Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310003L06Rik |
G |
A |
5: 88,120,457 (GRCm39) |
D405N |
probably benign |
Het |
4921517D22Rik |
T |
G |
13: 59,838,718 (GRCm39) |
E38A |
probably damaging |
Het |
4930433I11Rik |
A |
T |
7: 40,642,786 (GRCm39) |
I152F |
probably benign |
Het |
Aass |
A |
T |
6: 23,107,690 (GRCm39) |
D364E |
probably benign |
Het |
Adamts2 |
A |
G |
11: 50,628,014 (GRCm39) |
D238G |
probably benign |
Het |
Albfm1 |
T |
A |
5: 90,714,362 (GRCm39) |
L124H |
probably benign |
Het |
Aoc1l1 |
A |
G |
6: 48,952,195 (GRCm39) |
D40G |
probably damaging |
Het |
Aplf |
G |
A |
6: 87,623,237 (GRCm39) |
L302F |
probably damaging |
Het |
Apol7b |
G |
T |
15: 77,311,982 (GRCm39) |
|
probably benign |
Het |
Arhgef12 |
A |
G |
9: 42,931,992 (GRCm39) |
V165A |
probably benign |
Het |
Ascc3 |
T |
C |
10: 50,589,329 (GRCm39) |
S1017P |
probably damaging |
Het |
B230104I21Rik |
T |
A |
4: 154,434,204 (GRCm39) |
|
probably benign |
Het |
Bfsp2 |
C |
A |
9: 103,357,082 (GRCm39) |
C115F |
probably damaging |
Het |
Bhmt2 |
A |
T |
13: 93,799,798 (GRCm39) |
W213R |
probably benign |
Het |
Capn5 |
A |
T |
7: 97,775,648 (GRCm39) |
V431E |
probably damaging |
Het |
Ccdc88c |
A |
G |
12: 100,896,802 (GRCm39) |
Y1390H |
probably damaging |
Het |
Ccr3 |
A |
G |
9: 123,828,718 (GRCm39) |
T18A |
probably damaging |
Het |
Cdh5 |
T |
C |
8: 104,869,301 (GRCm39) |
S676P |
probably benign |
Het |
Ceacam5 |
A |
G |
7: 17,491,669 (GRCm39) |
T680A |
possibly damaging |
Het |
Cebpd |
G |
A |
16: 15,705,978 (GRCm39) |
G264S |
probably benign |
Het |
Cfd |
T |
C |
10: 79,726,782 (GRCm39) |
V8A |
probably benign |
Het |
Cops9 |
C |
T |
1: 92,569,588 (GRCm39) |
|
probably benign |
Het |
Cpne6 |
T |
C |
14: 55,754,467 (GRCm39) |
Y533H |
probably damaging |
Het |
Cyp2c67 |
T |
A |
19: 39,604,168 (GRCm39) |
H396L |
probably benign |
Het |
Cyp2j9 |
G |
A |
4: 96,456,972 (GRCm39) |
P500S |
possibly damaging |
Het |
Cyp4a12a |
A |
T |
4: 115,184,610 (GRCm39) |
|
probably null |
Het |
Dbt |
G |
A |
3: 116,317,036 (GRCm39) |
D71N |
probably damaging |
Het |
Ddx41 |
G |
T |
13: 55,679,868 (GRCm39) |
Q440K |
probably benign |
Het |
Elovl4 |
A |
G |
9: 83,662,738 (GRCm39) |
F174S |
probably damaging |
Het |
Emcn |
C |
G |
3: 137,129,187 (GRCm39) |
P193R |
probably damaging |
Het |
Etnk1 |
T |
C |
6: 143,113,364 (GRCm39) |
|
probably null |
Het |
Fads3 |
A |
C |
19: 10,019,252 (GRCm39) |
S53R |
probably damaging |
Het |
Fam193a |
A |
G |
5: 34,616,372 (GRCm39) |
E849G |
probably damaging |
Het |
Fat3 |
A |
G |
9: 15,907,803 (GRCm39) |
V2733A |
probably benign |
Het |
Frem3 |
T |
A |
8: 81,340,587 (GRCm39) |
M960K |
probably benign |
Het |
Frmd6 |
A |
T |
12: 70,919,349 (GRCm39) |
I62L |
probably benign |
Het |
Glmp |
T |
C |
3: 88,232,530 (GRCm39) |
|
probably benign |
Het |
Gm17421 |
T |
C |
12: 113,333,161 (GRCm39) |
|
noncoding transcript |
Het |
Gm27013 |
T |
A |
6: 130,499,186 (GRCm39) |
|
noncoding transcript |
Het |
Gtf2ird1 |
A |
G |
5: 134,424,576 (GRCm39) |
V390A |
probably damaging |
Het |
Hps3 |
A |
G |
3: 20,066,890 (GRCm39) |
Y559H |
probably benign |
Het |
Hsh2d |
G |
A |
8: 72,954,304 (GRCm39) |
D229N |
probably benign |
Het |
Itpr3 |
A |
G |
17: 27,304,121 (GRCm39) |
D114G |
probably benign |
Het |
Jmjd4 |
G |
A |
11: 59,346,406 (GRCm39) |
A408T |
probably benign |
Het |
Kcnh4 |
G |
T |
11: 100,646,000 (GRCm39) |
A316D |
probably damaging |
Het |
Klrg1 |
T |
A |
6: 122,250,492 (GRCm39) |
|
probably null |
Het |
Lancl2 |
T |
A |
6: 57,709,262 (GRCm39) |
Y355N |
probably damaging |
Het |
Ltb |
T |
C |
17: 35,414,206 (GRCm39) |
S115P |
probably benign |
Het |
Mccc2 |
T |
G |
13: 100,136,762 (GRCm39) |
R64S |
probably benign |
Het |
Mgam2-ps |
T |
A |
6: 40,809,596 (GRCm39) |
|
noncoding transcript |
Het |
Mrrf |
T |
G |
2: 36,038,042 (GRCm39) |
N104K |
possibly damaging |
Het |
Nipa1 |
C |
A |
7: 55,629,436 (GRCm39) |
V226L |
possibly damaging |
Het |
Numa1 |
T |
A |
7: 101,645,244 (GRCm39) |
L290Q |
probably damaging |
Het |
Ofcc1 |
T |
A |
13: 40,433,949 (GRCm39) |
H52L |
probably damaging |
Het |
Ogfod3 |
G |
A |
11: 121,086,027 (GRCm39) |
A189V |
probably benign |
Het |
Or14c39 |
T |
A |
7: 86,343,796 (GRCm39) |
I44N |
probably damaging |
Het |
Or5b21 |
A |
T |
19: 12,839,180 (GRCm39) |
I14F |
probably benign |
Het |
Or5d46 |
A |
G |
2: 88,170,179 (GRCm39) |
D90G |
probably damaging |
Het |
Or9i1b |
G |
A |
19: 13,897,022 (GRCm39) |
V213I |
probably benign |
Het |
P2ry12 |
G |
A |
3: 59,125,318 (GRCm39) |
S119L |
probably benign |
Het |
Pde7b |
T |
A |
10: 20,314,531 (GRCm39) |
N192Y |
probably damaging |
Het |
Pfkl |
T |
C |
10: 77,833,428 (GRCm39) |
N258S |
probably damaging |
Het |
Phykpl |
G |
A |
11: 51,477,420 (GRCm39) |
A71T |
probably damaging |
Het |
Ppp1r16a |
T |
C |
15: 76,577,393 (GRCm39) |
|
probably benign |
Het |
Pramel15 |
T |
C |
4: 144,099,781 (GRCm39) |
N328S |
possibly damaging |
Het |
Pramel32 |
T |
C |
4: 88,547,452 (GRCm39) |
K160R |
probably damaging |
Het |
Rapgef6 |
A |
G |
11: 54,585,326 (GRCm39) |
I1570V |
probably benign |
Het |
Rbm34 |
T |
C |
8: 127,697,655 (GRCm39) |
S19G |
probably benign |
Het |
Rnf10 |
T |
C |
5: 115,393,501 (GRCm39) |
|
probably null |
Het |
Rnf34 |
A |
G |
5: 122,988,365 (GRCm39) |
|
probably null |
Het |
Setd4 |
A |
G |
16: 93,386,838 (GRCm39) |
S287P |
probably benign |
Het |
Shc3 |
C |
T |
13: 51,605,606 (GRCm39) |
V225I |
probably benign |
Het |
Sipa1l3 |
C |
T |
7: 29,070,427 (GRCm39) |
V1030I |
probably damaging |
Het |
Siva1 |
G |
T |
12: 112,611,498 (GRCm39) |
R33L |
probably damaging |
Het |
Slc4a5 |
C |
T |
6: 83,249,115 (GRCm39) |
T573I |
probably damaging |
Het |
Sorcs1 |
C |
T |
19: 50,666,578 (GRCm39) |
R110Q |
possibly damaging |
Het |
Sorcs1 |
T |
C |
19: 50,218,740 (GRCm39) |
I581V |
possibly damaging |
Het |
Sorl1 |
T |
C |
9: 41,903,617 (GRCm39) |
D1545G |
probably damaging |
Het |
Tas2r124 |
T |
G |
6: 132,732,509 (GRCm39) |
S273A |
probably damaging |
Het |
Tcf15 |
T |
C |
2: 151,985,813 (GRCm39) |
F90L |
probably damaging |
Het |
Trim59 |
G |
A |
3: 68,944,453 (GRCm39) |
R296C |
probably benign |
Het |
Tulp1 |
A |
T |
17: 28,572,546 (GRCm39) |
D229E |
probably benign |
Het |
Ush1c |
T |
A |
7: 45,845,157 (GRCm39) |
N886I |
probably benign |
Het |
Usp9y |
A |
T |
Y: 1,444,559 (GRCm39) |
S127T |
probably damaging |
Het |
Vmn1r19 |
T |
A |
6: 57,382,219 (GRCm39) |
Y257* |
probably null |
Het |
Vmn2r109 |
A |
T |
17: 20,774,153 (GRCm39) |
Y401N |
probably damaging |
Het |
Vmn2r69 |
A |
C |
7: 85,060,508 (GRCm39) |
S359A |
probably benign |
Het |
Zfp37 |
A |
T |
4: 62,109,740 (GRCm39) |
N479K |
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 |
R1765:Prune2
|
UTSW |
19 |
17,102,962 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
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 |
|