Other mutations in this stock |
Total: 121 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
G |
11: 9,278,096 (GRCm39) |
E3092G |
probably damaging |
Het |
Abhd12b |
C |
G |
12: 70,215,838 (GRCm39) |
S170C |
probably damaging |
Het |
Abtb2 |
A |
T |
2: 103,547,644 (GRCm39) |
D1006V |
probably benign |
Het |
Abtb3 |
A |
C |
10: 85,490,414 (GRCm39) |
I1027L |
probably damaging |
Het |
Adgrl1 |
A |
G |
8: 84,662,202 (GRCm39) |
H1021R |
probably benign |
Het |
Ago3 |
A |
T |
4: 126,241,665 (GRCm39) |
|
probably null |
Het |
Ahnak |
A |
G |
19: 8,989,863 (GRCm39) |
|
probably benign |
Het |
Akap6 |
CA |
C |
12: 52,934,406 (GRCm39) |
|
probably null |
Het |
Amotl2 |
T |
G |
9: 102,597,322 (GRCm39) |
|
probably null |
Het |
Ankrd34b |
T |
A |
13: 92,574,813 (GRCm39) |
I15N |
probably damaging |
Het |
Ap3d1 |
C |
T |
10: 80,557,420 (GRCm39) |
|
probably null |
Het |
Appl2 |
A |
T |
10: 83,436,855 (GRCm39) |
D635E |
probably damaging |
Het |
Arid1b |
C |
T |
17: 5,389,496 (GRCm39) |
P1681S |
probably damaging |
Het |
Atp10a |
T |
C |
7: 58,440,843 (GRCm39) |
M496T |
probably benign |
Het |
Atp2c2 |
A |
G |
8: 120,475,891 (GRCm39) |
K595E |
probably damaging |
Het |
Atpaf2 |
T |
C |
11: 60,295,238 (GRCm39) |
H204R |
probably damaging |
Het |
Atr |
G |
A |
9: 95,744,850 (GRCm39) |
V56I |
probably benign |
Het |
Bod1l |
G |
A |
5: 41,991,006 (GRCm39) |
T183I |
probably benign |
Het |
Ccdc168 |
T |
C |
1: 44,098,203 (GRCm39) |
D965G |
possibly damaging |
Het |
Ccdc171 |
A |
T |
4: 83,599,253 (GRCm39) |
E689D |
probably damaging |
Het |
Cdc73 |
T |
A |
1: 143,503,613 (GRCm39) |
Q346L |
probably benign |
Het |
Cert1 |
T |
C |
13: 96,748,773 (GRCm39) |
V281A |
probably benign |
Het |
Chd2 |
A |
T |
7: 73,134,184 (GRCm39) |
M721K |
possibly damaging |
Het |
Col22a1 |
T |
A |
15: 71,673,774 (GRCm39) |
T981S |
unknown |
Het |
Cpox |
G |
A |
16: 58,492,986 (GRCm39) |
A207T |
probably damaging |
Het |
Cym |
G |
A |
3: 107,123,413 (GRCm39) |
T160I |
possibly damaging |
Het |
D130043K22Rik |
T |
C |
13: 25,062,023 (GRCm39) |
I664T |
probably damaging |
Het |
Ddx4 |
C |
T |
13: 112,750,230 (GRCm39) |
|
probably null |
Het |
Ddx4 |
A |
T |
13: 112,787,894 (GRCm39) |
V15E |
probably benign |
Het |
Depdc1a |
G |
A |
3: 159,232,273 (GRCm39) |
E675K |
probably damaging |
Het |
Dglucy |
A |
T |
12: 100,816,602 (GRCm39) |
M415L |
probably benign |
Het |
Dlg4 |
C |
T |
11: 69,917,780 (GRCm39) |
P21L |
probably damaging |
Het |
Dmxl1 |
A |
T |
18: 49,996,059 (GRCm39) |
N395I |
probably damaging |
Het |
Dzank1 |
A |
T |
2: 144,346,319 (GRCm39) |
C249S |
probably damaging |
Het |
Efnb2 |
A |
T |
8: 8,673,104 (GRCm39) |
|
probably null |
Het |
Ercc6l2 |
T |
G |
13: 63,982,552 (GRCm39) |
I244S |
probably damaging |
Het |
Ewsr1 |
A |
T |
11: 5,020,423 (GRCm39) |
M584K |
unknown |
Het |
Fam193b |
A |
G |
13: 55,691,284 (GRCm39) |
S197P |
probably damaging |
Het |
Fanca |
A |
G |
8: 124,014,941 (GRCm39) |
V689A |
probably damaging |
Het |
Fbxo31 |
A |
T |
8: 122,279,178 (GRCm39) |
Y436* |
probably null |
Het |
Fbxo31 |
A |
G |
8: 122,279,180 (GRCm39) |
Y436H |
probably damaging |
Het |
Fcna |
T |
A |
2: 25,515,338 (GRCm39) |
D215V |
probably damaging |
Het |
Foxj3 |
A |
T |
4: 119,478,857 (GRCm39) |
S438C |
unknown |
Het |
Gcm2 |
T |
C |
13: 41,256,970 (GRCm39) |
K260E |
possibly damaging |
Het |
Gcnt4 |
A |
T |
13: 97,083,914 (GRCm39) |
L403F |
possibly damaging |
Het |
Gdf10 |
A |
G |
14: 33,653,870 (GRCm39) |
T126A |
probably benign |
Het |
Ggcx |
A |
G |
6: 72,405,875 (GRCm39) |
K569E |
probably benign |
Het |
Gm10250 |
C |
T |
15: 5,150,578 (GRCm39) |
|
probably benign |
Het |
Gpnmb |
G |
T |
6: 49,022,417 (GRCm39) |
|
probably null |
Het |
Ifi44 |
G |
A |
3: 151,451,229 (GRCm39) |
P241S |
probably damaging |
Het |
Irs1 |
T |
C |
1: 82,265,184 (GRCm39) |
T1011A |
probably benign |
Het |
Jag2 |
A |
T |
12: 112,877,869 (GRCm39) |
S595T |
probably benign |
Het |
Kif5a |
T |
A |
10: 127,066,823 (GRCm39) |
Q960L |
probably benign |
Het |
Kifc2 |
A |
G |
15: 76,548,548 (GRCm39) |
E430G |
possibly damaging |
Het |
Lama3 |
T |
A |
18: 12,544,627 (GRCm39) |
C323* |
probably null |
Het |
Lgsn |
T |
C |
1: 31,242,823 (GRCm39) |
Y302H |
probably benign |
Het |
Lmbrd1 |
G |
A |
1: 24,784,056 (GRCm39) |
|
probably null |
Het |
Lrpap1 |
A |
G |
5: 35,256,622 (GRCm39) |
V120A |
probably damaging |
Het |
Macrod2 |
T |
A |
2: 140,261,858 (GRCm39) |
D46E |
possibly damaging |
Het |
Mbd4 |
C |
A |
6: 115,822,283 (GRCm39) |
R63L |
possibly damaging |
Het |
Mfsd10 |
T |
C |
5: 34,792,293 (GRCm39) |
|
probably benign |
Het |
Mib2 |
G |
T |
4: 155,744,229 (GRCm39) |
S144R |
probably benign |
Het |
Muc5b |
T |
A |
7: 141,401,453 (GRCm39) |
C566* |
probably null |
Het |
Ndufs1 |
C |
A |
1: 63,200,108 (GRCm39) |
G268V |
probably damaging |
Het |
Nfs1 |
A |
G |
2: 155,976,369 (GRCm39) |
V175A |
possibly damaging |
Het |
Ngb |
G |
A |
12: 87,146,999 (GRCm39) |
H73Y |
probably benign |
Het |
Npepps |
G |
A |
11: 97,117,652 (GRCm39) |
T549I |
probably damaging |
Het |
Nr1h2 |
A |
G |
7: 44,199,923 (GRCm39) |
V329A |
possibly damaging |
Het |
Nsun6 |
T |
C |
2: 15,041,137 (GRCm39) |
I151M |
possibly damaging |
Het |
Ofcc1 |
T |
C |
13: 40,155,368 (GRCm39) |
|
probably null |
Het |
Or1e31 |
C |
T |
11: 73,689,665 (GRCm39) |
C306Y |
probably benign |
Het |
Or2y16 |
T |
A |
11: 49,334,696 (GRCm39) |
F6Y |
probably benign |
Het |
Or2z8 |
A |
G |
8: 72,811,938 (GRCm39) |
N138S |
probably benign |
Het |
Or51h1 |
T |
A |
7: 102,308,041 (GRCm39) |
N4K |
possibly damaging |
Het |
Or5an1c |
C |
T |
19: 12,218,936 (GRCm39) |
V30I |
probably benign |
Het |
Or8b46 |
A |
G |
9: 38,450,371 (GRCm39) |
Y60C |
probably damaging |
Het |
Parp6 |
A |
G |
9: 59,542,267 (GRCm39) |
|
probably null |
Het |
Pcnt |
C |
A |
10: 76,245,411 (GRCm39) |
R1075S |
possibly damaging |
Het |
Pla2g4f |
T |
C |
2: 120,133,757 (GRCm39) |
E548G |
probably damaging |
Het |
Polrmt |
G |
T |
10: 79,575,357 (GRCm39) |
H725N |
probably benign |
Het |
Pou2f3 |
T |
C |
9: 43,051,153 (GRCm39) |
T178A |
probably damaging |
Het |
Prtn3 |
C |
A |
10: 79,717,899 (GRCm39) |
P169H |
probably damaging |
Het |
Ptprd |
A |
G |
4: 76,009,769 (GRCm39) |
I764T |
probably benign |
Het |
Ptprh |
A |
T |
7: 4,572,576 (GRCm39) |
H467Q |
probably benign |
Het |
Raph1 |
A |
T |
1: 60,528,273 (GRCm39) |
I996N |
probably damaging |
Het |
Rasa4 |
G |
A |
5: 136,120,083 (GRCm39) |
W53* |
probably null |
Het |
Rasgrp1 |
C |
T |
2: 117,115,356 (GRCm39) |
R744Q |
probably benign |
Het |
Rmnd5a |
T |
C |
6: 71,390,333 (GRCm39) |
E141G |
probably damaging |
Het |
Rps12 |
T |
C |
10: 23,662,688 (GRCm39) |
I51M |
possibly damaging |
Het |
Scn10a |
T |
G |
9: 119,451,976 (GRCm39) |
S1316R |
possibly damaging |
Het |
Sdhb |
A |
G |
4: 140,704,777 (GRCm39) |
H246R |
possibly damaging |
Het |
Setx |
G |
A |
2: 29,034,058 (GRCm39) |
R332Q |
probably damaging |
Het |
Siglec1 |
A |
C |
2: 130,917,843 (GRCm39) |
S1011R |
probably damaging |
Het |
Sin3b |
A |
C |
8: 73,452,271 (GRCm39) |
I126L |
probably benign |
Het |
Slc11a1 |
T |
G |
1: 74,423,247 (GRCm39) |
L366R |
probably damaging |
Het |
Slc12a1 |
C |
T |
2: 125,002,999 (GRCm39) |
R177* |
probably null |
Het |
Slc30a1 |
A |
C |
1: 191,641,160 (GRCm39) |
K269Q |
probably benign |
Het |
Slco1a5 |
T |
C |
6: 142,194,533 (GRCm39) |
Y370C |
possibly damaging |
Het |
Slf2 |
T |
A |
19: 44,923,364 (GRCm39) |
|
probably null |
Het |
Sltm |
A |
G |
9: 70,496,339 (GRCm39) |
H958R |
probably damaging |
Het |
Snrnp40 |
A |
G |
4: 130,256,549 (GRCm39) |
I91M |
probably damaging |
Het |
Spta1 |
A |
T |
1: 174,058,232 (GRCm39) |
Q1900L |
probably benign |
Het |
Srgn |
C |
T |
10: 62,333,631 (GRCm39) |
E49K |
possibly damaging |
Het |
Ssu2 |
A |
C |
6: 112,353,411 (GRCm39) |
C238G |
probably damaging |
Het |
Terf2 |
G |
T |
8: 107,803,307 (GRCm39) |
H425Q |
probably benign |
Het |
Thra |
G |
A |
11: 98,646,990 (GRCm39) |
S37N |
probably benign |
Het |
Toporsl |
A |
G |
4: 52,610,845 (GRCm39) |
D246G |
probably damaging |
Het |
Ubap2l |
G |
A |
3: 89,928,210 (GRCm39) |
T553M |
probably damaging |
Het |
Usp10 |
A |
G |
8: 120,667,930 (GRCm39) |
Y77C |
probably benign |
Het |
Vmn1r204 |
T |
G |
13: 22,740,867 (GRCm39) |
F166C |
probably benign |
Het |
Vmn2r14 |
T |
C |
5: 109,369,370 (GRCm39) |
I68V |
probably benign |
Het |
Wls |
C |
T |
3: 159,603,082 (GRCm39) |
T165I |
probably benign |
Het |
Wsb1 |
A |
G |
11: 79,131,199 (GRCm39) |
M399T |
probably benign |
Het |
Xbp1 |
C |
T |
11: 5,471,167 (GRCm39) |
T58M |
probably damaging |
Het |
Zbtb46 |
A |
T |
2: 181,032,929 (GRCm39) |
D577E |
probably benign |
Het |
Zfp366 |
A |
G |
13: 99,382,991 (GRCm39) |
D718G |
probably damaging |
Het |
Zfp408 |
A |
T |
2: 91,475,369 (GRCm39) |
V595E |
possibly damaging |
Het |
Zfp493 |
T |
A |
13: 67,934,322 (GRCm39) |
W60R |
probably null |
Het |
Zfp606 |
A |
T |
7: 12,227,932 (GRCm39) |
K626N |
probably damaging |
Het |
Zfp820 |
A |
T |
17: 22,037,966 (GRCm39) |
L454Q |
probably benign |
Het |
Zswim5 |
A |
G |
4: 116,830,169 (GRCm39) |
I515V |
probably benign |
Het |
|
Other mutations in Utrn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00333:Utrn
|
APN |
10 |
12,547,574 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00469:Utrn
|
APN |
10 |
12,282,273 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00518:Utrn
|
APN |
10 |
12,542,587 (GRCm39) |
splice site |
probably benign |
|
IGL00560:Utrn
|
APN |
10 |
12,331,211 (GRCm39) |
nonsense |
probably null |
|
IGL00589:Utrn
|
APN |
10 |
12,554,362 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL00662:Utrn
|
APN |
10 |
12,540,705 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00754:Utrn
|
APN |
10 |
12,539,236 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00772:Utrn
|
APN |
10 |
12,524,929 (GRCm39) |
missense |
probably benign |
|
IGL00775:Utrn
|
APN |
10 |
12,620,974 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00782:Utrn
|
APN |
10 |
12,528,555 (GRCm39) |
missense |
probably benign |
0.13 |
IGL00962:Utrn
|
APN |
10 |
12,357,078 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01584:Utrn
|
APN |
10 |
12,602,111 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01677:Utrn
|
APN |
10 |
12,619,901 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01695:Utrn
|
APN |
10 |
12,621,086 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01743:Utrn
|
APN |
10 |
12,587,301 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01815:Utrn
|
APN |
10 |
12,528,460 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01901:Utrn
|
APN |
10 |
12,516,672 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01982:Utrn
|
APN |
10 |
12,623,773 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01983:Utrn
|
APN |
10 |
12,545,525 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02031:Utrn
|
APN |
10 |
12,610,948 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02106:Utrn
|
APN |
10 |
12,289,717 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02134:Utrn
|
APN |
10 |
12,519,163 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02209:Utrn
|
APN |
10 |
12,559,039 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02217:Utrn
|
APN |
10 |
12,627,303 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02250:Utrn
|
APN |
10 |
12,312,135 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02307:Utrn
|
APN |
10 |
12,625,809 (GRCm39) |
nonsense |
probably null |
|
IGL02386:Utrn
|
APN |
10 |
12,297,352 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02494:Utrn
|
APN |
10 |
12,585,798 (GRCm39) |
missense |
probably benign |
|
IGL02631:Utrn
|
APN |
10 |
12,585,807 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02729:Utrn
|
APN |
10 |
12,596,554 (GRCm39) |
unclassified |
probably benign |
|
IGL02736:Utrn
|
APN |
10 |
12,297,384 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02832:Utrn
|
APN |
10 |
12,613,937 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02926:Utrn
|
APN |
10 |
12,566,504 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03184:Utrn
|
APN |
10 |
12,585,910 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03194:Utrn
|
APN |
10 |
12,282,173 (GRCm39) |
splice site |
probably benign |
|
IGL03346:Utrn
|
APN |
10 |
12,401,096 (GRCm39) |
missense |
probably benign |
0.22 |
retiring
|
UTSW |
10 |
12,516,764 (GRCm39) |
missense |
probably damaging |
1.00 |
shrinking_violet
|
UTSW |
10 |
12,587,329 (GRCm39) |
critical splice acceptor site |
probably null |
|
Wallflower
|
UTSW |
10 |
12,623,719 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4548:Utrn
|
UTSW |
10 |
12,509,685 (GRCm39) |
critical splice donor site |
probably benign |
|
I2288:Utrn
|
UTSW |
10 |
12,297,384 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4677001:Utrn
|
UTSW |
10 |
12,542,448 (GRCm39) |
missense |
probably benign |
0.06 |
R0022:Utrn
|
UTSW |
10 |
12,585,700 (GRCm39) |
splice site |
probably benign |
|
R0024:Utrn
|
UTSW |
10 |
12,281,755 (GRCm39) |
missense |
probably benign |
0.00 |
R0024:Utrn
|
UTSW |
10 |
12,281,755 (GRCm39) |
missense |
probably benign |
0.00 |
R0026:Utrn
|
UTSW |
10 |
12,601,940 (GRCm39) |
splice site |
probably benign |
|
R0026:Utrn
|
UTSW |
10 |
12,601,940 (GRCm39) |
splice site |
probably benign |
|
R0091:Utrn
|
UTSW |
10 |
12,610,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R0112:Utrn
|
UTSW |
10 |
12,562,209 (GRCm39) |
nonsense |
probably null |
|
R0126:Utrn
|
UTSW |
10 |
12,587,219 (GRCm39) |
missense |
probably benign |
0.02 |
R0184:Utrn
|
UTSW |
10 |
12,543,362 (GRCm39) |
missense |
probably benign |
|
R0219:Utrn
|
UTSW |
10 |
12,560,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R0369:Utrn
|
UTSW |
10 |
12,509,766 (GRCm39) |
missense |
probably benign |
0.37 |
R0390:Utrn
|
UTSW |
10 |
12,585,804 (GRCm39) |
missense |
probably benign |
0.05 |
R0391:Utrn
|
UTSW |
10 |
12,401,077 (GRCm39) |
splice site |
probably benign |
|
R0408:Utrn
|
UTSW |
10 |
12,259,934 (GRCm39) |
makesense |
probably null |
|
R0409:Utrn
|
UTSW |
10 |
12,519,345 (GRCm39) |
missense |
probably benign |
0.01 |
R0441:Utrn
|
UTSW |
10 |
12,564,038 (GRCm39) |
missense |
probably null |
0.88 |
R0504:Utrn
|
UTSW |
10 |
12,278,639 (GRCm39) |
missense |
probably benign |
0.02 |
R0730:Utrn
|
UTSW |
10 |
12,573,902 (GRCm39) |
splice site |
probably benign |
|
R1078:Utrn
|
UTSW |
10 |
12,331,310 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1171:Utrn
|
UTSW |
10 |
12,357,052 (GRCm39) |
missense |
probably damaging |
0.99 |
R1191:Utrn
|
UTSW |
10 |
12,509,777 (GRCm39) |
missense |
probably benign |
0.02 |
R1203:Utrn
|
UTSW |
10 |
12,362,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R1401:Utrn
|
UTSW |
10 |
12,524,897 (GRCm39) |
missense |
probably benign |
|
R1418:Utrn
|
UTSW |
10 |
12,589,094 (GRCm39) |
missense |
probably benign |
|
R1439:Utrn
|
UTSW |
10 |
12,619,793 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1441:Utrn
|
UTSW |
10 |
12,559,039 (GRCm39) |
missense |
probably damaging |
0.97 |
R1445:Utrn
|
UTSW |
10 |
12,554,318 (GRCm39) |
splice site |
probably benign |
|
R1509:Utrn
|
UTSW |
10 |
12,331,185 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1546:Utrn
|
UTSW |
10 |
12,312,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R1585:Utrn
|
UTSW |
10 |
12,312,029 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1621:Utrn
|
UTSW |
10 |
12,589,027 (GRCm39) |
missense |
probably benign |
0.24 |
R1637:Utrn
|
UTSW |
10 |
12,312,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R1703:Utrn
|
UTSW |
10 |
12,603,473 (GRCm39) |
splice site |
probably benign |
|
R1725:Utrn
|
UTSW |
10 |
12,539,263 (GRCm39) |
missense |
probably damaging |
0.99 |
R1735:Utrn
|
UTSW |
10 |
12,585,882 (GRCm39) |
missense |
probably benign |
|
R1770:Utrn
|
UTSW |
10 |
12,351,040 (GRCm39) |
missense |
probably damaging |
0.98 |
R1778:Utrn
|
UTSW |
10 |
12,312,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Utrn
|
UTSW |
10 |
12,339,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R1818:Utrn
|
UTSW |
10 |
12,585,708 (GRCm39) |
critical splice donor site |
probably null |
|
R1829:Utrn
|
UTSW |
10 |
12,351,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R1919:Utrn
|
UTSW |
10 |
12,331,224 (GRCm39) |
missense |
probably benign |
0.15 |
R1964:Utrn
|
UTSW |
10 |
12,560,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R2080:Utrn
|
UTSW |
10 |
12,612,826 (GRCm39) |
missense |
probably benign |
0.36 |
R2092:Utrn
|
UTSW |
10 |
12,554,442 (GRCm39) |
missense |
probably benign |
0.12 |
R2107:Utrn
|
UTSW |
10 |
12,312,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R2108:Utrn
|
UTSW |
10 |
12,312,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R2760:Utrn
|
UTSW |
10 |
12,566,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R2884:Utrn
|
UTSW |
10 |
12,615,105 (GRCm39) |
splice site |
probably null |
|
R2885:Utrn
|
UTSW |
10 |
12,615,105 (GRCm39) |
splice site |
probably null |
|
R2886:Utrn
|
UTSW |
10 |
12,615,105 (GRCm39) |
splice site |
probably null |
|
R2903:Utrn
|
UTSW |
10 |
12,519,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R2944:Utrn
|
UTSW |
10 |
12,519,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R2945:Utrn
|
UTSW |
10 |
12,362,135 (GRCm39) |
missense |
possibly damaging |
0.50 |
R3438:Utrn
|
UTSW |
10 |
12,357,062 (GRCm39) |
missense |
probably damaging |
0.98 |
R3683:Utrn
|
UTSW |
10 |
12,542,579 (GRCm39) |
missense |
probably benign |
0.10 |
R3735:Utrn
|
UTSW |
10 |
12,354,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R3907:Utrn
|
UTSW |
10 |
12,585,926 (GRCm39) |
splice site |
probably benign |
|
R3923:Utrn
|
UTSW |
10 |
12,615,223 (GRCm39) |
missense |
probably benign |
0.23 |
R3925:Utrn
|
UTSW |
10 |
12,573,786 (GRCm39) |
missense |
probably benign |
|
R3926:Utrn
|
UTSW |
10 |
12,573,786 (GRCm39) |
missense |
probably benign |
|
R3938:Utrn
|
UTSW |
10 |
12,625,774 (GRCm39) |
critical splice donor site |
probably null |
|
R3941:Utrn
|
UTSW |
10 |
12,587,329 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3958:Utrn
|
UTSW |
10 |
12,625,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R4091:Utrn
|
UTSW |
10 |
12,585,915 (GRCm39) |
missense |
probably benign |
0.10 |
R4454:Utrn
|
UTSW |
10 |
12,603,584 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4585:Utrn
|
UTSW |
10 |
12,564,050 (GRCm39) |
missense |
probably benign |
0.01 |
R4667:Utrn
|
UTSW |
10 |
12,573,797 (GRCm39) |
missense |
probably benign |
0.22 |
R4684:Utrn
|
UTSW |
10 |
12,620,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R4785:Utrn
|
UTSW |
10 |
12,530,489 (GRCm39) |
missense |
probably benign |
0.39 |
R4799:Utrn
|
UTSW |
10 |
12,625,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R4829:Utrn
|
UTSW |
10 |
12,539,205 (GRCm39) |
missense |
probably benign |
0.00 |
R4878:Utrn
|
UTSW |
10 |
12,603,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R4955:Utrn
|
UTSW |
10 |
12,737,311 (GRCm39) |
critical splice donor site |
probably null |
|
R4967:Utrn
|
UTSW |
10 |
12,331,164 (GRCm39) |
missense |
probably damaging |
0.99 |
R5071:Utrn
|
UTSW |
10 |
12,259,948 (GRCm39) |
splice site |
probably null |
|
R5072:Utrn
|
UTSW |
10 |
12,259,948 (GRCm39) |
splice site |
probably null |
|
R5186:Utrn
|
UTSW |
10 |
12,604,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R5213:Utrn
|
UTSW |
10 |
12,512,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R5296:Utrn
|
UTSW |
10 |
12,277,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R5309:Utrn
|
UTSW |
10 |
12,603,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R5312:Utrn
|
UTSW |
10 |
12,603,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R5399:Utrn
|
UTSW |
10 |
12,516,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R5407:Utrn
|
UTSW |
10 |
12,556,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5411:Utrn
|
UTSW |
10 |
12,524,929 (GRCm39) |
missense |
probably benign |
|
R5428:Utrn
|
UTSW |
10 |
12,569,175 (GRCm39) |
missense |
probably benign |
0.09 |
R5595:Utrn
|
UTSW |
10 |
12,558,062 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5602:Utrn
|
UTSW |
10 |
12,625,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R5608:Utrn
|
UTSW |
10 |
12,547,581 (GRCm39) |
missense |
probably benign |
0.00 |
R5678:Utrn
|
UTSW |
10 |
12,317,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R5726:Utrn
|
UTSW |
10 |
12,545,550 (GRCm39) |
missense |
probably benign |
|
R5804:Utrn
|
UTSW |
10 |
12,297,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5916:Utrn
|
UTSW |
10 |
12,540,795 (GRCm39) |
missense |
probably damaging |
0.97 |
R5941:Utrn
|
UTSW |
10 |
12,362,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R6014:Utrn
|
UTSW |
10 |
12,566,620 (GRCm39) |
missense |
probably benign |
0.01 |
R6015:Utrn
|
UTSW |
10 |
12,354,168 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6028:Utrn
|
UTSW |
10 |
12,530,460 (GRCm39) |
missense |
probably benign |
0.00 |
R6158:Utrn
|
UTSW |
10 |
12,566,566 (GRCm39) |
missense |
probably benign |
0.04 |
R6181:Utrn
|
UTSW |
10 |
12,615,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R6300:Utrn
|
UTSW |
10 |
12,377,220 (GRCm39) |
missense |
probably benign |
0.35 |
R6367:Utrn
|
UTSW |
10 |
12,623,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R6377:Utrn
|
UTSW |
10 |
12,619,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R6434:Utrn
|
UTSW |
10 |
12,401,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R6498:Utrn
|
UTSW |
10 |
12,317,837 (GRCm39) |
missense |
probably benign |
|
R6579:Utrn
|
UTSW |
10 |
12,623,750 (GRCm39) |
missense |
probably benign |
0.05 |
R6704:Utrn
|
UTSW |
10 |
12,621,035 (GRCm39) |
missense |
probably damaging |
0.99 |
R6736:Utrn
|
UTSW |
10 |
12,497,047 (GRCm39) |
missense |
probably benign |
0.09 |
R6755:Utrn
|
UTSW |
10 |
12,574,831 (GRCm39) |
missense |
probably benign |
0.00 |
R6793:Utrn
|
UTSW |
10 |
12,574,844 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6793:Utrn
|
UTSW |
10 |
12,516,669 (GRCm39) |
critical splice donor site |
probably null |
|
R6835:Utrn
|
UTSW |
10 |
12,603,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R6919:Utrn
|
UTSW |
10 |
12,569,214 (GRCm39) |
nonsense |
probably null |
|
R6920:Utrn
|
UTSW |
10 |
12,626,214 (GRCm39) |
missense |
probably damaging |
0.98 |
R7037:Utrn
|
UTSW |
10 |
12,702,514 (GRCm39) |
splice site |
probably null |
|
R7038:Utrn
|
UTSW |
10 |
12,558,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R7055:Utrn
|
UTSW |
10 |
12,623,665 (GRCm39) |
missense |
probably benign |
0.23 |
R7072:Utrn
|
UTSW |
10 |
12,340,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R7090:Utrn
|
UTSW |
10 |
12,560,260 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7211:Utrn
|
UTSW |
10 |
12,277,079 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7248:Utrn
|
UTSW |
10 |
12,604,562 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7305:Utrn
|
UTSW |
10 |
12,261,280 (GRCm39) |
missense |
probably benign |
|
R7334:Utrn
|
UTSW |
10 |
12,603,753 (GRCm39) |
splice site |
probably null |
|
R7348:Utrn
|
UTSW |
10 |
12,623,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R7375:Utrn
|
UTSW |
10 |
12,516,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R7436:Utrn
|
UTSW |
10 |
12,315,535 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7476:Utrn
|
UTSW |
10 |
12,516,695 (GRCm39) |
missense |
probably benign |
|
R7514:Utrn
|
UTSW |
10 |
12,573,833 (GRCm39) |
missense |
probably benign |
0.00 |
R7527:Utrn
|
UTSW |
10 |
12,277,126 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7735:Utrn
|
UTSW |
10 |
12,619,787 (GRCm39) |
critical splice donor site |
probably null |
|
R7748:Utrn
|
UTSW |
10 |
12,490,252 (GRCm39) |
missense |
probably benign |
0.01 |
R7778:Utrn
|
UTSW |
10 |
12,362,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R7824:Utrn
|
UTSW |
10 |
12,362,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R7826:Utrn
|
UTSW |
10 |
12,277,050 (GRCm39) |
splice site |
probably null |
|
R7872:Utrn
|
UTSW |
10 |
12,573,873 (GRCm39) |
missense |
probably benign |
|
R7915:Utrn
|
UTSW |
10 |
12,340,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R7922:Utrn
|
UTSW |
10 |
12,543,271 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8081:Utrn
|
UTSW |
10 |
12,423,803 (GRCm39) |
start gained |
probably benign |
|
R8132:Utrn
|
UTSW |
10 |
12,558,154 (GRCm39) |
missense |
probably damaging |
0.99 |
R8167:Utrn
|
UTSW |
10 |
12,547,558 (GRCm39) |
nonsense |
probably null |
|
R8186:Utrn
|
UTSW |
10 |
12,573,867 (GRCm39) |
missense |
probably benign |
|
R8331:Utrn
|
UTSW |
10 |
12,490,363 (GRCm39) |
missense |
probably benign |
0.00 |
R8352:Utrn
|
UTSW |
10 |
12,689,253 (GRCm39) |
missense |
probably benign |
0.34 |
R8408:Utrn
|
UTSW |
10 |
12,545,887 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8452:Utrn
|
UTSW |
10 |
12,689,253 (GRCm39) |
missense |
probably benign |
0.34 |
R8478:Utrn
|
UTSW |
10 |
12,524,892 (GRCm39) |
missense |
probably benign |
|
R8489:Utrn
|
UTSW |
10 |
12,587,190 (GRCm39) |
missense |
probably benign |
0.05 |
R8516:Utrn
|
UTSW |
10 |
12,362,254 (GRCm39) |
missense |
probably damaging |
0.99 |
R8520:Utrn
|
UTSW |
10 |
12,545,930 (GRCm39) |
nonsense |
probably null |
|
R8550:Utrn
|
UTSW |
10 |
12,689,329 (GRCm39) |
intron |
probably benign |
|
R8856:Utrn
|
UTSW |
10 |
12,543,351 (GRCm39) |
missense |
probably benign |
|
R8881:Utrn
|
UTSW |
10 |
12,423,737 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9180:Utrn
|
UTSW |
10 |
12,545,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R9186:Utrn
|
UTSW |
10 |
12,490,318 (GRCm39) |
missense |
probably benign |
|
R9216:Utrn
|
UTSW |
10 |
12,689,229 (GRCm39) |
missense |
probably benign |
0.19 |
R9251:Utrn
|
UTSW |
10 |
12,512,531 (GRCm39) |
missense |
probably benign |
0.01 |
R9273:Utrn
|
UTSW |
10 |
12,509,707 (GRCm39) |
missense |
probably damaging |
0.97 |
R9307:Utrn
|
UTSW |
10 |
12,554,475 (GRCm39) |
missense |
probably benign |
0.02 |
R9344:Utrn
|
UTSW |
10 |
12,560,275 (GRCm39) |
missense |
probably benign |
0.17 |
R9419:Utrn
|
UTSW |
10 |
12,564,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R9435:Utrn
|
UTSW |
10 |
12,519,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R9623:Utrn
|
UTSW |
10 |
12,282,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R9650:Utrn
|
UTSW |
10 |
12,613,929 (GRCm39) |
missense |
probably benign |
0.00 |
R9653:Utrn
|
UTSW |
10 |
12,539,189 (GRCm39) |
missense |
probably benign |
0.41 |
R9653:Utrn
|
UTSW |
10 |
12,497,123 (GRCm39) |
missense |
probably benign |
0.17 |
R9672:Utrn
|
UTSW |
10 |
12,603,613 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9678:Utrn
|
UTSW |
10 |
12,615,159 (GRCm39) |
missense |
probably benign |
0.00 |
R9741:Utrn
|
UTSW |
10 |
12,702,564 (GRCm39) |
missense |
probably benign |
|
R9765:Utrn
|
UTSW |
10 |
12,610,921 (GRCm39) |
missense |
probably damaging |
0.99 |
R9799:Utrn
|
UTSW |
10 |
12,585,736 (GRCm39) |
missense |
probably benign |
0.01 |
RF009:Utrn
|
UTSW |
10 |
12,509,689 (GRCm39) |
nonsense |
probably null |
|
V1662:Utrn
|
UTSW |
10 |
12,297,384 (GRCm39) |
missense |
probably damaging |
1.00 |
X0018:Utrn
|
UTSW |
10 |
12,610,942 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Utrn
|
UTSW |
10 |
12,564,173 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1176:Utrn
|
UTSW |
10 |
12,558,104 (GRCm39) |
nonsense |
probably null |
|
Z1177:Utrn
|
UTSW |
10 |
12,497,123 (GRCm39) |
missense |
probably benign |
0.17 |
Z1177:Utrn
|
UTSW |
10 |
12,401,150 (GRCm39) |
nonsense |
probably null |
|
Z1186:Utrn
|
UTSW |
10 |
12,545,491 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1189:Utrn
|
UTSW |
10 |
12,545,491 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1191:Utrn
|
UTSW |
10 |
12,545,491 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1192:Utrn
|
UTSW |
10 |
12,545,491 (GRCm39) |
missense |
probably damaging |
1.00 |
|