Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810010H24Rik |
T |
C |
11: 106,919,324 (GRCm39) |
V223A |
probably damaging |
Het |
2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
Ahctf1 |
A |
T |
1: 179,611,675 (GRCm39) |
I565N |
possibly damaging |
Het |
Ank1 |
C |
T |
8: 23,572,300 (GRCm39) |
T70I |
probably damaging |
Het |
Atg16l1 |
C |
A |
1: 87,701,902 (GRCm39) |
S248* |
probably null |
Het |
Atp13a5 |
A |
T |
16: 29,169,566 (GRCm39) |
L42Q |
probably damaging |
Het |
Atxn1 |
T |
C |
13: 45,710,545 (GRCm39) |
N796D |
probably damaging |
Het |
C3 |
T |
A |
17: 57,530,236 (GRCm39) |
Y455F |
probably benign |
Het |
Card11 |
A |
T |
5: 140,862,275 (GRCm39) |
D1007E |
possibly damaging |
Het |
Cbr2 |
T |
C |
11: 120,621,697 (GRCm39) |
D60G |
possibly damaging |
Het |
Cgn |
T |
A |
3: 94,683,455 (GRCm39) |
E400V |
probably null |
Het |
Chil3 |
T |
A |
3: 106,057,477 (GRCm39) |
Y229F |
possibly damaging |
Het |
Clcn2 |
G |
A |
16: 20,525,965 (GRCm39) |
P785S |
probably damaging |
Het |
Clk1 |
T |
C |
1: 58,453,642 (GRCm39) |
I315V |
probably benign |
Het |
Cops6 |
A |
G |
5: 138,160,459 (GRCm39) |
D102G |
probably benign |
Het |
Dennd5a |
A |
G |
7: 109,513,983 (GRCm39) |
I743T |
possibly damaging |
Het |
Dnaaf5 |
T |
A |
5: 139,149,012 (GRCm39) |
L437Q |
probably damaging |
Het |
Dnah12 |
T |
A |
14: 26,431,326 (GRCm39) |
D381E |
probably benign |
Het |
Dnah8 |
G |
A |
17: 30,967,542 (GRCm39) |
D2585N |
probably benign |
Het |
Draxin |
C |
A |
4: 148,192,436 (GRCm39) |
R292L |
probably damaging |
Het |
Dst |
T |
C |
1: 34,289,728 (GRCm39) |
V5776A |
probably damaging |
Het |
Eddm13 |
G |
A |
7: 6,269,332 (GRCm39) |
|
probably benign |
Het |
Ercc4 |
G |
A |
16: 12,941,445 (GRCm39) |
|
probably benign |
Het |
Eya1 |
T |
A |
1: 14,254,582 (GRCm39) |
N417Y |
probably damaging |
Het |
Fam149b |
T |
A |
14: 20,413,439 (GRCm39) |
H219Q |
possibly damaging |
Het |
Fam227b |
G |
A |
2: 125,958,043 (GRCm39) |
P241S |
probably damaging |
Het |
Fat1 |
A |
T |
8: 45,484,300 (GRCm39) |
|
probably null |
Het |
Fbxl18 |
A |
G |
5: 142,872,435 (GRCm39) |
S267P |
probably damaging |
Het |
Fer1l4 |
T |
C |
2: 155,873,135 (GRCm39) |
Y1315C |
probably damaging |
Het |
Fgd2 |
T |
C |
17: 29,593,954 (GRCm39) |
|
probably null |
Het |
Gm7251 |
T |
A |
13: 49,958,656 (GRCm39) |
|
noncoding transcript |
Het |
Golt1a |
T |
C |
1: 133,248,006 (GRCm39) |
V78A |
probably damaging |
Het |
Gsn |
T |
A |
2: 35,188,933 (GRCm39) |
Y440N |
probably damaging |
Het |
Gtf2ird2 |
G |
T |
5: 134,245,824 (GRCm39) |
S694I |
possibly damaging |
Het |
H2-Ob |
T |
A |
17: 34,460,253 (GRCm39) |
|
probably null |
Het |
Hsp90b1 |
T |
C |
10: 86,532,617 (GRCm39) |
D353G |
probably benign |
Het |
Ilk |
A |
G |
7: 105,391,456 (GRCm39) |
D374G |
probably damaging |
Het |
Invs |
G |
A |
4: 48,421,807 (GRCm39) |
R813Q |
probably damaging |
Het |
Itga7 |
G |
A |
10: 128,785,316 (GRCm39) |
V836M |
possibly damaging |
Het |
Itln1 |
T |
A |
1: 171,360,958 (GRCm39) |
K45* |
probably null |
Het |
Ivd |
A |
G |
2: 118,710,946 (GRCm39) |
Y385C |
probably damaging |
Het |
Ivns1abp |
T |
A |
1: 151,238,953 (GRCm39) |
M589K |
possibly damaging |
Het |
Jakmip3 |
C |
T |
7: 138,621,951 (GRCm39) |
R284W |
probably damaging |
Het |
Kank3 |
T |
C |
17: 34,041,044 (GRCm39) |
L512P |
probably damaging |
Het |
Kcnn2 |
T |
A |
18: 45,818,352 (GRCm39) |
I483N |
possibly damaging |
Het |
Klk1b4 |
A |
G |
7: 43,860,492 (GRCm39) |
N170S |
probably benign |
Het |
Klk1b9 |
A |
C |
7: 43,445,419 (GRCm39) |
D203A |
probably damaging |
Het |
Lbr |
A |
T |
1: 181,647,453 (GRCm39) |
Y199* |
probably null |
Het |
Lcn6 |
T |
A |
2: 25,567,082 (GRCm39) |
|
probably null |
Het |
Lrriq1 |
T |
C |
10: 103,025,784 (GRCm39) |
D946G |
probably damaging |
Het |
Ltbp1 |
T |
A |
17: 75,373,152 (GRCm39) |
L265H |
probably damaging |
Het |
Maml3 |
A |
T |
3: 51,598,196 (GRCm39) |
N183K |
possibly damaging |
Het |
Mprip |
T |
C |
11: 59,650,721 (GRCm39) |
V1475A |
possibly damaging |
Het |
Myh4 |
C |
A |
11: 67,147,189 (GRCm39) |
S1611R |
probably benign |
Het |
Nagpa |
A |
T |
16: 5,013,743 (GRCm39) |
M365K |
probably benign |
Het |
Nckap5l |
G |
T |
15: 99,324,457 (GRCm39) |
P682Q |
probably benign |
Het |
Nudt12 |
T |
C |
17: 59,303,499 (GRCm39) |
|
probably benign |
Het |
Nup153 |
T |
C |
13: 46,840,879 (GRCm39) |
T910A |
possibly damaging |
Het |
Or1e31 |
T |
A |
11: 73,690,473 (GRCm39) |
T37S |
possibly damaging |
Het |
Or5ae2 |
T |
C |
7: 84,505,646 (GRCm39) |
V23A |
probably damaging |
Het |
Or7c74 |
A |
G |
2: 37,160,937 (GRCm39) |
|
noncoding transcript |
Het |
Or8k53 |
A |
T |
2: 86,177,647 (GRCm39) |
F154L |
probably benign |
Het |
Pate14 |
T |
C |
9: 36,549,120 (GRCm39) |
N47D |
probably benign |
Het |
Pbx2 |
T |
A |
17: 34,813,673 (GRCm39) |
C224* |
probably null |
Het |
Pcdha6 |
A |
G |
18: 37,100,960 (GRCm39) |
D51G |
probably damaging |
Het |
Pnpla1 |
C |
T |
17: 29,104,558 (GRCm39) |
T538I |
possibly damaging |
Het |
Pnpla2 |
T |
C |
7: 141,039,204 (GRCm39) |
|
probably null |
Het |
Psme2b |
C |
T |
11: 48,836,654 (GRCm39) |
E98K |
probably benign |
Het |
Rimbp2 |
T |
C |
5: 128,880,985 (GRCm39) |
Y134C |
probably damaging |
Het |
Ryr1 |
G |
A |
7: 28,802,234 (GRCm39) |
|
probably null |
Het |
Sh3tc1 |
G |
T |
5: 35,857,633 (GRCm39) |
A1185D |
probably damaging |
Het |
Sin3b |
G |
A |
8: 73,471,184 (GRCm39) |
S377N |
probably benign |
Het |
Slc28a2 |
T |
C |
2: 122,288,371 (GRCm39) |
M554T |
possibly damaging |
Het |
Snhg11 |
T |
C |
2: 158,218,872 (GRCm39) |
|
probably benign |
Het |
Spink5 |
A |
T |
18: 44,139,479 (GRCm39) |
N614I |
probably damaging |
Het |
Tert |
T |
C |
13: 73,794,428 (GRCm39) |
|
probably null |
Het |
Thap4 |
T |
C |
1: 93,677,598 (GRCm39) |
Y396C |
probably damaging |
Het |
Tle2 |
T |
C |
10: 81,420,531 (GRCm39) |
L348P |
probably damaging |
Het |
Tmem104 |
T |
C |
11: 115,134,312 (GRCm39) |
S283P |
probably damaging |
Het |
Tnn |
T |
C |
1: 159,953,949 (GRCm39) |
E602G |
possibly damaging |
Het |
Tpm4 |
A |
G |
8: 72,900,938 (GRCm39) |
K190R |
probably benign |
Het |
Ttf2 |
T |
C |
3: 100,870,485 (GRCm39) |
E196G |
probably benign |
Het |
Ugt3a1 |
T |
C |
15: 9,365,373 (GRCm39) |
W329R |
probably damaging |
Het |
Unc13a |
G |
A |
8: 72,094,121 (GRCm39) |
Q1327* |
probably null |
Het |
Vmn1r194 |
C |
T |
13: 22,429,058 (GRCm39) |
T225I |
probably benign |
Het |
Vmn1r215 |
T |
C |
13: 23,260,721 (GRCm39) |
S254P |
probably damaging |
Het |
Vmn2r109 |
T |
C |
17: 20,775,451 (GRCm39) |
E92G |
probably damaging |
Het |
Ythdc2 |
A |
G |
18: 44,987,809 (GRCm39) |
M625V |
probably benign |
Het |
Zfp106 |
A |
G |
2: 120,341,015 (GRCm39) |
W1832R |
probably damaging |
Het |
Zfp189 |
G |
A |
4: 49,530,438 (GRCm39) |
G514S |
probably damaging |
Het |
Zfp768 |
T |
C |
7: 126,942,875 (GRCm39) |
R418G |
probably damaging |
Het |
Zmynd11 |
C |
T |
13: 9,739,479 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Ranbp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Ranbp2
|
APN |
10 |
58,313,078 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00336:Ranbp2
|
APN |
10 |
58,287,806 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00486:Ranbp2
|
APN |
10 |
58,313,434 (GRCm39) |
missense |
probably benign |
0.06 |
IGL00800:Ranbp2
|
APN |
10 |
58,326,526 (GRCm39) |
missense |
probably benign |
|
IGL00834:Ranbp2
|
APN |
10 |
58,289,145 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00852:Ranbp2
|
APN |
10 |
58,313,723 (GRCm39) |
missense |
probably benign |
|
IGL00984:Ranbp2
|
APN |
10 |
58,297,786 (GRCm39) |
nonsense |
probably null |
|
IGL01299:Ranbp2
|
APN |
10 |
58,328,639 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01325:Ranbp2
|
APN |
10 |
58,312,120 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01444:Ranbp2
|
APN |
10 |
58,311,122 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL01545:Ranbp2
|
APN |
10 |
58,314,703 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL01619:Ranbp2
|
APN |
10 |
58,299,900 (GRCm39) |
splice site |
probably null |
|
IGL01782:Ranbp2
|
APN |
10 |
58,314,131 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02020:Ranbp2
|
APN |
10 |
58,315,769 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02096:Ranbp2
|
APN |
10 |
58,297,789 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02182:Ranbp2
|
APN |
10 |
58,321,582 (GRCm39) |
nonsense |
probably null |
|
IGL02211:Ranbp2
|
APN |
10 |
58,314,064 (GRCm39) |
missense |
probably benign |
|
IGL02249:Ranbp2
|
APN |
10 |
58,315,900 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02268:Ranbp2
|
APN |
10 |
58,329,475 (GRCm39) |
unclassified |
probably benign |
|
IGL02421:Ranbp2
|
APN |
10 |
58,316,376 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03080:Ranbp2
|
APN |
10 |
58,312,613 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03119:Ranbp2
|
APN |
10 |
58,287,825 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03206:Ranbp2
|
APN |
10 |
58,301,369 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03237:Ranbp2
|
APN |
10 |
58,328,783 (GRCm39) |
missense |
probably damaging |
0.98 |
En_passant
|
UTSW |
10 |
58,287,839 (GRCm39) |
missense |
probably damaging |
1.00 |
red_river
|
UTSW |
10 |
58,301,489 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02799:Ranbp2
|
UTSW |
10 |
58,316,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R0058:Ranbp2
|
UTSW |
10 |
58,316,353 (GRCm39) |
missense |
probably damaging |
0.98 |
R0058:Ranbp2
|
UTSW |
10 |
58,316,353 (GRCm39) |
missense |
probably damaging |
0.98 |
R0145:Ranbp2
|
UTSW |
10 |
58,315,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R0309:Ranbp2
|
UTSW |
10 |
58,315,690 (GRCm39) |
missense |
probably benign |
0.04 |
R0375:Ranbp2
|
UTSW |
10 |
58,313,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R0441:Ranbp2
|
UTSW |
10 |
58,321,590 (GRCm39) |
missense |
probably benign |
0.40 |
R0494:Ranbp2
|
UTSW |
10 |
58,303,254 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0542:Ranbp2
|
UTSW |
10 |
58,314,236 (GRCm39) |
missense |
probably benign |
0.02 |
R0565:Ranbp2
|
UTSW |
10 |
58,312,158 (GRCm39) |
missense |
probably benign |
0.41 |
R0608:Ranbp2
|
UTSW |
10 |
58,329,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R0661:Ranbp2
|
UTSW |
10 |
58,314,555 (GRCm39) |
missense |
probably benign |
|
R0670:Ranbp2
|
UTSW |
10 |
58,316,520 (GRCm39) |
missense |
probably benign |
0.01 |
R0760:Ranbp2
|
UTSW |
10 |
58,312,613 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0811:Ranbp2
|
UTSW |
10 |
58,301,351 (GRCm39) |
missense |
probably benign |
0.01 |
R0812:Ranbp2
|
UTSW |
10 |
58,301,351 (GRCm39) |
missense |
probably benign |
0.01 |
R1180:Ranbp2
|
UTSW |
10 |
58,301,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R1196:Ranbp2
|
UTSW |
10 |
58,312,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R1216:Ranbp2
|
UTSW |
10 |
58,319,034 (GRCm39) |
splice site |
probably benign |
|
R1374:Ranbp2
|
UTSW |
10 |
58,321,715 (GRCm39) |
splice site |
probably benign |
|
R1541:Ranbp2
|
UTSW |
10 |
58,318,916 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1589:Ranbp2
|
UTSW |
10 |
58,299,808 (GRCm39) |
missense |
probably benign |
0.01 |
R1711:Ranbp2
|
UTSW |
10 |
58,296,341 (GRCm39) |
missense |
probably benign |
0.11 |
R1761:Ranbp2
|
UTSW |
10 |
58,321,563 (GRCm39) |
missense |
probably benign |
0.02 |
R1831:Ranbp2
|
UTSW |
10 |
58,315,044 (GRCm39) |
nonsense |
probably null |
|
R1840:Ranbp2
|
UTSW |
10 |
58,314,588 (GRCm39) |
missense |
probably benign |
0.41 |
R1869:Ranbp2
|
UTSW |
10 |
58,328,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R1871:Ranbp2
|
UTSW |
10 |
58,328,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R1892:Ranbp2
|
UTSW |
10 |
58,299,921 (GRCm39) |
missense |
probably benign |
0.36 |
R2270:Ranbp2
|
UTSW |
10 |
58,291,749 (GRCm39) |
missense |
probably benign |
0.06 |
R2363:Ranbp2
|
UTSW |
10 |
58,314,758 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3844:Ranbp2
|
UTSW |
10 |
58,313,717 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3937:Ranbp2
|
UTSW |
10 |
58,312,294 (GRCm39) |
missense |
probably benign |
0.00 |
R3938:Ranbp2
|
UTSW |
10 |
58,312,294 (GRCm39) |
missense |
probably benign |
0.00 |
R4025:Ranbp2
|
UTSW |
10 |
58,316,378 (GRCm39) |
missense |
probably benign |
0.23 |
R4183:Ranbp2
|
UTSW |
10 |
58,301,488 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4247:Ranbp2
|
UTSW |
10 |
58,314,686 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4334:Ranbp2
|
UTSW |
10 |
58,299,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R4656:Ranbp2
|
UTSW |
10 |
58,289,244 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4746:Ranbp2
|
UTSW |
10 |
58,328,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R4852:Ranbp2
|
UTSW |
10 |
58,312,878 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4863:Ranbp2
|
UTSW |
10 |
58,328,243 (GRCm39) |
missense |
probably damaging |
0.99 |
R5014:Ranbp2
|
UTSW |
10 |
58,299,942 (GRCm39) |
missense |
probably benign |
0.40 |
R5145:Ranbp2
|
UTSW |
10 |
58,315,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R5178:Ranbp2
|
UTSW |
10 |
58,312,607 (GRCm39) |
missense |
probably benign |
0.01 |
R5199:Ranbp2
|
UTSW |
10 |
58,300,265 (GRCm39) |
missense |
probably benign |
|
R5294:Ranbp2
|
UTSW |
10 |
58,314,490 (GRCm39) |
missense |
probably benign |
0.23 |
R5508:Ranbp2
|
UTSW |
10 |
58,315,827 (GRCm39) |
missense |
probably damaging |
0.97 |
R5511:Ranbp2
|
UTSW |
10 |
58,329,561 (GRCm39) |
missense |
probably benign |
0.29 |
R5575:Ranbp2
|
UTSW |
10 |
58,328,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R5617:Ranbp2
|
UTSW |
10 |
58,301,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R5630:Ranbp2
|
UTSW |
10 |
58,314,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R5733:Ranbp2
|
UTSW |
10 |
58,321,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R5751:Ranbp2
|
UTSW |
10 |
58,300,086 (GRCm39) |
splice site |
probably null |
|
R5767:Ranbp2
|
UTSW |
10 |
58,312,647 (GRCm39) |
missense |
probably benign |
0.02 |
R6122:Ranbp2
|
UTSW |
10 |
58,301,351 (GRCm39) |
missense |
probably benign |
0.02 |
R6147:Ranbp2
|
UTSW |
10 |
58,315,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R6286:Ranbp2
|
UTSW |
10 |
58,315,394 (GRCm39) |
missense |
probably benign |
0.02 |
R6344:Ranbp2
|
UTSW |
10 |
58,319,708 (GRCm39) |
splice site |
probably null |
|
R6452:Ranbp2
|
UTSW |
10 |
58,313,979 (GRCm39) |
missense |
probably benign |
0.00 |
R6487:Ranbp2
|
UTSW |
10 |
58,321,563 (GRCm39) |
missense |
probably benign |
0.02 |
R6620:Ranbp2
|
UTSW |
10 |
58,291,629 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6759:Ranbp2
|
UTSW |
10 |
58,293,559 (GRCm39) |
nonsense |
probably null |
|
R7010:Ranbp2
|
UTSW |
10 |
58,290,393 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7071:Ranbp2
|
UTSW |
10 |
58,328,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R7083:Ranbp2
|
UTSW |
10 |
58,315,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R7088:Ranbp2
|
UTSW |
10 |
58,299,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R7102:Ranbp2
|
UTSW |
10 |
58,299,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R7194:Ranbp2
|
UTSW |
10 |
58,312,591 (GRCm39) |
missense |
probably benign |
0.05 |
R7217:Ranbp2
|
UTSW |
10 |
58,287,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R7318:Ranbp2
|
UTSW |
10 |
58,318,909 (GRCm39) |
nonsense |
probably null |
|
R7341:Ranbp2
|
UTSW |
10 |
58,321,619 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7398:Ranbp2
|
UTSW |
10 |
58,303,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R7424:Ranbp2
|
UTSW |
10 |
58,315,016 (GRCm39) |
missense |
probably damaging |
0.98 |
R7727:Ranbp2
|
UTSW |
10 |
58,291,260 (GRCm39) |
missense |
probably benign |
0.09 |
R7795:Ranbp2
|
UTSW |
10 |
58,319,729 (GRCm39) |
nonsense |
probably null |
|
R7812:Ranbp2
|
UTSW |
10 |
58,303,224 (GRCm39) |
missense |
probably benign |
|
R7845:Ranbp2
|
UTSW |
10 |
58,282,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R7875:Ranbp2
|
UTSW |
10 |
58,314,277 (GRCm39) |
nonsense |
probably null |
|
R7934:Ranbp2
|
UTSW |
10 |
58,312,297 (GRCm39) |
missense |
probably damaging |
0.98 |
R8022:Ranbp2
|
UTSW |
10 |
58,321,683 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8050:Ranbp2
|
UTSW |
10 |
58,315,441 (GRCm39) |
missense |
probably damaging |
0.99 |
R8100:Ranbp2
|
UTSW |
10 |
58,326,470 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8194:Ranbp2
|
UTSW |
10 |
58,291,747 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8258:Ranbp2
|
UTSW |
10 |
58,291,755 (GRCm39) |
missense |
probably benign |
0.04 |
R8259:Ranbp2
|
UTSW |
10 |
58,291,755 (GRCm39) |
missense |
probably benign |
0.04 |
R8461:Ranbp2
|
UTSW |
10 |
58,312,216 (GRCm39) |
missense |
probably damaging |
0.97 |
R8722:Ranbp2
|
UTSW |
10 |
58,312,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R8755:Ranbp2
|
UTSW |
10 |
58,300,969 (GRCm39) |
nonsense |
probably null |
|
R8794:Ranbp2
|
UTSW |
10 |
58,328,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R8879:Ranbp2
|
UTSW |
10 |
58,313,711 (GRCm39) |
missense |
probably benign |
0.10 |
R8994:Ranbp2
|
UTSW |
10 |
58,315,891 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9023:Ranbp2
|
UTSW |
10 |
58,315,343 (GRCm39) |
nonsense |
probably null |
|
R9124:Ranbp2
|
UTSW |
10 |
58,328,719 (GRCm39) |
missense |
probably benign |
0.01 |
R9133:Ranbp2
|
UTSW |
10 |
58,313,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R9145:Ranbp2
|
UTSW |
10 |
58,291,736 (GRCm39) |
missense |
probably benign |
0.03 |
R9190:Ranbp2
|
UTSW |
10 |
58,313,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R9369:Ranbp2
|
UTSW |
10 |
58,316,486 (GRCm39) |
missense |
probably benign |
0.04 |
R9394:Ranbp2
|
UTSW |
10 |
58,291,698 (GRCm39) |
missense |
probably damaging |
0.97 |
R9642:Ranbp2
|
UTSW |
10 |
58,318,907 (GRCm39) |
missense |
probably damaging |
0.99 |
R9673:Ranbp2
|
UTSW |
10 |
58,300,963 (GRCm39) |
missense |
probably damaging |
1.00 |
X0018:Ranbp2
|
UTSW |
10 |
58,314,406 (GRCm39) |
missense |
probably benign |
0.13 |
X0022:Ranbp2
|
UTSW |
10 |
58,300,977 (GRCm39) |
missense |
probably benign |
0.33 |
Z1088:Ranbp2
|
UTSW |
10 |
58,328,715 (GRCm39) |
missense |
probably benign |
0.35 |
Z1088:Ranbp2
|
UTSW |
10 |
58,313,805 (GRCm39) |
frame shift |
probably null |
|
Z1088:Ranbp2
|
UTSW |
10 |
58,313,794 (GRCm39) |
frame shift |
probably null |
|
Z1176:Ranbp2
|
UTSW |
10 |
58,297,708 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ranbp2
|
UTSW |
10 |
58,329,713 (GRCm39) |
nonsense |
probably null |
|
|