Other mutations in this stock |
Total: 122 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A4gnt |
T |
C |
9: 99,502,412 (GRCm39) |
S191P |
probably damaging |
Het |
Ak2 |
C |
T |
4: 128,901,990 (GRCm39) |
A221V |
probably damaging |
Het |
Akap9 |
T |
A |
5: 4,011,010 (GRCm39) |
V571E |
probably damaging |
Het |
Amph |
G |
T |
13: 19,309,205 (GRCm39) |
E428* |
probably null |
Het |
Armh3 |
C |
T |
19: 45,967,106 (GRCm39) |
R12Q |
probably damaging |
Het |
Arnt2 |
T |
A |
7: 83,993,078 (GRCm39) |
D154V |
probably damaging |
Het |
Arrdc1 |
G |
A |
2: 24,816,364 (GRCm39) |
Q202* |
probably null |
Het |
Ate1 |
A |
G |
7: 130,112,643 (GRCm39) |
C72R |
probably damaging |
Het |
Atox1 |
A |
G |
11: 55,345,724 (GRCm39) |
V22A |
possibly damaging |
Het |
Bbs12 |
A |
T |
3: 37,373,215 (GRCm39) |
M3L |
probably damaging |
Het |
Bfsp1 |
A |
G |
2: 143,704,598 (GRCm39) |
V85A |
probably benign |
Het |
Bltp2 |
T |
A |
11: 78,159,575 (GRCm39) |
C541* |
probably null |
Het |
Caskin2 |
C |
A |
11: 115,694,456 (GRCm39) |
V382F |
probably benign |
Het |
Ccdc39 |
T |
A |
3: 33,874,045 (GRCm39) |
M596L |
probably damaging |
Het |
Cd22 |
C |
T |
7: 30,569,530 (GRCm39) |
V529M |
probably damaging |
Het |
Cd22 |
A |
C |
7: 30,575,581 (GRCm39) |
Y154D |
probably benign |
Het |
Cdadc1 |
T |
A |
14: 59,818,783 (GRCm39) |
E348D |
probably damaging |
Het |
Cdhr2 |
T |
C |
13: 54,868,631 (GRCm39) |
V531A |
probably damaging |
Het |
Cdk11b |
A |
G |
4: 155,726,061 (GRCm39) |
|
probably benign |
Het |
Cebpa |
G |
T |
7: 34,818,947 (GRCm39) |
R35L |
probably damaging |
Het |
Chat |
T |
C |
14: 32,168,830 (GRCm39) |
N235S |
probably benign |
Het |
Col12a1 |
T |
A |
9: 79,524,987 (GRCm39) |
I2725F |
possibly damaging |
Het |
Cracr2b |
A |
G |
7: 141,045,193 (GRCm39) |
E231G |
probably damaging |
Het |
Cryaa |
G |
T |
17: 31,900,029 (GRCm39) |
A151S |
probably benign |
Het |
Cspg4b |
T |
A |
13: 113,454,628 (GRCm39) |
W225R |
probably damaging |
Het |
Dab1 |
A |
T |
4: 104,535,938 (GRCm39) |
I116F |
probably damaging |
Het |
Ddx43 |
C |
A |
9: 78,303,386 (GRCm39) |
N75K |
probably benign |
Het |
Dmbt1 |
T |
G |
7: 130,700,863 (GRCm39) |
C1014G |
possibly damaging |
Het |
Dner |
C |
A |
1: 84,383,710 (GRCm39) |
C558F |
probably damaging |
Het |
Dsc2 |
A |
G |
18: 20,165,456 (GRCm39) |
V839A |
possibly damaging |
Het |
Dsg3 |
C |
T |
18: 20,660,794 (GRCm39) |
R378* |
probably null |
Het |
Ecpas |
G |
T |
4: 58,824,270 (GRCm39) |
P1116T |
probably damaging |
Het |
Emilin1 |
C |
T |
5: 31,075,082 (GRCm39) |
P441L |
possibly damaging |
Het |
Epha6 |
T |
C |
16: 59,476,160 (GRCm39) |
M1069V |
probably damaging |
Het |
F930017D23Rik |
A |
C |
10: 43,480,416 (GRCm39) |
|
noncoding transcript |
Het |
Faf1 |
A |
T |
4: 109,568,005 (GRCm39) |
N22Y |
probably damaging |
Het |
Flrt3 |
A |
T |
2: 140,503,373 (GRCm39) |
V85E |
probably damaging |
Het |
Gadl1 |
T |
A |
9: 115,770,448 (GRCm39) |
I87N |
probably damaging |
Het |
Galnt14 |
A |
G |
17: 73,819,148 (GRCm39) |
F314S |
probably damaging |
Het |
Gba2 |
A |
T |
4: 43,574,029 (GRCm39) |
Y141* |
probably null |
Het |
Gdap1 |
A |
T |
1: 17,215,689 (GRCm39) |
|
probably benign |
Het |
Gfod1 |
A |
T |
13: 43,456,719 (GRCm39) |
|
probably null |
Het |
Gm14295 |
C |
T |
2: 176,502,474 (GRCm39) |
R655* |
probably null |
Het |
Gm4353 |
A |
G |
7: 115,682,934 (GRCm39) |
S216P |
probably damaging |
Het |
Gm6605 |
T |
A |
7: 38,147,706 (GRCm39) |
|
noncoding transcript |
Het |
Hectd1 |
A |
T |
12: 51,841,227 (GRCm39) |
D634E |
probably damaging |
Het |
Helz2 |
A |
G |
2: 180,882,337 (GRCm39) |
I152T |
probably damaging |
Het |
Hivep1 |
A |
G |
13: 42,313,600 (GRCm39) |
K1947E |
possibly damaging |
Het |
Ifrd1 |
A |
T |
12: 40,263,244 (GRCm39) |
F144L |
probably benign |
Het |
Inhca |
T |
C |
9: 103,145,513 (GRCm39) |
M395V |
probably benign |
Het |
Itgae |
A |
T |
11: 73,009,448 (GRCm39) |
Q544L |
probably benign |
Het |
Jmjd1c |
A |
T |
10: 67,054,205 (GRCm39) |
E323D |
probably damaging |
Het |
Kdm5a |
G |
T |
6: 120,358,578 (GRCm39) |
R207L |
probably benign |
Het |
Kif5b |
C |
T |
18: 6,226,377 (GRCm39) |
|
probably null |
Het |
Lbp |
T |
C |
2: 158,166,499 (GRCm39) |
V351A |
probably benign |
Het |
Lss |
A |
T |
10: 76,381,932 (GRCm39) |
|
probably null |
Het |
Madd |
A |
C |
2: 90,991,831 (GRCm39) |
|
probably benign |
Het |
Map6 |
G |
A |
7: 98,966,679 (GRCm39) |
V503I |
probably damaging |
Het |
Mark1 |
A |
G |
1: 184,660,260 (GRCm39) |
L22P |
probably damaging |
Het |
Mcfd2 |
T |
C |
17: 87,563,404 (GRCm39) |
N130D |
probably damaging |
Het |
Mcm3ap |
A |
G |
10: 76,305,902 (GRCm39) |
N5S |
probably benign |
Het |
Mdm4 |
A |
T |
1: 132,940,389 (GRCm39) |
F48I |
probably damaging |
Het |
Mga |
A |
T |
2: 119,795,461 (GRCm39) |
|
probably benign |
Het |
Mknk2 |
A |
T |
10: 80,507,391 (GRCm39) |
|
probably null |
Het |
Mmp15 |
T |
C |
8: 96,097,407 (GRCm39) |
Y459H |
possibly damaging |
Het |
Mthfd1l |
A |
G |
10: 4,053,288 (GRCm39) |
K879R |
probably benign |
Het |
Nasp |
T |
C |
4: 116,468,323 (GRCm39) |
N221D |
probably benign |
Het |
Ndc80 |
T |
C |
17: 71,821,213 (GRCm39) |
E245G |
probably benign |
Het |
Nmral1 |
C |
T |
16: 4,534,193 (GRCm39) |
E83K |
probably damaging |
Het |
Noa1 |
T |
A |
5: 77,452,034 (GRCm39) |
Q550L |
possibly damaging |
Het |
Nutm1 |
A |
T |
2: 112,086,097 (GRCm39) |
Y211* |
probably null |
Het |
Or10n1 |
G |
T |
9: 39,525,071 (GRCm39) |
M69I |
probably benign |
Het |
Or10v1 |
T |
A |
19: 11,873,921 (GRCm39) |
Y179N |
probably damaging |
Het |
Or2ag18 |
A |
C |
7: 106,404,975 (GRCm39) |
H231Q |
probably benign |
Het |
Or4l1 |
T |
C |
14: 50,166,478 (GRCm39) |
I174M |
possibly damaging |
Het |
Or5b118 |
A |
G |
19: 13,448,605 (GRCm39) |
I90M |
probably damaging |
Het |
Otoa |
T |
C |
7: 120,730,551 (GRCm39) |
F584L |
probably damaging |
Het |
Palb2 |
G |
A |
7: 121,723,748 (GRCm39) |
T304I |
possibly damaging |
Het |
Pcolce2 |
A |
T |
9: 95,552,229 (GRCm39) |
M121L |
probably benign |
Het |
Pcsk5 |
T |
C |
19: 17,432,236 (GRCm39) |
T1460A |
probably benign |
Het |
Pdzrn4 |
A |
T |
15: 92,668,041 (GRCm39) |
D731V |
probably damaging |
Het |
Pex11b |
C |
A |
3: 96,543,037 (GRCm39) |
Q12K |
possibly damaging |
Het |
Pigw |
G |
C |
11: 84,768,136 (GRCm39) |
Q398E |
probably benign |
Het |
Pkd1 |
A |
G |
17: 24,788,888 (GRCm39) |
E882G |
possibly damaging |
Het |
Pkhd1 |
A |
T |
1: 20,683,036 (GRCm39) |
N55K |
possibly damaging |
Het |
Plch2 |
A |
T |
4: 155,127,298 (GRCm39) |
|
probably benign |
Het |
Plcl1 |
T |
A |
1: 55,790,504 (GRCm39) |
L1058Q |
probably benign |
Het |
Ppfia2 |
T |
C |
10: 106,673,190 (GRCm39) |
S511P |
possibly damaging |
Het |
Ppfibp2 |
T |
C |
7: 107,338,437 (GRCm39) |
L676P |
probably damaging |
Het |
Ppp6c |
T |
G |
2: 39,116,186 (GRCm39) |
D23A |
probably damaging |
Het |
Prss30 |
G |
A |
17: 24,193,642 (GRCm39) |
|
probably benign |
Het |
Ptprz1 |
T |
C |
6: 23,049,674 (GRCm39) |
|
probably null |
Het |
Rec114 |
T |
A |
9: 58,560,188 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
T |
C |
13: 11,680,764 (GRCm39) |
|
probably null |
Het |
Ryr3 |
A |
T |
2: 112,493,349 (GRCm39) |
I3715N |
possibly damaging |
Het |
Scin |
T |
C |
12: 40,130,947 (GRCm39) |
Y322C |
probably damaging |
Het |
Scn3a |
A |
G |
2: 65,291,652 (GRCm39) |
V1698A |
probably damaging |
Het |
Scn5a |
G |
A |
9: 119,314,717 (GRCm39) |
S1996L |
probably damaging |
Het |
Serpinb2 |
A |
G |
1: 107,450,525 (GRCm39) |
K174R |
possibly damaging |
Het |
Slc16a4 |
T |
C |
3: 107,208,027 (GRCm39) |
I179T |
probably benign |
Het |
Slc35b1 |
T |
G |
11: 95,276,718 (GRCm39) |
F102V |
possibly damaging |
Het |
Slc66a2 |
G |
T |
18: 80,334,930 (GRCm39) |
A232S |
probably benign |
Het |
Slc6a15 |
A |
G |
10: 103,245,595 (GRCm39) |
D526G |
probably benign |
Het |
Spata16 |
A |
G |
3: 26,978,519 (GRCm39) |
D495G |
probably damaging |
Het |
Stk11ip |
G |
A |
1: 75,506,228 (GRCm39) |
E583K |
possibly damaging |
Het |
Stk-ps1 |
T |
G |
17: 36,709,044 (GRCm39) |
|
noncoding transcript |
Het |
Sufu |
T |
A |
19: 46,385,651 (GRCm39) |
I37N |
probably damaging |
Het |
Tacr1 |
C |
T |
6: 82,469,535 (GRCm39) |
P140S |
probably damaging |
Het |
Tas1r3 |
G |
A |
4: 155,944,927 (GRCm39) |
R765C |
probably damaging |
Het |
Tenm3 |
C |
T |
8: 48,795,291 (GRCm39) |
|
probably null |
Het |
Tex36 |
A |
T |
7: 133,196,952 (GRCm39) |
I55N |
probably damaging |
Het |
Tmem150c |
T |
C |
5: 100,227,887 (GRCm39) |
Y192C |
probably damaging |
Het |
Tmem237 |
A |
G |
1: 59,159,445 (GRCm39) |
|
probably benign |
Het |
Trim11 |
A |
G |
11: 58,872,889 (GRCm39) |
E191G |
probably damaging |
Het |
Ttll3 |
C |
T |
6: 113,386,003 (GRCm39) |
A612V |
possibly damaging |
Het |
Ttn |
G |
A |
2: 76,807,466 (GRCm39) |
A89V |
probably damaging |
Het |
Usp37 |
A |
G |
1: 74,507,431 (GRCm39) |
F529L |
probably damaging |
Het |
Vmn1r217 |
A |
C |
13: 23,298,698 (GRCm39) |
V68G |
probably benign |
Het |
Vwf |
T |
C |
6: 125,568,151 (GRCm39) |
S349P |
probably damaging |
Het |
Wt1 |
G |
A |
2: 104,961,502 (GRCm39) |
|
probably null |
Het |
Zcchc7 |
T |
A |
4: 44,895,838 (GRCm39) |
L262H |
probably damaging |
Het |
Zfp873 |
A |
G |
10: 81,895,991 (GRCm39) |
S241G |
probably benign |
Het |
|
Other mutations in Mycbp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Mycbp2
|
APN |
14 |
103,460,486 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00518:Mycbp2
|
APN |
14 |
103,393,244 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00650:Mycbp2
|
APN |
14 |
103,380,664 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00653:Mycbp2
|
APN |
14 |
103,380,664 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00742:Mycbp2
|
APN |
14 |
103,438,788 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00755:Mycbp2
|
APN |
14 |
103,432,057 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL00793:Mycbp2
|
APN |
14 |
103,364,189 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL00916:Mycbp2
|
APN |
14 |
103,528,719 (GRCm39) |
splice site |
probably benign |
|
IGL00960:Mycbp2
|
APN |
14 |
103,466,820 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL00977:Mycbp2
|
APN |
14 |
103,410,078 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01349:Mycbp2
|
APN |
14 |
103,359,983 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01369:Mycbp2
|
APN |
14 |
103,392,946 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL01410:Mycbp2
|
APN |
14 |
103,466,928 (GRCm39) |
splice site |
probably null |
|
IGL01586:Mycbp2
|
APN |
14 |
103,378,305 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01593:Mycbp2
|
APN |
14 |
103,528,723 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01693:Mycbp2
|
APN |
14 |
103,365,415 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01730:Mycbp2
|
APN |
14 |
103,372,640 (GRCm39) |
nonsense |
probably null |
|
IGL01820:Mycbp2
|
APN |
14 |
103,425,937 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01974:Mycbp2
|
APN |
14 |
103,380,647 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02071:Mycbp2
|
APN |
14 |
103,392,343 (GRCm39) |
nonsense |
probably null |
|
IGL02178:Mycbp2
|
APN |
14 |
103,461,802 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02324:Mycbp2
|
APN |
14 |
103,479,643 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02442:Mycbp2
|
APN |
14 |
103,551,811 (GRCm39) |
missense |
probably benign |
|
IGL02607:Mycbp2
|
APN |
14 |
103,522,709 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02679:Mycbp2
|
APN |
14 |
103,442,621 (GRCm39) |
missense |
probably benign |
|
IGL02702:Mycbp2
|
APN |
14 |
103,457,560 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02709:Mycbp2
|
APN |
14 |
103,392,697 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02736:Mycbp2
|
APN |
14 |
103,351,678 (GRCm39) |
splice site |
probably benign |
|
IGL02866:Mycbp2
|
APN |
14 |
103,367,428 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02939:Mycbp2
|
APN |
14 |
103,414,715 (GRCm39) |
missense |
probably benign |
|
IGL03082:Mycbp2
|
APN |
14 |
103,441,805 (GRCm39) |
missense |
probably benign |
0.23 |
IGL03142:Mycbp2
|
APN |
14 |
103,536,212 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03155:Mycbp2
|
APN |
14 |
103,392,889 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03236:Mycbp2
|
APN |
14 |
103,536,134 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03256:Mycbp2
|
APN |
14 |
103,426,025 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL03303:Mycbp2
|
APN |
14 |
103,485,194 (GRCm39) |
missense |
probably damaging |
1.00 |
compost
|
UTSW |
14 |
103,393,889 (GRCm39) |
missense |
probably damaging |
1.00 |
decompose
|
UTSW |
14 |
103,457,415 (GRCm39) |
missense |
probably benign |
0.12 |
moulder
|
UTSW |
14 |
103,426,028 (GRCm39) |
missense |
probably damaging |
1.00 |
N/A - 293:Mycbp2
|
UTSW |
14 |
103,461,898 (GRCm39) |
splice site |
probably benign |
|
R0040:Mycbp2
|
UTSW |
14 |
103,461,708 (GRCm39) |
missense |
probably benign |
0.11 |
R0040:Mycbp2
|
UTSW |
14 |
103,461,708 (GRCm39) |
missense |
probably benign |
0.11 |
R0057:Mycbp2
|
UTSW |
14 |
103,389,578 (GRCm39) |
missense |
probably damaging |
0.97 |
R0063:Mycbp2
|
UTSW |
14 |
103,394,070 (GRCm39) |
unclassified |
probably benign |
|
R0097:Mycbp2
|
UTSW |
14 |
103,393,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R0097:Mycbp2
|
UTSW |
14 |
103,393,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R0268:Mycbp2
|
UTSW |
14 |
103,551,761 (GRCm39) |
nonsense |
probably null |
|
R0388:Mycbp2
|
UTSW |
14 |
103,394,103 (GRCm39) |
missense |
probably benign |
0.01 |
R0410:Mycbp2
|
UTSW |
14 |
103,372,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R0530:Mycbp2
|
UTSW |
14 |
103,419,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R0591:Mycbp2
|
UTSW |
14 |
103,433,827 (GRCm39) |
unclassified |
probably benign |
|
R0671:Mycbp2
|
UTSW |
14 |
103,432,024 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0755:Mycbp2
|
UTSW |
14 |
103,412,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R0817:Mycbp2
|
UTSW |
14 |
103,466,854 (GRCm39) |
missense |
probably damaging |
0.99 |
R0818:Mycbp2
|
UTSW |
14 |
103,466,854 (GRCm39) |
missense |
probably damaging |
0.99 |
R0819:Mycbp2
|
UTSW |
14 |
103,466,854 (GRCm39) |
missense |
probably damaging |
0.99 |
R0881:Mycbp2
|
UTSW |
14 |
103,457,449 (GRCm39) |
missense |
probably benign |
|
R0903:Mycbp2
|
UTSW |
14 |
103,513,293 (GRCm39) |
missense |
probably damaging |
0.99 |
R0940:Mycbp2
|
UTSW |
14 |
103,500,129 (GRCm39) |
unclassified |
probably benign |
|
R0961:Mycbp2
|
UTSW |
14 |
103,422,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R1004:Mycbp2
|
UTSW |
14 |
103,378,353 (GRCm39) |
missense |
probably benign |
0.00 |
R1138:Mycbp2
|
UTSW |
14 |
103,412,262 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1170:Mycbp2
|
UTSW |
14 |
103,437,588 (GRCm39) |
nonsense |
probably null |
|
R1211:Mycbp2
|
UTSW |
14 |
103,357,999 (GRCm39) |
missense |
probably benign |
0.31 |
R1268:Mycbp2
|
UTSW |
14 |
103,446,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R1298:Mycbp2
|
UTSW |
14 |
103,393,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R1341:Mycbp2
|
UTSW |
14 |
103,536,303 (GRCm39) |
splice site |
probably benign |
|
R1469:Mycbp2
|
UTSW |
14 |
103,425,956 (GRCm39) |
missense |
probably damaging |
0.99 |
R1469:Mycbp2
|
UTSW |
14 |
103,425,956 (GRCm39) |
missense |
probably damaging |
0.99 |
R1513:Mycbp2
|
UTSW |
14 |
103,441,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R1528:Mycbp2
|
UTSW |
14 |
103,470,033 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1564:Mycbp2
|
UTSW |
14 |
103,407,287 (GRCm39) |
splice site |
probably null |
|
R1565:Mycbp2
|
UTSW |
14 |
103,489,945 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1656:Mycbp2
|
UTSW |
14 |
103,485,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R1694:Mycbp2
|
UTSW |
14 |
103,464,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R1709:Mycbp2
|
UTSW |
14 |
103,461,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R1728:Mycbp2
|
UTSW |
14 |
103,392,614 (GRCm39) |
missense |
probably damaging |
0.98 |
R1751:Mycbp2
|
UTSW |
14 |
103,485,841 (GRCm39) |
missense |
probably damaging |
0.98 |
R1767:Mycbp2
|
UTSW |
14 |
103,485,841 (GRCm39) |
missense |
probably damaging |
0.98 |
R1772:Mycbp2
|
UTSW |
14 |
103,419,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R1784:Mycbp2
|
UTSW |
14 |
103,392,614 (GRCm39) |
missense |
probably damaging |
0.98 |
R1823:Mycbp2
|
UTSW |
14 |
103,489,945 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1824:Mycbp2
|
UTSW |
14 |
103,489,945 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1844:Mycbp2
|
UTSW |
14 |
103,393,150 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1916:Mycbp2
|
UTSW |
14 |
103,422,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R1944:Mycbp2
|
UTSW |
14 |
103,466,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R1983:Mycbp2
|
UTSW |
14 |
103,383,407 (GRCm39) |
missense |
probably damaging |
0.97 |
R2002:Mycbp2
|
UTSW |
14 |
103,485,839 (GRCm39) |
missense |
probably damaging |
0.98 |
R2031:Mycbp2
|
UTSW |
14 |
103,426,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R2035:Mycbp2
|
UTSW |
14 |
103,497,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R2048:Mycbp2
|
UTSW |
14 |
103,469,960 (GRCm39) |
critical splice donor site |
probably null |
|
R2113:Mycbp2
|
UTSW |
14 |
103,457,512 (GRCm39) |
missense |
probably damaging |
0.99 |
R2128:Mycbp2
|
UTSW |
14 |
103,438,666 (GRCm39) |
missense |
probably benign |
0.01 |
R2134:Mycbp2
|
UTSW |
14 |
103,446,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R2135:Mycbp2
|
UTSW |
14 |
103,446,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R2135:Mycbp2
|
UTSW |
14 |
103,383,378 (GRCm39) |
missense |
probably benign |
|
R2146:Mycbp2
|
UTSW |
14 |
103,393,358 (GRCm39) |
missense |
probably damaging |
0.97 |
R2147:Mycbp2
|
UTSW |
14 |
103,393,358 (GRCm39) |
missense |
probably damaging |
0.97 |
R2148:Mycbp2
|
UTSW |
14 |
103,393,358 (GRCm39) |
missense |
probably damaging |
0.97 |
R2150:Mycbp2
|
UTSW |
14 |
103,393,358 (GRCm39) |
missense |
probably damaging |
0.97 |
R2163:Mycbp2
|
UTSW |
14 |
103,407,291 (GRCm39) |
critical splice donor site |
probably null |
|
R2248:Mycbp2
|
UTSW |
14 |
103,407,295 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2265:Mycbp2
|
UTSW |
14 |
103,500,185 (GRCm39) |
missense |
probably benign |
0.39 |
R2272:Mycbp2
|
UTSW |
14 |
103,381,774 (GRCm39) |
missense |
probably null |
0.66 |
R2379:Mycbp2
|
UTSW |
14 |
103,412,386 (GRCm39) |
missense |
probably benign |
|
R2495:Mycbp2
|
UTSW |
14 |
103,437,554 (GRCm39) |
missense |
probably damaging |
0.99 |
R2508:Mycbp2
|
UTSW |
14 |
103,368,681 (GRCm39) |
missense |
probably damaging |
0.99 |
R2510:Mycbp2
|
UTSW |
14 |
103,392,691 (GRCm39) |
missense |
probably damaging |
0.96 |
R2851:Mycbp2
|
UTSW |
14 |
103,381,769 (GRCm39) |
missense |
probably damaging |
0.99 |
R2852:Mycbp2
|
UTSW |
14 |
103,381,769 (GRCm39) |
missense |
probably damaging |
0.99 |
R2965:Mycbp2
|
UTSW |
14 |
103,534,794 (GRCm39) |
missense |
probably benign |
0.00 |
R3156:Mycbp2
|
UTSW |
14 |
103,446,179 (GRCm39) |
splice site |
probably benign |
|
R3404:Mycbp2
|
UTSW |
14 |
103,437,550 (GRCm39) |
missense |
probably damaging |
0.99 |
R3410:Mycbp2
|
UTSW |
14 |
103,372,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R3429:Mycbp2
|
UTSW |
14 |
103,466,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R3706:Mycbp2
|
UTSW |
14 |
103,393,850 (GRCm39) |
missense |
probably benign |
0.31 |
R3772:Mycbp2
|
UTSW |
14 |
103,371,224 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3778:Mycbp2
|
UTSW |
14 |
103,434,721 (GRCm39) |
missense |
probably damaging |
0.99 |
R3883:Mycbp2
|
UTSW |
14 |
103,532,686 (GRCm39) |
missense |
probably damaging |
0.97 |
R3884:Mycbp2
|
UTSW |
14 |
103,532,686 (GRCm39) |
missense |
probably damaging |
0.97 |
R3887:Mycbp2
|
UTSW |
14 |
103,412,233 (GRCm39) |
missense |
probably damaging |
0.98 |
R3923:Mycbp2
|
UTSW |
14 |
103,364,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R3926:Mycbp2
|
UTSW |
14 |
103,441,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R3959:Mycbp2
|
UTSW |
14 |
103,532,688 (GRCm39) |
missense |
probably benign |
0.00 |
R3966:Mycbp2
|
UTSW |
14 |
103,376,161 (GRCm39) |
splice site |
probably benign |
|
R4021:Mycbp2
|
UTSW |
14 |
103,389,593 (GRCm39) |
missense |
probably damaging |
0.97 |
R4363:Mycbp2
|
UTSW |
14 |
103,485,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R4405:Mycbp2
|
UTSW |
14 |
103,360,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R4407:Mycbp2
|
UTSW |
14 |
103,524,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R4410:Mycbp2
|
UTSW |
14 |
103,372,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R4434:Mycbp2
|
UTSW |
14 |
103,371,225 (GRCm39) |
missense |
probably damaging |
0.99 |
R4448:Mycbp2
|
UTSW |
14 |
103,425,938 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4452:Mycbp2
|
UTSW |
14 |
103,393,094 (GRCm39) |
missense |
probably damaging |
0.99 |
R4573:Mycbp2
|
UTSW |
14 |
103,583,733 (GRCm39) |
missense |
probably benign |
0.05 |
R4589:Mycbp2
|
UTSW |
14 |
103,414,749 (GRCm39) |
missense |
probably benign |
0.04 |
R4621:Mycbp2
|
UTSW |
14 |
103,457,415 (GRCm39) |
missense |
probably benign |
0.12 |
R4622:Mycbp2
|
UTSW |
14 |
103,457,415 (GRCm39) |
missense |
probably benign |
0.12 |
R4729:Mycbp2
|
UTSW |
14 |
103,426,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R4770:Mycbp2
|
UTSW |
14 |
103,457,380 (GRCm39) |
missense |
probably benign |
0.41 |
R4790:Mycbp2
|
UTSW |
14 |
103,466,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R4884:Mycbp2
|
UTSW |
14 |
103,448,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R4885:Mycbp2
|
UTSW |
14 |
103,383,382 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4956:Mycbp2
|
UTSW |
14 |
103,524,675 (GRCm39) |
missense |
probably damaging |
0.99 |
R4980:Mycbp2
|
UTSW |
14 |
103,497,821 (GRCm39) |
splice site |
probably null |
|
R4994:Mycbp2
|
UTSW |
14 |
103,407,430 (GRCm39) |
missense |
probably benign |
|
R5029:Mycbp2
|
UTSW |
14 |
103,393,946 (GRCm39) |
missense |
probably benign |
0.21 |
R5038:Mycbp2
|
UTSW |
14 |
103,534,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R5044:Mycbp2
|
UTSW |
14 |
103,376,671 (GRCm39) |
critical splice donor site |
probably null |
|
R5231:Mycbp2
|
UTSW |
14 |
103,583,650 (GRCm39) |
critical splice donor site |
probably null |
|
R5305:Mycbp2
|
UTSW |
14 |
103,583,757 (GRCm39) |
missense |
probably benign |
0.00 |
R5322:Mycbp2
|
UTSW |
14 |
103,423,119 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5376:Mycbp2
|
UTSW |
14 |
103,479,868 (GRCm39) |
nonsense |
probably null |
|
R5414:Mycbp2
|
UTSW |
14 |
103,543,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R5453:Mycbp2
|
UTSW |
14 |
103,438,837 (GRCm39) |
missense |
probably damaging |
0.99 |
R5462:Mycbp2
|
UTSW |
14 |
103,437,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R5499:Mycbp2
|
UTSW |
14 |
103,479,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R5502:Mycbp2
|
UTSW |
14 |
103,411,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R5524:Mycbp2
|
UTSW |
14 |
103,532,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R5533:Mycbp2
|
UTSW |
14 |
103,520,081 (GRCm39) |
nonsense |
probably null |
|
R5569:Mycbp2
|
UTSW |
14 |
103,372,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R5574:Mycbp2
|
UTSW |
14 |
103,380,203 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5579:Mycbp2
|
UTSW |
14 |
103,528,769 (GRCm39) |
missense |
probably damaging |
0.98 |
R5590:Mycbp2
|
UTSW |
14 |
103,360,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R5592:Mycbp2
|
UTSW |
14 |
103,432,113 (GRCm39) |
missense |
probably benign |
0.02 |
R5643:Mycbp2
|
UTSW |
14 |
103,524,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R5644:Mycbp2
|
UTSW |
14 |
103,524,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R5645:Mycbp2
|
UTSW |
14 |
103,426,051 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5645:Mycbp2
|
UTSW |
14 |
103,426,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R5646:Mycbp2
|
UTSW |
14 |
103,407,346 (GRCm39) |
missense |
probably benign |
0.09 |
R5648:Mycbp2
|
UTSW |
14 |
103,528,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R5651:Mycbp2
|
UTSW |
14 |
103,520,101 (GRCm39) |
missense |
probably null |
0.99 |
R5668:Mycbp2
|
UTSW |
14 |
103,357,955 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5745:Mycbp2
|
UTSW |
14 |
103,393,889 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5751:Mycbp2
|
UTSW |
14 |
103,385,986 (GRCm39) |
missense |
probably damaging |
0.99 |
R5756:Mycbp2
|
UTSW |
14 |
103,371,410 (GRCm39) |
missense |
probably damaging |
0.99 |
R5837:Mycbp2
|
UTSW |
14 |
103,361,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R5984:Mycbp2
|
UTSW |
14 |
103,364,120 (GRCm39) |
missense |
probably damaging |
0.98 |
R6005:Mycbp2
|
UTSW |
14 |
103,394,159 (GRCm39) |
missense |
probably benign |
|
R6063:Mycbp2
|
UTSW |
14 |
103,372,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R6091:Mycbp2
|
UTSW |
14 |
103,460,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R6120:Mycbp2
|
UTSW |
14 |
103,513,323 (GRCm39) |
missense |
probably benign |
0.01 |
R6129:Mycbp2
|
UTSW |
14 |
103,522,836 (GRCm39) |
missense |
probably benign |
0.21 |
R6147:Mycbp2
|
UTSW |
14 |
103,392,945 (GRCm39) |
nonsense |
probably null |
|
R6161:Mycbp2
|
UTSW |
14 |
103,536,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R6187:Mycbp2
|
UTSW |
14 |
103,384,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R6208:Mycbp2
|
UTSW |
14 |
103,532,664 (GRCm39) |
missense |
probably benign |
0.11 |
R6228:Mycbp2
|
UTSW |
14 |
103,497,665 (GRCm39) |
missense |
probably benign |
0.24 |
R6301:Mycbp2
|
UTSW |
14 |
103,392,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R6311:Mycbp2
|
UTSW |
14 |
103,500,176 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6329:Mycbp2
|
UTSW |
14 |
103,393,288 (GRCm39) |
missense |
probably benign |
0.00 |
R6439:Mycbp2
|
UTSW |
14 |
103,392,911 (GRCm39) |
missense |
probably benign |
0.00 |
R6462:Mycbp2
|
UTSW |
14 |
103,373,993 (GRCm39) |
critical splice donor site |
probably null |
|
R6528:Mycbp2
|
UTSW |
14 |
103,380,317 (GRCm39) |
missense |
probably damaging |
0.99 |
R6736:Mycbp2
|
UTSW |
14 |
103,429,003 (GRCm39) |
missense |
probably null |
1.00 |
R6821:Mycbp2
|
UTSW |
14 |
103,376,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R6851:Mycbp2
|
UTSW |
14 |
103,497,630 (GRCm39) |
critical splice donor site |
probably null |
|
R6948:Mycbp2
|
UTSW |
14 |
103,522,703 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6977:Mycbp2
|
UTSW |
14 |
103,392,342 (GRCm39) |
missense |
probably damaging |
0.99 |
R6985:Mycbp2
|
UTSW |
14 |
103,444,117 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7035:Mycbp2
|
UTSW |
14 |
103,412,417 (GRCm39) |
missense |
probably benign |
|
R7054:Mycbp2
|
UTSW |
14 |
103,393,534 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7108:Mycbp2
|
UTSW |
14 |
103,360,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R7117:Mycbp2
|
UTSW |
14 |
103,391,513 (GRCm39) |
missense |
probably benign |
0.21 |
R7137:Mycbp2
|
UTSW |
14 |
103,520,115 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7169:Mycbp2
|
UTSW |
14 |
103,497,636 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7218:Mycbp2
|
UTSW |
14 |
103,371,282 (GRCm39) |
missense |
probably benign |
|
R7234:Mycbp2
|
UTSW |
14 |
103,452,773 (GRCm39) |
missense |
probably damaging |
0.98 |
R7238:Mycbp2
|
UTSW |
14 |
103,393,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R7244:Mycbp2
|
UTSW |
14 |
103,446,345 (GRCm39) |
missense |
probably damaging |
0.98 |
R7265:Mycbp2
|
UTSW |
14 |
103,434,679 (GRCm39) |
critical splice donor site |
probably null |
|
R7286:Mycbp2
|
UTSW |
14 |
103,358,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R7332:Mycbp2
|
UTSW |
14 |
103,434,793 (GRCm39) |
missense |
probably damaging |
0.97 |
R7332:Mycbp2
|
UTSW |
14 |
103,393,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R7384:Mycbp2
|
UTSW |
14 |
103,513,829 (GRCm39) |
missense |
probably damaging |
0.99 |
R7392:Mycbp2
|
UTSW |
14 |
103,480,564 (GRCm39) |
missense |
probably damaging |
0.99 |
R7392:Mycbp2
|
UTSW |
14 |
103,389,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R7409:Mycbp2
|
UTSW |
14 |
103,526,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R7486:Mycbp2
|
UTSW |
14 |
103,434,690 (GRCm39) |
missense |
probably damaging |
0.97 |
R7643:Mycbp2
|
UTSW |
14 |
103,583,701 (GRCm39) |
missense |
probably benign |
|
R7661:Mycbp2
|
UTSW |
14 |
103,450,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R7663:Mycbp2
|
UTSW |
14 |
103,429,045 (GRCm39) |
missense |
probably damaging |
0.99 |
R7730:Mycbp2
|
UTSW |
14 |
103,360,791 (GRCm39) |
missense |
probably damaging |
0.99 |
R7757:Mycbp2
|
UTSW |
14 |
103,429,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R7773:Mycbp2
|
UTSW |
14 |
103,485,840 (GRCm39) |
missense |
probably damaging |
0.97 |
R7787:Mycbp2
|
UTSW |
14 |
103,364,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R7822:Mycbp2
|
UTSW |
14 |
103,376,851 (GRCm39) |
missense |
probably benign |
0.00 |
R7838:Mycbp2
|
UTSW |
14 |
103,414,729 (GRCm39) |
missense |
probably benign |
0.10 |
R7841:Mycbp2
|
UTSW |
14 |
103,384,267 (GRCm39) |
critical splice donor site |
probably null |
|
R7858:Mycbp2
|
UTSW |
14 |
103,393,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R7873:Mycbp2
|
UTSW |
14 |
103,393,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R7911:Mycbp2
|
UTSW |
14 |
103,437,621 (GRCm39) |
missense |
probably damaging |
0.99 |
R7942:Mycbp2
|
UTSW |
14 |
103,392,674 (GRCm39) |
missense |
probably damaging |
0.99 |
R7951:Mycbp2
|
UTSW |
14 |
103,452,898 (GRCm39) |
missense |
probably damaging |
0.99 |
R7958:Mycbp2
|
UTSW |
14 |
103,367,400 (GRCm39) |
missense |
probably benign |
0.00 |
R8235:Mycbp2
|
UTSW |
14 |
103,436,110 (GRCm39) |
missense |
probably damaging |
0.99 |
R8246:Mycbp2
|
UTSW |
14 |
103,392,640 (GRCm39) |
missense |
probably damaging |
0.99 |
R8338:Mycbp2
|
UTSW |
14 |
103,372,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R8343:Mycbp2
|
UTSW |
14 |
103,398,111 (GRCm39) |
splice site |
probably null |
|
R8361:Mycbp2
|
UTSW |
14 |
103,376,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R8490:Mycbp2
|
UTSW |
14 |
103,446,267 (GRCm39) |
missense |
probably benign |
0.00 |
R8524:Mycbp2
|
UTSW |
14 |
103,392,895 (GRCm39) |
missense |
probably benign |
0.23 |
R8525:Mycbp2
|
UTSW |
14 |
103,450,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R8711:Mycbp2
|
UTSW |
14 |
103,407,430 (GRCm39) |
missense |
probably benign |
0.08 |
R8735:Mycbp2
|
UTSW |
14 |
103,460,586 (GRCm39) |
missense |
probably damaging |
0.99 |
R8825:Mycbp2
|
UTSW |
14 |
103,466,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R8928:Mycbp2
|
UTSW |
14 |
103,393,781 (GRCm39) |
missense |
probably benign |
|
R8974:Mycbp2
|
UTSW |
14 |
103,361,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R8987:Mycbp2
|
UTSW |
14 |
103,446,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R9021:Mycbp2
|
UTSW |
14 |
103,551,752 (GRCm39) |
missense |
probably benign |
0.08 |
R9062:Mycbp2
|
UTSW |
14 |
103,479,796 (GRCm39) |
missense |
probably benign |
0.00 |
R9077:Mycbp2
|
UTSW |
14 |
103,469,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R9208:Mycbp2
|
UTSW |
14 |
103,532,664 (GRCm39) |
missense |
probably benign |
0.01 |
R9285:Mycbp2
|
UTSW |
14 |
103,434,753 (GRCm39) |
missense |
probably damaging |
0.97 |
R9290:Mycbp2
|
UTSW |
14 |
103,425,960 (GRCm39) |
missense |
probably damaging |
0.99 |
R9362:Mycbp2
|
UTSW |
14 |
103,497,642 (GRCm39) |
missense |
probably damaging |
0.97 |
R9520:Mycbp2
|
UTSW |
14 |
103,497,705 (GRCm39) |
missense |
probably benign |
0.02 |
R9557:Mycbp2
|
UTSW |
14 |
103,372,697 (GRCm39) |
missense |
probably benign |
0.03 |
R9639:Mycbp2
|
UTSW |
14 |
103,433,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R9666:Mycbp2
|
UTSW |
14 |
103,371,474 (GRCm39) |
missense |
probably damaging |
0.98 |
R9732:Mycbp2
|
UTSW |
14 |
103,448,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R9736:Mycbp2
|
UTSW |
14 |
103,434,852 (GRCm39) |
missense |
probably damaging |
0.96 |
R9739:Mycbp2
|
UTSW |
14 |
103,520,229 (GRCm39) |
missense |
probably benign |
0.11 |
R9755:Mycbp2
|
UTSW |
14 |
103,551,806 (GRCm39) |
missense |
probably benign |
|
X0024:Mycbp2
|
UTSW |
14 |
103,384,378 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Mycbp2
|
UTSW |
14 |
103,583,685 (GRCm39) |
missense |
probably benign |
|
Z1176:Mycbp2
|
UTSW |
14 |
103,394,073 (GRCm39) |
missense |
probably benign |
0.06 |
Z1177:Mycbp2
|
UTSW |
14 |
103,407,309 (GRCm39) |
missense |
possibly damaging |
0.83 |
Z1177:Mycbp2
|
UTSW |
14 |
103,372,559 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Mycbp2
|
UTSW |
14 |
103,364,499 (GRCm39) |
critical splice donor site |
probably null |
|
|