Other mutations in this stock |
Total: 113 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
T |
C |
11: 119,909,681 (GRCm39) |
D28G |
probably benign |
Het |
Abcg1 |
T |
A |
17: 31,311,369 (GRCm39) |
S125T |
probably damaging |
Het |
Actbl2 |
T |
C |
13: 111,392,717 (GRCm39) |
S351P |
possibly damaging |
Het |
Ankrd34b |
A |
G |
13: 92,575,569 (GRCm39) |
|
probably null |
Het |
BC051665 |
C |
T |
13: 60,930,468 (GRCm39) |
V295I |
probably benign |
Het |
C1qtnf2 |
A |
G |
11: 43,381,983 (GRCm39) |
N265S |
probably damaging |
Het |
Ccdc14 |
C |
T |
16: 34,542,220 (GRCm39) |
R573* |
probably null |
Het |
Cd55b |
A |
T |
1: 130,337,612 (GRCm39) |
Y247N |
probably damaging |
Het |
Celsr2 |
A |
T |
3: 108,320,907 (GRCm39) |
V635E |
probably benign |
Het |
Clec16a |
T |
C |
16: 10,377,551 (GRCm39) |
|
probably benign |
Het |
Clec4b1 |
A |
G |
6: 123,042,904 (GRCm39) |
Y41C |
probably damaging |
Het |
Cntn5 |
A |
T |
9: 10,172,126 (GRCm39) |
D19E |
probably benign |
Het |
Cop1 |
A |
G |
1: 159,060,375 (GRCm39) |
N53S |
probably damaging |
Het |
Cplane1 |
G |
A |
15: 8,248,700 (GRCm39) |
E1750K |
probably damaging |
Het |
Csad |
A |
T |
15: 102,097,102 (GRCm39) |
M1K |
probably null |
Het |
Cyb5rl |
A |
G |
4: 106,938,142 (GRCm39) |
I200V |
probably benign |
Het |
Cyp26a1 |
A |
G |
19: 37,686,790 (GRCm39) |
T81A |
probably damaging |
Het |
Cyp2d12 |
A |
T |
15: 82,443,237 (GRCm39) |
H433L |
probably benign |
Het |
D7Ertd443e |
T |
A |
7: 133,951,208 (GRCm39) |
|
probably null |
Het |
Dennd1b |
A |
G |
1: 139,097,908 (GRCm39) |
|
probably benign |
Het |
Dmap1 |
G |
T |
4: 117,532,495 (GRCm39) |
T357K |
probably damaging |
Het |
Dzip1 |
G |
T |
14: 119,118,456 (GRCm39) |
T759K |
probably benign |
Het |
Elmo2 |
A |
G |
2: 165,140,607 (GRCm39) |
V300A |
probably damaging |
Het |
Eml5 |
T |
C |
12: 98,810,364 (GRCm39) |
D864G |
possibly damaging |
Het |
Ep400 |
A |
G |
5: 110,816,511 (GRCm39) |
V2670A |
probably damaging |
Het |
Epha3 |
T |
A |
16: 63,423,988 (GRCm39) |
I534F |
probably damaging |
Het |
Epha4 |
A |
C |
1: 77,359,628 (GRCm39) |
Y742D |
probably damaging |
Het |
Ergic2 |
A |
G |
6: 148,106,272 (GRCm39) |
|
probably null |
Het |
Ero1a |
A |
T |
14: 45,536,545 (GRCm39) |
|
probably null |
Het |
Fam229a |
A |
G |
4: 129,385,279 (GRCm39) |
D70G |
probably damaging |
Het |
Fbn2 |
C |
T |
18: 58,226,431 (GRCm39) |
R781Q |
probably damaging |
Het |
Fbxo16 |
A |
T |
14: 65,508,163 (GRCm39) |
|
probably benign |
Het |
Fbxo39 |
T |
A |
11: 72,208,111 (GRCm39) |
S154R |
probably benign |
Het |
Fer |
T |
A |
17: 64,298,575 (GRCm39) |
|
probably null |
Het |
Filip1l |
A |
T |
16: 57,391,410 (GRCm39) |
D428V |
probably damaging |
Het |
Filip1l |
A |
G |
16: 57,391,025 (GRCm39) |
I538V |
possibly damaging |
Het |
Fsip2 |
T |
C |
2: 82,809,954 (GRCm39) |
I2091T |
possibly damaging |
Het |
Glyat |
A |
C |
19: 12,628,762 (GRCm39) |
T186P |
possibly damaging |
Het |
Gm10604 |
A |
G |
4: 11,980,083 (GRCm39) |
S74P |
unknown |
Het |
Gm4787 |
T |
G |
12: 81,425,911 (GRCm39) |
K82N |
possibly damaging |
Het |
Hectd4 |
T |
C |
5: 121,358,683 (GRCm39) |
I50T |
unknown |
Het |
Hectd4 |
T |
C |
5: 121,402,030 (GRCm39) |
S373P |
possibly damaging |
Het |
Hmcn1 |
A |
T |
1: 150,562,618 (GRCm39) |
C2313* |
probably null |
Het |
Hrob |
T |
C |
11: 102,146,122 (GRCm39) |
Y133H |
possibly damaging |
Het |
Igfn1 |
A |
T |
1: 135,897,054 (GRCm39) |
S1171T |
probably benign |
Het |
Ints8 |
T |
C |
4: 11,241,642 (GRCm39) |
D267G |
probably benign |
Het |
Itln1 |
A |
G |
1: 171,356,727 (GRCm39) |
C251R |
probably damaging |
Het |
Jcad |
C |
T |
18: 4,674,026 (GRCm39) |
T596M |
probably damaging |
Het |
Kcnj16 |
C |
T |
11: 110,916,409 (GRCm39) |
T357M |
probably benign |
Het |
Kif13a |
G |
A |
13: 46,967,676 (GRCm39) |
T346M |
probably damaging |
Het |
Klhl24 |
G |
A |
16: 19,938,917 (GRCm39) |
A491T |
probably benign |
Het |
Kntc1 |
C |
T |
5: 123,916,410 (GRCm39) |
Q748* |
probably null |
Het |
Krt25 |
T |
A |
11: 99,208,122 (GRCm39) |
K369* |
probably null |
Het |
Krt75 |
C |
T |
15: 101,476,466 (GRCm39) |
R433Q |
probably benign |
Het |
Krt76 |
A |
G |
15: 101,793,293 (GRCm39) |
F582L |
unknown |
Het |
Lysmd1 |
G |
A |
3: 95,045,708 (GRCm39) |
V182I |
probably benign |
Het |
Mab21l2 |
T |
A |
3: 86,454,862 (GRCm39) |
E46V |
probably damaging |
Het |
Magi2 |
A |
T |
5: 20,563,934 (GRCm39) |
K355N |
probably damaging |
Het |
Marchf10 |
T |
C |
11: 105,276,398 (GRCm39) |
D630G |
probably damaging |
Het |
Mast4 |
A |
T |
13: 102,875,147 (GRCm39) |
I1215N |
probably damaging |
Het |
Nckap1 |
G |
A |
2: 80,360,562 (GRCm39) |
T523I |
probably benign |
Het |
Nexmif |
T |
A |
X: 103,127,999 (GRCm39) |
D1306V |
probably damaging |
Het |
Nfkb1 |
A |
C |
3: 135,295,090 (GRCm39) |
I918R |
possibly damaging |
Het |
Nt5el |
A |
G |
13: 105,246,250 (GRCm39) |
I270M |
probably benign |
Het |
Nup50 |
A |
T |
15: 84,817,859 (GRCm39) |
T93S |
probably benign |
Het |
Nwd2 |
T |
C |
5: 63,961,717 (GRCm39) |
Y434H |
probably benign |
Het |
Or13a28 |
T |
C |
7: 140,218,397 (GRCm39) |
V261A |
probably benign |
Het |
Osbpl1a |
C |
A |
18: 13,038,088 (GRCm39) |
V288L |
probably benign |
Het |
Pan3 |
A |
G |
5: 147,463,846 (GRCm39) |
E562G |
possibly damaging |
Het |
Pappa |
T |
A |
4: 65,099,126 (GRCm39) |
Y548* |
probably null |
Het |
Phf3 |
A |
T |
1: 30,849,870 (GRCm39) |
L1181Q |
probably damaging |
Het |
Phip |
T |
C |
9: 82,797,392 (GRCm39) |
H537R |
possibly damaging |
Het |
Pkhd1l1 |
T |
C |
15: 44,348,824 (GRCm39) |
I240T |
probably damaging |
Het |
Pole |
G |
A |
5: 110,438,368 (GRCm39) |
|
probably null |
Het |
Polq |
T |
A |
16: 36,832,304 (GRCm39) |
S15T |
unknown |
Het |
Prrt2 |
T |
C |
7: 126,619,396 (GRCm39) |
E23G |
possibly damaging |
Het |
Prss37 |
A |
T |
6: 40,494,760 (GRCm39) |
|
probably null |
Het |
Psd |
A |
T |
19: 46,313,352 (GRCm39) |
M6K |
possibly damaging |
Het |
Psmd1 |
A |
G |
1: 86,017,719 (GRCm39) |
E510G |
possibly damaging |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Pxdn |
T |
A |
12: 30,053,405 (GRCm39) |
I1194N |
probably damaging |
Het |
Rbp3 |
C |
T |
14: 33,677,975 (GRCm39) |
T641M |
probably damaging |
Het |
Rgmb |
C |
A |
17: 16,027,909 (GRCm39) |
R270L |
probably benign |
Het |
Rpgrip1l |
A |
G |
8: 92,007,344 (GRCm39) |
|
probably null |
Het |
Rps2 |
G |
A |
17: 24,939,353 (GRCm39) |
|
probably benign |
Het |
Rsbn1l |
G |
T |
5: 21,107,364 (GRCm39) |
A550E |
probably damaging |
Het |
S1pr4 |
C |
T |
10: 81,335,138 (GRCm39) |
R112H |
probably benign |
Het |
Scfd2 |
T |
C |
5: 74,691,838 (GRCm39) |
N148S |
probably damaging |
Het |
Scin |
C |
T |
12: 40,131,705 (GRCm39) |
M276I |
probably benign |
Het |
Sec24d |
T |
C |
3: 123,147,255 (GRCm39) |
I708T |
possibly damaging |
Het |
Skint11 |
T |
A |
4: 114,086,009 (GRCm39) |
F41I |
possibly damaging |
Het |
Slc15a4 |
A |
T |
5: 127,694,303 (GRCm39) |
F44Y |
possibly damaging |
Het |
Slc6a18 |
A |
G |
13: 73,823,925 (GRCm39) |
Y72H |
probably benign |
Het |
Slc7a11 |
A |
T |
3: 50,332,195 (GRCm39) |
|
probably null |
Het |
Slc7a14 |
G |
T |
3: 31,291,650 (GRCm39) |
N209K |
possibly damaging |
Het |
Sstr2 |
T |
C |
11: 113,515,257 (GRCm39) |
C59R |
probably damaging |
Het |
Stab1 |
A |
G |
14: 30,884,997 (GRCm39) |
|
probably null |
Het |
Stag1 |
G |
T |
9: 100,748,263 (GRCm39) |
S475I |
probably damaging |
Het |
Stxbp5l |
A |
G |
16: 36,936,029 (GRCm39) |
Y1183H |
probably damaging |
Het |
Svep1 |
A |
T |
4: 58,135,628 (GRCm39) |
|
probably null |
Het |
Tm9sf2 |
A |
G |
14: 122,396,096 (GRCm39) |
T653A |
probably benign |
Het |
Tmeff1 |
T |
C |
4: 48,662,059 (GRCm39) |
S366P |
possibly damaging |
Het |
Tnnt2 |
G |
T |
1: 135,779,803 (GRCm39) |
W300L |
probably damaging |
Het |
Traj32 |
A |
G |
14: 54,423,560 (GRCm39) |
|
probably benign |
Het |
Trp53bp2 |
A |
T |
1: 182,269,204 (GRCm39) |
M223L |
probably benign |
Het |
Tsga10 |
G |
A |
1: 37,854,758 (GRCm39) |
T246M |
probably damaging |
Het |
Txn2 |
A |
T |
15: 77,810,870 (GRCm39) |
|
probably benign |
Het |
Ubr3 |
T |
A |
2: 69,768,542 (GRCm39) |
F450I |
probably damaging |
Het |
Usp47 |
T |
C |
7: 111,703,677 (GRCm39) |
|
probably null |
Het |
Vars2 |
C |
T |
17: 35,975,685 (GRCm39) |
R244Q |
probably damaging |
Het |
Xrra1 |
T |
A |
7: 99,546,803 (GRCm39) |
F251L |
probably damaging |
Het |
Zfp804a |
G |
A |
2: 82,087,863 (GRCm39) |
R564Q |
probably benign |
Het |
Zfp983 |
T |
C |
17: 21,877,883 (GRCm39) |
C29R |
probably damaging |
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 |
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 |
|