Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc4 |
T |
C |
14: 118,856,339 (GRCm39) |
I334V |
probably benign |
Het |
Adamts5 |
C |
T |
16: 85,696,156 (GRCm39) |
A334T |
probably damaging |
Het |
Adcy4 |
G |
C |
14: 56,010,900 (GRCm39) |
F672L |
probably benign |
Het |
Adgrl1 |
A |
G |
8: 84,656,444 (GRCm39) |
Y254C |
probably damaging |
Het |
Adnp2 |
A |
G |
18: 80,174,065 (GRCm39) |
S115P |
probably damaging |
Het |
Aox1 |
A |
T |
1: 58,134,356 (GRCm39) |
S1110C |
probably damaging |
Het |
Arhgap44 |
G |
T |
11: 64,915,064 (GRCm39) |
N401K |
probably damaging |
Het |
Atp23 |
A |
T |
10: 126,735,494 (GRCm39) |
N63K |
possibly damaging |
Het |
Atp8b1 |
G |
C |
18: 64,664,453 (GRCm39) |
I1238M |
probably benign |
Het |
Ccdc38 |
A |
T |
10: 93,391,448 (GRCm39) |
|
probably null |
Het |
Celsr2 |
T |
C |
3: 108,304,051 (GRCm39) |
D2364G |
probably null |
Het |
Celsr3 |
G |
A |
9: 108,715,671 (GRCm39) |
D2116N |
probably benign |
Het |
Cenpf |
A |
G |
1: 189,389,279 (GRCm39) |
S1518P |
probably damaging |
Het |
Clcn3 |
C |
A |
8: 61,372,387 (GRCm39) |
V758L |
possibly damaging |
Het |
Cmklr2 |
A |
G |
1: 63,222,626 (GRCm39) |
V203A |
probably benign |
Het |
Ctsf |
T |
C |
19: 4,908,505 (GRCm39) |
L288P |
probably damaging |
Het |
Cwh43 |
A |
G |
5: 73,575,484 (GRCm39) |
T334A |
probably damaging |
Het |
Cyp3a57 |
A |
T |
5: 145,286,135 (GRCm39) |
|
probably null |
Het |
Ddr1 |
C |
T |
17: 35,997,400 (GRCm39) |
A531T |
probably benign |
Het |
Dennd1a |
A |
G |
2: 37,691,138 (GRCm39) |
I260T |
probably benign |
Het |
Dgkh |
T |
C |
14: 78,865,201 (GRCm39) |
H47R |
probably damaging |
Het |
Dync1h1 |
G |
A |
12: 110,632,422 (GRCm39) |
V4514I |
possibly damaging |
Het |
Dync2h1 |
A |
T |
9: 7,116,638 (GRCm39) |
M66K |
probably benign |
Het |
Fam186a |
T |
G |
15: 99,843,253 (GRCm39) |
Y997S |
possibly damaging |
Het |
Fam8a1 |
T |
A |
13: 46,827,814 (GRCm39) |
L334H |
probably damaging |
Het |
Fat4 |
C |
T |
3: 39,057,117 (GRCm39) |
T4271I |
probably damaging |
Het |
Fdxacb1 |
T |
A |
9: 50,679,705 (GRCm39) |
L41Q |
probably damaging |
Het |
Fgfr2 |
C |
T |
7: 129,863,593 (GRCm39) |
V18M |
probably damaging |
Het |
Gpa33 |
A |
C |
1: 165,992,714 (GRCm39) |
|
probably null |
Het |
Gpr107 |
A |
G |
2: 31,075,601 (GRCm39) |
I371V |
probably benign |
Het |
H1f6 |
A |
G |
13: 23,880,219 (GRCm39) |
K124R |
probably benign |
Het |
Hectd2 |
T |
C |
19: 36,581,720 (GRCm39) |
V420A |
probably damaging |
Het |
Iglc3 |
A |
G |
16: 18,884,420 (GRCm39) |
|
probably benign |
Het |
Igtp |
A |
G |
11: 58,097,455 (GRCm39) |
T209A |
probably benign |
Het |
Itgb7 |
T |
A |
15: 102,124,638 (GRCm39) |
N793I |
possibly damaging |
Het |
Kansl1 |
G |
A |
11: 104,228,992 (GRCm39) |
R870C |
probably damaging |
Het |
Kcnh6 |
C |
T |
11: 105,899,811 (GRCm39) |
R27C |
probably damaging |
Het |
Kif2b |
T |
A |
11: 91,466,656 (GRCm39) |
E542D |
possibly damaging |
Het |
Klhl24 |
C |
A |
16: 19,938,997 (GRCm39) |
Y517* |
probably null |
Het |
Klhl25 |
A |
G |
7: 75,515,895 (GRCm39) |
D267G |
probably benign |
Het |
Krr1 |
C |
A |
10: 111,813,288 (GRCm39) |
F195L |
possibly damaging |
Het |
Lsr |
C |
T |
7: 30,658,456 (GRCm39) |
G95D |
probably damaging |
Het |
Matcap2 |
A |
G |
9: 22,335,786 (GRCm39) |
T135A |
probably benign |
Het |
Med15 |
A |
T |
16: 17,473,055 (GRCm39) |
I504N |
probably damaging |
Het |
Mypn |
T |
A |
10: 62,971,580 (GRCm39) |
Q820L |
probably damaging |
Het |
Nlrp4f |
A |
T |
13: 65,330,803 (GRCm39) |
H863Q |
probably benign |
Het |
Nudt9 |
G |
A |
5: 104,207,646 (GRCm39) |
V213M |
probably benign |
Het |
Or5ak4 |
T |
A |
2: 85,161,717 (GRCm39) |
N175I |
probably damaging |
Het |
Or5k14 |
A |
G |
16: 58,692,847 (GRCm39) |
L222P |
probably damaging |
Het |
Or7g16 |
A |
G |
9: 18,726,922 (GRCm39) |
S223P |
probably damaging |
Het |
Or8c13 |
T |
C |
9: 38,092,111 (GRCm39) |
T3A |
probably benign |
Het |
Orc2 |
A |
G |
1: 58,505,231 (GRCm39) |
F475L |
probably damaging |
Het |
Oxa1l |
T |
A |
14: 54,604,289 (GRCm39) |
L183* |
probably null |
Het |
Pcdh20 |
T |
C |
14: 88,704,760 (GRCm39) |
T847A |
probably damaging |
Het |
Pcdha6 |
G |
A |
18: 37,101,889 (GRCm39) |
|
probably null |
Het |
Pip5k1a |
T |
C |
3: 94,974,750 (GRCm39) |
N376S |
probably benign |
Het |
Pkd1l1 |
T |
C |
11: 8,859,889 (GRCm39) |
E573G |
probably benign |
Het |
Pkp1 |
T |
A |
1: 135,810,335 (GRCm39) |
|
probably null |
Het |
Pum1 |
T |
C |
4: 130,491,438 (GRCm39) |
I643T |
possibly damaging |
Het |
Rapgef3 |
A |
G |
15: 97,656,318 (GRCm39) |
S328P |
probably benign |
Het |
Raver1 |
A |
G |
9: 21,001,608 (GRCm39) |
V75A |
probably damaging |
Het |
Rbm28 |
T |
C |
6: 29,135,408 (GRCm39) |
E511G |
probably damaging |
Het |
Satb1 |
T |
A |
17: 52,049,823 (GRCm39) |
T544S |
probably damaging |
Het |
Sdcbp2 |
T |
C |
2: 151,431,135 (GRCm39) |
V248A |
probably benign |
Het |
Sema7a |
A |
G |
9: 57,867,942 (GRCm39) |
D506G |
probably damaging |
Het |
Septin8 |
A |
G |
11: 53,428,044 (GRCm39) |
E286G |
probably damaging |
Het |
Sh3pxd2b |
A |
G |
11: 32,372,812 (GRCm39) |
I660V |
probably damaging |
Het |
Stk38l |
G |
T |
6: 146,674,826 (GRCm39) |
D364Y |
possibly damaging |
Het |
Sycp2 |
T |
C |
2: 178,000,498 (GRCm39) |
|
probably null |
Het |
Tbc1d31 |
T |
A |
15: 57,815,062 (GRCm39) |
S580T |
probably damaging |
Het |
Tcerg1l |
G |
A |
7: 137,881,775 (GRCm39) |
R305C |
probably damaging |
Het |
Tek |
T |
A |
4: 94,743,561 (GRCm39) |
Y859N |
probably damaging |
Het |
Tjp1 |
A |
T |
7: 64,962,191 (GRCm39) |
|
probably null |
Het |
Tmem132d |
A |
T |
5: 127,861,859 (GRCm39) |
I754N |
possibly damaging |
Het |
Togaram1 |
G |
A |
12: 65,063,424 (GRCm39) |
V1580I |
probably benign |
Het |
Troap |
A |
G |
15: 98,980,145 (GRCm39) |
T442A |
probably benign |
Het |
Ttn |
A |
T |
2: 76,712,097 (GRCm39) |
|
probably benign |
Het |
Twnk |
T |
A |
19: 44,995,732 (GRCm39) |
V55E |
possibly damaging |
Het |
Uggt1 |
A |
T |
1: 36,255,234 (GRCm39) |
Y225* |
probably null |
Het |
Vmn2r109 |
A |
G |
17: 20,760,781 (GRCm39) |
*859Q |
probably null |
Het |
Vmn2r17 |
A |
T |
5: 109,577,430 (GRCm39) |
I494L |
probably benign |
Het |
Vmn2r88 |
T |
C |
14: 51,656,029 (GRCm39) |
V746A |
probably damaging |
Het |
Yae1d1 |
A |
G |
13: 18,166,291 (GRCm39) |
L57P |
probably damaging |
Het |
Zfp26 |
G |
A |
9: 20,349,137 (GRCm39) |
R476* |
probably null |
Het |
Zmynd8 |
T |
A |
2: 165,649,618 (GRCm39) |
Q816L |
probably damaging |
Het |
Zswim8 |
A |
T |
14: 20,763,495 (GRCm39) |
H414L |
possibly damaging |
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 |
|
R4999:Mug1
|
UTSW |
6 |
121,855,902 (GRCm39) |
nonsense |
probably null |
|
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 |
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 |
|