Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931406B18Rik |
A |
G |
7: 43,145,057 (GRCm39) |
V367A |
possibly damaging |
Het |
Abcb5 |
A |
T |
12: 118,904,104 (GRCm39) |
S200R |
possibly damaging |
Het |
Adam29 |
T |
C |
8: 56,326,100 (GRCm39) |
D118G |
probably damaging |
Het |
Adh4 |
A |
G |
3: 138,134,906 (GRCm39) |
D360G |
probably benign |
Het |
Ankle2 |
A |
G |
5: 110,399,476 (GRCm39) |
Q611R |
possibly damaging |
Het |
Ankra2 |
C |
T |
13: 98,409,881 (GRCm39) |
|
probably benign |
Het |
Ap1g2 |
T |
A |
14: 55,343,504 (GRCm39) |
I28F |
probably damaging |
Het |
Baz2a |
C |
T |
10: 127,961,015 (GRCm39) |
T1608I |
possibly damaging |
Het |
Cacnb4 |
T |
C |
2: 52,364,894 (GRCm39) |
D123G |
probably damaging |
Het |
Cage1 |
G |
A |
13: 38,212,123 (GRCm39) |
T51M |
probably benign |
Het |
Ccdc63 |
A |
G |
5: 122,260,876 (GRCm39) |
V216A |
probably benign |
Het |
Ccnd2 |
A |
G |
6: 127,125,841 (GRCm39) |
V65A |
probably damaging |
Het |
Cfap20dc |
A |
G |
14: 8,511,113 (GRCm38) |
S434P |
probably damaging |
Het |
Chd3 |
T |
A |
11: 69,245,230 (GRCm39) |
T1163S |
possibly damaging |
Het |
Cmbl |
A |
G |
15: 31,589,823 (GRCm39) |
|
probably benign |
Het |
Cobl |
G |
T |
11: 12,204,241 (GRCm39) |
N813K |
possibly damaging |
Het |
Cog5 |
G |
A |
12: 31,840,921 (GRCm39) |
V249M |
probably damaging |
Het |
Cps1 |
A |
G |
1: 67,182,080 (GRCm39) |
N98S |
probably damaging |
Het |
Cracd |
A |
G |
5: 77,005,463 (GRCm39) |
D608G |
unknown |
Het |
D630045J12Rik |
A |
T |
6: 38,126,648 (GRCm39) |
I1454N |
probably damaging |
Het |
Elmo2 |
A |
G |
2: 165,136,237 (GRCm39) |
V603A |
possibly damaging |
Het |
F12 |
A |
G |
13: 55,569,332 (GRCm39) |
|
probably benign |
Het |
Ficd |
G |
A |
5: 113,874,990 (GRCm39) |
V20I |
probably benign |
Het |
Gatad2b |
G |
T |
3: 90,249,244 (GRCm39) |
G94V |
probably benign |
Het |
Gm4845 |
G |
A |
1: 141,184,403 (GRCm39) |
|
noncoding transcript |
Het |
Hrnr |
G |
A |
3: 93,227,908 (GRCm39) |
V9I |
possibly damaging |
Het |
Kifc3 |
A |
G |
8: 95,829,040 (GRCm39) |
S584P |
probably damaging |
Het |
Klk1b24 |
C |
A |
7: 43,840,790 (GRCm39) |
Q73K |
probably benign |
Het |
Lrp10 |
C |
A |
14: 54,706,619 (GRCm39) |
N518K |
possibly damaging |
Het |
Lsr |
A |
G |
7: 30,658,706 (GRCm39) |
V247A |
possibly damaging |
Het |
Mfsd6 |
A |
T |
1: 52,748,862 (GRCm39) |
M1K |
probably null |
Het |
Mprip |
T |
A |
11: 59,631,941 (GRCm39) |
|
probably null |
Het |
Myo3b |
G |
T |
2: 70,257,160 (GRCm39) |
|
probably benign |
Het |
Oprd1 |
A |
G |
4: 131,844,696 (GRCm39) |
F104S |
possibly damaging |
Het |
Or1l4 |
T |
C |
2: 37,091,883 (GRCm39) |
V210A |
probably benign |
Het |
Or2g1 |
T |
A |
17: 38,107,162 (GRCm39) |
Y276N |
probably damaging |
Het |
Or4b1d |
A |
T |
2: 89,969,006 (GRCm39) |
I159N |
possibly damaging |
Het |
Or5ar1 |
T |
C |
2: 85,671,416 (GRCm39) |
T240A |
probably damaging |
Het |
Or5b109 |
C |
T |
19: 13,212,418 (GRCm39) |
S268L |
probably damaging |
Het |
Palb2 |
A |
G |
7: 121,712,479 (GRCm39) |
V591A |
probably damaging |
Het |
Pcdhb18 |
A |
T |
18: 37,623,786 (GRCm39) |
D372V |
probably damaging |
Het |
Phc3 |
A |
G |
3: 30,991,002 (GRCm39) |
V405A |
probably damaging |
Het |
Phf20l1 |
A |
T |
15: 66,513,796 (GRCm39) |
|
probably benign |
Het |
Pik3ip1 |
A |
G |
11: 3,283,259 (GRCm39) |
K57E |
possibly damaging |
Het |
Pkhd1l1 |
G |
A |
15: 44,455,372 (GRCm39) |
M4044I |
probably benign |
Het |
Pkhd1l1 |
T |
C |
15: 44,460,298 (GRCm39) |
V4169A |
probably benign |
Het |
Pklr |
A |
T |
3: 89,049,963 (GRCm39) |
I313F |
probably damaging |
Het |
Plxna4 |
T |
A |
6: 32,179,160 (GRCm39) |
T952S |
probably benign |
Het |
Pop4 |
A |
T |
7: 37,962,730 (GRCm39) |
I178N |
probably damaging |
Het |
Prorp |
A |
G |
12: 55,351,429 (GRCm39) |
D246G |
probably damaging |
Het |
Prss40 |
A |
C |
1: 34,597,182 (GRCm39) |
V122G |
probably damaging |
Het |
Rapgef2 |
C |
A |
3: 78,981,614 (GRCm39) |
|
probably null |
Het |
Rbm19 |
A |
G |
5: 120,269,311 (GRCm39) |
D538G |
probably damaging |
Het |
Rnf44 |
G |
A |
13: 54,829,803 (GRCm39) |
R312* |
probably null |
Het |
Rock1 |
T |
C |
18: 10,070,215 (GRCm39) |
|
probably benign |
Het |
Rrp1b |
A |
G |
17: 32,275,875 (GRCm39) |
E474G |
probably damaging |
Het |
Ryr2 |
T |
A |
13: 11,699,365 (GRCm39) |
I2959F |
probably damaging |
Het |
Sidt2 |
A |
G |
9: 45,850,803 (GRCm39) |
S801P |
probably damaging |
Het |
Skint6 |
T |
C |
4: 112,870,153 (GRCm39) |
I602V |
probably benign |
Het |
Slc6a19 |
C |
A |
13: 73,848,590 (GRCm39) |
V55L |
probably damaging |
Het |
Smarca4 |
C |
T |
9: 21,547,132 (GRCm39) |
T219I |
probably benign |
Het |
Trappc11 |
C |
A |
8: 47,966,964 (GRCm39) |
V440F |
probably damaging |
Het |
Vmn1r236 |
G |
A |
17: 21,507,108 (GRCm39) |
W75* |
probably null |
Het |
Vmn2r52 |
A |
G |
7: 9,892,799 (GRCm39) |
F780S |
probably benign |
Het |
Vmn2r82 |
G |
T |
10: 79,217,149 (GRCm39) |
A494S |
possibly damaging |
Het |
Vwa3b |
A |
T |
1: 37,084,049 (GRCm39) |
K74M |
probably damaging |
Het |
Zfp13 |
T |
C |
17: 23,799,819 (GRCm39) |
T82A |
probably benign |
Het |
Zfp82 |
T |
C |
7: 29,756,890 (GRCm39) |
E64G |
probably benign |
Het |
|
Other mutations in Wrn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00659:Wrn
|
APN |
8 |
33,812,405 (GRCm39) |
splice site |
probably benign |
|
IGL00661:Wrn
|
APN |
8 |
33,809,173 (GRCm39) |
splice site |
probably benign |
|
IGL01472:Wrn
|
APN |
8 |
33,819,200 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01544:Wrn
|
APN |
8 |
33,814,554 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01599:Wrn
|
APN |
8 |
33,731,039 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL01688:Wrn
|
APN |
8 |
33,800,730 (GRCm39) |
splice site |
probably benign |
|
IGL01916:Wrn
|
APN |
8 |
33,747,252 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL01925:Wrn
|
APN |
8 |
33,809,208 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02068:Wrn
|
APN |
8 |
33,800,777 (GRCm39) |
missense |
probably benign |
0.38 |
IGL02084:Wrn
|
APN |
8 |
33,775,207 (GRCm39) |
missense |
probably benign |
|
IGL02167:Wrn
|
APN |
8 |
33,807,583 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02230:Wrn
|
APN |
8 |
33,807,591 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02717:Wrn
|
APN |
8 |
33,833,601 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02982:Wrn
|
APN |
8 |
33,833,094 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03088:Wrn
|
APN |
8 |
33,758,851 (GRCm39) |
splice site |
probably benign |
|
IGL03179:Wrn
|
APN |
8 |
33,800,734 (GRCm39) |
splice site |
probably null |
|
IGL03306:Wrn
|
APN |
8 |
33,826,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R0004:Wrn
|
UTSW |
8 |
33,807,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R0190:Wrn
|
UTSW |
8 |
33,731,011 (GRCm39) |
missense |
probably benign |
0.02 |
R0441:Wrn
|
UTSW |
8 |
33,758,778 (GRCm39) |
missense |
probably benign |
0.24 |
R0463:Wrn
|
UTSW |
8 |
33,770,843 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0538:Wrn
|
UTSW |
8 |
33,826,119 (GRCm39) |
missense |
probably damaging |
0.99 |
R0682:Wrn
|
UTSW |
8 |
33,757,848 (GRCm39) |
missense |
probably benign |
0.00 |
R0729:Wrn
|
UTSW |
8 |
33,738,946 (GRCm39) |
splice site |
probably null |
|
R0744:Wrn
|
UTSW |
8 |
33,785,034 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0836:Wrn
|
UTSW |
8 |
33,785,034 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1168:Wrn
|
UTSW |
8 |
33,806,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R1301:Wrn
|
UTSW |
8 |
33,782,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R1352:Wrn
|
UTSW |
8 |
33,784,944 (GRCm39) |
missense |
probably benign |
0.25 |
R1396:Wrn
|
UTSW |
8 |
33,758,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R1432:Wrn
|
UTSW |
8 |
33,809,169 (GRCm39) |
splice site |
probably benign |
|
R1523:Wrn
|
UTSW |
8 |
33,782,744 (GRCm39) |
missense |
probably benign |
0.23 |
R1625:Wrn
|
UTSW |
8 |
33,819,158 (GRCm39) |
missense |
probably benign |
0.01 |
R1664:Wrn
|
UTSW |
8 |
33,770,794 (GRCm39) |
splice site |
probably null |
|
R1773:Wrn
|
UTSW |
8 |
33,833,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R1864:Wrn
|
UTSW |
8 |
33,778,892 (GRCm39) |
missense |
probably damaging |
0.99 |
R1868:Wrn
|
UTSW |
8 |
33,747,249 (GRCm39) |
missense |
probably benign |
0.03 |
R2011:Wrn
|
UTSW |
8 |
33,726,432 (GRCm39) |
missense |
probably benign |
0.02 |
R2075:Wrn
|
UTSW |
8 |
33,812,357 (GRCm39) |
missense |
probably benign |
0.00 |
R2091:Wrn
|
UTSW |
8 |
33,757,853 (GRCm39) |
missense |
probably benign |
|
R2213:Wrn
|
UTSW |
8 |
33,747,043 (GRCm39) |
missense |
probably benign |
0.05 |
R2255:Wrn
|
UTSW |
8 |
33,819,230 (GRCm39) |
missense |
probably benign |
0.13 |
R2276:Wrn
|
UTSW |
8 |
33,814,584 (GRCm39) |
missense |
probably benign |
0.02 |
R3177:Wrn
|
UTSW |
8 |
33,807,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R3277:Wrn
|
UTSW |
8 |
33,807,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R3779:Wrn
|
UTSW |
8 |
33,731,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R3827:Wrn
|
UTSW |
8 |
33,814,548 (GRCm39) |
missense |
probably benign |
0.00 |
R4111:Wrn
|
UTSW |
8 |
33,842,183 (GRCm39) |
missense |
probably benign |
0.02 |
R4392:Wrn
|
UTSW |
8 |
33,741,860 (GRCm39) |
missense |
probably damaging |
0.99 |
R4458:Wrn
|
UTSW |
8 |
33,785,026 (GRCm39) |
missense |
probably damaging |
0.99 |
R4650:Wrn
|
UTSW |
8 |
33,745,537 (GRCm39) |
missense |
probably benign |
0.05 |
R4656:Wrn
|
UTSW |
8 |
33,826,019 (GRCm39) |
splice site |
probably null |
|
R4657:Wrn
|
UTSW |
8 |
33,826,019 (GRCm39) |
splice site |
probably null |
|
R4667:Wrn
|
UTSW |
8 |
33,814,366 (GRCm39) |
missense |
probably benign |
0.00 |
R4735:Wrn
|
UTSW |
8 |
33,775,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R4933:Wrn
|
UTSW |
8 |
33,812,371 (GRCm39) |
missense |
probably benign |
0.01 |
R5104:Wrn
|
UTSW |
8 |
33,757,895 (GRCm39) |
splice site |
probably null |
|
R5166:Wrn
|
UTSW |
8 |
33,842,100 (GRCm39) |
critical splice donor site |
probably null |
|
R5279:Wrn
|
UTSW |
8 |
33,731,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R5400:Wrn
|
UTSW |
8 |
33,784,945 (GRCm39) |
missense |
probably benign |
0.02 |
R5575:Wrn
|
UTSW |
8 |
33,826,158 (GRCm39) |
missense |
probably benign |
0.02 |
R5695:Wrn
|
UTSW |
8 |
33,814,346 (GRCm39) |
missense |
probably benign |
0.26 |
R5729:Wrn
|
UTSW |
8 |
33,758,806 (GRCm39) |
missense |
probably benign |
0.02 |
R6044:Wrn
|
UTSW |
8 |
33,726,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R6139:Wrn
|
UTSW |
8 |
33,843,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R6158:Wrn
|
UTSW |
8 |
33,809,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R6192:Wrn
|
UTSW |
8 |
33,774,682 (GRCm39) |
missense |
probably benign |
0.12 |
R6243:Wrn
|
UTSW |
8 |
33,774,682 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6354:Wrn
|
UTSW |
8 |
33,833,666 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6429:Wrn
|
UTSW |
8 |
33,833,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R6490:Wrn
|
UTSW |
8 |
33,809,248 (GRCm39) |
missense |
probably benign |
0.01 |
R6529:Wrn
|
UTSW |
8 |
33,826,004 (GRCm39) |
splice site |
probably null |
|
R6535:Wrn
|
UTSW |
8 |
33,826,131 (GRCm39) |
missense |
probably damaging |
0.99 |
R7001:Wrn
|
UTSW |
8 |
33,842,157 (GRCm39) |
missense |
probably benign |
0.04 |
R7114:Wrn
|
UTSW |
8 |
33,775,149 (GRCm39) |
frame shift |
probably null |
|
R7198:Wrn
|
UTSW |
8 |
33,814,346 (GRCm39) |
missense |
probably benign |
0.00 |
R7200:Wrn
|
UTSW |
8 |
33,812,376 (GRCm39) |
missense |
probably benign |
0.00 |
R7227:Wrn
|
UTSW |
8 |
33,738,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R7299:Wrn
|
UTSW |
8 |
33,782,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R7374:Wrn
|
UTSW |
8 |
33,758,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R7402:Wrn
|
UTSW |
8 |
33,738,994 (GRCm39) |
missense |
probably benign |
0.00 |
R7404:Wrn
|
UTSW |
8 |
33,738,994 (GRCm39) |
missense |
probably benign |
0.00 |
R7405:Wrn
|
UTSW |
8 |
33,738,994 (GRCm39) |
missense |
probably benign |
0.00 |
R7464:Wrn
|
UTSW |
8 |
33,826,024 (GRCm39) |
critical splice donor site |
probably null |
|
R7474:Wrn
|
UTSW |
8 |
33,819,209 (GRCm39) |
missense |
probably damaging |
0.96 |
R7609:Wrn
|
UTSW |
8 |
33,800,741 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7729:Wrn
|
UTSW |
8 |
33,814,454 (GRCm39) |
missense |
probably benign |
0.21 |
R7830:Wrn
|
UTSW |
8 |
33,759,082 (GRCm39) |
missense |
probably damaging |
0.97 |
R7998:Wrn
|
UTSW |
8 |
33,782,671 (GRCm39) |
missense |
probably benign |
0.10 |
R8239:Wrn
|
UTSW |
8 |
33,819,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R8262:Wrn
|
UTSW |
8 |
33,814,274 (GRCm39) |
missense |
probably benign |
0.07 |
R8410:Wrn
|
UTSW |
8 |
33,759,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R8480:Wrn
|
UTSW |
8 |
33,778,796 (GRCm39) |
missense |
probably benign |
0.10 |
R8530:Wrn
|
UTSW |
8 |
33,770,852 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8540:Wrn
|
UTSW |
8 |
33,842,154 (GRCm39) |
missense |
probably damaging |
0.96 |
R8708:Wrn
|
UTSW |
8 |
33,782,671 (GRCm39) |
missense |
probably damaging |
0.96 |
R8783:Wrn
|
UTSW |
8 |
33,826,041 (GRCm39) |
missense |
probably null |
1.00 |
R8870:Wrn
|
UTSW |
8 |
33,819,220 (GRCm39) |
missense |
probably benign |
0.01 |
R8876:Wrn
|
UTSW |
8 |
33,814,422 (GRCm39) |
missense |
probably benign |
0.00 |
R9050:Wrn
|
UTSW |
8 |
33,833,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R9329:Wrn
|
UTSW |
8 |
33,731,006 (GRCm39) |
missense |
probably benign |
|
R9595:Wrn
|
UTSW |
8 |
33,758,961 (GRCm39) |
missense |
probably benign |
|
R9621:Wrn
|
UTSW |
8 |
33,814,301 (GRCm39) |
missense |
probably benign |
0.01 |
R9623:Wrn
|
UTSW |
8 |
33,774,644 (GRCm39) |
critical splice donor site |
probably null |
|
R9797:Wrn
|
UTSW |
8 |
33,758,950 (GRCm39) |
missense |
probably benign |
0.02 |
RF010:Wrn
|
UTSW |
8 |
33,778,793 (GRCm39) |
missense |
probably benign |
0.13 |
X0017:Wrn
|
UTSW |
8 |
33,770,810 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Wrn
|
UTSW |
8 |
33,824,237 (GRCm39) |
missense |
probably damaging |
0.98 |
|