Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1600012P17Rik |
T |
C |
1: 158,797,126 (GRCm39) |
|
noncoding transcript |
Het |
2310030G06Rik |
T |
C |
9: 50,651,967 (GRCm39) |
E87G |
probably damaging |
Het |
Aknad1 |
A |
T |
3: 108,682,547 (GRCm39) |
H541L |
possibly damaging |
Het |
Asb15 |
A |
G |
6: 24,567,236 (GRCm39) |
E519G |
possibly damaging |
Het |
Atad2 |
T |
C |
15: 57,971,758 (GRCm39) |
D373G |
probably benign |
Het |
Bbs12 |
G |
A |
3: 37,374,529 (GRCm39) |
V326M |
probably damaging |
Het |
Birc6 |
T |
C |
17: 74,936,484 (GRCm39) |
I2617T |
probably damaging |
Het |
Casz1 |
T |
C |
4: 149,023,438 (GRCm39) |
L495P |
probably damaging |
Het |
Ccdc30 |
T |
A |
4: 119,190,785 (GRCm39) |
I481F |
probably damaging |
Het |
Cept1 |
A |
T |
3: 106,446,677 (GRCm39) |
Y56* |
probably null |
Het |
Cfap54 |
A |
C |
10: 92,897,315 (GRCm39) |
|
probably null |
Het |
Cyp2j8 |
G |
T |
4: 96,358,886 (GRCm39) |
D344E |
probably damaging |
Het |
Dido1 |
A |
T |
2: 180,331,368 (GRCm39) |
W27R |
probably damaging |
Het |
Disp3 |
A |
G |
4: 148,356,575 (GRCm39) |
I95T |
probably damaging |
Het |
Engase |
G |
T |
11: 118,377,920 (GRCm39) |
V237F |
possibly damaging |
Het |
Ephb6 |
G |
A |
6: 41,595,094 (GRCm39) |
E703K |
probably damaging |
Het |
Fnip1 |
T |
A |
11: 54,356,997 (GRCm39) |
F35L |
probably damaging |
Het |
Fnip1 |
A |
T |
11: 54,390,352 (GRCm39) |
T440S |
probably benign |
Het |
Fras1 |
T |
A |
5: 96,879,477 (GRCm39) |
H2431Q |
probably benign |
Het |
Fzd4 |
A |
T |
7: 89,056,924 (GRCm39) |
T324S |
probably damaging |
Het |
Gm10192 |
C |
G |
4: 97,071,345 (GRCm39) |
S20T |
probably null |
Het |
Gpr84 |
A |
T |
15: 103,217,027 (GRCm39) |
V350E |
probably damaging |
Het |
Gsto2 |
T |
C |
19: 47,863,312 (GRCm39) |
Y63H |
probably damaging |
Het |
Gtpbp6 |
T |
C |
5: 110,252,186 (GRCm39) |
T449A |
probably damaging |
Het |
Herc2 |
G |
A |
7: 55,820,388 (GRCm39) |
V2876I |
probably benign |
Het |
Hnrnpa3 |
A |
G |
2: 75,492,351 (GRCm39) |
I152V |
possibly damaging |
Het |
Hpse2 |
T |
C |
19: 42,777,510 (GRCm39) |
D552G |
possibly damaging |
Het |
Itfg1 |
A |
G |
8: 86,459,070 (GRCm39) |
V460A |
possibly damaging |
Het |
Jhy |
G |
A |
9: 40,822,494 (GRCm39) |
A548V |
probably benign |
Het |
Klhl21 |
T |
A |
4: 152,094,268 (GRCm39) |
L290Q |
possibly damaging |
Het |
Knl1 |
T |
C |
2: 118,902,417 (GRCm39) |
S1373P |
probably benign |
Het |
Kpna2 |
A |
C |
11: 106,881,085 (GRCm39) |
M426R |
probably benign |
Het |
Krt9 |
C |
T |
11: 100,081,675 (GRCm39) |
V285I |
probably damaging |
Het |
Lpar1 |
T |
G |
4: 58,437,346 (GRCm39) |
H361P |
possibly damaging |
Het |
Macf1 |
T |
C |
4: 123,349,237 (GRCm39) |
T2100A |
probably benign |
Het |
Mfsd13b |
T |
C |
7: 120,590,549 (GRCm39) |
F97L |
probably damaging |
Het |
Mmp15 |
A |
G |
8: 96,098,958 (GRCm39) |
K595R |
probably benign |
Het |
Mrps25 |
C |
T |
6: 92,152,085 (GRCm39) |
G145D |
probably damaging |
Het |
Muc4 |
T |
A |
16: 32,574,916 (GRCm39) |
|
probably benign |
Het |
Napa |
A |
T |
7: 15,849,196 (GRCm39) |
K245N |
probably benign |
Het |
Or10p1 |
C |
A |
10: 129,444,043 (GRCm39) |
M102I |
probably damaging |
Het |
Or14c39 |
A |
G |
7: 86,344,329 (GRCm39) |
T222A |
probably benign |
Het |
Or2y1c |
A |
T |
11: 49,361,112 (GRCm39) |
I45F |
probably damaging |
Het |
Or4g17 |
G |
A |
2: 111,210,082 (GRCm39) |
V246M |
probably damaging |
Het |
Or4k39 |
T |
A |
2: 111,239,225 (GRCm39) |
|
noncoding transcript |
Het |
Or5au1 |
T |
A |
14: 52,272,921 (GRCm39) |
I216F |
possibly damaging |
Het |
Or8c20 |
A |
G |
9: 38,260,577 (GRCm39) |
Y60C |
probably damaging |
Het |
Or8k35 |
A |
G |
2: 86,424,381 (GRCm39) |
S264P |
possibly damaging |
Het |
Papss2 |
A |
T |
19: 32,616,378 (GRCm39) |
T195S |
probably benign |
Het |
Parp4 |
T |
A |
14: 56,848,267 (GRCm39) |
H694Q |
probably damaging |
Het |
Patj |
C |
T |
4: 98,293,807 (GRCm39) |
R20* |
probably null |
Het |
Pcdhgb8 |
T |
A |
18: 37,895,419 (GRCm39) |
V163E |
probably damaging |
Het |
Pkd2l1 |
T |
A |
19: 44,144,060 (GRCm39) |
T338S |
probably benign |
Het |
Ppargc1b |
A |
T |
18: 61,444,328 (GRCm39) |
S278R |
possibly damaging |
Het |
Ppl |
T |
C |
16: 4,906,846 (GRCm39) |
T1150A |
probably benign |
Het |
Ralgds |
A |
G |
2: 28,442,164 (GRCm39) |
D858G |
probably damaging |
Het |
Rassf2 |
G |
A |
2: 131,844,783 (GRCm39) |
|
probably benign |
Het |
Ring1 |
T |
C |
17: 34,240,971 (GRCm39) |
|
probably benign |
Het |
Rusc1 |
A |
C |
3: 88,998,949 (GRCm39) |
S278A |
probably benign |
Het |
Samd9l |
T |
C |
6: 3,375,623 (GRCm39) |
N546S |
probably benign |
Het |
Sct |
A |
C |
7: 140,858,954 (GRCm39) |
|
probably benign |
Het |
Slc22a12 |
T |
G |
19: 6,588,474 (GRCm39) |
H348P |
probably benign |
Het |
Slc25a15 |
A |
G |
8: 22,873,248 (GRCm39) |
S143P |
probably damaging |
Het |
Slc26a11 |
C |
A |
11: 119,247,657 (GRCm39) |
|
probably benign |
Het |
Slc6a20b |
A |
G |
9: 123,427,625 (GRCm39) |
M428T |
probably damaging |
Het |
Smim17 |
G |
A |
7: 6,432,321 (GRCm39) |
V88M |
probably damaging |
Het |
Smoc1 |
G |
T |
12: 81,214,425 (GRCm39) |
W269L |
probably damaging |
Het |
Sox5 |
C |
T |
6: 143,807,109 (GRCm39) |
|
probably null |
Het |
Sp100 |
A |
G |
1: 85,629,179 (GRCm39) |
*483W |
probably null |
Het |
Sptbn5 |
T |
A |
2: 119,907,703 (GRCm39) |
|
noncoding transcript |
Het |
Sun5 |
G |
A |
2: 153,707,283 (GRCm39) |
R132* |
probably null |
Het |
Tedc2 |
A |
G |
17: 24,435,354 (GRCm39) |
V345A |
probably benign |
Het |
Tlr6 |
T |
A |
5: 65,111,739 (GRCm39) |
R389S |
probably benign |
Het |
Ttc17 |
G |
T |
2: 94,202,113 (GRCm39) |
H396Q |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,773,383 (GRCm39) |
S2340P |
probably damaging |
Het |
Vmn1r219 |
C |
T |
13: 23,346,999 (GRCm39) |
Q63* |
probably null |
Het |
Vmn1r224 |
A |
G |
17: 20,639,902 (GRCm39) |
T160A |
possibly damaging |
Het |
Vmn2r11 |
T |
C |
5: 109,195,436 (GRCm39) |
N630S |
probably damaging |
Het |
Zfp1005 |
T |
A |
2: 150,109,549 (GRCm39) |
C80S |
possibly damaging |
Het |
Zfp747 |
A |
G |
7: 126,973,498 (GRCm39) |
V224A |
possibly damaging |
Het |
Zfp804b |
T |
C |
5: 6,822,250 (GRCm39) |
N271S |
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 |
|
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 |
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 |
|