Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aco1 |
A |
G |
4: 40,197,566 (GRCm39) |
K857E |
probably benign |
Het |
Adam20 |
A |
G |
8: 41,249,080 (GRCm39) |
N397D |
probably benign |
Het |
Adgrf3 |
T |
G |
5: 30,404,211 (GRCm39) |
D347A |
probably damaging |
Het |
Ang6 |
C |
T |
14: 44,239,330 (GRCm39) |
E133K |
possibly damaging |
Het |
Arhgap23 |
T |
A |
11: 97,354,234 (GRCm39) |
W205R |
probably damaging |
Het |
Arhgef40 |
C |
A |
14: 52,235,080 (GRCm39) |
R1086S |
probably damaging |
Het |
Atr |
G |
T |
9: 95,787,870 (GRCm39) |
A1488S |
probably benign |
Het |
Cabin1 |
A |
T |
10: 75,579,184 (GRCm39) |
|
probably null |
Het |
Cby2 |
C |
T |
14: 75,820,850 (GRCm39) |
V292I |
probably benign |
Het |
Cdh22 |
A |
C |
2: 164,985,614 (GRCm39) |
F324C |
probably damaging |
Het |
Cep350 |
T |
C |
1: 155,724,374 (GRCm39) |
I3075V |
probably damaging |
Het |
Chd9 |
A |
T |
8: 91,683,323 (GRCm39) |
K588* |
probably null |
Het |
Clns1a |
A |
T |
7: 97,346,066 (GRCm39) |
I44F |
probably damaging |
Het |
Colgalt1 |
T |
C |
8: 72,063,995 (GRCm39) |
I51T |
possibly damaging |
Het |
Cpt2 |
C |
T |
4: 107,761,452 (GRCm39) |
E217K |
possibly damaging |
Het |
Ctss |
A |
G |
3: 95,454,105 (GRCm39) |
|
probably null |
Het |
Cyp1a1 |
A |
G |
9: 57,609,980 (GRCm39) |
T465A |
probably benign |
Het |
Dbn1 |
A |
G |
13: 55,629,160 (GRCm39) |
|
probably null |
Het |
Dennd1b |
A |
G |
1: 139,018,143 (GRCm39) |
|
probably null |
Het |
Dnajc1 |
A |
C |
2: 18,298,838 (GRCm39) |
Y49* |
probably null |
Het |
Dock10 |
T |
A |
1: 80,520,918 (GRCm39) |
I1188L |
probably damaging |
Het |
Dsg1c |
T |
G |
18: 20,416,096 (GRCm39) |
|
probably null |
Het |
Efcab6 |
G |
A |
15: 83,851,822 (GRCm39) |
T352I |
possibly damaging |
Het |
Eps8l3 |
T |
C |
3: 107,786,902 (GRCm39) |
L26P |
possibly damaging |
Het |
Fbxw26 |
A |
G |
9: 109,553,946 (GRCm39) |
V231A |
probably benign |
Het |
Fetub |
G |
A |
16: 22,754,419 (GRCm39) |
E209K |
possibly damaging |
Het |
Galc |
A |
T |
12: 98,212,556 (GRCm39) |
|
probably null |
Het |
Gm6871 |
A |
T |
7: 41,222,892 (GRCm39) |
N65K |
probably benign |
Het |
Gstp3 |
A |
G |
19: 4,107,540 (GRCm39) |
I208T |
probably benign |
Het |
Gtpbp3 |
A |
G |
8: 71,945,272 (GRCm39) |
Y448C |
probably benign |
Het |
Hdac7 |
G |
T |
15: 97,705,857 (GRCm39) |
Q385K |
probably damaging |
Het |
Hemgn |
C |
T |
4: 46,396,655 (GRCm39) |
V194M |
possibly damaging |
Het |
Idh2 |
G |
C |
7: 79,748,625 (GRCm39) |
T113R |
probably benign |
Het |
Jarid2 |
A |
C |
13: 45,056,219 (GRCm39) |
K336T |
possibly damaging |
Het |
Kcnj4 |
C |
T |
15: 79,369,216 (GRCm39) |
V255M |
probably damaging |
Het |
Ldhb |
C |
A |
6: 142,439,934 (GRCm39) |
W202L |
probably damaging |
Het |
Lmbrd2 |
T |
A |
15: 9,177,838 (GRCm39) |
Y512* |
probably null |
Het |
Lrp1 |
A |
G |
10: 127,431,152 (GRCm39) |
|
probably null |
Het |
Map3k12 |
G |
A |
15: 102,411,970 (GRCm39) |
P365S |
probably damaging |
Het |
Map3k5 |
G |
A |
10: 19,979,909 (GRCm39) |
D806N |
probably benign |
Het |
Matn3 |
A |
G |
12: 9,017,662 (GRCm39) |
E438G |
possibly damaging |
Het |
Mcmbp |
G |
A |
7: 128,325,698 (GRCm39) |
L97F |
probably damaging |
Het |
Mmp3 |
A |
T |
9: 7,453,662 (GRCm39) |
I428L |
probably benign |
Het |
Mphosph8 |
T |
C |
14: 56,934,616 (GRCm39) |
V855A |
probably damaging |
Het |
Mycbp2 |
T |
A |
14: 103,393,150 (GRCm39) |
H3027L |
possibly damaging |
Het |
Notch1 |
G |
T |
2: 26,350,446 (GRCm39) |
H2231Q |
probably benign |
Het |
Npas2 |
A |
T |
1: 39,364,456 (GRCm39) |
H266L |
probably damaging |
Het |
Oas3 |
A |
G |
5: 120,898,045 (GRCm39) |
S833P |
probably damaging |
Het |
Or1j15 |
T |
C |
2: 36,458,789 (GRCm39) |
Y60H |
probably damaging |
Het |
Or5ak24 |
T |
C |
2: 85,260,265 (GRCm39) |
T303A |
probably benign |
Het |
Or5w17 |
A |
C |
2: 87,584,334 (GRCm39) |
M1R |
probably null |
Het |
Or6c65 |
G |
A |
10: 129,603,725 (GRCm39) |
R120H |
probably benign |
Het |
Pak4 |
C |
T |
7: 28,264,690 (GRCm39) |
V71I |
possibly damaging |
Het |
Pitpnm1 |
T |
C |
19: 4,162,395 (GRCm39) |
V1075A |
probably damaging |
Het |
Pkp3 |
G |
A |
7: 140,668,415 (GRCm39) |
V555M |
probably damaging |
Het |
Plekhm2 |
T |
C |
4: 141,359,685 (GRCm39) |
T381A |
probably benign |
Het |
Plppr3 |
A |
G |
10: 79,702,244 (GRCm39) |
|
probably null |
Het |
Ppp2r5e |
A |
T |
12: 75,516,540 (GRCm39) |
F216I |
possibly damaging |
Het |
Ppp3ca |
T |
A |
3: 136,627,672 (GRCm39) |
V412D |
probably benign |
Het |
Prss50 |
A |
G |
9: 110,687,081 (GRCm39) |
|
probably benign |
Het |
Psph |
A |
C |
5: 129,843,532 (GRCm39) |
I174R |
probably damaging |
Het |
Ptov1 |
A |
G |
7: 44,514,991 (GRCm39) |
Y207H |
possibly damaging |
Het |
Ptprs |
A |
G |
17: 56,741,510 (GRCm39) |
S585P |
probably damaging |
Het |
Rnf146 |
A |
T |
10: 29,223,720 (GRCm39) |
H55Q |
probably damaging |
Het |
Rnf213 |
T |
A |
11: 119,332,009 (GRCm39) |
M2407K |
probably damaging |
Het |
Rnls |
A |
C |
19: 33,179,931 (GRCm39) |
L55R |
possibly damaging |
Het |
Rptor |
T |
C |
11: 119,647,146 (GRCm39) |
C246R |
probably damaging |
Het |
Rrp12 |
C |
T |
19: 41,866,222 (GRCm39) |
|
probably null |
Het |
Samd3 |
A |
G |
10: 26,127,672 (GRCm39) |
D223G |
probably damaging |
Het |
Sdad1 |
G |
A |
5: 92,453,155 (GRCm39) |
Q68* |
probably null |
Het |
Selenov |
G |
A |
7: 27,989,847 (GRCm39) |
T219M |
probably damaging |
Het |
Shd |
A |
G |
17: 56,278,554 (GRCm39) |
D39G |
possibly damaging |
Het |
Slc26a10 |
A |
T |
10: 127,014,279 (GRCm39) |
V245E |
probably damaging |
Het |
Slit1 |
A |
G |
19: 41,614,012 (GRCm39) |
L820P |
probably damaging |
Het |
Snap23 |
T |
C |
2: 120,421,163 (GRCm39) |
F96L |
probably benign |
Het |
Speer1k |
T |
C |
5: 10,998,994 (GRCm39) |
|
probably benign |
Het |
Spef1l |
A |
T |
7: 139,556,005 (GRCm39) |
I212N |
probably benign |
Het |
Stkld1 |
A |
G |
2: 26,840,115 (GRCm39) |
H395R |
probably damaging |
Het |
Syt13 |
G |
A |
2: 92,771,165 (GRCm39) |
G84D |
probably damaging |
Het |
Terb2 |
T |
A |
2: 122,016,990 (GRCm39) |
L37Q |
probably damaging |
Het |
Themis |
A |
G |
10: 28,657,753 (GRCm39) |
Y107C |
probably damaging |
Het |
Top2a |
T |
A |
11: 98,906,895 (GRCm39) |
T249S |
probably benign |
Het |
Tspo2 |
A |
T |
17: 48,756,148 (GRCm39) |
F71Y |
probably damaging |
Het |
Ttc21b |
T |
A |
2: 66,053,921 (GRCm39) |
K753* |
probably null |
Het |
Ttk |
A |
G |
9: 83,736,915 (GRCm39) |
Y458C |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,586,017 (GRCm39) |
R21905G |
probably damaging |
Het |
Ugt3a1 |
T |
A |
15: 9,351,254 (GRCm39) |
F88I |
probably benign |
Het |
Vmn1r119 |
A |
G |
7: 20,746,121 (GRCm39) |
L87P |
probably damaging |
Het |
Vmn1r36 |
A |
G |
6: 66,693,747 (GRCm39) |
F6L |
probably benign |
Het |
Vmn2r15 |
T |
A |
5: 109,434,860 (GRCm39) |
K615* |
probably null |
Het |
Wdr18 |
G |
A |
10: 79,802,561 (GRCm39) |
|
probably null |
Het |
Wdr6 |
A |
T |
9: 108,453,176 (GRCm39) |
W236R |
probably damaging |
Het |
Zbtb48 |
T |
C |
4: 152,110,955 (GRCm39) |
T187A |
probably benign |
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 |
R1663:Nbea
|
UTSW |
3 |
55,553,407 (GRCm39) |
missense |
possibly damaging |
0.95 |
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 |
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 |
|