Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
T |
C |
6: 121,639,405 (GRCm39) |
|
probably null |
Het |
Abtb2 |
A |
G |
2: 103,397,480 (GRCm39) |
I137V |
probably benign |
Het |
Ank1 |
T |
A |
8: 23,613,993 (GRCm39) |
N1545K |
probably damaging |
Het |
Arl6 |
T |
C |
16: 59,439,153 (GRCm39) |
|
probably benign |
Het |
Avl9 |
T |
A |
6: 56,713,487 (GRCm39) |
D248E |
probably benign |
Het |
Becn1 |
T |
C |
11: 101,192,562 (GRCm39) |
E40G |
probably damaging |
Het |
Bod1l |
G |
T |
5: 41,976,040 (GRCm39) |
A1758E |
possibly damaging |
Het |
Btbd16 |
C |
T |
7: 130,381,324 (GRCm39) |
T19I |
probably damaging |
Het |
Casc3 |
T |
A |
11: 98,713,325 (GRCm39) |
N246K |
possibly damaging |
Het |
Celf1 |
G |
T |
2: 90,835,035 (GRCm39) |
|
probably benign |
Het |
Chrm3 |
G |
T |
13: 9,928,780 (GRCm39) |
N85K |
probably damaging |
Het |
Cluh |
T |
A |
11: 74,556,764 (GRCm39) |
Y935N |
probably damaging |
Het |
Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
Col6a5 |
T |
C |
9: 105,802,993 (GRCm39) |
D1324G |
unknown |
Het |
Ctcfl |
T |
C |
2: 172,960,340 (GRCm39) |
D81G |
possibly damaging |
Het |
D630003M21Rik |
C |
T |
2: 158,044,987 (GRCm39) |
|
probably benign |
Het |
Ddx39a |
C |
T |
8: 84,449,105 (GRCm39) |
R298C |
possibly damaging |
Het |
Dnmt3b |
T |
G |
2: 153,503,377 (GRCm39) |
N9K |
possibly damaging |
Het |
Dock8 |
T |
C |
19: 25,096,823 (GRCm39) |
L577P |
probably benign |
Het |
Drc1 |
A |
T |
5: 30,486,487 (GRCm39) |
N13I |
possibly damaging |
Het |
Eml4 |
T |
A |
17: 83,729,081 (GRCm39) |
N85K |
probably damaging |
Het |
Epb41l4a |
T |
C |
18: 33,931,853 (GRCm39) |
T581A |
probably damaging |
Het |
Epha3 |
T |
C |
16: 63,433,307 (GRCm39) |
D446G |
possibly damaging |
Het |
Fam209 |
G |
T |
2: 172,315,900 (GRCm39) |
G92C |
probably damaging |
Het |
Fam98c |
T |
A |
7: 28,852,146 (GRCm39) |
R340* |
probably null |
Het |
Fbxw10 |
T |
G |
11: 62,738,307 (GRCm39) |
|
probably null |
Het |
Galr1 |
A |
G |
18: 82,423,695 (GRCm39) |
L194P |
probably benign |
Het |
Gar1 |
T |
C |
3: 129,623,122 (GRCm39) |
H89R |
probably damaging |
Het |
Gbp4 |
T |
A |
5: 105,267,362 (GRCm39) |
Y519F |
probably benign |
Het |
Gm28042 |
T |
A |
2: 119,866,944 (GRCm39) |
S196T |
probably benign |
Het |
Grid2 |
T |
C |
6: 64,510,571 (GRCm39) |
Y734H |
probably benign |
Het |
Grm6 |
T |
A |
11: 50,750,144 (GRCm39) |
I466N |
possibly damaging |
Het |
Hectd3 |
T |
C |
4: 116,854,237 (GRCm39) |
|
probably benign |
Het |
Hpse2 |
A |
C |
19: 42,920,099 (GRCm39) |
|
probably null |
Het |
Hspb7 |
T |
C |
4: 141,151,302 (GRCm39) |
I148T |
probably damaging |
Het |
Htr1d |
C |
A |
4: 136,170,788 (GRCm39) |
T339K |
probably damaging |
Het |
Ip6k1 |
T |
A |
9: 107,923,093 (GRCm39) |
D408E |
probably damaging |
Het |
Irs2 |
A |
T |
8: 11,057,568 (GRCm39) |
M288K |
probably damaging |
Het |
Kansl3 |
A |
T |
1: 36,392,897 (GRCm39) |
C225S |
probably damaging |
Het |
Knop1 |
C |
A |
7: 118,445,061 (GRCm39) |
R301L |
probably benign |
Het |
Lama5 |
T |
C |
2: 179,832,199 (GRCm39) |
H1714R |
probably benign |
Het |
Mettl14 |
G |
A |
3: 123,165,043 (GRCm39) |
T316I |
probably damaging |
Het |
Mmp15 |
A |
T |
8: 96,098,945 (GRCm39) |
N591Y |
probably benign |
Het |
Mprip |
T |
A |
11: 59,627,899 (GRCm39) |
D93E |
possibly damaging |
Het |
Mtmr14 |
T |
A |
6: 113,237,627 (GRCm39) |
|
probably benign |
Het |
Muc6 |
C |
T |
7: 141,238,255 (GRCm39) |
C75Y |
probably damaging |
Het |
Naip1 |
A |
T |
13: 100,563,418 (GRCm39) |
H582Q |
possibly damaging |
Het |
Nbeal2 |
G |
A |
9: 110,471,211 (GRCm39) |
R264* |
probably null |
Het |
Neb |
T |
C |
2: 52,139,388 (GRCm39) |
K140E |
probably damaging |
Het |
Nfya |
A |
G |
17: 48,706,026 (GRCm39) |
V48A |
possibly damaging |
Het |
Ngf |
G |
T |
3: 102,417,119 (GRCm39) |
|
probably benign |
Het |
Nsmce2 |
T |
G |
15: 59,250,806 (GRCm39) |
S26A |
probably damaging |
Het |
Or52s19 |
T |
C |
7: 103,007,613 (GRCm39) |
T263A |
possibly damaging |
Het |
Or5m13b |
T |
A |
2: 85,754,362 (GRCm39) |
I250N |
possibly damaging |
Het |
Or7e177 |
T |
G |
9: 20,212,387 (GRCm39) |
M297R |
probably damaging |
Het |
Pax1 |
A |
G |
2: 147,215,654 (GRCm39) |
S424G |
probably benign |
Het |
Pcdhb19 |
A |
T |
18: 37,630,235 (GRCm39) |
Q10L |
probably benign |
Het |
Pdcl |
T |
C |
2: 37,242,142 (GRCm39) |
I203V |
probably benign |
Het |
Pknox1 |
T |
A |
17: 31,823,764 (GRCm39) |
N379K |
probably benign |
Het |
Plxna1 |
C |
T |
6: 89,297,692 (GRCm39) |
A1831T |
possibly damaging |
Het |
Prodh |
T |
G |
16: 17,895,677 (GRCm39) |
Q360P |
probably damaging |
Het |
Pygo2 |
T |
C |
3: 89,340,610 (GRCm39) |
V299A |
probably damaging |
Het |
Raf1 |
C |
T |
6: 115,609,934 (GRCm39) |
G202S |
probably benign |
Het |
Rgs11 |
T |
A |
17: 26,426,433 (GRCm39) |
|
probably null |
Het |
Rmc1 |
C |
T |
18: 12,322,328 (GRCm39) |
R594C |
probably damaging |
Het |
Rnf13 |
A |
G |
3: 57,709,889 (GRCm39) |
D144G |
probably damaging |
Het |
Rtel1 |
T |
C |
2: 180,962,839 (GRCm39) |
C31R |
probably damaging |
Het |
Rubcnl |
T |
A |
14: 75,279,898 (GRCm39) |
I427K |
probably damaging |
Het |
Sec23ip |
C |
T |
7: 128,380,775 (GRCm39) |
|
probably benign |
Het |
Slc25a26 |
T |
A |
6: 94,569,507 (GRCm39) |
|
probably null |
Het |
Slc6a7 |
A |
G |
18: 61,135,183 (GRCm39) |
|
probably benign |
Het |
Slco6b1 |
A |
T |
1: 96,915,562 (GRCm39) |
|
noncoding transcript |
Het |
Spata17 |
A |
G |
1: 186,844,798 (GRCm39) |
V111A |
probably damaging |
Het |
Spata22 |
T |
A |
11: 73,221,979 (GRCm39) |
M1K |
probably null |
Het |
Svep1 |
C |
T |
4: 58,116,608 (GRCm39) |
D881N |
possibly damaging |
Het |
Sypl2 |
T |
A |
3: 108,126,411 (GRCm39) |
N67I |
possibly damaging |
Het |
Tasor |
A |
G |
14: 27,193,725 (GRCm39) |
D975G |
probably benign |
Het |
Tenm3 |
T |
C |
8: 48,689,755 (GRCm39) |
Y1944C |
probably damaging |
Het |
Tm9sf4 |
G |
T |
2: 153,037,233 (GRCm39) |
V365L |
probably benign |
Het |
Tmc3 |
T |
C |
7: 83,256,950 (GRCm39) |
V401A |
probably damaging |
Het |
Trpm2 |
C |
T |
10: 77,761,659 (GRCm39) |
G997D |
probably damaging |
Het |
Unc5b |
A |
T |
10: 60,608,076 (GRCm39) |
S675T |
probably damaging |
Het |
Vmn1r217 |
A |
G |
13: 23,298,107 (GRCm39) |
M265T |
probably benign |
Het |
Vps54 |
T |
A |
11: 21,250,259 (GRCm39) |
D548E |
probably benign |
Het |
Wdfy3 |
A |
G |
5: 102,065,277 (GRCm39) |
V1297A |
probably benign |
Het |
Wdr46 |
T |
A |
17: 34,159,997 (GRCm39) |
F70I |
probably benign |
Het |
Zdbf2 |
C |
T |
1: 63,343,165 (GRCm39) |
Q515* |
probably null |
Het |
Zfp710 |
T |
A |
7: 79,731,721 (GRCm39) |
C299* |
probably null |
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 |
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 |
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 |
|
|