Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310034C09Rik |
T |
A |
16: 88,556,373 (GRCm39) |
S196T |
probably benign |
Het |
Abcc5 |
T |
C |
16: 20,186,803 (GRCm39) |
D977G |
probably damaging |
Het |
Acot2 |
T |
C |
12: 84,034,698 (GRCm39) |
V8A |
probably benign |
Het |
Adamts9 |
T |
A |
6: 92,857,679 (GRCm39) |
I870F |
possibly damaging |
Het |
Adgrl3 |
G |
A |
5: 81,942,407 (GRCm39) |
V1414I |
probably damaging |
Het |
Aggf1 |
T |
C |
13: 95,504,934 (GRCm39) |
K275R |
probably benign |
Het |
Alpk1 |
T |
C |
3: 127,466,195 (GRCm39) |
I1104V |
possibly damaging |
Het |
Angptl7 |
A |
T |
4: 148,582,539 (GRCm39) |
I119N |
probably damaging |
Het |
Ank3 |
A |
T |
10: 69,824,065 (GRCm39) |
E129D |
possibly damaging |
Het |
Brd4 |
A |
G |
17: 32,420,134 (GRCm39) |
F1008S |
unknown |
Het |
Car2 |
T |
C |
3: 14,953,025 (GRCm39) |
S56P |
probably damaging |
Het |
Casp3 |
A |
G |
8: 47,085,420 (GRCm39) |
Y41C |
probably benign |
Het |
Ces4a |
A |
T |
8: 105,873,297 (GRCm39) |
T381S |
probably benign |
Het |
Clstn1 |
A |
G |
4: 149,710,558 (GRCm39) |
T77A |
possibly damaging |
Het |
Cul7 |
G |
T |
17: 46,966,521 (GRCm39) |
V615L |
probably benign |
Het |
Dnpep |
A |
G |
1: 75,293,384 (GRCm39) |
F24L |
probably damaging |
Het |
Efcab3 |
T |
A |
11: 104,855,174 (GRCm39) |
|
probably null |
Het |
Emsy |
G |
A |
7: 98,239,905 (GRCm39) |
R1263W |
probably damaging |
Het |
Fam124b |
A |
T |
1: 80,191,282 (GRCm39) |
C34S |
possibly damaging |
Het |
Fan1 |
C |
A |
7: 64,022,512 (GRCm39) |
G247V |
probably benign |
Het |
Fbxl9 |
C |
A |
8: 106,041,916 (GRCm39) |
R304L |
possibly damaging |
Het |
Glipr1l3 |
T |
G |
10: 111,977,777 (GRCm39) |
H218P |
probably benign |
Het |
Gm14305 |
T |
A |
2: 176,412,703 (GRCm39) |
S198R |
probably benign |
Het |
Gm14326 |
T |
C |
2: 177,590,274 (GRCm39) |
Y29C |
probably damaging |
Het |
Gm45713 |
C |
T |
7: 44,783,426 (GRCm39) |
V147I |
probably benign |
Het |
Gpr149 |
C |
T |
3: 62,438,160 (GRCm39) |
D666N |
probably damaging |
Het |
Gpr183 |
A |
G |
14: 122,192,152 (GRCm39) |
I123T |
possibly damaging |
Het |
Il7r |
A |
T |
15: 9,513,013 (GRCm39) |
H165Q |
probably damaging |
Het |
Krt73 |
A |
G |
15: 101,710,480 (GRCm39) |
F85L |
probably benign |
Het |
Lrrc8d |
A |
G |
5: 105,960,657 (GRCm39) |
T356A |
probably damaging |
Het |
Marco |
A |
G |
1: 120,421,771 (GRCm39) |
|
probably null |
Het |
Mettl14 |
T |
A |
3: 123,177,253 (GRCm39) |
E49D |
possibly damaging |
Het |
Mrap |
T |
A |
16: 90,546,110 (GRCm39) |
|
probably null |
Het |
Mrps34 |
C |
T |
17: 25,114,852 (GRCm39) |
A152V |
probably benign |
Het |
Nfasc |
T |
A |
1: 132,501,511 (GRCm39) |
Y1163F |
unknown |
Het |
Nfic |
T |
C |
10: 81,256,334 (GRCm39) |
D110G |
probably damaging |
Het |
Nip7 |
T |
C |
8: 107,783,751 (GRCm39) |
V28A |
possibly damaging |
Het |
Odam |
T |
C |
5: 88,040,287 (GRCm39) |
F251S |
possibly damaging |
Het |
Olfm5 |
T |
A |
7: 103,810,979 (GRCm39) |
Q53L |
probably null |
Het |
P2ry13 |
T |
G |
3: 59,117,545 (GRCm39) |
M78L |
probably benign |
Het |
Pacs1 |
T |
C |
19: 5,202,727 (GRCm39) |
E385G |
probably damaging |
Het |
Pip5k1b |
C |
T |
19: 24,337,343 (GRCm39) |
G315D |
probably damaging |
Het |
Pla2g4a |
C |
A |
1: 149,762,022 (GRCm39) |
R145L |
probably damaging |
Het |
Pramel26 |
A |
G |
4: 143,537,290 (GRCm39) |
L347S |
probably benign |
Het |
Rars1 |
T |
C |
11: 35,719,579 (GRCm39) |
Q81R |
probably benign |
Het |
Rassf7 |
A |
G |
7: 140,797,847 (GRCm39) |
N296D |
probably damaging |
Het |
Rcsd1 |
C |
T |
1: 165,485,262 (GRCm39) |
A94T |
probably benign |
Het |
Rgs8 |
T |
C |
1: 153,566,668 (GRCm39) |
F73S |
probably damaging |
Het |
Rilpl2 |
A |
C |
5: 124,616,043 (GRCm39) |
Y36D |
probably damaging |
Het |
Rpl10l |
A |
G |
12: 66,331,004 (GRCm39) |
V43A |
probably benign |
Het |
Sesn2 |
T |
C |
4: 132,224,200 (GRCm39) |
I403V |
probably damaging |
Het |
Slc10a4 |
C |
T |
5: 73,164,453 (GRCm39) |
S15L |
unknown |
Het |
Slc7a5 |
T |
C |
8: 122,633,879 (GRCm39) |
Y156C |
probably damaging |
Het |
Spata18 |
A |
G |
5: 73,826,008 (GRCm39) |
H105R |
|
Het |
Specc1l |
A |
G |
10: 75,081,636 (GRCm39) |
D344G |
probably damaging |
Het |
Syne1 |
A |
G |
10: 5,112,461 (GRCm39) |
V415A |
probably benign |
Het |
Thbs4 |
T |
G |
13: 92,912,070 (GRCm39) |
D220A |
probably benign |
Het |
Tmco5 |
T |
C |
2: 116,716,752 (GRCm39) |
S152P |
probably benign |
Het |
Tmem35b |
A |
T |
4: 127,022,734 (GRCm39) |
D125V |
probably damaging |
Het |
Trim17 |
A |
G |
11: 58,857,634 (GRCm39) |
E155G |
possibly damaging |
Het |
Vmn2r11 |
A |
C |
5: 109,195,481 (GRCm39) |
V615G |
probably benign |
Het |
Vmn2r88 |
A |
T |
14: 51,655,906 (GRCm39) |
Q705L |
|
Het |
Vmn2r93 |
A |
G |
17: 18,525,583 (GRCm39) |
R414G |
probably benign |
Het |
Xirp2 |
T |
C |
2: 67,339,193 (GRCm39) |
L478P |
probably damaging |
Het |
|
Other mutations in Brca2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00332:Brca2
|
APN |
5 |
150,463,363 (GRCm39) |
missense |
probably benign |
0.18 |
IGL00392:Brca2
|
APN |
5 |
150,464,705 (GRCm39) |
missense |
probably benign |
0.02 |
IGL00557:Brca2
|
APN |
5 |
150,484,003 (GRCm39) |
missense |
probably benign |
|
IGL00798:Brca2
|
APN |
5 |
150,462,928 (GRCm39) |
missense |
probably benign |
0.30 |
IGL00933:Brca2
|
APN |
5 |
150,465,869 (GRCm39) |
missense |
probably benign |
0.04 |
IGL00964:Brca2
|
APN |
5 |
150,455,775 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01152:Brca2
|
APN |
5 |
150,465,855 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01577:Brca2
|
APN |
5 |
150,465,085 (GRCm39) |
nonsense |
probably null |
|
IGL01585:Brca2
|
APN |
5 |
150,462,981 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL01732:Brca2
|
APN |
5 |
150,465,852 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01809:Brca2
|
APN |
5 |
150,454,526 (GRCm39) |
splice site |
probably null |
|
IGL01911:Brca2
|
APN |
5 |
150,491,078 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02113:Brca2
|
APN |
5 |
150,464,444 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02313:Brca2
|
APN |
5 |
150,462,126 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02342:Brca2
|
APN |
5 |
150,466,289 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02508:Brca2
|
APN |
5 |
150,466,773 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02532:Brca2
|
APN |
5 |
150,474,327 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02646:Brca2
|
APN |
5 |
150,484,255 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02738:Brca2
|
APN |
5 |
150,490,500 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02833:Brca2
|
APN |
5 |
150,465,255 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02871:Brca2
|
APN |
5 |
150,466,017 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02995:Brca2
|
APN |
5 |
150,452,953 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03105:Brca2
|
APN |
5 |
150,483,950 (GRCm39) |
missense |
probably benign |
0.02 |
BB007:Brca2
|
UTSW |
5 |
150,481,975 (GRCm39) |
missense |
probably damaging |
0.96 |
BB017:Brca2
|
UTSW |
5 |
150,481,975 (GRCm39) |
missense |
probably damaging |
0.96 |
R0219:Brca2
|
UTSW |
5 |
150,446,640 (GRCm39) |
splice site |
probably benign |
|
R0416:Brca2
|
UTSW |
5 |
150,492,857 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0441:Brca2
|
UTSW |
5 |
150,465,322 (GRCm39) |
missense |
probably damaging |
0.96 |
R0548:Brca2
|
UTSW |
5 |
150,468,400 (GRCm39) |
missense |
probably damaging |
0.96 |
R0745:Brca2
|
UTSW |
5 |
150,468,347 (GRCm39) |
splice site |
probably benign |
|
R0799:Brca2
|
UTSW |
5 |
150,483,658 (GRCm39) |
missense |
probably damaging |
0.99 |
R1165:Brca2
|
UTSW |
5 |
150,466,212 (GRCm39) |
missense |
probably damaging |
0.98 |
R1247:Brca2
|
UTSW |
5 |
150,464,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R1403:Brca2
|
UTSW |
5 |
150,466,114 (GRCm39) |
missense |
probably benign |
0.22 |
R1403:Brca2
|
UTSW |
5 |
150,466,114 (GRCm39) |
missense |
probably benign |
0.22 |
R1444:Brca2
|
UTSW |
5 |
150,465,915 (GRCm39) |
missense |
probably benign |
|
R1466:Brca2
|
UTSW |
5 |
150,475,723 (GRCm39) |
missense |
probably damaging |
0.99 |
R1466:Brca2
|
UTSW |
5 |
150,475,723 (GRCm39) |
missense |
probably damaging |
0.99 |
R1584:Brca2
|
UTSW |
5 |
150,475,723 (GRCm39) |
missense |
probably damaging |
0.99 |
R1599:Brca2
|
UTSW |
5 |
150,472,178 (GRCm39) |
nonsense |
probably null |
|
R1600:Brca2
|
UTSW |
5 |
150,484,295 (GRCm39) |
splice site |
probably benign |
|
R1822:Brca2
|
UTSW |
5 |
150,463,663 (GRCm39) |
missense |
probably benign |
0.06 |
R1824:Brca2
|
UTSW |
5 |
150,460,387 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2037:Brca2
|
UTSW |
5 |
150,464,134 (GRCm39) |
missense |
probably benign |
|
R2131:Brca2
|
UTSW |
5 |
150,480,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R2203:Brca2
|
UTSW |
5 |
150,462,967 (GRCm39) |
missense |
possibly damaging |
0.58 |
R2208:Brca2
|
UTSW |
5 |
150,455,809 (GRCm39) |
missense |
probably damaging |
0.96 |
R2293:Brca2
|
UTSW |
5 |
150,483,999 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2517:Brca2
|
UTSW |
5 |
150,463,137 (GRCm39) |
missense |
probably benign |
0.04 |
R2566:Brca2
|
UTSW |
5 |
150,465,227 (GRCm39) |
missense |
probably benign |
0.03 |
R3422:Brca2
|
UTSW |
5 |
150,466,586 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3917:Brca2
|
UTSW |
5 |
150,464,292 (GRCm39) |
missense |
probably damaging |
0.96 |
R3946:Brca2
|
UTSW |
5 |
150,460,169 (GRCm39) |
missense |
probably damaging |
0.96 |
R4176:Brca2
|
UTSW |
5 |
150,463,098 (GRCm39) |
nonsense |
probably null |
|
R4255:Brca2
|
UTSW |
5 |
150,464,634 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4450:Brca2
|
UTSW |
5 |
150,459,518 (GRCm39) |
missense |
probably damaging |
0.96 |
R4603:Brca2
|
UTSW |
5 |
150,459,630 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4681:Brca2
|
UTSW |
5 |
150,475,863 (GRCm39) |
splice site |
probably null |
|
R4755:Brca2
|
UTSW |
5 |
150,483,452 (GRCm39) |
splice site |
probably null |
|
R4762:Brca2
|
UTSW |
5 |
150,454,581 (GRCm39) |
missense |
probably benign |
0.00 |
R4824:Brca2
|
UTSW |
5 |
150,463,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R4887:Brca2
|
UTSW |
5 |
150,480,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R5020:Brca2
|
UTSW |
5 |
150,483,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R5159:Brca2
|
UTSW |
5 |
150,465,573 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5216:Brca2
|
UTSW |
5 |
150,466,445 (GRCm39) |
missense |
probably damaging |
0.99 |
R5269:Brca2
|
UTSW |
5 |
150,462,688 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5274:Brca2
|
UTSW |
5 |
150,463,154 (GRCm39) |
missense |
probably benign |
0.00 |
R5589:Brca2
|
UTSW |
5 |
150,480,597 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5619:Brca2
|
UTSW |
5 |
150,480,579 (GRCm39) |
missense |
probably damaging |
0.96 |
R5641:Brca2
|
UTSW |
5 |
150,480,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R5686:Brca2
|
UTSW |
5 |
150,464,369 (GRCm39) |
missense |
probably benign |
0.00 |
R5730:Brca2
|
UTSW |
5 |
150,492,470 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5763:Brca2
|
UTSW |
5 |
150,471,471 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5877:Brca2
|
UTSW |
5 |
150,466,686 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5893:Brca2
|
UTSW |
5 |
150,492,603 (GRCm39) |
missense |
probably benign |
0.02 |
R5900:Brca2
|
UTSW |
5 |
150,464,597 (GRCm39) |
missense |
probably benign |
0.01 |
R5926:Brca2
|
UTSW |
5 |
150,458,087 (GRCm39) |
missense |
probably benign |
0.07 |
R5966:Brca2
|
UTSW |
5 |
150,466,716 (GRCm39) |
missense |
probably damaging |
0.99 |
R6025:Brca2
|
UTSW |
5 |
150,465,040 (GRCm39) |
frame shift |
probably null |
|
R6062:Brca2
|
UTSW |
5 |
150,480,354 (GRCm39) |
missense |
probably damaging |
0.96 |
R6141:Brca2
|
UTSW |
5 |
150,464,102 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6244:Brca2
|
UTSW |
5 |
150,490,443 (GRCm39) |
missense |
probably benign |
0.08 |
R6508:Brca2
|
UTSW |
5 |
150,460,058 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6519:Brca2
|
UTSW |
5 |
150,464,444 (GRCm39) |
missense |
probably damaging |
0.99 |
R6611:Brca2
|
UTSW |
5 |
150,459,658 (GRCm39) |
missense |
probably damaging |
0.99 |
R6698:Brca2
|
UTSW |
5 |
150,455,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R6856:Brca2
|
UTSW |
5 |
150,463,673 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6912:Brca2
|
UTSW |
5 |
150,465,207 (GRCm39) |
missense |
probably damaging |
0.99 |
R7002:Brca2
|
UTSW |
5 |
150,463,383 (GRCm39) |
missense |
probably benign |
|
R7025:Brca2
|
UTSW |
5 |
150,463,943 (GRCm39) |
missense |
probably benign |
0.39 |
R7151:Brca2
|
UTSW |
5 |
150,464,901 (GRCm39) |
missense |
probably benign |
0.12 |
R7202:Brca2
|
UTSW |
5 |
150,455,819 (GRCm39) |
missense |
probably benign |
0.03 |
R7365:Brca2
|
UTSW |
5 |
150,455,802 (GRCm39) |
missense |
probably damaging |
0.99 |
R7510:Brca2
|
UTSW |
5 |
150,460,156 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7612:Brca2
|
UTSW |
5 |
150,464,076 (GRCm39) |
missense |
probably benign |
0.03 |
R7890:Brca2
|
UTSW |
5 |
150,462,846 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7930:Brca2
|
UTSW |
5 |
150,481,975 (GRCm39) |
missense |
probably damaging |
0.96 |
R7940:Brca2
|
UTSW |
5 |
150,462,198 (GRCm39) |
missense |
probably benign |
|
R8054:Brca2
|
UTSW |
5 |
150,459,969 (GRCm39) |
missense |
probably benign |
0.02 |
R8056:Brca2
|
UTSW |
5 |
150,492,771 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8080:Brca2
|
UTSW |
5 |
150,463,357 (GRCm39) |
missense |
probably benign |
0.11 |
R8094:Brca2
|
UTSW |
5 |
150,459,634 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8306:Brca2
|
UTSW |
5 |
150,460,128 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8401:Brca2
|
UTSW |
5 |
150,475,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R8523:Brca2
|
UTSW |
5 |
150,483,613 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8784:Brca2
|
UTSW |
5 |
150,472,126 (GRCm39) |
nonsense |
probably null |
|
R8791:Brca2
|
UTSW |
5 |
150,466,061 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8832:Brca2
|
UTSW |
5 |
150,465,611 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8838:Brca2
|
UTSW |
5 |
150,465,005 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8845:Brca2
|
UTSW |
5 |
150,466,847 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8898:Brca2
|
UTSW |
5 |
150,492,498 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8914:Brca2
|
UTSW |
5 |
150,465,208 (GRCm39) |
missense |
probably damaging |
0.96 |
R8935:Brca2
|
UTSW |
5 |
150,492,446 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9014:Brca2
|
UTSW |
5 |
150,465,219 (GRCm39) |
missense |
probably benign |
|
R9023:Brca2
|
UTSW |
5 |
150,465,360 (GRCm39) |
missense |
probably benign |
0.07 |
R9094:Brca2
|
UTSW |
5 |
150,475,770 (GRCm39) |
missense |
probably benign |
0.08 |
R9195:Brca2
|
UTSW |
5 |
150,463,418 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9198:Brca2
|
UTSW |
5 |
150,459,977 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9314:Brca2
|
UTSW |
5 |
150,474,359 (GRCm39) |
missense |
probably damaging |
0.96 |
R9408:Brca2
|
UTSW |
5 |
150,464,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R9459:Brca2
|
UTSW |
5 |
150,464,094 (GRCm39) |
missense |
probably damaging |
0.98 |
R9512:Brca2
|
UTSW |
5 |
150,454,546 (GRCm39) |
missense |
probably benign |
0.40 |
R9622:Brca2
|
UTSW |
5 |
150,480,410 (GRCm39) |
missense |
probably damaging |
0.96 |
R9777:Brca2
|
UTSW |
5 |
150,480,579 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1088:Brca2
|
UTSW |
5 |
150,466,228 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1186:Brca2
|
UTSW |
5 |
150,460,048 (GRCm39) |
missense |
probably damaging |
0.98 |
|