Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310009B15Rik |
T |
A |
1: 138,784,394 (GRCm39) |
E54D |
possibly damaging |
Het |
Abcb6 |
C |
A |
1: 75,154,002 (GRCm39) |
G367W |
probably damaging |
Het |
Asprv1 |
A |
G |
6: 86,605,405 (GRCm39) |
M84V |
probably damaging |
Het |
Aspscr1 |
T |
C |
11: 120,592,333 (GRCm39) |
V291A |
probably damaging |
Het |
B4galnt4 |
T |
C |
7: 140,651,633 (GRCm39) |
F980L |
probably damaging |
Het |
Bpi |
G |
A |
2: 158,113,941 (GRCm39) |
V280I |
possibly damaging |
Het |
Bptf |
T |
C |
11: 106,986,706 (GRCm39) |
D581G |
probably damaging |
Het |
Cap2 |
T |
A |
13: 46,793,302 (GRCm39) |
Y223N |
possibly damaging |
Het |
Ccdc141 |
A |
C |
2: 76,888,324 (GRCm39) |
I480M |
possibly damaging |
Het |
Ccn4 |
C |
A |
15: 66,778,489 (GRCm39) |
Y103* |
probably null |
Het |
Ccnh |
T |
A |
13: 85,337,758 (GRCm39) |
V35E |
probably benign |
Het |
Cd6 |
G |
T |
19: 10,771,589 (GRCm39) |
S433* |
probably null |
Het |
Ceacam10 |
A |
C |
7: 24,480,477 (GRCm39) |
I83L |
probably benign |
Het |
Chek2 |
T |
C |
5: 111,003,705 (GRCm39) |
|
probably null |
Het |
Chia1 |
A |
T |
3: 106,029,765 (GRCm39) |
D73V |
probably damaging |
Het |
Commd2 |
G |
A |
3: 57,554,215 (GRCm39) |
T162I |
probably benign |
Het |
Creb3l3 |
C |
T |
10: 80,921,881 (GRCm39) |
A316T |
probably benign |
Het |
Cul4a |
A |
G |
8: 13,173,526 (GRCm39) |
K1R |
probably benign |
Het |
Cyp2c23 |
T |
C |
19: 44,005,176 (GRCm39) |
|
probably null |
Het |
D630045J12Rik |
T |
C |
6: 38,173,776 (GRCm39) |
T131A |
possibly damaging |
Het |
Dctn4 |
A |
C |
18: 60,683,308 (GRCm39) |
K295N |
probably damaging |
Het |
Dync1i1 |
A |
G |
6: 5,767,048 (GRCm39) |
K91E |
possibly damaging |
Het |
Dzip1l |
A |
G |
9: 99,524,704 (GRCm39) |
D275G |
probably damaging |
Het |
Enam |
C |
A |
5: 88,649,402 (GRCm39) |
P304T |
probably damaging |
Het |
Enpep |
A |
G |
3: 129,125,812 (GRCm39) |
Y107H |
probably damaging |
Het |
Exd2 |
T |
C |
12: 80,527,350 (GRCm39) |
L27P |
probably damaging |
Het |
Fam135b |
T |
A |
15: 71,335,904 (GRCm39) |
D430V |
probably benign |
Het |
Fam222b |
C |
T |
11: 78,045,429 (GRCm39) |
T202I |
possibly damaging |
Het |
Fmod |
T |
A |
1: 133,968,912 (GRCm39) |
N317K |
probably damaging |
Het |
Frem2 |
A |
G |
3: 53,448,514 (GRCm39) |
F2301L |
probably damaging |
Het |
Frem3 |
T |
C |
8: 81,338,088 (GRCm39) |
F127S |
probably damaging |
Het |
Gbp7 |
A |
G |
3: 142,243,848 (GRCm39) |
S132G |
probably benign |
Het |
Gm4787 |
A |
G |
12: 81,424,830 (GRCm39) |
C443R |
probably damaging |
Het |
Grik2 |
T |
C |
10: 49,411,437 (GRCm39) |
M5V |
possibly damaging |
Het |
Helb |
T |
C |
10: 119,920,754 (GRCm39) |
D1063G |
probably benign |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Krt90 |
G |
A |
15: 101,463,768 (GRCm39) |
L429F |
probably damaging |
Het |
Lrr1 |
C |
A |
12: 69,221,236 (GRCm39) |
T126K |
probably benign |
Het |
Mgat4e |
C |
A |
1: 134,469,766 (GRCm39) |
D93Y |
probably damaging |
Het |
Mllt3 |
A |
T |
4: 87,759,018 (GRCm39) |
S343R |
possibly damaging |
Het |
Mms19 |
T |
A |
19: 41,932,997 (GRCm39) |
S1031C |
probably damaging |
Het |
Mtrf1 |
C |
T |
14: 79,649,090 (GRCm39) |
H237Y |
probably damaging |
Het |
Nckap1l |
T |
A |
15: 103,381,483 (GRCm39) |
L408Q |
probably damaging |
Het |
Oit3 |
A |
T |
10: 59,259,904 (GRCm39) |
C500S |
probably damaging |
Het |
Or11g1 |
T |
G |
14: 50,651,333 (GRCm39) |
L111V |
possibly damaging |
Het |
Or13c3 |
A |
G |
4: 52,856,076 (GRCm39) |
S146P |
possibly damaging |
Het |
Or4a39 |
C |
T |
2: 89,236,599 (GRCm39) |
V275I |
probably benign |
Het |
Or5d36 |
T |
A |
2: 87,900,956 (GRCm39) |
I257L |
probably benign |
Het |
Otud7a |
T |
C |
7: 63,385,663 (GRCm39) |
S376P |
possibly damaging |
Het |
Pabpc2 |
A |
T |
18: 39,907,322 (GRCm39) |
K196* |
probably null |
Het |
Paqr8 |
T |
A |
1: 21,005,637 (GRCm39) |
C264S |
probably benign |
Het |
Pgm1 |
T |
A |
4: 99,839,176 (GRCm39) |
F459Y |
probably benign |
Het |
Phip |
C |
A |
9: 82,790,922 (GRCm39) |
V675L |
probably benign |
Het |
Pnma1 |
T |
G |
12: 84,194,497 (GRCm39) |
T69P |
probably benign |
Het |
Ppp1r14bl |
T |
C |
1: 23,140,951 (GRCm39) |
E121G |
probably damaging |
Het |
Ptpn12 |
A |
T |
5: 21,210,383 (GRCm39) |
C242* |
probably null |
Het |
Rabep1 |
T |
A |
11: 70,799,294 (GRCm39) |
V306E |
probably benign |
Het |
Ros1 |
C |
T |
10: 51,992,093 (GRCm39) |
D1377N |
probably benign |
Het |
Ryr3 |
T |
C |
2: 112,794,750 (GRCm39) |
T121A |
possibly damaging |
Het |
Scaf11 |
G |
A |
15: 96,318,302 (GRCm39) |
Q421* |
probably null |
Het |
Shcbp1 |
G |
A |
8: 4,794,512 (GRCm39) |
T427M |
probably damaging |
Het |
Shprh |
G |
A |
10: 11,046,220 (GRCm39) |
R979H |
probably damaging |
Het |
Slc22a27 |
C |
T |
19: 7,903,241 (GRCm39) |
C163Y |
probably benign |
Het |
Slc27a1 |
A |
G |
8: 72,033,319 (GRCm39) |
D287G |
probably damaging |
Het |
Slc27a1 |
C |
T |
8: 72,033,453 (GRCm39) |
T310M |
possibly damaging |
Het |
Slc29a3 |
A |
G |
10: 60,552,105 (GRCm39) |
V313A |
probably benign |
Het |
Slc35f2 |
A |
T |
9: 53,679,069 (GRCm39) |
M1L |
probably benign |
Het |
Sltm |
G |
C |
9: 70,488,647 (GRCm39) |
R599T |
probably damaging |
Het |
Spic |
T |
A |
10: 88,511,752 (GRCm39) |
Q168L |
probably damaging |
Het |
Spink6 |
G |
A |
18: 44,215,428 (GRCm39) |
|
probably null |
Het |
Stac2 |
T |
C |
11: 97,932,198 (GRCm39) |
E235G |
possibly damaging |
Het |
Szt2 |
G |
A |
4: 118,246,388 (GRCm39) |
Q957* |
probably null |
Het |
Them7 |
A |
T |
2: 105,208,991 (GRCm39) |
T104S |
possibly damaging |
Het |
Tmed4 |
T |
A |
11: 6,221,716 (GRCm39) |
I207F |
possibly damaging |
Het |
Tmem248 |
A |
G |
5: 130,265,731 (GRCm39) |
E178G |
probably benign |
Het |
Tomm40l |
G |
A |
1: 171,047,131 (GRCm39) |
R296* |
probably null |
Het |
Trim80 |
C |
A |
11: 115,338,964 (GRCm39) |
T598N |
possibly damaging |
Het |
Trim9 |
T |
C |
12: 70,295,047 (GRCm39) |
N688D |
probably damaging |
Het |
Vil1 |
C |
T |
1: 74,460,425 (GRCm39) |
A194V |
probably damaging |
Het |
Vmn2r61 |
A |
T |
7: 41,916,565 (GRCm39) |
M393L |
probably damaging |
Het |
Vmn2r63 |
C |
T |
7: 42,577,544 (GRCm39) |
M331I |
probably benign |
Het |
Vps33b |
G |
T |
7: 79,939,796 (GRCm39) |
A516S |
probably damaging |
Het |
Zc3h6 |
G |
A |
2: 128,844,160 (GRCm39) |
G235R |
probably damaging |
Het |
Zfp612 |
T |
A |
8: 110,815,304 (GRCm39) |
D170E |
probably benign |
Het |
Zfp746 |
A |
G |
6: 48,041,490 (GRCm39) |
I412T |
probably benign |
Het |
|
Other mutations in Dnah1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Dnah1
|
APN |
14 |
31,009,830 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00227:Dnah1
|
APN |
14 |
31,008,853 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00491:Dnah1
|
APN |
14 |
30,983,796 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00787:Dnah1
|
APN |
14 |
31,022,020 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL00809:Dnah1
|
APN |
14 |
31,022,766 (GRCm39) |
nonsense |
probably null |
|
IGL00911:Dnah1
|
APN |
14 |
31,026,391 (GRCm39) |
splice site |
probably null |
|
IGL00949:Dnah1
|
APN |
14 |
31,029,047 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00976:Dnah1
|
APN |
14 |
31,000,095 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01484:Dnah1
|
APN |
14 |
31,021,897 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01629:Dnah1
|
APN |
14 |
31,014,277 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01716:Dnah1
|
APN |
14 |
30,985,335 (GRCm39) |
missense |
probably benign |
0.34 |
IGL01893:Dnah1
|
APN |
14 |
30,988,427 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01933:Dnah1
|
APN |
14 |
31,032,872 (GRCm39) |
missense |
probably benign |
0.40 |
IGL01938:Dnah1
|
APN |
14 |
31,005,844 (GRCm39) |
missense |
probably benign |
|
IGL02032:Dnah1
|
APN |
14 |
30,996,326 (GRCm39) |
missense |
probably benign |
|
IGL02052:Dnah1
|
APN |
14 |
30,990,743 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02097:Dnah1
|
APN |
14 |
31,026,958 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02127:Dnah1
|
APN |
14 |
31,026,885 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02143:Dnah1
|
APN |
14 |
31,005,246 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02158:Dnah1
|
APN |
14 |
31,022,924 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02442:Dnah1
|
APN |
14 |
31,009,835 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02525:Dnah1
|
APN |
14 |
31,027,790 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02558:Dnah1
|
APN |
14 |
30,996,336 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02633:Dnah1
|
APN |
14 |
31,006,772 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02720:Dnah1
|
APN |
14 |
30,984,177 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02728:Dnah1
|
APN |
14 |
31,005,955 (GRCm39) |
missense |
probably benign |
0.44 |
IGL02738:Dnah1
|
APN |
14 |
31,014,597 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02863:Dnah1
|
APN |
14 |
31,017,250 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02944:Dnah1
|
APN |
14 |
31,022,828 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03110:Dnah1
|
APN |
14 |
30,988,674 (GRCm39) |
missense |
probably benign |
0.40 |
IGL03201:Dnah1
|
APN |
14 |
31,022,906 (GRCm39) |
missense |
probably benign |
0.13 |
IGL03215:Dnah1
|
APN |
14 |
30,996,348 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03230:Dnah1
|
APN |
14 |
30,992,023 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03248:Dnah1
|
APN |
14 |
30,991,846 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03267:Dnah1
|
APN |
14 |
31,008,545 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03299:Dnah1
|
APN |
14 |
31,037,079 (GRCm39) |
nonsense |
probably null |
|
IGL03301:Dnah1
|
APN |
14 |
31,014,649 (GRCm39) |
missense |
probably damaging |
1.00 |
ergonomic
|
UTSW |
14 |
31,022,705 (GRCm39) |
missense |
possibly damaging |
0.91 |
Faraday
|
UTSW |
14 |
31,032,839 (GRCm39) |
missense |
probably null |
0.05 |
K3955:Dnah1
|
UTSW |
14 |
30,988,416 (GRCm39) |
missense |
probably benign |
|
PIT1430001:Dnah1
|
UTSW |
14 |
30,984,537 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4382001:Dnah1
|
UTSW |
14 |
31,006,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R0043:Dnah1
|
UTSW |
14 |
30,996,362 (GRCm39) |
missense |
probably damaging |
0.97 |
R0092:Dnah1
|
UTSW |
14 |
30,993,566 (GRCm39) |
missense |
probably benign |
0.00 |
R0100:Dnah1
|
UTSW |
14 |
30,984,109 (GRCm39) |
critical splice donor site |
probably null |
|
R0100:Dnah1
|
UTSW |
14 |
30,984,109 (GRCm39) |
critical splice donor site |
probably null |
|
R0101:Dnah1
|
UTSW |
14 |
31,005,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R0119:Dnah1
|
UTSW |
14 |
30,998,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R0136:Dnah1
|
UTSW |
14 |
30,998,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R0144:Dnah1
|
UTSW |
14 |
30,989,831 (GRCm39) |
splice site |
probably benign |
|
R0279:Dnah1
|
UTSW |
14 |
31,024,332 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0299:Dnah1
|
UTSW |
14 |
30,998,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R0316:Dnah1
|
UTSW |
14 |
31,000,108 (GRCm39) |
missense |
probably benign |
0.00 |
R0739:Dnah1
|
UTSW |
14 |
30,987,872 (GRCm39) |
nonsense |
probably null |
|
R0789:Dnah1
|
UTSW |
14 |
31,026,548 (GRCm39) |
missense |
probably benign |
|
R0826:Dnah1
|
UTSW |
14 |
31,025,864 (GRCm39) |
missense |
probably benign |
0.02 |
R1102:Dnah1
|
UTSW |
14 |
31,018,414 (GRCm39) |
nonsense |
probably null |
|
R1116:Dnah1
|
UTSW |
14 |
31,029,824 (GRCm39) |
missense |
probably benign |
0.13 |
R1229:Dnah1
|
UTSW |
14 |
31,032,808 (GRCm39) |
missense |
probably benign |
0.11 |
R1447:Dnah1
|
UTSW |
14 |
31,028,855 (GRCm39) |
missense |
probably benign |
0.06 |
R1449:Dnah1
|
UTSW |
14 |
30,985,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R1462:Dnah1
|
UTSW |
14 |
30,990,738 (GRCm39) |
splice site |
probably benign |
|
R1482:Dnah1
|
UTSW |
14 |
31,016,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R1500:Dnah1
|
UTSW |
14 |
31,038,715 (GRCm39) |
missense |
probably benign |
|
R1512:Dnah1
|
UTSW |
14 |
31,014,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R1591:Dnah1
|
UTSW |
14 |
30,994,289 (GRCm39) |
missense |
probably benign |
0.01 |
R1598:Dnah1
|
UTSW |
14 |
31,023,219 (GRCm39) |
missense |
probably benign |
0.07 |
R1644:Dnah1
|
UTSW |
14 |
31,024,249 (GRCm39) |
splice site |
probably benign |
|
R1672:Dnah1
|
UTSW |
14 |
30,998,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R1713:Dnah1
|
UTSW |
14 |
31,001,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R1769:Dnah1
|
UTSW |
14 |
31,032,839 (GRCm39) |
missense |
probably null |
0.05 |
R1796:Dnah1
|
UTSW |
14 |
30,983,050 (GRCm39) |
missense |
probably benign |
0.00 |
R1902:Dnah1
|
UTSW |
14 |
31,041,716 (GRCm39) |
missense |
probably damaging |
0.99 |
R1903:Dnah1
|
UTSW |
14 |
31,041,716 (GRCm39) |
missense |
probably damaging |
0.99 |
R1905:Dnah1
|
UTSW |
14 |
30,986,587 (GRCm39) |
missense |
probably benign |
0.06 |
R1908:Dnah1
|
UTSW |
14 |
30,984,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R1972:Dnah1
|
UTSW |
14 |
30,987,348 (GRCm39) |
nonsense |
probably null |
|
R1973:Dnah1
|
UTSW |
14 |
30,987,348 (GRCm39) |
nonsense |
probably null |
|
R2004:Dnah1
|
UTSW |
14 |
31,023,813 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2051:Dnah1
|
UTSW |
14 |
31,001,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R2062:Dnah1
|
UTSW |
14 |
30,993,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R2188:Dnah1
|
UTSW |
14 |
31,001,121 (GRCm39) |
missense |
probably damaging |
0.98 |
R2240:Dnah1
|
UTSW |
14 |
31,021,931 (GRCm39) |
missense |
probably benign |
0.00 |
R2862:Dnah1
|
UTSW |
14 |
31,006,719 (GRCm39) |
missense |
probably benign |
0.21 |
R2894:Dnah1
|
UTSW |
14 |
31,020,718 (GRCm39) |
missense |
possibly damaging |
0.67 |
R3120:Dnah1
|
UTSW |
14 |
30,988,779 (GRCm39) |
nonsense |
probably null |
|
R3410:Dnah1
|
UTSW |
14 |
30,991,774 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3411:Dnah1
|
UTSW |
14 |
30,991,774 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3435:Dnah1
|
UTSW |
14 |
31,038,631 (GRCm39) |
missense |
probably damaging |
0.96 |
R3615:Dnah1
|
UTSW |
14 |
31,037,105 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3616:Dnah1
|
UTSW |
14 |
31,037,105 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3741:Dnah1
|
UTSW |
14 |
30,987,424 (GRCm39) |
splice site |
probably benign |
|
R3805:Dnah1
|
UTSW |
14 |
31,016,720 (GRCm39) |
missense |
possibly damaging |
0.67 |
R3894:Dnah1
|
UTSW |
14 |
31,028,985 (GRCm39) |
missense |
probably benign |
|
R4007:Dnah1
|
UTSW |
14 |
31,025,741 (GRCm39) |
splice site |
probably benign |
|
R4201:Dnah1
|
UTSW |
14 |
30,984,227 (GRCm39) |
missense |
probably benign |
0.00 |
R4232:Dnah1
|
UTSW |
14 |
31,026,873 (GRCm39) |
missense |
probably benign |
|
R4372:Dnah1
|
UTSW |
14 |
31,026,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R4391:Dnah1
|
UTSW |
14 |
31,016,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R4423:Dnah1
|
UTSW |
14 |
31,006,718 (GRCm39) |
missense |
probably benign |
0.00 |
R4526:Dnah1
|
UTSW |
14 |
31,007,955 (GRCm39) |
missense |
probably benign |
0.05 |
R4650:Dnah1
|
UTSW |
14 |
31,006,844 (GRCm39) |
splice site |
probably null |
|
R4723:Dnah1
|
UTSW |
14 |
30,994,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R4783:Dnah1
|
UTSW |
14 |
30,985,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R4784:Dnah1
|
UTSW |
14 |
30,985,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R4785:Dnah1
|
UTSW |
14 |
30,985,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R4843:Dnah1
|
UTSW |
14 |
30,986,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R4879:Dnah1
|
UTSW |
14 |
31,022,705 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4897:Dnah1
|
UTSW |
14 |
30,989,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R4911:Dnah1
|
UTSW |
14 |
31,017,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R4985:Dnah1
|
UTSW |
14 |
31,008,855 (GRCm39) |
missense |
probably null |
1.00 |
R5070:Dnah1
|
UTSW |
14 |
31,004,375 (GRCm39) |
missense |
probably benign |
0.05 |
R5128:Dnah1
|
UTSW |
14 |
31,018,152 (GRCm39) |
splice site |
probably null |
|
R5409:Dnah1
|
UTSW |
14 |
30,985,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R5436:Dnah1
|
UTSW |
14 |
31,038,704 (GRCm39) |
missense |
probably benign |
|
R5481:Dnah1
|
UTSW |
14 |
31,030,828 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5550:Dnah1
|
UTSW |
14 |
31,038,665 (GRCm39) |
missense |
probably benign |
0.00 |
R5555:Dnah1
|
UTSW |
14 |
31,012,776 (GRCm39) |
missense |
probably damaging |
0.99 |
R5566:Dnah1
|
UTSW |
14 |
30,996,323 (GRCm39) |
missense |
probably benign |
0.35 |
R5623:Dnah1
|
UTSW |
14 |
31,007,980 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5701:Dnah1
|
UTSW |
14 |
30,996,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R5751:Dnah1
|
UTSW |
14 |
31,032,863 (GRCm39) |
missense |
probably benign |
0.00 |
R5823:Dnah1
|
UTSW |
14 |
30,988,375 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6030:Dnah1
|
UTSW |
14 |
30,989,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R6030:Dnah1
|
UTSW |
14 |
30,989,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R6090:Dnah1
|
UTSW |
14 |
30,991,382 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6139:Dnah1
|
UTSW |
14 |
31,007,984 (GRCm39) |
missense |
probably benign |
0.02 |
R6145:Dnah1
|
UTSW |
14 |
31,022,927 (GRCm39) |
missense |
probably benign |
0.07 |
R6306:Dnah1
|
UTSW |
14 |
31,026,544 (GRCm39) |
missense |
probably damaging |
0.97 |
R6376:Dnah1
|
UTSW |
14 |
30,997,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R6451:Dnah1
|
UTSW |
14 |
31,022,765 (GRCm39) |
missense |
probably benign |
0.08 |
R6549:Dnah1
|
UTSW |
14 |
30,991,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R6748:Dnah1
|
UTSW |
14 |
31,021,945 (GRCm39) |
missense |
probably damaging |
0.99 |
R6826:Dnah1
|
UTSW |
14 |
31,008,247 (GRCm39) |
missense |
probably benign |
0.00 |
R6870:Dnah1
|
UTSW |
14 |
30,993,018 (GRCm39) |
nonsense |
probably null |
|
R6932:Dnah1
|
UTSW |
14 |
31,009,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R6944:Dnah1
|
UTSW |
14 |
30,990,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R7033:Dnah1
|
UTSW |
14 |
30,986,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R7078:Dnah1
|
UTSW |
14 |
31,019,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R7133:Dnah1
|
UTSW |
14 |
31,008,033 (GRCm39) |
missense |
probably benign |
|
R7136:Dnah1
|
UTSW |
14 |
31,020,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R7203:Dnah1
|
UTSW |
14 |
30,996,339 (GRCm39) |
missense |
probably benign |
|
R7241:Dnah1
|
UTSW |
14 |
30,986,896 (GRCm39) |
missense |
probably benign |
0.00 |
R7260:Dnah1
|
UTSW |
14 |
30,991,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R7264:Dnah1
|
UTSW |
14 |
30,991,851 (GRCm39) |
missense |
probably benign |
|
R7291:Dnah1
|
UTSW |
14 |
31,020,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R7293:Dnah1
|
UTSW |
14 |
31,009,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R7300:Dnah1
|
UTSW |
14 |
30,991,798 (GRCm39) |
missense |
probably benign |
0.05 |
R7319:Dnah1
|
UTSW |
14 |
31,018,551 (GRCm39) |
missense |
probably benign |
0.02 |
R7323:Dnah1
|
UTSW |
14 |
31,020,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R7472:Dnah1
|
UTSW |
14 |
31,022,748 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7472:Dnah1
|
UTSW |
14 |
30,983,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R7499:Dnah1
|
UTSW |
14 |
31,037,079 (GRCm39) |
nonsense |
probably null |
|
R7526:Dnah1
|
UTSW |
14 |
31,009,833 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7560:Dnah1
|
UTSW |
14 |
31,026,940 (GRCm39) |
missense |
probably benign |
|
R7574:Dnah1
|
UTSW |
14 |
31,041,865 (GRCm39) |
missense |
probably benign |
0.00 |
R7617:Dnah1
|
UTSW |
14 |
31,006,739 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7620:Dnah1
|
UTSW |
14 |
31,025,863 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7692:Dnah1
|
UTSW |
14 |
31,014,295 (GRCm39) |
missense |
probably benign |
0.00 |
R7702:Dnah1
|
UTSW |
14 |
31,032,866 (GRCm39) |
missense |
probably benign |
|
R7786:Dnah1
|
UTSW |
14 |
30,984,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R7984:Dnah1
|
UTSW |
14 |
30,989,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R8002:Dnah1
|
UTSW |
14 |
31,020,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R8022:Dnah1
|
UTSW |
14 |
30,986,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R8032:Dnah1
|
UTSW |
14 |
30,993,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R8099:Dnah1
|
UTSW |
14 |
31,024,321 (GRCm39) |
missense |
probably benign |
0.00 |
R8171:Dnah1
|
UTSW |
14 |
31,019,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R8263:Dnah1
|
UTSW |
14 |
31,015,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R8274:Dnah1
|
UTSW |
14 |
31,017,531 (GRCm39) |
missense |
probably benign |
0.00 |
R8345:Dnah1
|
UTSW |
14 |
30,986,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R8348:Dnah1
|
UTSW |
14 |
31,015,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R8353:Dnah1
|
UTSW |
14 |
31,005,159 (GRCm39) |
missense |
probably benign |
|
R8356:Dnah1
|
UTSW |
14 |
30,994,972 (GRCm39) |
missense |
probably benign |
0.00 |
R8376:Dnah1
|
UTSW |
14 |
31,023,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R8448:Dnah1
|
UTSW |
14 |
31,015,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R8461:Dnah1
|
UTSW |
14 |
31,027,915 (GRCm39) |
missense |
probably benign |
0.00 |
R8534:Dnah1
|
UTSW |
14 |
31,023,805 (GRCm39) |
missense |
probably benign |
0.16 |
R8544:Dnah1
|
UTSW |
14 |
30,990,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R8679:Dnah1
|
UTSW |
14 |
30,989,767 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8716:Dnah1
|
UTSW |
14 |
30,989,941 (GRCm39) |
critical splice donor site |
probably benign |
|
R8750:Dnah1
|
UTSW |
14 |
31,026,924 (GRCm39) |
missense |
probably benign |
0.30 |
R8790:Dnah1
|
UTSW |
14 |
31,018,232 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8808:Dnah1
|
UTSW |
14 |
31,008,771 (GRCm39) |
missense |
probably benign |
|
R8821:Dnah1
|
UTSW |
14 |
31,018,455 (GRCm39) |
missense |
probably benign |
|
R8887:Dnah1
|
UTSW |
14 |
31,032,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R8948:Dnah1
|
UTSW |
14 |
31,012,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R8950:Dnah1
|
UTSW |
14 |
31,012,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R8955:Dnah1
|
UTSW |
14 |
31,007,950 (GRCm39) |
missense |
probably benign |
|
R8987:Dnah1
|
UTSW |
14 |
31,033,704 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8998:Dnah1
|
UTSW |
14 |
31,018,235 (GRCm39) |
missense |
probably benign |
0.12 |
R8999:Dnah1
|
UTSW |
14 |
31,018,235 (GRCm39) |
missense |
probably benign |
0.12 |
R9015:Dnah1
|
UTSW |
14 |
30,986,316 (GRCm39) |
missense |
probably damaging |
0.96 |
R9031:Dnah1
|
UTSW |
14 |
31,001,128 (GRCm39) |
missense |
probably benign |
|
R9088:Dnah1
|
UTSW |
14 |
30,987,970 (GRCm39) |
missense |
probably benign |
0.04 |
R9096:Dnah1
|
UTSW |
14 |
30,983,027 (GRCm39) |
missense |
probably damaging |
0.99 |
R9117:Dnah1
|
UTSW |
14 |
31,033,581 (GRCm39) |
splice site |
probably benign |
|
R9157:Dnah1
|
UTSW |
14 |
30,987,970 (GRCm39) |
missense |
probably damaging |
0.97 |
R9296:Dnah1
|
UTSW |
14 |
30,996,011 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9313:Dnah1
|
UTSW |
14 |
30,987,970 (GRCm39) |
missense |
probably damaging |
0.97 |
R9325:Dnah1
|
UTSW |
14 |
30,998,160 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9352:Dnah1
|
UTSW |
14 |
31,038,620 (GRCm39) |
missense |
probably benign |
0.00 |
R9411:Dnah1
|
UTSW |
14 |
31,018,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R9429:Dnah1
|
UTSW |
14 |
30,997,499 (GRCm39) |
nonsense |
probably null |
|
R9452:Dnah1
|
UTSW |
14 |
31,018,448 (GRCm39) |
missense |
probably benign |
0.35 |
R9562:Dnah1
|
UTSW |
14 |
30,986,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R9565:Dnah1
|
UTSW |
14 |
30,986,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R9616:Dnah1
|
UTSW |
14 |
31,026,400 (GRCm39) |
missense |
probably null |
0.20 |
R9621:Dnah1
|
UTSW |
14 |
31,016,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R9677:Dnah1
|
UTSW |
14 |
31,029,821 (GRCm39) |
missense |
probably benign |
0.00 |
R9723:Dnah1
|
UTSW |
14 |
30,987,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R9758:Dnah1
|
UTSW |
14 |
30,985,395 (GRCm39) |
missense |
probably damaging |
0.98 |
RF006:Dnah1
|
UTSW |
14 |
31,029,832 (GRCm39) |
missense |
probably benign |
0.08 |
Z1088:Dnah1
|
UTSW |
14 |
31,026,768 (GRCm39) |
missense |
probably benign |
0.17 |
|