Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
T |
C |
7: 119,917,236 (GRCm39) |
I1467T |
probably damaging |
Het |
Abtb3 |
A |
G |
10: 85,223,629 (GRCm39) |
E146G |
unknown |
Het |
Adgrf3 |
T |
A |
5: 30,409,378 (GRCm39) |
K38* |
probably null |
Het |
Ahdc1 |
T |
A |
4: 132,789,198 (GRCm39) |
C146* |
probably null |
Het |
Ahnak |
A |
T |
19: 8,995,163 (GRCm39) |
K5482N |
probably damaging |
Het |
Arhgap23 |
C |
T |
11: 97,342,819 (GRCm39) |
A367V |
possibly damaging |
Het |
Arvcf |
T |
C |
16: 18,223,948 (GRCm39) |
S960P |
probably damaging |
Het |
Asb14 |
C |
A |
14: 26,622,394 (GRCm39) |
P74Q |
probably benign |
Het |
Atad5 |
T |
C |
11: 79,980,601 (GRCm39) |
V2A |
probably damaging |
Het |
Baz2a |
A |
G |
10: 127,954,428 (GRCm39) |
I691M |
possibly damaging |
Het |
Calr4 |
T |
A |
4: 109,101,254 (GRCm39) |
N152K |
possibly damaging |
Het |
Ccnb2 |
C |
T |
9: 70,318,128 (GRCm39) |
A215T |
probably damaging |
Het |
Cdh16 |
C |
T |
8: 105,340,780 (GRCm39) |
D140N |
unknown |
Het |
Ces1g |
T |
C |
8: 94,029,595 (GRCm39) |
T546A |
probably benign |
Het |
Cfap74 |
G |
T |
4: 155,510,654 (GRCm39) |
|
probably null |
Het |
Cfap91 |
T |
C |
16: 38,155,959 (GRCm39) |
Y88C |
probably benign |
Het |
Col5a1 |
G |
T |
2: 27,842,390 (GRCm39) |
D422Y |
unknown |
Het |
Cyp2c66 |
A |
T |
19: 39,130,348 (GRCm39) |
Y61F |
probably damaging |
Het |
Dnah12 |
G |
A |
14: 26,500,869 (GRCm39) |
|
probably null |
Het |
Dnah6 |
A |
G |
6: 73,158,688 (GRCm39) |
|
probably null |
Het |
Dop1a |
T |
G |
9: 86,386,220 (GRCm39) |
|
probably null |
Het |
Fam163a |
A |
G |
1: 155,954,834 (GRCm39) |
F106L |
probably damaging |
Het |
Gfy |
T |
C |
7: 44,827,596 (GRCm39) |
T167A |
probably benign |
Het |
Gm6525 |
A |
T |
3: 84,082,341 (GRCm39) |
R87S |
probably benign |
Het |
Gramd1c |
C |
A |
16: 43,879,584 (GRCm39) |
A19S |
possibly damaging |
Het |
Herc2 |
T |
C |
7: 55,781,034 (GRCm39) |
V1233A |
probably damaging |
Het |
Hibch |
G |
A |
1: 52,892,874 (GRCm39) |
|
probably null |
Het |
Ibsp |
A |
T |
5: 104,450,027 (GRCm39) |
S9C |
probably benign |
Het |
Il17ra |
A |
G |
6: 120,452,572 (GRCm39) |
I252V |
probably benign |
Het |
Ino80 |
A |
T |
2: 119,204,918 (GRCm39) |
M1536K |
probably benign |
Het |
Ipo11 |
A |
T |
13: 107,012,078 (GRCm39) |
L568Q |
probably damaging |
Het |
Kcnu1 |
T |
G |
8: 26,409,609 (GRCm39) |
|
probably null |
Het |
Kdm5b |
T |
G |
1: 134,552,497 (GRCm39) |
S1158A |
probably benign |
Het |
Kmt2a |
T |
C |
9: 44,759,012 (GRCm39) |
T946A |
probably benign |
Het |
Kmt2e |
A |
T |
5: 23,697,292 (GRCm39) |
|
probably benign |
Het |
Krba1 |
G |
A |
6: 48,389,261 (GRCm39) |
V594M |
probably damaging |
Het |
Lamb1 |
T |
C |
12: 31,374,314 (GRCm39) |
L1559P |
probably damaging |
Het |
Lig1 |
C |
T |
7: 13,025,175 (GRCm39) |
P227S |
probably benign |
Het |
Lims2 |
T |
A |
18: 32,090,017 (GRCm39) |
D255E |
probably benign |
Het |
Marchf3 |
C |
T |
18: 56,909,161 (GRCm39) |
C208Y |
probably benign |
Het |
Mei1 |
A |
G |
15: 81,976,843 (GRCm39) |
E142G |
|
Het |
Melk |
G |
T |
4: 44,351,106 (GRCm39) |
R549L |
probably benign |
Het |
Muc6 |
AGGCGCAGAAACCCTGGC |
AGGC |
7: 141,214,363 (GRCm39) |
|
probably null |
Het |
Myorg |
T |
C |
4: 41,498,268 (GRCm39) |
Y454C |
probably damaging |
Het |
Nae1 |
T |
C |
8: 105,250,215 (GRCm39) |
Y226C |
possibly damaging |
Het |
Nap1l1 |
T |
C |
10: 111,326,964 (GRCm39) |
F175S |
probably damaging |
Het |
Ndn |
T |
C |
7: 61,998,709 (GRCm39) |
L185P |
probably damaging |
Het |
Ndst3 |
T |
A |
3: 123,465,388 (GRCm39) |
I195F |
possibly damaging |
Het |
Ndufaf1 |
A |
T |
2: 119,488,907 (GRCm39) |
S206T |
probably benign |
Het |
Nek10 |
C |
A |
14: 14,836,171 (GRCm38) |
H131N |
probably benign |
Het |
Obsl1 |
T |
A |
1: 75,466,360 (GRCm39) |
D1456V |
possibly damaging |
Het |
Or10a2 |
A |
G |
7: 106,673,448 (GRCm39) |
N138D |
probably benign |
Het |
Or10ak7 |
C |
T |
4: 118,791,215 (GRCm39) |
V277I |
probably benign |
Het |
Or52s6 |
T |
A |
7: 103,092,292 (GRCm39) |
T13S |
probably benign |
Het |
Otog |
C |
T |
7: 45,937,474 (GRCm39) |
L1728F |
probably damaging |
Het |
Pcx |
A |
T |
19: 4,652,361 (GRCm39) |
M150L |
possibly damaging |
Het |
Pole |
A |
G |
5: 110,444,973 (GRCm39) |
D443G |
possibly damaging |
Het |
Prr14 |
G |
T |
7: 127,075,648 (GRCm39) |
R552L |
probably damaging |
Het |
Rasgrf1 |
T |
G |
9: 89,899,125 (GRCm39) |
S1156A |
possibly damaging |
Het |
Rfc4 |
T |
A |
16: 22,946,359 (GRCm39) |
|
probably benign |
Het |
Rfx5 |
G |
T |
3: 94,866,272 (GRCm39) |
A524S |
unknown |
Het |
Ryr3 |
G |
A |
2: 112,596,664 (GRCm39) |
P2497S |
probably damaging |
Het |
Scg3 |
T |
C |
9: 75,590,992 (GRCm39) |
T6A |
probably benign |
Het |
Slc26a9 |
A |
T |
1: 131,690,526 (GRCm39) |
D510V |
possibly damaging |
Het |
Stpg3 |
A |
G |
2: 25,104,586 (GRCm39) |
F10L |
probably damaging |
Het |
Tmc5 |
T |
A |
7: 118,239,179 (GRCm39) |
H357Q |
possibly damaging |
Het |
Tmem40 |
A |
T |
6: 115,707,420 (GRCm39) |
L253H |
probably damaging |
Het |
Tmie |
A |
G |
9: 110,696,632 (GRCm39) |
V83A |
probably damaging |
Het |
Uck2 |
A |
T |
1: 167,054,084 (GRCm39) |
I218N |
probably damaging |
Het |
Vtn |
A |
G |
11: 78,391,626 (GRCm39) |
D310G |
possibly damaging |
Het |
Wdr49 |
A |
T |
3: 75,240,580 (GRCm39) |
S430T |
probably benign |
Het |
Wtip |
A |
G |
7: 33,832,087 (GRCm39) |
V133A |
probably benign |
Het |
Zbtb9 |
T |
A |
17: 27,193,666 (GRCm39) |
V357E |
probably damaging |
Het |
Zfp953 |
G |
A |
13: 67,491,706 (GRCm39) |
T82M |
probably benign |
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 |
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 |
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 |
|