386 (GRCm38) |
splice site |
probably null |
|
R6376:Dnah14
|
UTSW |
1 |
181,605,894 (GRCm38) |
missense |
possibly damaging |
0.79 |
R6389:Dnah14
|
UTSW |
1 |
181,651,202 (GRCm38) |
critical splice donor site |
probably null |
|
R6433:Dnah14
|
UTSW |
1 |
181,651,657 (GRCm38) |
missense |
probably damaging |
0.99 |
R6454:Dnah14
|
UTSW |
1 |
181,783,705 (GRCm38) |
missense |
probably damaging |
1.00 |
R6476:Dnah14
|
UTSW |
1 |
181,744,768 (GRCm38) |
missense |
probably benign |
0.26 |
R6523:Dnah14
|
UTSW |
1 |
181,643,621 (GRCm38) |
missense |
probably benign |
0.00 |
R6529:Dnah14
|
UTSW |
1 |
181,666,469 (GRCm38) |
missense |
probably damaging |
0.98 |
R6538:Dnah14
|
UTSW |
1 |
181,584,985 (GRCm38) |
missense |
unknown |
|
R6546:Dnah14
|
UTSW |
1 |
181,738,987 (GRCm38) |
missense |
probably damaging |
1.00 |
R6752:Dnah14
|
UTSW |
1 |
181,593,452 (GRCm38) |
missense |
probably benign |
0.07 |
R6762:Dnah14
|
UTSW |
1 |
181,757,259 (GRCm38) |
missense |
probably damaging |
1.00 |
R6786:Dnah14
|
UTSW |
1 |
181,641,405 (GRCm38) |
missense |
probably benign |
0.21 |
R6849:Dnah14
|
UTSW |
1 |
181,808,945 (GRCm38) |
missense |
probably benign |
0.00 |
R6877:Dnah14
|
UTSW |
1 |
181,628,432 (GRCm38) |
missense |
possibly damaging |
0.82 |
R6912:Dnah14
|
UTSW |
1 |
181,750,183 (GRCm38) |
missense |
possibly damaging |
0.83 |
R6919:Dnah14
|
UTSW |
1 |
181,585,066 (GRCm38) |
missense |
probably benign |
0.04 |
R6924:Dnah14
|
UTSW |
1 |
181,627,952 (GRCm38) |
missense |
probably benign |
0.04 |
R6957:Dnah14
|
UTSW |
1 |
181,785,175 (GRCm38) |
missense |
possibly damaging |
0.92 |
R6980:Dnah14
|
UTSW |
1 |
181,648,230 (GRCm38) |
missense |
probably benign |
0.00 |
R7018:Dnah14
|
UTSW |
1 |
181,626,944 (GRCm38) |
missense |
possibly damaging |
0.55 |
R7046:Dnah14
|
UTSW |
1 |
181,623,003 (GRCm38) |
missense |
probably benign |
0.01 |
R7058:Dnah14
|
UTSW |
1 |
181,698,049 (GRCm38) |
missense |
probably benign |
0.00 |
R7068:Dnah14
|
UTSW |
1 |
181,769,790 (GRCm38) |
missense |
probably benign |
0.35 |
R7115:Dnah14
|
UTSW |
1 |
181,720,145 (GRCm38) |
missense |
probably damaging |
1.00 |
R7130:Dnah14
|
UTSW |
1 |
181,745,958 (GRCm38) |
nonsense |
probably null |
|
R7165:Dnah14
|
UTSW |
1 |
181,704,535 (GRCm38) |
missense |
probably benign |
0.00 |
R7169:Dnah14
|
UTSW |
1 |
181,702,365 (GRCm38) |
missense |
probably benign |
0.00 |
R7184:Dnah14
|
UTSW |
1 |
181,704,529 (GRCm38) |
nonsense |
probably null |
|
R7232:Dnah14
|
UTSW |
1 |
181,757,363 (GRCm38) |
missense |
probably damaging |
1.00 |
R7260:Dnah14
|
UTSW |
1 |
181,706,744 (GRCm38) |
missense |
probably damaging |
0.99 |
R7276:Dnah14
|
UTSW |
1 |
181,685,807 (GRCm38) |
missense |
probably benign |
0.41 |
R7290:Dnah14
|
UTSW |
1 |
181,628,174 (GRCm38) |
missense |
probably benign |
0.20 |
R7314:Dnah14
|
UTSW |
1 |
181,785,254 (GRCm38) |
splice site |
probably null |
|
R7326:Dnah14
|
UTSW |
1 |
181,598,403 (GRCm38) |
missense |
probably benign |
0.02 |
R7336:Dnah14
|
UTSW |
1 |
181,797,734 (GRCm38) |
missense |
probably damaging |
0.96 |
R7363:Dnah14
|
UTSW |
1 |
181,690,524 (GRCm38) |
splice site |
probably null |
|
R7371:Dnah14
|
UTSW |
1 |
181,626,885 (GRCm38) |
missense |
probably benign |
0.05 |
R7376:Dnah14
|
UTSW |
1 |
181,763,402 (GRCm38) |
missense |
probably benign |
0.03 |
R7418:Dnah14
|
UTSW |
1 |
181,616,742 (GRCm38) |
missense |
possibly damaging |
0.92 |
R7473:Dnah14
|
UTSW |
1 |
181,752,139 (GRCm38) |
missense |
probably damaging |
0.99 |
R7514:Dnah14
|
UTSW |
1 |
181,628,067 (GRCm38) |
missense |
probably damaging |
0.96 |
R7555:Dnah14
|
UTSW |
1 |
181,770,054 (GRCm38) |
missense |
probably benign |
0.26 |
R7641:Dnah14
|
UTSW |
1 |
181,707,533 (GRCm38) |
missense |
probably benign |
0.01 |
R7663:Dnah14
|
UTSW |
1 |
181,752,155 (GRCm38) |
splice site |
probably null |
|
R7674:Dnah14
|
UTSW |
1 |
181,707,533 (GRCm38) |
missense |
probably benign |
0.01 |
R7680:Dnah14
|
UTSW |
1 |
181,685,800 (GRCm38) |
missense |
probably benign |
0.15 |
R7709:Dnah14
|
UTSW |
1 |
181,702,484 (GRCm38) |
critical splice donor site |
probably null |
|
R7842:Dnah14
|
UTSW |
1 |
181,627,898 (GRCm38) |
missense |
probably damaging |
0.99 |
R7861:Dnah14
|
UTSW |
1 |
181,616,759 (GRCm38) |
missense |
probably damaging |
1.00 |
R7988:Dnah14
|
UTSW |
1 |
181,783,574 (GRCm38) |
missense |
probably damaging |
0.97 |
R8016:Dnah14
|
UTSW |
1 |
181,648,311 (GRCm38) |
missense |
probably benign |
0.05 |
R8042:Dnah14
|
UTSW |
1 |
181,643,631 (GRCm38) |
critical splice donor site |
probably null |
|
R8071:Dnah14
|
UTSW |
1 |
181,615,894 (GRCm38) |
missense |
possibly damaging |
0.84 |
R8086:Dnah14
|
UTSW |
1 |
181,766,232 (GRCm38) |
missense |
probably damaging |
1.00 |
R8095:Dnah14
|
UTSW |
1 |
181,806,032 (GRCm38) |
nonsense |
probably null |
|
R8139:Dnah14
|
UTSW |
1 |
181,755,288 (GRCm38) |
missense |
probably damaging |
1.00 |
R8176:Dnah14
|
UTSW |
1 |
181,657,033 (GRCm38) |
missense |
probably damaging |
0.96 |
R8193:Dnah14
|
UTSW |
1 |
181,688,205 (GRCm38) |
missense |
probably damaging |
1.00 |
R8197:Dnah14
|
UTSW |
1 |
181,690,101 (GRCm38) |
missense |
possibly damaging |
0.94 |
R8209:Dnah14
|
UTSW |
1 |
181,795,545 (GRCm38) |
missense |
possibly damaging |
0.69 |
R8226:Dnah14
|
UTSW |
1 |
181,795,545 (GRCm38) |
missense |
possibly damaging |
0.69 |
R8251:Dnah14
|
UTSW |
1 |
181,664,865 (GRCm38) |
missense |
probably damaging |
1.00 |
R8264:Dnah14
|
UTSW |
1 |
181,744,792 (GRCm38) |
missense |
probably damaging |
0.99 |
R8284:Dnah14
|
UTSW |
1 |
181,773,811 (GRCm38) |
missense |
probably benign |
0.03 |
R8289:Dnah14
|
UTSW |
1 |
181,716,215 (GRCm38) |
nonsense |
probably null |
|
R8323:Dnah14
|
UTSW |
1 |
181,704,544 (GRCm38) |
missense |
probably benign |
0.01 |
R8442:Dnah14
|
UTSW |
1 |
181,741,284 (GRCm38) |
missense |
probably damaging |
0.97 |
R8458:Dnah14
|
UTSW |
1 |
181,806,012 (GRCm38) |
missense |
|
|
R8507:Dnah14
|
UTSW |
1 |
181,641,414 (GRCm38) |
missense |
probably benign |
0.02 |
R8509:Dnah14
|
UTSW |
1 |
181,814,655 (GRCm38) |
missense |
|
|
R8520:Dnah14
|
UTSW |
1 |
181,653,638 (GRCm38) |
missense |
probably damaging |
1.00 |
R8530:Dnah14
|
UTSW |
1 |
181,664,946 (GRCm38) |
missense |
probably damaging |
1.00 |
R8703:Dnah14
|
UTSW |
1 |
181,666,011 (GRCm38) |
nonsense |
probably null |
|
R8710:Dnah14
|
UTSW |
1 |
181,690,311 (GRCm38) |
missense |
probably benign |
0.04 |
R8752:Dnah14
|
UTSW |
1 |
181,628,016 (GRCm38) |
missense |
probably benign |
0.00 |
R8792:Dnah14
|
UTSW |
1 |
181,814,624 (GRCm38) |
missense |
|
|
R8797:Dnah14
|
UTSW |
1 |
181,637,847 (GRCm38) |
missense |
probably benign |
0.19 |
R8821:Dnah14
|
UTSW |
1 |
181,792,004 (GRCm38) |
nonsense |
probably null |
|
R8834:Dnah14
|
UTSW |
1 |
181,616,750 (GRCm38) |
missense |
possibly damaging |
0.83 |
R8913:Dnah14
|
UTSW |
1 |
181,725,498 (GRCm38) |
missense |
probably benign |
0.01 |
R8925:Dnah14
|
UTSW |
1 |
181,680,756 (GRCm38) |
missense |
probably damaging |
1.00 |
R8927:Dnah14
|
UTSW |
1 |
181,680,756 (GRCm38) |
missense |
probably damaging |
1.00 |
R8934:Dnah14
|
UTSW |
1 |
181,622,723 (GRCm38) |
missense |
possibly damaging |
0.84 |
R9090:Dnah14
|
UTSW |
1 |
181,769,760 (GRCm38) |
missense |
probably benign |
0.33 |
R9169:Dnah14
|
UTSW |
1 |
181,605,816 (GRCm38) |
missense |
probably benign |
0.06 |
R9199:Dnah14
|
UTSW |
1 |
181,651,001 (GRCm38) |
missense |
possibly damaging |
0.50 |
R9212:Dnah14
|
UTSW |
1 |
181,801,287 (GRCm38) |
missense |
possibly damaging |
0.95 |
R9213:Dnah14
|
UTSW |
1 |
181,616,640 (GRCm38) |
critical splice donor site |
probably null |
|
R9271:Dnah14
|
UTSW |
1 |
181,769,760 (GRCm38) |
missense |
probably benign |
0.33 |
R9282:Dnah14
|
UTSW |
1 |
181,814,512 (GRCm38) |
missense |
|
|
R9350:Dnah14
|
UTSW |
1 |
181,734,804 (GRCm38) |
missense |
possibly damaging |
0.79 |
R9358:Dnah14
|
UTSW |
1 |
181,709,033 (GRCm38) |
missense |
probably benign |
0.01 |
R9436:Dnah14
|
UTSW |
1 |
181,680,783 (GRCm38) |
missense |
probably damaging |
1.00 |
R9484:Dnah14
|
UTSW |
1 |
181,797,746 (GRCm38) |
missense |
probably benign |
0.01 |
R9484:Dnah14
|
UTSW |
1 |
181,690,208 (GRCm38) |
missense |
probably benign |
0.45 |
R9486:Dnah14
|
UTSW |
1 |
181,680,929 (GRCm38) |
missense |
possibly damaging |
0.68 |
R9546:Dnah14
|
UTSW |
1 |
181,593,427 (GRCm38) |
critical splice acceptor site |
probably null |
|
R9547:Dnah14
|
UTSW |
1 |
181,593,427 (GRCm38) |
critical splice acceptor site |
probably null |
|
R9578:Dnah14
|
UTSW |
1 |
181,674,442 (GRCm38) |
missense |
probably benign |
0.16 |
R9654:Dnah14
|
UTSW |
1 |
181,766,339 (GRCm38) |
missense |
probably benign |
0.01 |
R9681:Dnah14
|
UTSW |
1 |
181,734,849 (GRCm38) |
missense |
possibly damaging |
0.91 |
R9683:Dnah14
|
UTSW |
1 |
181,598,944 (GRCm38) |
missense |
probably benign |
0.01 |
R9687:Dnah14
|
UTSW |
1 |
181,598,413 (GRCm38) |
missense |
probably benign |
0.01 |
R9718:Dnah14
|
UTSW |
1 |
181,622,979 (GRCm38) |
missense |
probably benign |
0.08 |
R9751:Dnah14
|
UTSW |
1 |
181,792,045 (GRCm38) |
missense |
probably damaging |
1.00 |
R9757:Dnah14
|
UTSW |
1 |
181,685,784 (GRCm38) |
missense |
probably benign |
0.03 |
RF007:Dnah14
|
UTSW |
1 |
181,685,809 (GRCm38) |
missense |
probably benign |
0.00 |
RF012:Dnah14
|
UTSW |
1 |
181,627,898 (GRCm38) |
missense |
probably damaging |
0.99 |
Z1176:Dnah14
|
UTSW |
1 |
181,757,351 (GRCm38) |
missense |
possibly damaging |
0.83 |
Z1177:Dnah14
|
UTSW |
1 |
181,690,320 (GRCm38) |
missense |
probably benign |
0.03 |
Z1177:Dnah14
|
UTSW |
1 |
181,766,304 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1177:Dnah14
|
UTSW |
1 |
181,763,334 (GRCm38) |
missense |
probably damaging |
1.00 |
|