Other mutations in this stock |
Total: 133 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc8 |
T |
C |
7: 45,824,795 (GRCm39) |
K134R |
possibly damaging |
Het |
Adamts17 |
T |
C |
7: 66,774,820 (GRCm39) |
S980P |
probably damaging |
Het |
Adap2 |
T |
A |
11: 80,061,508 (GRCm39) |
I221K |
probably damaging |
Het |
Adgrv1 |
C |
T |
13: 81,539,876 (GRCm39) |
R5681Q |
probably damaging |
Het |
Adipor1 |
T |
A |
1: 134,350,841 (GRCm39) |
L30Q |
probably benign |
Het |
Agpat5 |
A |
G |
8: 18,928,181 (GRCm39) |
T249A |
probably benign |
Het |
Agxt2 |
G |
T |
15: 10,392,021 (GRCm39) |
G329V |
probably damaging |
Het |
Ankrd28 |
A |
G |
14: 31,427,233 (GRCm39) |
V801A |
possibly damaging |
Het |
Ap1g2 |
A |
G |
14: 55,337,229 (GRCm39) |
V702A |
possibly damaging |
Het |
Arid3a |
A |
G |
10: 79,786,540 (GRCm39) |
Q429R |
probably damaging |
Het |
Arsb |
T |
A |
13: 93,998,658 (GRCm39) |
L322Q |
probably damaging |
Het |
Ash1l |
A |
G |
3: 88,891,729 (GRCm39) |
T1203A |
probably damaging |
Het |
Atad2 |
T |
A |
15: 57,960,101 (GRCm39) |
N1308Y |
possibly damaging |
Het |
Atp10b |
A |
T |
11: 43,121,245 (GRCm39) |
R969S |
probably benign |
Het |
Bmp10 |
T |
C |
6: 87,410,702 (GRCm39) |
I165T |
possibly damaging |
Het |
Ccdc121rt2 |
C |
A |
5: 112,597,667 (GRCm39) |
C71* |
probably null |
Het |
Ccne1 |
A |
G |
7: 37,805,702 (GRCm39) |
|
probably null |
Het |
Cenpe |
A |
G |
3: 134,953,240 (GRCm39) |
N1565D |
probably damaging |
Het |
Chd1 |
A |
T |
17: 15,982,748 (GRCm39) |
E1404D |
probably benign |
Het |
Chd7 |
G |
A |
4: 8,847,200 (GRCm39) |
E1648K |
probably damaging |
Het |
Chodl |
T |
C |
16: 78,738,314 (GRCm39) |
I94T |
possibly damaging |
Het |
Chsy3 |
T |
C |
18: 59,542,584 (GRCm39) |
F574S |
probably damaging |
Het |
Clpb |
A |
T |
7: 101,412,863 (GRCm39) |
I317F |
probably damaging |
Het |
Cnga3 |
T |
A |
1: 37,300,954 (GRCm39) |
V558D |
possibly damaging |
Het |
Col9a1 |
C |
T |
1: 24,261,554 (GRCm39) |
P573S |
probably damaging |
Het |
Crat |
A |
T |
2: 30,303,073 (GRCm39) |
D71E |
probably benign |
Het |
Cspg4 |
A |
G |
9: 56,794,385 (GRCm39) |
T707A |
probably benign |
Het |
Ctsr |
T |
A |
13: 61,310,259 (GRCm39) |
R132S |
probably benign |
Het |
Ctu2 |
T |
C |
8: 123,206,024 (GRCm39) |
L255P |
probably damaging |
Het |
Cyp2c69 |
T |
C |
19: 39,837,810 (GRCm39) |
Y424C |
probably damaging |
Het |
Ddx27 |
A |
T |
2: 166,876,029 (GRCm39) |
K726N |
probably damaging |
Het |
Dennd4a |
A |
G |
9: 64,749,772 (GRCm39) |
Q121R |
probably damaging |
Het |
Dis3 |
A |
G |
14: 99,335,026 (GRCm39) |
F192S |
probably benign |
Het |
Ect2l |
C |
T |
10: 18,020,383 (GRCm39) |
S487N |
probably benign |
Het |
Eml1 |
T |
A |
12: 108,487,655 (GRCm39) |
F524L |
possibly damaging |
Het |
Espl1 |
T |
C |
15: 102,213,477 (GRCm39) |
I601T |
probably benign |
Het |
Fbxo40 |
C |
A |
16: 36,789,713 (GRCm39) |
V466L |
probably damaging |
Het |
Frmpd1 |
C |
T |
4: 45,283,711 (GRCm39) |
T844M |
probably damaging |
Het |
Frs2 |
T |
A |
10: 116,917,011 (GRCm39) |
|
probably benign |
Het |
Fuom |
G |
T |
7: 139,679,521 (GRCm39) |
T133K |
probably benign |
Het |
Garnl3 |
T |
A |
2: 32,895,212 (GRCm39) |
H619L |
probably damaging |
Het |
Gm4861 |
G |
T |
3: 137,257,876 (GRCm39) |
N36K |
unknown |
Het |
Gps2 |
G |
T |
11: 69,806,195 (GRCm39) |
M153I |
probably benign |
Het |
Gtf2ird1 |
A |
G |
5: 134,444,099 (GRCm39) |
V52A |
probably damaging |
Het |
Gtpbp8 |
A |
T |
16: 44,565,785 (GRCm39) |
D137E |
probably benign |
Het |
Haus4 |
A |
G |
14: 54,781,733 (GRCm39) |
C213R |
probably damaging |
Het |
Hdc |
T |
A |
2: 126,448,317 (GRCm39) |
H142L |
possibly damaging |
Het |
Hephl1 |
T |
C |
9: 14,965,283 (GRCm39) |
D1069G |
possibly damaging |
Het |
Herc6 |
T |
A |
6: 57,602,926 (GRCm39) |
V535D |
probably damaging |
Het |
Hipk3 |
A |
T |
2: 104,260,533 (GRCm39) |
H1082Q |
possibly damaging |
Het |
Hps5 |
A |
T |
7: 46,422,691 (GRCm39) |
V513D |
probably damaging |
Het |
Ifna13 |
T |
A |
4: 88,562,412 (GRCm39) |
I71F |
probably damaging |
Het |
Il1rl2 |
T |
C |
1: 40,402,484 (GRCm39) |
I426T |
probably damaging |
Het |
Irf5 |
A |
T |
6: 29,536,738 (GRCm39) |
D483V |
probably benign |
Het |
Jakmip3 |
A |
G |
7: 138,621,867 (GRCm39) |
R256G |
probably damaging |
Het |
Jazf1 |
T |
C |
6: 52,754,600 (GRCm39) |
I159V |
probably damaging |
Het |
Kmo |
A |
G |
1: 175,479,154 (GRCm39) |
D230G |
possibly damaging |
Het |
Lrrc74b |
A |
G |
16: 17,371,058 (GRCm39) |
V213A |
probably benign |
Het |
LTO1 |
A |
G |
7: 144,470,205 (GRCm39) |
S45G |
probably damaging |
Het |
Ly6g5b |
T |
C |
17: 35,333,704 (GRCm39) |
D36G |
possibly damaging |
Het |
Mab21l4 |
T |
C |
1: 93,079,730 (GRCm39) |
*453W |
probably null |
Het |
Macc1 |
T |
G |
12: 119,409,466 (GRCm39) |
L78R |
probably damaging |
Het |
Mettl4 |
A |
T |
17: 95,055,285 (GRCm39) |
D51E |
possibly damaging |
Het |
Mfap1a |
G |
A |
2: 121,332,835 (GRCm39) |
L199F |
possibly damaging |
Het |
Mmp17 |
G |
T |
5: 129,679,190 (GRCm39) |
R363L |
probably damaging |
Het |
Mrc1 |
G |
A |
2: 14,324,052 (GRCm39) |
A1130T |
possibly damaging |
Het |
Mrpl15 |
C |
T |
1: 4,847,805 (GRCm39) |
A165T |
probably damaging |
Het |
Mrpl45 |
G |
A |
11: 97,206,770 (GRCm39) |
|
probably null |
Het |
Ms4a3 |
C |
T |
19: 11,613,204 (GRCm39) |
A85T |
possibly damaging |
Het |
Mttp |
A |
T |
3: 137,830,882 (GRCm39) |
D77E |
probably benign |
Het |
Myl3 |
G |
A |
9: 110,595,802 (GRCm39) |
E100K |
probably damaging |
Het |
Nbea |
T |
A |
3: 55,992,743 (GRCm39) |
N288Y |
probably damaging |
Het |
Ncoa7 |
A |
G |
10: 30,574,166 (GRCm39) |
V181A |
probably benign |
Het |
Oat |
C |
T |
7: 132,159,934 (GRCm39) |
V429M |
probably benign |
Het |
Or2ak6 |
A |
T |
11: 58,593,449 (GRCm39) |
*307C |
probably null |
Het |
Or4x6 |
T |
G |
2: 89,949,427 (GRCm39) |
I172L |
probably damaging |
Het |
Or5d36 |
A |
T |
2: 87,901,300 (GRCm39) |
L142Q |
probably damaging |
Het |
Or5p80 |
T |
C |
7: 108,230,045 (GRCm39) |
I282T |
probably benign |
Het |
Or5w19 |
G |
A |
2: 87,698,805 (GRCm39) |
V157I |
probably benign |
Het |
Or6b13 |
A |
G |
7: 139,782,144 (GRCm39) |
F180L |
probably benign |
Het |
Or6c69b |
T |
A |
10: 129,626,759 (GRCm39) |
K233M |
probably damaging |
Het |
Or8b55 |
A |
G |
9: 38,727,146 (GRCm39) |
T116A |
probably benign |
Het |
Or8s16 |
T |
A |
15: 98,211,261 (GRCm39) |
M57L |
probably damaging |
Het |
Otof |
A |
G |
5: 30,533,713 (GRCm39) |
S1464P |
probably benign |
Het |
Otogl |
A |
T |
10: 107,613,436 (GRCm39) |
Y2010N |
probably damaging |
Het |
Pgap3 |
C |
T |
11: 98,291,040 (GRCm39) |
|
probably null |
Het |
Pgbd5 |
T |
A |
8: 125,100,988 (GRCm39) |
K332* |
probably null |
Het |
Pgs1 |
C |
T |
11: 117,896,553 (GRCm39) |
P410L |
probably damaging |
Het |
Pkhd1l1 |
G |
A |
15: 44,363,434 (GRCm39) |
S618N |
probably benign |
Het |
Plcb1 |
A |
T |
2: 135,228,222 (GRCm39) |
D1073V |
probably damaging |
Het |
Pola2 |
T |
A |
19: 6,001,208 (GRCm39) |
T309S |
probably benign |
Het |
Polg2 |
T |
A |
11: 106,669,787 (GRCm39) |
H161L |
probably damaging |
Het |
Postn |
T |
A |
3: 54,285,033 (GRCm39) |
|
probably null |
Het |
Ppt1 |
G |
T |
4: 122,739,784 (GRCm39) |
C128F |
probably damaging |
Het |
Ptpn12 |
G |
A |
5: 21,198,261 (GRCm39) |
P678S |
probably damaging |
Het |
Rcan3 |
A |
T |
4: 135,139,812 (GRCm39) |
|
probably null |
Het |
Rgs22 |
T |
C |
15: 36,101,950 (GRCm39) |
N216S |
probably benign |
Het |
Rgs7bp |
T |
A |
13: 105,088,090 (GRCm39) |
D228V |
probably damaging |
Het |
Rhobtb2 |
A |
T |
14: 70,034,062 (GRCm39) |
S388T |
probably benign |
Het |
Rnps1 |
C |
T |
17: 24,639,364 (GRCm39) |
R138C |
unknown |
Het |
Rpl38 |
T |
C |
11: 114,562,602 (GRCm39) |
V36A |
probably benign |
Het |
Rps7 |
G |
T |
12: 28,681,752 (GRCm39) |
H126Q |
possibly damaging |
Het |
Sec24b |
G |
T |
3: 129,785,010 (GRCm39) |
Q999K |
possibly damaging |
Het |
Slc19a3 |
A |
G |
1: 82,997,089 (GRCm39) |
V373A |
possibly damaging |
Het |
Spats2l |
T |
A |
1: 57,924,941 (GRCm39) |
V113E |
probably benign |
Het |
Ss18l1 |
A |
T |
2: 179,705,138 (GRCm39) |
T377S |
unknown |
Het |
Surf1 |
A |
G |
2: 26,805,982 (GRCm39) |
F38L |
probably benign |
Het |
Ticrr |
G |
A |
7: 79,325,142 (GRCm39) |
R556H |
probably damaging |
Het |
Tmem184b |
A |
G |
15: 79,250,014 (GRCm39) |
S254P |
probably damaging |
Het |
Tnfrsf4 |
G |
T |
4: 156,100,692 (GRCm39) |
R237L |
possibly damaging |
Het |
Tnk2 |
C |
A |
16: 32,482,560 (GRCm39) |
|
probably benign |
Het |
Tnks |
A |
T |
8: 35,305,684 (GRCm39) |
D1191E |
probably damaging |
Het |
Tnr |
C |
A |
1: 159,722,607 (GRCm39) |
Y1017* |
probably null |
Het |
Tomm34 |
A |
G |
2: 163,902,926 (GRCm39) |
I128T |
probably benign |
Het |
Trim2 |
G |
A |
3: 84,085,099 (GRCm39) |
S540F |
possibly damaging |
Het |
Trio |
A |
T |
15: 27,732,977 (GRCm39) |
I2968N |
probably damaging |
Het |
Ttc24 |
T |
C |
3: 87,982,181 (GRCm39) |
E17G |
probably benign |
Het |
Ttc41 |
A |
G |
10: 86,612,078 (GRCm39) |
H1117R |
probably benign |
Het |
Ttn |
A |
T |
2: 76,565,752 (GRCm39) |
V28200D |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,592,730 (GRCm39) |
S20801T |
possibly damaging |
Het |
Ube3d |
C |
T |
9: 86,330,840 (GRCm39) |
C114Y |
probably damaging |
Het |
Ugt2b37 |
A |
C |
5: 87,388,716 (GRCm39) |
L499R |
probably damaging |
Het |
Vmn1r81 |
T |
C |
7: 11,994,589 (GRCm39) |
I6M |
possibly damaging |
Het |
Vmn2r97 |
A |
T |
17: 19,149,593 (GRCm39) |
Y327F |
probably benign |
Het |
Vps13b |
T |
C |
15: 35,709,653 (GRCm39) |
S1867P |
probably damaging |
Het |
Wdr11 |
T |
C |
7: 129,208,331 (GRCm39) |
V362A |
probably benign |
Het |
Zan |
T |
A |
5: 137,387,201 (GRCm39) |
M4951L |
unknown |
Het |
Zcwpw1 |
T |
A |
5: 137,809,884 (GRCm39) |
L337Q |
probably damaging |
Het |
Zfp2 |
A |
T |
11: 50,790,809 (GRCm39) |
D411E |
possibly damaging |
Het |
Zfp628 |
C |
T |
7: 4,923,767 (GRCm39) |
T663I |
probably benign |
Het |
Zfpm1 |
T |
A |
8: 123,061,663 (GRCm39) |
|
probably null |
Het |
Zfyve19 |
T |
C |
2: 119,041,693 (GRCm39) |
S87P |
probably benign |
Het |
Zswim9 |
T |
A |
7: 12,994,141 (GRCm39) |
K672* |
probably null |
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 |
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 |
|