Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700123K08Rik |
G |
A |
5: 138,562,447 (GRCm39) |
T98M |
probably damaging |
Het |
4932414N04Rik |
G |
T |
2: 68,541,392 (GRCm39) |
K10N |
possibly damaging |
Het |
Aadat |
T |
A |
8: 60,960,173 (GRCm39) |
S40T |
probably benign |
Het |
Abca13 |
A |
G |
11: 9,278,098 (GRCm39) |
I3093V |
probably benign |
Het |
Acacb |
A |
T |
5: 114,383,951 (GRCm39) |
Q2160L |
probably damaging |
Het |
Acp6 |
G |
T |
3: 97,075,333 (GRCm39) |
S189I |
probably benign |
Het |
Actr5 |
A |
T |
2: 158,474,213 (GRCm39) |
M339L |
probably benign |
Het |
Adcy1 |
A |
T |
11: 7,111,885 (GRCm39) |
K917* |
probably null |
Het |
Adgrg5 |
C |
T |
8: 95,668,695 (GRCm39) |
R504C |
probably benign |
Het |
Ago1 |
T |
C |
4: 126,354,246 (GRCm39) |
H188R |
probably benign |
Het |
Akap9 |
T |
A |
5: 4,025,685 (GRCm39) |
C23* |
probably null |
Het |
Ank3 |
T |
C |
10: 69,733,920 (GRCm39) |
I728T |
probably damaging |
Het |
Ankrd50 |
A |
G |
3: 38,508,642 (GRCm39) |
S1242P |
probably benign |
Het |
Arhgap29 |
G |
A |
3: 121,775,509 (GRCm39) |
R84H |
probably benign |
Het |
Arhgef10 |
A |
G |
8: 14,995,320 (GRCm39) |
D7G |
probably null |
Het |
Arid4b |
A |
G |
13: 14,362,230 (GRCm39) |
E898G |
probably damaging |
Het |
Atrnl1 |
A |
G |
19: 57,680,281 (GRCm39) |
N727S |
probably benign |
Het |
Baalc |
G |
T |
15: 38,796,629 (GRCm39) |
|
probably benign |
Het |
Cdc25c |
G |
C |
18: 34,871,292 (GRCm39) |
L275V |
probably damaging |
Het |
Chpf2 |
G |
T |
5: 24,796,274 (GRCm39) |
V407L |
probably benign |
Het |
Chrnb3 |
C |
A |
8: 27,876,839 (GRCm39) |
N84K |
probably damaging |
Het |
Cnot1 |
A |
G |
8: 96,451,221 (GRCm39) |
F2171L |
possibly damaging |
Het |
Csmd3 |
C |
T |
15: 48,485,389 (GRCm39) |
|
probably null |
Het |
Cux1 |
T |
A |
5: 136,361,512 (GRCm39) |
Q138L |
probably damaging |
Het |
Cyp2c65 |
A |
G |
19: 39,070,675 (GRCm39) |
N286S |
probably benign |
Het |
Dclre1b |
T |
C |
3: 103,716,356 (GRCm39) |
S17G |
possibly damaging |
Het |
Dlgap5 |
A |
G |
14: 47,648,941 (GRCm39) |
S221P |
probably benign |
Het |
Dnah1 |
T |
G |
14: 31,001,080 (GRCm39) |
T2422P |
probably damaging |
Het |
Enpp1 |
A |
G |
10: 24,587,702 (GRCm39) |
|
probably null |
Het |
Erbb2 |
T |
C |
11: 98,310,998 (GRCm39) |
C53R |
probably damaging |
Het |
Exoc8 |
A |
G |
8: 125,622,219 (GRCm39) |
V716A |
probably benign |
Het |
Fam193a |
T |
A |
5: 34,619,494 (GRCm39) |
D766E |
probably benign |
Het |
Fbxo43 |
C |
A |
15: 36,162,278 (GRCm39) |
G310W |
probably damaging |
Het |
Fcgbp |
C |
T |
7: 27,819,785 (GRCm39) |
T2504I |
probably damaging |
Het |
Fnbp4 |
C |
T |
2: 90,587,876 (GRCm39) |
P418L |
probably benign |
Het |
Gjd2 |
T |
C |
2: 113,841,539 (GRCm39) |
T313A |
probably damaging |
Het |
Gm12695 |
T |
A |
4: 96,658,008 (GRCm39) |
R54W |
probably damaging |
Het |
Gm128 |
T |
C |
3: 95,148,051 (GRCm39) |
D81G |
possibly damaging |
Het |
Gm21834 |
A |
G |
17: 58,048,763 (GRCm39) |
V151A |
possibly damaging |
Het |
Grhl1 |
T |
A |
12: 24,636,151 (GRCm39) |
|
probably null |
Het |
Hcn1 |
C |
T |
13: 118,112,619 (GRCm39) |
T861I |
probably damaging |
Het |
Herc6 |
C |
A |
6: 57,602,961 (GRCm39) |
Q547K |
probably benign |
Het |
Iqgap3 |
T |
C |
3: 88,027,474 (GRCm39) |
L699P |
probably damaging |
Het |
Kank4 |
T |
C |
4: 98,668,339 (GRCm39) |
D36G |
probably damaging |
Het |
Kcnk5 |
A |
T |
14: 20,192,277 (GRCm39) |
S295T |
probably damaging |
Het |
Krt18 |
T |
C |
15: 101,937,935 (GRCm39) |
V144A |
probably benign |
Het |
Krtap9-5 |
A |
G |
11: 99,840,030 (GRCm39) |
I244V |
unknown |
Het |
Leng1 |
T |
G |
7: 3,668,400 (GRCm39) |
N16T |
probably damaging |
Het |
Lss |
A |
G |
10: 76,367,712 (GRCm39) |
K15E |
possibly damaging |
Het |
Mastl |
G |
T |
2: 23,022,836 (GRCm39) |
A629E |
possibly damaging |
Het |
Mavs |
G |
C |
2: 131,082,370 (GRCm39) |
A85P |
possibly damaging |
Het |
Nav3 |
T |
C |
10: 109,660,536 (GRCm39) |
D678G |
probably damaging |
Het |
Nsd3 |
T |
G |
8: 26,181,116 (GRCm39) |
S906A |
probably damaging |
Het |
Nsfl1c |
A |
G |
2: 151,345,002 (GRCm39) |
N118S |
probably damaging |
Het |
Nup205 |
T |
A |
6: 35,207,451 (GRCm39) |
M1501K |
probably benign |
Het |
Or4p7 |
C |
T |
2: 88,221,882 (GRCm39) |
T97M |
possibly damaging |
Het |
Or6n1 |
T |
A |
1: 173,916,785 (GRCm39) |
Y60N |
possibly damaging |
Het |
Pax8 |
A |
G |
2: 24,326,520 (GRCm39) |
S281P |
probably benign |
Het |
Pds5b |
T |
G |
5: 150,671,655 (GRCm39) |
I433R |
probably damaging |
Het |
Peg3 |
T |
C |
7: 6,715,720 (GRCm39) |
N117D |
probably damaging |
Het |
Pfkm |
A |
T |
15: 98,029,573 (GRCm39) |
D728V |
probably benign |
Het |
Phkb |
T |
C |
8: 86,776,450 (GRCm39) |
|
probably null |
Het |
Pkp4 |
T |
C |
2: 59,165,248 (GRCm39) |
V704A |
probably benign |
Het |
Ppfia2 |
T |
A |
10: 106,673,160 (GRCm39) |
S501T |
probably damaging |
Het |
Ptpru |
T |
C |
4: 131,546,398 (GRCm39) |
E284G |
possibly damaging |
Het |
Ror1 |
C |
T |
4: 100,265,065 (GRCm39) |
R180* |
probably null |
Het |
Ryr3 |
T |
A |
2: 112,586,986 (GRCm39) |
Y2666F |
probably damaging |
Het |
Sec23a |
C |
A |
12: 59,037,754 (GRCm39) |
|
probably null |
Het |
Sertad3 |
C |
T |
7: 27,175,694 (GRCm39) |
Q43* |
probably null |
Het |
Setd2 |
C |
T |
9: 110,379,958 (GRCm39) |
H1258Y |
probably benign |
Het |
Sharpin |
A |
G |
15: 76,232,407 (GRCm39) |
S177P |
probably benign |
Het |
Skap1 |
T |
C |
11: 96,432,289 (GRCm39) |
F86S |
possibly damaging |
Het |
Slc8a2 |
T |
C |
7: 15,874,940 (GRCm39) |
I396T |
probably damaging |
Het |
Slc9a2 |
T |
C |
1: 40,765,597 (GRCm39) |
F329S |
probably damaging |
Het |
Slx4ip |
C |
T |
2: 136,908,125 (GRCm39) |
L161F |
possibly damaging |
Het |
Sox4 |
A |
G |
13: 29,136,764 (GRCm39) |
S81P |
probably damaging |
Het |
Ssc4d |
G |
T |
5: 135,999,118 (GRCm39) |
S28R |
probably benign |
Het |
St8sia2 |
C |
T |
7: 73,592,950 (GRCm39) |
G369S |
possibly damaging |
Het |
Swt1 |
T |
C |
1: 151,248,081 (GRCm39) |
Y836C |
probably damaging |
Het |
Taar7d |
A |
G |
10: 23,903,904 (GRCm39) |
D262G |
probably benign |
Het |
Taar8b |
T |
A |
10: 23,967,212 (GRCm39) |
L327F |
probably benign |
Het |
Tars1 |
A |
T |
15: 11,393,280 (GRCm39) |
L138* |
probably null |
Het |
Tbcd |
A |
T |
11: 121,344,496 (GRCm39) |
D75V |
probably damaging |
Het |
Tesc |
A |
G |
5: 118,184,394 (GRCm39) |
I25V |
probably damaging |
Het |
Tmem132e |
G |
T |
11: 82,331,264 (GRCm39) |
S407I |
probably damaging |
Het |
Tmem50b |
C |
A |
16: 91,377,180 (GRCm39) |
A95S |
possibly damaging |
Het |
Tnr |
T |
C |
1: 159,719,603 (GRCm39) |
I960T |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Tpcn1 |
G |
C |
5: 120,681,453 (GRCm39) |
P532A |
probably damaging |
Het |
Tpsb2 |
T |
C |
17: 25,585,539 (GRCm39) |
|
probably benign |
Het |
Triobp |
C |
A |
15: 78,888,740 (GRCm39) |
H1948Q |
probably damaging |
Het |
Tshb |
T |
C |
3: 102,684,857 (GRCm39) |
I116V |
probably benign |
Het |
Ttc13 |
A |
T |
8: 125,398,950 (GRCm39) |
|
probably null |
Het |
Vmn2r18 |
A |
T |
5: 151,486,016 (GRCm39) |
C493S |
possibly damaging |
Het |
Vmn2r2 |
T |
C |
3: 64,024,766 (GRCm39) |
K605R |
possibly damaging |
Het |
Vmn2r37 |
T |
C |
7: 9,220,792 (GRCm39) |
Y357C |
probably damaging |
Het |
Zc3h6 |
T |
G |
2: 128,857,538 (GRCm39) |
S686A |
possibly damaging |
Het |
Zfp608 |
G |
A |
18: 55,121,386 (GRCm39) |
P67L |
probably benign |
Het |
Zyg11a |
T |
C |
4: 108,049,244 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Usp34 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Usp34
|
APN |
11 |
23,386,020 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00477:Usp34
|
APN |
11 |
23,418,879 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01307:Usp34
|
APN |
11 |
23,367,676 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01313:Usp34
|
APN |
11 |
23,423,206 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01794:Usp34
|
APN |
11 |
23,386,020 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01826:Usp34
|
APN |
11 |
23,386,020 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01827:Usp34
|
APN |
11 |
23,386,020 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01830:Usp34
|
APN |
11 |
23,386,020 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01867:Usp34
|
APN |
11 |
23,334,411 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL01939:Usp34
|
APN |
11 |
23,295,141 (GRCm39) |
splice site |
probably benign |
|
IGL01977:Usp34
|
APN |
11 |
23,402,661 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01985:Usp34
|
APN |
11 |
23,402,565 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02011:Usp34
|
APN |
11 |
23,421,554 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02302:Usp34
|
APN |
11 |
23,417,243 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02423:Usp34
|
APN |
11 |
23,304,900 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02491:Usp34
|
APN |
11 |
23,382,630 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02532:Usp34
|
APN |
11 |
23,320,291 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02561:Usp34
|
APN |
11 |
23,301,652 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02706:Usp34
|
APN |
11 |
23,338,659 (GRCm39) |
splice site |
probably benign |
|
IGL02891:Usp34
|
APN |
11 |
23,437,166 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03079:Usp34
|
APN |
11 |
23,382,247 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL03089:Usp34
|
APN |
11 |
23,396,958 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03175:Usp34
|
APN |
11 |
23,438,686 (GRCm39) |
missense |
probably benign |
|
IGL03256:Usp34
|
APN |
11 |
23,370,090 (GRCm39) |
nonsense |
probably null |
|
IGL03280:Usp34
|
APN |
11 |
23,304,897 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03289:Usp34
|
APN |
11 |
23,343,818 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03408:Usp34
|
APN |
11 |
23,396,957 (GRCm39) |
missense |
possibly damaging |
0.92 |
Chub
|
UTSW |
11 |
23,414,686 (GRCm39) |
missense |
probably damaging |
0.99 |
Cicione
|
UTSW |
11 |
23,439,033 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5571_Usp34_680
|
UTSW |
11 |
23,407,975 (GRCm39) |
missense |
probably damaging |
0.99 |
R5713_Usp34_003
|
UTSW |
11 |
23,293,515 (GRCm39) |
missense |
possibly damaging |
0.94 |
Roebuck
|
UTSW |
11 |
23,436,810 (GRCm39) |
splice site |
probably benign |
|
stoat
|
UTSW |
11 |
23,437,203 (GRCm39) |
missense |
|
|
tunnelvision
|
UTSW |
11 |
23,396,968 (GRCm39) |
missense |
|
|
I2288:Usp34
|
UTSW |
11 |
23,382,473 (GRCm39) |
splice site |
probably benign |
|
R0047:Usp34
|
UTSW |
11 |
23,414,403 (GRCm39) |
missense |
probably benign |
0.34 |
R0047:Usp34
|
UTSW |
11 |
23,414,403 (GRCm39) |
missense |
probably benign |
0.34 |
R0099:Usp34
|
UTSW |
11 |
23,313,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Usp34
|
UTSW |
11 |
23,383,206 (GRCm39) |
missense |
probably damaging |
0.99 |
R0240:Usp34
|
UTSW |
11 |
23,383,206 (GRCm39) |
missense |
probably damaging |
0.99 |
R0403:Usp34
|
UTSW |
11 |
23,283,838 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0432:Usp34
|
UTSW |
11 |
23,351,505 (GRCm39) |
missense |
probably damaging |
0.99 |
R0446:Usp34
|
UTSW |
11 |
23,417,207 (GRCm39) |
missense |
probably damaging |
0.97 |
R0455:Usp34
|
UTSW |
11 |
23,396,741 (GRCm39) |
splice site |
probably benign |
|
R0470:Usp34
|
UTSW |
11 |
23,386,001 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0472:Usp34
|
UTSW |
11 |
23,334,509 (GRCm39) |
splice site |
probably benign |
|
R0512:Usp34
|
UTSW |
11 |
23,401,997 (GRCm39) |
missense |
probably benign |
0.04 |
R0557:Usp34
|
UTSW |
11 |
23,353,848 (GRCm39) |
missense |
probably damaging |
0.98 |
R0562:Usp34
|
UTSW |
11 |
23,382,406 (GRCm39) |
splice site |
probably benign |
|
R0656:Usp34
|
UTSW |
11 |
23,422,967 (GRCm39) |
missense |
probably damaging |
0.99 |
R0693:Usp34
|
UTSW |
11 |
23,402,637 (GRCm39) |
missense |
probably damaging |
0.97 |
R0739:Usp34
|
UTSW |
11 |
23,417,243 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1061:Usp34
|
UTSW |
11 |
23,334,420 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1078:Usp34
|
UTSW |
11 |
23,383,175 (GRCm39) |
splice site |
probably benign |
|
R1223:Usp34
|
UTSW |
11 |
23,396,464 (GRCm39) |
splice site |
probably null |
|
R1295:Usp34
|
UTSW |
11 |
23,334,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R1430:Usp34
|
UTSW |
11 |
23,409,151 (GRCm39) |
missense |
probably damaging |
0.97 |
R1445:Usp34
|
UTSW |
11 |
23,301,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R1468:Usp34
|
UTSW |
11 |
23,391,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Usp34
|
UTSW |
11 |
23,391,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R1471:Usp34
|
UTSW |
11 |
23,438,862 (GRCm39) |
missense |
probably benign |
0.20 |
R1475:Usp34
|
UTSW |
11 |
23,423,253 (GRCm39) |
missense |
probably damaging |
0.99 |
R1628:Usp34
|
UTSW |
11 |
23,438,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R1631:Usp34
|
UTSW |
11 |
23,410,651 (GRCm39) |
missense |
probably damaging |
0.99 |
R1655:Usp34
|
UTSW |
11 |
23,325,051 (GRCm39) |
missense |
probably benign |
0.05 |
R1741:Usp34
|
UTSW |
11 |
23,314,103 (GRCm39) |
missense |
probably benign |
0.00 |
R1854:Usp34
|
UTSW |
11 |
23,376,153 (GRCm39) |
missense |
probably benign |
0.24 |
R1867:Usp34
|
UTSW |
11 |
23,311,593 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1869:Usp34
|
UTSW |
11 |
23,314,479 (GRCm39) |
missense |
probably benign |
0.37 |
R1870:Usp34
|
UTSW |
11 |
23,314,479 (GRCm39) |
missense |
probably benign |
0.37 |
R1871:Usp34
|
UTSW |
11 |
23,314,479 (GRCm39) |
missense |
probably benign |
0.37 |
R1967:Usp34
|
UTSW |
11 |
23,314,503 (GRCm39) |
missense |
probably benign |
0.01 |
R2132:Usp34
|
UTSW |
11 |
23,414,556 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2156:Usp34
|
UTSW |
11 |
23,332,602 (GRCm39) |
missense |
probably damaging |
0.98 |
R2205:Usp34
|
UTSW |
11 |
23,335,147 (GRCm39) |
missense |
probably damaging |
0.97 |
R2342:Usp34
|
UTSW |
11 |
23,353,599 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3431:Usp34
|
UTSW |
11 |
23,320,466 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3812:Usp34
|
UTSW |
11 |
23,414,517 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3872:Usp34
|
UTSW |
11 |
23,439,033 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3873:Usp34
|
UTSW |
11 |
23,439,033 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3874:Usp34
|
UTSW |
11 |
23,439,033 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3875:Usp34
|
UTSW |
11 |
23,439,033 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3925:Usp34
|
UTSW |
11 |
23,293,640 (GRCm39) |
missense |
probably benign |
0.28 |
R3972:Usp34
|
UTSW |
11 |
23,407,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R4018:Usp34
|
UTSW |
11 |
23,439,033 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4042:Usp34
|
UTSW |
11 |
23,439,033 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4155:Usp34
|
UTSW |
11 |
23,367,676 (GRCm39) |
missense |
probably damaging |
0.99 |
R4197:Usp34
|
UTSW |
11 |
23,394,189 (GRCm39) |
missense |
probably damaging |
0.98 |
R4352:Usp34
|
UTSW |
11 |
23,270,727 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4379:Usp34
|
UTSW |
11 |
23,334,499 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4444:Usp34
|
UTSW |
11 |
23,385,998 (GRCm39) |
missense |
probably damaging |
0.98 |
R4475:Usp34
|
UTSW |
11 |
23,407,975 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4501:Usp34
|
UTSW |
11 |
23,351,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R4527:Usp34
|
UTSW |
11 |
23,371,257 (GRCm39) |
missense |
possibly damaging |
0.57 |
R4603:Usp34
|
UTSW |
11 |
23,414,633 (GRCm39) |
missense |
probably damaging |
0.97 |
R4612:Usp34
|
UTSW |
11 |
23,382,268 (GRCm39) |
missense |
probably damaging |
0.99 |
R4673:Usp34
|
UTSW |
11 |
23,314,480 (GRCm39) |
small deletion |
probably benign |
|
R4707:Usp34
|
UTSW |
11 |
23,437,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R4736:Usp34
|
UTSW |
11 |
23,343,749 (GRCm39) |
splice site |
probably null |
|
R4867:Usp34
|
UTSW |
11 |
23,401,999 (GRCm39) |
missense |
probably benign |
0.28 |
R4879:Usp34
|
UTSW |
11 |
23,323,410 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4977:Usp34
|
UTSW |
11 |
23,438,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R5004:Usp34
|
UTSW |
11 |
23,414,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R5057:Usp34
|
UTSW |
11 |
23,408,086 (GRCm39) |
intron |
probably benign |
|
R5068:Usp34
|
UTSW |
11 |
23,410,665 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5304:Usp34
|
UTSW |
11 |
23,293,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R5320:Usp34
|
UTSW |
11 |
23,283,739 (GRCm39) |
missense |
probably benign |
|
R5327:Usp34
|
UTSW |
11 |
23,418,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R5328:Usp34
|
UTSW |
11 |
23,438,659 (GRCm39) |
missense |
probably benign |
0.04 |
R5328:Usp34
|
UTSW |
11 |
23,414,616 (GRCm39) |
missense |
probably benign |
0.01 |
R5390:Usp34
|
UTSW |
11 |
23,394,202 (GRCm39) |
critical splice donor site |
probably null |
|
R5434:Usp34
|
UTSW |
11 |
23,362,271 (GRCm39) |
missense |
probably damaging |
0.99 |
R5523:Usp34
|
UTSW |
11 |
23,299,198 (GRCm39) |
missense |
probably benign |
0.39 |
R5567:Usp34
|
UTSW |
11 |
23,438,336 (GRCm39) |
missense |
probably damaging |
0.97 |
R5571:Usp34
|
UTSW |
11 |
23,407,975 (GRCm39) |
missense |
probably damaging |
0.99 |
R5645:Usp34
|
UTSW |
11 |
23,325,024 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5713:Usp34
|
UTSW |
11 |
23,293,515 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5719:Usp34
|
UTSW |
11 |
23,304,846 (GRCm39) |
missense |
probably benign |
0.00 |
R5813:Usp34
|
UTSW |
11 |
23,371,340 (GRCm39) |
missense |
probably benign |
0.38 |
R5921:Usp34
|
UTSW |
11 |
23,414,686 (GRCm39) |
missense |
probably damaging |
0.99 |
R5928:Usp34
|
UTSW |
11 |
23,386,040 (GRCm39) |
missense |
probably damaging |
0.98 |
R5944:Usp34
|
UTSW |
11 |
23,313,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R6198:Usp34
|
UTSW |
11 |
23,434,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R6229:Usp34
|
UTSW |
11 |
23,396,778 (GRCm39) |
missense |
probably damaging |
0.99 |
R6306:Usp34
|
UTSW |
11 |
23,362,260 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6320:Usp34
|
UTSW |
11 |
23,402,520 (GRCm39) |
missense |
probably damaging |
0.98 |
R6341:Usp34
|
UTSW |
11 |
23,331,353 (GRCm39) |
missense |
probably damaging |
0.97 |
R6374:Usp34
|
UTSW |
11 |
23,388,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R6398:Usp34
|
UTSW |
11 |
23,438,666 (GRCm39) |
missense |
probably benign |
|
R6438:Usp34
|
UTSW |
11 |
23,314,266 (GRCm39) |
missense |
probably benign |
0.02 |
R6668:Usp34
|
UTSW |
11 |
23,410,659 (GRCm39) |
missense |
probably damaging |
0.97 |
R6700:Usp34
|
UTSW |
11 |
23,389,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R6783:Usp34
|
UTSW |
11 |
23,362,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R6821:Usp34
|
UTSW |
11 |
23,317,491 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6855:Usp34
|
UTSW |
11 |
23,402,569 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6916:Usp34
|
UTSW |
11 |
23,408,023 (GRCm39) |
missense |
probably damaging |
0.98 |
R7020:Usp34
|
UTSW |
11 |
23,343,954 (GRCm39) |
missense |
probably benign |
0.05 |
R7026:Usp34
|
UTSW |
11 |
23,311,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R7085:Usp34
|
UTSW |
11 |
23,313,097 (GRCm39) |
missense |
|
|
R7101:Usp34
|
UTSW |
11 |
23,376,183 (GRCm39) |
missense |
|
|
R7168:Usp34
|
UTSW |
11 |
23,414,585 (GRCm39) |
missense |
|
|
R7192:Usp34
|
UTSW |
11 |
23,410,571 (GRCm39) |
missense |
|
|
R7264:Usp34
|
UTSW |
11 |
23,283,566 (GRCm39) |
missense |
probably benign |
0.00 |
R7325:Usp34
|
UTSW |
11 |
23,369,052 (GRCm39) |
missense |
|
|
R7343:Usp34
|
UTSW |
11 |
23,438,868 (GRCm39) |
missense |
|
|
R7358:Usp34
|
UTSW |
11 |
23,311,683 (GRCm39) |
missense |
probably damaging |
0.99 |
R7369:Usp34
|
UTSW |
11 |
23,382,361 (GRCm39) |
missense |
|
|
R7389:Usp34
|
UTSW |
11 |
23,295,200 (GRCm39) |
missense |
|
|
R7459:Usp34
|
UTSW |
11 |
23,314,458 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7517:Usp34
|
UTSW |
11 |
23,396,968 (GRCm39) |
missense |
|
|
R7729:Usp34
|
UTSW |
11 |
23,399,268 (GRCm39) |
missense |
|
|
R7777:Usp34
|
UTSW |
11 |
23,332,638 (GRCm39) |
missense |
|
|
R7810:Usp34
|
UTSW |
11 |
23,362,314 (GRCm39) |
missense |
|
|
R7836:Usp34
|
UTSW |
11 |
23,396,614 (GRCm39) |
missense |
|
|
R7862:Usp34
|
UTSW |
11 |
23,414,718 (GRCm39) |
missense |
|
|
R7993:Usp34
|
UTSW |
11 |
23,327,622 (GRCm39) |
missense |
|
|
R8050:Usp34
|
UTSW |
11 |
23,396,787 (GRCm39) |
missense |
|
|
R8054:Usp34
|
UTSW |
11 |
23,311,295 (GRCm39) |
missense |
|
|
R8239:Usp34
|
UTSW |
11 |
23,396,750 (GRCm39) |
missense |
|
|
R8266:Usp34
|
UTSW |
11 |
23,436,810 (GRCm39) |
splice site |
probably benign |
|
R8347:Usp34
|
UTSW |
11 |
23,362,345 (GRCm39) |
missense |
|
|
R8409:Usp34
|
UTSW |
11 |
23,407,811 (GRCm39) |
missense |
|
|
R8692:Usp34
|
UTSW |
11 |
23,379,325 (GRCm39) |
missense |
|
|
R8694:Usp34
|
UTSW |
11 |
23,434,161 (GRCm39) |
missense |
|
|
R8734:Usp34
|
UTSW |
11 |
23,394,184 (GRCm39) |
missense |
|
|
R8806:Usp34
|
UTSW |
11 |
23,434,143 (GRCm39) |
missense |
|
|
R8914:Usp34
|
UTSW |
11 |
23,293,604 (GRCm39) |
missense |
|
|
R8987:Usp34
|
UTSW |
11 |
23,414,267 (GRCm39) |
missense |
|
|
R9013:Usp34
|
UTSW |
11 |
23,320,302 (GRCm39) |
missense |
|
|
R9108:Usp34
|
UTSW |
11 |
23,320,528 (GRCm39) |
missense |
|
|
R9264:Usp34
|
UTSW |
11 |
23,439,064 (GRCm39) |
missense |
|
|
R9301:Usp34
|
UTSW |
11 |
23,422,951 (GRCm39) |
missense |
|
|
R9375:Usp34
|
UTSW |
11 |
23,437,203 (GRCm39) |
missense |
|
|
R9385:Usp34
|
UTSW |
11 |
23,399,223 (GRCm39) |
missense |
|
|
R9500:Usp34
|
UTSW |
11 |
23,331,337 (GRCm39) |
missense |
probably damaging |
0.99 |
R9566:Usp34
|
UTSW |
11 |
23,317,529 (GRCm39) |
missense |
|
|
R9629:Usp34
|
UTSW |
11 |
23,314,364 (GRCm39) |
missense |
|
|
R9679:Usp34
|
UTSW |
11 |
23,394,369 (GRCm39) |
missense |
|
|
R9680:Usp34
|
UTSW |
11 |
23,317,385 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9686:Usp34
|
UTSW |
11 |
23,424,351 (GRCm39) |
missense |
|
|
R9752:Usp34
|
UTSW |
11 |
23,409,182 (GRCm39) |
missense |
probably benign |
0.11 |
X0023:Usp34
|
UTSW |
11 |
23,325,028 (GRCm39) |
missense |
possibly damaging |
0.73 |
X0057:Usp34
|
UTSW |
11 |
23,407,824 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1176:Usp34
|
UTSW |
11 |
23,423,221 (GRCm39) |
missense |
probably damaging |
1.00 |
|