Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy8 |
T |
G |
15: 64,626,735 (GRCm39) |
|
probably null |
Het |
Adgrv1 |
A |
G |
13: 81,705,200 (GRCm39) |
F1537L |
probably damaging |
Het |
Aggf1 |
T |
C |
13: 95,501,231 (GRCm39) |
S384G |
probably benign |
Het |
Anxa8 |
A |
T |
14: 33,816,722 (GRCm39) |
D204V |
possibly damaging |
Het |
Asap3 |
A |
T |
4: 135,954,883 (GRCm39) |
E71V |
possibly damaging |
Het |
BC024139 |
T |
C |
15: 76,003,946 (GRCm39) |
*773W |
probably null |
Het |
Bckdhb |
T |
C |
9: 83,835,814 (GRCm39) |
V106A |
possibly damaging |
Het |
Cep250 |
A |
G |
2: 155,823,379 (GRCm39) |
D1010G |
probably benign |
Het |
Chrd |
T |
A |
16: 20,553,486 (GRCm39) |
L243Q |
probably damaging |
Het |
Cib2 |
G |
T |
9: 54,457,175 (GRCm39) |
L30I |
possibly damaging |
Het |
Cpsf7 |
T |
A |
19: 10,510,248 (GRCm39) |
L113* |
probably null |
Het |
Cubn |
T |
A |
2: 13,449,840 (GRCm39) |
I895L |
probably benign |
Het |
Cyp24a1 |
C |
A |
2: 170,329,899 (GRCm39) |
R351I |
probably benign |
Het |
Cyp2a12 |
A |
T |
7: 26,733,581 (GRCm39) |
D320V |
possibly damaging |
Het |
Dact1 |
C |
G |
12: 71,364,713 (GRCm39) |
P498R |
probably benign |
Het |
Diaph1 |
T |
A |
18: 38,009,436 (GRCm39) |
|
probably null |
Het |
Dop1b |
A |
T |
16: 93,552,373 (GRCm39) |
I271F |
possibly damaging |
Het |
Elp1 |
A |
G |
4: 56,787,939 (GRCm39) |
Y331H |
probably damaging |
Het |
Erich3 |
C |
A |
3: 154,433,074 (GRCm39) |
F349L |
probably damaging |
Het |
Fam187b |
G |
C |
7: 30,688,715 (GRCm39) |
V358L |
probably benign |
Het |
Fat4 |
T |
A |
3: 39,038,088 (GRCm39) |
H3913Q |
probably benign |
Het |
Fbxw7 |
G |
C |
3: 84,865,934 (GRCm39) |
E118D |
probably benign |
Het |
Fgf1 |
A |
G |
18: 38,980,161 (GRCm39) |
I71T |
probably damaging |
Het |
Fryl |
A |
T |
5: 73,222,560 (GRCm39) |
I2007K |
probably damaging |
Het |
Galnt2 |
C |
G |
8: 125,050,750 (GRCm39) |
P130A |
probably benign |
Het |
H1f10 |
G |
A |
6: 87,958,284 (GRCm39) |
R19C |
probably damaging |
Het |
Hmga2 |
A |
C |
10: 120,311,929 (GRCm39) |
S14A |
possibly damaging |
Het |
Hoxb4 |
C |
T |
11: 96,209,480 (GRCm39) |
|
probably benign |
Het |
Hr |
A |
T |
14: 70,802,814 (GRCm39) |
I756F |
probably damaging |
Het |
Hspa1b |
A |
T |
17: 35,177,161 (GRCm39) |
S275T |
probably benign |
Het |
Kcnh1 |
T |
C |
1: 192,187,597 (GRCm39) |
*99R |
probably null |
Het |
Kit |
C |
A |
5: 75,813,309 (GRCm39) |
L864I |
probably benign |
Het |
Klk14 |
A |
T |
7: 43,343,880 (GRCm39) |
K196* |
probably null |
Het |
Lmod1 |
A |
G |
1: 135,252,905 (GRCm39) |
N53S |
probably damaging |
Het |
Myh13 |
T |
C |
11: 67,246,984 (GRCm39) |
M1235T |
probably benign |
Het |
Neurl3 |
T |
A |
1: 36,307,785 (GRCm39) |
K175* |
probably null |
Het |
Nlgn2 |
T |
A |
11: 69,716,750 (GRCm39) |
K597M |
probably damaging |
Het |
Npdc1 |
T |
C |
2: 25,299,121 (GRCm39) |
M306T |
probably damaging |
Het |
Obscn |
C |
T |
11: 58,958,769 (GRCm39) |
|
probably null |
Het |
Or1p1b |
T |
C |
11: 74,130,522 (GRCm39) |
L44P |
probably damaging |
Het |
Or52m2 |
G |
A |
7: 102,263,693 (GRCm39) |
L168F |
probably damaging |
Het |
Or8b49 |
T |
C |
9: 38,506,201 (GRCm39) |
I228T |
possibly damaging |
Het |
Pbrm1 |
A |
T |
14: 30,806,747 (GRCm39) |
Y1042F |
probably damaging |
Het |
Pclo |
T |
A |
5: 14,727,921 (GRCm39) |
|
probably benign |
Het |
Peg10 |
CATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAGGATC |
CATC |
6: 4,756,431 (GRCm39) |
|
probably benign |
Het |
Phf12 |
C |
T |
11: 77,913,337 (GRCm39) |
Q430* |
probably null |
Het |
Plaat5 |
A |
T |
19: 7,616,861 (GRCm39) |
|
probably benign |
Het |
Pld3 |
C |
T |
7: 27,235,322 (GRCm39) |
R302H |
probably damaging |
Het |
Plekha5 |
T |
C |
6: 140,471,584 (GRCm39) |
S112P |
probably benign |
Het |
Pmfbp1 |
T |
A |
8: 110,256,939 (GRCm39) |
S548T |
possibly damaging |
Het |
Ppa1 |
A |
T |
10: 61,503,382 (GRCm39) |
I220F |
probably damaging |
Het |
Ppp2r3d |
A |
G |
9: 124,439,078 (GRCm38) |
|
probably benign |
Het |
Psmg2 |
A |
T |
18: 67,781,927 (GRCm39) |
E164D |
possibly damaging |
Het |
Rarb |
T |
C |
14: 16,443,824 (GRCm38) |
R155G |
probably damaging |
Het |
Rnf215 |
T |
C |
11: 4,086,609 (GRCm39) |
L162S |
probably damaging |
Het |
Rsf1 |
GGCG |
GGCGACGGCCGCG |
7: 97,229,113 (GRCm39) |
|
probably benign |
Het |
Rtkn2 |
G |
A |
10: 67,862,462 (GRCm39) |
V330M |
probably damaging |
Het |
Slc16a4 |
A |
T |
3: 107,218,814 (GRCm39) |
I472F |
probably benign |
Het |
Snx14 |
T |
C |
9: 88,276,435 (GRCm39) |
N617D |
possibly damaging |
Het |
Spire2 |
T |
C |
8: 124,083,466 (GRCm39) |
V150A |
probably damaging |
Het |
Sptbn1 |
C |
A |
11: 30,064,787 (GRCm39) |
R1904M |
probably damaging |
Het |
Swap70 |
A |
G |
7: 109,880,510 (GRCm39) |
E575G |
possibly damaging |
Het |
Tbxas1 |
A |
T |
6: 38,896,087 (GRCm39) |
M1L |
possibly damaging |
Het |
Tenm3 |
A |
T |
8: 48,709,872 (GRCm39) |
V1688D |
probably damaging |
Het |
Tgfbr3 |
A |
T |
5: 107,297,780 (GRCm39) |
S207T |
probably damaging |
Het |
Timm44 |
A |
G |
8: 4,317,282 (GRCm39) |
F248L |
probably damaging |
Het |
Tmem161a |
T |
C |
8: 70,633,849 (GRCm39) |
L170P |
probably damaging |
Het |
Tmem63a |
A |
T |
1: 180,788,035 (GRCm39) |
Y263F |
possibly damaging |
Het |
Tnfsf9 |
C |
A |
17: 57,412,513 (GRCm39) |
L28I |
probably benign |
Het |
Tph2 |
T |
A |
10: 115,010,011 (GRCm39) |
N183I |
probably benign |
Het |
Ttyh1 |
T |
C |
7: 4,125,528 (GRCm39) |
I60T |
probably damaging |
Het |
Ubn1 |
T |
G |
16: 4,882,411 (GRCm39) |
S48A |
probably damaging |
Het |
Ubr5 |
T |
C |
15: 37,989,842 (GRCm39) |
N2019S |
probably benign |
Het |
Wbp2 |
T |
C |
11: 115,977,736 (GRCm39) |
N6D |
probably benign |
Het |
Wdr59 |
T |
A |
8: 112,185,672 (GRCm39) |
E810V |
possibly damaging |
Het |
Wiz |
T |
C |
17: 32,579,395 (GRCm39) |
D220G |
probably damaging |
Het |
Yipf7 |
A |
G |
5: 69,674,413 (GRCm39) |
L244P |
probably damaging |
Het |
Zdhhc17 |
T |
C |
10: 110,790,972 (GRCm39) |
T366A |
possibly damaging |
Het |
Zfp169 |
A |
T |
13: 48,644,472 (GRCm39) |
|
probably benign |
Het |
Zfp707 |
C |
T |
15: 75,841,572 (GRCm39) |
|
probably benign |
Het |
Zfp788 |
A |
G |
7: 41,298,984 (GRCm39) |
H540R |
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 |
53,601,059 (GRCm39) |
critical splice donor site |
probably null |
|
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 |
|
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 |
|