Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930444P10Rik |
A |
G |
1: 16,139,022 (GRCm39) |
|
probably null |
Het |
Abca4 |
T |
A |
3: 121,899,019 (GRCm39) |
V667D |
probably damaging |
Het |
Aco1 |
A |
G |
4: 40,176,507 (GRCm39) |
I224V |
probably damaging |
Het |
Arel1 |
C |
T |
12: 84,978,541 (GRCm39) |
V364M |
probably damaging |
Het |
Arhgap42 |
A |
G |
9: 9,009,435 (GRCm39) |
V484A |
probably damaging |
Het |
Asap2 |
T |
C |
12: 21,302,766 (GRCm39) |
F681L |
probably benign |
Het |
Atrn |
C |
A |
2: 130,817,874 (GRCm39) |
D809E |
probably damaging |
Het |
Ccdc70 |
G |
A |
8: 22,463,266 (GRCm39) |
V19M |
possibly damaging |
Het |
Ccp110 |
G |
T |
7: 118,329,235 (GRCm39) |
E73* |
probably null |
Het |
Cfap57 |
A |
C |
4: 118,453,045 (GRCm39) |
S553A |
probably benign |
Het |
Cftr |
A |
G |
6: 18,221,613 (GRCm39) |
K212E |
probably benign |
Het |
Chkb |
A |
T |
15: 89,312,368 (GRCm39) |
Y216N |
probably damaging |
Het |
Cntnap2 |
G |
T |
6: 45,897,768 (GRCm39) |
D149Y |
probably damaging |
Het |
Cpd |
A |
G |
11: 76,737,048 (GRCm39) |
|
probably null |
Het |
Creb3l1 |
C |
T |
2: 91,813,571 (GRCm39) |
D489N |
probably benign |
Het |
Crhbp |
A |
G |
13: 95,578,753 (GRCm39) |
F123L |
probably damaging |
Het |
Cryab |
T |
C |
9: 50,665,909 (GRCm39) |
V100A |
possibly damaging |
Het |
Csmd2 |
T |
C |
4: 128,415,723 (GRCm39) |
I2684T |
probably benign |
Het |
Ctbp2 |
G |
T |
7: 132,616,378 (GRCm39) |
P186T |
possibly damaging |
Het |
Ctnna2 |
T |
C |
6: 76,892,745 (GRCm39) |
N814S |
possibly damaging |
Het |
Dntt |
T |
C |
19: 41,028,295 (GRCm39) |
V197A |
probably damaging |
Het |
Fam135a |
G |
A |
1: 24,059,758 (GRCm39) |
A1187V |
possibly damaging |
Het |
Filip1l |
A |
T |
16: 57,390,778 (GRCm39) |
Q455H |
probably benign |
Het |
Grm2 |
T |
C |
9: 106,531,189 (GRCm39) |
E100G |
probably damaging |
Het |
Gtf2ird2 |
G |
A |
5: 134,246,306 (GRCm39) |
V855M |
probably damaging |
Het |
Heatr9 |
A |
T |
11: 83,409,618 (GRCm39) |
I118N |
possibly damaging |
Het |
Htra3 |
T |
C |
5: 35,828,469 (GRCm39) |
H137R |
probably benign |
Het |
Iars1 |
A |
G |
13: 49,863,137 (GRCm39) |
S530G |
probably damaging |
Het |
Klhdc4 |
T |
A |
8: 122,523,342 (GRCm39) |
M510L |
probably benign |
Het |
Lipc |
T |
C |
9: 70,724,013 (GRCm39) |
T204A |
probably benign |
Het |
Lrp1 |
A |
G |
10: 127,389,648 (GRCm39) |
V3129A |
probably damaging |
Het |
Macf1 |
G |
A |
4: 123,388,702 (GRCm39) |
T1120I |
probably benign |
Het |
Maco1 |
A |
G |
4: 134,555,444 (GRCm39) |
I343T |
probably benign |
Het |
Map4 |
T |
C |
9: 109,867,445 (GRCm39) |
|
probably benign |
Het |
Mbtps1 |
A |
T |
8: 120,260,087 (GRCm39) |
V420D |
probably damaging |
Het |
Mta2 |
G |
T |
19: 8,927,747 (GRCm39) |
D523Y |
probably benign |
Het |
Mtcl2 |
C |
T |
2: 156,864,776 (GRCm39) |
G1144D |
probably benign |
Het |
Muc4 |
A |
G |
16: 32,576,670 (GRCm39) |
|
probably benign |
Het |
Myo1e |
T |
A |
9: 70,260,594 (GRCm39) |
I584N |
probably damaging |
Het |
Nolc1 |
T |
C |
19: 46,067,359 (GRCm39) |
V80A |
probably damaging |
Het |
Nop56 |
G |
T |
2: 130,117,645 (GRCm39) |
V91L |
probably benign |
Het |
Or5b99 |
A |
T |
19: 12,976,583 (GRCm39) |
M78L |
probably benign |
Het |
Or5h23 |
A |
T |
16: 58,906,765 (GRCm39) |
L27Q |
probably damaging |
Het |
Or6f2 |
T |
C |
7: 139,756,933 (GRCm39) |
V300A |
probably damaging |
Het |
Osbpl3 |
T |
C |
6: 50,313,277 (GRCm39) |
E107G |
probably damaging |
Het |
Pde3a |
T |
A |
6: 141,195,751 (GRCm39) |
C146S |
probably benign |
Het |
Pfkm |
A |
G |
15: 98,026,123 (GRCm39) |
M573V |
probably damaging |
Het |
Pkd1l2 |
C |
T |
8: 117,774,113 (GRCm39) |
|
probably null |
Het |
Plekhg3 |
T |
C |
12: 76,612,021 (GRCm39) |
I374T |
possibly damaging |
Het |
Ppig |
T |
A |
2: 69,571,830 (GRCm39) |
V183D |
unknown |
Het |
Prom1 |
T |
G |
5: 44,194,876 (GRCm39) |
I290L |
probably benign |
Het |
Rufy3 |
T |
A |
5: 88,785,085 (GRCm39) |
M387K |
probably damaging |
Het |
Selenoo |
G |
A |
15: 88,978,387 (GRCm39) |
R270H |
probably damaging |
Het |
Sema3d |
T |
A |
5: 12,558,054 (GRCm39) |
|
probably null |
Het |
Sema6c |
C |
T |
3: 95,075,674 (GRCm39) |
T175I |
probably damaging |
Het |
Serpina3k |
T |
C |
12: 104,307,305 (GRCm39) |
I179T |
probably damaging |
Het |
Sf3b3 |
T |
C |
8: 111,567,835 (GRCm39) |
T207A |
probably benign |
Het |
Slc22a26 |
C |
A |
19: 7,779,546 (GRCm39) |
R90L |
probably damaging |
Het |
Slitrk5 |
T |
C |
14: 111,917,648 (GRCm39) |
V424A |
probably damaging |
Het |
Smarca2 |
G |
T |
19: 26,698,255 (GRCm39) |
E89* |
probably null |
Het |
Stab2 |
T |
A |
10: 86,773,773 (GRCm39) |
S853C |
probably damaging |
Het |
Stk17b |
A |
T |
1: 53,800,306 (GRCm39) |
|
probably null |
Het |
Taar5 |
T |
A |
10: 23,847,445 (GRCm39) |
I281N |
possibly damaging |
Het |
Tars3 |
A |
T |
7: 65,308,683 (GRCm39) |
E284D |
probably damaging |
Het |
Tbx15 |
C |
A |
3: 99,223,649 (GRCm39) |
T279K |
probably damaging |
Het |
Tfr2 |
G |
A |
5: 137,585,187 (GRCm39) |
V740I |
probably benign |
Het |
Tlr12 |
T |
C |
4: 128,511,473 (GRCm39) |
E259G |
probably benign |
Het |
Tmem145 |
A |
G |
7: 25,008,459 (GRCm39) |
T302A |
probably benign |
Het |
Trappc14 |
T |
A |
5: 138,259,884 (GRCm39) |
T391S |
probably damaging |
Het |
Trpa1 |
G |
T |
1: 14,946,085 (GRCm39) |
H1015Q |
probably benign |
Het |
Tspan8 |
A |
G |
10: 115,653,534 (GRCm39) |
Y10C |
possibly damaging |
Het |
Ttll7 |
A |
G |
3: 146,600,224 (GRCm39) |
N44S |
probably damaging |
Het |
Uba7 |
T |
C |
9: 107,857,038 (GRCm39) |
|
probably null |
Het |
Ube2j2 |
G |
A |
4: 156,030,841 (GRCm39) |
M1I |
probably null |
Het |
Ubr5 |
C |
A |
15: 38,009,912 (GRCm39) |
A1022S |
probably benign |
Het |
Usf1 |
T |
G |
1: 171,243,331 (GRCm39) |
I36S |
probably damaging |
Het |
Vmn1r181 |
A |
T |
7: 23,683,790 (GRCm39) |
D85V |
probably damaging |
Het |
Vmn1r3 |
A |
T |
4: 3,185,009 (GRCm39) |
Y99* |
probably null |
Het |
Vmn1r72 |
T |
C |
7: 11,404,300 (GRCm39) |
I49M |
possibly damaging |
Het |
Vmn2r99 |
A |
G |
17: 19,582,397 (GRCm39) |
M1V |
probably null |
Het |
Vsig10 |
T |
A |
5: 117,482,040 (GRCm39) |
V410E |
probably damaging |
Het |
Zc3h7b |
A |
G |
15: 81,663,334 (GRCm39) |
Y442C |
probably damaging |
Het |
Zfyve26 |
G |
T |
12: 79,327,159 (GRCm39) |
Y730* |
probably null |
Het |
|
Other mutations in Mug1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00158:Mug1
|
APN |
6 |
121,842,768 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00485:Mug1
|
APN |
6 |
121,864,375 (GRCm39) |
missense |
probably benign |
0.17 |
IGL00816:Mug1
|
APN |
6 |
121,859,597 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01140:Mug1
|
APN |
6 |
121,859,693 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01141:Mug1
|
APN |
6 |
121,847,458 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01384:Mug1
|
APN |
6 |
121,826,433 (GRCm39) |
splice site |
probably benign |
|
IGL01659:Mug1
|
APN |
6 |
121,847,619 (GRCm39) |
splice site |
probably benign |
|
IGL02049:Mug1
|
APN |
6 |
121,848,295 (GRCm39) |
missense |
probably benign |
|
IGL02151:Mug1
|
APN |
6 |
121,861,649 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02315:Mug1
|
APN |
6 |
121,817,126 (GRCm39) |
missense |
probably benign |
|
IGL02629:Mug1
|
APN |
6 |
121,817,024 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL02642:Mug1
|
APN |
6 |
121,859,544 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02807:Mug1
|
APN |
6 |
121,863,531 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02932:Mug1
|
APN |
6 |
121,864,386 (GRCm39) |
missense |
probably benign |
0.35 |
IGL03232:Mug1
|
APN |
6 |
121,855,494 (GRCm39) |
missense |
probably benign |
0.00 |
R1462_Mug1_304
|
UTSW |
6 |
121,859,588 (GRCm39) |
missense |
probably benign |
0.41 |
R2341_Mug1_749
|
UTSW |
6 |
121,861,588 (GRCm39) |
missense |
probably benign |
0.06 |
R4261_Mug1_652
|
UTSW |
6 |
121,850,693 (GRCm39) |
missense |
probably benign |
|
R6173_mug1_139
|
UTSW |
6 |
121,840,752 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03050:Mug1
|
UTSW |
6 |
121,857,530 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0101:Mug1
|
UTSW |
6 |
121,861,206 (GRCm39) |
missense |
possibly damaging |
0.59 |
R0194:Mug1
|
UTSW |
6 |
121,817,066 (GRCm39) |
missense |
probably damaging |
0.98 |
R0196:Mug1
|
UTSW |
6 |
121,815,684 (GRCm39) |
critical splice donor site |
probably null |
|
R0325:Mug1
|
UTSW |
6 |
121,826,801 (GRCm39) |
missense |
probably benign |
|
R0332:Mug1
|
UTSW |
6 |
121,826,856 (GRCm39) |
splice site |
probably null |
|
R0377:Mug1
|
UTSW |
6 |
121,834,320 (GRCm39) |
missense |
probably benign |
0.02 |
R0393:Mug1
|
UTSW |
6 |
121,826,809 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0414:Mug1
|
UTSW |
6 |
121,833,513 (GRCm39) |
missense |
probably benign |
0.00 |
R0457:Mug1
|
UTSW |
6 |
121,838,514 (GRCm39) |
missense |
probably benign |
0.06 |
R0479:Mug1
|
UTSW |
6 |
121,817,186 (GRCm39) |
missense |
probably benign |
|
R0519:Mug1
|
UTSW |
6 |
121,828,383 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0535:Mug1
|
UTSW |
6 |
121,828,413 (GRCm39) |
missense |
probably benign |
|
R0745:Mug1
|
UTSW |
6 |
121,864,386 (GRCm39) |
missense |
probably benign |
0.35 |
R0939:Mug1
|
UTSW |
6 |
121,861,308 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0975:Mug1
|
UTSW |
6 |
121,855,498 (GRCm39) |
missense |
probably damaging |
0.99 |
R1033:Mug1
|
UTSW |
6 |
121,857,510 (GRCm39) |
missense |
probably damaging |
0.99 |
R1086:Mug1
|
UTSW |
6 |
121,862,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R1116:Mug1
|
UTSW |
6 |
121,847,604 (GRCm39) |
missense |
probably benign |
|
R1131:Mug1
|
UTSW |
6 |
121,838,144 (GRCm39) |
missense |
probably benign |
0.18 |
R1249:Mug1
|
UTSW |
6 |
121,826,420 (GRCm39) |
missense |
probably benign |
0.07 |
R1364:Mug1
|
UTSW |
6 |
121,858,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R1418:Mug1
|
UTSW |
6 |
121,815,635 (GRCm39) |
missense |
probably benign |
0.00 |
R1462:Mug1
|
UTSW |
6 |
121,859,588 (GRCm39) |
missense |
probably benign |
0.41 |
R1462:Mug1
|
UTSW |
6 |
121,859,588 (GRCm39) |
missense |
probably benign |
0.41 |
R1494:Mug1
|
UTSW |
6 |
121,856,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R1639:Mug1
|
UTSW |
6 |
121,857,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R1901:Mug1
|
UTSW |
6 |
121,858,780 (GRCm39) |
missense |
probably benign |
|
R1902:Mug1
|
UTSW |
6 |
121,858,780 (GRCm39) |
missense |
probably benign |
|
R2087:Mug1
|
UTSW |
6 |
121,833,250 (GRCm39) |
missense |
probably benign |
0.00 |
R2168:Mug1
|
UTSW |
6 |
121,847,458 (GRCm39) |
missense |
probably benign |
0.08 |
R2249:Mug1
|
UTSW |
6 |
121,847,469 (GRCm39) |
missense |
probably benign |
|
R2341:Mug1
|
UTSW |
6 |
121,861,588 (GRCm39) |
missense |
probably benign |
0.06 |
R2888:Mug1
|
UTSW |
6 |
121,858,802 (GRCm39) |
missense |
probably benign |
0.44 |
R2892:Mug1
|
UTSW |
6 |
121,817,029 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3703:Mug1
|
UTSW |
6 |
121,865,515 (GRCm39) |
splice site |
probably benign |
|
R3789:Mug1
|
UTSW |
6 |
121,861,587 (GRCm39) |
missense |
probably benign |
0.03 |
R3790:Mug1
|
UTSW |
6 |
121,861,587 (GRCm39) |
missense |
probably benign |
0.03 |
R3950:Mug1
|
UTSW |
6 |
121,855,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R4261:Mug1
|
UTSW |
6 |
121,850,693 (GRCm39) |
missense |
probably benign |
|
R4402:Mug1
|
UTSW |
6 |
121,856,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R4589:Mug1
|
UTSW |
6 |
121,834,310 (GRCm39) |
missense |
probably benign |
0.19 |
R4707:Mug1
|
UTSW |
6 |
121,861,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R4766:Mug1
|
UTSW |
6 |
121,861,213 (GRCm39) |
missense |
probably benign |
0.01 |
R4840:Mug1
|
UTSW |
6 |
121,862,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R4984:Mug1
|
UTSW |
6 |
121,815,576 (GRCm39) |
utr 5 prime |
probably benign |
|
R5198:Mug1
|
UTSW |
6 |
121,851,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R5220:Mug1
|
UTSW |
6 |
121,838,092 (GRCm39) |
missense |
probably benign |
0.03 |
R5253:Mug1
|
UTSW |
6 |
121,865,872 (GRCm39) |
missense |
probably benign |
0.03 |
R5273:Mug1
|
UTSW |
6 |
121,850,748 (GRCm39) |
missense |
probably damaging |
0.99 |
R5285:Mug1
|
UTSW |
6 |
121,818,066 (GRCm39) |
missense |
probably benign |
0.45 |
R5387:Mug1
|
UTSW |
6 |
121,861,353 (GRCm39) |
missense |
probably damaging |
0.99 |
R5560:Mug1
|
UTSW |
6 |
121,838,032 (GRCm39) |
missense |
probably damaging |
0.96 |
R5652:Mug1
|
UTSW |
6 |
121,817,140 (GRCm39) |
missense |
probably benign |
|
R5704:Mug1
|
UTSW |
6 |
121,828,392 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5732:Mug1
|
UTSW |
6 |
121,855,452 (GRCm39) |
missense |
probably benign |
0.00 |
R6053:Mug1
|
UTSW |
6 |
121,842,697 (GRCm39) |
missense |
probably benign |
0.00 |
R6173:Mug1
|
UTSW |
6 |
121,840,752 (GRCm39) |
missense |
probably damaging |
0.99 |
R6578:Mug1
|
UTSW |
6 |
121,864,411 (GRCm39) |
missense |
probably benign |
0.00 |
R6647:Mug1
|
UTSW |
6 |
121,817,200 (GRCm39) |
missense |
probably benign |
0.02 |
R6681:Mug1
|
UTSW |
6 |
121,815,683 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6925:Mug1
|
UTSW |
6 |
121,858,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R7014:Mug1
|
UTSW |
6 |
121,838,084 (GRCm39) |
missense |
probably benign |
0.22 |
R7031:Mug1
|
UTSW |
6 |
121,815,673 (GRCm39) |
missense |
probably benign |
0.00 |
R7034:Mug1
|
UTSW |
6 |
121,850,603 (GRCm39) |
missense |
probably benign |
0.00 |
R7156:Mug1
|
UTSW |
6 |
121,861,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R7156:Mug1
|
UTSW |
6 |
121,857,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R7179:Mug1
|
UTSW |
6 |
121,834,379 (GRCm39) |
missense |
probably benign |
0.00 |
R7211:Mug1
|
UTSW |
6 |
121,857,498 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7318:Mug1
|
UTSW |
6 |
121,847,611 (GRCm39) |
critical splice donor site |
probably null |
|
R7462:Mug1
|
UTSW |
6 |
121,852,399 (GRCm39) |
missense |
probably benign |
0.00 |
R7479:Mug1
|
UTSW |
6 |
121,855,467 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7588:Mug1
|
UTSW |
6 |
121,852,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R7611:Mug1
|
UTSW |
6 |
121,852,387 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7659:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7660:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7661:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7663:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7664:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7666:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7788:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7789:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7794:Mug1
|
UTSW |
6 |
121,833,247 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7809:Mug1
|
UTSW |
6 |
121,855,944 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7836:Mug1
|
UTSW |
6 |
121,847,611 (GRCm39) |
critical splice donor site |
probably null |
|
R7867:Mug1
|
UTSW |
6 |
121,850,593 (GRCm39) |
missense |
probably benign |
|
R7904:Mug1
|
UTSW |
6 |
121,828,424 (GRCm39) |
missense |
probably benign |
|
R7937:Mug1
|
UTSW |
6 |
121,838,128 (GRCm39) |
missense |
probably benign |
0.00 |
R7981:Mug1
|
UTSW |
6 |
121,858,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R7999:Mug1
|
UTSW |
6 |
121,857,855 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8070:Mug1
|
UTSW |
6 |
121,852,838 (GRCm39) |
missense |
probably benign |
0.26 |
R8071:Mug1
|
UTSW |
6 |
121,850,631 (GRCm39) |
missense |
probably benign |
|
R8151:Mug1
|
UTSW |
6 |
121,818,117 (GRCm39) |
missense |
probably benign |
0.01 |
R8491:Mug1
|
UTSW |
6 |
121,859,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R8714:Mug1
|
UTSW |
6 |
121,859,681 (GRCm39) |
missense |
probably benign |
0.01 |
R8734:Mug1
|
UTSW |
6 |
121,848,340 (GRCm39) |
missense |
probably benign |
0.00 |
R8738:Mug1
|
UTSW |
6 |
121,817,208 (GRCm39) |
splice site |
probably benign |
|
R8807:Mug1
|
UTSW |
6 |
121,851,434 (GRCm39) |
missense |
probably benign |
0.27 |
R8931:Mug1
|
UTSW |
6 |
121,861,296 (GRCm39) |
missense |
probably benign |
|
R8940:Mug1
|
UTSW |
6 |
121,858,642 (GRCm39) |
missense |
|
|
R9156:Mug1
|
UTSW |
6 |
121,851,390 (GRCm39) |
missense |
probably damaging |
0.99 |
R9314:Mug1
|
UTSW |
6 |
121,834,296 (GRCm39) |
missense |
probably damaging |
0.97 |
R9315:Mug1
|
UTSW |
6 |
121,850,730 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9330:Mug1
|
UTSW |
6 |
121,859,723 (GRCm39) |
missense |
probably benign |
0.14 |
R9334:Mug1
|
UTSW |
6 |
121,838,490 (GRCm39) |
missense |
probably benign |
0.01 |
R9357:Mug1
|
UTSW |
6 |
121,852,450 (GRCm39) |
missense |
probably benign |
0.02 |
R9515:Mug1
|
UTSW |
6 |
121,861,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R9549:Mug1
|
UTSW |
6 |
121,858,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Mug1
|
UTSW |
6 |
121,861,587 (GRCm39) |
missense |
probably benign |
0.03 |
R9663:Mug1
|
UTSW |
6 |
121,859,699 (GRCm39) |
missense |
probably benign |
0.03 |
R9663:Mug1
|
UTSW |
6 |
121,857,463 (GRCm39) |
missense |
probably benign |
0.08 |
R9681:Mug1
|
UTSW |
6 |
121,833,254 (GRCm39) |
missense |
probably benign |
0.01 |
R9777:Mug1
|
UTSW |
6 |
121,857,864 (GRCm39) |
missense |
probably damaging |
1.00 |
RF017:Mug1
|
UTSW |
6 |
121,861,533 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Mug1
|
UTSW |
6 |
121,838,174 (GRCm39) |
missense |
possibly damaging |
0.48 |
Z1176:Mug1
|
UTSW |
6 |
121,857,452 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Mug1
|
UTSW |
6 |
121,818,253 (GRCm39) |
missense |
probably benign |
0.32 |
Z1177:Mug1
|
UTSW |
6 |
121,856,258 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1177:Mug1
|
UTSW |
6 |
121,840,767 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Mug1
|
UTSW |
6 |
121,863,527 (GRCm39) |
missense |
probably damaging |
0.98 |
|