Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3110001I22Rik |
C |
T |
16: 13,677,759 (GRCm38) |
R241C |
probably damaging |
Het |
A430078G23Rik |
G |
A |
8: 3,384,936 (GRCm38) |
V194M |
probably damaging |
Het |
A4gnt |
A |
G |
9: 99,620,417 (GRCm38) |
E210G |
possibly damaging |
Het |
Accsl |
T |
C |
2: 93,861,018 (GRCm38) |
T372A |
probably benign |
Het |
Adgrf5 |
T |
A |
17: 43,450,560 (GRCm38) |
S1049T |
probably damaging |
Het |
Agmo |
G |
A |
12: 37,414,940 (GRCm38) |
R405K |
probably benign |
Het |
Akap3 |
A |
G |
6: 126,865,068 (GRCm38) |
T217A |
probably benign |
Het |
Ankfy1 |
T |
A |
11: 72,712,281 (GRCm38) |
N45K |
probably benign |
Het |
Ankrd11 |
G |
A |
8: 122,895,433 (GRCm38) |
T560I |
probably benign |
Het |
Aqp1 |
T |
C |
6: 55,345,819 (GRCm38) |
Y186H |
possibly damaging |
Het |
Arnt |
T |
C |
3: 95,483,775 (GRCm38) |
V320A |
probably benign |
Het |
B230217C12Rik |
T |
C |
11: 97,841,400 (GRCm38) |
L2P |
unknown |
Het |
Bco1 |
C |
A |
8: 117,131,068 (GRCm38) |
S477R |
possibly damaging |
Het |
Brd4 |
A |
G |
17: 32,211,224 (GRCm38) |
S703P |
possibly damaging |
Het |
Ceacam3 |
T |
A |
7: 17,158,350 (GRCm38) |
N339K |
|
Het |
Cebpb |
A |
G |
2: 167,689,206 (GRCm38) |
D62G |
probably damaging |
Het |
Clca4a |
T |
C |
3: 144,952,785 (GRCm38) |
I890V |
probably benign |
Het |
Cyp2d9 |
A |
G |
15: 82,455,432 (GRCm38) |
|
probably null |
Het |
Cyth1 |
T |
C |
11: 118,169,053 (GRCm38) |
T374A |
possibly damaging |
Het |
Dennd3 |
A |
T |
15: 73,562,367 (GRCm38) |
H962L |
probably damaging |
Het |
Dhtkd1 |
T |
G |
2: 5,924,112 (GRCm38) |
L249F |
probably benign |
Het |
E2f4 |
A |
G |
8: 105,298,633 (GRCm38) |
D115G |
probably damaging |
Het |
Exoc3l4 |
G |
C |
12: 111,430,748 (GRCm38) |
D688H |
possibly damaging |
Het |
Fan1 |
C |
T |
7: 64,372,696 (GRCm38) |
V270I |
probably benign |
Het |
Fat2 |
A |
T |
11: 55,310,706 (GRCm38) |
I514N |
probably damaging |
Het |
Fndc1 |
G |
A |
17: 7,773,439 (GRCm38) |
T475I |
unknown |
Het |
Fstl5 |
T |
A |
3: 76,661,762 (GRCm38) |
I574N |
probably damaging |
Het |
Fzd4 |
T |
C |
7: 89,408,050 (GRCm38) |
V435A |
possibly damaging |
Het |
Fzd6 |
T |
C |
15: 39,033,932 (GRCm38) |
F492S |
probably damaging |
Het |
Gm4924 |
T |
A |
10: 82,377,527 (GRCm38) |
N386K |
unknown |
Het |
Gm8994 |
A |
G |
6: 136,328,873 (GRCm38) |
I111V |
probably benign |
Het |
Hbp1 |
A |
T |
12: 31,933,368 (GRCm38) |
D362E |
possibly damaging |
Het |
Hectd4 |
A |
C |
5: 121,307,014 (GRCm38) |
M105L |
probably benign |
Het |
Hivep2 |
C |
T |
10: 14,149,714 (GRCm38) |
P2424L |
probably benign |
Het |
Hspa4 |
A |
T |
11: 53,266,964 (GRCm38) |
|
probably null |
Het |
Igf2bp3 |
A |
G |
6: 49,134,731 (GRCm38) |
V122A |
probably damaging |
Het |
Ikzf2 |
A |
T |
1: 69,539,143 (GRCm38) |
N402K |
possibly damaging |
Het |
Ip6k1 |
T |
C |
9: 108,044,728 (GRCm38) |
F207S |
probably damaging |
Het |
Kbtbd8 |
C |
A |
6: 95,118,578 (GRCm38) |
N24K |
probably benign |
Het |
Krtap10-4 |
T |
G |
10: 77,826,820 (GRCm38) |
T75P |
unknown |
Het |
Macf1 |
C |
A |
4: 123,444,879 (GRCm38) |
S4355I |
probably benign |
Het |
Muc5b |
A |
T |
7: 141,857,305 (GRCm38) |
|
probably null |
Het |
Myo3a |
G |
A |
2: 22,282,589 (GRCm38) |
V179M |
probably damaging |
Het |
Nup210 |
G |
T |
6: 91,071,888 (GRCm38) |
T462K |
possibly damaging |
Het |
Olfr1106 |
T |
C |
2: 87,049,234 (GRCm38) |
M1V |
probably null |
Het |
Olfr365 |
A |
G |
2: 37,201,549 (GRCm38) |
M103V |
probably benign |
Het |
Olfr561 |
A |
G |
7: 102,774,934 (GRCm38) |
I137V |
probably benign |
Het |
Olfr743 |
T |
A |
14: 50,533,684 (GRCm38) |
S91T |
probably damaging |
Het |
Olfr920 |
A |
G |
9: 38,756,246 (GRCm38) |
Q186R |
possibly damaging |
Het |
Ostn |
G |
A |
16: 27,346,918 (GRCm38) |
R119Q |
probably damaging |
Het |
Pcdhga11 |
A |
T |
18: 37,756,511 (GRCm38) |
N191Y |
probably benign |
Het |
Pcsk6 |
A |
T |
7: 66,033,893 (GRCm38) |
Q752L |
probably benign |
Het |
Pfas |
T |
C |
11: 69,000,045 (GRCm38) |
T347A |
probably damaging |
Het |
Pkd1 |
A |
T |
17: 24,573,898 (GRCm38) |
R1520W |
probably damaging |
Het |
Prpf8 |
T |
C |
11: 75,508,906 (GRCm38) |
S2264P |
probably damaging |
Het |
Ptcd1 |
C |
A |
5: 145,151,364 (GRCm38) |
R612S |
probably benign |
Het |
Ptch2 |
T |
A |
4: 117,108,295 (GRCm38) |
F359Y |
probably benign |
Het |
Ptprr |
A |
C |
10: 116,237,295 (GRCm38) |
D474A |
probably damaging |
Het |
Pum1 |
C |
A |
4: 130,762,963 (GRCm38) |
Q846K |
probably benign |
Het |
Slc22a14 |
C |
T |
9: 119,170,611 (GRCm38) |
A505T |
possibly damaging |
Het |
Smpdl3a |
A |
G |
10: 57,802,554 (GRCm38) |
Y151C |
probably damaging |
Het |
Snrnp200 |
A |
G |
2: 127,229,102 (GRCm38) |
N1101S |
probably benign |
Het |
Sprr2b |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
3: 92,317,519 (GRCm38) |
|
probably benign |
Het |
Sptlc1 |
A |
G |
13: 53,333,957 (GRCm38) |
V450A |
probably benign |
Het |
Sqle |
A |
G |
15: 59,315,972 (GRCm38) |
Y43C |
probably benign |
Het |
Srgap3 |
T |
C |
6: 112,766,897 (GRCm38) |
H460R |
probably benign |
Het |
Syt15 |
A |
T |
14: 34,223,067 (GRCm38) |
E190D |
possibly damaging |
Het |
Tbc1d10b |
T |
C |
7: 127,198,821 (GRCm38) |
K716R |
probably benign |
Het |
Tbx20 |
T |
C |
9: 24,770,697 (GRCm38) |
I120M |
probably damaging |
Het |
Tgm1 |
T |
G |
14: 55,710,521 (GRCm38) |
I274L |
probably benign |
Het |
Tmem156 |
C |
T |
5: 65,075,562 (GRCm38) |
|
probably null |
Het |
Tnk2 |
A |
G |
16: 32,670,134 (GRCm38) |
D264G |
possibly damaging |
Het |
Tsc22d4 |
A |
G |
5: 137,758,694 (GRCm38) |
S306G |
possibly damaging |
Het |
Tut1 |
T |
A |
19: 8,959,262 (GRCm38) |
V150D |
probably benign |
Het |
Uchl5 |
T |
C |
1: 143,794,537 (GRCm38) |
F143L |
|
Het |
Vmn1r23 |
T |
C |
6: 57,926,334 (GRCm38) |
K153R |
probably benign |
Het |
Zfp236 |
A |
T |
18: 82,680,673 (GRCm38) |
D94E |
probably benign |
Het |
Zfp759 |
T |
C |
13: 67,139,626 (GRCm38) |
Y414H |
possibly damaging |
Het |
|
Other mutations in Dnah7b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Dnah7b
|
APN |
1 |
46,142,149 (GRCm38) |
missense |
probably benign |
0.04 |
IGL00796:Dnah7b
|
APN |
1 |
46,211,337 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL00825:Dnah7b
|
APN |
1 |
46,224,651 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00910:Dnah7b
|
APN |
1 |
46,066,729 (GRCm38) |
unclassified |
probably benign |
|
IGL00950:Dnah7b
|
APN |
1 |
46,214,322 (GRCm38) |
missense |
probably benign |
0.07 |
IGL01142:Dnah7b
|
APN |
1 |
46,195,378 (GRCm38) |
critical splice donor site |
probably null |
|
IGL01350:Dnah7b
|
APN |
1 |
46,081,432 (GRCm38) |
splice site |
probably benign |
|
IGL01392:Dnah7b
|
APN |
1 |
46,126,788 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01403:Dnah7b
|
APN |
1 |
46,116,300 (GRCm38) |
splice site |
probably benign |
|
IGL01460:Dnah7b
|
APN |
1 |
46,139,704 (GRCm38) |
missense |
possibly damaging |
0.82 |
IGL01576:Dnah7b
|
APN |
1 |
46,268,653 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01693:Dnah7b
|
APN |
1 |
46,358,147 (GRCm38) |
missense |
probably benign |
0.29 |
IGL01838:Dnah7b
|
APN |
1 |
46,358,137 (GRCm38) |
nonsense |
probably null |
|
IGL01906:Dnah7b
|
APN |
1 |
46,175,453 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01960:Dnah7b
|
APN |
1 |
46,124,337 (GRCm38) |
splice site |
probably benign |
|
IGL01989:Dnah7b
|
APN |
1 |
46,289,534 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02127:Dnah7b
|
APN |
1 |
46,139,875 (GRCm38) |
missense |
probably benign |
|
IGL02213:Dnah7b
|
APN |
1 |
46,233,592 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL02267:Dnah7b
|
APN |
1 |
46,226,930 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02349:Dnah7b
|
APN |
1 |
46,099,503 (GRCm38) |
nonsense |
probably null |
|
IGL02381:Dnah7b
|
APN |
1 |
46,277,120 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02473:Dnah7b
|
APN |
1 |
46,234,193 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02484:Dnah7b
|
APN |
1 |
46,195,318 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02590:Dnah7b
|
APN |
1 |
46,123,777 (GRCm38) |
missense |
probably benign |
0.02 |
IGL02655:Dnah7b
|
APN |
1 |
46,116,301 (GRCm38) |
splice site |
probably benign |
|
IGL02704:Dnah7b
|
APN |
1 |
46,142,133 (GRCm38) |
missense |
probably benign |
0.03 |
IGL02719:Dnah7b
|
APN |
1 |
46,099,608 (GRCm38) |
splice site |
probably benign |
|
IGL02745:Dnah7b
|
APN |
1 |
46,195,029 (GRCm38) |
splice site |
probably benign |
|
IGL02818:Dnah7b
|
APN |
1 |
46,290,808 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02892:Dnah7b
|
APN |
1 |
46,119,298 (GRCm38) |
missense |
possibly damaging |
0.79 |
IGL03285:Dnah7b
|
APN |
1 |
46,182,375 (GRCm38) |
missense |
probably benign |
0.00 |
IGL03354:Dnah7b
|
APN |
1 |
46,085,689 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03355:Dnah7b
|
APN |
1 |
46,119,304 (GRCm38) |
missense |
probably benign |
0.18 |
BB001:Dnah7b
|
UTSW |
1 |
46,219,430 (GRCm38) |
missense |
probably benign |
0.04 |
BB011:Dnah7b
|
UTSW |
1 |
46,219,430 (GRCm38) |
missense |
probably benign |
0.04 |
PIT4305001:Dnah7b
|
UTSW |
1 |
46,373,348 (GRCm38) |
missense |
probably damaging |
1.00 |
R0116:Dnah7b
|
UTSW |
1 |
46,213,360 (GRCm38) |
missense |
possibly damaging |
0.94 |
R0145:Dnah7b
|
UTSW |
1 |
46,223,178 (GRCm38) |
missense |
probably damaging |
1.00 |
R0230:Dnah7b
|
UTSW |
1 |
46,219,348 (GRCm38) |
missense |
probably damaging |
1.00 |
R0302:Dnah7b
|
UTSW |
1 |
46,123,777 (GRCm38) |
missense |
probably benign |
0.26 |
R0313:Dnah7b
|
UTSW |
1 |
46,207,643 (GRCm38) |
missense |
probably damaging |
1.00 |
R0317:Dnah7b
|
UTSW |
1 |
46,134,656 (GRCm38) |
missense |
probably damaging |
1.00 |
R0347:Dnah7b
|
UTSW |
1 |
46,240,944 (GRCm38) |
missense |
probably damaging |
1.00 |
R0352:Dnah7b
|
UTSW |
1 |
46,277,126 (GRCm38) |
missense |
probably damaging |
0.98 |
R0363:Dnah7b
|
UTSW |
1 |
46,236,788 (GRCm38) |
missense |
probably damaging |
0.99 |
R0379:Dnah7b
|
UTSW |
1 |
46,140,176 (GRCm38) |
missense |
probably benign |
0.00 |
R0502:Dnah7b
|
UTSW |
1 |
46,219,544 (GRCm38) |
missense |
probably damaging |
0.96 |
R0602:Dnah7b
|
UTSW |
1 |
46,324,842 (GRCm38) |
missense |
probably damaging |
1.00 |
R0631:Dnah7b
|
UTSW |
1 |
46,240,992 (GRCm38) |
missense |
probably benign |
0.02 |
R0664:Dnah7b
|
UTSW |
1 |
46,324,842 (GRCm38) |
missense |
probably damaging |
1.00 |
R0882:Dnah7b
|
UTSW |
1 |
46,340,132 (GRCm38) |
missense |
probably benign |
0.00 |
R0931:Dnah7b
|
UTSW |
1 |
46,099,612 (GRCm38) |
splice site |
probably benign |
|
R1035:Dnah7b
|
UTSW |
1 |
46,124,448 (GRCm38) |
missense |
probably benign |
|
R1147:Dnah7b
|
UTSW |
1 |
46,340,266 (GRCm38) |
missense |
probably damaging |
0.99 |
R1147:Dnah7b
|
UTSW |
1 |
46,340,266 (GRCm38) |
missense |
probably damaging |
0.99 |
R1166:Dnah7b
|
UTSW |
1 |
46,325,810 (GRCm38) |
missense |
probably damaging |
1.00 |
R1219:Dnah7b
|
UTSW |
1 |
46,340,120 (GRCm38) |
missense |
probably benign |
0.00 |
R1318:Dnah7b
|
UTSW |
1 |
46,099,509 (GRCm38) |
missense |
possibly damaging |
0.80 |
R1334:Dnah7b
|
UTSW |
1 |
46,322,335 (GRCm38) |
missense |
probably damaging |
0.99 |
R1429:Dnah7b
|
UTSW |
1 |
46,289,656 (GRCm38) |
missense |
possibly damaging |
0.84 |
R1440:Dnah7b
|
UTSW |
1 |
46,078,593 (GRCm38) |
splice site |
probably benign |
|
R1484:Dnah7b
|
UTSW |
1 |
46,137,543 (GRCm38) |
missense |
probably benign |
0.00 |
R1529:Dnah7b
|
UTSW |
1 |
46,177,281 (GRCm38) |
missense |
probably damaging |
1.00 |
R1544:Dnah7b
|
UTSW |
1 |
46,066,797 (GRCm38) |
missense |
unknown |
|
R1607:Dnah7b
|
UTSW |
1 |
46,290,646 (GRCm38) |
missense |
probably damaging |
1.00 |
R1609:Dnah7b
|
UTSW |
1 |
46,352,966 (GRCm38) |
missense |
probably damaging |
1.00 |
R1652:Dnah7b
|
UTSW |
1 |
46,175,390 (GRCm38) |
nonsense |
probably null |
|
R1681:Dnah7b
|
UTSW |
1 |
46,324,712 (GRCm38) |
nonsense |
probably null |
|
R1716:Dnah7b
|
UTSW |
1 |
46,191,783 (GRCm38) |
missense |
probably damaging |
1.00 |
R1753:Dnah7b
|
UTSW |
1 |
46,322,335 (GRCm38) |
missense |
probably damaging |
0.99 |
R1834:Dnah7b
|
UTSW |
1 |
46,233,759 (GRCm38) |
missense |
possibly damaging |
0.90 |
R1838:Dnah7b
|
UTSW |
1 |
46,277,105 (GRCm38) |
missense |
probably damaging |
1.00 |
R1838:Dnah7b
|
UTSW |
1 |
46,116,177 (GRCm38) |
missense |
probably benign |
0.04 |
R1898:Dnah7b
|
UTSW |
1 |
46,236,714 (GRCm38) |
missense |
probably benign |
0.02 |
R1962:Dnah7b
|
UTSW |
1 |
46,242,103 (GRCm38) |
missense |
possibly damaging |
0.95 |
R2001:Dnah7b
|
UTSW |
1 |
46,142,087 (GRCm38) |
missense |
possibly damaging |
0.69 |
R2049:Dnah7b
|
UTSW |
1 |
46,268,670 (GRCm38) |
missense |
probably damaging |
1.00 |
R2076:Dnah7b
|
UTSW |
1 |
46,242,321 (GRCm38) |
nonsense |
probably null |
|
R2083:Dnah7b
|
UTSW |
1 |
46,241,067 (GRCm38) |
missense |
possibly damaging |
0.90 |
R2140:Dnah7b
|
UTSW |
1 |
46,268,670 (GRCm38) |
missense |
probably damaging |
1.00 |
R2141:Dnah7b
|
UTSW |
1 |
46,268,670 (GRCm38) |
missense |
probably damaging |
1.00 |
R2142:Dnah7b
|
UTSW |
1 |
46,268,670 (GRCm38) |
missense |
probably damaging |
1.00 |
R2165:Dnah7b
|
UTSW |
1 |
46,097,992 (GRCm38) |
splice site |
probably benign |
|
R2172:Dnah7b
|
UTSW |
1 |
46,124,512 (GRCm38) |
missense |
probably benign |
0.12 |
R2239:Dnah7b
|
UTSW |
1 |
46,201,184 (GRCm38) |
splice site |
probably benign |
|
R2247:Dnah7b
|
UTSW |
1 |
46,277,063 (GRCm38) |
missense |
probably damaging |
1.00 |
R2267:Dnah7b
|
UTSW |
1 |
46,233,915 (GRCm38) |
missense |
probably damaging |
1.00 |
R2405:Dnah7b
|
UTSW |
1 |
46,362,954 (GRCm38) |
missense |
probably benign |
0.31 |
R2509:Dnah7b
|
UTSW |
1 |
46,195,287 (GRCm38) |
missense |
probably damaging |
0.96 |
R2895:Dnah7b
|
UTSW |
1 |
46,139,741 (GRCm38) |
missense |
probably damaging |
1.00 |
R2965:Dnah7b
|
UTSW |
1 |
46,207,572 (GRCm38) |
missense |
probably damaging |
1.00 |
R3013:Dnah7b
|
UTSW |
1 |
46,188,687 (GRCm38) |
critical splice donor site |
probably null |
|
R3022:Dnah7b
|
UTSW |
1 |
46,182,423 (GRCm38) |
missense |
probably damaging |
0.99 |
R3056:Dnah7b
|
UTSW |
1 |
46,268,709 (GRCm38) |
missense |
possibly damaging |
0.95 |
R3107:Dnah7b
|
UTSW |
1 |
46,352,873 (GRCm38) |
missense |
probably benign |
0.00 |
R3735:Dnah7b
|
UTSW |
1 |
46,299,875 (GRCm38) |
missense |
probably benign |
0.05 |
R3898:Dnah7b
|
UTSW |
1 |
46,243,257 (GRCm38) |
missense |
probably damaging |
1.00 |
R3944:Dnah7b
|
UTSW |
1 |
46,137,485 (GRCm38) |
missense |
probably damaging |
1.00 |
R3983:Dnah7b
|
UTSW |
1 |
46,233,711 (GRCm38) |
missense |
possibly damaging |
0.88 |
R4041:Dnah7b
|
UTSW |
1 |
46,081,495 (GRCm38) |
missense |
probably benign |
|
R4172:Dnah7b
|
UTSW |
1 |
46,226,946 (GRCm38) |
missense |
probably damaging |
1.00 |
R4210:Dnah7b
|
UTSW |
1 |
46,137,418 (GRCm38) |
missense |
possibly damaging |
0.63 |
R4306:Dnah7b
|
UTSW |
1 |
46,221,772 (GRCm38) |
missense |
probably damaging |
0.99 |
R4391:Dnah7b
|
UTSW |
1 |
46,337,594 (GRCm38) |
splice site |
probably null |
|
R4414:Dnah7b
|
UTSW |
1 |
46,126,680 (GRCm38) |
missense |
probably benign |
0.00 |
R4495:Dnah7b
|
UTSW |
1 |
46,085,632 (GRCm38) |
missense |
probably benign |
0.00 |
R4660:Dnah7b
|
UTSW |
1 |
46,289,536 (GRCm38) |
missense |
probably damaging |
1.00 |
R4670:Dnah7b
|
UTSW |
1 |
46,078,524 (GRCm38) |
missense |
probably damaging |
1.00 |
R4675:Dnah7b
|
UTSW |
1 |
46,217,157 (GRCm38) |
missense |
possibly damaging |
0.89 |
R4685:Dnah7b
|
UTSW |
1 |
46,211,328 (GRCm38) |
missense |
probably damaging |
1.00 |
R4727:Dnah7b
|
UTSW |
1 |
46,207,656 (GRCm38) |
missense |
probably damaging |
1.00 |
R4735:Dnah7b
|
UTSW |
1 |
46,066,955 (GRCm38) |
missense |
unknown |
|
R4780:Dnah7b
|
UTSW |
1 |
46,353,014 (GRCm38) |
missense |
probably benign |
|
R4828:Dnah7b
|
UTSW |
1 |
46,128,112 (GRCm38) |
missense |
possibly damaging |
0.59 |
R4859:Dnah7b
|
UTSW |
1 |
46,356,602 (GRCm38) |
missense |
probably damaging |
1.00 |
R4865:Dnah7b
|
UTSW |
1 |
46,195,074 (GRCm38) |
missense |
probably damaging |
1.00 |
R4871:Dnah7b
|
UTSW |
1 |
46,081,444 (GRCm38) |
missense |
probably benign |
0.21 |
R4881:Dnah7b
|
UTSW |
1 |
46,201,318 (GRCm38) |
missense |
probably damaging |
1.00 |
R4902:Dnah7b
|
UTSW |
1 |
46,290,775 (GRCm38) |
missense |
probably benign |
0.04 |
R4960:Dnah7b
|
UTSW |
1 |
46,233,726 (GRCm38) |
missense |
probably benign |
|
R5000:Dnah7b
|
UTSW |
1 |
46,099,503 (GRCm38) |
nonsense |
probably null |
|
R5005:Dnah7b
|
UTSW |
1 |
46,242,028 (GRCm38) |
missense |
probably damaging |
0.99 |
R5026:Dnah7b
|
UTSW |
1 |
46,187,363 (GRCm38) |
missense |
probably damaging |
0.99 |
R5080:Dnah7b
|
UTSW |
1 |
46,182,380 (GRCm38) |
nonsense |
probably null |
|
R5174:Dnah7b
|
UTSW |
1 |
46,243,349 (GRCm38) |
missense |
possibly damaging |
0.83 |
R5178:Dnah7b
|
UTSW |
1 |
46,358,216 (GRCm38) |
missense |
possibly damaging |
0.50 |
R5244:Dnah7b
|
UTSW |
1 |
46,233,858 (GRCm38) |
missense |
probably damaging |
1.00 |
R5250:Dnah7b
|
UTSW |
1 |
46,373,354 (GRCm38) |
missense |
probably damaging |
1.00 |
R5350:Dnah7b
|
UTSW |
1 |
46,233,689 (GRCm38) |
missense |
probably benign |
0.16 |
R5380:Dnah7b
|
UTSW |
1 |
46,217,191 (GRCm38) |
missense |
probably benign |
0.18 |
R5387:Dnah7b
|
UTSW |
1 |
46,188,659 (GRCm38) |
missense |
probably damaging |
1.00 |
R5423:Dnah7b
|
UTSW |
1 |
46,358,271 (GRCm38) |
missense |
probably benign |
0.01 |
R5426:Dnah7b
|
UTSW |
1 |
46,242,206 (GRCm38) |
missense |
possibly damaging |
0.82 |
R5451:Dnah7b
|
UTSW |
1 |
46,242,019 (GRCm38) |
missense |
possibly damaging |
0.73 |
R5459:Dnah7b
|
UTSW |
1 |
46,109,312 (GRCm38) |
missense |
probably null |
|
R5479:Dnah7b
|
UTSW |
1 |
46,223,105 (GRCm38) |
missense |
probably damaging |
1.00 |
R5583:Dnah7b
|
UTSW |
1 |
46,242,199 (GRCm38) |
missense |
probably benign |
0.06 |
R5637:Dnah7b
|
UTSW |
1 |
46,356,514 (GRCm38) |
missense |
possibly damaging |
0.95 |
R5641:Dnah7b
|
UTSW |
1 |
46,268,764 (GRCm38) |
splice site |
probably null |
|
R5659:Dnah7b
|
UTSW |
1 |
46,352,849 (GRCm38) |
missense |
probably damaging |
1.00 |
R5739:Dnah7b
|
UTSW |
1 |
46,233,992 (GRCm38) |
missense |
probably damaging |
1.00 |
R5759:Dnah7b
|
UTSW |
1 |
46,277,120 (GRCm38) |
missense |
probably damaging |
1.00 |
R5821:Dnah7b
|
UTSW |
1 |
46,142,132 (GRCm38) |
missense |
possibly damaging |
0.91 |
R5874:Dnah7b
|
UTSW |
1 |
46,191,725 (GRCm38) |
missense |
probably damaging |
1.00 |
R5892:Dnah7b
|
UTSW |
1 |
46,337,593 (GRCm38) |
critical splice donor site |
probably null |
|
R5918:Dnah7b
|
UTSW |
1 |
46,221,643 (GRCm38) |
missense |
probably benign |
|
R5941:Dnah7b
|
UTSW |
1 |
46,187,290 (GRCm38) |
missense |
probably damaging |
1.00 |
R5965:Dnah7b
|
UTSW |
1 |
46,362,987 (GRCm38) |
missense |
probably damaging |
1.00 |
R5987:Dnah7b
|
UTSW |
1 |
46,119,398 (GRCm38) |
splice site |
probably null |
|
R6041:Dnah7b
|
UTSW |
1 |
46,289,645 (GRCm38) |
missense |
probably benign |
0.04 |
R6043:Dnah7b
|
UTSW |
1 |
46,139,789 (GRCm38) |
missense |
probably benign |
|
R6049:Dnah7b
|
UTSW |
1 |
46,085,602 (GRCm38) |
missense |
probably benign |
|
R6131:Dnah7b
|
UTSW |
1 |
46,253,466 (GRCm38) |
missense |
probably damaging |
1.00 |
R6168:Dnah7b
|
UTSW |
1 |
46,290,703 (GRCm38) |
missense |
probably damaging |
1.00 |
R6195:Dnah7b
|
UTSW |
1 |
46,204,269 (GRCm38) |
missense |
probably damaging |
1.00 |
R6219:Dnah7b
|
UTSW |
1 |
46,233,585 (GRCm38) |
missense |
probably benign |
0.03 |
R6226:Dnah7b
|
UTSW |
1 |
46,126,668 (GRCm38) |
missense |
probably benign |
0.01 |
R6233:Dnah7b
|
UTSW |
1 |
46,204,269 (GRCm38) |
missense |
probably damaging |
1.00 |
R6247:Dnah7b
|
UTSW |
1 |
46,225,888 (GRCm38) |
missense |
probably benign |
|
R6273:Dnah7b
|
UTSW |
1 |
46,242,316 (GRCm38) |
missense |
possibly damaging |
0.94 |
R6279:Dnah7b
|
UTSW |
1 |
46,325,886 (GRCm38) |
missense |
probably damaging |
1.00 |
R6300:Dnah7b
|
UTSW |
1 |
46,325,886 (GRCm38) |
missense |
probably damaging |
1.00 |
R6330:Dnah7b
|
UTSW |
1 |
46,340,175 (GRCm38) |
missense |
probably damaging |
1.00 |
R6476:Dnah7b
|
UTSW |
1 |
46,242,204 (GRCm38) |
nonsense |
probably null |
|
R6494:Dnah7b
|
UTSW |
1 |
46,099,431 (GRCm38) |
missense |
probably damaging |
1.00 |
R6762:Dnah7b
|
UTSW |
1 |
46,224,742 (GRCm38) |
missense |
probably benign |
0.12 |
R6800:Dnah7b
|
UTSW |
1 |
46,340,217 (GRCm38) |
missense |
possibly damaging |
0.90 |
R6838:Dnah7b
|
UTSW |
1 |
46,191,788 (GRCm38) |
missense |
probably damaging |
1.00 |
R6937:Dnah7b
|
UTSW |
1 |
46,195,120 (GRCm38) |
missense |
probably damaging |
1.00 |
R6940:Dnah7b
|
UTSW |
1 |
46,119,268 (GRCm38) |
missense |
probably benign |
0.12 |
R6969:Dnah7b
|
UTSW |
1 |
46,358,238 (GRCm38) |
missense |
probably damaging |
1.00 |
R6993:Dnah7b
|
UTSW |
1 |
46,195,139 (GRCm38) |
critical splice donor site |
probably null |
|
R7040:Dnah7b
|
UTSW |
1 |
46,236,809 (GRCm38) |
missense |
probably benign |
0.01 |
R7117:Dnah7b
|
UTSW |
1 |
46,352,813 (GRCm38) |
critical splice acceptor site |
probably null |
|
R7135:Dnah7b
|
UTSW |
1 |
46,139,710 (GRCm38) |
missense |
probably damaging |
0.99 |
R7153:Dnah7b
|
UTSW |
1 |
46,126,804 (GRCm38) |
missense |
probably benign |
0.05 |
R7189:Dnah7b
|
UTSW |
1 |
46,242,142 (GRCm38) |
missense |
probably damaging |
1.00 |
R7237:Dnah7b
|
UTSW |
1 |
46,139,966 (GRCm38) |
missense |
probably damaging |
0.98 |
R7243:Dnah7b
|
UTSW |
1 |
46,083,754 (GRCm38) |
missense |
probably benign |
|
R7244:Dnah7b
|
UTSW |
1 |
46,277,143 (GRCm38) |
missense |
probably damaging |
0.99 |
R7248:Dnah7b
|
UTSW |
1 |
46,142,085 (GRCm38) |
missense |
possibly damaging |
0.83 |
R7318:Dnah7b
|
UTSW |
1 |
46,195,372 (GRCm38) |
missense |
probably damaging |
1.00 |
R7375:Dnah7b
|
UTSW |
1 |
46,303,634 (GRCm38) |
missense |
probably damaging |
1.00 |
R7483:Dnah7b
|
UTSW |
1 |
46,175,419 (GRCm38) |
missense |
probably damaging |
1.00 |
R7486:Dnah7b
|
UTSW |
1 |
46,290,734 (GRCm38) |
missense |
probably damaging |
1.00 |
R7498:Dnah7b
|
UTSW |
1 |
46,325,765 (GRCm38) |
missense |
probably damaging |
1.00 |
R7501:Dnah7b
|
UTSW |
1 |
46,356,554 (GRCm38) |
missense |
probably damaging |
1.00 |
R7513:Dnah7b
|
UTSW |
1 |
46,124,346 (GRCm38) |
missense |
probably benign |
0.06 |
R7547:Dnah7b
|
UTSW |
1 |
46,214,413 (GRCm38) |
missense |
possibly damaging |
0.82 |
R7620:Dnah7b
|
UTSW |
1 |
46,268,634 (GRCm38) |
missense |
probably damaging |
1.00 |
R7670:Dnah7b
|
UTSW |
1 |
46,109,302 (GRCm38) |
missense |
probably benign |
|
R7676:Dnah7b
|
UTSW |
1 |
46,234,164 (GRCm38) |
nonsense |
probably null |
|
R7760:Dnah7b
|
UTSW |
1 |
46,201,253 (GRCm38) |
missense |
probably damaging |
1.00 |
R7768:Dnah7b
|
UTSW |
1 |
46,137,474 (GRCm38) |
missense |
probably benign |
|
R7807:Dnah7b
|
UTSW |
1 |
46,214,367 (GRCm38) |
missense |
probably benign |
|
R7895:Dnah7b
|
UTSW |
1 |
46,249,950 (GRCm38) |
missense |
probably damaging |
1.00 |
R7911:Dnah7b
|
UTSW |
1 |
46,139,678 (GRCm38) |
missense |
probably damaging |
1.00 |
R7924:Dnah7b
|
UTSW |
1 |
46,219,430 (GRCm38) |
missense |
probably benign |
0.04 |
R7944:Dnah7b
|
UTSW |
1 |
46,227,003 (GRCm38) |
missense |
probably benign |
|
R7946:Dnah7b
|
UTSW |
1 |
46,233,579 (GRCm38) |
missense |
probably damaging |
1.00 |
R7983:Dnah7b
|
UTSW |
1 |
46,243,424 (GRCm38) |
missense |
probably damaging |
1.00 |
R8012:Dnah7b
|
UTSW |
1 |
46,243,365 (GRCm38) |
missense |
probably damaging |
1.00 |
R8069:Dnah7b
|
UTSW |
1 |
46,224,706 (GRCm38) |
nonsense |
probably null |
|
R8094:Dnah7b
|
UTSW |
1 |
46,126,804 (GRCm38) |
missense |
probably benign |
0.01 |
R8137:Dnah7b
|
UTSW |
1 |
46,233,753 (GRCm38) |
missense |
probably damaging |
1.00 |
R8167:Dnah7b
|
UTSW |
1 |
46,253,511 (GRCm38) |
missense |
possibly damaging |
0.95 |
R8268:Dnah7b
|
UTSW |
1 |
46,356,576 (GRCm38) |
missense |
probably benign |
0.43 |
R8309:Dnah7b
|
UTSW |
1 |
46,139,872 (GRCm38) |
missense |
probably damaging |
1.00 |
R8313:Dnah7b
|
UTSW |
1 |
46,175,296 (GRCm38) |
missense |
possibly damaging |
0.81 |
R8410:Dnah7b
|
UTSW |
1 |
46,356,659 (GRCm38) |
critical splice donor site |
probably null |
|
R8438:Dnah7b
|
UTSW |
1 |
46,188,679 (GRCm38) |
missense |
probably damaging |
1.00 |
R8446:Dnah7b
|
UTSW |
1 |
46,290,715 (GRCm38) |
missense |
probably damaging |
1.00 |
R8471:Dnah7b
|
UTSW |
1 |
46,099,490 (GRCm38) |
missense |
possibly damaging |
0.92 |
R8551:Dnah7b
|
UTSW |
1 |
46,116,200 (GRCm38) |
missense |
possibly damaging |
0.94 |
R8711:Dnah7b
|
UTSW |
1 |
46,175,438 (GRCm38) |
missense |
probably damaging |
1.00 |
R8745:Dnah7b
|
UTSW |
1 |
46,182,464 (GRCm38) |
missense |
possibly damaging |
0.82 |
R8765:Dnah7b
|
UTSW |
1 |
46,352,999 (GRCm38) |
missense |
possibly damaging |
0.91 |
R8797:Dnah7b
|
UTSW |
1 |
46,123,646 (GRCm38) |
missense |
probably damaging |
1.00 |
R8805:Dnah7b
|
UTSW |
1 |
46,234,145 (GRCm38) |
missense |
possibly damaging |
0.90 |
R8830:Dnah7b
|
UTSW |
1 |
46,191,793 (GRCm38) |
missense |
probably damaging |
1.00 |
R8861:Dnah7b
|
UTSW |
1 |
46,241,076 (GRCm38) |
missense |
possibly damaging |
0.82 |
R8905:Dnah7b
|
UTSW |
1 |
46,253,374 (GRCm38) |
missense |
probably damaging |
0.99 |
R9009:Dnah7b
|
UTSW |
1 |
46,223,072 (GRCm38) |
missense |
probably benign |
0.00 |
R9058:Dnah7b
|
UTSW |
1 |
46,243,415 (GRCm38) |
missense |
probably damaging |
1.00 |
R9130:Dnah7b
|
UTSW |
1 |
46,134,514 (GRCm38) |
missense |
probably benign |
0.01 |
R9131:Dnah7b
|
UTSW |
1 |
46,227,020 (GRCm38) |
missense |
probably damaging |
1.00 |
R9181:Dnah7b
|
UTSW |
1 |
46,142,034 (GRCm38) |
missense |
probably damaging |
1.00 |
R9182:Dnah7b
|
UTSW |
1 |
46,290,878 (GRCm38) |
missense |
probably benign |
0.06 |
R9223:Dnah7b
|
UTSW |
1 |
46,322,260 (GRCm38) |
missense |
probably benign |
0.12 |
R9391:Dnah7b
|
UTSW |
1 |
46,233,754 (GRCm38) |
nonsense |
probably null |
|
R9392:Dnah7b
|
UTSW |
1 |
46,123,738 (GRCm38) |
nonsense |
probably null |
|
R9456:Dnah7b
|
UTSW |
1 |
46,126,793 (GRCm38) |
missense |
possibly damaging |
0.82 |
R9498:Dnah7b
|
UTSW |
1 |
46,214,404 (GRCm38) |
missense |
probably benign |
0.27 |
R9553:Dnah7b
|
UTSW |
1 |
46,225,796 (GRCm38) |
missense |
probably damaging |
0.99 |
R9598:Dnah7b
|
UTSW |
1 |
46,253,461 (GRCm38) |
missense |
possibly damaging |
0.67 |
R9653:Dnah7b
|
UTSW |
1 |
46,213,384 (GRCm38) |
missense |
possibly damaging |
0.55 |
R9781:Dnah7b
|
UTSW |
1 |
46,337,594 (GRCm38) |
splice site |
probably null |
|
RF020:Dnah7b
|
UTSW |
1 |
46,373,261 (GRCm38) |
missense |
possibly damaging |
0.84 |
V8831:Dnah7b
|
UTSW |
1 |
46,373,298 (GRCm38) |
nonsense |
probably null |
|
X0023:Dnah7b
|
UTSW |
1 |
46,303,577 (GRCm38) |
missense |
probably benign |
0.04 |
|