Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3100002H09Rik |
A |
G |
4: 124,504,316 (GRCm39) |
S79P |
unknown |
Het |
Aadacl4fm2 |
C |
G |
4: 144,281,863 (GRCm39) |
A310P |
probably damaging |
Het |
Adamts20 |
T |
A |
15: 94,238,947 (GRCm39) |
D757V |
probably damaging |
Het |
Adamts9 |
C |
T |
6: 92,784,144 (GRCm39) |
G1570D |
probably damaging |
Het |
Adamtsl3 |
A |
G |
7: 82,077,642 (GRCm39) |
Y109C |
possibly damaging |
Het |
Agl |
G |
A |
3: 116,566,121 (GRCm39) |
R335C |
|
Het |
Ankfy1 |
C |
A |
11: 72,646,532 (GRCm39) |
T805K |
possibly damaging |
Het |
Cast |
A |
T |
13: 74,892,780 (GRCm39) |
V96E |
probably damaging |
Het |
Cdh17 |
G |
T |
4: 11,795,685 (GRCm39) |
E422* |
probably null |
Het |
Cox4i1 |
T |
A |
8: 121,396,110 (GRCm39) |
L21H |
possibly damaging |
Het |
Cwc22 |
T |
C |
2: 77,726,694 (GRCm39) |
E795G |
probably benign |
Het |
Cwf19l2 |
C |
A |
9: 3,430,723 (GRCm39) |
Q352K |
probably benign |
Het |
Cyp2d9 |
T |
C |
15: 82,339,276 (GRCm39) |
V226A |
probably benign |
Het |
Dnah12 |
A |
G |
14: 26,414,757 (GRCm39) |
I53V |
probably benign |
Het |
Dnah7a |
T |
C |
1: 53,674,476 (GRCm39) |
I434V |
probably benign |
Het |
Dock8 |
C |
T |
19: 25,055,448 (GRCm39) |
Q137* |
probably null |
Het |
Eif4b |
T |
G |
15: 102,002,116 (GRCm39) |
V515G |
unknown |
Het |
Far2 |
T |
A |
6: 148,067,133 (GRCm39) |
N339K |
probably benign |
Het |
Gpr22 |
T |
C |
12: 31,759,829 (GRCm39) |
T98A |
probably damaging |
Het |
Hamp2 |
A |
G |
7: 30,621,974 (GRCm39) |
C72R |
probably damaging |
Het |
Hmgn1 |
G |
A |
16: 95,928,540 (GRCm39) |
P16S |
possibly damaging |
Het |
Hspd1 |
A |
G |
1: 55,120,922 (GRCm39) |
S256P |
probably benign |
Het |
Iqcn |
T |
C |
8: 71,162,372 (GRCm39) |
C522R |
possibly damaging |
Het |
Iqgap2 |
T |
C |
13: 95,796,713 (GRCm39) |
H1147R |
probably damaging |
Het |
Itgb1 |
T |
A |
8: 129,439,887 (GRCm39) |
|
probably benign |
Het |
Klhl29 |
A |
T |
12: 5,140,681 (GRCm39) |
W654R |
probably damaging |
Het |
Krtap22-2 |
T |
A |
16: 88,807,514 (GRCm39) |
Y28F |
unknown |
Het |
Lcp2 |
T |
A |
11: 34,004,354 (GRCm39) |
|
probably benign |
Het |
Myom3 |
A |
G |
4: 135,523,607 (GRCm39) |
E908G |
possibly damaging |
Het |
Nup54 |
A |
G |
5: 92,570,267 (GRCm39) |
|
probably benign |
Het |
Or1p1 |
T |
A |
11: 74,180,054 (GRCm39) |
I194N |
possibly damaging |
Het |
Or4a74 |
C |
T |
2: 89,440,366 (GRCm39) |
V27I |
probably benign |
Het |
Or51af1 |
T |
C |
7: 103,141,519 (GRCm39) |
T189A |
probably benign |
Het |
Or5ae1 |
T |
A |
7: 84,565,671 (GRCm39) |
I228N |
probably damaging |
Het |
Pak4 |
A |
C |
7: 28,261,969 (GRCm39) |
D453E |
probably benign |
Het |
Pkd1l1 |
T |
C |
11: 8,805,567 (GRCm39) |
T2120A |
|
Het |
Pkhd1l1 |
T |
A |
15: 44,381,570 (GRCm39) |
S1099T |
probably benign |
Het |
Pld2 |
C |
T |
11: 70,444,275 (GRCm39) |
R524W |
probably damaging |
Het |
Polr1a |
T |
A |
6: 71,951,832 (GRCm39) |
D1466E |
probably benign |
Het |
Pxdn |
C |
T |
12: 30,056,601 (GRCm39) |
L1271F |
probably damaging |
Het |
Rp1l1 |
A |
C |
14: 64,269,295 (GRCm39) |
D1627A |
probably damaging |
Het |
Sephs1 |
T |
C |
2: 4,889,402 (GRCm39) |
V60A |
probably benign |
Het |
Sipa1 |
C |
T |
19: 5,710,980 (GRCm39) |
R10Q |
probably damaging |
Het |
Sp4 |
T |
C |
12: 118,263,189 (GRCm39) |
T286A |
possibly damaging |
Het |
Spag5 |
T |
A |
11: 78,192,738 (GRCm39) |
S23R |
probably benign |
Het |
Spag9 |
T |
A |
11: 93,958,916 (GRCm39) |
N313K |
probably benign |
Het |
Stag1 |
T |
A |
9: 100,772,975 (GRCm39) |
|
probably benign |
Het |
Stkld1 |
T |
A |
2: 26,835,817 (GRCm39) |
H217Q |
probably benign |
Het |
Stxbp2 |
T |
A |
8: 3,683,914 (GRCm39) |
F104I |
possibly damaging |
Het |
Tcf12 |
A |
G |
9: 71,765,787 (GRCm39) |
V575A |
possibly damaging |
Het |
Tcf12 |
A |
T |
9: 71,830,069 (GRCm39) |
S131T |
probably benign |
Het |
Tg |
T |
A |
15: 66,553,786 (GRCm39) |
S400R |
probably benign |
Het |
Tomm40 |
T |
C |
7: 19,444,703 (GRCm39) |
T200A |
possibly damaging |
Het |
Trio |
T |
C |
15: 27,919,323 (GRCm39) |
E71G |
unknown |
Het |
Zfp292 |
A |
T |
4: 34,805,982 (GRCm39) |
V2359E |
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 |
R1758:Muc5ac
|
UTSW |
7 |
141,355,268 (GRCm39) |
missense |
possibly damaging |
0.86 |
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 |
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 |
|
|