Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca2 |
T |
A |
2: 25,324,345 (GRCm39) |
L234M |
probably benign |
Het |
Abca3 |
G |
A |
17: 24,596,753 (GRCm39) |
S402N |
probably benign |
Het |
Acad12 |
A |
T |
5: 121,745,544 (GRCm39) |
V249D |
probably benign |
Het |
Acp4 |
T |
C |
7: 43,904,428 (GRCm39) |
I212V |
probably benign |
Het |
Actl6a |
T |
A |
3: 32,772,723 (GRCm39) |
V233D |
probably damaging |
Het |
Aire |
T |
A |
10: 77,866,124 (GRCm39) |
Q533L |
probably damaging |
Het |
Aldh3b3 |
T |
C |
19: 4,018,517 (GRCm39) |
S411P |
probably benign |
Het |
Amer2 |
A |
G |
14: 60,617,206 (GRCm39) |
K467R |
probably damaging |
Het |
Apol9b |
A |
T |
15: 77,619,962 (GRCm39) |
I253F |
probably benign |
Het |
Arid1b |
A |
G |
17: 5,329,476 (GRCm39) |
|
probably null |
Het |
Atp6v0a4 |
T |
C |
6: 38,044,764 (GRCm39) |
T494A |
probably benign |
Het |
Atp6v1b2 |
A |
G |
8: 69,554,613 (GRCm39) |
D106G |
probably benign |
Het |
Avpr1b |
T |
C |
1: 131,527,839 (GRCm39) |
S121P |
probably damaging |
Het |
Bcl11a |
A |
C |
11: 24,114,724 (GRCm39) |
E689A |
probably damaging |
Het |
Brpf3 |
T |
G |
17: 29,040,297 (GRCm39) |
L906R |
probably benign |
Het |
Btn1a1 |
T |
C |
13: 23,644,638 (GRCm39) |
K287E |
probably benign |
Het |
Cacna1i |
A |
G |
15: 80,255,730 (GRCm39) |
H871R |
probably damaging |
Het |
Cd14 |
A |
T |
18: 36,858,567 (GRCm39) |
L296Q |
probably damaging |
Het |
Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
Colgalt1 |
G |
T |
8: 72,075,823 (GRCm39) |
W490L |
probably damaging |
Het |
Ctnna2 |
A |
G |
6: 77,613,732 (GRCm39) |
I273T |
possibly damaging |
Het |
Egfem1 |
T |
C |
3: 29,722,482 (GRCm39) |
Y404H |
possibly damaging |
Het |
Esm1 |
A |
T |
13: 113,353,230 (GRCm39) |
N171Y |
probably damaging |
Het |
Exoc1 |
T |
G |
5: 76,708,169 (GRCm39) |
|
probably null |
Het |
Fam243 |
A |
G |
16: 92,117,919 (GRCm39) |
V123A |
probably damaging |
Het |
Fcho1 |
A |
G |
8: 72,163,890 (GRCm39) |
I580T |
probably benign |
Het |
Fgfr1 |
A |
G |
8: 26,060,226 (GRCm39) |
H552R |
probably damaging |
Het |
Fsbp |
A |
G |
4: 11,583,906 (GRCm39) |
R202G |
probably damaging |
Het |
Gabra6 |
A |
G |
11: 42,207,388 (GRCm39) |
V231A |
probably damaging |
Het |
Gmeb1 |
A |
G |
4: 131,959,338 (GRCm39) |
S239P |
probably benign |
Het |
Gnpat |
T |
A |
8: 125,603,745 (GRCm39) |
Y208N |
probably damaging |
Het |
Il21 |
T |
C |
3: 37,279,674 (GRCm39) |
K114R |
possibly damaging |
Het |
Inhbc |
T |
C |
10: 127,206,162 (GRCm39) |
D35G |
possibly damaging |
Het |
Inpp4b |
A |
T |
8: 82,497,440 (GRCm39) |
T87S |
probably damaging |
Het |
Kcns2 |
T |
C |
15: 34,839,663 (GRCm39) |
I342T |
possibly damaging |
Het |
Ky |
A |
T |
9: 102,419,126 (GRCm39) |
T378S |
possibly damaging |
Het |
Lcat |
CAT |
C |
8: 106,668,446 (GRCm39) |
|
probably null |
Het |
Lrrc8d |
T |
C |
5: 105,960,523 (GRCm39) |
V311A |
probably benign |
Het |
Mief1 |
A |
G |
15: 80,133,803 (GRCm39) |
I287V |
probably damaging |
Het |
Mrpl47 |
A |
G |
3: 32,784,233 (GRCm39) |
V179A |
probably benign |
Het |
Mtcl1 |
T |
C |
17: 66,687,178 (GRCm39) |
K576R |
probably damaging |
Het |
Myh10 |
C |
A |
11: 68,703,884 (GRCm39) |
A1902E |
probably damaging |
Het |
Nlrp3 |
A |
G |
11: 59,449,228 (GRCm39) |
T837A |
possibly damaging |
Het |
Nr1i3 |
T |
C |
1: 171,044,963 (GRCm39) |
Y132H |
probably damaging |
Het |
Oit3 |
T |
C |
10: 59,263,762 (GRCm39) |
|
probably null |
Het |
Or12j4 |
A |
T |
7: 140,046,773 (GRCm39) |
I220F |
probably damaging |
Het |
Or2z2 |
A |
T |
11: 58,346,088 (GRCm39) |
M229K |
probably damaging |
Het |
Or4c100 |
A |
T |
2: 88,356,159 (GRCm39) |
R77S |
probably damaging |
Het |
Or5b113 |
T |
C |
19: 13,342,717 (GRCm39) |
S242P |
probably damaging |
Het |
Or5h25 |
T |
A |
16: 58,930,944 (GRCm39) |
I10F |
probably benign |
Het |
Or6k14 |
A |
G |
1: 173,927,599 (GRCm39) |
T192A |
probably benign |
Het |
Or7a42 |
T |
A |
10: 78,791,531 (GRCm39) |
V164E |
probably damaging |
Het |
Or9k2 |
G |
A |
10: 129,999,033 (GRCm39) |
T54I |
probably benign |
Het |
Pdlim4 |
T |
C |
11: 53,946,699 (GRCm39) |
E196G |
possibly damaging |
Het |
Pigs |
A |
G |
11: 78,228,673 (GRCm39) |
Y293C |
probably damaging |
Het |
Pkd1l2 |
A |
T |
8: 117,757,458 (GRCm39) |
S1527T |
possibly damaging |
Het |
Pkd2l1 |
A |
T |
19: 44,144,040 (GRCm39) |
Y344* |
probably null |
Het |
Pmp2 |
T |
C |
3: 10,247,284 (GRCm39) |
|
probably null |
Het |
Polr3e |
T |
C |
7: 120,538,521 (GRCm39) |
|
probably null |
Het |
Ppp3ca |
C |
G |
3: 136,587,209 (GRCm39) |
I230M |
probably benign |
Het |
Ppp5c |
T |
C |
7: 16,739,235 (GRCm39) |
H463R |
probably benign |
Het |
Ptger1 |
A |
G |
8: 84,395,926 (GRCm39) |
N328D |
probably benign |
Het |
Rhno1 |
A |
T |
6: 128,334,822 (GRCm39) |
I167N |
probably benign |
Het |
Rictor |
C |
A |
15: 6,764,849 (GRCm39) |
P34H |
probably damaging |
Het |
Rnf10 |
A |
C |
5: 115,383,924 (GRCm39) |
S630R |
probably damaging |
Het |
Rnf168 |
A |
G |
16: 32,117,942 (GRCm39) |
Q501R |
probably benign |
Het |
Rngtt |
T |
G |
4: 33,329,634 (GRCm39) |
|
probably null |
Het |
Samd9l |
G |
T |
6: 3,373,126 (GRCm39) |
F1378L |
probably damaging |
Het |
Slc9c1 |
T |
A |
16: 45,409,872 (GRCm39) |
M864K |
probably benign |
Het |
Slitrk5 |
T |
C |
14: 111,917,951 (GRCm39) |
F525S |
probably damaging |
Het |
Sox6 |
T |
C |
7: 115,076,290 (GRCm39) |
M784V |
probably benign |
Het |
Spata31e4 |
A |
T |
13: 50,855,123 (GRCm39) |
T254S |
probably damaging |
Het |
Spint2 |
C |
T |
7: 28,959,791 (GRCm39) |
|
probably null |
Het |
Ssh1 |
A |
T |
5: 114,093,906 (GRCm39) |
I276N |
probably damaging |
Het |
Trank1 |
T |
A |
9: 111,221,939 (GRCm39) |
V2892D |
probably benign |
Het |
Ttn |
C |
A |
2: 76,581,384 (GRCm39) |
E21424* |
probably null |
Het |
Usp17lc |
T |
C |
7: 103,068,055 (GRCm39) |
I450T |
probably benign |
Het |
Vcan |
A |
G |
13: 89,852,854 (GRCm39) |
V702A |
probably benign |
Het |
Vmn1r36 |
TA |
TAA |
6: 66,693,517 (GRCm39) |
|
probably null |
Het |
Vmn2r51 |
G |
T |
7: 9,833,873 (GRCm39) |
D388E |
probably benign |
Het |
Zfp106 |
A |
C |
2: 120,364,245 (GRCm39) |
S721A |
probably damaging |
Het |
Zfp106 |
G |
A |
2: 120,364,244 (GRCm39) |
S721L |
probably damaging |
Het |
Zfp189 |
T |
A |
4: 49,529,342 (GRCm39) |
H148Q |
possibly damaging |
Het |
Zfp352 |
A |
T |
4: 90,112,046 (GRCm39) |
Y62F |
probably benign |
Het |
Zfp839 |
T |
C |
12: 110,821,891 (GRCm39) |
V235A |
probably damaging |
Het |
Zfp871 |
T |
C |
17: 32,994,308 (GRCm39) |
Y289C |
probably damaging |
Het |
|
Other mutations in Dnah7a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00479:Dnah7a
|
APN |
1 |
53,458,843 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00510:Dnah7a
|
APN |
1 |
53,540,701 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00545:Dnah7a
|
APN |
1 |
53,496,905 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01320:Dnah7a
|
APN |
1 |
53,473,205 (GRCm39) |
missense |
probably benign |
0.32 |
IGL01322:Dnah7a
|
APN |
1 |
53,473,205 (GRCm39) |
missense |
probably benign |
0.32 |
IGL01357:Dnah7a
|
APN |
1 |
53,701,540 (GRCm39) |
missense |
probably benign |
|
IGL01417:Dnah7a
|
APN |
1 |
53,623,759 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01508:Dnah7a
|
APN |
1 |
53,666,231 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01511:Dnah7a
|
APN |
1 |
53,458,754 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01545:Dnah7a
|
APN |
1 |
53,557,941 (GRCm39) |
missense |
probably benign |
|
IGL01575:Dnah7a
|
APN |
1 |
53,466,979 (GRCm39) |
splice site |
probably benign |
|
IGL01667:Dnah7a
|
APN |
1 |
53,586,451 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01712:Dnah7a
|
APN |
1 |
53,462,429 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01824:Dnah7a
|
APN |
1 |
53,543,429 (GRCm39) |
missense |
probably benign |
|
IGL01829:Dnah7a
|
APN |
1 |
53,657,227 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL01861:Dnah7a
|
APN |
1 |
53,623,608 (GRCm39) |
splice site |
probably benign |
|
IGL01861:Dnah7a
|
APN |
1 |
53,679,508 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01984:Dnah7a
|
APN |
1 |
53,741,174 (GRCm39) |
splice site |
probably null |
|
IGL02056:Dnah7a
|
APN |
1 |
53,543,501 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02069:Dnah7a
|
APN |
1 |
53,601,053 (GRCm39) |
splice site |
probably benign |
|
IGL02072:Dnah7a
|
APN |
1 |
53,644,986 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02110:Dnah7a
|
APN |
1 |
53,450,739 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL02120:Dnah7a
|
APN |
1 |
53,534,876 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02128:Dnah7a
|
APN |
1 |
53,476,672 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02135:Dnah7a
|
APN |
1 |
53,662,632 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02151:Dnah7a
|
APN |
1 |
53,512,023 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02156:Dnah7a
|
APN |
1 |
53,458,882 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02270:Dnah7a
|
APN |
1 |
53,512,052 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02282:Dnah7a
|
APN |
1 |
53,682,669 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02328:Dnah7a
|
APN |
1 |
53,564,096 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02370:Dnah7a
|
APN |
1 |
53,674,556 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02420:Dnah7a
|
APN |
1 |
53,725,702 (GRCm39) |
missense |
probably benign |
|
IGL02458:Dnah7a
|
APN |
1 |
53,657,487 (GRCm39) |
nonsense |
probably null |
|
IGL02489:Dnah7a
|
APN |
1 |
53,686,481 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02554:Dnah7a
|
APN |
1 |
53,657,205 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02578:Dnah7a
|
APN |
1 |
53,472,074 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02646:Dnah7a
|
APN |
1 |
53,564,194 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02675:Dnah7a
|
APN |
1 |
53,543,183 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02688:Dnah7a
|
APN |
1 |
53,483,631 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02858:Dnah7a
|
APN |
1 |
53,512,118 (GRCm39) |
splice site |
probably benign |
|
IGL02874:Dnah7a
|
APN |
1 |
53,644,973 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02887:Dnah7a
|
APN |
1 |
53,561,519 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02894:Dnah7a
|
APN |
1 |
53,616,487 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02926:Dnah7a
|
APN |
1 |
53,535,109 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL03113:Dnah7a
|
APN |
1 |
53,472,163 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL03156:Dnah7a
|
APN |
1 |
53,644,983 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03195:Dnah7a
|
APN |
1 |
53,458,766 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03209:Dnah7a
|
APN |
1 |
53,725,773 (GRCm39) |
splice site |
probably benign |
|
IGL03214:Dnah7a
|
APN |
1 |
53,561,368 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03242:Dnah7a
|
APN |
1 |
53,659,882 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03251:Dnah7a
|
APN |
1 |
53,686,433 (GRCm39) |
missense |
probably benign |
|
IGL03265:Dnah7a
|
APN |
1 |
53,568,007 (GRCm39) |
missense |
probably benign |
|
IGL03277:Dnah7a
|
APN |
1 |
53,669,481 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03278:Dnah7a
|
APN |
1 |
53,536,124 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03356:Dnah7a
|
APN |
1 |
53,543,093 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4378001:Dnah7a
|
UTSW |
1 |
53,570,362 (GRCm39) |
missense |
probably damaging |
0.99 |
R0046:Dnah7a
|
UTSW |
1 |
53,496,033 (GRCm39) |
splice site |
probably null |
|
R0051:Dnah7a
|
UTSW |
1 |
53,560,245 (GRCm39) |
splice site |
probably benign |
|
R0082:Dnah7a
|
UTSW |
1 |
53,557,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R0111:Dnah7a
|
UTSW |
1 |
53,507,843 (GRCm39) |
missense |
probably benign |
0.03 |
R0122:Dnah7a
|
UTSW |
1 |
53,436,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R0245:Dnah7a
|
UTSW |
1 |
53,540,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R0278:Dnah7a
|
UTSW |
1 |
53,543,305 (GRCm39) |
missense |
probably benign |
0.00 |
R0309:Dnah7a
|
UTSW |
1 |
53,444,849 (GRCm39) |
missense |
probably damaging |
0.97 |
R0334:Dnah7a
|
UTSW |
1 |
53,472,213 (GRCm39) |
missense |
possibly damaging |
0.61 |
R0392:Dnah7a
|
UTSW |
1 |
53,543,357 (GRCm39) |
missense |
probably damaging |
0.97 |
R0452:Dnah7a
|
UTSW |
1 |
53,644,978 (GRCm39) |
missense |
probably benign |
0.00 |
R0511:Dnah7a
|
UTSW |
1 |
53,536,285 (GRCm39) |
missense |
probably benign |
|
R0576:Dnah7a
|
UTSW |
1 |
53,675,246 (GRCm39) |
missense |
probably benign |
0.12 |
R0592:Dnah7a
|
UTSW |
1 |
53,495,771 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0628:Dnah7a
|
UTSW |
1 |
53,536,264 (GRCm39) |
missense |
probably benign |
0.18 |
R0689:Dnah7a
|
UTSW |
1 |
53,659,840 (GRCm39) |
nonsense |
probably null |
|
R0735:Dnah7a
|
UTSW |
1 |
53,583,670 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0800:Dnah7a
|
UTSW |
1 |
53,604,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R0829:Dnah7a
|
UTSW |
1 |
53,543,238 (GRCm39) |
missense |
probably benign |
0.07 |
R0842:Dnah7a
|
UTSW |
1 |
53,540,833 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0879:Dnah7a
|
UTSW |
1 |
53,467,019 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1331:Dnah7a
|
UTSW |
1 |
53,507,828 (GRCm39) |
missense |
probably damaging |
0.99 |
R1418:Dnah7a
|
UTSW |
1 |
53,686,395 (GRCm39) |
splice site |
probably benign |
|
R1421:Dnah7a
|
UTSW |
1 |
53,580,032 (GRCm39) |
splice site |
probably benign |
|
R1445:Dnah7a
|
UTSW |
1 |
53,567,956 (GRCm39) |
missense |
probably benign |
0.02 |
R1473:Dnah7a
|
UTSW |
1 |
53,535,173 (GRCm39) |
missense |
probably benign |
0.00 |
R1538:Dnah7a
|
UTSW |
1 |
53,535,148 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1742:Dnah7a
|
UTSW |
1 |
53,495,843 (GRCm39) |
missense |
probably benign |
0.39 |
R1754:Dnah7a
|
UTSW |
1 |
53,543,344 (GRCm39) |
missense |
probably benign |
0.18 |
R1773:Dnah7a
|
UTSW |
1 |
53,472,046 (GRCm39) |
splice site |
probably null |
|
R1779:Dnah7a
|
UTSW |
1 |
53,616,382 (GRCm39) |
missense |
probably benign |
|
R1816:Dnah7a
|
UTSW |
1 |
53,670,901 (GRCm39) |
splice site |
probably benign |
|
R1817:Dnah7a
|
UTSW |
1 |
53,598,307 (GRCm39) |
missense |
probably benign |
|
R1818:Dnah7a
|
UTSW |
1 |
53,598,307 (GRCm39) |
missense |
probably benign |
|
R1819:Dnah7a
|
UTSW |
1 |
53,598,307 (GRCm39) |
missense |
probably benign |
|
R1873:Dnah7a
|
UTSW |
1 |
53,495,691 (GRCm39) |
splice site |
probably benign |
|
R1875:Dnah7a
|
UTSW |
1 |
53,495,691 (GRCm39) |
splice site |
probably benign |
|
R1884:Dnah7a
|
UTSW |
1 |
53,580,159 (GRCm39) |
missense |
probably damaging |
0.99 |
R1902:Dnah7a
|
UTSW |
1 |
53,574,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R1903:Dnah7a
|
UTSW |
1 |
53,574,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R1908:Dnah7a
|
UTSW |
1 |
53,670,721 (GRCm39) |
missense |
probably benign |
|
R1959:Dnah7a
|
UTSW |
1 |
53,724,142 (GRCm39) |
missense |
probably benign |
0.00 |
R1960:Dnah7a
|
UTSW |
1 |
53,724,142 (GRCm39) |
missense |
probably benign |
0.00 |
R1985:Dnah7a
|
UTSW |
1 |
53,543,093 (GRCm39) |
missense |
probably benign |
0.01 |
R1992:Dnah7a
|
UTSW |
1 |
53,621,835 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2037:Dnah7a
|
UTSW |
1 |
53,621,741 (GRCm39) |
missense |
probably benign |
0.00 |
R2074:Dnah7a
|
UTSW |
1 |
53,496,855 (GRCm39) |
missense |
probably benign |
0.45 |
R2076:Dnah7a
|
UTSW |
1 |
53,542,968 (GRCm39) |
missense |
probably benign |
0.01 |
R2124:Dnah7a
|
UTSW |
1 |
53,536,101 (GRCm39) |
missense |
possibly damaging |
0.58 |
R2191:Dnah7a
|
UTSW |
1 |
53,645,034 (GRCm39) |
missense |
possibly damaging |
0.54 |
R2211:Dnah7a
|
UTSW |
1 |
53,518,932 (GRCm39) |
missense |
probably benign |
0.21 |
R2220:Dnah7a
|
UTSW |
1 |
53,560,333 (GRCm39) |
missense |
probably benign |
|
R2355:Dnah7a
|
UTSW |
1 |
53,621,661 (GRCm39) |
missense |
probably benign |
0.00 |
R2495:Dnah7a
|
UTSW |
1 |
53,645,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R2901:Dnah7a
|
UTSW |
1 |
53,467,031 (GRCm39) |
missense |
probably damaging |
0.99 |
R2911:Dnah7a
|
UTSW |
1 |
53,466,983 (GRCm39) |
critical splice donor site |
probably null |
|
R2993:Dnah7a
|
UTSW |
1 |
53,542,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R3522:Dnah7a
|
UTSW |
1 |
53,657,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R3683:Dnah7a
|
UTSW |
1 |
53,483,675 (GRCm39) |
missense |
probably benign |
|
R3723:Dnah7a
|
UTSW |
1 |
53,486,505 (GRCm39) |
missense |
probably benign |
0.04 |
R3847:Dnah7a
|
UTSW |
1 |
53,540,815 (GRCm39) |
missense |
probably benign |
0.01 |
R4002:Dnah7a
|
UTSW |
1 |
53,670,840 (GRCm39) |
missense |
probably benign |
|
R4009:Dnah7a
|
UTSW |
1 |
53,564,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R4063:Dnah7a
|
UTSW |
1 |
53,464,376 (GRCm39) |
missense |
probably benign |
|
R4193:Dnah7a
|
UTSW |
1 |
53,486,493 (GRCm39) |
missense |
probably benign |
0.00 |
R4236:Dnah7a
|
UTSW |
1 |
53,486,524 (GRCm39) |
missense |
probably benign |
0.00 |
R4399:Dnah7a
|
UTSW |
1 |
53,557,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R4469:Dnah7a
|
UTSW |
1 |
53,483,685 (GRCm39) |
missense |
probably benign |
0.01 |
R4494:Dnah7a
|
UTSW |
1 |
53,488,197 (GRCm39) |
missense |
probably benign |
0.01 |
R4569:Dnah7a
|
UTSW |
1 |
53,450,818 (GRCm39) |
missense |
probably benign |
0.01 |
R4609:Dnah7a
|
UTSW |
1 |
53,495,816 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4632:Dnah7a
|
UTSW |
1 |
53,467,110 (GRCm39) |
missense |
probably damaging |
0.97 |
R4703:Dnah7a
|
UTSW |
1 |
53,486,476 (GRCm39) |
critical splice donor site |
probably null |
|
R4781:Dnah7a
|
UTSW |
1 |
53,464,367 (GRCm39) |
missense |
probably benign |
0.28 |
R4854:Dnah7a
|
UTSW |
1 |
53,745,888 (GRCm39) |
utr 5 prime |
probably benign |
|
R4932:Dnah7a
|
UTSW |
1 |
53,542,737 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4976:Dnah7a
|
UTSW |
1 |
53,737,851 (GRCm39) |
missense |
probably benign |
|
R5000:Dnah7a
|
UTSW |
1 |
53,606,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R5023:Dnah7a
|
UTSW |
1 |
53,686,407 (GRCm39) |
nonsense |
probably null |
|
R5026:Dnah7a
|
UTSW |
1 |
53,701,657 (GRCm39) |
missense |
probably damaging |
0.99 |
R5050:Dnah7a
|
UTSW |
1 |
53,536,255 (GRCm39) |
missense |
probably benign |
0.01 |
R5119:Dnah7a
|
UTSW |
1 |
53,737,851 (GRCm39) |
missense |
probably benign |
|
R5151:Dnah7a
|
UTSW |
1 |
53,659,929 (GRCm39) |
missense |
probably benign |
0.00 |
R5155:Dnah7a
|
UTSW |
1 |
53,682,654 (GRCm39) |
missense |
probably benign |
0.01 |
R5180:Dnah7a
|
UTSW |
1 |
53,462,446 (GRCm39) |
missense |
probably damaging |
0.97 |
R5228:Dnah7a
|
UTSW |
1 |
53,476,768 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5237:Dnah7a
|
UTSW |
1 |
53,486,690 (GRCm39) |
splice site |
probably null |
|
R5267:Dnah7a
|
UTSW |
1 |
53,518,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R5334:Dnah7a
|
UTSW |
1 |
53,542,805 (GRCm39) |
missense |
probably benign |
0.00 |
R5358:Dnah7a
|
UTSW |
1 |
53,586,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R5401:Dnah7a
|
UTSW |
1 |
53,670,812 (GRCm39) |
missense |
probably benign |
0.01 |
R5412:Dnah7a
|
UTSW |
1 |
53,674,503 (GRCm39) |
missense |
probably benign |
|
R5496:Dnah7a
|
UTSW |
1 |
53,496,927 (GRCm39) |
missense |
probably benign |
|
R5531:Dnah7a
|
UTSW |
1 |
53,458,907 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5536:Dnah7a
|
UTSW |
1 |
53,464,412 (GRCm39) |
missense |
probably benign |
|
R5543:Dnah7a
|
UTSW |
1 |
53,543,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R5597:Dnah7a
|
UTSW |
1 |
53,573,611 (GRCm39) |
missense |
probably benign |
0.00 |
R5609:Dnah7a
|
UTSW |
1 |
53,621,753 (GRCm39) |
missense |
probably benign |
0.03 |
R5643:Dnah7a
|
UTSW |
1 |
53,444,866 (GRCm39) |
missense |
probably benign |
|
R5644:Dnah7a
|
UTSW |
1 |
53,580,138 (GRCm39) |
missense |
probably benign |
0.33 |
R5689:Dnah7a
|
UTSW |
1 |
53,444,857 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5715:Dnah7a
|
UTSW |
1 |
53,452,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R5780:Dnah7a
|
UTSW |
1 |
53,522,478 (GRCm39) |
missense |
probably benign |
0.03 |
R5893:Dnah7a
|
UTSW |
1 |
53,496,944 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5946:Dnah7a
|
UTSW |
1 |
53,598,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R5995:Dnah7a
|
UTSW |
1 |
53,659,829 (GRCm39) |
missense |
probably benign |
0.00 |
R6102:Dnah7a
|
UTSW |
1 |
53,598,299 (GRCm39) |
missense |
probably benign |
0.00 |
R6108:Dnah7a
|
UTSW |
1 |
53,496,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R6133:Dnah7a
|
UTSW |
1 |
53,458,814 (GRCm39) |
missense |
probably benign |
0.05 |
R6168:Dnah7a
|
UTSW |
1 |
53,450,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R6175:Dnah7a
|
UTSW |
1 |
53,472,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R6211:Dnah7a
|
UTSW |
1 |
53,458,795 (GRCm39) |
missense |
probably damaging |
0.99 |
R6282:Dnah7a
|
UTSW |
1 |
53,542,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R6329:Dnah7a
|
UTSW |
1 |
53,580,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R6344:Dnah7a
|
UTSW |
1 |
53,436,349 (GRCm39) |
missense |
probably benign |
0.02 |
R6530:Dnah7a
|
UTSW |
1 |
53,542,856 (GRCm39) |
missense |
probably benign |
0.04 |
R6574:Dnah7a
|
UTSW |
1 |
53,495,693 (GRCm39) |
critical splice donor site |
probably null |
|
R6608:Dnah7a
|
UTSW |
1 |
53,564,277 (GRCm39) |
missense |
probably benign |
|
R6625:Dnah7a
|
UTSW |
1 |
53,604,916 (GRCm39) |
missense |
probably benign |
0.05 |
R6661:Dnah7a
|
UTSW |
1 |
53,662,609 (GRCm39) |
missense |
probably benign |
0.00 |
R6681:Dnah7a
|
UTSW |
1 |
53,560,385 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6747:Dnah7a
|
UTSW |
1 |
53,675,221 (GRCm39) |
missense |
probably benign |
0.01 |
R6774:Dnah7a
|
UTSW |
1 |
53,737,810 (GRCm39) |
missense |
probably benign |
|
R6823:Dnah7a
|
UTSW |
1 |
53,495,863 (GRCm39) |
missense |
probably benign |
|
R6900:Dnah7a
|
UTSW |
1 |
53,701,510 (GRCm39) |
missense |
probably damaging |
0.97 |
R6940:Dnah7a
|
UTSW |
1 |
53,670,836 (GRCm39) |
missense |
probably benign |
0.09 |
R6956:Dnah7a
|
UTSW |
1 |
53,616,446 (GRCm39) |
missense |
probably benign |
0.02 |
R6978:Dnah7a
|
UTSW |
1 |
53,701,526 (GRCm39) |
missense |
probably null |
|
R6988:Dnah7a
|
UTSW |
1 |
53,621,784 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7026:Dnah7a
|
UTSW |
1 |
53,543,448 (GRCm39) |
missense |
probably benign |
|
R7027:Dnah7a
|
UTSW |
1 |
53,670,665 (GRCm39) |
missense |
probably benign |
0.01 |
R7033:Dnah7a
|
UTSW |
1 |
53,518,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R7072:Dnah7a
|
UTSW |
1 |
53,458,912 (GRCm39) |
missense |
probably benign |
0.00 |
R7096:Dnah7a
|
UTSW |
1 |
53,522,599 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7142:Dnah7a
|
UTSW |
1 |
53,452,927 (GRCm39) |
nonsense |
probably null |
|
R7144:Dnah7a
|
UTSW |
1 |
53,737,867 (GRCm39) |
splice site |
probably null |
|
R7167:Dnah7a
|
UTSW |
1 |
53,542,935 (GRCm39) |
missense |
probably benign |
0.00 |
R7182:Dnah7a
|
UTSW |
1 |
53,659,620 (GRCm39) |
splice site |
probably null |
|
R7196:Dnah7a
|
UTSW |
1 |
53,724,000 (GRCm39) |
missense |
probably benign |
0.00 |
R7206:Dnah7a
|
UTSW |
1 |
53,737,792 (GRCm39) |
nonsense |
probably null |
|
R7215:Dnah7a
|
UTSW |
1 |
53,657,509 (GRCm39) |
missense |
probably damaging |
0.99 |
R7224:Dnah7a
|
UTSW |
1 |
53,436,420 (GRCm39) |
missense |
probably benign |
0.00 |
R7264:Dnah7a
|
UTSW |
1 |
53,557,973 (GRCm39) |
missense |
probably benign |
|
R7282:Dnah7a
|
UTSW |
1 |
53,724,059 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7365:Dnah7a
|
UTSW |
1 |
53,536,297 (GRCm39) |
missense |
probably benign |
|
R7392:Dnah7a
|
UTSW |
1 |
53,540,820 (GRCm39) |
missense |
probably benign |
0.00 |
R7454:Dnah7a
|
UTSW |
1 |
53,557,923 (GRCm39) |
missense |
probably benign |
|
R7471:Dnah7a
|
UTSW |
1 |
53,458,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R7547:Dnah7a
|
UTSW |
1 |
53,702,996 (GRCm39) |
missense |
probably benign |
0.00 |
R7554:Dnah7a
|
UTSW |
1 |
53,567,857 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7655:Dnah7a
|
UTSW |
1 |
53,535,164 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7656:Dnah7a
|
UTSW |
1 |
53,535,164 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7666:Dnah7a
|
UTSW |
1 |
53,586,456 (GRCm39) |
missense |
probably benign |
0.00 |
R7721:Dnah7a
|
UTSW |
1 |
53,670,842 (GRCm39) |
missense |
probably benign |
|
R7813:Dnah7a
|
UTSW |
1 |
53,657,245 (GRCm39) |
missense |
probably benign |
|
R7839:Dnah7a
|
UTSW |
1 |
53,606,334 (GRCm39) |
missense |
probably benign |
0.08 |
R7959:Dnah7a
|
UTSW |
1 |
53,682,621 (GRCm39) |
missense |
probably benign |
0.00 |
R7984:Dnah7a
|
UTSW |
1 |
53,543,377 (GRCm39) |
missense |
probably benign |
0.01 |
R7985:Dnah7a
|
UTSW |
1 |
53,557,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R8116:Dnah7a
|
UTSW |
1 |
53,543,049 (GRCm39) |
missense |
probably benign |
|
R8140:Dnah7a
|
UTSW |
1 |
53,540,748 (GRCm39) |
missense |
probably benign |
0.02 |
R8184:Dnah7a
|
UTSW |
1 |
53,666,194 (GRCm39) |
missense |
probably benign |
0.03 |
R8339:Dnah7a
|
UTSW |
1 |
53,724,178 (GRCm39) |
missense |
probably benign |
|
R8352:Dnah7a
|
UTSW |
1 |
53,466,986 (GRCm39) |
missense |
probably null |
0.01 |
R8423:Dnah7a
|
UTSW |
1 |
53,512,063 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8428:Dnah7a
|
UTSW |
1 |
53,512,112 (GRCm39) |
missense |
probably damaging |
0.98 |
R8432:Dnah7a
|
UTSW |
1 |
53,657,195 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8452:Dnah7a
|
UTSW |
1 |
53,466,986 (GRCm39) |
missense |
probably null |
0.01 |
R8458:Dnah7a
|
UTSW |
1 |
53,657,142 (GRCm39) |
missense |
probably benign |
0.01 |
R8493:Dnah7a
|
UTSW |
1 |
53,512,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R8498:Dnah7a
|
UTSW |
1 |
53,657,139 (GRCm39) |
missense |
probably benign |
0.01 |
R8502:Dnah7a
|
UTSW |
1 |
53,679,520 (GRCm39) |
missense |
probably benign |
0.39 |
R8692:Dnah7a
|
UTSW |
1 |
53,472,175 (GRCm39) |
missense |
probably benign |
0.00 |
R8700:Dnah7a
|
UTSW |
1 |
53,535,088 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8709:Dnah7a
|
UTSW |
1 |
53,674,476 (GRCm39) |
missense |
probably benign |
|
R8856:Dnah7a
|
UTSW |
1 |
53,462,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R8875:Dnah7a
|
UTSW |
1 |
53,682,682 (GRCm39) |
missense |
probably benign |
0.10 |
R8967:Dnah7a
|
UTSW |
1 |
53,682,594 (GRCm39) |
splice site |
probably benign |
|
R8982:Dnah7a
|
UTSW |
1 |
53,570,301 (GRCm39) |
missense |
probably benign |
|
R8984:Dnah7a
|
UTSW |
1 |
53,674,436 (GRCm39) |
nonsense |
probably null |
|
R8993:Dnah7a
|
UTSW |
1 |
53,543,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R9008:Dnah7a
|
UTSW |
1 |
53,701,501 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9022:Dnah7a
|
UTSW |
1 |
53,512,116 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9028:Dnah7a
|
UTSW |
1 |
53,560,297 (GRCm39) |
missense |
probably benign |
0.00 |
R9077:Dnah7a
|
UTSW |
1 |
53,741,218 (GRCm39) |
missense |
unknown |
|
R9167:Dnah7a
|
UTSW |
1 |
53,657,370 (GRCm39) |
missense |
probably benign |
0.00 |
R9206:Dnah7a
|
UTSW |
1 |
53,540,757 (GRCm39) |
missense |
probably benign |
0.11 |
R9226:Dnah7a
|
UTSW |
1 |
53,560,326 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9251:Dnah7a
|
UTSW |
1 |
53,621,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R9265:Dnah7a
|
UTSW |
1 |
53,674,505 (GRCm39) |
missense |
probably benign |
|
R9350:Dnah7a
|
UTSW |
1 |
53,436,307 (GRCm39) |
missense |
probably benign |
0.19 |
R9369:Dnah7a
|
UTSW |
1 |
53,564,222 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9369:Dnah7a
|
UTSW |
1 |
53,543,421 (GRCm39) |
missense |
probably benign |
|
R9372:Dnah7a
|
UTSW |
1 |
53,543,474 (GRCm39) |
missense |
probably benign |
|
R9376:Dnah7a
|
UTSW |
1 |
53,568,058 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9378:Dnah7a
|
UTSW |
1 |
53,621,776 (GRCm39) |
missense |
probably benign |
0.32 |
R9401:Dnah7a
|
UTSW |
1 |
53,568,026 (GRCm39) |
missense |
probably benign |
0.01 |
R9431:Dnah7a
|
UTSW |
1 |
53,450,812 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9529:Dnah7a
|
UTSW |
1 |
53,561,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R9701:Dnah7a
|
UTSW |
1 |
53,561,388 (GRCm39) |
missense |
probably benign |
0.03 |
R9712:Dnah7a
|
UTSW |
1 |
53,598,299 (GRCm39) |
missense |
probably benign |
0.00 |
R9799:Dnah7a
|
UTSW |
1 |
53,557,968 (GRCm39) |
missense |
probably benign |
0.00 |
R9802:Dnah7a
|
UTSW |
1 |
53,561,388 (GRCm39) |
missense |
probably benign |
0.03 |
X0027:Dnah7a
|
UTSW |
1 |
53,512,089 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Dnah7a
|
UTSW |
1 |
53,507,802 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dnah7a
|
UTSW |
1 |
53,522,622 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dnah7a
|
UTSW |
1 |
53,458,858 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Dnah7a
|
UTSW |
1 |
53,598,261 (GRCm39) |
missense |
probably benign |
0.21 |
Z1177:Dnah7a
|
UTSW |
1 |
53,450,815 (GRCm39) |
missense |
probably benign |
0.08 |
Z1177:Dnah7a
|
UTSW |
1 |
53,682,616 (GRCm39) |
missense |
possibly damaging |
0.92 |
|