Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522H14Rik |
A |
G |
4: 109,362,768 (GRCm39) |
S184P |
probably damaging |
Het |
Adgb |
A |
G |
10: 10,271,115 (GRCm39) |
F817L |
probably damaging |
Het |
Anxa10 |
T |
C |
8: 62,545,618 (GRCm39) |
D38G |
probably damaging |
Het |
Atp8b2 |
G |
A |
3: 89,849,091 (GRCm39) |
A1081V |
probably benign |
Het |
Baz1a |
G |
A |
12: 55,021,983 (GRCm39) |
R100C |
probably damaging |
Het |
Ceacam18 |
A |
C |
7: 43,288,689 (GRCm39) |
T147P |
possibly damaging |
Het |
Cep170b |
C |
T |
12: 112,702,806 (GRCm39) |
T423I |
probably damaging |
Het |
Chd6 |
A |
G |
2: 160,883,978 (GRCm39) |
L89S |
probably damaging |
Het |
Chrm3 |
A |
T |
13: 9,928,461 (GRCm39) |
W192R |
probably damaging |
Het |
Cnn1 |
C |
A |
9: 22,019,150 (GRCm39) |
A202E |
probably damaging |
Het |
Dcaf7 |
T |
A |
11: 105,942,628 (GRCm39) |
F192I |
probably damaging |
Het |
Eif2b5 |
T |
C |
16: 20,321,335 (GRCm39) |
V296A |
possibly damaging |
Het |
Entpd7 |
A |
G |
19: 43,710,184 (GRCm39) |
|
probably benign |
Het |
Esr1 |
A |
G |
10: 4,951,260 (GRCm39) |
E546G |
possibly damaging |
Het |
Etaa1 |
C |
A |
11: 17,896,492 (GRCm39) |
G542C |
probably damaging |
Het |
Exosc8 |
A |
T |
3: 54,641,522 (GRCm39) |
|
probably null |
Het |
Fras1 |
T |
A |
5: 96,874,472 (GRCm39) |
|
probably null |
Het |
G930045G22Rik |
T |
C |
6: 50,823,698 (GRCm39) |
|
noncoding transcript |
Het |
Gm22697+Rbm27 |
AGGTCCAGGCCCAGGCCCTGGTCCTGGCCCTGGCCCTGGTCCCGGCCCAGGCCC |
AGGTCCCGGCCCAGGCCC |
18: 42,434,948 (GRCm39) |
|
probably benign |
Het |
Gpr155 |
T |
C |
2: 73,194,508 (GRCm39) |
|
probably null |
Het |
Has1 |
A |
G |
17: 18,070,247 (GRCm39) |
Y225H |
probably damaging |
Het |
Hk3 |
A |
G |
13: 55,162,274 (GRCm39) |
F110S |
probably damaging |
Het |
Iars1 |
A |
G |
13: 49,876,478 (GRCm39) |
K848E |
possibly damaging |
Het |
Il22ra1 |
C |
A |
4: 135,477,771 (GRCm39) |
H281N |
probably damaging |
Het |
Inpp4b |
G |
T |
8: 82,583,403 (GRCm39) |
|
probably benign |
Het |
Itga11 |
A |
G |
9: 62,667,652 (GRCm39) |
N662D |
probably benign |
Het |
Kif20b |
A |
T |
19: 34,914,190 (GRCm39) |
T355S |
possibly damaging |
Het |
Kif21a |
T |
C |
15: 90,878,570 (GRCm39) |
T237A |
probably damaging |
Het |
Klc1 |
T |
C |
12: 111,743,321 (GRCm39) |
L216P |
probably damaging |
Het |
Krt84 |
G |
A |
15: 101,434,398 (GRCm39) |
S523F |
possibly damaging |
Het |
Lama3 |
A |
G |
18: 12,665,256 (GRCm39) |
D2330G |
possibly damaging |
Het |
Lamb2 |
G |
A |
9: 108,358,622 (GRCm39) |
|
probably null |
Het |
Limch1 |
T |
A |
5: 67,156,599 (GRCm39) |
S511R |
probably damaging |
Het |
Lnx2 |
C |
A |
5: 146,964,152 (GRCm39) |
V468L |
probably benign |
Het |
Lrriq1 |
A |
T |
10: 103,006,509 (GRCm39) |
C1205* |
probably null |
Het |
Lsm4 |
A |
G |
8: 71,130,456 (GRCm39) |
Y25C |
probably damaging |
Het |
Macc1 |
T |
C |
12: 119,410,156 (GRCm39) |
M308T |
probably benign |
Het |
Miip |
T |
C |
4: 147,949,691 (GRCm39) |
S174G |
probably benign |
Het |
Mroh9 |
T |
G |
1: 162,873,625 (GRCm39) |
E510A |
probably damaging |
Het |
Msh2 |
C |
T |
17: 87,980,064 (GRCm39) |
A14V |
probably benign |
Het |
Nkx2-3 |
A |
T |
19: 43,602,895 (GRCm39) |
Q167L |
probably damaging |
Het |
Nup160 |
T |
C |
2: 90,540,432 (GRCm39) |
Y854H |
probably damaging |
Het |
Or10a3n |
A |
G |
7: 108,492,972 (GRCm39) |
I214T |
probably damaging |
Het |
Or51a10 |
A |
G |
7: 103,699,376 (GRCm39) |
Y62H |
probably damaging |
Het |
Or5an10 |
T |
A |
19: 12,276,023 (GRCm39) |
I158L |
probably benign |
Het |
Pate9 |
A |
G |
9: 36,445,736 (GRCm39) |
S72P |
possibly damaging |
Het |
Phldb1 |
G |
A |
9: 44,626,730 (GRCm39) |
P572S |
probably damaging |
Het |
Plcb2 |
A |
T |
2: 118,554,261 (GRCm39) |
M64K |
possibly damaging |
Het |
Prr12 |
T |
A |
7: 44,683,616 (GRCm39) |
N1683Y |
probably benign |
Het |
Prrg4 |
C |
A |
2: 104,663,088 (GRCm39) |
A173S |
probably benign |
Het |
Pygl |
T |
A |
12: 70,243,784 (GRCm39) |
I553F |
possibly damaging |
Het |
Rasd1 |
T |
C |
11: 59,854,920 (GRCm39) |
M187V |
probably benign |
Het |
Rasgrf1 |
A |
G |
9: 89,835,973 (GRCm39) |
I234V |
probably benign |
Het |
Rps6ka4 |
C |
A |
19: 6,816,730 (GRCm39) |
V118L |
probably benign |
Het |
Sbspon |
C |
A |
1: 15,953,983 (GRCm39) |
R99L |
probably damaging |
Het |
Sdhaf3 |
T |
C |
6: 6,956,126 (GRCm39) |
Y34H |
probably damaging |
Het |
Setd2 |
A |
G |
9: 110,378,932 (GRCm39) |
S632G |
probably benign |
Het |
Shc2 |
T |
A |
10: 79,461,945 (GRCm39) |
M367L |
probably benign |
Het |
Slc26a5 |
T |
A |
5: 22,018,974 (GRCm39) |
K590* |
probably null |
Het |
Slc39a12 |
T |
C |
2: 14,456,803 (GRCm39) |
V597A |
probably benign |
Het |
Slc45a3 |
G |
A |
1: 131,905,262 (GRCm39) |
G81D |
probably damaging |
Het |
Spata2l |
T |
C |
8: 123,960,041 (GRCm39) |
N416S |
probably benign |
Het |
Tdrd6 |
A |
C |
17: 43,938,000 (GRCm39) |
V1016G |
possibly damaging |
Het |
Tet2 |
A |
G |
3: 133,191,641 (GRCm39) |
V931A |
probably benign |
Het |
Tmem190 |
A |
G |
7: 4,787,120 (GRCm39) |
D108G |
probably damaging |
Het |
Trip11 |
T |
A |
12: 101,850,651 (GRCm39) |
K853* |
probably null |
Het |
Vmn2r111 |
A |
T |
17: 22,788,042 (GRCm39) |
D436E |
probably benign |
Het |
Zfp704 |
A |
T |
3: 9,536,099 (GRCm39) |
S140R |
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 |
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 |
|
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 |
|