Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010315B03Rik |
T |
C |
9: 124,055,701 (GRCm39) |
K408E |
probably damaging |
Het |
2010315B03Rik |
T |
A |
9: 124,055,783 (GRCm39) |
K380N |
probably damaging |
Het |
9230104M06Rik |
C |
T |
12: 112,964,359 (GRCm39) |
|
probably benign |
Het |
Ahi1 |
T |
A |
10: 20,846,810 (GRCm39) |
C413* |
probably null |
Het |
Alms1 |
T |
A |
6: 85,599,464 (GRCm39) |
M1430K |
possibly damaging |
Het |
Ankrd52 |
G |
T |
10: 128,225,220 (GRCm39) |
A894S |
probably benign |
Het |
Arhgap33 |
C |
A |
7: 30,226,654 (GRCm39) |
V494L |
probably damaging |
Het |
Atic |
G |
T |
1: 71,608,130 (GRCm39) |
V275F |
probably damaging |
Het |
Atoh1 |
T |
A |
6: 64,706,668 (GRCm39) |
V121E |
probably damaging |
Het |
Atp5pd |
T |
A |
11: 115,306,864 (GRCm39) |
|
probably null |
Het |
Baiap2l2 |
A |
T |
15: 79,146,174 (GRCm39) |
|
probably null |
Het |
Brca2 |
A |
T |
5: 150,465,227 (GRCm39) |
T1664S |
probably benign |
Het |
Cdh15 |
G |
A |
8: 123,588,763 (GRCm39) |
R279Q |
probably damaging |
Het |
Celf3 |
ACAGCAGCAGCAGCAGCAGCAGCA |
ACAGCAGCAGCAGCAGCAGCA |
3: 94,395,537 (GRCm39) |
|
probably benign |
Het |
Cep350 |
A |
T |
1: 155,835,464 (GRCm39) |
|
probably null |
Het |
Ces2g |
T |
C |
8: 105,692,621 (GRCm39) |
|
probably null |
Het |
Csmd3 |
CCTTTGCGCTT |
CCTT |
15: 47,604,632 (GRCm39) |
|
probably null |
Het |
Cyp2d34 |
A |
G |
15: 82,500,368 (GRCm39) |
F457S |
probably damaging |
Het |
Disp3 |
T |
A |
4: 148,325,880 (GRCm39) |
T1293S |
probably damaging |
Het |
Dock10 |
T |
A |
1: 80,517,970 (GRCm39) |
I1348F |
possibly damaging |
Het |
Dsp |
A |
T |
13: 38,380,380 (GRCm39) |
H1776L |
probably damaging |
Het |
Efhd1 |
A |
T |
1: 87,237,477 (GRCm39) |
Q228L |
possibly damaging |
Het |
Entpd2 |
T |
A |
2: 25,289,295 (GRCm39) |
I259N |
probably benign |
Het |
Fam149b |
A |
T |
14: 20,425,578 (GRCm39) |
M138L |
probably damaging |
Het |
Fastkd5 |
T |
C |
2: 130,458,285 (GRCm39) |
K102E |
probably benign |
Het |
Fzd7 |
C |
A |
1: 59,523,695 (GRCm39) |
T526K |
possibly damaging |
Het |
G6pd2 |
T |
A |
5: 61,966,330 (GRCm39) |
I35N |
probably damaging |
Het |
Gars1 |
T |
A |
6: 55,042,548 (GRCm39) |
M427K |
probably damaging |
Het |
Gimap4 |
C |
T |
6: 48,667,799 (GRCm39) |
R57C |
probably damaging |
Het |
Gm11232 |
C |
A |
4: 71,676,022 (GRCm39) |
W41L |
probably benign |
Het |
Gm15737 |
T |
A |
6: 92,856,701 (GRCm39) |
C43* |
probably null |
Het |
Gpr180 |
T |
C |
14: 118,377,185 (GRCm39) |
V62A |
probably benign |
Het |
H2-M11 |
C |
T |
17: 36,859,042 (GRCm39) |
T194I |
possibly damaging |
Het |
Jakmip3 |
A |
T |
7: 138,591,197 (GRCm39) |
E27V |
possibly damaging |
Het |
Kcnq3 |
T |
C |
15: 65,903,276 (GRCm39) |
T145A |
probably damaging |
Het |
Krt8 |
A |
G |
15: 101,906,459 (GRCm39) |
M350T |
probably benign |
Het |
Krtap4-9 |
T |
A |
11: 99,676,492 (GRCm39) |
|
probably benign |
Het |
Lbr |
G |
T |
1: 181,663,692 (GRCm39) |
D109E |
probably damaging |
Het |
Ldc1 |
A |
T |
4: 130,103,681 (GRCm39) |
L420Q |
probably benign |
Het |
Med23 |
A |
G |
10: 24,764,473 (GRCm39) |
H42R |
probably damaging |
Het |
Mgat5 |
A |
T |
1: 127,234,741 (GRCm39) |
M77L |
probably benign |
Het |
Mlf1 |
A |
T |
3: 67,291,919 (GRCm39) |
N28I |
possibly damaging |
Het |
Mroh3 |
A |
C |
1: 136,125,864 (GRCm39) |
L343R |
probably damaging |
Het |
Mrpl37 |
T |
A |
4: 106,921,690 (GRCm39) |
I180F |
possibly damaging |
Het |
Mrps27 |
T |
A |
13: 99,536,836 (GRCm39) |
C116* |
probably null |
Het |
Myh7 |
A |
T |
14: 55,220,699 (GRCm39) |
D1033E |
probably damaging |
Het |
Myo16 |
A |
T |
8: 10,644,820 (GRCm39) |
E1717D |
probably benign |
Het |
Myo1g |
T |
A |
11: 6,462,539 (GRCm39) |
|
probably null |
Het |
Or51ag1 |
A |
G |
7: 103,155,367 (GRCm39) |
M262T |
probably benign |
Het |
Or6c217 |
A |
C |
10: 129,737,964 (GRCm39) |
L205R |
probably damaging |
Het |
Pan2 |
T |
C |
10: 128,149,766 (GRCm39) |
L576P |
probably damaging |
Het |
Parp8 |
A |
G |
13: 117,032,223 (GRCm39) |
S278P |
possibly damaging |
Het |
Pdk2 |
A |
G |
11: 94,918,028 (GRCm39) |
|
probably null |
Het |
Phf1 |
T |
C |
17: 27,156,062 (GRCm39) |
S450P |
probably damaging |
Het |
Pkd1l2 |
T |
C |
8: 117,746,233 (GRCm39) |
Y1919C |
probably damaging |
Het |
Postn |
T |
A |
3: 54,284,374 (GRCm39) |
S614T |
probably damaging |
Het |
Psmg1 |
A |
T |
16: 95,783,395 (GRCm39) |
Y213* |
probably null |
Het |
Rab11b |
T |
A |
17: 33,966,692 (GRCm39) |
T203S |
probably benign |
Het |
Rad54l2 |
T |
A |
9: 106,580,825 (GRCm39) |
T899S |
possibly damaging |
Het |
Ramp2 |
TTGCTGCTGCTGCTGCTGCTGCTG |
TTGCTGCTGCTGCTGCTGCTG |
11: 101,137,371 (GRCm39) |
|
probably benign |
Het |
Rapgef6 |
A |
G |
11: 54,578,537 (GRCm39) |
T1028A |
possibly damaging |
Het |
Rbm6 |
A |
G |
9: 107,669,197 (GRCm39) |
S58P |
possibly damaging |
Het |
Rreb1 |
G |
T |
13: 38,113,768 (GRCm39) |
A376S |
possibly damaging |
Het |
Rsbn1l |
T |
A |
5: 21,124,767 (GRCm39) |
N345I |
probably benign |
Het |
Sf3b2 |
A |
T |
19: 5,325,118 (GRCm39) |
S785T |
possibly damaging |
Het |
Sh2b1 |
C |
T |
7: 126,068,098 (GRCm39) |
D519N |
probably damaging |
Het |
Slitrk6 |
T |
C |
14: 110,987,704 (GRCm39) |
T668A |
probably benign |
Het |
Stkld1 |
T |
A |
2: 26,840,650 (GRCm39) |
I444N |
probably damaging |
Het |
Sucla2 |
A |
T |
14: 73,790,244 (GRCm39) |
|
probably benign |
Het |
Tmem67 |
T |
A |
4: 12,079,918 (GRCm39) |
L190F |
probably damaging |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Trem2 |
G |
A |
17: 48,658,863 (GRCm39) |
W191* |
probably null |
Het |
Ube2d4 |
A |
T |
15: 58,718,528 (GRCm39) |
|
noncoding transcript |
Het |
Uimc1 |
G |
T |
13: 55,223,617 (GRCm39) |
D218E |
probably damaging |
Het |
Wdr62 |
A |
T |
7: 29,973,424 (GRCm39) |
V95E |
probably damaging |
Het |
Zfhx4 |
T |
C |
3: 5,310,203 (GRCm39) |
V862A |
probably damaging |
Het |
Zfp462 |
T |
A |
4: 55,008,522 (GRCm39) |
S163T |
probably benign |
Het |
Zfp704 |
T |
C |
3: 9,674,553 (GRCm39) |
D76G |
unknown |
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 |
R1702:Muc6
|
UTSW |
7 |
141,236,752 (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 |
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 |
|