Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam3 |
T |
A |
8: 25,177,949 (GRCm39) |
T11S |
probably benign |
Het |
Adgb |
T |
C |
10: 10,215,419 (GRCm39) |
M1529V |
possibly damaging |
Het |
Ankrd36 |
T |
A |
11: 5,570,126 (GRCm39) |
D531E |
possibly damaging |
Het |
Ankzf1 |
C |
T |
1: 75,172,914 (GRCm39) |
P337S |
probably damaging |
Het |
Apc |
A |
G |
18: 34,401,378 (GRCm39) |
I55V |
probably damaging |
Het |
Aplnr |
A |
G |
2: 84,967,038 (GRCm39) |
D21G |
possibly damaging |
Het |
Apol10b |
A |
T |
15: 77,472,914 (GRCm39) |
F47I |
probably damaging |
Het |
Arhgef5 |
G |
A |
6: 43,253,899 (GRCm39) |
A1131T |
probably damaging |
Het |
Arrb2 |
A |
T |
11: 70,328,429 (GRCm39) |
Q83L |
probably damaging |
Het |
Atf7ip |
A |
G |
6: 136,580,322 (GRCm39) |
Q1082R |
possibly damaging |
Het |
Atl2 |
A |
G |
17: 80,172,140 (GRCm39) |
S28P |
probably damaging |
Het |
Brd7 |
T |
C |
8: 89,084,651 (GRCm39) |
K89E |
possibly damaging |
Het |
Cc2d1b |
A |
G |
4: 108,480,744 (GRCm39) |
T55A |
probably damaging |
Het |
Ccdc18 |
A |
G |
5: 108,363,956 (GRCm39) |
E1217G |
probably damaging |
Het |
Cdc42ep4 |
A |
T |
11: 113,620,277 (GRCm39) |
M38K |
probably damaging |
Het |
Cldn14 |
A |
G |
16: 93,716,166 (GRCm39) |
S227P |
probably damaging |
Het |
Clspn |
T |
A |
4: 126,459,768 (GRCm39) |
C332S |
probably benign |
Het |
Col5a1 |
T |
C |
2: 27,841,488 (GRCm39) |
S370P |
unknown |
Het |
Comp |
T |
C |
8: 70,826,250 (GRCm39) |
L10P |
possibly damaging |
Het |
Dcc |
A |
T |
18: 71,959,123 (GRCm39) |
N216K |
probably damaging |
Het |
Dcstamp |
C |
T |
15: 39,618,340 (GRCm39) |
Q250* |
probably null |
Het |
Drd5 |
T |
C |
5: 38,478,198 (GRCm39) |
F397S |
probably benign |
Het |
Dst |
T |
C |
1: 34,202,466 (GRCm39) |
S265P |
probably damaging |
Het |
Dync2i1 |
T |
C |
12: 116,193,230 (GRCm39) |
Q574R |
probably benign |
Het |
Enam |
A |
T |
5: 88,651,853 (GRCm39) |
S1046C |
probably damaging |
Het |
Eno3 |
T |
C |
11: 70,553,100 (GRCm39) |
|
probably null |
Het |
Fam13a |
G |
A |
6: 58,931,357 (GRCm39) |
R408* |
probably null |
Het |
Gipc2 |
T |
A |
3: 151,799,801 (GRCm39) |
M310L |
probably benign |
Het |
Gm14496 |
T |
C |
2: 181,639,230 (GRCm39) |
V440A |
probably benign |
Het |
Gzmg |
A |
T |
14: 56,394,265 (GRCm39) |
C210S |
probably damaging |
Het |
Helb |
G |
T |
10: 119,941,338 (GRCm39) |
A450E |
probably damaging |
Het |
Hepacam2 |
A |
T |
6: 3,483,439 (GRCm39) |
I190N |
possibly damaging |
Het |
Hk3 |
A |
T |
13: 55,154,388 (GRCm39) |
S773T |
probably benign |
Het |
Hnrnpc |
A |
G |
14: 52,312,852 (GRCm39) |
S221P |
probably damaging |
Het |
Ifna9 |
T |
C |
4: 88,510,220 (GRCm39) |
T135A |
probably benign |
Het |
Igfn1 |
C |
T |
1: 135,896,046 (GRCm39) |
G1507R |
probably benign |
Het |
Kank3 |
A |
G |
17: 34,037,349 (GRCm39) |
T218A |
probably benign |
Het |
Kcp |
G |
T |
6: 29,498,964 (GRCm39) |
R337S |
possibly damaging |
Het |
Krt74 |
A |
T |
15: 101,665,109 (GRCm39) |
|
noncoding transcript |
Het |
Lrp1 |
A |
T |
10: 127,392,790 (GRCm39) |
D2758E |
probably damaging |
Het |
Ly75 |
T |
C |
2: 60,144,578 (GRCm39) |
E1295G |
probably damaging |
Het |
Mccc1 |
C |
A |
3: 36,033,082 (GRCm39) |
W354L |
probably damaging |
Het |
Mmp1a |
C |
T |
9: 7,465,657 (GRCm39) |
T198M |
probably benign |
Het |
Mtmr2 |
C |
T |
9: 13,714,797 (GRCm39) |
T519I |
probably damaging |
Het |
Nbn |
T |
A |
4: 15,970,903 (GRCm39) |
D295E |
probably benign |
Het |
Ndufb8 |
T |
C |
19: 44,538,820 (GRCm39) |
Y167C |
probably damaging |
Het |
Nisch |
A |
G |
14: 30,913,478 (GRCm39) |
|
probably benign |
Het |
Notch3 |
C |
T |
17: 32,375,093 (GRCm39) |
G407D |
probably damaging |
Het |
Nucb1 |
A |
G |
7: 45,148,288 (GRCm39) |
F175S |
probably damaging |
Het |
Or1l8 |
T |
G |
2: 36,817,346 (GRCm39) |
Y260S |
probably damaging |
Het |
Or6c6c |
G |
A |
10: 129,541,160 (GRCm39) |
V138M |
probably benign |
Het |
Or7g12 |
T |
A |
9: 18,900,006 (GRCm39) |
C241S |
probably damaging |
Het |
Or8b44 |
T |
G |
9: 38,410,868 (GRCm39) |
I301R |
unknown |
Het |
Pip5k1c |
T |
C |
10: 81,148,349 (GRCm39) |
V425A |
probably damaging |
Het |
Pnisr |
T |
A |
4: 21,873,857 (GRCm39) |
|
probably benign |
Het |
Prkag1 |
A |
G |
15: 98,713,776 (GRCm39) |
V18A |
probably damaging |
Het |
Rad50 |
T |
C |
11: 53,559,050 (GRCm39) |
N1063S |
probably benign |
Het |
Rnf170 |
C |
T |
8: 26,619,171 (GRCm39) |
H132Y |
probably damaging |
Het |
Rnf213 |
A |
G |
11: 119,328,498 (GRCm39) |
D1977G |
probably benign |
Het |
Sema3a |
G |
A |
5: 13,607,092 (GRCm39) |
|
probably null |
Het |
Setx |
T |
A |
2: 29,016,917 (GRCm39) |
C7S |
probably damaging |
Het |
Slc23a2 |
A |
G |
2: 131,907,384 (GRCm39) |
I417T |
probably damaging |
Het |
Spink6 |
T |
G |
18: 44,204,588 (GRCm39) |
F18C |
unknown |
Het |
Sptbn1 |
T |
C |
11: 30,070,783 (GRCm39) |
Q1538R |
possibly damaging |
Het |
Strn3 |
A |
G |
12: 51,699,609 (GRCm39) |
Y188H |
probably damaging |
Het |
Tecpr1 |
C |
A |
5: 144,134,762 (GRCm39) |
K1040N |
probably benign |
Het |
Tll1 |
T |
A |
8: 64,470,720 (GRCm39) |
Y901F |
probably benign |
Het |
Tmem81 |
C |
T |
1: 132,435,635 (GRCm39) |
A147V |
probably benign |
Het |
Tnpo3 |
T |
C |
6: 29,565,758 (GRCm39) |
D532G |
probably benign |
Het |
Vmn2r19 |
T |
A |
6: 123,313,411 (GRCm39) |
I827N |
probably benign |
Het |
Wdr35 |
A |
G |
12: 9,070,000 (GRCm39) |
K857R |
probably benign |
Het |
Zfp110 |
A |
G |
7: 12,582,569 (GRCm39) |
T406A |
probably benign |
Het |
Zfp52 |
T |
C |
17: 21,782,084 (GRCm39) |
L644P |
possibly damaging |
Het |
Zfp605 |
G |
A |
5: 110,275,451 (GRCm39) |
V190I |
probably benign |
Het |
Zfp964 |
A |
G |
8: 70,116,733 (GRCm39) |
|
probably null |
Het |
Zmynd8 |
A |
G |
2: 165,649,805 (GRCm39) |
S779P |
probably benign |
Het |
Zswim5 |
T |
A |
4: 116,844,092 (GRCm39) |
N1043K |
probably damaging |
Het |
|
Other mutations in Nbea |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00540:Nbea
|
APN |
3 |
55,535,914 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00541:Nbea
|
APN |
3 |
55,875,510 (GRCm39) |
missense |
probably benign |
0.02 |
IGL00584:Nbea
|
APN |
3 |
55,989,869 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00648:Nbea
|
APN |
3 |
55,916,681 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00785:Nbea
|
APN |
3 |
55,862,814 (GRCm39) |
missense |
probably benign |
|
IGL00899:Nbea
|
APN |
3 |
55,550,266 (GRCm39) |
missense |
probably benign |
0.32 |
IGL00955:Nbea
|
APN |
3 |
55,912,893 (GRCm39) |
missense |
possibly damaging |
0.45 |
IGL01296:Nbea
|
APN |
3 |
55,938,957 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01299:Nbea
|
APN |
3 |
55,598,315 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01393:Nbea
|
APN |
3 |
55,912,729 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01550:Nbea
|
APN |
3 |
55,712,669 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02023:Nbea
|
APN |
3 |
55,588,437 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02034:Nbea
|
APN |
3 |
55,875,577 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02061:Nbea
|
APN |
3 |
55,625,308 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL02082:Nbea
|
APN |
3 |
55,875,588 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02113:Nbea
|
APN |
3 |
55,899,913 (GRCm39) |
missense |
probably benign |
|
IGL02188:Nbea
|
APN |
3 |
55,891,258 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02319:Nbea
|
APN |
3 |
55,893,159 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02406:Nbea
|
APN |
3 |
55,993,687 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02494:Nbea
|
APN |
3 |
55,712,772 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02550:Nbea
|
APN |
3 |
55,926,835 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02706:Nbea
|
APN |
3 |
55,944,699 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02718:Nbea
|
APN |
3 |
55,539,483 (GRCm39) |
nonsense |
probably null |
|
IGL02822:Nbea
|
APN |
3 |
55,926,868 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02885:Nbea
|
APN |
3 |
55,539,407 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03000:Nbea
|
APN |
3 |
55,912,048 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03081:Nbea
|
APN |
3 |
55,987,339 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03091:Nbea
|
APN |
3 |
55,992,725 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03368:Nbea
|
APN |
3 |
55,987,351 (GRCm39) |
missense |
probably damaging |
0.98 |
Neches
|
UTSW |
3 |
55,860,455 (GRCm39) |
critical splice donor site |
probably null |
|
scotland
|
UTSW |
3 |
55,534,329 (GRCm39) |
missense |
probably damaging |
1.00 |
Wales
|
UTSW |
3 |
55,998,540 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4340:Nbea
|
UTSW |
3 |
55,916,633 (GRCm39) |
critical splice donor site |
probably benign |
|
G4846:Nbea
|
UTSW |
3 |
55,994,918 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02835:Nbea
|
UTSW |
3 |
55,625,290 (GRCm39) |
missense |
possibly damaging |
0.88 |
LCD18:Nbea
|
UTSW |
3 |
55,608,948 (GRCm39) |
intron |
probably benign |
|
R0087:Nbea
|
UTSW |
3 |
55,998,444 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0220:Nbea
|
UTSW |
3 |
55,912,724 (GRCm39) |
missense |
probably benign |
0.30 |
R0324:Nbea
|
UTSW |
3 |
55,965,369 (GRCm39) |
critical splice donor site |
probably null |
|
R0330:Nbea
|
UTSW |
3 |
55,550,238 (GRCm39) |
missense |
probably benign |
0.27 |
R0391:Nbea
|
UTSW |
3 |
55,944,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R0394:Nbea
|
UTSW |
3 |
55,937,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R0419:Nbea
|
UTSW |
3 |
55,726,715 (GRCm39) |
missense |
probably benign |
0.05 |
R0503:Nbea
|
UTSW |
3 |
55,550,257 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0521:Nbea
|
UTSW |
3 |
55,915,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R0595:Nbea
|
UTSW |
3 |
55,535,917 (GRCm39) |
missense |
probably benign |
0.18 |
R0894:Nbea
|
UTSW |
3 |
55,916,761 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1072:Nbea
|
UTSW |
3 |
55,993,617 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1125:Nbea
|
UTSW |
3 |
55,764,427 (GRCm39) |
nonsense |
probably null |
|
R1169:Nbea
|
UTSW |
3 |
55,875,744 (GRCm39) |
missense |
probably benign |
0.00 |
R1241:Nbea
|
UTSW |
3 |
55,965,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R1269:Nbea
|
UTSW |
3 |
55,912,202 (GRCm39) |
missense |
probably benign |
0.05 |
R1406:Nbea
|
UTSW |
3 |
55,944,702 (GRCm39) |
missense |
probably benign |
0.00 |
R1406:Nbea
|
UTSW |
3 |
55,944,702 (GRCm39) |
missense |
probably benign |
0.00 |
R1457:Nbea
|
UTSW |
3 |
55,992,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R1482:Nbea
|
UTSW |
3 |
55,987,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R1483:Nbea
|
UTSW |
3 |
55,910,211 (GRCm39) |
missense |
probably benign |
0.25 |
R1502:Nbea
|
UTSW |
3 |
55,912,310 (GRCm39) |
missense |
probably benign |
0.03 |
R1544:Nbea
|
UTSW |
3 |
55,966,248 (GRCm39) |
missense |
probably damaging |
0.99 |
R1629:Nbea
|
UTSW |
3 |
55,910,312 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1647:Nbea
|
UTSW |
3 |
55,537,650 (GRCm39) |
missense |
probably damaging |
0.97 |
R1722:Nbea
|
UTSW |
3 |
55,573,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R1757:Nbea
|
UTSW |
3 |
55,537,610 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1771:Nbea
|
UTSW |
3 |
55,841,940 (GRCm39) |
missense |
probably benign |
0.00 |
R1796:Nbea
|
UTSW |
3 |
55,551,129 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1844:Nbea
|
UTSW |
3 |
55,989,857 (GRCm39) |
missense |
probably damaging |
0.97 |
R1872:Nbea
|
UTSW |
3 |
55,550,310 (GRCm39) |
missense |
probably benign |
0.12 |
R1938:Nbea
|
UTSW |
3 |
55,992,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R1940:Nbea
|
UTSW |
3 |
55,860,521 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2062:Nbea
|
UTSW |
3 |
55,993,578 (GRCm39) |
splice site |
probably benign |
|
R2066:Nbea
|
UTSW |
3 |
55,875,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R2097:Nbea
|
UTSW |
3 |
55,630,638 (GRCm39) |
missense |
probably damaging |
0.96 |
R2181:Nbea
|
UTSW |
3 |
55,937,360 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2274:Nbea
|
UTSW |
3 |
55,895,506 (GRCm39) |
splice site |
probably null |
|
R2345:Nbea
|
UTSW |
3 |
55,992,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R2423:Nbea
|
UTSW |
3 |
55,992,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R2434:Nbea
|
UTSW |
3 |
55,554,881 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2880:Nbea
|
UTSW |
3 |
55,554,779 (GRCm39) |
missense |
probably benign |
0.04 |
R2881:Nbea
|
UTSW |
3 |
55,554,779 (GRCm39) |
missense |
probably benign |
0.04 |
R2940:Nbea
|
UTSW |
3 |
55,842,045 (GRCm39) |
missense |
probably benign |
0.24 |
R3500:Nbea
|
UTSW |
3 |
55,588,431 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3765:Nbea
|
UTSW |
3 |
55,912,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R3790:Nbea
|
UTSW |
3 |
55,912,450 (GRCm39) |
missense |
probably benign |
|
R3808:Nbea
|
UTSW |
3 |
55,625,269 (GRCm39) |
missense |
probably benign |
0.02 |
R3845:Nbea
|
UTSW |
3 |
55,993,713 (GRCm39) |
splice site |
probably benign |
|
R4182:Nbea
|
UTSW |
3 |
55,915,848 (GRCm39) |
missense |
probably damaging |
0.99 |
R4385:Nbea
|
UTSW |
3 |
55,908,059 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4419:Nbea
|
UTSW |
3 |
55,917,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R4426:Nbea
|
UTSW |
3 |
55,989,800 (GRCm39) |
missense |
probably damaging |
0.98 |
R4451:Nbea
|
UTSW |
3 |
55,899,753 (GRCm39) |
critical splice donor site |
probably null |
|
R4456:Nbea
|
UTSW |
3 |
55,551,205 (GRCm39) |
missense |
probably benign |
0.00 |
R4604:Nbea
|
UTSW |
3 |
55,631,069 (GRCm39) |
missense |
probably benign |
0.18 |
R4687:Nbea
|
UTSW |
3 |
55,965,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R4758:Nbea
|
UTSW |
3 |
55,912,824 (GRCm39) |
missense |
probably benign |
|
R4840:Nbea
|
UTSW |
3 |
55,618,091 (GRCm39) |
missense |
probably benign |
0.37 |
R4888:Nbea
|
UTSW |
3 |
55,912,776 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4954:Nbea
|
UTSW |
3 |
55,943,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R4972:Nbea
|
UTSW |
3 |
55,992,667 (GRCm39) |
missense |
probably damaging |
0.99 |
R4980:Nbea
|
UTSW |
3 |
55,860,466 (GRCm39) |
missense |
probably benign |
0.00 |
R4980:Nbea
|
UTSW |
3 |
55,554,772 (GRCm39) |
splice site |
probably null |
|
R5104:Nbea
|
UTSW |
3 |
55,987,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R5139:Nbea
|
UTSW |
3 |
55,534,384 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5166:Nbea
|
UTSW |
3 |
55,926,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R5347:Nbea
|
UTSW |
3 |
55,948,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R5350:Nbea
|
UTSW |
3 |
55,926,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R5418:Nbea
|
UTSW |
3 |
55,553,410 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5586:Nbea
|
UTSW |
3 |
55,539,392 (GRCm39) |
missense |
probably benign |
0.08 |
R5627:Nbea
|
UTSW |
3 |
55,899,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R5683:Nbea
|
UTSW |
3 |
55,536,007 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5765:Nbea
|
UTSW |
3 |
55,912,719 (GRCm39) |
missense |
probably benign |
0.15 |
R5853:Nbea
|
UTSW |
3 |
55,899,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R5858:Nbea
|
UTSW |
3 |
55,860,455 (GRCm39) |
critical splice donor site |
probably null |
|
R5955:Nbea
|
UTSW |
3 |
55,588,404 (GRCm39) |
missense |
probably benign |
0.00 |
R5976:Nbea
|
UTSW |
3 |
55,761,268 (GRCm39) |
missense |
probably benign |
0.30 |
R6039:Nbea
|
UTSW |
3 |
55,912,538 (GRCm39) |
missense |
probably benign |
0.00 |
R6039:Nbea
|
UTSW |
3 |
55,912,538 (GRCm39) |
missense |
probably benign |
0.00 |
R6043:Nbea
|
UTSW |
3 |
55,693,896 (GRCm39) |
missense |
probably benign |
0.32 |
R6122:Nbea
|
UTSW |
3 |
55,937,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R6218:Nbea
|
UTSW |
3 |
55,535,905 (GRCm39) |
missense |
probably damaging |
0.97 |
R6331:Nbea
|
UTSW |
3 |
55,908,037 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6334:Nbea
|
UTSW |
3 |
55,944,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R6393:Nbea
|
UTSW |
3 |
55,998,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R6411:Nbea
|
UTSW |
3 |
55,712,778 (GRCm39) |
missense |
probably benign |
0.01 |
R6457:Nbea
|
UTSW |
3 |
55,907,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R6476:Nbea
|
UTSW |
3 |
55,912,227 (GRCm39) |
missense |
probably benign |
0.00 |
R6488:Nbea
|
UTSW |
3 |
55,625,264 (GRCm39) |
missense |
probably damaging |
0.99 |
R6700:Nbea
|
UTSW |
3 |
55,989,869 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6702:Nbea
|
UTSW |
3 |
55,912,923 (GRCm39) |
missense |
probably benign |
0.06 |
R6752:Nbea
|
UTSW |
3 |
55,944,640 (GRCm39) |
missense |
probably benign |
|
R6752:Nbea
|
UTSW |
3 |
55,875,730 (GRCm39) |
missense |
probably benign |
0.02 |
R6804:Nbea
|
UTSW |
3 |
55,994,874 (GRCm39) |
missense |
probably benign |
0.37 |
R6901:Nbea
|
UTSW |
3 |
55,926,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R6933:Nbea
|
UTSW |
3 |
55,631,031 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7124:Nbea
|
UTSW |
3 |
55,899,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R7211:Nbea
|
UTSW |
3 |
55,912,322 (GRCm39) |
missense |
probably benign |
0.05 |
R7308:Nbea
|
UTSW |
3 |
55,998,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R7405:Nbea
|
UTSW |
3 |
55,712,687 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7669:Nbea
|
UTSW |
3 |
55,625,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R7762:Nbea
|
UTSW |
3 |
55,557,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R7833:Nbea
|
UTSW |
3 |
55,910,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R7885:Nbea
|
UTSW |
3 |
55,573,110 (GRCm39) |
missense |
probably damaging |
0.97 |
R7935:Nbea
|
UTSW |
3 |
55,966,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R8050:Nbea
|
UTSW |
3 |
55,895,402 (GRCm39) |
missense |
probably damaging |
0.99 |
R8108:Nbea
|
UTSW |
3 |
55,726,736 (GRCm39) |
missense |
probably benign |
0.11 |
R8290:Nbea
|
UTSW |
3 |
55,966,056 (GRCm39) |
nonsense |
probably null |
|
R8314:Nbea
|
UTSW |
3 |
55,916,672 (GRCm39) |
missense |
probably damaging |
0.99 |
R8321:Nbea
|
UTSW |
3 |
56,090,518 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8376:Nbea
|
UTSW |
3 |
55,551,076 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8410:Nbea
|
UTSW |
3 |
55,944,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R8556:Nbea
|
UTSW |
3 |
55,554,807 (GRCm39) |
missense |
probably benign |
0.25 |
R8753:Nbea
|
UTSW |
3 |
55,534,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R8844:Nbea
|
UTSW |
3 |
55,998,415 (GRCm39) |
missense |
probably damaging |
0.97 |
R8884:Nbea
|
UTSW |
3 |
55,712,720 (GRCm39) |
missense |
probably benign |
0.00 |
R8886:Nbea
|
UTSW |
3 |
55,966,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R8890:Nbea
|
UTSW |
3 |
55,926,784 (GRCm39) |
splice site |
probably benign |
|
R9004:Nbea
|
UTSW |
3 |
55,910,359 (GRCm39) |
missense |
probably benign |
0.01 |
R9022:Nbea
|
UTSW |
3 |
55,551,110 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9080:Nbea
|
UTSW |
3 |
55,912,516 (GRCm39) |
nonsense |
probably null |
|
R9087:Nbea
|
UTSW |
3 |
55,550,157 (GRCm39) |
critical splice donor site |
probably null |
|
R9104:Nbea
|
UTSW |
3 |
55,862,809 (GRCm39) |
missense |
probably benign |
|
R9165:Nbea
|
UTSW |
3 |
55,912,289 (GRCm39) |
missense |
probably benign |
0.15 |
R9219:Nbea
|
UTSW |
3 |
55,998,393 (GRCm39) |
frame shift |
probably null |
|
R9221:Nbea
|
UTSW |
3 |
55,998,393 (GRCm39) |
frame shift |
probably null |
|
R9222:Nbea
|
UTSW |
3 |
55,998,393 (GRCm39) |
frame shift |
probably null |
|
R9260:Nbea
|
UTSW |
3 |
55,891,233 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9263:Nbea
|
UTSW |
3 |
55,998,393 (GRCm39) |
frame shift |
probably null |
|
R9265:Nbea
|
UTSW |
3 |
55,998,393 (GRCm39) |
frame shift |
probably null |
|
R9294:Nbea
|
UTSW |
3 |
55,998,513 (GRCm39) |
missense |
probably benign |
0.00 |
R9360:Nbea
|
UTSW |
3 |
55,943,319 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9387:Nbea
|
UTSW |
3 |
55,898,460 (GRCm39) |
missense |
probably benign |
0.12 |
R9428:Nbea
|
UTSW |
3 |
55,998,393 (GRCm39) |
frame shift |
probably null |
|
R9435:Nbea
|
UTSW |
3 |
55,943,309 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9507:Nbea
|
UTSW |
3 |
55,573,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R9514:Nbea
|
UTSW |
3 |
55,937,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R9516:Nbea
|
UTSW |
3 |
55,937,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R9674:Nbea
|
UTSW |
3 |
55,966,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R9688:Nbea
|
UTSW |
3 |
55,557,165 (GRCm39) |
missense |
probably benign |
0.42 |
R9709:Nbea
|
UTSW |
3 |
55,693,879 (GRCm39) |
nonsense |
probably null |
|
RF051:Nbea
|
UTSW |
3 |
55,916,633 (GRCm39) |
critical splice donor site |
probably benign |
|
X0018:Nbea
|
UTSW |
3 |
55,943,469 (GRCm39) |
missense |
probably benign |
0.39 |
Z1088:Nbea
|
UTSW |
3 |
55,630,584 (GRCm39) |
missense |
probably benign |
0.34 |
Z1177:Nbea
|
UTSW |
3 |
55,938,971 (GRCm39) |
missense |
probably damaging |
1.00 |
|