Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010B08Rik |
A |
T |
2: 173,561,706 (GRCm39) |
H5L |
unknown |
Het |
Aatk |
A |
G |
11: 119,901,733 (GRCm39) |
S888P |
probably damaging |
Het |
Ahnak |
A |
T |
19: 8,985,786 (GRCm39) |
K2357* |
probably null |
Het |
Arl9 |
T |
A |
5: 77,155,139 (GRCm39) |
L90Q |
probably damaging |
Het |
Atosa |
A |
G |
9: 74,924,349 (GRCm39) |
D864G |
possibly damaging |
Het |
Atxn2 |
T |
C |
5: 121,949,055 (GRCm39) |
V1144A |
probably damaging |
Het |
Batf3 |
C |
T |
1: 190,830,623 (GRCm39) |
|
probably benign |
Het |
Bltp3b |
C |
A |
10: 89,626,593 (GRCm39) |
T429K |
probably benign |
Het |
Cabin1 |
T |
A |
10: 75,575,239 (GRCm39) |
Q602L |
probably damaging |
Het |
Cadps |
T |
C |
14: 12,597,418 (GRCm38) |
E424G |
probably damaging |
Het |
Camta1 |
A |
G |
4: 151,216,004 (GRCm39) |
L972P |
possibly damaging |
Het |
Ccdc159 |
A |
G |
9: 21,840,672 (GRCm39) |
N80D |
possibly damaging |
Het |
Cdh1 |
A |
C |
8: 107,388,604 (GRCm39) |
E553D |
possibly damaging |
Het |
Cdk14 |
T |
A |
5: 5,423,477 (GRCm39) |
E35V |
probably benign |
Het |
Cfap70 |
A |
G |
14: 20,450,546 (GRCm39) |
L995P |
probably damaging |
Het |
Col18a1 |
T |
A |
10: 76,916,673 (GRCm39) |
E334V |
unknown |
Het |
Colec12 |
T |
A |
18: 9,877,000 (GRCm39) |
I741K |
unknown |
Het |
Crot |
A |
G |
5: 9,024,170 (GRCm39) |
V342A |
probably benign |
Het |
Ctnnal1 |
A |
G |
4: 56,865,036 (GRCm39) |
S27P |
possibly damaging |
Het |
Cyp2j9 |
A |
G |
4: 96,460,193 (GRCm39) |
S437P |
probably damaging |
Het |
Dennd4c |
A |
T |
4: 86,743,160 (GRCm39) |
T1001S |
probably benign |
Het |
Dffa |
G |
A |
4: 149,202,276 (GRCm39) |
V227I |
probably benign |
Het |
Dnaaf5 |
T |
A |
5: 139,159,909 (GRCm39) |
H602Q |
probably benign |
Het |
Efcab7 |
G |
T |
4: 99,761,902 (GRCm39) |
K397N |
probably damaging |
Het |
Egfl6 |
C |
T |
X: 165,319,235 (GRCm39) |
V379I |
probably benign |
Het |
Fadd |
G |
A |
7: 144,134,384 (GRCm39) |
T167I |
probably benign |
Het |
Fam184b |
T |
C |
5: 45,796,484 (GRCm39) |
D33G |
probably damaging |
Het |
Fam237b |
C |
T |
5: 5,625,549 (GRCm39) |
Q82* |
probably null |
Het |
Fam83h |
G |
A |
15: 75,877,976 (GRCm39) |
R141W |
probably damaging |
Het |
Fanci |
G |
A |
7: 79,076,954 (GRCm39) |
R564Q |
probably damaging |
Het |
Fat3 |
A |
T |
9: 15,908,054 (GRCm39) |
D2649E |
possibly damaging |
Het |
Fcrl1 |
A |
G |
3: 87,291,918 (GRCm39) |
T46A |
possibly damaging |
Het |
Fig4 |
C |
T |
10: 41,143,763 (GRCm39) |
G232D |
probably benign |
Het |
Frem3 |
A |
T |
8: 81,341,145 (GRCm39) |
H1146L |
probably damaging |
Het |
Fyttd1 |
T |
A |
16: 32,715,472 (GRCm39) |
F133L |
probably benign |
Het |
Gata2 |
A |
G |
6: 88,179,505 (GRCm39) |
N326D |
probably damaging |
Het |
Gm7298 |
A |
T |
6: 121,764,491 (GRCm39) |
T1457S |
probably damaging |
Het |
Hdac1-ps |
A |
T |
17: 78,799,075 (GRCm39) |
Y22F |
probably benign |
Het |
Heatr5b |
C |
T |
17: 79,141,524 (GRCm39) |
|
probably null |
Het |
Hfm1 |
T |
A |
5: 107,066,329 (GRCm39) |
D33V |
possibly damaging |
Het |
Hmcn2 |
G |
A |
2: 31,292,450 (GRCm39) |
A2447T |
possibly damaging |
Het |
Hs3st3b1 |
A |
G |
11: 63,812,331 (GRCm39) |
F128S |
probably benign |
Het |
Hs3st6 |
G |
T |
17: 24,972,226 (GRCm39) |
R56L |
possibly damaging |
Het |
Hsd17b3 |
C |
T |
13: 64,212,171 (GRCm39) |
M168I |
probably damaging |
Het |
Ighv1-34 |
G |
T |
12: 114,814,885 (GRCm39) |
D92E |
possibly damaging |
Het |
Itgb4 |
A |
T |
11: 115,885,171 (GRCm39) |
I1018F |
possibly damaging |
Het |
Itih3 |
T |
C |
14: 30,637,605 (GRCm39) |
D518G |
possibly damaging |
Het |
Kcnma1 |
C |
T |
14: 23,501,666 (GRCm39) |
|
probably null |
Het |
Klhl11 |
A |
T |
11: 100,363,506 (GRCm39) |
S17T |
probably benign |
Het |
Lilra6 |
T |
C |
7: 3,917,521 (GRCm39) |
E158G |
possibly damaging |
Het |
Loxl1 |
A |
G |
9: 58,220,037 (GRCm39) |
W45R |
probably damaging |
Het |
Lratd1 |
T |
C |
12: 14,200,190 (GRCm39) |
N179S |
probably benign |
Het |
Lrfn1 |
G |
T |
7: 28,166,255 (GRCm39) |
V550F |
probably damaging |
Het |
Lrp1 |
T |
C |
10: 127,409,368 (GRCm39) |
K1584E |
probably benign |
Het |
Lrp4 |
C |
G |
2: 91,338,914 (GRCm39) |
P1782A |
possibly damaging |
Het |
Map3k1 |
A |
G |
13: 111,885,478 (GRCm39) |
S1480P |
probably damaging |
Het |
Mark4 |
G |
T |
7: 19,160,015 (GRCm39) |
N748K |
probably benign |
Het |
Mrpl38 |
G |
A |
11: 116,025,900 (GRCm39) |
T142M |
probably damaging |
Het |
Mrpl41 |
T |
C |
2: 24,864,481 (GRCm39) |
T64A |
probably benign |
Het |
Mrps2 |
G |
A |
2: 28,359,764 (GRCm39) |
R207K |
possibly damaging |
Het |
Myo5a |
A |
T |
9: 75,099,726 (GRCm39) |
E96D |
|
Het |
Nbas |
A |
T |
12: 13,633,417 (GRCm39) |
E2274V |
probably damaging |
Het |
Or4x13 |
T |
C |
2: 90,231,338 (GRCm39) |
F111S |
probably damaging |
Het |
Or51a8 |
T |
C |
7: 102,549,652 (GRCm39) |
I26T |
probably benign |
Het |
Or51ac3 |
T |
C |
7: 103,213,850 (GRCm39) |
D212G |
probably damaging |
Het |
Or5m10b |
T |
C |
2: 85,699,278 (GRCm39) |
L114P |
possibly damaging |
Het |
Or5m10b |
T |
A |
2: 85,699,819 (GRCm39) |
N294K |
probably damaging |
Het |
Or6c35 |
T |
A |
10: 129,169,368 (GRCm39) |
I206N |
possibly damaging |
Het |
Pcdhga12 |
T |
A |
18: 37,900,288 (GRCm39) |
D373E |
probably damaging |
Het |
Pgd |
A |
C |
4: 149,235,596 (GRCm39) |
F395V |
probably damaging |
Het |
Pi16 |
A |
G |
17: 29,538,363 (GRCm39) |
M59V |
possibly damaging |
Het |
Pik3r5 |
A |
T |
11: 68,381,720 (GRCm39) |
T255S |
probably benign |
Het |
Plch2 |
A |
T |
4: 155,068,516 (GRCm39) |
V1370E |
probably benign |
Het |
Plec |
A |
G |
15: 76,067,153 (GRCm39) |
I1309T |
unknown |
Het |
Ppp2r3d |
A |
T |
9: 124,440,831 (GRCm38) |
S22R |
|
Het |
Pramel26 |
A |
G |
4: 143,542,609 (GRCm39) |
C4R |
probably damaging |
Het |
Ptk2b |
C |
A |
14: 66,413,154 (GRCm39) |
E342* |
probably null |
Het |
Ptpn23 |
T |
C |
9: 110,215,226 (GRCm39) |
|
probably null |
Het |
Rfx8 |
A |
C |
1: 39,722,850 (GRCm39) |
S256A |
probably damaging |
Het |
Rnf115 |
C |
T |
3: 96,665,337 (GRCm39) |
T69I |
probably damaging |
Het |
Rnf213 |
A |
G |
11: 119,370,457 (GRCm39) |
Y4753C |
|
Het |
S100a10 |
A |
C |
3: 93,471,590 (GRCm39) |
D58A |
possibly damaging |
Het |
Serpina12 |
T |
C |
12: 104,004,317 (GRCm39) |
K105R |
probably benign |
Het |
Slc20a2 |
G |
A |
8: 23,028,900 (GRCm39) |
G124S |
probably damaging |
Het |
Stab2 |
ACC |
AC |
10: 86,692,561 (GRCm39) |
|
probably null |
Het |
Stard9 |
C |
A |
2: 120,526,635 (GRCm39) |
T964N |
probably benign |
Het |
Stxbp5 |
T |
A |
10: 9,774,938 (GRCm39) |
I72F |
probably damaging |
Het |
Sumf2 |
T |
A |
5: 129,891,482 (GRCm39) |
M282K |
possibly damaging |
Het |
Tle7 |
T |
C |
8: 110,837,580 (GRCm39) |
F375L |
probably damaging |
Het |
Tmem135 |
G |
C |
7: 88,797,186 (GRCm39) |
L357V |
probably benign |
Het |
Tmem185b |
G |
T |
1: 119,454,613 (GRCm39) |
V125L |
probably benign |
Het |
Tmtc1 |
A |
G |
6: 148,144,714 (GRCm39) |
M887T |
probably damaging |
Het |
Tnfaip8 |
C |
T |
18: 50,223,512 (GRCm39) |
Q83* |
probably null |
Het |
Tnks |
A |
G |
8: 35,306,089 (GRCm39) |
V1162A |
probably damaging |
Het |
Tomm70a |
T |
A |
16: 56,961,072 (GRCm39) |
Y342N |
possibly damaging |
Het |
Tpo |
T |
A |
12: 30,125,875 (GRCm39) |
D828V |
probably damaging |
Het |
Ugt8a |
A |
T |
3: 125,708,338 (GRCm39) |
N257K |
probably damaging |
Het |
Unc13d |
AATGCCTCCCATGCC |
AATGCCTCCCATGCCTCCCATGCC |
11: 115,958,998 (GRCm39) |
|
probably benign |
Het |
Vim |
T |
A |
2: 13,579,703 (GRCm39) |
M154K |
probably damaging |
Het |
Virma |
G |
T |
4: 11,486,045 (GRCm39) |
M1I |
probably null |
Het |
Zfp715 |
A |
T |
7: 42,950,653 (GRCm39) |
M100K |
probably benign |
Het |
Zfp748 |
A |
T |
13: 67,690,647 (GRCm39) |
C204* |
probably null |
Het |
Zmynd8 |
A |
T |
2: 165,680,772 (GRCm39) |
D236E |
probably damaging |
Het |
|
Other mutations in Brpf3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00906:Brpf3
|
APN |
17 |
29,055,674 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01397:Brpf3
|
APN |
17 |
29,036,606 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01608:Brpf3
|
APN |
17 |
29,040,491 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02073:Brpf3
|
APN |
17 |
29,026,370 (GRCm39) |
missense |
probably benign |
|
IGL02540:Brpf3
|
APN |
17 |
29,047,328 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02838:Brpf3
|
APN |
17 |
29,054,758 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02888:Brpf3
|
APN |
17 |
29,047,365 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02969:Brpf3
|
APN |
17 |
29,040,279 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03036:Brpf3
|
APN |
17 |
29,043,022 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03084:Brpf3
|
APN |
17 |
29,054,751 (GRCm39) |
missense |
probably damaging |
0.98 |
R0448:Brpf3
|
UTSW |
17 |
29,025,010 (GRCm39) |
missense |
probably benign |
0.10 |
R0898:Brpf3
|
UTSW |
17 |
29,025,964 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1268:Brpf3
|
UTSW |
17 |
29,055,530 (GRCm39) |
missense |
probably damaging |
0.98 |
R1639:Brpf3
|
UTSW |
17 |
29,043,042 (GRCm39) |
critical splice donor site |
probably null |
|
R1754:Brpf3
|
UTSW |
17 |
29,040,297 (GRCm39) |
missense |
probably benign |
0.00 |
R1867:Brpf3
|
UTSW |
17 |
29,026,342 (GRCm39) |
missense |
probably benign |
|
R1954:Brpf3
|
UTSW |
17 |
29,025,533 (GRCm39) |
missense |
probably benign |
|
R2000:Brpf3
|
UTSW |
17 |
29,040,531 (GRCm39) |
missense |
probably benign |
0.20 |
R2064:Brpf3
|
UTSW |
17 |
29,040,338 (GRCm39) |
missense |
probably benign |
|
R2209:Brpf3
|
UTSW |
17 |
29,047,394 (GRCm39) |
missense |
probably damaging |
0.98 |
R2413:Brpf3
|
UTSW |
17 |
29,024,924 (GRCm39) |
start gained |
probably benign |
|
R3977:Brpf3
|
UTSW |
17 |
29,026,016 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4067:Brpf3
|
UTSW |
17 |
29,040,233 (GRCm39) |
missense |
probably benign |
|
R4291:Brpf3
|
UTSW |
17 |
29,042,949 (GRCm39) |
missense |
probably benign |
0.00 |
R4369:Brpf3
|
UTSW |
17 |
29,055,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R4371:Brpf3
|
UTSW |
17 |
29,055,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R4741:Brpf3
|
UTSW |
17 |
29,036,758 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4773:Brpf3
|
UTSW |
17 |
29,040,233 (GRCm39) |
missense |
probably benign |
0.00 |
R4824:Brpf3
|
UTSW |
17 |
29,025,460 (GRCm39) |
missense |
probably benign |
|
R5360:Brpf3
|
UTSW |
17 |
29,029,536 (GRCm39) |
missense |
probably benign |
|
R5923:Brpf3
|
UTSW |
17 |
29,025,610 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6181:Brpf3
|
UTSW |
17 |
29,029,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R6278:Brpf3
|
UTSW |
17 |
29,040,258 (GRCm39) |
missense |
probably benign |
0.00 |
R6702:Brpf3
|
UTSW |
17 |
29,029,633 (GRCm39) |
missense |
probably benign |
0.01 |
R6884:Brpf3
|
UTSW |
17 |
29,050,324 (GRCm39) |
missense |
probably benign |
0.03 |
R6920:Brpf3
|
UTSW |
17 |
29,042,970 (GRCm39) |
missense |
probably benign |
0.34 |
R6976:Brpf3
|
UTSW |
17 |
29,054,751 (GRCm39) |
missense |
probably damaging |
0.98 |
R7099:Brpf3
|
UTSW |
17 |
29,025,611 (GRCm39) |
missense |
probably benign |
0.06 |
R7108:Brpf3
|
UTSW |
17 |
29,036,099 (GRCm39) |
missense |
probably benign |
0.01 |
R7193:Brpf3
|
UTSW |
17 |
29,055,665 (GRCm39) |
makesense |
probably null |
|
R7316:Brpf3
|
UTSW |
17 |
29,033,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R7326:Brpf3
|
UTSW |
17 |
29,025,267 (GRCm39) |
missense |
probably benign |
0.00 |
R7403:Brpf3
|
UTSW |
17 |
29,040,330 (GRCm39) |
missense |
probably benign |
|
R7666:Brpf3
|
UTSW |
17 |
29,029,546 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7686:Brpf3
|
UTSW |
17 |
29,025,908 (GRCm39) |
missense |
probably damaging |
0.98 |
R7691:Brpf3
|
UTSW |
17 |
29,025,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R8054:Brpf3
|
UTSW |
17 |
29,055,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R8165:Brpf3
|
UTSW |
17 |
29,025,248 (GRCm39) |
missense |
probably benign |
0.01 |
R8200:Brpf3
|
UTSW |
17 |
29,025,248 (GRCm39) |
missense |
probably benign |
0.01 |
R8698:Brpf3
|
UTSW |
17 |
29,037,436 (GRCm39) |
missense |
probably damaging |
0.99 |
R8722:Brpf3
|
UTSW |
17 |
29,029,510 (GRCm39) |
missense |
probably benign |
0.42 |
R8738:Brpf3
|
UTSW |
17 |
29,040,214 (GRCm39) |
missense |
probably benign |
|
R9044:Brpf3
|
UTSW |
17 |
29,025,871 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9250:Brpf3
|
UTSW |
17 |
29,054,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R9349:Brpf3
|
UTSW |
17 |
29,040,276 (GRCm39) |
missense |
probably benign |
0.00 |
R9496:Brpf3
|
UTSW |
17 |
29,040,453 (GRCm39) |
missense |
probably benign |
|
R9564:Brpf3
|
UTSW |
17 |
29,026,152 (GRCm39) |
missense |
probably benign |
|
R9720:Brpf3
|
UTSW |
17 |
29,026,330 (GRCm39) |
missense |
probably benign |
0.13 |
Z1177:Brpf3
|
UTSW |
17 |
29,040,452 (GRCm39) |
missense |
probably benign |
|
|