Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933412E24Rik |
G |
T |
15: 59,887,194 (GRCm39) |
C415* |
probably null |
Het |
Adamtsl2 |
A |
C |
2: 26,992,842 (GRCm39) |
I652L |
probably benign |
Het |
Adgrl4 |
T |
C |
3: 151,248,872 (GRCm39) |
I720T |
probably damaging |
Het |
Agrn |
A |
T |
4: 156,261,284 (GRCm39) |
C604* |
probably null |
Het |
Amh |
AGCGCCTTGG |
AG |
10: 80,641,419 (GRCm39) |
|
probably null |
Het |
B3galt2 |
C |
A |
1: 143,522,207 (GRCm39) |
N114K |
probably benign |
Het |
Bud23 |
A |
T |
5: 135,084,897 (GRCm39) |
M59K |
probably benign |
Het |
C3 |
C |
T |
17: 57,531,401 (GRCm39) |
|
probably null |
Het |
C9orf72 |
A |
C |
4: 35,197,098 (GRCm39) |
H322Q |
probably damaging |
Het |
Cc2d2a |
A |
T |
5: 43,871,873 (GRCm39) |
D903V |
probably damaging |
Het |
Ccdc9b |
G |
A |
2: 118,591,128 (GRCm39) |
A135V |
probably benign |
Het |
Cd84 |
A |
G |
1: 171,700,317 (GRCm39) |
T145A |
possibly damaging |
Het |
Cdan1 |
A |
C |
2: 120,551,230 (GRCm39) |
L1097V |
probably damaging |
Het |
Cdc26 |
T |
A |
4: 62,313,155 (GRCm39) |
N62I |
probably benign |
Het |
Cdc27 |
G |
T |
11: 104,425,607 (GRCm39) |
Q70K |
probably damaging |
Het |
Cenpq |
A |
T |
17: 41,235,178 (GRCm39) |
|
probably null |
Het |
Cep295 |
T |
C |
9: 15,239,200 (GRCm39) |
S1858G |
probably damaging |
Het |
Clasp1 |
T |
C |
1: 118,433,261 (GRCm39) |
S247P |
probably damaging |
Het |
Cyp2w1 |
C |
T |
5: 139,339,623 (GRCm39) |
T71I |
probably damaging |
Het |
Dcaf1 |
T |
C |
9: 106,741,793 (GRCm39) |
F1336S |
probably damaging |
Het |
Dennd6b |
G |
A |
15: 89,074,506 (GRCm39) |
Q104* |
probably null |
Het |
Dglucy |
T |
A |
12: 100,816,361 (GRCm39) |
|
probably null |
Het |
Dnajc9 |
A |
G |
14: 20,438,158 (GRCm39) |
V148A |
possibly damaging |
Het |
Dnmbp |
T |
A |
19: 43,890,579 (GRCm39) |
D396V |
possibly damaging |
Het |
Dock10 |
T |
A |
1: 80,583,540 (GRCm39) |
I221F |
probably damaging |
Het |
Dscam |
T |
C |
16: 96,486,579 (GRCm39) |
N1032S |
probably benign |
Het |
Dsg4 |
A |
C |
18: 20,589,888 (GRCm39) |
Y346S |
probably benign |
Het |
Dync1i2 |
A |
G |
2: 71,079,759 (GRCm39) |
H417R |
probably benign |
Het |
Dysf |
G |
A |
6: 84,167,884 (GRCm39) |
|
probably null |
Het |
Elovl1 |
A |
G |
4: 118,287,707 (GRCm39) |
M1V |
probably null |
Het |
Eva1c |
A |
G |
16: 90,701,135 (GRCm39) |
S257G |
probably benign |
Het |
Eya2 |
A |
T |
2: 165,566,723 (GRCm39) |
D258V |
probably damaging |
Het |
Fam193a |
A |
G |
5: 34,593,841 (GRCm39) |
T113A |
probably damaging |
Het |
Fbxw15 |
G |
A |
9: 109,387,314 (GRCm39) |
S227F |
probably damaging |
Het |
Fstl5 |
G |
T |
3: 76,500,783 (GRCm39) |
R404L |
possibly damaging |
Het |
Glud1 |
T |
C |
14: 34,047,541 (GRCm39) |
|
probably benign |
Het |
Gm10770 |
A |
C |
2: 150,021,258 (GRCm39) |
H86Q |
probably damaging |
Het |
Gzme |
C |
T |
14: 56,355,871 (GRCm39) |
G147D |
probably damaging |
Het |
Herc3 |
T |
C |
6: 58,865,645 (GRCm39) |
V746A |
probably damaging |
Het |
Hmga1 |
A |
G |
17: 27,778,592 (GRCm39) |
E17G |
probably damaging |
Het |
Kdelr2 |
A |
T |
5: 143,406,567 (GRCm39) |
K206* |
probably null |
Het |
Kng2 |
A |
G |
16: 22,806,993 (GRCm39) |
|
probably null |
Het |
Lrrc41 |
G |
A |
4: 115,946,248 (GRCm39) |
R321H |
possibly damaging |
Het |
Mapkapk2 |
A |
T |
1: 130,986,498 (GRCm39) |
M1K |
probably null |
Het |
Me2 |
A |
G |
18: 73,924,929 (GRCm39) |
F263L |
probably damaging |
Het |
Mkks |
A |
G |
2: 136,722,287 (GRCm39) |
L290P |
probably damaging |
Het |
Mmp12 |
T |
A |
9: 7,354,772 (GRCm39) |
I255N |
probably damaging |
Het |
Mogs |
A |
G |
6: 83,093,784 (GRCm39) |
D251G |
probably benign |
Het |
Morf4l1 |
T |
A |
9: 89,984,401 (GRCm39) |
Y65F |
possibly damaging |
Het |
Neb |
T |
C |
2: 52,094,676 (GRCm39) |
D5169G |
probably damaging |
Het |
Nin |
A |
G |
12: 70,089,665 (GRCm39) |
L1250P |
probably damaging |
Het |
Nomo1 |
G |
T |
7: 45,715,717 (GRCm39) |
G721V |
possibly damaging |
Het |
Notch2 |
T |
G |
3: 98,029,242 (GRCm39) |
C1002G |
probably damaging |
Het |
Npat |
T |
C |
9: 53,481,522 (GRCm39) |
Y1077H |
probably benign |
Het |
Or1e1c |
T |
A |
11: 73,266,170 (GRCm39) |
N198K |
probably damaging |
Het |
Or4g17 |
G |
A |
2: 111,209,491 (GRCm39) |
V49I |
probably benign |
Het |
Or4p21 |
A |
T |
2: 88,276,367 (GRCm39) |
F305Y |
probably damaging |
Het |
Or5h25 |
A |
G |
16: 58,930,118 (GRCm39) |
L285P |
probably damaging |
Het |
Or8c16 |
T |
C |
9: 38,130,548 (GRCm39) |
I143T |
probably benign |
Het |
Otop2 |
A |
T |
11: 115,215,504 (GRCm39) |
I142F |
probably benign |
Het |
Pacsin3 |
A |
G |
2: 91,093,460 (GRCm39) |
E279G |
possibly damaging |
Het |
Pafah2 |
A |
G |
4: 134,140,758 (GRCm39) |
T243A |
probably benign |
Het |
Pcdhgc5 |
A |
G |
18: 37,954,913 (GRCm39) |
H729R |
probably benign |
Het |
Plcd1 |
T |
C |
9: 118,900,874 (GRCm39) |
D756G |
probably damaging |
Het |
Rit2 |
C |
T |
18: 31,449,951 (GRCm39) |
G16S |
probably damaging |
Het |
Sec24c |
A |
G |
14: 20,738,922 (GRCm39) |
|
probably benign |
Het |
Skint5 |
G |
T |
4: 113,434,858 (GRCm39) |
T1037K |
unknown |
Het |
Slc28a2 |
T |
A |
2: 122,290,876 (GRCm39) |
|
probably null |
Het |
Slc41a2 |
G |
A |
10: 83,137,130 (GRCm39) |
A259V |
probably damaging |
Het |
Slc6a17 |
T |
A |
3: 107,380,895 (GRCm39) |
I537F |
possibly damaging |
Het |
Slco1a7 |
T |
C |
6: 141,700,084 (GRCm39) |
|
probably benign |
Het |
Smchd1 |
A |
T |
17: 71,707,196 (GRCm39) |
|
probably benign |
Het |
Smg1 |
T |
C |
7: 117,738,938 (GRCm39) |
I3489V |
probably benign |
Het |
Sytl3 |
T |
C |
17: 6,967,082 (GRCm39) |
L142P |
probably damaging |
Het |
Tektl1 |
A |
T |
10: 78,584,502 (GRCm39) |
M340K |
probably benign |
Het |
Tfr2 |
C |
T |
5: 137,581,707 (GRCm39) |
T598I |
probably damaging |
Het |
Tmc2 |
A |
G |
2: 130,102,145 (GRCm39) |
Q770R |
probably benign |
Het |
Tnc |
C |
T |
4: 63,932,231 (GRCm39) |
V728M |
probably damaging |
Het |
Trim68 |
A |
T |
7: 102,329,597 (GRCm39) |
M177K |
possibly damaging |
Het |
Trmt11 |
T |
C |
10: 30,435,184 (GRCm39) |
D325G |
probably benign |
Het |
Ube3a |
C |
T |
7: 58,935,862 (GRCm39) |
T582I |
probably damaging |
Het |
Usp13 |
G |
A |
3: 32,969,919 (GRCm39) |
E682K |
probably benign |
Het |
Usp9y |
A |
G |
Y: 1,384,454 (GRCm39) |
V688A |
possibly damaging |
Het |
Uts2r |
A |
G |
11: 121,052,095 (GRCm39) |
T320A |
possibly damaging |
Het |
Vmn1r34 |
A |
T |
6: 66,614,480 (GRCm39) |
M86K |
probably damaging |
Het |
Vsig10 |
A |
G |
5: 117,456,880 (GRCm39) |
|
probably benign |
Het |
Zbtb41 |
T |
A |
1: 139,368,132 (GRCm39) |
C607S |
probably benign |
Het |
|
Other mutations in Prune2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00234:Prune2
|
APN |
19 |
17,145,708 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00848:Prune2
|
APN |
19 |
17,096,482 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00862:Prune2
|
APN |
19 |
17,096,713 (GRCm39) |
missense |
probably benign |
0.41 |
IGL00915:Prune2
|
APN |
19 |
16,993,617 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01084:Prune2
|
APN |
19 |
17,095,573 (GRCm39) |
missense |
probably benign |
0.19 |
IGL01109:Prune2
|
APN |
19 |
17,101,243 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01372:Prune2
|
APN |
19 |
17,102,433 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01650:Prune2
|
APN |
19 |
17,145,656 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01752:Prune2
|
APN |
19 |
17,101,267 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01812:Prune2
|
APN |
19 |
16,981,141 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01902:Prune2
|
APN |
19 |
17,096,002 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02195:Prune2
|
APN |
19 |
17,096,921 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02502:Prune2
|
APN |
19 |
17,101,245 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02569:Prune2
|
APN |
19 |
17,156,223 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02693:Prune2
|
APN |
19 |
17,101,855 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02737:Prune2
|
APN |
19 |
17,170,775 (GRCm39) |
nonsense |
probably null |
|
IGL02794:Prune2
|
APN |
19 |
17,096,725 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02985:Prune2
|
APN |
19 |
16,993,723 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03349:Prune2
|
APN |
19 |
17,100,710 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Prune2
|
UTSW |
19 |
17,102,646 (GRCm39) |
missense |
probably benign |
0.00 |
R0060:Prune2
|
UTSW |
19 |
16,981,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R0098:Prune2
|
UTSW |
19 |
17,101,267 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0098:Prune2
|
UTSW |
19 |
17,101,267 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0165:Prune2
|
UTSW |
19 |
17,099,974 (GRCm39) |
missense |
probably benign |
0.00 |
R0277:Prune2
|
UTSW |
19 |
17,098,753 (GRCm39) |
missense |
probably damaging |
0.99 |
R0321:Prune2
|
UTSW |
19 |
17,099,818 (GRCm39) |
missense |
probably benign |
0.39 |
R0321:Prune2
|
UTSW |
19 |
17,098,291 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0374:Prune2
|
UTSW |
19 |
17,098,274 (GRCm39) |
missense |
probably benign |
0.00 |
R0380:Prune2
|
UTSW |
19 |
17,101,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R0396:Prune2
|
UTSW |
19 |
17,100,444 (GRCm39) |
missense |
probably benign |
0.35 |
R0408:Prune2
|
UTSW |
19 |
17,099,674 (GRCm39) |
missense |
probably benign |
0.00 |
R0421:Prune2
|
UTSW |
19 |
17,100,675 (GRCm39) |
missense |
probably benign |
0.02 |
R0480:Prune2
|
UTSW |
19 |
16,984,156 (GRCm39) |
splice site |
probably benign |
|
R0531:Prune2
|
UTSW |
19 |
16,984,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R0546:Prune2
|
UTSW |
19 |
16,998,030 (GRCm39) |
splice site |
probably benign |
|
R0554:Prune2
|
UTSW |
19 |
17,102,582 (GRCm39) |
nonsense |
probably null |
|
R0659:Prune2
|
UTSW |
19 |
17,100,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R0699:Prune2
|
UTSW |
19 |
17,101,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R0781:Prune2
|
UTSW |
19 |
17,102,586 (GRCm39) |
missense |
probably benign |
|
R1110:Prune2
|
UTSW |
19 |
17,102,586 (GRCm39) |
missense |
probably benign |
|
R1178:Prune2
|
UTSW |
19 |
17,100,469 (GRCm39) |
missense |
probably benign |
0.22 |
R1181:Prune2
|
UTSW |
19 |
17,100,469 (GRCm39) |
missense |
probably benign |
0.22 |
R1337:Prune2
|
UTSW |
19 |
17,096,971 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1356:Prune2
|
UTSW |
19 |
17,189,681 (GRCm39) |
missense |
probably benign |
0.40 |
R1385:Prune2
|
UTSW |
19 |
17,102,312 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1659:Prune2
|
UTSW |
19 |
17,098,015 (GRCm39) |
missense |
possibly damaging |
0.59 |
R1738:Prune2
|
UTSW |
19 |
17,102,374 (GRCm39) |
missense |
probably benign |
0.01 |
R1756:Prune2
|
UTSW |
19 |
17,101,068 (GRCm39) |
missense |
probably benign |
0.01 |
R1782:Prune2
|
UTSW |
19 |
17,099,537 (GRCm39) |
missense |
probably benign |
0.00 |
R1817:Prune2
|
UTSW |
19 |
17,099,445 (GRCm39) |
missense |
probably benign |
0.00 |
R1838:Prune2
|
UTSW |
19 |
17,177,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R1851:Prune2
|
UTSW |
19 |
17,176,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R1852:Prune2
|
UTSW |
19 |
17,176,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R1866:Prune2
|
UTSW |
19 |
17,100,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R1911:Prune2
|
UTSW |
19 |
17,091,038 (GRCm39) |
missense |
probably benign |
0.02 |
R1983:Prune2
|
UTSW |
19 |
16,998,006 (GRCm39) |
missense |
probably damaging |
0.97 |
R2014:Prune2
|
UTSW |
19 |
17,097,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R2066:Prune2
|
UTSW |
19 |
17,098,042 (GRCm39) |
missense |
possibly damaging |
0.57 |
R2088:Prune2
|
UTSW |
19 |
17,097,109 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2111:Prune2
|
UTSW |
19 |
17,185,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R2128:Prune2
|
UTSW |
19 |
17,099,786 (GRCm39) |
missense |
probably benign |
0.00 |
R2165:Prune2
|
UTSW |
19 |
17,097,546 (GRCm39) |
missense |
probably benign |
0.19 |
R2241:Prune2
|
UTSW |
19 |
17,100,456 (GRCm39) |
missense |
probably damaging |
0.96 |
R2278:Prune2
|
UTSW |
19 |
17,095,919 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2504:Prune2
|
UTSW |
19 |
16,977,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R2508:Prune2
|
UTSW |
19 |
17,099,986 (GRCm39) |
missense |
probably benign |
0.43 |
R3055:Prune2
|
UTSW |
19 |
17,102,407 (GRCm39) |
missense |
probably damaging |
0.98 |
R3086:Prune2
|
UTSW |
19 |
17,098,777 (GRCm39) |
missense |
possibly damaging |
0.75 |
R3104:Prune2
|
UTSW |
19 |
17,096,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R3105:Prune2
|
UTSW |
19 |
17,096,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R3547:Prune2
|
UTSW |
19 |
17,101,712 (GRCm39) |
missense |
probably damaging |
0.96 |
R3702:Prune2
|
UTSW |
19 |
17,156,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R3753:Prune2
|
UTSW |
19 |
17,102,818 (GRCm39) |
missense |
probably benign |
0.38 |
R3933:Prune2
|
UTSW |
19 |
17,101,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R3935:Prune2
|
UTSW |
19 |
17,177,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R4022:Prune2
|
UTSW |
19 |
16,977,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R4042:Prune2
|
UTSW |
19 |
16,981,190 (GRCm39) |
critical splice donor site |
probably null |
|
R4164:Prune2
|
UTSW |
19 |
16,981,098 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4453:Prune2
|
UTSW |
19 |
17,099,274 (GRCm39) |
missense |
probably benign |
0.00 |
R4642:Prune2
|
UTSW |
19 |
16,998,019 (GRCm39) |
critical splice donor site |
probably null |
|
R4661:Prune2
|
UTSW |
19 |
16,977,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R4666:Prune2
|
UTSW |
19 |
17,097,552 (GRCm39) |
nonsense |
probably null |
|
R4823:Prune2
|
UTSW |
19 |
17,097,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R4897:Prune2
|
UTSW |
19 |
17,099,219 (GRCm39) |
missense |
probably benign |
0.03 |
R4922:Prune2
|
UTSW |
19 |
17,100,116 (GRCm39) |
missense |
probably benign |
0.00 |
R4962:Prune2
|
UTSW |
19 |
17,099,637 (GRCm39) |
missense |
probably benign |
0.11 |
R5026:Prune2
|
UTSW |
19 |
17,176,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R5042:Prune2
|
UTSW |
19 |
17,097,161 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5124:Prune2
|
UTSW |
19 |
17,177,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R5133:Prune2
|
UTSW |
19 |
16,980,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R5184:Prune2
|
UTSW |
19 |
17,193,721 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5234:Prune2
|
UTSW |
19 |
17,096,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R5339:Prune2
|
UTSW |
19 |
17,098,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R5363:Prune2
|
UTSW |
19 |
17,095,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R5382:Prune2
|
UTSW |
19 |
16,981,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R5436:Prune2
|
UTSW |
19 |
16,998,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R5480:Prune2
|
UTSW |
19 |
17,098,311 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5635:Prune2
|
UTSW |
19 |
17,095,573 (GRCm39) |
missense |
probably benign |
0.19 |
R5678:Prune2
|
UTSW |
19 |
17,096,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R5814:Prune2
|
UTSW |
19 |
16,993,725 (GRCm39) |
splice site |
probably null |
|
R5894:Prune2
|
UTSW |
19 |
17,098,755 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6011:Prune2
|
UTSW |
19 |
17,096,080 (GRCm39) |
missense |
probably benign |
0.35 |
R6207:Prune2
|
UTSW |
19 |
17,095,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R6218:Prune2
|
UTSW |
19 |
17,098,926 (GRCm39) |
missense |
probably benign |
0.00 |
R6573:Prune2
|
UTSW |
19 |
17,098,522 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6573:Prune2
|
UTSW |
19 |
17,098,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R6734:Prune2
|
UTSW |
19 |
16,981,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R6805:Prune2
|
UTSW |
19 |
17,097,954 (GRCm39) |
missense |
probably benign |
|
R6837:Prune2
|
UTSW |
19 |
17,156,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R6850:Prune2
|
UTSW |
19 |
17,099,552 (GRCm39) |
missense |
probably benign |
0.00 |
R6858:Prune2
|
UTSW |
19 |
17,095,470 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6874:Prune2
|
UTSW |
19 |
17,100,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R6954:Prune2
|
UTSW |
19 |
16,977,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R7098:Prune2
|
UTSW |
19 |
17,097,966 (GRCm39) |
missense |
probably benign |
0.39 |
R7102:Prune2
|
UTSW |
19 |
17,098,577 (GRCm39) |
missense |
probably benign |
0.24 |
R7246:Prune2
|
UTSW |
19 |
17,098,732 (GRCm39) |
missense |
probably damaging |
0.99 |
R7284:Prune2
|
UTSW |
19 |
17,097,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R7295:Prune2
|
UTSW |
19 |
17,097,261 (GRCm39) |
missense |
probably benign |
0.01 |
R7371:Prune2
|
UTSW |
19 |
17,096,734 (GRCm39) |
missense |
probably benign |
0.02 |
R7651:Prune2
|
UTSW |
19 |
17,097,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R7830:Prune2
|
UTSW |
19 |
17,100,038 (GRCm39) |
missense |
probably benign |
0.21 |
R7872:Prune2
|
UTSW |
19 |
17,096,798 (GRCm39) |
missense |
probably benign |
0.05 |
R7881:Prune2
|
UTSW |
19 |
17,100,393 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7966:Prune2
|
UTSW |
19 |
17,156,223 (GRCm39) |
missense |
probably damaging |
0.99 |
R7969:Prune2
|
UTSW |
19 |
17,179,034 (GRCm39) |
missense |
probably damaging |
0.98 |
R8092:Prune2
|
UTSW |
19 |
17,097,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R8110:Prune2
|
UTSW |
19 |
17,098,083 (GRCm39) |
missense |
probably benign |
0.22 |
R8115:Prune2
|
UTSW |
19 |
17,101,288 (GRCm39) |
missense |
probably benign |
0.02 |
R8129:Prune2
|
UTSW |
19 |
17,096,200 (GRCm39) |
missense |
probably benign |
0.01 |
R8169:Prune2
|
UTSW |
19 |
17,102,455 (GRCm39) |
missense |
probably benign |
0.10 |
R8171:Prune2
|
UTSW |
19 |
17,097,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R8176:Prune2
|
UTSW |
19 |
17,095,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R8200:Prune2
|
UTSW |
19 |
17,102,337 (GRCm39) |
missense |
probably benign |
0.01 |
R8217:Prune2
|
UTSW |
19 |
17,097,480 (GRCm39) |
missense |
probably benign |
0.01 |
R8258:Prune2
|
UTSW |
19 |
17,189,672 (GRCm39) |
missense |
unknown |
|
R8259:Prune2
|
UTSW |
19 |
17,189,672 (GRCm39) |
missense |
unknown |
|
R8289:Prune2
|
UTSW |
19 |
17,100,373 (GRCm39) |
missense |
probably benign |
0.43 |
R8329:Prune2
|
UTSW |
19 |
17,098,629 (GRCm39) |
missense |
probably benign |
0.02 |
R8342:Prune2
|
UTSW |
19 |
17,103,027 (GRCm39) |
missense |
probably benign |
0.01 |
R8558:Prune2
|
UTSW |
19 |
17,099,602 (GRCm39) |
missense |
probably damaging |
0.98 |
R8732:Prune2
|
UTSW |
19 |
17,097,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R8743:Prune2
|
UTSW |
19 |
17,096,920 (GRCm39) |
missense |
probably benign |
0.22 |
R8769:Prune2
|
UTSW |
19 |
17,100,442 (GRCm39) |
missense |
probably damaging |
0.96 |
R8862:Prune2
|
UTSW |
19 |
17,097,510 (GRCm39) |
missense |
probably benign |
0.04 |
R8936:Prune2
|
UTSW |
19 |
17,099,199 (GRCm39) |
missense |
probably benign |
0.24 |
R9040:Prune2
|
UTSW |
19 |
17,097,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R9084:Prune2
|
UTSW |
19 |
17,097,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R9224:Prune2
|
UTSW |
19 |
17,097,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R9273:Prune2
|
UTSW |
19 |
17,095,690 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9275:Prune2
|
UTSW |
19 |
17,101,144 (GRCm39) |
missense |
probably benign |
0.06 |
R9278:Prune2
|
UTSW |
19 |
17,101,144 (GRCm39) |
missense |
probably benign |
0.06 |
R9290:Prune2
|
UTSW |
19 |
17,145,691 (GRCm39) |
missense |
probably benign |
0.41 |
R9305:Prune2
|
UTSW |
19 |
17,097,625 (GRCm39) |
missense |
probably benign |
0.14 |
R9317:Prune2
|
UTSW |
19 |
17,099,034 (GRCm39) |
missense |
probably benign |
0.00 |
R9354:Prune2
|
UTSW |
19 |
17,099,986 (GRCm39) |
missense |
probably benign |
0.43 |
R9373:Prune2
|
UTSW |
19 |
17,099,502 (GRCm39) |
missense |
probably benign |
|
R9394:Prune2
|
UTSW |
19 |
16,981,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R9405:Prune2
|
UTSW |
19 |
17,193,708 (GRCm39) |
missense |
probably damaging |
0.99 |
R9476:Prune2
|
UTSW |
19 |
17,096,706 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9532:Prune2
|
UTSW |
19 |
17,099,794 (GRCm39) |
missense |
probably benign |
0.00 |
X0019:Prune2
|
UTSW |
19 |
17,098,881 (GRCm39) |
missense |
probably benign |
0.16 |
X0028:Prune2
|
UTSW |
19 |
17,100,249 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Prune2
|
UTSW |
19 |
17,099,739 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Prune2
|
UTSW |
19 |
17,096,154 (GRCm39) |
missense |
probably damaging |
1.00 |
|