Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933436I01Rik |
T |
A |
X: 66,964,308 (GRCm39) |
I184L |
probably benign |
Het |
9530002B09Rik |
T |
A |
4: 122,583,115 (GRCm39) |
|
probably benign |
Het |
Acadl |
C |
T |
1: 66,880,905 (GRCm39) |
|
probably null |
Het |
Acss1 |
G |
A |
2: 150,510,051 (GRCm39) |
Q23* |
probably null |
Het |
Afap1l1 |
A |
T |
18: 61,872,193 (GRCm39) |
|
probably null |
Het |
Akt3 |
A |
G |
1: 176,930,551 (GRCm39) |
S136P |
possibly damaging |
Het |
Amy2a1 |
T |
C |
3: 113,324,217 (GRCm39) |
I108V |
probably benign |
Het |
Ano5 |
T |
G |
7: 51,235,134 (GRCm39) |
L639R |
probably damaging |
Het |
Arhgap26 |
T |
C |
18: 39,439,781 (GRCm39) |
S71P |
probably damaging |
Het |
B3gnt2 |
A |
G |
11: 22,786,735 (GRCm39) |
L151P |
probably damaging |
Het |
Bach1 |
A |
T |
16: 87,526,513 (GRCm39) |
K658N |
probably damaging |
Het |
Bdnf |
C |
A |
2: 109,554,247 (GRCm39) |
T207K |
probably damaging |
Het |
Bod1l |
G |
T |
5: 41,962,499 (GRCm39) |
T2746K |
probably damaging |
Het |
Brwd1 |
A |
G |
16: 95,847,665 (GRCm39) |
S652P |
probably benign |
Het |
Ccnt1 |
A |
T |
15: 98,449,823 (GRCm39) |
H156Q |
probably benign |
Het |
Clasp2 |
T |
A |
9: 113,735,225 (GRCm39) |
I1021N |
possibly damaging |
Het |
Cnep1r1 |
G |
T |
8: 88,845,445 (GRCm39) |
|
probably benign |
Het |
Cntn6 |
C |
T |
6: 104,838,783 (GRCm39) |
R946* |
probably null |
Het |
Dnaaf3 |
T |
C |
7: 4,526,798 (GRCm39) |
I426M |
possibly damaging |
Het |
Dnajc13 |
A |
T |
9: 104,098,640 (GRCm39) |
I471N |
probably benign |
Het |
Ehd1 |
T |
C |
19: 6,348,108 (GRCm39) |
L362P |
probably benign |
Het |
Emx2 |
A |
G |
19: 59,450,130 (GRCm39) |
N149S |
probably benign |
Het |
Fbln7 |
G |
T |
2: 128,719,386 (GRCm39) |
R61L |
probably damaging |
Het |
Fgb |
C |
A |
3: 82,956,996 (GRCm39) |
D25Y |
probably benign |
Het |
Filip1 |
A |
G |
9: 79,727,498 (GRCm39) |
S374P |
probably damaging |
Het |
Fry |
T |
A |
5: 150,293,584 (GRCm39) |
|
probably benign |
Het |
Gm12695 |
T |
C |
4: 96,657,963 (GRCm39) |
T69A |
probably benign |
Het |
Gm2959 |
A |
G |
14: 42,235,658 (GRCm39) |
|
noncoding transcript |
Het |
Gm9912 |
T |
C |
3: 148,890,795 (GRCm39) |
T113A |
unknown |
Het |
Hdlbp |
A |
G |
1: 93,349,602 (GRCm39) |
|
probably benign |
Het |
Hunk |
G |
A |
16: 90,278,133 (GRCm39) |
|
probably null |
Het |
Ifnb1 |
T |
A |
4: 88,440,996 (GRCm39) |
I6F |
possibly damaging |
Het |
Il2rg |
A |
G |
X: 100,311,416 (GRCm39) |
L57P |
possibly damaging |
Het |
Ints1 |
A |
G |
5: 139,753,251 (GRCm39) |
V720A |
probably benign |
Het |
Invs |
T |
A |
4: 48,396,287 (GRCm39) |
L320Q |
probably damaging |
Het |
Jpt2 |
G |
A |
17: 25,167,713 (GRCm39) |
Q79* |
probably null |
Het |
Lingo2 |
A |
G |
4: 35,709,179 (GRCm39) |
L267P |
probably benign |
Het |
Lonp2 |
A |
G |
8: 87,392,403 (GRCm39) |
T490A |
probably damaging |
Het |
Meiob |
G |
T |
17: 25,037,290 (GRCm39) |
R56L |
probably damaging |
Het |
Mindy3 |
A |
T |
2: 12,424,060 (GRCm39) |
S2T |
probably damaging |
Het |
Mrm3 |
A |
T |
11: 76,141,147 (GRCm39) |
D385V |
probably damaging |
Het |
Mrto4 |
T |
C |
4: 139,076,334 (GRCm39) |
K86E |
probably benign |
Het |
Naf1 |
A |
G |
8: 67,340,432 (GRCm39) |
D414G |
probably damaging |
Het |
Nav1 |
C |
T |
1: 135,376,742 (GRCm39) |
R1694Q |
probably damaging |
Het |
Nipal4 |
T |
G |
11: 46,047,622 (GRCm39) |
D104A |
probably damaging |
Het |
Npas4 |
A |
G |
19: 5,037,442 (GRCm39) |
V284A |
probably damaging |
Het |
Nup133 |
C |
A |
8: 124,641,314 (GRCm39) |
D869Y |
probably damaging |
Het |
Obscn |
G |
A |
11: 59,026,558 (GRCm39) |
A215V |
possibly damaging |
Het |
Or4c113 |
A |
G |
2: 88,885,243 (GRCm39) |
Y176H |
probably damaging |
Het |
Or8b12i |
G |
T |
9: 20,082,850 (GRCm39) |
Q6K |
probably benign |
Het |
Or8g24 |
T |
C |
9: 38,989,510 (GRCm39) |
Y177C |
probably damaging |
Het |
Pgs1 |
G |
A |
11: 117,905,396 (GRCm39) |
|
probably benign |
Het |
Phc2 |
T |
C |
4: 128,640,929 (GRCm39) |
F672S |
probably damaging |
Het |
Phldb2 |
A |
T |
16: 45,591,121 (GRCm39) |
L970Q |
probably damaging |
Het |
Plxnb3 |
T |
A |
X: 72,815,357 (GRCm39) |
Y1845* |
probably null |
Het |
Ppip5k1 |
A |
G |
2: 121,173,352 (GRCm39) |
|
probably benign |
Het |
Prune2 |
A |
G |
19: 17,098,042 (GRCm39) |
D1182G |
possibly damaging |
Het |
Psg25 |
G |
A |
7: 18,263,487 (GRCm39) |
T112I |
probably damaging |
Het |
Sec61g |
T |
C |
11: 16,458,124 (GRCm39) |
T24A |
probably benign |
Het |
Skint1 |
T |
A |
4: 111,882,730 (GRCm39) |
V258D |
probably benign |
Het |
Sorbs1 |
T |
C |
19: 40,353,472 (GRCm39) |
|
probably null |
Het |
Sox2 |
C |
A |
3: 34,705,456 (GRCm39) |
Q298K |
possibly damaging |
Het |
Spatc1 |
T |
A |
15: 76,167,737 (GRCm39) |
|
probably null |
Het |
Szt2 |
T |
C |
4: 118,231,177 (GRCm39) |
M2529V |
unknown |
Het |
Thrap3 |
T |
C |
4: 126,069,189 (GRCm39) |
Y654C |
possibly damaging |
Het |
Tpp2 |
T |
G |
1: 44,017,598 (GRCm39) |
I734S |
possibly damaging |
Het |
Troap |
T |
C |
15: 98,980,344 (GRCm39) |
L508P |
probably benign |
Het |
Ttc28 |
C |
A |
5: 111,373,799 (GRCm39) |
F1078L |
probably benign |
Het |
Ttn |
T |
C |
2: 76,544,717 (GRCm39) |
N32795S |
probably damaging |
Het |
Ubap2 |
C |
T |
4: 41,199,872 (GRCm39) |
A752T |
probably benign |
Het |
Ugt2b36 |
T |
C |
5: 87,240,100 (GRCm39) |
E95G |
probably benign |
Het |
Vmn1r55 |
A |
G |
7: 5,150,048 (GRCm39) |
V125A |
possibly damaging |
Het |
Vstm2a |
A |
T |
11: 16,211,483 (GRCm39) |
I98F |
probably benign |
Het |
Zdhhc13 |
T |
A |
7: 48,466,175 (GRCm39) |
V284D |
probably benign |
Het |
Zfp668 |
C |
A |
7: 127,466,203 (GRCm39) |
R327L |
probably damaging |
Het |
Zgrf1 |
T |
C |
3: 127,406,999 (GRCm39) |
C1589R |
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 |
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 |
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 |
|
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 |
|