Other mutations in this stock |
Total: 116 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb9 |
T |
C |
5: 124,228,176 (GRCm39) |
T22A |
possibly damaging |
Het |
Abi3bp |
A |
G |
16: 56,417,173 (GRCm39) |
D419G |
probably benign |
Het |
Acoxl |
A |
T |
2: 127,696,691 (GRCm39) |
|
probably benign |
Het |
Acvr1 |
T |
C |
2: 58,352,983 (GRCm39) |
T326A |
possibly damaging |
Het |
Adgra2 |
T |
C |
8: 27,610,979 (GRCm39) |
L976P |
probably damaging |
Het |
Adora2b |
A |
G |
11: 62,155,886 (GRCm39) |
|
probably null |
Het |
Ak1 |
A |
T |
2: 32,521,182 (GRCm39) |
Q117L |
probably damaging |
Het |
Akr1c14 |
T |
A |
13: 4,128,029 (GRCm39) |
D143E |
probably damaging |
Het |
Ap4e1 |
A |
T |
2: 126,861,242 (GRCm39) |
H127L |
probably damaging |
Het |
Asxl3 |
T |
A |
18: 22,649,670 (GRCm39) |
I553N |
probably damaging |
Het |
Asxl3 |
T |
A |
18: 22,657,481 (GRCm39) |
N1830K |
possibly damaging |
Het |
Atp11a |
G |
A |
8: 12,863,144 (GRCm39) |
A108T |
probably damaging |
Het |
Bag6 |
A |
G |
17: 35,362,437 (GRCm39) |
T582A |
unknown |
Het |
Bbs9 |
T |
C |
9: 22,490,005 (GRCm39) |
S259P |
probably damaging |
Het |
Bean1 |
CT |
C |
8: 104,908,664 (GRCm39) |
|
probably null |
Het |
Bltp3a |
T |
A |
17: 28,104,902 (GRCm39) |
L532* |
probably null |
Het |
Blvrb |
T |
C |
7: 27,165,210 (GRCm39) |
S177P |
probably damaging |
Het |
C1s2 |
T |
A |
6: 124,602,642 (GRCm39) |
D523V |
probably benign |
Het |
Cacna2d1 |
C |
T |
5: 16,558,850 (GRCm39) |
T736I |
probably damaging |
Het |
Card9 |
T |
C |
2: 26,242,397 (GRCm39) |
N513S |
probably benign |
Het |
Casp2 |
A |
G |
6: 42,245,882 (GRCm39) |
T180A |
probably benign |
Het |
Cenpf |
A |
T |
1: 189,404,746 (GRCm39) |
L361Q |
probably damaging |
Het |
Cnbd2 |
T |
C |
2: 156,217,488 (GRCm39) |
I659T |
probably damaging |
Het |
Cped1 |
A |
T |
6: 21,987,012 (GRCm39) |
D68V |
probably damaging |
Het |
Cxcr1 |
T |
C |
1: 74,231,099 (GRCm39) |
I308V |
probably benign |
Het |
Dad1 |
A |
G |
14: 54,491,163 (GRCm39) |
L46P |
probably damaging |
Het |
Defb23 |
G |
A |
2: 152,301,422 (GRCm39) |
A50V |
probably benign |
Het |
Dhx33 |
C |
T |
11: 70,877,992 (GRCm39) |
A684T |
probably damaging |
Het |
Dnai3 |
T |
C |
3: 145,772,589 (GRCm39) |
T486A |
probably benign |
Het |
Epb41l4a |
T |
A |
18: 33,965,729 (GRCm39) |
N366I |
probably benign |
Het |
Erich3 |
A |
G |
3: 154,467,912 (GRCm39) |
E788G |
|
Het |
Fam241b |
T |
C |
10: 61,944,892 (GRCm39) |
N35S |
probably benign |
Het |
Fbxo24 |
T |
A |
5: 137,622,526 (GRCm39) |
Q80L |
probably benign |
Het |
Foxk1 |
T |
G |
5: 142,434,497 (GRCm39) |
F254V |
probably benign |
Het |
Gm10801 |
C |
CGTG |
2: 98,494,152 (GRCm39) |
|
probably null |
Het |
Gm12886 |
T |
C |
4: 121,274,743 (GRCm39) |
I46V |
probably benign |
Het |
Gm20834 |
G |
T |
Y: 10,323,354 (GRCm39) |
H27Q |
probably damaging |
Het |
Gm2888 |
A |
G |
14: 3,032,106 (GRCm38) |
N138S |
probably damaging |
Het |
Gm5773 |
T |
C |
3: 93,681,179 (GRCm39) |
C284R |
possibly damaging |
Het |
Gprin3 |
A |
T |
6: 59,330,273 (GRCm39) |
M678K |
probably benign |
Het |
Grm7 |
T |
C |
6: 111,472,729 (GRCm39) |
V856A |
probably benign |
Het |
Il18rap |
C |
T |
1: 40,582,177 (GRCm39) |
T366M |
probably benign |
Het |
Immt |
C |
T |
6: 71,851,403 (GRCm39) |
T588I |
probably damaging |
Het |
Ints1 |
G |
C |
5: 139,737,701 (GRCm39) |
N2145K |
possibly damaging |
Het |
Jade2 |
T |
C |
11: 51,715,951 (GRCm39) |
D418G |
probably benign |
Het |
Kdf1 |
T |
C |
4: 133,256,140 (GRCm39) |
Y286H |
probably damaging |
Het |
Kif18a |
A |
G |
2: 109,171,506 (GRCm39) |
Y861C |
possibly damaging |
Het |
Lama2 |
T |
A |
10: 27,298,515 (GRCm39) |
I194F |
probably damaging |
Het |
Lhx8 |
A |
G |
3: 154,034,063 (GRCm39) |
S33P |
probably benign |
Het |
Lmo7 |
T |
C |
14: 102,118,297 (GRCm39) |
I174T |
probably damaging |
Het |
Lrfn2 |
A |
T |
17: 49,376,976 (GRCm39) |
D19V |
possibly damaging |
Het |
Lrrk1 |
A |
T |
7: 65,928,357 (GRCm39) |
I1257N |
probably damaging |
Het |
Malrd1 |
T |
A |
2: 15,802,516 (GRCm39) |
H1076Q |
unknown |
Het |
Map3k14 |
A |
C |
11: 103,128,364 (GRCm39) |
M419R |
probably damaging |
Het |
Mcm10 |
G |
A |
2: 5,011,372 (GRCm39) |
R200C |
probably benign |
Het |
Mertk |
A |
G |
2: 128,604,035 (GRCm39) |
N390D |
probably benign |
Het |
Mitf |
T |
A |
6: 97,990,680 (GRCm39) |
I361N |
probably damaging |
Het |
Mrgprb1 |
T |
A |
7: 48,097,046 (GRCm39) |
I289F |
possibly damaging |
Het |
Nox4 |
G |
A |
7: 87,025,448 (GRCm39) |
R525Q |
probably benign |
Het |
Nphp3 |
T |
G |
9: 103,909,214 (GRCm39) |
L808R |
probably damaging |
Het |
Or14c42-ps1 |
G |
A |
7: 86,211,156 (GRCm39) |
C72Y |
unknown |
Het |
Or1e1 |
T |
C |
11: 73,245,316 (GRCm39) |
S246P |
probably damaging |
Het |
Or5an1 |
T |
A |
19: 12,260,808 (GRCm39) |
L132Q |
probably damaging |
Het |
Or5b113 |
T |
A |
19: 13,342,755 (GRCm39) |
S254R |
possibly damaging |
Het |
Pagr1a |
T |
C |
7: 126,615,954 (GRCm39) |
E47G |
probably benign |
Het |
Papss2 |
G |
T |
19: 32,618,764 (GRCm39) |
R274L |
probably damaging |
Het |
Pcdhga10 |
C |
A |
18: 37,880,960 (GRCm39) |
F240L |
probably damaging |
Het |
Pcsk5 |
T |
G |
19: 17,563,472 (GRCm39) |
E555A |
|
Het |
Peg10 |
C |
CTCA |
6: 4,756,453 (GRCm39) |
|
probably benign |
Het |
Pgrmc2 |
T |
A |
3: 41,023,099 (GRCm39) |
D206V |
probably damaging |
Het |
Pkd1 |
T |
C |
17: 24,790,976 (GRCm39) |
V1057A |
|
Het |
Plekha5 |
T |
C |
6: 140,480,239 (GRCm39) |
I113T |
probably damaging |
Het |
Prorp |
T |
A |
12: 55,426,189 (GRCm39) |
L513Q |
probably damaging |
Het |
Prss32 |
C |
T |
17: 24,078,199 (GRCm39) |
T295I |
possibly damaging |
Het |
Ptprk |
G |
T |
10: 28,456,413 (GRCm39) |
V1072F |
probably damaging |
Het |
Rasd2 |
T |
A |
8: 75,945,174 (GRCm39) |
M1K |
probably null |
Het |
Rhag |
T |
A |
17: 41,139,302 (GRCm39) |
M79K |
probably damaging |
Het |
Rnf19a |
C |
A |
15: 36,253,310 (GRCm39) |
|
probably null |
Het |
Rnf213 |
G |
T |
11: 119,299,573 (GRCm39) |
G101C |
|
Het |
Sap130 |
T |
A |
18: 31,780,116 (GRCm39) |
D45E |
probably benign |
Het |
Scel |
T |
A |
14: 103,839,626 (GRCm39) |
F510I |
probably benign |
Het |
Sertad2 |
A |
T |
11: 20,598,425 (GRCm39) |
E207V |
probably benign |
Het |
Shoc2 |
T |
A |
19: 53,976,310 (GRCm39) |
S67T |
probably benign |
Het |
Slc22a3 |
T |
C |
17: 12,645,619 (GRCm39) |
I441V |
possibly damaging |
Het |
Slfn5 |
A |
G |
11: 82,851,503 (GRCm39) |
D600G |
probably benign |
Het |
Smim7 |
G |
A |
8: 73,324,757 (GRCm39) |
T10M |
probably damaging |
Het |
Sntb2 |
A |
T |
8: 107,662,831 (GRCm39) |
Q133L |
possibly damaging |
Het |
Steap3 |
A |
C |
1: 120,162,048 (GRCm39) |
M408R |
probably benign |
Het |
Supt4a |
T |
C |
11: 87,633,624 (GRCm39) |
I60T |
probably benign |
Het |
Swt1 |
A |
C |
1: 151,244,239 (GRCm39) |
C899G |
possibly damaging |
Het |
Taok3 |
A |
G |
5: 117,344,744 (GRCm39) |
E157G |
probably damaging |
Het |
Taok3 |
C |
T |
5: 117,379,245 (GRCm39) |
L427F |
possibly damaging |
Het |
Taok3 |
T |
C |
5: 117,379,168 (GRCm39) |
V401A |
probably benign |
Het |
Tcf25 |
A |
G |
8: 124,108,182 (GRCm39) |
E79G |
probably benign |
Het |
Tigit |
G |
A |
16: 43,479,876 (GRCm39) |
L140F |
possibly damaging |
Het |
Tmem143 |
G |
T |
7: 45,546,802 (GRCm39) |
|
probably benign |
Het |
Tmem151b |
C |
T |
17: 45,856,355 (GRCm39) |
V362M |
possibly damaging |
Het |
Tmem230 |
A |
G |
2: 132,085,989 (GRCm39) |
F58L |
probably benign |
Het |
Trim25 |
T |
C |
11: 88,899,988 (GRCm39) |
M245T |
probably benign |
Het |
Trim36 |
A |
C |
18: 46,302,410 (GRCm39) |
V546G |
probably benign |
Het |
Triml1 |
T |
C |
8: 43,583,624 (GRCm39) |
N326D |
probably damaging |
Het |
Trp53bp2 |
T |
C |
1: 182,286,328 (GRCm39) |
V1056A |
probably damaging |
Het |
Trpa1 |
C |
A |
1: 14,952,435 (GRCm39) |
M865I |
probably damaging |
Het |
Ttbk1 |
A |
T |
17: 46,790,132 (GRCm39) |
Y104* |
probably null |
Het |
Tubg1 |
T |
A |
11: 101,014,257 (GRCm39) |
H139Q |
probably damaging |
Het |
Ufsp2 |
A |
G |
8: 46,447,050 (GRCm39) |
|
probably null |
Het |
Usp47 |
A |
T |
7: 111,652,431 (GRCm39) |
N36I |
probably benign |
Het |
Vmn1r32 |
G |
A |
6: 66,530,120 (GRCm39) |
R219* |
probably null |
Het |
Vmn2r59 |
G |
A |
7: 41,693,125 (GRCm39) |
P492S |
probably benign |
Het |
Vmn2r59 |
G |
C |
7: 41,693,127 (GRCm39) |
A491G |
|
Het |
Wdr76 |
T |
C |
2: 121,364,592 (GRCm39) |
Y299H |
probably damaging |
Het |
Wnt5a |
C |
T |
14: 28,240,309 (GRCm39) |
A153V |
probably benign |
Het |
Zfp202 |
T |
C |
9: 40,120,237 (GRCm39) |
V226A |
possibly damaging |
Het |
Zfp219 |
C |
T |
14: 52,244,598 (GRCm39) |
R527H |
probably damaging |
Het |
Zfp408 |
A |
T |
2: 91,475,528 (GRCm39) |
L542H |
probably damaging |
Het |
Zfyve9 |
A |
T |
4: 108,539,386 (GRCm39) |
C271* |
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 |
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 |
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 |
|
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 |
|
|