Other mutations in this stock |
Total: 113 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A330008L17Rik |
A |
G |
8: 100,450,057 (GRCm39) |
|
noncoding transcript |
Het |
Aff2 |
C |
A |
X: 68,791,141 (GRCm39) |
|
probably benign |
Het |
Aldh1a1 |
C |
A |
19: 20,604,010 (GRCm39) |
|
probably benign |
Het |
Anxa7 |
C |
T |
14: 20,519,479 (GRCm39) |
G113E |
probably damaging |
Het |
Apba2 |
A |
T |
7: 64,271,908 (GRCm39) |
|
probably benign |
Het |
Apc2 |
G |
C |
10: 80,135,808 (GRCm39) |
|
probably benign |
Het |
App |
C |
G |
16: 84,822,300 (GRCm39) |
|
probably benign |
Het |
Asic2 |
C |
A |
11: 80,876,570 (GRCm39) |
|
probably benign |
Het |
Btk |
T |
C |
X: 133,479,574 (GRCm39) |
|
probably benign |
Het |
Car12 |
C |
A |
9: 66,668,958 (GRCm39) |
|
probably benign |
Het |
Ccdc121 |
GAGAAG |
GAG |
5: 31,644,717 (GRCm39) |
|
probably benign |
Het |
Ccdc191 |
G |
A |
16: 43,742,164 (GRCm39) |
|
probably benign |
Het |
Ccdc34 |
N |
|
2: 110,016,318 (GRCm38) |
|
probably benign |
Het |
Cd164 |
G |
T |
10: 41,397,922 (GRCm39) |
A59S |
probably benign |
Het |
Cd22 |
C |
T |
7: 30,577,507 (GRCm39) |
R2H |
possibly damaging |
Het |
Cdv3 |
C |
A |
9: 103,242,553 (GRCm39) |
|
probably benign |
Het |
Cdv3 |
A |
T |
9: 103,242,542 (GRCm39) |
|
probably benign |
Het |
Celf2 |
N |
|
2: 6,779,076 (GRCm38) |
|
probably benign |
Het |
Cfap299 |
G |
A |
5: 98,855,367 (GRCm39) |
|
probably benign |
Het |
Clec18a |
C |
A |
8: 111,802,768 (GRCm39) |
|
probably benign |
Het |
Cnpy3 |
GGATGGAT |
GGATAGATAGATAGATAGATGGAT |
17: 47,048,462 (GRCm39) |
|
probably benign |
Het |
Cntn4 |
A |
G |
6: 106,530,901 (GRCm39) |
|
probably benign |
Het |
Cntnap5c |
G |
C |
17: 58,469,155 (GRCm39) |
|
probably benign |
Het |
Col2a1 |
C |
A |
15: 97,886,862 (GRCm39) |
|
probably null |
Het |
Cpne3 |
G |
T |
4: 19,563,382 (GRCm39) |
|
probably benign |
Het |
Cracd |
GGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG |
GGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG |
5: 76,806,589 (GRCm39) |
|
probably benign |
Het |
Dab1 |
T |
G |
4: 103,903,769 (GRCm39) |
|
probably benign |
Het |
Dapp1 |
G |
A |
3: 137,645,161 (GRCm39) |
|
probably benign |
Het |
Dcc |
G |
A |
18: 72,430,518 (GRCm39) |
|
probably benign |
Het |
Dcun1d1 |
GAAAAAAAAA |
GAAAAAAAAAA |
3: 35,992,154 (GRCm39) |
|
probably benign |
Het |
Dennd1b |
G |
A |
1: 139,042,502 (GRCm39) |
|
probably benign |
Het |
Dhdds |
TAA |
TA |
4: 133,697,674 (GRCm39) |
|
probably benign |
Het |
Dnah12 |
G |
T |
14: 26,571,342 (GRCm39) |
G2817V |
probably damaging |
Het |
Dnm3 |
CATATATATATATATATATATATA |
CATATATATATATATATATATA |
1: 162,234,130 (GRCm39) |
|
probably benign |
Het |
Dock10 |
N |
|
1: 80,716,623 (GRCm38) |
|
probably benign |
Het |
Dusp10 |
G |
T |
1: 183,769,253 (GRCm39) |
C73F |
probably damaging |
Het |
Fgf20 |
A |
C |
8: 40,745,359 (GRCm39) |
|
probably benign |
Het |
Ftsj3 |
G |
T |
11: 106,140,885 (GRCm39) |
|
probably benign |
Het |
Gls |
T |
G |
1: 52,222,526 (GRCm39) |
|
probably benign |
Het |
Gm12130 |
T |
C |
11: 38,397,750 (GRCm39) |
|
noncoding transcript |
Het |
Gm14936 |
G |
A |
X: 111,908,447 (GRCm39) |
|
noncoding transcript |
Het |
Gm16630 |
C |
T |
6: 48,118,203 (GRCm39) |
|
noncoding transcript |
Het |
Gm22194 |
AGTGTGTGTGTGTGTGTGTGTGTGTGTGTG |
AGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG |
10: 11,816,707 (GRCm39) |
|
noncoding transcript |
Het |
Gm26917 |
C |
G |
17: 40,154,862 (GRCm39) |
|
noncoding transcript |
Het |
Gm35048 |
GACACACACACACACACACACACACACACACACACACAC |
GACACACACACACACACACACACACACACACACACAC |
1: 90,449,248 (GRCm39) |
|
noncoding transcript |
Het |
Gm37311 |
G |
A |
16: 77,415,169 (GRCm39) |
|
noncoding transcript |
Het |
Gm37928 |
AACACACACACACACACACACACACACACACACA |
AACACACACACACACACACACACACACACACACACA |
3: 118,328,206 (GRCm39) |
|
noncoding transcript |
Het |
Gm4302 |
T |
C |
10: 100,177,306 (GRCm39) |
W197R |
probably benign |
Het |
H2-Q4 |
G |
A |
17: 35,599,381 (GRCm39) |
D155N |
probably damaging |
Het |
H2-T23 |
T |
C |
17: 36,342,108 (GRCm39) |
|
probably benign |
Het |
Hgs |
CTTTTTTT |
CTTTTTT |
11: 120,360,404 (GRCm39) |
|
probably benign |
Het |
Ighv5-9 |
C |
T |
12: 113,625,497 (GRCm39) |
S82N |
probably benign |
Het |
Il1rap |
C |
A |
16: 26,450,343 (GRCm39) |
|
probably benign |
Het |
Inhbc |
N |
|
10: 127,367,140 (GRCm38) |
|
probably benign |
Het |
Inpp4b |
C |
T |
8: 82,419,639 (GRCm39) |
|
probably benign |
Het |
Kars1 |
N |
|
8: 111,993,708 (GRCm38) |
|
probably benign |
Het |
Kcng4 |
G |
T |
8: 120,360,258 (GRCm39) |
Y39* |
probably null |
Het |
Kcnh7 |
A |
G |
2: 62,880,143 (GRCm39) |
|
probably benign |
Het |
Klhl1 |
G |
C |
14: 96,555,166 (GRCm39) |
|
probably benign |
Het |
Lrch1 |
C |
T |
14: 75,142,461 (GRCm39) |
|
probably benign |
Het |
Lrp1b |
G |
C |
2: 42,127,574 (GRCm39) |
|
probably benign |
Het |
Lsm8 |
G |
A |
6: 18,844,315 (GRCm39) |
|
probably benign |
Het |
Lsm8 |
G |
A |
6: 18,854,320 (GRCm39) |
|
probably benign |
Het |
Magi2 |
T |
C |
5: 20,159,509 (GRCm39) |
|
probably benign |
Het |
Matcap2 |
N |
|
9: 22,442,083 (GRCm38) |
|
probably benign |
Het |
Mef2c |
G |
A |
13: 83,753,942 (GRCm39) |
|
probably benign |
Het |
Mei4 |
A |
G |
9: 82,069,012 (GRCm39) |
|
probably benign |
Het |
Mid1 |
T |
A |
X: 168,788,560 (GRCm39) |
|
probably benign |
Het |
Mndal |
G |
C |
1: 173,707,784 (GRCm39) |
|
probably benign |
Het |
Mpped2 |
C |
A |
2: 106,551,773 (GRCm39) |
|
probably benign |
Het |
Mtarc2 |
TAGGCAGCCAATCAGAGCACTGCCTCTCAGCGCCAGGCAGCCAATCAGAGCACTGCCTCTCAGCGCCAGGCA |
TAGGCAGCCAATCAGAGCACTGCCTCTCAGCGCCAGGCA |
1: 184,554,985 (GRCm39) |
|
probably benign |
Het |
Mtf1 |
A |
G |
4: 124,723,109 (GRCm39) |
|
probably benign |
Het |
Mxd1 |
T |
C |
6: 86,644,388 (GRCm39) |
|
probably benign |
Het |
Ncor1 |
N |
|
11: 62,419,782 (GRCm38) |
|
probably benign |
Het |
Nox4 |
A |
G |
7: 86,892,275 (GRCm39) |
|
probably benign |
Het |
Ocln |
C |
T |
13: 100,657,075 (GRCm39) |
|
probably benign |
Het |
Ofcc1 |
G |
A |
13: 40,246,443 (GRCm39) |
|
probably benign |
Het |
Or5af2 |
T |
A |
11: 58,708,266 (GRCm39) |
V144D |
possibly damaging |
Het |
Paics |
N |
|
5: 76,956,744 (GRCm38) |
|
probably null |
Het |
Paqr8 |
G |
T |
1: 20,984,882 (GRCm39) |
|
probably benign |
Het |
Pate9 |
T |
C |
9: 36,444,849 (GRCm39) |
|
probably benign |
Het |
Pdss1 |
C |
T |
2: 22,790,980 (GRCm39) |
|
probably benign |
Het |
Piezo1 |
G |
A |
8: 123,222,308 (GRCm39) |
R503W |
probably damaging |
Het |
Pkhd1 |
G |
A |
1: 20,681,638 (GRCm39) |
|
probably benign |
Het |
Ppp1r3f |
C |
A |
X: 7,426,575 (GRCm39) |
G562V |
probably damaging |
Het |
Prr16 |
C |
T |
18: 51,333,396 (GRCm39) |
|
probably benign |
Het |
Prss38 |
T |
G |
11: 59,266,467 (GRCm39) |
|
probably benign |
Het |
Prxl2c |
G |
A |
13: 64,435,099 (GRCm39) |
|
probably benign |
Het |
Ptprk |
T |
C |
10: 28,450,983 (GRCm39) |
|
probably benign |
Het |
Pum1 |
N |
|
4: 130,730,549 (GRCm38) |
|
probably benign |
Het |
Rabgef1 |
N |
|
5: 130,187,586 (GRCm38) |
|
probably null |
Het |
Rgs16 |
G |
A |
1: 153,619,976 (GRCm39) |
|
probably benign |
Het |
Riok3 |
G |
T |
18: 12,263,039 (GRCm39) |
|
probably benign |
Het |
Rn18s-rs5 |
T |
C |
17: 40,159,446 (GRCm39) |
|
noncoding transcript |
Het |
Robo2 |
N |
|
16: 74,055,954 (GRCm38) |
|
probably benign |
Het |
Rps6ka3 |
A |
G |
X: 158,062,211 (GRCm39) |
|
probably benign |
Het |
Rptn |
T |
A |
3: 93,304,848 (GRCm39) |
L727Q |
probably benign |
Het |
Slc25a46 |
C |
A |
18: 31,730,366 (GRCm39) |
|
probably benign |
Het |
Spata31f1e |
T |
C |
4: 42,792,885 (GRCm39) |
T416A |
probably benign |
Het |
Spsb1 |
C |
T |
4: 150,036,943 (GRCm39) |
|
probably benign |
Het |
Tbc1d19 |
A |
C |
5: 53,974,051 (GRCm39) |
|
probably benign |
Het |
Trav7-4 |
C |
T |
14: 53,698,975 (GRCm39) |
L41F |
probably benign |
Het |
Trip12 |
N |
|
1: 84,754,482 (GRCm38) |
|
probably benign |
Het |
Ttc13 |
G |
A |
8: 125,402,605 (GRCm39) |
|
probably benign |
Het |
Ttll6 |
C |
T |
11: 96,046,084 (GRCm39) |
|
probably benign |
Het |
Unc5b |
C |
G |
10: 60,621,950 (GRCm39) |
|
probably benign |
Het |
Vmn2r87 |
C |
T |
10: 130,314,583 (GRCm39) |
M334I |
probably benign |
Het |
Vps13b |
G |
T |
15: 35,847,103 (GRCm39) |
A2629S |
probably damaging |
Het |
Wars2 |
N |
|
3: 99,214,774 (GRCm38) |
|
probably null |
Het |
Zdhhc3 |
AACACACACACACACACACACACACACACACAC |
AACACACACACACACACACACACACACACACACAC |
9: 122,912,087 (GRCm39) |
|
probably benign |
Het |
Zfp26 |
C |
A |
9: 20,349,842 (GRCm39) |
A241S |
probably benign |
Het |
Zfp442 |
C |
T |
2: 150,261,768 (GRCm39) |
|
probably benign |
Het |
Zfp808 |
C |
T |
13: 62,314,465 (GRCm39) |
|
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 |
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 |
|
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 |
|