Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700029H14Rik |
T |
C |
8: 13,612,237 (GRCm39) |
R38G |
possibly damaging |
Het |
4930590J08Rik |
T |
C |
6: 91,892,203 (GRCm39) |
V155A |
possibly damaging |
Het |
Adgb |
A |
G |
10: 10,302,349 (GRCm39) |
S406P |
probably damaging |
Het |
Adgrb2 |
C |
A |
4: 129,905,668 (GRCm39) |
T893N |
probably damaging |
Het |
Adgrf5 |
T |
C |
17: 43,735,484 (GRCm39) |
|
probably null |
Het |
Alms1 |
T |
A |
6: 85,605,487 (GRCm39) |
I2379N |
probably damaging |
Het |
Arap3 |
C |
T |
18: 38,122,965 (GRCm39) |
V512I |
probably benign |
Het |
Atf4 |
C |
T |
15: 80,141,414 (GRCm39) |
T268I |
probably benign |
Het |
Cblif |
G |
A |
19: 11,735,179 (GRCm39) |
M266I |
probably damaging |
Het |
Ccdc154 |
T |
C |
17: 25,382,156 (GRCm39) |
L25P |
probably damaging |
Het |
Ccdc9 |
G |
A |
7: 16,010,161 (GRCm39) |
S381F |
probably damaging |
Het |
Cdk17 |
C |
T |
10: 93,044,112 (GRCm39) |
T17M |
probably damaging |
Het |
Cep128 |
T |
C |
12: 91,314,352 (GRCm39) |
N142S |
probably benign |
Het |
Cep78 |
A |
G |
19: 15,936,900 (GRCm39) |
I602T |
probably damaging |
Het |
Clasp1 |
C |
T |
1: 118,475,755 (GRCm39) |
T935I |
probably damaging |
Het |
Cnr1 |
T |
C |
4: 33,945,000 (GRCm39) |
S463P |
probably damaging |
Het |
Cntnap1 |
T |
A |
11: 101,075,449 (GRCm39) |
W876R |
probably damaging |
Het |
Cntnap5c |
A |
G |
17: 58,349,545 (GRCm39) |
D286G |
probably damaging |
Het |
Copa |
C |
T |
1: 171,931,711 (GRCm39) |
R321C |
probably damaging |
Het |
Cspg4b |
A |
G |
13: 113,505,266 (GRCm39) |
T2132A |
possibly damaging |
Het |
Ctla2a |
T |
G |
13: 61,083,256 (GRCm39) |
E98A |
probably damaging |
Het |
Cux1 |
A |
T |
5: 136,421,176 (GRCm39) |
D183E |
probably damaging |
Het |
Cxcl15 |
A |
C |
5: 90,949,323 (GRCm39) |
T163P |
unknown |
Het |
Ddias |
T |
C |
7: 92,508,571 (GRCm39) |
N448S |
probably benign |
Het |
Dhx8 |
T |
C |
11: 101,657,564 (GRCm39) |
F1152S |
probably damaging |
Het |
Dnah12 |
C |
A |
14: 26,488,071 (GRCm39) |
Q992K |
probably benign |
Het |
Eno3 |
G |
T |
11: 70,552,251 (GRCm39) |
W301L |
possibly damaging |
Het |
Faap100 |
A |
T |
11: 120,268,059 (GRCm39) |
V238E |
probably damaging |
Het |
Fgf4 |
A |
G |
7: 144,416,049 (GRCm39) |
S137G |
probably benign |
Het |
Fhod3 |
A |
C |
18: 25,253,367 (GRCm39) |
D1439A |
possibly damaging |
Het |
Frem2 |
A |
G |
3: 53,560,778 (GRCm39) |
L1243P |
probably damaging |
Het |
Gkn3 |
T |
G |
6: 87,365,817 (GRCm39) |
M1L |
probably benign |
Het |
Gm10250 |
T |
C |
15: 5,150,509 (GRCm39) |
|
probably benign |
Het |
Gm12185 |
T |
C |
11: 48,798,859 (GRCm39) |
T545A |
possibly damaging |
Het |
Gm14226 |
T |
A |
2: 154,867,378 (GRCm39) |
L445H |
probably damaging |
Het |
Gm3404 |
A |
T |
5: 146,463,036 (GRCm39) |
M73L |
probably benign |
Het |
Gm973 |
G |
T |
1: 59,673,169 (GRCm39) |
R976S |
unknown |
Het |
Gpr146 |
A |
T |
5: 139,379,137 (GRCm39) |
H313L |
probably benign |
Het |
Gys2 |
T |
A |
6: 142,418,432 (GRCm39) |
E32D |
probably damaging |
Het |
Igsf10 |
G |
A |
3: 59,236,617 (GRCm39) |
T1188I |
probably benign |
Het |
Igsf9b |
A |
T |
9: 27,245,548 (GRCm39) |
T1172S |
possibly damaging |
Het |
Itga8 |
T |
A |
2: 12,270,144 (GRCm39) |
N114I |
possibly damaging |
Het |
Itsn2 |
T |
A |
12: 4,708,160 (GRCm39) |
V795E |
possibly damaging |
Het |
Kdm1b |
T |
A |
13: 47,214,244 (GRCm39) |
S197T |
probably benign |
Het |
Kif5c |
G |
A |
2: 49,613,145 (GRCm39) |
R161Q |
probably benign |
Het |
Krt33b |
T |
C |
11: 99,916,361 (GRCm39) |
Y232C |
probably damaging |
Het |
Lonrf2 |
G |
A |
1: 38,852,357 (GRCm39) |
P165S |
probably benign |
Het |
Lrp1 |
A |
T |
10: 127,424,453 (GRCm39) |
N744K |
possibly damaging |
Het |
Mcm10 |
C |
A |
2: 5,008,861 (GRCm39) |
L369F |
probably damaging |
Het |
Myom2 |
T |
C |
8: 15,115,795 (GRCm39) |
L70P |
probably benign |
Het |
Myt1l |
T |
A |
12: 29,877,241 (GRCm39) |
N297K |
unknown |
Het |
Ncr1 |
C |
T |
7: 4,343,807 (GRCm39) |
T98I |
probably benign |
Het |
Nek3 |
T |
C |
8: 22,650,278 (GRCm39) |
E78G |
probably damaging |
Het |
Nfatc3 |
T |
A |
8: 106,825,768 (GRCm39) |
N606K |
probably damaging |
Het |
Nup107 |
T |
G |
10: 117,597,248 (GRCm39) |
D669A |
probably damaging |
Het |
Or10ag52 |
A |
T |
2: 87,043,758 (GRCm39) |
Q174L |
probably benign |
Het |
Or10c1 |
A |
T |
17: 37,522,204 (GRCm39) |
I180N |
possibly damaging |
Het |
Or4c3 |
T |
C |
2: 89,851,673 (GRCm39) |
T246A |
probably benign |
Het |
Or8b55 |
A |
T |
9: 38,726,871 (GRCm39) |
H24L |
probably benign |
Het |
Pcnx1 |
T |
C |
12: 82,030,258 (GRCm39) |
V1711A |
probably benign |
Het |
Pik3c3 |
A |
G |
18: 30,410,063 (GRCm39) |
D99G |
probably damaging |
Het |
Pinx1 |
C |
A |
14: 64,157,024 (GRCm39) |
T317K |
probably benign |
Het |
Ppargc1b |
G |
T |
18: 61,431,857 (GRCm39) |
|
probably null |
Het |
Pradc1 |
T |
A |
6: 85,424,203 (GRCm39) |
I119F |
possibly damaging |
Het |
Psat1 |
G |
T |
19: 15,892,243 (GRCm39) |
T242K |
probably damaging |
Het |
Psma6 |
G |
A |
12: 55,454,317 (GRCm39) |
C28Y |
probably damaging |
Het |
Pyurf |
A |
T |
6: 57,668,817 (GRCm39) |
C58* |
probably null |
Het |
Rab3gap2 |
C |
A |
1: 185,016,081 (GRCm39) |
A1331E |
probably benign |
Het |
Rnase4 |
T |
C |
14: 51,342,722 (GRCm39) |
*149Q |
probably null |
Het |
Ruvbl2 |
T |
C |
7: 45,074,586 (GRCm39) |
K184R |
probably benign |
Het |
Scn7a |
T |
G |
2: 66,510,527 (GRCm39) |
M1292L |
probably benign |
Het |
Scn7a |
A |
T |
2: 66,531,231 (GRCm39) |
Y549N |
probably damaging |
Het |
Selp |
A |
G |
1: 163,959,854 (GRCm39) |
D370G |
possibly damaging |
Het |
Slc22a15 |
G |
A |
3: 101,767,769 (GRCm39) |
Q386* |
probably null |
Het |
Slc22a29 |
A |
G |
19: 8,195,126 (GRCm39) |
|
probably null |
Het |
Slc26a7 |
A |
C |
4: 14,548,491 (GRCm39) |
I266S |
possibly damaging |
Het |
Smpd4 |
T |
C |
16: 17,443,872 (GRCm39) |
S112P |
probably damaging |
Het |
Smpd4 |
T |
A |
16: 17,458,744 (GRCm39) |
L165Q |
probably damaging |
Het |
Snx33 |
A |
G |
9: 56,833,982 (GRCm39) |
I29T |
probably benign |
Het |
Spen |
G |
A |
4: 141,203,686 (GRCm39) |
P1647L |
unknown |
Het |
Strip2 |
T |
C |
6: 29,941,940 (GRCm39) |
|
probably null |
Het |
Swsap1 |
C |
T |
9: 21,867,280 (GRCm39) |
R75* |
probably null |
Het |
Tesl1 |
A |
G |
X: 23,772,990 (GRCm39) |
I164V |
probably benign |
Het |
Tmem210 |
C |
T |
2: 25,178,435 (GRCm39) |
T32I |
probably damaging |
Het |
Tnn |
C |
T |
1: 159,975,154 (GRCm39) |
R91H |
possibly damaging |
Het |
Tnni1 |
G |
A |
1: 135,736,420 (GRCm39) |
R94H |
probably damaging |
Het |
Tnrc6c |
T |
A |
11: 117,651,556 (GRCm39) |
V1693D |
probably benign |
Het |
Trip4 |
G |
A |
9: 65,782,259 (GRCm39) |
Q158* |
probably null |
Het |
Ttc39b |
T |
C |
4: 83,155,586 (GRCm39) |
E474G |
probably damaging |
Het |
Usp50 |
C |
A |
2: 126,617,782 (GRCm39) |
C221F |
probably damaging |
Het |
Vmn1r171 |
T |
C |
7: 23,331,781 (GRCm39) |
I2T |
probably benign |
Het |
Wdr62 |
T |
A |
7: 29,967,328 (GRCm39) |
I309F |
probably damaging |
Het |
Xdh |
A |
T |
17: 74,217,204 (GRCm39) |
V688E |
probably damaging |
Het |
Zfyve26 |
A |
G |
12: 79,285,718 (GRCm39) |
L2353P |
probably damaging |
Het |
Zgpat |
C |
A |
2: 181,020,633 (GRCm39) |
R269S |
probably damaging |
Het |
|
Other mutations in Muc5ac |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00899:Muc5ac
|
APN |
7 |
141,366,440 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01064:Muc5ac
|
APN |
7 |
141,361,210 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01155:Muc5ac
|
APN |
7 |
141,360,680 (GRCm39) |
splice site |
probably benign |
|
IGL01452:Muc5ac
|
APN |
7 |
141,371,292 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01590:Muc5ac
|
APN |
7 |
141,352,630 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02104:Muc5ac
|
APN |
7 |
141,364,815 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02152:Muc5ac
|
APN |
7 |
141,353,914 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02153:Muc5ac
|
APN |
7 |
141,372,537 (GRCm39) |
nonsense |
probably null |
|
IGL02178:Muc5ac
|
APN |
7 |
141,359,184 (GRCm39) |
splice site |
probably benign |
|
IGL02403:Muc5ac
|
APN |
7 |
141,357,187 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02576:Muc5ac
|
APN |
7 |
141,370,781 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02665:Muc5ac
|
APN |
7 |
141,344,823 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02704:Muc5ac
|
APN |
7 |
141,349,000 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02808:Muc5ac
|
APN |
7 |
141,359,512 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL03283:Muc5ac
|
APN |
7 |
141,367,518 (GRCm39) |
missense |
probably benign |
0.34 |
IGL03384:Muc5ac
|
APN |
7 |
141,366,140 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL03046:Muc5ac
|
UTSW |
7 |
141,348,950 (GRCm39) |
missense |
probably benign |
0.27 |
PIT4515001:Muc5ac
|
UTSW |
7 |
141,361,153 (GRCm39) |
missense |
probably damaging |
0.99 |
R0092:Muc5ac
|
UTSW |
7 |
141,372,367 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0145:Muc5ac
|
UTSW |
7 |
141,349,012 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0147:Muc5ac
|
UTSW |
7 |
141,364,776 (GRCm39) |
missense |
probably benign |
0.08 |
R0363:Muc5ac
|
UTSW |
7 |
141,354,697 (GRCm39) |
missense |
probably benign |
0.01 |
R0384:Muc5ac
|
UTSW |
7 |
141,365,988 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0440:Muc5ac
|
UTSW |
7 |
141,345,771 (GRCm39) |
nonsense |
probably null |
|
R0583:Muc5ac
|
UTSW |
7 |
141,361,345 (GRCm39) |
missense |
probably damaging |
0.99 |
R0616:Muc5ac
|
UTSW |
7 |
141,349,981 (GRCm39) |
missense |
probably benign |
0.02 |
R0682:Muc5ac
|
UTSW |
7 |
141,359,406 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0685:Muc5ac
|
UTSW |
7 |
141,361,446 (GRCm39) |
missense |
probably benign |
0.03 |
R0883:Muc5ac
|
UTSW |
7 |
141,350,002 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0924:Muc5ac
|
UTSW |
7 |
141,361,252 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1300:Muc5ac
|
UTSW |
7 |
141,370,666 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1315:Muc5ac
|
UTSW |
7 |
141,361,060 (GRCm39) |
missense |
probably damaging |
0.99 |
R1354:Muc5ac
|
UTSW |
7 |
141,361,114 (GRCm39) |
missense |
probably damaging |
0.99 |
R1484:Muc5ac
|
UTSW |
7 |
141,367,629 (GRCm39) |
splice site |
probably null |
|
R1599:Muc5ac
|
UTSW |
7 |
141,352,640 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1837:Muc5ac
|
UTSW |
7 |
141,360,823 (GRCm39) |
missense |
probably benign |
0.00 |
R1911:Muc5ac
|
UTSW |
7 |
141,350,041 (GRCm39) |
missense |
probably benign |
0.18 |
R1922:Muc5ac
|
UTSW |
7 |
141,347,426 (GRCm39) |
missense |
probably benign |
0.03 |
R1966:Muc5ac
|
UTSW |
7 |
141,357,113 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1994:Muc5ac
|
UTSW |
7 |
141,366,889 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2056:Muc5ac
|
UTSW |
7 |
141,345,772 (GRCm39) |
missense |
probably benign |
0.01 |
R2126:Muc5ac
|
UTSW |
7 |
141,364,479 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2170:Muc5ac
|
UTSW |
7 |
141,366,084 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2258:Muc5ac
|
UTSW |
7 |
141,344,745 (GRCm39) |
missense |
probably benign |
0.41 |
R2259:Muc5ac
|
UTSW |
7 |
141,344,745 (GRCm39) |
missense |
probably benign |
0.41 |
R2293:Muc5ac
|
UTSW |
7 |
141,360,936 (GRCm39) |
missense |
probably damaging |
0.99 |
R2435:Muc5ac
|
UTSW |
7 |
141,371,841 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2895:Muc5ac
|
UTSW |
7 |
141,344,877 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2910:Muc5ac
|
UTSW |
7 |
141,361,378 (GRCm39) |
missense |
probably damaging |
0.99 |
R3154:Muc5ac
|
UTSW |
7 |
141,346,473 (GRCm39) |
splice site |
probably null |
|
R3762:Muc5ac
|
UTSW |
7 |
141,361,212 (GRCm39) |
missense |
possibly damaging |
0.53 |
R3791:Muc5ac
|
UTSW |
7 |
141,352,238 (GRCm39) |
missense |
probably benign |
0.32 |
R3806:Muc5ac
|
UTSW |
7 |
141,367,471 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3825:Muc5ac
|
UTSW |
7 |
141,368,460 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3888:Muc5ac
|
UTSW |
7 |
141,344,961 (GRCm39) |
missense |
possibly damaging |
0.51 |
R3929:Muc5ac
|
UTSW |
7 |
141,356,629 (GRCm39) |
missense |
probably benign |
|
R3981:Muc5ac
|
UTSW |
7 |
141,367,512 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4034:Muc5ac
|
UTSW |
7 |
141,353,581 (GRCm39) |
critical splice donor site |
probably null |
|
R4043:Muc5ac
|
UTSW |
7 |
141,361,215 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4061:Muc5ac
|
UTSW |
7 |
141,364,867 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4106:Muc5ac
|
UTSW |
7 |
141,356,572 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4206:Muc5ac
|
UTSW |
7 |
141,370,847 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4613:Muc5ac
|
UTSW |
7 |
141,344,840 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4719:Muc5ac
|
UTSW |
7 |
141,343,500 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4751:Muc5ac
|
UTSW |
7 |
141,371,338 (GRCm39) |
missense |
probably benign |
0.00 |
R4789:Muc5ac
|
UTSW |
7 |
141,352,619 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4928:Muc5ac
|
UTSW |
7 |
141,371,639 (GRCm39) |
nonsense |
probably null |
|
R4971:Muc5ac
|
UTSW |
7 |
141,370,015 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4982:Muc5ac
|
UTSW |
7 |
141,363,193 (GRCm39) |
intron |
probably benign |
|
R5088:Muc5ac
|
UTSW |
7 |
141,350,056 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5141:Muc5ac
|
UTSW |
7 |
141,368,479 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5224:Muc5ac
|
UTSW |
7 |
141,347,708 (GRCm39) |
missense |
probably benign |
0.32 |
R5366:Muc5ac
|
UTSW |
7 |
141,361,287 (GRCm39) |
missense |
probably benign |
0.01 |
R5497:Muc5ac
|
UTSW |
7 |
141,361,380 (GRCm39) |
missense |
probably damaging |
0.99 |
R5507:Muc5ac
|
UTSW |
7 |
141,361,569 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5643:Muc5ac
|
UTSW |
7 |
141,347,452 (GRCm39) |
critical splice donor site |
probably null |
|
R5811:Muc5ac
|
UTSW |
7 |
141,352,721 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5946:Muc5ac
|
UTSW |
7 |
141,371,644 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5970:Muc5ac
|
UTSW |
7 |
141,344,406 (GRCm39) |
nonsense |
probably null |
|
R5977:Muc5ac
|
UTSW |
7 |
141,350,104 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6051:Muc5ac
|
UTSW |
7 |
141,365,594 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6126:Muc5ac
|
UTSW |
7 |
141,354,969 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6159:Muc5ac
|
UTSW |
7 |
141,369,323 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6256:Muc5ac
|
UTSW |
7 |
141,343,532 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6283:Muc5ac
|
UTSW |
7 |
141,370,601 (GRCm39) |
nonsense |
probably null |
|
R6341:Muc5ac
|
UTSW |
7 |
141,355,229 (GRCm39) |
missense |
probably damaging |
0.99 |
R6356:Muc5ac
|
UTSW |
7 |
141,366,416 (GRCm39) |
missense |
probably benign |
0.05 |
R6481:Muc5ac
|
UTSW |
7 |
141,362,808 (GRCm39) |
intron |
probably benign |
|
R6483:Muc5ac
|
UTSW |
7 |
141,356,591 (GRCm39) |
missense |
probably benign |
0.18 |
R6627:Muc5ac
|
UTSW |
7 |
141,362,427 (GRCm39) |
intron |
probably benign |
|
R6636:Muc5ac
|
UTSW |
7 |
141,372,342 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6637:Muc5ac
|
UTSW |
7 |
141,372,342 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6656:Muc5ac
|
UTSW |
7 |
141,357,065 (GRCm39) |
missense |
probably damaging |
0.98 |
R6721:Muc5ac
|
UTSW |
7 |
141,352,729 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6794:Muc5ac
|
UTSW |
7 |
141,363,289 (GRCm39) |
intron |
probably benign |
|
R6844:Muc5ac
|
UTSW |
7 |
141,363,481 (GRCm39) |
intron |
probably benign |
|
R6847:Muc5ac
|
UTSW |
7 |
141,363,481 (GRCm39) |
intron |
probably benign |
|
R6852:Muc5ac
|
UTSW |
7 |
141,370,644 (GRCm39) |
missense |
probably benign |
0.03 |
R6862:Muc5ac
|
UTSW |
7 |
141,363,481 (GRCm39) |
intron |
probably benign |
|
R6863:Muc5ac
|
UTSW |
7 |
141,363,481 (GRCm39) |
intron |
probably benign |
|
R6864:Muc5ac
|
UTSW |
7 |
141,363,481 (GRCm39) |
intron |
probably benign |
|
R6865:Muc5ac
|
UTSW |
7 |
141,363,481 (GRCm39) |
intron |
probably benign |
|
R6874:Muc5ac
|
UTSW |
7 |
141,363,481 (GRCm39) |
intron |
probably benign |
|
R6875:Muc5ac
|
UTSW |
7 |
141,363,481 (GRCm39) |
intron |
probably benign |
|
R6876:Muc5ac
|
UTSW |
7 |
141,363,481 (GRCm39) |
intron |
probably benign |
|
R6877:Muc5ac
|
UTSW |
7 |
141,363,481 (GRCm39) |
intron |
probably benign |
|
R6889:Muc5ac
|
UTSW |
7 |
141,363,481 (GRCm39) |
intron |
probably benign |
|
R6920:Muc5ac
|
UTSW |
7 |
141,347,035 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6998:Muc5ac
|
UTSW |
7 |
141,372,451 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7017:Muc5ac
|
UTSW |
7 |
141,363,424 (GRCm39) |
intron |
probably benign |
|
R7091:Muc5ac
|
UTSW |
7 |
141,363,424 (GRCm39) |
intron |
probably benign |
|
R7092:Muc5ac
|
UTSW |
7 |
141,363,424 (GRCm39) |
intron |
probably benign |
|
R7092:Muc5ac
|
UTSW |
7 |
141,363,385 (GRCm39) |
intron |
probably benign |
|
R7110:Muc5ac
|
UTSW |
7 |
141,353,559 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7117:Muc5ac
|
UTSW |
7 |
141,367,559 (GRCm39) |
nonsense |
probably null |
|
R7238:Muc5ac
|
UTSW |
7 |
141,363,424 (GRCm39) |
intron |
probably benign |
|
R7238:Muc5ac
|
UTSW |
7 |
141,363,254 (GRCm39) |
missense |
unknown |
|
R7396:Muc5ac
|
UTSW |
7 |
141,362,152 (GRCm39) |
missense |
unknown |
|
R7456:Muc5ac
|
UTSW |
7 |
141,346,904 (GRCm39) |
missense |
probably benign |
0.32 |
R7477:Muc5ac
|
UTSW |
7 |
141,370,019 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7530:Muc5ac
|
UTSW |
7 |
141,367,536 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7545:Muc5ac
|
UTSW |
7 |
141,362,405 (GRCm39) |
missense |
unknown |
|
R7604:Muc5ac
|
UTSW |
7 |
141,363,446 (GRCm39) |
missense |
unknown |
|
R7635:Muc5ac
|
UTSW |
7 |
141,359,413 (GRCm39) |
missense |
probably damaging |
0.98 |
R7635:Muc5ac
|
UTSW |
7 |
141,359,490 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7650:Muc5ac
|
UTSW |
7 |
141,363,159 (GRCm39) |
missense |
unknown |
|
R7651:Muc5ac
|
UTSW |
7 |
141,349,991 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7685:Muc5ac
|
UTSW |
7 |
141,363,120 (GRCm39) |
missense |
unknown |
|
R7720:Muc5ac
|
UTSW |
7 |
141,363,040 (GRCm39) |
missense |
unknown |
|
R7749:Muc5ac
|
UTSW |
7 |
141,363,040 (GRCm39) |
missense |
unknown |
|
R7750:Muc5ac
|
UTSW |
7 |
141,363,040 (GRCm39) |
missense |
unknown |
|
R7751:Muc5ac
|
UTSW |
7 |
141,363,040 (GRCm39) |
missense |
unknown |
|
R7754:Muc5ac
|
UTSW |
7 |
141,363,040 (GRCm39) |
missense |
unknown |
|
R7798:Muc5ac
|
UTSW |
7 |
141,347,778 (GRCm39) |
critical splice donor site |
probably null |
|
R7835:Muc5ac
|
UTSW |
7 |
141,363,040 (GRCm39) |
missense |
unknown |
|
R7837:Muc5ac
|
UTSW |
7 |
141,369,700 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7858:Muc5ac
|
UTSW |
7 |
141,357,166 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7866:Muc5ac
|
UTSW |
7 |
141,349,589 (GRCm39) |
missense |
probably benign |
0.00 |
R7874:Muc5ac
|
UTSW |
7 |
141,363,040 (GRCm39) |
missense |
unknown |
|
R7876:Muc5ac
|
UTSW |
7 |
141,363,040 (GRCm39) |
missense |
unknown |
|
R7877:Muc5ac
|
UTSW |
7 |
141,363,040 (GRCm39) |
missense |
unknown |
|
R7881:Muc5ac
|
UTSW |
7 |
141,363,040 (GRCm39) |
missense |
unknown |
|
R7884:Muc5ac
|
UTSW |
7 |
141,363,040 (GRCm39) |
missense |
unknown |
|
R7921:Muc5ac
|
UTSW |
7 |
141,363,424 (GRCm39) |
intron |
probably benign |
|
R7976:Muc5ac
|
UTSW |
7 |
141,363,528 (GRCm39) |
missense |
unknown |
|
R8104:Muc5ac
|
UTSW |
7 |
141,358,520 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8177:Muc5ac
|
UTSW |
7 |
141,361,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R8214:Muc5ac
|
UTSW |
7 |
141,356,685 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8292:Muc5ac
|
UTSW |
7 |
141,363,000 (GRCm39) |
missense |
unknown |
|
R8386:Muc5ac
|
UTSW |
7 |
141,361,371 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8400:Muc5ac
|
UTSW |
7 |
141,364,213 (GRCm39) |
missense |
probably damaging |
0.99 |
R8504:Muc5ac
|
UTSW |
7 |
141,360,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R8709:Muc5ac
|
UTSW |
7 |
141,370,663 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8725:Muc5ac
|
UTSW |
7 |
141,363,481 (GRCm39) |
intron |
probably benign |
|
R8727:Muc5ac
|
UTSW |
7 |
141,363,481 (GRCm39) |
intron |
probably benign |
|
R8754:Muc5ac
|
UTSW |
7 |
141,354,008 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8769:Muc5ac
|
UTSW |
7 |
141,372,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R8933:Muc5ac
|
UTSW |
7 |
141,343,493 (GRCm39) |
missense |
possibly damaging |
0.59 |
R8939:Muc5ac
|
UTSW |
7 |
141,347,091 (GRCm39) |
missense |
probably damaging |
0.98 |
R9049:Muc5ac
|
UTSW |
7 |
141,362,712 (GRCm39) |
missense |
unknown |
|
R9124:Muc5ac
|
UTSW |
7 |
141,363,529 (GRCm39) |
missense |
unknown |
|
R9131:Muc5ac
|
UTSW |
7 |
141,363,529 (GRCm39) |
missense |
unknown |
|
R9132:Muc5ac
|
UTSW |
7 |
141,363,529 (GRCm39) |
missense |
unknown |
|
R9135:Muc5ac
|
UTSW |
7 |
141,352,218 (GRCm39) |
missense |
probably damaging |
0.99 |
R9156:Muc5ac
|
UTSW |
7 |
141,363,529 (GRCm39) |
missense |
unknown |
|
R9157:Muc5ac
|
UTSW |
7 |
141,363,529 (GRCm39) |
missense |
unknown |
|
R9159:Muc5ac
|
UTSW |
7 |
141,363,529 (GRCm39) |
missense |
unknown |
|
R9160:Muc5ac
|
UTSW |
7 |
141,363,529 (GRCm39) |
missense |
unknown |
|
R9161:Muc5ac
|
UTSW |
7 |
141,353,026 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9175:Muc5ac
|
UTSW |
7 |
141,366,093 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9183:Muc5ac
|
UTSW |
7 |
141,352,637 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9218:Muc5ac
|
UTSW |
7 |
141,361,098 (GRCm39) |
missense |
probably damaging |
0.99 |
R9219:Muc5ac
|
UTSW |
7 |
141,370,800 (GRCm39) |
nonsense |
probably null |
|
R9239:Muc5ac
|
UTSW |
7 |
141,353,954 (GRCm39) |
missense |
probably damaging |
0.99 |
R9246:Muc5ac
|
UTSW |
7 |
141,364,215 (GRCm39) |
missense |
probably benign |
0.11 |
R9287:Muc5ac
|
UTSW |
7 |
141,361,626 (GRCm39) |
missense |
probably damaging |
0.99 |
R9320:Muc5ac
|
UTSW |
7 |
141,369,255 (GRCm39) |
missense |
probably benign |
0.01 |
R9327:Muc5ac
|
UTSW |
7 |
141,365,429 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9428:Muc5ac
|
UTSW |
7 |
141,362,559 (GRCm39) |
missense |
unknown |
|
R9430:Muc5ac
|
UTSW |
7 |
141,362,569 (GRCm39) |
missense |
unknown |
|
R9454:Muc5ac
|
UTSW |
7 |
141,362,431 (GRCm39) |
missense |
unknown |
|
R9483:Muc5ac
|
UTSW |
7 |
141,365,465 (GRCm39) |
nonsense |
probably null |
|
R9581:Muc5ac
|
UTSW |
7 |
141,363,799 (GRCm39) |
missense |
unknown |
|
R9610:Muc5ac
|
UTSW |
7 |
141,350,078 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9642:Muc5ac
|
UTSW |
7 |
141,349,601 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9684:Muc5ac
|
UTSW |
7 |
141,364,798 (GRCm39) |
missense |
probably benign |
0.41 |
R9760:Muc5ac
|
UTSW |
7 |
141,360,985 (GRCm39) |
missense |
probably benign |
0.05 |
R9778:Muc5ac
|
UTSW |
7 |
141,349,021 (GRCm39) |
nonsense |
probably null |
|
X0060:Muc5ac
|
UTSW |
7 |
141,357,070 (GRCm39) |
missense |
possibly damaging |
0.71 |
Z1088:Muc5ac
|
UTSW |
7 |
141,365,429 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1088:Muc5ac
|
UTSW |
7 |
141,363,481 (GRCm39) |
intron |
probably benign |
|
Z1177:Muc5ac
|
UTSW |
7 |
141,371,777 (GRCm39) |
missense |
probably benign |
0.33 |
Z1177:Muc5ac
|
UTSW |
7 |
141,362,961 (GRCm39) |
missense |
unknown |
|
|