Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700025G04Rik |
A |
G |
1: 151,856,163 (GRCm39) |
|
probably benign |
Het |
Akap9 |
G |
A |
5: 4,105,671 (GRCm39) |
S2914N |
probably benign |
Het |
Alk |
T |
C |
17: 72,207,729 (GRCm39) |
D1002G |
probably damaging |
Het |
Ap3d1 |
A |
G |
10: 80,568,674 (GRCm39) |
|
probably benign |
Het |
Asb15 |
T |
C |
6: 24,562,486 (GRCm39) |
|
probably benign |
Het |
Asxl3 |
C |
A |
18: 22,657,564 (GRCm39) |
P1858Q |
probably benign |
Het |
Bltp1 |
T |
C |
3: 37,098,780 (GRCm39) |
S1136P |
probably damaging |
Het |
Bud31 |
T |
A |
5: 145,079,388 (GRCm39) |
|
probably benign |
Het |
C1qtnf1 |
G |
T |
11: 118,339,095 (GRCm39) |
R255L |
probably damaging |
Het |
Cacna2d4 |
C |
T |
6: 119,284,247 (GRCm39) |
R745W |
probably damaging |
Het |
Cage1 |
C |
T |
13: 38,206,856 (GRCm39) |
E330K |
probably damaging |
Het |
Catsperz |
T |
A |
19: 6,902,317 (GRCm39) |
N59I |
probably benign |
Het |
Ccdc110 |
G |
T |
8: 46,394,922 (GRCm39) |
S271I |
probably benign |
Het |
Ccdc88b |
T |
A |
19: 6,830,581 (GRCm39) |
E787V |
probably damaging |
Het |
Ccna2 |
A |
T |
3: 36,623,119 (GRCm39) |
|
probably benign |
Het |
Cd36 |
T |
A |
5: 18,018,086 (GRCm39) |
D209V |
probably damaging |
Het |
Cers4 |
T |
A |
8: 4,569,475 (GRCm39) |
W161R |
probably damaging |
Het |
Ces2f |
T |
A |
8: 105,680,178 (GRCm39) |
H442Q |
probably damaging |
Het |
Chchd6 |
A |
C |
6: 89,361,669 (GRCm39) |
C245G |
probably damaging |
Het |
Cndp1 |
T |
G |
18: 84,629,750 (GRCm39) |
Q481P |
probably benign |
Het |
Col3a1 |
A |
G |
1: 45,366,761 (GRCm39) |
R234G |
unknown |
Het |
Col3a1 |
A |
T |
1: 45,386,884 (GRCm39) |
N232I |
probably damaging |
Het |
Colgalt2 |
A |
T |
1: 152,378,768 (GRCm39) |
D398V |
probably damaging |
Het |
Cxcl10 |
TACTCAC |
TACTCACTCAC |
5: 92,495,941 (GRCm39) |
|
probably null |
Het |
Dcdc2a |
C |
A |
13: 25,240,290 (GRCm39) |
Q13K |
probably benign |
Het |
Dzip3 |
A |
T |
16: 48,781,571 (GRCm39) |
I240N |
probably damaging |
Het |
Epb41l3 |
T |
A |
17: 69,566,175 (GRCm39) |
L452* |
probably null |
Het |
Fam193b |
C |
T |
13: 55,689,518 (GRCm39) |
A753T |
probably damaging |
Het |
Fam47e |
G |
C |
5: 92,713,781 (GRCm39) |
|
probably benign |
Het |
Fastkd1 |
A |
G |
2: 69,538,993 (GRCm39) |
|
probably benign |
Het |
Fmnl1 |
G |
A |
11: 103,088,196 (GRCm39) |
G69D |
probably benign |
Het |
Foxn2 |
A |
G |
17: 88,781,094 (GRCm39) |
|
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,821,844 (GRCm39) |
E5859G |
possibly damaging |
Het |
Gm9894 |
T |
A |
13: 67,912,820 (GRCm39) |
|
noncoding transcript |
Het |
H2-T13 |
T |
C |
17: 36,391,983 (GRCm39) |
N44S |
possibly damaging |
Het |
Helz2 |
T |
C |
2: 180,871,608 (GRCm39) |
Y2668C |
probably damaging |
Het |
Hhipl1 |
T |
A |
12: 108,277,952 (GRCm39) |
C93* |
probably null |
Het |
Lig1 |
C |
T |
7: 13,026,079 (GRCm39) |
A278V |
probably benign |
Het |
Lipn |
T |
A |
19: 34,049,158 (GRCm39) |
I108K |
probably benign |
Het |
Lsamp |
A |
G |
16: 41,971,592 (GRCm39) |
|
probably benign |
Het |
Map3k14 |
A |
G |
11: 103,129,743 (GRCm39) |
|
probably benign |
Het |
Mdm4 |
A |
T |
1: 132,919,558 (GRCm39) |
C436S |
probably damaging |
Het |
Mdm4 |
A |
G |
1: 132,940,430 (GRCm39) |
L33P |
probably damaging |
Het |
Meiob |
T |
C |
17: 25,055,458 (GRCm39) |
W422R |
probably damaging |
Het |
Mppe1 |
T |
C |
18: 67,360,777 (GRCm39) |
Y254C |
probably damaging |
Het |
Mterf1a |
A |
T |
5: 3,940,964 (GRCm39) |
N301K |
probably benign |
Het |
Mycbp2 |
A |
T |
14: 103,437,588 (GRCm39) |
Y2091* |
probably null |
Het |
Mylk |
G |
A |
16: 34,694,409 (GRCm39) |
R156H |
probably benign |
Het |
Myo15a |
G |
T |
11: 60,370,233 (GRCm39) |
D998Y |
probably benign |
Het |
Neb |
A |
T |
2: 52,086,369 (GRCm39) |
Y5235N |
probably damaging |
Het |
Nop58 |
A |
G |
1: 59,743,370 (GRCm39) |
|
probably benign |
Het |
Nr4a3 |
A |
G |
4: 48,083,324 (GRCm39) |
K619R |
probably benign |
Het |
Nr4a3 |
A |
G |
4: 48,051,564 (GRCm39) |
H135R |
probably damaging |
Het |
Nrg1 |
T |
C |
8: 32,327,695 (GRCm39) |
|
probably benign |
Het |
Odr4 |
T |
A |
1: 150,262,142 (GRCm39) |
E99D |
probably benign |
Het |
Or4f59 |
A |
T |
2: 111,872,560 (GRCm39) |
D272E |
probably benign |
Het |
Or5b122 |
T |
C |
19: 13,563,577 (GRCm39) |
V260A |
probably benign |
Het |
Or5m8 |
A |
T |
2: 85,823,040 (GRCm39) |
N293I |
probably damaging |
Het |
Or8g24 |
T |
A |
9: 38,989,525 (GRCm39) |
D172V |
possibly damaging |
Het |
Parp3 |
T |
C |
9: 106,353,204 (GRCm39) |
|
probably benign |
Het |
Pde2a |
A |
G |
7: 101,133,750 (GRCm39) |
E103G |
probably benign |
Het |
Pds5a |
A |
T |
5: 65,792,645 (GRCm39) |
|
probably benign |
Het |
Pip4k2c |
A |
G |
10: 127,047,262 (GRCm39) |
V40A |
unknown |
Het |
Pitrm1 |
T |
C |
13: 6,602,780 (GRCm39) |
|
probably benign |
Het |
Plk4 |
A |
G |
3: 40,756,282 (GRCm39) |
I64M |
probably damaging |
Het |
Ppp1r16a |
C |
T |
15: 76,577,869 (GRCm39) |
Q328* |
probably null |
Het |
Ppp2r1a |
T |
C |
17: 21,171,593 (GRCm39) |
|
probably benign |
Het |
Ppp4r3b |
T |
A |
11: 29,159,426 (GRCm39) |
N172K |
probably damaging |
Het |
Prkcg |
G |
A |
7: 3,368,177 (GRCm39) |
R357Q |
probably damaging |
Het |
Prmt3 |
T |
C |
7: 49,498,295 (GRCm39) |
|
probably null |
Het |
Prx |
T |
A |
7: 27,217,432 (GRCm39) |
C644* |
probably null |
Het |
Ptpru |
A |
G |
4: 131,535,838 (GRCm39) |
|
probably benign |
Het |
Rbm5 |
A |
T |
9: 107,619,696 (GRCm39) |
D738E |
probably damaging |
Het |
Recql5 |
A |
T |
11: 115,788,060 (GRCm39) |
Y420N |
probably damaging |
Het |
Rnf17 |
T |
C |
14: 56,663,088 (GRCm39) |
I152T |
probably benign |
Het |
Rnpepl1 |
A |
G |
1: 92,846,917 (GRCm39) |
S580G |
possibly damaging |
Het |
Ryr3 |
C |
T |
2: 112,777,332 (GRCm39) |
G275D |
probably damaging |
Het |
Serpinb9e |
T |
A |
13: 33,441,735 (GRCm39) |
Y222* |
probably null |
Het |
Shld2 |
A |
T |
14: 33,990,448 (GRCm39) |
S153T |
possibly damaging |
Het |
Slc10a1 |
T |
A |
12: 81,002,802 (GRCm39) |
I279F |
probably damaging |
Het |
Slc12a8 |
G |
T |
16: 33,483,347 (GRCm39) |
G584V |
probably damaging |
Het |
Slc35b3 |
T |
A |
13: 39,121,307 (GRCm39) |
Y311F |
probably benign |
Het |
Slc44a5 |
A |
G |
3: 153,963,357 (GRCm39) |
|
probably null |
Het |
Slc6a9 |
A |
G |
4: 117,722,003 (GRCm39) |
E422G |
possibly damaging |
Het |
Smpd2 |
A |
G |
10: 41,364,728 (GRCm39) |
|
probably null |
Het |
Spast |
A |
G |
17: 74,688,963 (GRCm39) |
|
probably null |
Het |
Spink5 |
A |
T |
18: 44,116,630 (GRCm39) |
E208V |
probably benign |
Het |
Stag1 |
T |
C |
9: 100,770,506 (GRCm39) |
|
probably benign |
Het |
Stambp |
A |
G |
6: 83,540,803 (GRCm39) |
|
probably null |
Het |
Sult3a2 |
A |
T |
10: 33,653,188 (GRCm39) |
M184K |
possibly damaging |
Het |
Tcp11 |
T |
C |
17: 28,290,636 (GRCm39) |
D162G |
probably damaging |
Het |
Themis |
A |
C |
10: 28,544,744 (GRCm39) |
E30A |
possibly damaging |
Het |
Tmc7 |
G |
A |
7: 118,150,483 (GRCm39) |
S350L |
probably benign |
Het |
Tmem131 |
A |
T |
1: 36,873,979 (GRCm39) |
Y271* |
probably null |
Het |
Trim35 |
T |
A |
14: 66,546,248 (GRCm39) |
S338R |
probably benign |
Het |
Trim42 |
C |
A |
9: 97,245,673 (GRCm39) |
V376F |
probably benign |
Het |
Tshr |
A |
T |
12: 91,504,871 (GRCm39) |
K11M |
probably damaging |
Het |
Vps8 |
A |
G |
16: 21,278,570 (GRCm39) |
|
probably benign |
Het |
Wdr11 |
T |
C |
7: 129,208,831 (GRCm39) |
|
probably benign |
Het |
Wdr26 |
A |
T |
1: 181,008,859 (GRCm39) |
|
probably benign |
Het |
Wdtc1 |
A |
G |
4: 133,024,857 (GRCm39) |
Y447H |
probably damaging |
Het |
Zfp687 |
C |
T |
3: 94,915,784 (GRCm39) |
C996Y |
probably damaging |
Het |
Zfp984 |
A |
T |
4: 147,840,446 (GRCm39) |
V135E |
probably benign |
Het |
Zranb2 |
T |
C |
3: 157,247,502 (GRCm39) |
|
probably benign |
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 |
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 |
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 |
|