Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
T |
C |
7: 119,917,236 (GRCm39) |
I1467T |
probably damaging |
Het |
Abtb3 |
A |
G |
10: 85,223,629 (GRCm39) |
E146G |
unknown |
Het |
Adgrf3 |
T |
A |
5: 30,409,378 (GRCm39) |
K38* |
probably null |
Het |
Ahdc1 |
T |
A |
4: 132,789,198 (GRCm39) |
C146* |
probably null |
Het |
Ahnak |
A |
T |
19: 8,995,163 (GRCm39) |
K5482N |
probably damaging |
Het |
Arhgap23 |
C |
T |
11: 97,342,819 (GRCm39) |
A367V |
possibly damaging |
Het |
Arvcf |
T |
C |
16: 18,223,948 (GRCm39) |
S960P |
probably damaging |
Het |
Asb14 |
C |
A |
14: 26,622,394 (GRCm39) |
P74Q |
probably benign |
Het |
Atad5 |
T |
C |
11: 79,980,601 (GRCm39) |
V2A |
probably damaging |
Het |
Baz2a |
A |
G |
10: 127,954,428 (GRCm39) |
I691M |
possibly damaging |
Het |
Brca2 |
A |
G |
5: 150,455,819 (GRCm39) |
T187A |
probably benign |
Het |
Calr4 |
T |
A |
4: 109,101,254 (GRCm39) |
N152K |
possibly damaging |
Het |
Ccnb2 |
C |
T |
9: 70,318,128 (GRCm39) |
A215T |
probably damaging |
Het |
Cdh16 |
C |
T |
8: 105,340,780 (GRCm39) |
D140N |
unknown |
Het |
Ces1g |
T |
C |
8: 94,029,595 (GRCm39) |
T546A |
probably benign |
Het |
Cfap74 |
G |
T |
4: 155,510,654 (GRCm39) |
|
probably null |
Het |
Cfap91 |
T |
C |
16: 38,155,959 (GRCm39) |
Y88C |
probably benign |
Het |
Col5a1 |
G |
T |
2: 27,842,390 (GRCm39) |
D422Y |
unknown |
Het |
Cyp2c66 |
A |
T |
19: 39,130,348 (GRCm39) |
Y61F |
probably damaging |
Het |
Dnah12 |
G |
A |
14: 26,500,869 (GRCm39) |
|
probably null |
Het |
Dnah6 |
A |
G |
6: 73,158,688 (GRCm39) |
|
probably null |
Het |
Dop1a |
T |
G |
9: 86,386,220 (GRCm39) |
|
probably null |
Het |
Fam163a |
A |
G |
1: 155,954,834 (GRCm39) |
F106L |
probably damaging |
Het |
Gfy |
T |
C |
7: 44,827,596 (GRCm39) |
T167A |
probably benign |
Het |
Gm6525 |
A |
T |
3: 84,082,341 (GRCm39) |
R87S |
probably benign |
Het |
Gramd1c |
C |
A |
16: 43,879,584 (GRCm39) |
A19S |
possibly damaging |
Het |
Herc2 |
T |
C |
7: 55,781,034 (GRCm39) |
V1233A |
probably damaging |
Het |
Hibch |
G |
A |
1: 52,892,874 (GRCm39) |
|
probably null |
Het |
Ibsp |
A |
T |
5: 104,450,027 (GRCm39) |
S9C |
probably benign |
Het |
Il17ra |
A |
G |
6: 120,452,572 (GRCm39) |
I252V |
probably benign |
Het |
Ino80 |
A |
T |
2: 119,204,918 (GRCm39) |
M1536K |
probably benign |
Het |
Ipo11 |
A |
T |
13: 107,012,078 (GRCm39) |
L568Q |
probably damaging |
Het |
Kcnu1 |
T |
G |
8: 26,409,609 (GRCm39) |
|
probably null |
Het |
Kdm5b |
T |
G |
1: 134,552,497 (GRCm39) |
S1158A |
probably benign |
Het |
Kmt2a |
T |
C |
9: 44,759,012 (GRCm39) |
T946A |
probably benign |
Het |
Kmt2e |
A |
T |
5: 23,697,292 (GRCm39) |
|
probably benign |
Het |
Krba1 |
G |
A |
6: 48,389,261 (GRCm39) |
V594M |
probably damaging |
Het |
Lamb1 |
T |
C |
12: 31,374,314 (GRCm39) |
L1559P |
probably damaging |
Het |
Lig1 |
C |
T |
7: 13,025,175 (GRCm39) |
P227S |
probably benign |
Het |
Lims2 |
T |
A |
18: 32,090,017 (GRCm39) |
D255E |
probably benign |
Het |
Marchf3 |
C |
T |
18: 56,909,161 (GRCm39) |
C208Y |
probably benign |
Het |
Mei1 |
A |
G |
15: 81,976,843 (GRCm39) |
E142G |
|
Het |
Melk |
G |
T |
4: 44,351,106 (GRCm39) |
R549L |
probably benign |
Het |
Myorg |
T |
C |
4: 41,498,268 (GRCm39) |
Y454C |
probably damaging |
Het |
Nae1 |
T |
C |
8: 105,250,215 (GRCm39) |
Y226C |
possibly damaging |
Het |
Nap1l1 |
T |
C |
10: 111,326,964 (GRCm39) |
F175S |
probably damaging |
Het |
Ndn |
T |
C |
7: 61,998,709 (GRCm39) |
L185P |
probably damaging |
Het |
Ndst3 |
T |
A |
3: 123,465,388 (GRCm39) |
I195F |
possibly damaging |
Het |
Ndufaf1 |
A |
T |
2: 119,488,907 (GRCm39) |
S206T |
probably benign |
Het |
Nek10 |
C |
A |
14: 14,836,171 (GRCm38) |
H131N |
probably benign |
Het |
Obsl1 |
T |
A |
1: 75,466,360 (GRCm39) |
D1456V |
possibly damaging |
Het |
Or10a2 |
A |
G |
7: 106,673,448 (GRCm39) |
N138D |
probably benign |
Het |
Or10ak7 |
C |
T |
4: 118,791,215 (GRCm39) |
V277I |
probably benign |
Het |
Or52s6 |
T |
A |
7: 103,092,292 (GRCm39) |
T13S |
probably benign |
Het |
Otog |
C |
T |
7: 45,937,474 (GRCm39) |
L1728F |
probably damaging |
Het |
Pcx |
A |
T |
19: 4,652,361 (GRCm39) |
M150L |
possibly damaging |
Het |
Pole |
A |
G |
5: 110,444,973 (GRCm39) |
D443G |
possibly damaging |
Het |
Prr14 |
G |
T |
7: 127,075,648 (GRCm39) |
R552L |
probably damaging |
Het |
Rasgrf1 |
T |
G |
9: 89,899,125 (GRCm39) |
S1156A |
possibly damaging |
Het |
Rfc4 |
T |
A |
16: 22,946,359 (GRCm39) |
|
probably benign |
Het |
Rfx5 |
G |
T |
3: 94,866,272 (GRCm39) |
A524S |
unknown |
Het |
Ryr3 |
G |
A |
2: 112,596,664 (GRCm39) |
P2497S |
probably damaging |
Het |
Scg3 |
T |
C |
9: 75,590,992 (GRCm39) |
T6A |
probably benign |
Het |
Slc26a9 |
A |
T |
1: 131,690,526 (GRCm39) |
D510V |
possibly damaging |
Het |
Stpg3 |
A |
G |
2: 25,104,586 (GRCm39) |
F10L |
probably damaging |
Het |
Tmc5 |
T |
A |
7: 118,239,179 (GRCm39) |
H357Q |
possibly damaging |
Het |
Tmem40 |
A |
T |
6: 115,707,420 (GRCm39) |
L253H |
probably damaging |
Het |
Tmie |
A |
G |
9: 110,696,632 (GRCm39) |
V83A |
probably damaging |
Het |
Uck2 |
A |
T |
1: 167,054,084 (GRCm39) |
I218N |
probably damaging |
Het |
Vtn |
A |
G |
11: 78,391,626 (GRCm39) |
D310G |
possibly damaging |
Het |
Wdr49 |
A |
T |
3: 75,240,580 (GRCm39) |
S430T |
probably benign |
Het |
Wtip |
A |
G |
7: 33,832,087 (GRCm39) |
V133A |
probably benign |
Het |
Zbtb9 |
T |
A |
17: 27,193,666 (GRCm39) |
V357E |
probably damaging |
Het |
Zfp953 |
G |
A |
13: 67,491,706 (GRCm39) |
T82M |
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 |
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 |
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 |
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 |
|