Other mutations in this stock |
Total: 117 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931414P19Rik |
G |
A |
14: 54,822,444 (GRCm39) |
R8* |
probably null |
Het |
Abhd17a |
A |
G |
10: 80,421,440 (GRCm39) |
|
probably null |
Het |
Acsm1 |
A |
G |
7: 119,255,262 (GRCm39) |
R415G |
probably damaging |
Het |
Acta1 |
G |
T |
8: 124,618,803 (GRCm39) |
T360N |
probably benign |
Het |
Adam6a |
T |
A |
12: 113,508,049 (GRCm39) |
S141T |
probably benign |
Het |
Adgrd1 |
G |
T |
5: 129,192,159 (GRCm39) |
K76N |
probably benign |
Het |
Afdn |
A |
G |
17: 14,030,695 (GRCm39) |
E202G |
probably damaging |
Het |
Agps |
T |
A |
2: 75,689,270 (GRCm39) |
M156K |
probably benign |
Het |
Agxt |
A |
G |
1: 93,065,037 (GRCm39) |
I149V |
probably benign |
Het |
Aoc1l1 |
T |
A |
6: 48,954,689 (GRCm39) |
L609* |
probably null |
Het |
Aqp2 |
A |
G |
15: 99,477,247 (GRCm39) |
T72A |
probably damaging |
Het |
Arhgap18 |
T |
A |
10: 26,725,938 (GRCm39) |
D54E |
probably benign |
Het |
Asb8 |
C |
A |
15: 98,033,950 (GRCm39) |
E202* |
probably null |
Het |
Bmp5 |
A |
G |
9: 75,801,072 (GRCm39) |
I401V |
probably damaging |
Het |
Bscl2 |
T |
C |
19: 8,822,684 (GRCm39) |
|
probably null |
Het |
Capn9 |
G |
A |
8: 125,332,450 (GRCm39) |
G430R |
possibly damaging |
Het |
Cd55 |
C |
T |
1: 130,377,160 (GRCm39) |
V333I |
probably benign |
Het |
Cep112 |
A |
G |
11: 108,497,151 (GRCm39) |
E697G |
probably damaging |
Het |
Cerk |
G |
A |
15: 86,027,009 (GRCm39) |
S167L |
probably benign |
Het |
Chrm3 |
T |
A |
13: 9,928,371 (GRCm39) |
I222F |
probably damaging |
Het |
Clcn6 |
A |
G |
4: 148,108,594 (GRCm39) |
F145S |
possibly damaging |
Het |
Cnksr1 |
A |
G |
4: 133,956,939 (GRCm39) |
Y488H |
probably damaging |
Het |
Cntrl |
CAGAG |
CAG |
2: 35,012,818 (GRCm39) |
|
probably null |
Het |
Commd10 |
A |
T |
18: 47,096,814 (GRCm39) |
T74S |
probably benign |
Het |
Cyp4f39 |
T |
C |
17: 32,701,112 (GRCm39) |
F201L |
probably benign |
Het |
Dennd4a |
A |
G |
9: 64,796,887 (GRCm39) |
T860A |
possibly damaging |
Het |
Dlg5 |
A |
T |
14: 24,204,715 (GRCm39) |
I1253N |
probably damaging |
Het |
Dnah7b |
T |
A |
1: 46,307,830 (GRCm39) |
M3048K |
probably damaging |
Het |
Dnah9 |
A |
G |
11: 65,935,509 (GRCm39) |
M1970T |
probably damaging |
Het |
Dsc3 |
A |
T |
18: 20,122,737 (GRCm39) |
D62E |
possibly damaging |
Het |
Dsel |
T |
C |
1: 111,787,187 (GRCm39) |
N1116S |
probably benign |
Het |
Dusp7 |
C |
T |
9: 106,251,096 (GRCm39) |
T407M |
probably damaging |
Het |
Efnb1 |
A |
G |
X: 98,191,123 (GRCm39) |
Y343C |
probably damaging |
Het |
Eif1ad8 |
A |
G |
12: 87,564,046 (GRCm39) |
D127G |
unknown |
Het |
Entpd5 |
A |
G |
12: 84,443,632 (GRCm39) |
I12T |
probably benign |
Het |
Espn |
T |
C |
4: 152,205,714 (GRCm39) |
E408G |
probably damaging |
Het |
Fhip1b |
A |
T |
7: 105,039,046 (GRCm39) |
D64E |
probably damaging |
Het |
Gdpd3 |
A |
G |
7: 126,367,766 (GRCm39) |
T200A |
probably damaging |
Het |
Gli1 |
A |
G |
10: 127,172,596 (GRCm39) |
L182P |
probably damaging |
Het |
Gm5134 |
G |
A |
10: 75,840,718 (GRCm39) |
A521T |
possibly damaging |
Het |
Gprasp1 |
G |
A |
X: 134,702,791 (GRCm39) |
E995K |
possibly damaging |
Het |
H2-M10.1 |
T |
C |
17: 36,636,108 (GRCm39) |
D153G |
possibly damaging |
Het |
Helb |
A |
T |
10: 119,941,926 (GRCm39) |
M254K |
possibly damaging |
Het |
I0C0044D17Rik |
A |
G |
4: 98,708,533 (GRCm39) |
|
probably benign |
Het |
Igfn1 |
AGGG |
AGG |
1: 135,902,590 (GRCm39) |
|
probably benign |
Het |
Igfn1 |
T |
A |
1: 135,898,376 (GRCm39) |
Q730L |
probably benign |
Het |
Jmjd1c |
T |
A |
10: 66,993,777 (GRCm39) |
L86* |
probably null |
Het |
Kat5 |
T |
A |
19: 5,655,713 (GRCm39) |
|
probably null |
Het |
Kif14 |
A |
G |
1: 136,414,818 (GRCm39) |
N768S |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,437,905 (GRCm39) |
E1199G |
possibly damaging |
Het |
Klhl29 |
A |
G |
12: 5,187,876 (GRCm39) |
S163P |
probably damaging |
Het |
Kmt2c |
C |
A |
5: 25,490,077 (GRCm39) |
Q4287H |
probably damaging |
Het |
Krt82 |
T |
A |
15: 101,453,591 (GRCm39) |
Q265L |
probably damaging |
Het |
Macf1 |
C |
T |
4: 123,248,895 (GRCm39) |
C7210Y |
probably damaging |
Het |
Mx2 |
G |
A |
16: 97,339,903 (GRCm39) |
E20K |
probably benign |
Het |
Myom2 |
T |
G |
8: 15,156,379 (GRCm39) |
I742S |
probably damaging |
Het |
Narf |
A |
T |
11: 121,141,195 (GRCm39) |
R310* |
probably null |
Het |
Nktr |
T |
A |
9: 121,570,760 (GRCm39) |
D167E |
probably damaging |
Het |
Nle1 |
A |
G |
11: 82,796,192 (GRCm39) |
W183R |
probably damaging |
Het |
Npas3 |
A |
G |
12: 54,108,871 (GRCm39) |
N425S |
probably damaging |
Het |
Obsl1 |
G |
A |
1: 75,486,756 (GRCm38) |
T1764M |
probably benign |
Het |
Optc |
A |
T |
1: 133,831,534 (GRCm39) |
|
probably null |
Het |
Or4a27 |
A |
T |
2: 88,559,089 (GRCm39) |
Y285N |
probably damaging |
Het |
Or4a68 |
C |
T |
2: 89,269,927 (GRCm39) |
R232H |
probably benign |
Het |
Or4d5 |
T |
A |
9: 40,012,415 (GRCm39) |
I124L |
probably benign |
Het |
Or6c69 |
A |
G |
10: 129,748,036 (GRCm39) |
V37A |
probably benign |
Het |
Or8g52 |
A |
T |
9: 39,631,411 (GRCm39) |
D296V |
probably damaging |
Het |
Or8s2 |
G |
A |
15: 98,276,277 (GRCm39) |
T238I |
possibly damaging |
Het |
Otol1 |
T |
A |
3: 69,926,169 (GRCm39) |
F115I |
probably benign |
Het |
Parp8 |
T |
A |
13: 117,031,422 (GRCm39) |
D430V |
probably benign |
Het |
Pex7 |
T |
A |
10: 19,770,061 (GRCm39) |
H123L |
probably damaging |
Het |
Pkhd1l1 |
T |
A |
15: 44,410,909 (GRCm39) |
|
probably benign |
Het |
Pkhd1l1 |
G |
A |
15: 44,445,137 (GRCm39) |
D3670N |
probably damaging |
Het |
Plec |
T |
C |
15: 76,067,374 (GRCm39) |
T1331A |
probably benign |
Het |
Plekha4 |
A |
G |
7: 45,203,222 (GRCm39) |
D704G |
probably benign |
Het |
Plxnb2 |
T |
A |
15: 89,043,205 (GRCm39) |
N1453I |
probably damaging |
Het |
Pms1 |
T |
A |
1: 53,321,147 (GRCm39) |
I29F |
probably damaging |
Het |
Ppp1r1a |
G |
A |
15: 103,439,833 (GRCm39) |
T153I |
probably damaging |
Het |
Pramel12 |
T |
A |
4: 143,143,441 (GRCm39) |
L69Q |
probably damaging |
Het |
Prelp |
C |
T |
1: 133,842,869 (GRCm39) |
R92K |
probably benign |
Het |
Ptpre |
A |
G |
7: 135,272,424 (GRCm39) |
|
probably benign |
Het |
Ptprt |
A |
T |
2: 161,376,465 (GRCm39) |
I1312N |
probably damaging |
Het |
Ren1 |
C |
G |
1: 133,278,516 (GRCm39) |
|
probably null |
Het |
Rims1 |
C |
T |
1: 22,635,516 (GRCm39) |
C155Y |
probably damaging |
Het |
Ro60 |
T |
C |
1: 143,635,772 (GRCm39) |
D458G |
probably benign |
Het |
Slitrk6 |
T |
G |
14: 110,988,226 (GRCm39) |
T494P |
probably benign |
Het |
Sltm |
G |
A |
9: 70,488,583 (GRCm39) |
G578S |
probably benign |
Het |
Smyd5 |
A |
G |
6: 85,421,300 (GRCm39) |
E338G |
probably benign |
Het |
Snx2 |
G |
A |
18: 53,327,516 (GRCm39) |
V81M |
probably damaging |
Het |
Sp2 |
G |
T |
11: 96,852,191 (GRCm39) |
N244K |
probably benign |
Het |
Sspo |
C |
A |
6: 48,437,697 (GRCm39) |
|
probably benign |
Het |
Sspo |
A |
C |
6: 48,440,465 (GRCm39) |
D1568A |
probably benign |
Het |
Ssrp1 |
T |
C |
2: 84,871,771 (GRCm39) |
|
probably benign |
Het |
Syt2 |
ACTCTCTCT |
ACTCTCTCTCT |
1: 134,674,479 (GRCm39) |
|
probably benign |
Het |
Syt7 |
G |
A |
19: 10,416,577 (GRCm39) |
R138Q |
probably benign |
Het |
Taar7f |
T |
C |
10: 23,926,323 (GRCm39) |
Y306H |
possibly damaging |
Het |
Tbccd1 |
T |
C |
16: 22,637,291 (GRCm39) |
|
probably null |
Het |
Tesl1 |
T |
A |
X: 23,773,549 (GRCm39) |
V350E |
probably benign |
Het |
Tex261 |
A |
G |
6: 83,749,241 (GRCm39) |
Y119H |
probably damaging |
Het |
Tmem131l |
T |
G |
3: 83,850,095 (GRCm39) |
E234D |
probably damaging |
Het |
Tnnt2 |
TG |
TGG |
1: 135,774,499 (GRCm39) |
|
probably benign |
Het |
Top6bl |
A |
G |
19: 4,748,633 (GRCm39) |
|
probably benign |
Het |
Ttn |
C |
T |
2: 76,643,683 (GRCm39) |
G11436R |
probably damaging |
Het |
Ubap1 |
C |
T |
4: 41,379,257 (GRCm39) |
A157V |
probably damaging |
Het |
Ubr4 |
C |
T |
4: 139,204,518 (GRCm39) |
T4810M |
probably damaging |
Het |
Uso1 |
G |
A |
5: 92,329,795 (GRCm39) |
G427R |
probably damaging |
Het |
Usp15 |
A |
T |
10: 122,955,042 (GRCm39) |
V912D |
probably damaging |
Het |
Vmn1r20 |
T |
C |
6: 57,408,943 (GRCm39) |
S90P |
probably damaging |
Het |
Vmn1r32 |
T |
C |
6: 66,530,545 (GRCm39) |
K77R |
probably damaging |
Het |
Vmn2r100 |
A |
G |
17: 19,742,312 (GRCm39) |
K229E |
probably benign |
Het |
Vmn2r106 |
A |
G |
17: 20,488,566 (GRCm39) |
V611A |
possibly damaging |
Het |
Xrcc6 |
T |
A |
15: 81,907,178 (GRCm39) |
F167I |
probably damaging |
Het |
Zbtb21 |
G |
T |
16: 97,751,355 (GRCm39) |
P804H |
probably damaging |
Het |
Zdhhc3 |
T |
C |
9: 122,929,602 (GRCm39) |
D11G |
probably damaging |
Het |
Zfhx3 |
A |
G |
8: 109,671,809 (GRCm39) |
T1324A |
probably benign |
Het |
Zfp281 |
GCGGCAGCTCCGGCAGC |
GCGGCAGCTCCGGCAGCTCCGGCAGC |
1: 136,553,091 (GRCm39) |
|
probably benign |
Het |
Zfp608 |
G |
T |
18: 55,028,637 (GRCm39) |
L1259I |
probably damaging |
Het |
|
Other mutations in Ipo9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00896:Ipo9
|
APN |
1 |
135,327,797 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01611:Ipo9
|
APN |
1 |
135,314,431 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL01941:Ipo9
|
APN |
1 |
135,335,811 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01944:Ipo9
|
APN |
1 |
135,333,624 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01959:Ipo9
|
APN |
1 |
135,348,093 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02649:Ipo9
|
APN |
1 |
135,313,672 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02697:Ipo9
|
APN |
1 |
135,318,314 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03286:Ipo9
|
APN |
1 |
135,334,816 (GRCm39) |
intron |
probably benign |
|
FR4304:Ipo9
|
UTSW |
1 |
135,314,017 (GRCm39) |
nonsense |
probably null |
|
FR4304:Ipo9
|
UTSW |
1 |
135,314,013 (GRCm39) |
small insertion |
probably benign |
|
FR4340:Ipo9
|
UTSW |
1 |
135,314,009 (GRCm39) |
small insertion |
probably benign |
|
FR4340:Ipo9
|
UTSW |
1 |
135,314,007 (GRCm39) |
small insertion |
probably benign |
|
FR4548:Ipo9
|
UTSW |
1 |
135,314,013 (GRCm39) |
small insertion |
probably benign |
|
FR4589:Ipo9
|
UTSW |
1 |
135,314,019 (GRCm39) |
small insertion |
probably benign |
|
FR4589:Ipo9
|
UTSW |
1 |
135,314,004 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Ipo9
|
UTSW |
1 |
135,314,019 (GRCm39) |
small insertion |
probably benign |
|
R0111:Ipo9
|
UTSW |
1 |
135,333,662 (GRCm39) |
missense |
probably damaging |
0.97 |
R0238:Ipo9
|
UTSW |
1 |
135,332,074 (GRCm39) |
splice site |
probably benign |
|
R0239:Ipo9
|
UTSW |
1 |
135,332,074 (GRCm39) |
splice site |
probably benign |
|
R0279:Ipo9
|
UTSW |
1 |
135,348,101 (GRCm39) |
intron |
probably benign |
|
R0704:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small deletion |
probably benign |
|
R1070:Ipo9
|
UTSW |
1 |
135,334,281 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1282:Ipo9
|
UTSW |
1 |
135,330,030 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1467:Ipo9
|
UTSW |
1 |
135,334,281 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1467:Ipo9
|
UTSW |
1 |
135,334,281 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1728:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R1728:Ipo9
|
UTSW |
1 |
135,314,009 (GRCm39) |
small insertion |
probably benign |
|
R1728:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R1729:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R1729:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R1730:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R1730:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R1739:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R1739:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R1762:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R1762:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R1783:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R1783:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R1784:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R1784:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R1785:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R1785:Ipo9
|
UTSW |
1 |
135,314,019 (GRCm39) |
small insertion |
probably benign |
|
R1785:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R1899:Ipo9
|
UTSW |
1 |
135,327,884 (GRCm39) |
missense |
probably damaging |
0.99 |
R2049:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R2130:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R2130:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R2131:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R2131:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R2133:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R2133:Ipo9
|
UTSW |
1 |
135,314,013 (GRCm39) |
small insertion |
probably benign |
|
R2133:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R2136:Ipo9
|
UTSW |
1 |
135,322,023 (GRCm39) |
missense |
probably damaging |
0.98 |
R2141:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R2141:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R2142:Ipo9
|
UTSW |
1 |
135,314,020 (GRCm39) |
small insertion |
probably benign |
|
R2142:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R2142:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R2142:Ipo9
|
UTSW |
1 |
135,314,013 (GRCm39) |
small insertion |
probably benign |
|
R2356:Ipo9
|
UTSW |
1 |
135,334,555 (GRCm39) |
missense |
probably benign |
0.00 |
R2923:Ipo9
|
UTSW |
1 |
135,327,867 (GRCm39) |
missense |
probably benign |
0.25 |
R3161:Ipo9
|
UTSW |
1 |
135,337,214 (GRCm39) |
missense |
probably benign |
0.43 |
R3162:Ipo9
|
UTSW |
1 |
135,337,214 (GRCm39) |
missense |
probably benign |
0.43 |
R3162:Ipo9
|
UTSW |
1 |
135,337,214 (GRCm39) |
missense |
probably benign |
0.43 |
R4086:Ipo9
|
UTSW |
1 |
135,316,428 (GRCm39) |
unclassified |
probably benign |
|
R4679:Ipo9
|
UTSW |
1 |
135,321,907 (GRCm39) |
missense |
probably benign |
|
R4816:Ipo9
|
UTSW |
1 |
135,334,288 (GRCm39) |
missense |
probably benign |
0.21 |
R4956:Ipo9
|
UTSW |
1 |
135,331,960 (GRCm39) |
critical splice donor site |
probably null |
|
R5052:Ipo9
|
UTSW |
1 |
135,316,349 (GRCm39) |
splice site |
probably null |
|
R5055:Ipo9
|
UTSW |
1 |
135,330,097 (GRCm39) |
nonsense |
probably null |
|
R5230:Ipo9
|
UTSW |
1 |
135,347,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R5240:Ipo9
|
UTSW |
1 |
135,317,344 (GRCm39) |
unclassified |
probably benign |
|
R5257:Ipo9
|
UTSW |
1 |
135,313,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R5340:Ipo9
|
UTSW |
1 |
135,313,170 (GRCm39) |
missense |
probably benign |
0.00 |
R5560:Ipo9
|
UTSW |
1 |
135,329,983 (GRCm39) |
missense |
probably damaging |
0.99 |
R5602:Ipo9
|
UTSW |
1 |
135,329,983 (GRCm39) |
missense |
probably damaging |
0.99 |
R5604:Ipo9
|
UTSW |
1 |
135,329,983 (GRCm39) |
missense |
probably damaging |
0.99 |
R5654:Ipo9
|
UTSW |
1 |
135,313,210 (GRCm39) |
nonsense |
probably null |
|
R6018:Ipo9
|
UTSW |
1 |
135,318,274 (GRCm39) |
critical splice donor site |
probably null |
|
R6128:Ipo9
|
UTSW |
1 |
135,318,311 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6841:Ipo9
|
UTSW |
1 |
135,314,046 (GRCm39) |
missense |
probably benign |
|
R7230:Ipo9
|
UTSW |
1 |
135,334,496 (GRCm39) |
critical splice donor site |
probably benign |
|
R7255:Ipo9
|
UTSW |
1 |
135,313,726 (GRCm39) |
missense |
probably benign |
0.01 |
R7383:Ipo9
|
UTSW |
1 |
135,316,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R7844:Ipo9
|
UTSW |
1 |
135,322,062 (GRCm39) |
missense |
probably benign |
0.00 |
R7889:Ipo9
|
UTSW |
1 |
135,334,591 (GRCm39) |
missense |
probably benign |
0.22 |
R8125:Ipo9
|
UTSW |
1 |
135,331,078 (GRCm39) |
missense |
probably benign |
0.00 |
R8823:Ipo9
|
UTSW |
1 |
135,347,077 (GRCm39) |
missense |
probably damaging |
0.99 |
R8889:Ipo9
|
UTSW |
1 |
135,314,544 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8892:Ipo9
|
UTSW |
1 |
135,314,544 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8906:Ipo9
|
UTSW |
1 |
135,321,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R8926:Ipo9
|
UTSW |
1 |
135,313,952 (GRCm39) |
splice site |
probably benign |
|
R9084:Ipo9
|
UTSW |
1 |
135,334,563 (GRCm39) |
missense |
probably benign |
0.01 |
R9215:Ipo9
|
UTSW |
1 |
135,347,033 (GRCm39) |
missense |
probably benign |
0.05 |
R9756:Ipo9
|
UTSW |
1 |
135,314,057 (GRCm39) |
missense |
probably benign |
0.00 |
Y5405:Ipo9
|
UTSW |
1 |
135,314,022 (GRCm39) |
small insertion |
probably benign |
|
Y5405:Ipo9
|
UTSW |
1 |
135,314,013 (GRCm39) |
small insertion |
probably benign |
|
Y5405:Ipo9
|
UTSW |
1 |
135,314,007 (GRCm39) |
small insertion |
probably benign |
|
|