Other mutations in this stock |
Total: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700006A11Rik |
T |
C |
3: 124,406,453 (GRCm38) |
I497V |
probably benign |
Het |
2010300C02Rik |
T |
C |
1: 37,625,300 (GRCm38) |
M506V |
probably benign |
Het |
4930571K23Rik |
C |
A |
7: 125,369,139 (GRCm38) |
|
noncoding transcript |
Het |
Abca17 |
G |
T |
17: 24,289,613 (GRCm38) |
|
probably benign |
Het |
Ablim1 |
C |
T |
19: 57,152,359 (GRCm38) |
R196Q |
probably damaging |
Het |
Acot11 |
T |
C |
4: 106,755,319 (GRCm38) |
I379V |
possibly damaging |
Het |
Acot4 |
G |
A |
12: 84,041,873 (GRCm38) |
G165D |
probably damaging |
Het |
Agrn |
A |
T |
4: 156,166,424 (GRCm38) |
|
probably null |
Het |
Ahctf1 |
T |
C |
1: 179,770,693 (GRCm38) |
S945G |
possibly damaging |
Het |
Akr1c13 |
C |
T |
13: 4,198,584 (GRCm38) |
R263C |
probably damaging |
Het |
Arfgap1 |
T |
A |
2: 180,974,053 (GRCm38) |
|
probably benign |
Het |
Arhgef3 |
A |
G |
14: 27,379,676 (GRCm38) |
K103R |
probably damaging |
Het |
Cabp1 |
A |
T |
5: 115,172,784 (GRCm38) |
N211K |
probably damaging |
Het |
Cacna1c |
T |
A |
6: 118,734,982 (GRCm38) |
D261V |
probably damaging |
Het |
Car11 |
G |
A |
7: 45,701,359 (GRCm38) |
G93E |
probably damaging |
Het |
Card10 |
A |
G |
15: 78,780,273 (GRCm38) |
I821T |
probably benign |
Het |
Cast |
T |
C |
13: 74,737,616 (GRCm38) |
I277V |
probably benign |
Het |
Cenpj |
T |
C |
14: 56,532,237 (GRCm38) |
K1165R |
probably null |
Het |
Cenpk |
A |
G |
13: 104,234,167 (GRCm38) |
|
probably null |
Het |
Cmya5 |
T |
C |
13: 93,093,558 (GRCm38) |
Q1674R |
probably benign |
Het |
Cnnm1 |
T |
A |
19: 43,441,886 (GRCm38) |
V481D |
probably damaging |
Het |
Csmd3 |
CCTTTGCGCTT |
CCTT |
15: 47,741,236 (GRCm38) |
|
probably null |
Het |
Cyp2c50 |
G |
A |
19: 40,090,569 (GRCm38) |
V119I |
probably benign |
Het |
Dnah8 |
G |
A |
17: 30,775,045 (GRCm38) |
D3379N |
probably benign |
Het |
Dnajc4 |
C |
T |
19: 6,990,743 (GRCm38) |
R55H |
probably damaging |
Het |
Ebf4 |
C |
T |
2: 130,306,562 (GRCm38) |
R98* |
probably null |
Het |
Epha4 |
G |
A |
1: 77,511,702 (GRCm38) |
A47V |
possibly damaging |
Het |
Ercc8 |
T |
C |
13: 108,183,717 (GRCm38) |
|
probably benign |
Het |
Exo1 |
T |
C |
1: 175,905,833 (GRCm38) |
F75S |
probably damaging |
Het |
Fam168a |
G |
T |
7: 100,834,184 (GRCm38) |
|
probably null |
Het |
Fat3 |
G |
A |
9: 15,925,014 (GRCm38) |
R4065W |
possibly damaging |
Het |
Gm10639 |
T |
A |
9: 78,294,807 (GRCm38) |
M1K |
probably null |
Het |
Gm13103 |
G |
A |
4: 143,851,991 (GRCm38) |
V274I |
probably benign |
Het |
Gm5431 |
T |
A |
11: 48,888,709 (GRCm38) |
N740I |
probably benign |
Het |
Gm5900 |
T |
A |
7: 104,950,364 (GRCm38) |
|
noncoding transcript |
Het |
Gpi1 |
A |
G |
7: 34,205,923 (GRCm38) |
S359P |
probably damaging |
Het |
Gpr156 |
A |
G |
16: 37,947,787 (GRCm38) |
R22G |
probably benign |
Het |
Greb1 |
A |
G |
12: 16,724,922 (GRCm38) |
V158A |
probably damaging |
Het |
Grin2c |
T |
A |
11: 115,251,068 (GRCm38) |
K842* |
probably null |
Het |
Hnf4a |
T |
A |
2: 163,566,241 (GRCm38) |
L329Q |
probably damaging |
Het |
Hsp90ab1 |
A |
G |
17: 45,569,341 (GRCm38) |
L92P |
probably damaging |
Het |
Ido1 |
T |
A |
8: 24,584,485 (GRCm38) |
R290* |
probably null |
Het |
Ifnlr1 |
G |
T |
4: 135,705,248 (GRCm38) |
D332Y |
probably damaging |
Het |
Ift172 |
T |
C |
5: 31,262,968 (GRCm38) |
N1108S |
probably benign |
Het |
Igkv3-9 |
T |
A |
6: 70,588,744 (GRCm38) |
M109K |
probably benign |
Het |
Igsf10 |
T |
C |
3: 59,331,866 (GRCm38) |
D298G |
probably damaging |
Het |
Iqck |
T |
G |
7: 118,876,282 (GRCm38) |
M98R |
probably benign |
Het |
Klk1b1 |
T |
C |
7: 43,969,379 (GRCm38) |
V60A |
probably damaging |
Het |
Krtap1-3 |
C |
T |
11: 99,590,827 (GRCm38) |
E165K |
unknown |
Het |
Lair1 |
A |
G |
7: 4,010,783 (GRCm38) |
L155P |
probably damaging |
Het |
Mast4 |
G |
T |
13: 102,853,842 (GRCm38) |
S57Y |
probably damaging |
Het |
Mical3 |
T |
C |
6: 121,034,157 (GRCm38) |
H360R |
probably damaging |
Het |
Muc5b |
A |
T |
7: 141,859,061 (GRCm38) |
N1915Y |
unknown |
Het |
Myh1 |
A |
G |
11: 67,205,597 (GRCm38) |
I301V |
probably benign |
Het |
Nck2 |
T |
A |
1: 43,554,233 (GRCm38) |
V200E |
probably damaging |
Het |
Olfr10 |
T |
G |
11: 49,318,221 (GRCm38) |
L225R |
probably damaging |
Het |
Olfr1214 |
T |
G |
2: 88,987,431 (GRCm38) |
Y257S |
probably damaging |
Het |
Olfr1271 |
T |
C |
2: 90,265,686 (GRCm38) |
Y248C |
possibly damaging |
Het |
Olfr1282 |
C |
T |
2: 111,335,731 (GRCm38) |
V116I |
probably damaging |
Het |
Olfr1313 |
T |
A |
2: 112,072,492 (GRCm38) |
L30F |
probably benign |
Het |
Olfr1453 |
T |
A |
19: 13,027,694 (GRCm38) |
I212F |
probably damaging |
Het |
Olfr668 |
G |
A |
7: 104,925,687 (GRCm38) |
H26Y |
probably benign |
Het |
Olfr870 |
A |
G |
9: 20,171,229 (GRCm38) |
L114P |
probably damaging |
Het |
Otoa |
C |
T |
7: 121,160,472 (GRCm38) |
T1099I |
probably benign |
Het |
Pask |
T |
A |
1: 93,330,763 (GRCm38) |
I288F |
possibly damaging |
Het |
Pcnx4 |
T |
C |
12: 72,566,972 (GRCm38) |
W564R |
probably damaging |
Het |
Pitpnm2 |
T |
C |
5: 124,136,326 (GRCm38) |
E240G |
probably damaging |
Het |
Ppp1r16b |
A |
G |
2: 158,761,463 (GRCm38) |
Y436C |
possibly damaging |
Het |
Prkca |
T |
C |
11: 107,979,206 (GRCm38) |
Y37C |
probably damaging |
Het |
Rad18 |
T |
G |
6: 112,675,922 (GRCm38) |
H238P |
possibly damaging |
Het |
Rap1b |
T |
A |
10: 117,818,539 (GRCm38) |
Q1L |
probably damaging |
Het |
Rgs9 |
T |
C |
11: 109,268,972 (GRCm38) |
Y178C |
probably benign |
Het |
Rpl3l |
A |
T |
17: 24,732,386 (GRCm38) |
D87V |
possibly damaging |
Het |
Scrn2 |
T |
C |
11: 97,033,166 (GRCm38) |
V292A |
possibly damaging |
Het |
Sdad1 |
A |
G |
5: 92,305,825 (GRCm38) |
Y35H |
probably benign |
Het |
Sez6l2 |
T |
C |
7: 126,953,772 (GRCm38) |
S177P |
probably benign |
Het |
Sh3bp1 |
C |
T |
15: 78,911,506 (GRCm38) |
P612S |
probably damaging |
Het |
Shank1 |
T |
C |
7: 44,351,724 (GRCm38) |
S956P |
unknown |
Het |
Shank1 |
G |
A |
7: 44,352,123 (GRCm38) |
A1089T |
unknown |
Het |
Shprh |
G |
A |
10: 11,166,724 (GRCm38) |
C817Y |
probably damaging |
Het |
Spata22 |
C |
T |
11: 73,345,767 (GRCm38) |
P300S |
probably damaging |
Het |
Sstr2 |
A |
T |
11: 113,624,923 (GRCm38) |
I223F |
probably damaging |
Het |
Stom |
C |
T |
2: 35,320,342 (GRCm38) |
A217T |
probably damaging |
Het |
Stpg1 |
T |
C |
4: 135,536,649 (GRCm38) |
V341A |
probably benign |
Het |
Tagap |
A |
G |
17: 7,928,754 (GRCm38) |
T99A |
probably benign |
Het |
Tas1r2 |
A |
G |
4: 139,659,851 (GRCm38) |
N207S |
probably damaging |
Het |
Thbs2 |
A |
G |
17: 14,685,843 (GRCm38) |
V265A |
probably benign |
Het |
Thyn1 |
A |
G |
9: 27,000,020 (GRCm38) |
R3G |
possibly damaging |
Het |
Tia1 |
T |
A |
6: 86,424,330 (GRCm38) |
|
probably null |
Het |
Tktl2 |
A |
G |
8: 66,512,852 (GRCm38) |
E354G |
probably benign |
Het |
Tmc8 |
A |
G |
11: 117,792,685 (GRCm38) |
T689A |
possibly damaging |
Het |
Tmem11 |
A |
T |
11: 60,864,981 (GRCm38) |
|
probably null |
Het |
Tmem55b |
A |
T |
14: 50,929,658 (GRCm38) |
Y129* |
probably null |
Het |
Tmem57 |
A |
G |
4: 134,804,388 (GRCm38) |
S657P |
probably damaging |
Het |
Tnik |
T |
C |
3: 28,667,915 (GRCm38) |
V1310A |
probably damaging |
Het |
Trappc10 |
A |
G |
10: 78,211,523 (GRCm38) |
S380P |
possibly damaging |
Het |
Trim8 |
C |
T |
19: 46,515,295 (GRCm38) |
P429S |
probably benign |
Het |
Ttc25 |
T |
G |
11: 100,553,535 (GRCm38) |
L222R |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,857,412 (GRCm38) |
|
probably benign |
Het |
Ulk2 |
T |
C |
11: 61,787,514 (GRCm38) |
Y793C |
probably benign |
Het |
Vill |
G |
A |
9: 119,070,302 (GRCm38) |
V337M |
possibly damaging |
Het |
Vps53 |
C |
A |
11: 76,066,835 (GRCm38) |
V364F |
possibly damaging |
Het |
Wdr66 |
A |
G |
5: 123,256,106 (GRCm38) |
K353E |
probably benign |
Het |
Zan |
A |
T |
5: 137,456,586 (GRCm38) |
I1396N |
unknown |
Het |
Zfa-ps |
A |
C |
10: 52,544,243 (GRCm38) |
|
noncoding transcript |
Het |
Zfp426 |
T |
C |
9: 20,470,681 (GRCm38) |
T337A |
possibly damaging |
Het |
Zfp536 |
T |
C |
7: 37,567,978 (GRCm38) |
E671G |
possibly damaging |
Het |
Zfp985 |
A |
G |
4: 147,582,986 (GRCm38) |
T104A |
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 |
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 |
|
R7731:Dnah7b
|
UTSW |
1 |
46,139,745 (GRCm38) |
missense |
probably benign |
0.00 |
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 |
|