Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgb |
A |
C |
10: 10,283,214 (GRCm39) |
M164R |
possibly damaging |
Het |
Alg10b |
T |
A |
15: 90,111,656 (GRCm39) |
C167S |
probably benign |
Het |
Ap2m1 |
C |
A |
16: 20,358,113 (GRCm39) |
R44S |
probably damaging |
Het |
Atrip |
T |
C |
9: 108,902,964 (GRCm39) |
S37G |
probably benign |
Het |
Bicra |
C |
T |
7: 15,705,987 (GRCm39) |
V1485M |
probably benign |
Het |
C1qtnf7 |
A |
T |
5: 43,673,313 (GRCm39) |
|
probably benign |
Het |
Ccdc7a |
C |
T |
8: 129,618,860 (GRCm39) |
A895T |
possibly damaging |
Het |
Cep290 |
T |
C |
10: 100,354,529 (GRCm39) |
M871T |
probably benign |
Het |
Col19a1 |
A |
G |
1: 24,318,904 (GRCm39) |
V1062A |
unknown |
Het |
Col24a1 |
T |
A |
3: 145,021,103 (GRCm39) |
Y491* |
probably null |
Het |
Cyp2c66 |
A |
T |
19: 39,102,520 (GRCm39) |
I50F |
probably benign |
Het |
Dbn1 |
C |
A |
13: 55,625,639 (GRCm39) |
R261L |
probably benign |
Het |
Dlat |
G |
A |
9: 50,562,208 (GRCm39) |
A272V |
probably damaging |
Het |
Dlgap3 |
A |
T |
4: 127,130,127 (GRCm39) |
E967V |
possibly damaging |
Het |
Dnhd1 |
A |
G |
7: 105,369,456 (GRCm39) |
M4360V |
probably benign |
Het |
Dock7 |
C |
T |
4: 98,877,464 (GRCm39) |
R1058Q |
unknown |
Het |
Dpp4 |
T |
A |
2: 62,195,340 (GRCm39) |
I313F |
probably benign |
Het |
Dus1l |
C |
T |
11: 120,683,858 (GRCm39) |
V197I |
possibly damaging |
Het |
Eef2k |
TATTCATTCATTCATTCATTCATTCATTCA |
TATTCATTCATTCATTCATTCATTCA |
7: 120,499,453 (GRCm39) |
|
probably benign |
Het |
Fat3 |
A |
G |
9: 15,826,537 (GRCm39) |
S324P |
probably benign |
Het |
Fkbp9 |
C |
T |
6: 56,855,181 (GRCm39) |
H567Y |
possibly damaging |
Het |
Galnt10 |
C |
A |
11: 57,672,065 (GRCm39) |
P452T |
probably damaging |
Het |
Glb1 |
A |
T |
9: 114,246,084 (GRCm39) |
D45V |
probably damaging |
Het |
Grm1 |
A |
T |
10: 10,573,826 (GRCm39) |
V904E |
possibly damaging |
Het |
Gsdma3 |
T |
G |
11: 98,526,071 (GRCm39) |
V274G |
probably damaging |
Het |
Gsn |
A |
G |
2: 35,194,600 (GRCm39) |
E681G |
probably damaging |
Het |
Hpdl |
A |
G |
4: 116,678,062 (GRCm39) |
L133P |
probably damaging |
Het |
Ighv1-75 |
A |
G |
12: 115,797,655 (GRCm39) |
L89P |
probably damaging |
Het |
Igsf21 |
T |
A |
4: 139,755,407 (GRCm39) |
Q416L |
probably damaging |
Het |
Il23a |
G |
C |
10: 128,132,829 (GRCm39) |
R143G |
probably benign |
Het |
Ildr1 |
A |
G |
16: 36,528,659 (GRCm39) |
T35A |
probably benign |
Het |
Ints13 |
G |
T |
6: 146,463,326 (GRCm39) |
H235Q |
probably damaging |
Het |
Lama4 |
C |
T |
10: 38,924,101 (GRCm39) |
T503I |
probably benign |
Het |
Mapk13 |
T |
A |
17: 28,997,075 (GRCm39) |
L289Q |
probably damaging |
Het |
Med13l |
T |
C |
5: 118,887,024 (GRCm39) |
S1642P |
probably benign |
Het |
Megf6 |
T |
A |
4: 154,343,617 (GRCm39) |
S713R |
probably damaging |
Het |
Mical3 |
A |
G |
6: 120,959,529 (GRCm39) |
V922A |
possibly damaging |
Het |
Mug1 |
C |
T |
6: 121,857,864 (GRCm39) |
T1119M |
probably damaging |
Het |
Myo18a |
T |
A |
11: 77,733,080 (GRCm39) |
M1370K |
possibly damaging |
Het |
Ndufa12 |
A |
G |
10: 94,056,692 (GRCm39) |
E140G |
probably damaging |
Het |
Nek4 |
T |
A |
14: 30,706,401 (GRCm39) |
D696E |
probably benign |
Het |
Oas1f |
A |
G |
5: 120,994,429 (GRCm39) |
T317A |
probably benign |
Het |
Or14c39 |
T |
C |
7: 86,343,988 (GRCm39) |
V108A |
probably benign |
Het |
Or2r11 |
A |
G |
6: 42,437,029 (GRCm39) |
I308T |
probably benign |
Het |
Or6c210 |
T |
C |
10: 129,495,705 (GRCm39) |
I10T |
probably benign |
Het |
Pcdh17 |
C |
T |
14: 84,683,683 (GRCm39) |
P50L |
probably benign |
Het |
Pgs1 |
A |
G |
11: 117,894,256 (GRCm39) |
E261G |
probably benign |
Het |
Pira12 |
T |
G |
7: 3,897,612 (GRCm39) |
R494S |
probably damaging |
Het |
Ppp1r1a |
T |
C |
15: 103,439,857 (GRCm39) |
E145G |
possibly damaging |
Het |
Ppp1r37 |
T |
C |
7: 19,295,783 (GRCm39) |
E58G |
probably benign |
Het |
Ptprc |
A |
T |
1: 138,047,901 (GRCm39) |
V77E |
|
Het |
Rhag |
A |
G |
17: 41,139,416 (GRCm39) |
E117G |
probably benign |
Het |
Sh3d19 |
C |
T |
3: 86,028,483 (GRCm39) |
S653L |
probably benign |
Het |
Sirpd |
C |
A |
3: 15,385,813 (GRCm39) |
E30* |
probably null |
Het |
Slc35a5 |
C |
T |
16: 44,972,939 (GRCm39) |
|
probably null |
Het |
Smc4 |
C |
T |
3: 68,929,655 (GRCm39) |
R510* |
probably null |
Het |
Sorcs1 |
A |
G |
19: 50,248,190 (GRCm39) |
|
probably null |
Het |
Sp140 |
A |
G |
1: 85,569,461 (GRCm39) |
N357S |
probably damaging |
Het |
Spic |
T |
A |
10: 88,514,421 (GRCm39) |
T60S |
possibly damaging |
Het |
Steap1 |
C |
A |
5: 5,786,517 (GRCm39) |
A307S |
probably benign |
Het |
Stk3 |
A |
T |
15: 35,114,791 (GRCm39) |
S40R |
probably damaging |
Het |
Taar1 |
T |
C |
10: 23,796,676 (GRCm39) |
C125R |
probably damaging |
Het |
Tep1 |
T |
A |
14: 51,076,443 (GRCm39) |
K1664* |
probably null |
Het |
Tmem198b |
C |
A |
10: 128,638,273 (GRCm39) |
V97L |
possibly damaging |
Het |
Xirp2 |
C |
A |
2: 67,347,379 (GRCm39) |
P3207T |
possibly damaging |
Het |
Zbtb38 |
C |
G |
9: 96,570,355 (GRCm39) |
S243T |
possibly damaging |
Het |
Zbtb38 |
T |
A |
9: 96,570,356 (GRCm39) |
S243C |
probably damaging |
Het |
Zfp692 |
C |
T |
11: 58,199,638 (GRCm39) |
R76W |
probably benign |
Het |
Zwilch |
A |
T |
9: 64,054,170 (GRCm39) |
L509H |
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 |
R7682:Brca2
|
UTSW |
5 |
150,466,618 (GRCm39) |
missense |
probably benign |
|
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 |
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 |
|