Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700016H13Rik |
T |
A |
5: 103,797,360 (GRCm39) |
I50F |
possibly damaging |
Het |
Abcc3 |
T |
C |
11: 94,248,075 (GRCm39) |
D1175G |
probably null |
Het |
Accs |
C |
A |
2: 93,666,077 (GRCm39) |
*503L |
probably null |
Het |
Adgra2 |
A |
G |
8: 27,604,485 (GRCm39) |
E520G |
probably damaging |
Het |
Aldh7a1 |
C |
A |
18: 56,681,525 (GRCm39) |
C215F |
probably benign |
Het |
Apbb1ip |
A |
C |
2: 22,706,990 (GRCm39) |
D9A |
unknown |
Het |
Atad2 |
G |
A |
15: 57,989,176 (GRCm39) |
A228V |
probably benign |
Het |
Atp10a |
T |
C |
7: 58,438,107 (GRCm39) |
S430P |
probably damaging |
Het |
Atp1a3 |
T |
C |
7: 24,700,573 (GRCm39) |
D6G |
unknown |
Het |
Brca1 |
A |
T |
11: 101,417,248 (GRCm39) |
N295K |
possibly damaging |
Het |
Caly |
C |
A |
7: 139,661,301 (GRCm39) |
|
probably benign |
Het |
Ces1h |
A |
G |
8: 94,084,053 (GRCm39) |
Y386H |
unknown |
Het |
Col14a1 |
A |
G |
15: 55,308,012 (GRCm39) |
D1044G |
unknown |
Het |
Csf2rb |
A |
G |
15: 78,233,357 (GRCm39) |
D888G |
probably damaging |
Het |
Cux1 |
T |
C |
5: 136,281,458 (GRCm39) |
E568G |
possibly damaging |
Het |
Dhrs7b |
T |
A |
11: 60,746,568 (GRCm39) |
L219Q |
probably damaging |
Het |
Dlg5 |
G |
A |
14: 24,295,280 (GRCm39) |
P80L |
probably damaging |
Het |
Dnajc24 |
A |
T |
2: 105,832,380 (GRCm39) |
M1K |
probably null |
Het |
Dusp12 |
C |
T |
1: 170,702,095 (GRCm39) |
W301* |
probably null |
Het |
Dyrk1a |
G |
T |
16: 94,492,575 (GRCm39) |
G603* |
probably null |
Het |
Eif4g1 |
T |
A |
16: 20,498,452 (GRCm39) |
V403E |
probably benign |
Het |
Epn3 |
T |
C |
11: 94,387,100 (GRCm39) |
E90G |
probably damaging |
Het |
Etl4 |
A |
G |
2: 20,810,721 (GRCm39) |
S1303G |
probably benign |
Het |
Evpl |
A |
T |
11: 116,118,895 (GRCm39) |
Y627N |
probably damaging |
Het |
Fbxw25 |
A |
T |
9: 109,493,625 (GRCm39) |
L22* |
probably null |
Het |
Fcamr |
T |
A |
1: 130,742,375 (GRCm39) |
N587K |
probably benign |
Het |
Fgd6 |
A |
G |
10: 93,939,193 (GRCm39) |
N946S |
probably benign |
Het |
Fndc3b |
A |
T |
3: 27,523,148 (GRCm39) |
I477N |
possibly damaging |
Het |
Grifin |
C |
T |
5: 140,550,280 (GRCm39) |
A54T |
probably benign |
Het |
Gtf2b |
A |
G |
3: 142,487,105 (GRCm39) |
I180M |
probably damaging |
Het |
Invs |
A |
T |
4: 48,397,559 (GRCm39) |
D378V |
possibly damaging |
Het |
Itgb6 |
T |
C |
2: 60,458,788 (GRCm39) |
E378G |
probably damaging |
Het |
Khdc1a |
T |
C |
1: 21,420,623 (GRCm39) |
I81T |
possibly damaging |
Het |
Kif20b |
T |
A |
19: 34,917,322 (GRCm39) |
D617E |
probably damaging |
Het |
Kifc3 |
T |
A |
8: 95,834,165 (GRCm39) |
|
probably null |
Het |
Kirrel3 |
C |
T |
9: 34,931,419 (GRCm39) |
H403Y |
possibly damaging |
Het |
Klf15 |
G |
A |
6: 90,443,820 (GRCm39) |
V132I |
probably benign |
Het |
Kmt2a |
A |
G |
9: 44,730,031 (GRCm39) |
S3429P |
unknown |
Het |
Lama1 |
T |
G |
17: 68,116,216 (GRCm39) |
L2361R |
|
Het |
Lrp1b |
T |
C |
2: 40,587,570 (GRCm39) |
D3895G |
|
Het |
Mcoln3 |
A |
C |
3: 145,830,546 (GRCm39) |
E92A |
possibly damaging |
Het |
Myo3b |
T |
C |
2: 69,939,032 (GRCm39) |
M135T |
probably damaging |
Het |
Mysm1 |
A |
G |
4: 94,835,204 (GRCm39) |
*820Q |
probably null |
Het |
Ncoa7 |
A |
G |
10: 30,567,056 (GRCm39) |
S541P |
probably benign |
Het |
Nup54 |
T |
C |
5: 92,578,952 (GRCm39) |
T33A |
unknown |
Het |
Or10al2 |
C |
A |
17: 37,983,408 (GRCm39) |
Q165K |
possibly damaging |
Het |
Or13a17 |
T |
G |
7: 140,271,484 (GRCm39) |
I222S |
probably damaging |
Het |
Or1s2 |
T |
C |
19: 13,758,810 (GRCm39) |
V276A |
possibly damaging |
Het |
Or4k42 |
T |
A |
2: 111,320,369 (GRCm39) |
I45F |
probably damaging |
Het |
Or51a5 |
T |
A |
7: 102,771,899 (GRCm39) |
I27F |
probably benign |
Het |
Otud6b |
A |
G |
4: 14,826,414 (GRCm39) |
C18R |
probably benign |
Het |
Pde4d |
A |
G |
13: 110,071,858 (GRCm39) |
E284G |
probably damaging |
Het |
Peg10 |
CATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAGGATC |
CATC |
6: 4,756,431 (GRCm39) |
|
probably benign |
Het |
Pidd1 |
C |
A |
7: 141,020,055 (GRCm39) |
W598L |
probably damaging |
Het |
Pira2 |
A |
T |
7: 3,847,543 (GRCm39) |
C49S |
probably damaging |
Het |
Pramel11 |
T |
C |
4: 143,624,288 (GRCm39) |
M70V |
possibly damaging |
Het |
Prdx1 |
T |
G |
4: 116,550,935 (GRCm39) |
D135E |
probably benign |
Het |
Rab15 |
T |
A |
12: 76,849,903 (GRCm39) |
Y88F |
probably damaging |
Het |
Rem2 |
C |
A |
14: 54,715,256 (GRCm39) |
H144Q |
probably damaging |
Het |
Sel1l3 |
T |
C |
5: 53,301,406 (GRCm39) |
D737G |
probably damaging |
Het |
Srd5a3 |
C |
T |
5: 76,295,666 (GRCm39) |
Q119* |
probably null |
Het |
Suclg2 |
G |
T |
6: 95,571,703 (GRCm39) |
Q120K |
probably benign |
Het |
Tacc2 |
T |
A |
7: 130,227,161 (GRCm39) |
M1282K |
probably benign |
Het |
Tbc1d5 |
T |
A |
17: 51,063,720 (GRCm39) |
Q620L |
probably damaging |
Het |
Tdrd3 |
G |
T |
14: 87,709,590 (GRCm39) |
A91S |
probably damaging |
Het |
Thsd7b |
T |
A |
1: 130,087,435 (GRCm39) |
F1184Y |
probably benign |
Het |
Trim28 |
T |
A |
7: 12,762,339 (GRCm39) |
V321E |
possibly damaging |
Het |
Trim5 |
C |
A |
7: 103,915,675 (GRCm39) |
|
probably null |
Het |
Ugt2b37 |
A |
T |
5: 87,390,299 (GRCm39) |
Y382* |
probably null |
Het |
Usp40 |
C |
T |
1: 87,909,852 (GRCm39) |
G534D |
probably damaging |
Het |
Usp53 |
A |
T |
3: 122,728,112 (GRCm39) |
H823Q |
probably benign |
Het |
Vmn2r12 |
T |
A |
5: 109,235,829 (GRCm39) |
M508L |
probably benign |
Het |
Vmn2r56 |
T |
A |
7: 12,449,351 (GRCm39) |
I296F |
probably benign |
Het |
Vps13a |
T |
C |
19: 16,632,668 (GRCm39) |
S2563G |
probably damaging |
Het |
Wdr59 |
A |
G |
8: 112,220,912 (GRCm39) |
F207L |
|
Het |
Zan |
A |
G |
5: 137,405,295 (GRCm39) |
S3777P |
unknown |
Het |
Zfp277 |
T |
C |
12: 40,365,880 (GRCm39) |
N530D |
possibly damaging |
Het |
Zfp365 |
G |
A |
10: 67,745,749 (GRCm39) |
R10W |
probably damaging |
Het |
Zfp384 |
A |
T |
6: 125,013,288 (GRCm39) |
H452L |
probably damaging |
Het |
Zftraf1 |
C |
T |
15: 76,532,386 (GRCm39) |
D241N |
probably benign |
Het |
Zfyve28 |
A |
T |
5: 34,374,487 (GRCm39) |
L509Q |
probably damaging |
Het |
|
Other mutations in Dnah14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01086:Dnah14
|
APN |
1 |
181,579,611 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01764:Dnah14
|
APN |
1 |
181,572,342 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03218:Dnah14
|
APN |
1 |
181,582,834 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03290:Dnah14
|
APN |
1 |
181,591,543 (GRCm39) |
splice site |
probably benign |
|
IGL03384:Dnah14
|
APN |
1 |
181,573,514 (GRCm39) |
missense |
probably benign |
0.03 |
R0009:Dnah14
|
UTSW |
1 |
181,596,972 (GRCm39) |
splice site |
probably benign |
|
R0125:Dnah14
|
UTSW |
1 |
181,579,628 (GRCm39) |
missense |
probably damaging |
0.99 |
R0579:Dnah14
|
UTSW |
1 |
181,572,312 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0973:Dnah14
|
UTSW |
1 |
181,579,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R0973:Dnah14
|
UTSW |
1 |
181,579,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R0974:Dnah14
|
UTSW |
1 |
181,579,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R1609:Dnah14
|
UTSW |
1 |
181,577,742 (GRCm39) |
missense |
probably damaging |
0.97 |
R1860:Dnah14
|
UTSW |
1 |
181,591,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R2050:Dnah14
|
UTSW |
1 |
181,580,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R2974:Dnah14
|
UTSW |
1 |
181,582,806 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4715:Dnah14
|
UTSW |
1 |
181,584,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R5076:Dnah14
|
UTSW |
1 |
181,584,799 (GRCm39) |
missense |
probably benign |
0.01 |
R5424:Dnah14
|
UTSW |
1 |
181,590,875 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5808:Dnah14
|
UTSW |
1 |
181,568,724 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5997:Dnah14
|
UTSW |
1 |
181,597,670 (GRCm39) |
missense |
probably benign |
0.00 |
R6052:Dnah14
|
UTSW |
1 |
181,494,052 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6061:Dnah14
|
UTSW |
1 |
181,536,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R6089:Dnah14
|
UTSW |
1 |
181,577,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R6092:Dnah14
|
UTSW |
1 |
181,449,398 (GRCm39) |
missense |
probably benign |
0.13 |
R6145:Dnah14
|
UTSW |
1 |
181,493,982 (GRCm39) |
missense |
probably benign |
0.00 |
R6163:Dnah14
|
UTSW |
1 |
181,493,926 (GRCm39) |
missense |
probably benign |
0.33 |
R6246:Dnah14
|
UTSW |
1 |
181,508,453 (GRCm39) |
missense |
probably benign |
0.00 |
R6302:Dnah14
|
UTSW |
1 |
181,428,771 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6306:Dnah14
|
UTSW |
1 |
181,412,589 (GRCm39) |
frame shift |
probably null |
|
R6326:Dnah14
|
UTSW |
1 |
181,611,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R6348:Dnah14
|
UTSW |
1 |
181,454,285 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6367:Dnah14
|
UTSW |
1 |
181,582,951 (GRCm39) |
splice site |
probably null |
|
R6376:Dnah14
|
UTSW |
1 |
181,433,459 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6389:Dnah14
|
UTSW |
1 |
181,478,767 (GRCm39) |
critical splice donor site |
probably null |
|
R6433:Dnah14
|
UTSW |
1 |
181,479,222 (GRCm39) |
missense |
probably damaging |
0.99 |
R6454:Dnah14
|
UTSW |
1 |
181,611,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R6476:Dnah14
|
UTSW |
1 |
181,572,333 (GRCm39) |
missense |
probably benign |
0.26 |
R6523:Dnah14
|
UTSW |
1 |
181,471,186 (GRCm39) |
missense |
probably benign |
0.00 |
R6529:Dnah14
|
UTSW |
1 |
181,494,034 (GRCm39) |
missense |
probably damaging |
0.98 |
R6538:Dnah14
|
UTSW |
1 |
181,412,550 (GRCm39) |
missense |
unknown |
|
R6546:Dnah14
|
UTSW |
1 |
181,566,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R6752:Dnah14
|
UTSW |
1 |
181,421,017 (GRCm39) |
missense |
probably benign |
0.07 |
R6762:Dnah14
|
UTSW |
1 |
181,584,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R6786:Dnah14
|
UTSW |
1 |
181,468,970 (GRCm39) |
missense |
probably benign |
0.21 |
R6849:Dnah14
|
UTSW |
1 |
181,636,510 (GRCm39) |
missense |
probably benign |
0.00 |
R6877:Dnah14
|
UTSW |
1 |
181,455,997 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6912:Dnah14
|
UTSW |
1 |
181,577,748 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6919:Dnah14
|
UTSW |
1 |
181,412,631 (GRCm39) |
missense |
probably benign |
0.04 |
R6924:Dnah14
|
UTSW |
1 |
181,455,517 (GRCm39) |
missense |
probably benign |
0.04 |
R6957:Dnah14
|
UTSW |
1 |
181,612,740 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6980:Dnah14
|
UTSW |
1 |
181,475,795 (GRCm39) |
missense |
probably benign |
0.00 |
R7018:Dnah14
|
UTSW |
1 |
181,454,509 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7046:Dnah14
|
UTSW |
1 |
181,450,568 (GRCm39) |
missense |
probably benign |
0.01 |
R7058:Dnah14
|
UTSW |
1 |
181,525,614 (GRCm39) |
missense |
probably benign |
0.00 |
R7068:Dnah14
|
UTSW |
1 |
181,597,355 (GRCm39) |
missense |
probably benign |
0.35 |
R7115:Dnah14
|
UTSW |
1 |
181,547,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R7130:Dnah14
|
UTSW |
1 |
181,573,523 (GRCm39) |
nonsense |
probably null |
|
R7165:Dnah14
|
UTSW |
1 |
181,532,100 (GRCm39) |
missense |
probably benign |
0.00 |
R7169:Dnah14
|
UTSW |
1 |
181,529,930 (GRCm39) |
missense |
probably benign |
0.00 |
R7184:Dnah14
|
UTSW |
1 |
181,532,094 (GRCm39) |
nonsense |
probably null |
|
R7232:Dnah14
|
UTSW |
1 |
181,584,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R7260:Dnah14
|
UTSW |
1 |
181,534,309 (GRCm39) |
missense |
probably damaging |
0.99 |
R7276:Dnah14
|
UTSW |
1 |
181,513,372 (GRCm39) |
missense |
probably benign |
0.41 |
R7290:Dnah14
|
UTSW |
1 |
181,455,739 (GRCm39) |
missense |
probably benign |
0.20 |
R7314:Dnah14
|
UTSW |
1 |
181,612,819 (GRCm39) |
splice site |
probably null |
|
R7326:Dnah14
|
UTSW |
1 |
181,425,968 (GRCm39) |
missense |
probably benign |
0.02 |
R7336:Dnah14
|
UTSW |
1 |
181,625,299 (GRCm39) |
missense |
probably damaging |
0.96 |
R7363:Dnah14
|
UTSW |
1 |
181,518,089 (GRCm39) |
splice site |
probably null |
|
R7371:Dnah14
|
UTSW |
1 |
181,454,450 (GRCm39) |
missense |
probably benign |
0.05 |
R7376:Dnah14
|
UTSW |
1 |
181,590,967 (GRCm39) |
missense |
probably benign |
0.03 |
R7418:Dnah14
|
UTSW |
1 |
181,444,307 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7473:Dnah14
|
UTSW |
1 |
181,579,704 (GRCm39) |
missense |
probably damaging |
0.99 |
R7514:Dnah14
|
UTSW |
1 |
181,455,632 (GRCm39) |
missense |
probably damaging |
0.96 |
R7555:Dnah14
|
UTSW |
1 |
181,597,619 (GRCm39) |
missense |
probably benign |
0.26 |
R7641:Dnah14
|
UTSW |
1 |
181,535,098 (GRCm39) |
missense |
probably benign |
0.01 |
R7663:Dnah14
|
UTSW |
1 |
181,579,720 (GRCm39) |
splice site |
probably null |
|
R7674:Dnah14
|
UTSW |
1 |
181,535,098 (GRCm39) |
missense |
probably benign |
0.01 |
R7680:Dnah14
|
UTSW |
1 |
181,513,365 (GRCm39) |
missense |
probably benign |
0.15 |
R7709:Dnah14
|
UTSW |
1 |
181,530,049 (GRCm39) |
critical splice donor site |
probably null |
|
R7842:Dnah14
|
UTSW |
1 |
181,455,463 (GRCm39) |
missense |
probably damaging |
0.99 |
R7988:Dnah14
|
UTSW |
1 |
181,611,139 (GRCm39) |
missense |
probably damaging |
0.97 |
R8016:Dnah14
|
UTSW |
1 |
181,475,876 (GRCm39) |
missense |
probably benign |
0.05 |
R8042:Dnah14
|
UTSW |
1 |
181,471,196 (GRCm39) |
critical splice donor site |
probably null |
|
R8071:Dnah14
|
UTSW |
1 |
181,443,459 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8086:Dnah14
|
UTSW |
1 |
181,593,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R8095:Dnah14
|
UTSW |
1 |
181,633,597 (GRCm39) |
nonsense |
probably null |
|
R8139:Dnah14
|
UTSW |
1 |
181,582,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R8176:Dnah14
|
UTSW |
1 |
181,484,598 (GRCm39) |
missense |
probably damaging |
0.96 |
R8193:Dnah14
|
UTSW |
1 |
181,515,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R8197:Dnah14
|
UTSW |
1 |
181,517,666 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8209:Dnah14
|
UTSW |
1 |
181,623,110 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8226:Dnah14
|
UTSW |
1 |
181,623,110 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8251:Dnah14
|
UTSW |
1 |
181,492,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R8264:Dnah14
|
UTSW |
1 |
181,572,357 (GRCm39) |
missense |
probably damaging |
0.99 |
R8284:Dnah14
|
UTSW |
1 |
181,601,376 (GRCm39) |
missense |
probably benign |
0.03 |
R8289:Dnah14
|
UTSW |
1 |
181,543,780 (GRCm39) |
nonsense |
probably null |
|
R8323:Dnah14
|
UTSW |
1 |
181,532,109 (GRCm39) |
missense |
probably benign |
0.01 |
R8442:Dnah14
|
UTSW |
1 |
181,568,849 (GRCm39) |
missense |
probably damaging |
0.97 |
R8458:Dnah14
|
UTSW |
1 |
181,633,577 (GRCm39) |
missense |
|
|
R8507:Dnah14
|
UTSW |
1 |
181,468,979 (GRCm39) |
missense |
probably benign |
0.02 |
R8509:Dnah14
|
UTSW |
1 |
181,642,220 (GRCm39) |
missense |
|
|
R8520:Dnah14
|
UTSW |
1 |
181,481,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R8530:Dnah14
|
UTSW |
1 |
181,492,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R8703:Dnah14
|
UTSW |
1 |
181,493,576 (GRCm39) |
nonsense |
probably null |
|
R8710:Dnah14
|
UTSW |
1 |
181,517,876 (GRCm39) |
missense |
probably benign |
0.04 |
R8752:Dnah14
|
UTSW |
1 |
181,455,581 (GRCm39) |
missense |
probably benign |
0.00 |
R8792:Dnah14
|
UTSW |
1 |
181,642,189 (GRCm39) |
missense |
|
|
R8797:Dnah14
|
UTSW |
1 |
181,465,412 (GRCm39) |
missense |
probably benign |
0.19 |
R8821:Dnah14
|
UTSW |
1 |
181,619,569 (GRCm39) |
nonsense |
probably null |
|
R8834:Dnah14
|
UTSW |
1 |
181,444,315 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8913:Dnah14
|
UTSW |
1 |
181,553,063 (GRCm39) |
missense |
probably benign |
0.01 |
R8925:Dnah14
|
UTSW |
1 |
181,508,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R8927:Dnah14
|
UTSW |
1 |
181,508,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R8934:Dnah14
|
UTSW |
1 |
181,450,288 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9090:Dnah14
|
UTSW |
1 |
181,597,325 (GRCm39) |
missense |
probably benign |
0.33 |
R9169:Dnah14
|
UTSW |
1 |
181,433,381 (GRCm39) |
missense |
probably benign |
0.06 |
R9199:Dnah14
|
UTSW |
1 |
181,478,566 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9212:Dnah14
|
UTSW |
1 |
181,628,852 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9213:Dnah14
|
UTSW |
1 |
181,444,205 (GRCm39) |
critical splice donor site |
probably null |
|
R9271:Dnah14
|
UTSW |
1 |
181,597,325 (GRCm39) |
missense |
probably benign |
0.33 |
R9282:Dnah14
|
UTSW |
1 |
181,642,077 (GRCm39) |
missense |
|
|
R9350:Dnah14
|
UTSW |
1 |
181,562,369 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9358:Dnah14
|
UTSW |
1 |
181,536,598 (GRCm39) |
missense |
probably benign |
0.01 |
R9436:Dnah14
|
UTSW |
1 |
181,508,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R9484:Dnah14
|
UTSW |
1 |
181,625,311 (GRCm39) |
missense |
probably benign |
0.01 |
R9484:Dnah14
|
UTSW |
1 |
181,517,773 (GRCm39) |
missense |
probably benign |
0.45 |
R9486:Dnah14
|
UTSW |
1 |
181,508,494 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9546:Dnah14
|
UTSW |
1 |
181,420,992 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9547:Dnah14
|
UTSW |
1 |
181,420,992 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9578:Dnah14
|
UTSW |
1 |
181,502,007 (GRCm39) |
missense |
probably benign |
0.16 |
R9654:Dnah14
|
UTSW |
1 |
181,593,904 (GRCm39) |
missense |
probably benign |
0.01 |
R9681:Dnah14
|
UTSW |
1 |
181,562,414 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9683:Dnah14
|
UTSW |
1 |
181,426,509 (GRCm39) |
missense |
probably benign |
0.01 |
R9687:Dnah14
|
UTSW |
1 |
181,425,978 (GRCm39) |
missense |
probably benign |
0.01 |
R9718:Dnah14
|
UTSW |
1 |
181,450,544 (GRCm39) |
missense |
probably benign |
0.08 |
R9751:Dnah14
|
UTSW |
1 |
181,619,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R9757:Dnah14
|
UTSW |
1 |
181,513,349 (GRCm39) |
missense |
probably benign |
0.03 |
RF007:Dnah14
|
UTSW |
1 |
181,513,374 (GRCm39) |
missense |
probably benign |
0.00 |
RF012:Dnah14
|
UTSW |
1 |
181,455,463 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Dnah14
|
UTSW |
1 |
181,584,916 (GRCm39) |
missense |
possibly damaging |
0.83 |
Z1177:Dnah14
|
UTSW |
1 |
181,517,885 (GRCm39) |
missense |
probably benign |
0.03 |
Z1177:Dnah14
|
UTSW |
1 |
181,593,869 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Dnah14
|
UTSW |
1 |
181,590,899 (GRCm39) |
missense |
probably damaging |
1.00 |
|