Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca15 |
T |
C |
7: 119,981,925 (GRCm39) |
V1080A |
probably benign |
Het |
Abcg4 |
A |
C |
9: 44,186,370 (GRCm39) |
V553G |
probably damaging |
Het |
Ache |
T |
C |
5: 137,289,251 (GRCm39) |
V319A |
possibly damaging |
Het |
Acsm2 |
T |
A |
7: 119,172,787 (GRCm39) |
M134K |
possibly damaging |
Het |
Ank2 |
A |
T |
3: 126,749,548 (GRCm39) |
S494T |
probably benign |
Het |
Asic3 |
A |
T |
5: 24,620,454 (GRCm39) |
T202S |
probably damaging |
Het |
Baiap3 |
T |
A |
17: 25,463,779 (GRCm39) |
H886L |
probably damaging |
Het |
Bltp2 |
T |
A |
11: 78,179,854 (GRCm39) |
C2126S |
probably damaging |
Het |
Cidea |
T |
A |
18: 67,499,491 (GRCm39) |
I126K |
probably damaging |
Het |
Cmklr1 |
T |
G |
5: 113,751,903 (GRCm39) |
K366T |
probably benign |
Het |
Cntrl |
A |
T |
2: 35,061,848 (GRCm39) |
|
probably null |
Het |
Crhr2 |
A |
G |
6: 55,069,520 (GRCm39) |
F378S |
probably damaging |
Het |
Deaf1 |
C |
G |
7: 140,894,867 (GRCm39) |
R303T |
probably damaging |
Het |
Dnah9 |
T |
A |
11: 65,976,021 (GRCm39) |
N1343Y |
possibly damaging |
Het |
Dop1b |
A |
G |
16: 93,544,509 (GRCm39) |
K99E |
possibly damaging |
Het |
Dpp4 |
A |
T |
2: 62,216,773 (GRCm39) |
|
probably null |
Het |
Dst |
T |
C |
1: 34,206,421 (GRCm39) |
V598A |
probably damaging |
Het |
Ece2 |
C |
T |
16: 20,449,996 (GRCm39) |
R136C |
probably damaging |
Het |
Efcab3 |
C |
T |
11: 104,581,832 (GRCm39) |
P58L |
probably benign |
Het |
Egf |
C |
A |
3: 129,484,460 (GRCm39) |
V453L |
probably benign |
Het |
Egr3 |
T |
A |
14: 70,317,216 (GRCm39) |
F342L |
probably damaging |
Het |
Eif2ak2 |
A |
T |
17: 79,164,063 (GRCm39) |
I434N |
probably damaging |
Het |
Emc1 |
A |
G |
4: 139,102,512 (GRCm39) |
T936A |
probably damaging |
Het |
Fmod |
A |
T |
1: 133,968,500 (GRCm39) |
E180V |
probably damaging |
Het |
Gabrg3 |
T |
C |
7: 56,634,848 (GRCm39) |
T112A |
probably damaging |
Het |
Gak |
T |
C |
5: 108,754,242 (GRCm39) |
|
probably null |
Het |
Gas2 |
T |
A |
7: 51,603,089 (GRCm39) |
|
probably null |
Het |
Gm2381 |
T |
A |
7: 42,469,655 (GRCm39) |
Q156H |
probably benign |
Het |
Golga2 |
T |
A |
2: 32,189,287 (GRCm39) |
S273T |
probably damaging |
Het |
Homez |
T |
A |
14: 55,094,452 (GRCm39) |
T419S |
probably damaging |
Het |
Igfbp6 |
T |
A |
15: 102,056,617 (GRCm39) |
Y184* |
probably null |
Het |
Il11 |
A |
G |
7: 4,776,733 (GRCm39) |
S86P |
probably damaging |
Het |
Itgal |
A |
G |
7: 126,904,197 (GRCm39) |
N270S |
probably benign |
Het |
Lama2 |
T |
C |
10: 27,066,525 (GRCm39) |
R1119G |
probably benign |
Het |
Lamp3 |
G |
T |
16: 19,494,822 (GRCm39) |
N294K |
probably benign |
Het |
Mars1 |
T |
C |
10: 127,145,948 (GRCm39) |
I113M |
possibly damaging |
Het |
Mgat5b |
A |
G |
11: 116,839,485 (GRCm39) |
T334A |
possibly damaging |
Het |
Mis18bp1 |
A |
G |
12: 65,208,518 (GRCm39) |
I65T |
probably benign |
Het |
Mmrn2 |
A |
T |
14: 34,119,871 (GRCm39) |
N247I |
probably benign |
Het |
Mx2 |
A |
G |
16: 97,359,883 (GRCm39) |
H551R |
probably benign |
Het |
Mylk |
T |
A |
16: 34,742,314 (GRCm39) |
V942E |
probably benign |
Het |
Nes |
A |
G |
3: 87,883,286 (GRCm39) |
E515G |
probably benign |
Het |
Nfatc3 |
T |
G |
8: 106,818,792 (GRCm39) |
S503R |
probably damaging |
Het |
Nkain3 |
C |
A |
4: 20,158,339 (GRCm39) |
|
probably null |
Het |
Noxa1 |
A |
G |
2: 24,982,596 (GRCm39) |
V73A |
probably damaging |
Het |
Nup160 |
A |
T |
2: 90,514,302 (GRCm39) |
E83D |
probably damaging |
Het |
Or12j3 |
A |
T |
7: 139,952,655 (GRCm39) |
Y289* |
probably null |
Het |
Or4z4 |
C |
A |
19: 12,076,530 (GRCm39) |
V158L |
probably benign |
Het |
Or5ac23 |
C |
A |
16: 59,149,504 (GRCm39) |
V123L |
probably benign |
Het |
Or8b56 |
A |
G |
9: 38,739,839 (GRCm39) |
Y284C |
probably damaging |
Het |
Plxnb2 |
A |
G |
15: 89,046,187 (GRCm39) |
|
probably null |
Het |
Rundc3b |
A |
G |
5: 8,562,318 (GRCm39) |
V350A |
probably benign |
Het |
Scn1a |
C |
T |
2: 66,148,567 (GRCm39) |
D993N |
probably damaging |
Het |
Sec24c |
G |
T |
14: 20,736,641 (GRCm39) |
G226V |
probably null |
Het |
Septin11 |
T |
A |
5: 93,304,783 (GRCm39) |
I200N |
probably damaging |
Het |
Shank3 |
G |
T |
15: 89,384,099 (GRCm39) |
G14C |
probably damaging |
Het |
Skic3 |
A |
G |
13: 76,270,862 (GRCm39) |
K153R |
possibly damaging |
Het |
Slc25a39 |
T |
C |
11: 102,297,452 (GRCm39) |
D5G |
possibly damaging |
Het |
Stoml3 |
A |
T |
3: 53,412,852 (GRCm39) |
T169S |
probably benign |
Het |
Taf1b |
T |
A |
12: 24,559,125 (GRCm39) |
I83K |
possibly damaging |
Het |
Tarbp1 |
T |
A |
8: 127,154,957 (GRCm39) |
Q1389L |
probably damaging |
Het |
Thbs1 |
T |
A |
2: 117,943,923 (GRCm39) |
D180E |
probably benign |
Het |
Tmc5 |
T |
A |
7: 118,271,462 (GRCm39) |
V925D |
probably benign |
Het |
Tmem62 |
T |
C |
2: 120,809,708 (GRCm39) |
V130A |
probably damaging |
Het |
Tpp2 |
C |
T |
1: 44,029,708 (GRCm39) |
P997L |
probably damaging |
Het |
Trip12 |
A |
T |
1: 84,722,784 (GRCm39) |
I127N |
probably damaging |
Het |
Upp2 |
T |
C |
2: 58,661,562 (GRCm39) |
F142L |
possibly damaging |
Het |
Usf3 |
C |
T |
16: 44,039,995 (GRCm39) |
Q1492* |
probably null |
Het |
Vcp |
T |
C |
4: 42,990,840 (GRCm39) |
D205G |
probably damaging |
Het |
Vmn1r180 |
G |
A |
7: 23,652,394 (GRCm39) |
V186I |
possibly damaging |
Het |
Washc2 |
T |
C |
6: 116,206,267 (GRCm39) |
S496P |
probably damaging |
Het |
Wee2 |
T |
C |
6: 40,441,135 (GRCm39) |
I480T |
probably benign |
Het |
Xylt2 |
T |
A |
11: 94,559,571 (GRCm39) |
H357L |
probably damaging |
Het |
Zbed4 |
T |
C |
15: 88,665,056 (GRCm39) |
S375P |
probably damaging |
Het |
Zfp442 |
A |
T |
2: 150,251,100 (GRCm39) |
Y266* |
probably null |
Het |
Zfp600 |
A |
G |
4: 146,133,497 (GRCm39) |
T722A |
probably benign |
Het |
Zfp976 |
T |
A |
7: 42,265,424 (GRCm39) |
H55L |
possibly damaging |
Het |
|
Other mutations in Muc6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Muc6
|
APN |
7 |
141,218,497 (GRCm39) |
missense |
probably benign |
0.06 |
IGL00466:Muc6
|
APN |
7 |
141,232,169 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00990:Muc6
|
APN |
7 |
141,638,890 (GRCm38) |
missense |
possibly damaging |
0.85 |
IGL01013:Muc6
|
APN |
7 |
141,234,333 (GRCm39) |
nonsense |
probably null |
|
IGL01021:Muc6
|
APN |
7 |
141,217,075 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01061:Muc6
|
APN |
7 |
141,234,720 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01294:Muc6
|
APN |
7 |
141,232,926 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01449:Muc6
|
APN |
7 |
141,218,527 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01474:Muc6
|
APN |
7 |
141,237,572 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01539:Muc6
|
APN |
7 |
141,236,306 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01541:Muc6
|
APN |
7 |
141,236,069 (GRCm39) |
nonsense |
probably null |
|
IGL01810:Muc6
|
APN |
7 |
141,237,327 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01941:Muc6
|
APN |
7 |
141,218,497 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01954:Muc6
|
APN |
7 |
141,218,497 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02096:Muc6
|
APN |
7 |
141,226,117 (GRCm39) |
intron |
probably benign |
|
IGL02192:Muc6
|
APN |
7 |
141,217,717 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02217:Muc6
|
APN |
7 |
141,235,889 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02234:Muc6
|
APN |
7 |
141,226,842 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02302:Muc6
|
APN |
7 |
141,227,763 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02331:Muc6
|
APN |
7 |
141,226,726 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02531:Muc6
|
APN |
7 |
141,216,853 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02639:Muc6
|
APN |
7 |
141,235,843 (GRCm39) |
splice site |
probably benign |
|
IGL02851:Muc6
|
APN |
7 |
141,234,627 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03026:Muc6
|
APN |
7 |
141,226,414 (GRCm39) |
intron |
probably benign |
|
IGL03070:Muc6
|
APN |
7 |
141,230,834 (GRCm39) |
splice site |
probably benign |
|
IGL03108:Muc6
|
APN |
7 |
141,217,402 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03350:Muc6
|
APN |
7 |
141,238,324 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03366:Muc6
|
APN |
7 |
141,234,349 (GRCm39) |
missense |
probably damaging |
1.00 |
anticipation
|
UTSW |
7 |
141,214,363 (GRCm39) |
frame shift |
probably null |
|
F5770:Muc6
|
UTSW |
7 |
141,233,880 (GRCm39) |
missense |
probably benign |
0.11 |
IGL03147:Muc6
|
UTSW |
7 |
141,218,313 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0001:Muc6
|
UTSW |
7 |
141,227,841 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0005:Muc6
|
UTSW |
7 |
141,218,685 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0147:Muc6
|
UTSW |
7 |
141,238,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R0153:Muc6
|
UTSW |
7 |
141,214,029 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0227:Muc6
|
UTSW |
7 |
141,223,981 (GRCm39) |
intron |
probably benign |
|
R0234:Muc6
|
UTSW |
7 |
141,235,939 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0234:Muc6
|
UTSW |
7 |
141,235,939 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0304:Muc6
|
UTSW |
7 |
141,218,313 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0379:Muc6
|
UTSW |
7 |
141,216,868 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0385:Muc6
|
UTSW |
7 |
141,218,313 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0423:Muc6
|
UTSW |
7 |
141,238,548 (GRCm39) |
missense |
probably benign |
0.01 |
R0499:Muc6
|
UTSW |
7 |
141,226,735 (GRCm39) |
missense |
probably benign |
|
R0503:Muc6
|
UTSW |
7 |
141,218,685 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0757:Muc6
|
UTSW |
7 |
141,218,497 (GRCm39) |
missense |
probably benign |
0.06 |
R0792:Muc6
|
UTSW |
7 |
141,223,981 (GRCm39) |
intron |
probably benign |
|
R0880:Muc6
|
UTSW |
7 |
141,217,270 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1136:Muc6
|
UTSW |
7 |
141,218,685 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1170:Muc6
|
UTSW |
7 |
141,230,500 (GRCm39) |
missense |
probably damaging |
0.99 |
R1174:Muc6
|
UTSW |
7 |
141,234,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R1175:Muc6
|
UTSW |
7 |
141,234,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R1189:Muc6
|
UTSW |
7 |
141,232,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R1259:Muc6
|
UTSW |
7 |
141,226,464 (GRCm39) |
intron |
probably benign |
|
R1293:Muc6
|
UTSW |
7 |
141,238,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R1295:Muc6
|
UTSW |
7 |
141,238,144 (GRCm39) |
missense |
probably benign |
0.04 |
R1296:Muc6
|
UTSW |
7 |
141,238,144 (GRCm39) |
missense |
probably benign |
0.04 |
R1471:Muc6
|
UTSW |
7 |
141,234,176 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1472:Muc6
|
UTSW |
7 |
141,238,144 (GRCm39) |
missense |
probably benign |
0.04 |
R1548:Muc6
|
UTSW |
7 |
141,218,685 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1548:Muc6
|
UTSW |
7 |
141,238,368 (GRCm39) |
splice site |
probably benign |
|
R1576:Muc6
|
UTSW |
7 |
141,214,437 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1689:Muc6
|
UTSW |
7 |
141,234,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R1792:Muc6
|
UTSW |
7 |
141,214,371 (GRCm39) |
missense |
probably benign |
0.41 |
R1924:Muc6
|
UTSW |
7 |
141,218,313 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1938:Muc6
|
UTSW |
7 |
141,217,011 (GRCm39) |
missense |
probably damaging |
0.99 |
R1964:Muc6
|
UTSW |
7 |
141,226,330 (GRCm39) |
intron |
probably benign |
|
R1964:Muc6
|
UTSW |
7 |
141,226,329 (GRCm39) |
nonsense |
probably null |
|
R1975:Muc6
|
UTSW |
7 |
141,234,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R2031:Muc6
|
UTSW |
7 |
141,218,313 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2104:Muc6
|
UTSW |
7 |
141,213,991 (GRCm39) |
missense |
probably benign |
0.23 |
R2201:Muc6
|
UTSW |
7 |
141,236,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R2218:Muc6
|
UTSW |
7 |
141,233,227 (GRCm39) |
missense |
probably benign |
0.41 |
R2245:Muc6
|
UTSW |
7 |
141,218,313 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2261:Muc6
|
UTSW |
7 |
141,218,313 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2271:Muc6
|
UTSW |
7 |
141,217,423 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2272:Muc6
|
UTSW |
7 |
141,217,423 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2284:Muc6
|
UTSW |
7 |
141,217,837 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2310:Muc6
|
UTSW |
7 |
141,217,444 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2566:Muc6
|
UTSW |
7 |
141,226,651 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2975:Muc6
|
UTSW |
7 |
141,216,951 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3406:Muc6
|
UTSW |
7 |
141,218,313 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3423:Muc6
|
UTSW |
7 |
141,218,313 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3548:Muc6
|
UTSW |
7 |
141,218,313 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3693:Muc6
|
UTSW |
7 |
141,234,946 (GRCm39) |
splice site |
probably benign |
|
R3872:Muc6
|
UTSW |
7 |
141,226,867 (GRCm39) |
missense |
probably benign |
|
R4029:Muc6
|
UTSW |
7 |
141,218,313 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4084:Muc6
|
UTSW |
7 |
141,234,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R4126:Muc6
|
UTSW |
7 |
141,218,313 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4410:Muc6
|
UTSW |
7 |
141,217,576 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4508:Muc6
|
UTSW |
7 |
141,226,356 (GRCm39) |
intron |
probably benign |
|
R4509:Muc6
|
UTSW |
7 |
141,218,313 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4518:Muc6
|
UTSW |
7 |
141,230,489 (GRCm39) |
missense |
probably benign |
0.03 |
R4594:Muc6
|
UTSW |
7 |
141,218,685 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4677:Muc6
|
UTSW |
7 |
141,224,212 (GRCm39) |
intron |
probably benign |
|
R4678:Muc6
|
UTSW |
7 |
141,230,554 (GRCm39) |
missense |
probably benign |
0.09 |
R4737:Muc6
|
UTSW |
7 |
141,218,685 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4737:Muc6
|
UTSW |
7 |
141,226,426 (GRCm39) |
intron |
probably benign |
|
R4981:Muc6
|
UTSW |
7 |
141,218,313 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5008:Muc6
|
UTSW |
7 |
141,223,981 (GRCm39) |
intron |
probably benign |
|
R5012:Muc6
|
UTSW |
7 |
141,216,570 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5017:Muc6
|
UTSW |
7 |
141,226,795 (GRCm39) |
missense |
probably benign |
|
R5027:Muc6
|
UTSW |
7 |
141,216,349 (GRCm39) |
missense |
probably benign |
0.01 |
R5058:Muc6
|
UTSW |
7 |
141,230,491 (GRCm39) |
missense |
probably benign |
0.01 |
R5069:Muc6
|
UTSW |
7 |
141,237,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R5126:Muc6
|
UTSW |
7 |
141,237,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R5168:Muc6
|
UTSW |
7 |
141,223,981 (GRCm39) |
intron |
probably benign |
|
R5179:Muc6
|
UTSW |
7 |
141,218,685 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5198:Muc6
|
UTSW |
7 |
141,218,685 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5262:Muc6
|
UTSW |
7 |
141,237,375 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5381:Muc6
|
UTSW |
7 |
141,217,836 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5454:Muc6
|
UTSW |
7 |
141,235,078 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5467:Muc6
|
UTSW |
7 |
141,216,448 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5540:Muc6
|
UTSW |
7 |
141,235,850 (GRCm39) |
critical splice donor site |
probably null |
|
R5800:Muc6
|
UTSW |
7 |
141,226,690 (GRCm39) |
splice site |
probably benign |
|
R5808:Muc6
|
UTSW |
7 |
141,226,360 (GRCm39) |
intron |
probably benign |
|
R5865:Muc6
|
UTSW |
7 |
141,236,769 (GRCm39) |
missense |
probably damaging |
0.97 |
R5919:Muc6
|
UTSW |
7 |
141,227,837 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6024:Muc6
|
UTSW |
7 |
141,227,841 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6064:Muc6
|
UTSW |
7 |
141,234,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R6126:Muc6
|
UTSW |
7 |
141,218,685 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6229:Muc6
|
UTSW |
7 |
141,226,792 (GRCm39) |
missense |
probably benign |
|
R6236:Muc6
|
UTSW |
7 |
141,218,685 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6245:Muc6
|
UTSW |
7 |
141,235,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R6254:Muc6
|
UTSW |
7 |
141,237,380 (GRCm39) |
missense |
probably benign |
0.09 |
R6418:Muc6
|
UTSW |
7 |
141,224,032 (GRCm39) |
intron |
probably benign |
|
R6609:Muc6
|
UTSW |
7 |
141,226,700 (GRCm39) |
splice site |
probably benign |
|
R6610:Muc6
|
UTSW |
7 |
141,226,700 (GRCm39) |
splice site |
probably benign |
|
R6611:Muc6
|
UTSW |
7 |
141,226,700 (GRCm39) |
splice site |
probably benign |
|
R6623:Muc6
|
UTSW |
7 |
141,223,981 (GRCm39) |
intron |
probably benign |
|
R6626:Muc6
|
UTSW |
7 |
141,223,981 (GRCm39) |
intron |
probably benign |
|
R6817:Muc6
|
UTSW |
7 |
141,237,326 (GRCm39) |
missense |
probably damaging |
0.99 |
R6923:Muc6
|
UTSW |
7 |
141,217,453 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6989:Muc6
|
UTSW |
7 |
141,226,246 (GRCm39) |
intron |
probably benign |
|
R7001:Muc6
|
UTSW |
7 |
141,217,320 (GRCm39) |
missense |
probably damaging |
0.99 |
R7046:Muc6
|
UTSW |
7 |
141,226,456 (GRCm39) |
intron |
probably benign |
|
R7097:Muc6
|
UTSW |
7 |
141,214,363 (GRCm39) |
frame shift |
probably null |
|
R7099:Muc6
|
UTSW |
7 |
141,214,363 (GRCm39) |
frame shift |
probably null |
|
R7101:Muc6
|
UTSW |
7 |
141,214,363 (GRCm39) |
frame shift |
probably null |
|
R7107:Muc6
|
UTSW |
7 |
141,214,363 (GRCm39) |
frame shift |
probably null |
|
R7108:Muc6
|
UTSW |
7 |
141,214,363 (GRCm39) |
frame shift |
probably null |
|
R7112:Muc6
|
UTSW |
7 |
141,235,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R7202:Muc6
|
UTSW |
7 |
141,214,363 (GRCm39) |
frame shift |
probably null |
|
R7204:Muc6
|
UTSW |
7 |
141,214,363 (GRCm39) |
frame shift |
probably null |
|
R7205:Muc6
|
UTSW |
7 |
141,214,363 (GRCm39) |
frame shift |
probably null |
|
R7222:Muc6
|
UTSW |
7 |
141,214,428 (GRCm39) |
missense |
unknown |
|
R7230:Muc6
|
UTSW |
7 |
141,235,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R7278:Muc6
|
UTSW |
7 |
141,226,842 (GRCm39) |
missense |
probably benign |
0.09 |
R7483:Muc6
|
UTSW |
7 |
141,224,245 (GRCm39) |
missense |
unknown |
|
R7501:Muc6
|
UTSW |
7 |
141,217,659 (GRCm39) |
missense |
probably damaging |
0.98 |
R7601:Muc6
|
UTSW |
7 |
141,216,454 (GRCm39) |
missense |
unknown |
|
R7641:Muc6
|
UTSW |
7 |
141,224,247 (GRCm39) |
missense |
unknown |
|
R7644:Muc6
|
UTSW |
7 |
141,217,659 (GRCm39) |
missense |
probably damaging |
0.98 |
R7645:Muc6
|
UTSW |
7 |
141,234,923 (GRCm39) |
missense |
probably benign |
0.40 |
R7659:Muc6
|
UTSW |
7 |
141,216,973 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7674:Muc6
|
UTSW |
7 |
141,224,247 (GRCm39) |
missense |
unknown |
|
R7679:Muc6
|
UTSW |
7 |
141,217,659 (GRCm39) |
missense |
probably damaging |
0.98 |
R7680:Muc6
|
UTSW |
7 |
141,217,659 (GRCm39) |
missense |
probably damaging |
0.98 |
R7689:Muc6
|
UTSW |
7 |
141,217,659 (GRCm39) |
missense |
probably damaging |
0.98 |
R7690:Muc6
|
UTSW |
7 |
141,217,659 (GRCm39) |
missense |
probably damaging |
0.98 |
R7760:Muc6
|
UTSW |
7 |
141,237,322 (GRCm39) |
splice site |
probably null |
|
R7806:Muc6
|
UTSW |
7 |
141,217,387 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7809:Muc6
|
UTSW |
7 |
141,226,638 (GRCm39) |
missense |
probably benign |
0.02 |
R7848:Muc6
|
UTSW |
7 |
141,232,188 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7859:Muc6
|
UTSW |
7 |
141,231,687 (GRCm39) |
missense |
probably damaging |
0.96 |
R8054:Muc6
|
UTSW |
7 |
141,231,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R8085:Muc6
|
UTSW |
7 |
141,226,729 (GRCm39) |
missense |
unknown |
|
R8130:Muc6
|
UTSW |
7 |
141,233,354 (GRCm39) |
missense |
probably damaging |
0.97 |
R8210:Muc6
|
UTSW |
7 |
141,235,673 (GRCm39) |
critical splice donor site |
probably null |
|
R8273:Muc6
|
UTSW |
7 |
141,226,795 (GRCm39) |
missense |
unknown |
|
R8294:Muc6
|
UTSW |
7 |
141,217,263 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8329:Muc6
|
UTSW |
7 |
141,226,525 (GRCm39) |
missense |
unknown |
|
R8379:Muc6
|
UTSW |
7 |
141,230,579 (GRCm39) |
nonsense |
probably null |
|
R8537:Muc6
|
UTSW |
7 |
141,234,184 (GRCm39) |
missense |
probably benign |
0.03 |
R8736:Muc6
|
UTSW |
7 |
141,228,439 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8767:Muc6
|
UTSW |
7 |
141,229,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R8902:Muc6
|
UTSW |
7 |
141,233,791 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9009:Muc6
|
UTSW |
7 |
141,217,018 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9010:Muc6
|
UTSW |
7 |
141,226,351 (GRCm39) |
missense |
unknown |
|
R9023:Muc6
|
UTSW |
7 |
141,237,432 (GRCm39) |
nonsense |
probably null |
|
R9058:Muc6
|
UTSW |
7 |
141,218,154 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9257:Muc6
|
UTSW |
7 |
141,226,738 (GRCm39) |
missense |
unknown |
|
R9495:Muc6
|
UTSW |
7 |
141,237,398 (GRCm39) |
missense |
probably damaging |
0.98 |
R9563:Muc6
|
UTSW |
7 |
141,217,783 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9645:Muc6
|
UTSW |
7 |
141,217,783 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9659:Muc6
|
UTSW |
7 |
141,232,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R9733:Muc6
|
UTSW |
7 |
141,216,310 (GRCm39) |
missense |
unknown |
|
R9787:Muc6
|
UTSW |
7 |
141,227,748 (GRCm39) |
nonsense |
probably null |
|
R9788:Muc6
|
UTSW |
7 |
141,232,100 (GRCm39) |
missense |
probably damaging |
1.00 |
V7581:Muc6
|
UTSW |
7 |
141,233,880 (GRCm39) |
missense |
probably benign |
0.11 |
V7583:Muc6
|
UTSW |
7 |
141,233,880 (GRCm39) |
missense |
probably benign |
0.11 |
X0026:Muc6
|
UTSW |
7 |
141,237,964 (GRCm39) |
missense |
possibly damaging |
0.94 |
X0058:Muc6
|
UTSW |
7 |
141,218,313 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1177:Muc6
|
UTSW |
7 |
141,237,656 (GRCm39) |
missense |
probably benign |
0.20 |
Z1177:Muc6
|
UTSW |
7 |
141,236,701 (GRCm39) |
missense |
probably benign |
0.29 |
Z1177:Muc6
|
UTSW |
7 |
141,217,827 (GRCm39) |
missense |
possibly damaging |
0.72 |
|