Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam39 |
A |
G |
8: 41,279,610 (GRCm39) |
N667S |
probably benign |
Het |
Ap4e1 |
T |
A |
2: 126,908,508 (GRCm39) |
C1085* |
probably null |
Het |
BC035044 |
A |
T |
6: 128,861,997 (GRCm39) |
|
probably benign |
Het |
Bltp2 |
A |
G |
11: 78,164,084 (GRCm39) |
M1142V |
possibly damaging |
Het |
Capn11 |
T |
C |
17: 45,941,692 (GRCm39) |
D693G |
probably damaging |
Het |
Cavin4 |
A |
T |
4: 48,663,917 (GRCm39) |
H99L |
possibly damaging |
Het |
Ccdc86 |
T |
C |
19: 10,925,945 (GRCm39) |
K218R |
possibly damaging |
Het |
Ccno |
T |
C |
13: 113,126,379 (GRCm39) |
S283P |
probably damaging |
Het |
Ccser2 |
A |
T |
14: 36,662,276 (GRCm39) |
S303T |
probably benign |
Het |
Cd53 |
T |
A |
3: 106,674,680 (GRCm39) |
N129I |
probably damaging |
Het |
Cd63 |
G |
A |
10: 128,747,933 (GRCm39) |
|
probably null |
Het |
Cyp2j6 |
G |
C |
4: 96,424,323 (GRCm39) |
L145V |
probably damaging |
Het |
Daam2 |
A |
G |
17: 49,776,694 (GRCm39) |
M797T |
probably damaging |
Het |
Dennd2b |
A |
C |
7: 109,156,095 (GRCm39) |
D218E |
probably benign |
Het |
Dmgdh |
G |
A |
13: 93,888,794 (GRCm39) |
V811I |
possibly damaging |
Het |
Dpysl4 |
A |
T |
7: 138,670,250 (GRCm39) |
T123S |
probably damaging |
Het |
Erap1 |
A |
G |
13: 74,814,345 (GRCm39) |
E428G |
possibly damaging |
Het |
Fam124b |
T |
A |
1: 80,177,902 (GRCm39) |
T366S |
possibly damaging |
Het |
Fbxw22 |
T |
C |
9: 109,215,747 (GRCm39) |
D167G |
probably damaging |
Het |
Flrt2 |
C |
T |
12: 95,746,012 (GRCm39) |
Q117* |
probably null |
Het |
Ftsj3 |
A |
T |
11: 106,144,166 (GRCm39) |
|
probably null |
Het |
Ggn |
A |
G |
7: 28,872,474 (GRCm39) |
Y618C |
probably damaging |
Het |
Glis1 |
T |
A |
4: 107,484,710 (GRCm39) |
S402T |
probably benign |
Het |
Gm4781 |
T |
A |
10: 100,232,349 (GRCm39) |
|
noncoding transcript |
Het |
Gm7168 |
T |
A |
17: 14,168,858 (GRCm39) |
I75K |
probably damaging |
Het |
Gm7298 |
C |
T |
6: 121,737,782 (GRCm39) |
H348Y |
probably benign |
Het |
Gria1 |
G |
T |
11: 57,133,618 (GRCm39) |
R499L |
probably damaging |
Het |
Gtf2ird2 |
C |
T |
5: 134,245,389 (GRCm39) |
T549M |
probably damaging |
Het |
H2-M10.6 |
T |
A |
17: 37,125,178 (GRCm39) |
V323E |
probably damaging |
Het |
Hoxb3 |
G |
A |
11: 96,236,929 (GRCm39) |
V336I |
probably benign |
Het |
Il12b |
G |
A |
11: 44,303,453 (GRCm39) |
A327T |
probably benign |
Het |
Inpp4a |
C |
A |
1: 37,419,183 (GRCm39) |
P588T |
probably benign |
Het |
Kctd12 |
C |
A |
14: 103,219,027 (GRCm39) |
D284Y |
probably damaging |
Het |
Kif28 |
C |
A |
1: 179,525,337 (GRCm39) |
|
probably null |
Het |
Krt1c |
T |
C |
15: 101,723,479 (GRCm39) |
N332S |
probably benign |
Het |
Lama2 |
G |
A |
10: 26,857,495 (GRCm39) |
T3118I |
probably benign |
Het |
Lgi1 |
T |
C |
19: 38,253,404 (GRCm39) |
L25P |
probably damaging |
Het |
Lhx3 |
T |
A |
2: 26,091,503 (GRCm39) |
M269L |
probably benign |
Het |
Lmtk2 |
A |
T |
5: 144,112,160 (GRCm39) |
E960V |
probably damaging |
Het |
Loxl4 |
A |
T |
19: 42,596,791 (GRCm39) |
D60E |
probably damaging |
Het |
Lrp2 |
T |
A |
2: 69,333,868 (GRCm39) |
N1458Y |
possibly damaging |
Het |
Ltn1 |
A |
T |
16: 87,224,677 (GRCm39) |
S16T |
probably damaging |
Het |
Mllt6 |
G |
A |
11: 97,569,362 (GRCm39) |
A875T |
possibly damaging |
Het |
Mrgprb4 |
A |
T |
7: 47,848,574 (GRCm39) |
I118N |
probably damaging |
Het |
Mrps7 |
A |
G |
11: 115,495,707 (GRCm39) |
T82A |
possibly damaging |
Het |
Mug2 |
A |
G |
6: 122,056,565 (GRCm39) |
E1170G |
probably benign |
Het |
Nav2 |
A |
G |
7: 49,107,915 (GRCm39) |
H647R |
probably benign |
Het |
Ndc1 |
A |
T |
4: 107,268,395 (GRCm39) |
I644L |
possibly damaging |
Het |
Or4c108 |
T |
G |
2: 88,804,226 (GRCm39) |
N3T |
probably damaging |
Het |
Or8g33 |
A |
T |
9: 39,338,008 (GRCm39) |
Y120N |
probably damaging |
Het |
Padi4 |
A |
G |
4: 140,483,784 (GRCm39) |
M352T |
possibly damaging |
Het |
Pals1 |
C |
T |
12: 78,864,084 (GRCm39) |
H216Y |
probably benign |
Het |
Pcdhgc3 |
C |
A |
18: 37,939,990 (GRCm39) |
D130E |
probably damaging |
Het |
Pde6a |
A |
T |
18: 61,417,163 (GRCm39) |
|
probably null |
Het |
Pdpn |
C |
T |
4: 143,025,792 (GRCm39) |
G12R |
probably damaging |
Het |
Pot1a |
A |
T |
6: 25,771,620 (GRCm39) |
D200E |
probably benign |
Het |
Ppa1 |
A |
T |
10: 61,503,431 (GRCm39) |
D236V |
probably benign |
Het |
Ptprn2 |
T |
A |
12: 116,822,739 (GRCm39) |
S273T |
probably benign |
Het |
Rasgrf2 |
T |
C |
13: 92,165,609 (GRCm39) |
E297G |
probably damaging |
Het |
Rgl1 |
T |
C |
1: 152,394,923 (GRCm39) |
N750S |
probably damaging |
Het |
Rinl |
A |
G |
7: 28,496,365 (GRCm39) |
N449D |
probably benign |
Het |
Samd8 |
T |
A |
14: 21,825,093 (GRCm39) |
H79Q |
probably benign |
Het |
Scn11a |
T |
C |
9: 119,583,933 (GRCm39) |
I1561V |
probably benign |
Het |
Slc39a12 |
T |
C |
2: 14,400,938 (GRCm39) |
L105P |
probably benign |
Het |
Slc7a12 |
A |
T |
3: 14,546,200 (GRCm39) |
|
probably null |
Het |
Slco1a4 |
A |
G |
6: 141,763,546 (GRCm39) |
I390T |
possibly damaging |
Het |
Snta1 |
T |
C |
2: 154,219,102 (GRCm39) |
N411S |
probably benign |
Het |
Srgap2 |
T |
C |
1: 131,277,279 (GRCm39) |
T323A |
probably benign |
Het |
Ssh2 |
G |
T |
11: 77,344,291 (GRCm39) |
V759L |
probably benign |
Het |
Swap70 |
G |
T |
7: 109,869,188 (GRCm39) |
R327L |
probably damaging |
Het |
Tbc1d4 |
C |
A |
14: 101,696,206 (GRCm39) |
C914F |
probably benign |
Het |
Tbx3 |
A |
G |
5: 119,812,132 (GRCm39) |
D144G |
probably damaging |
Het |
Tgfbr2 |
T |
C |
9: 115,939,212 (GRCm39) |
K205R |
possibly damaging |
Het |
Tmem94 |
A |
T |
11: 115,681,857 (GRCm39) |
|
probably null |
Het |
Usf3 |
T |
A |
16: 44,041,468 (GRCm39) |
F1983I |
probably damaging |
Het |
Ush2a |
T |
A |
1: 188,132,068 (GRCm39) |
C763* |
probably null |
Het |
Vmn1r115 |
A |
C |
7: 20,578,640 (GRCm39) |
L91V |
probably damaging |
Het |
Vmn1r201 |
A |
T |
13: 22,659,499 (GRCm39) |
I238F |
possibly damaging |
Het |
Vmn1r28 |
T |
A |
6: 58,242,476 (GRCm39) |
S106R |
probably damaging |
Het |
Vmn1r82 |
T |
C |
7: 12,039,012 (GRCm39) |
V95A |
probably damaging |
Het |
Vrk3 |
A |
T |
7: 44,419,035 (GRCm39) |
N371I |
possibly damaging |
Het |
Wnt8b |
C |
A |
19: 44,500,082 (GRCm39) |
A223E |
probably benign |
Het |
Xirp2 |
T |
C |
2: 67,335,921 (GRCm39) |
|
probably null |
Het |
Xpo7 |
T |
C |
14: 70,920,243 (GRCm39) |
N642S |
probably benign |
Het |
Ythdc1 |
G |
A |
5: 86,975,953 (GRCm39) |
R520H |
possibly damaging |
Het |
Zfp367 |
T |
C |
13: 64,283,204 (GRCm39) |
E316G |
probably damaging |
Het |
Zfp488 |
T |
A |
14: 33,692,751 (GRCm39) |
R137S |
possibly damaging |
Het |
Zfp532 |
G |
T |
18: 65,789,542 (GRCm39) |
V994L |
probably benign |
Het |
|
Other mutations in Nbeal2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Nbeal2
|
APN |
9 |
110,464,937 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00784:Nbeal2
|
APN |
9 |
110,458,831 (GRCm39) |
splice site |
probably benign |
|
IGL00826:Nbeal2
|
APN |
9 |
110,455,971 (GRCm39) |
missense |
probably benign |
|
IGL00885:Nbeal2
|
APN |
9 |
110,467,729 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01348:Nbeal2
|
APN |
9 |
110,458,214 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01511:Nbeal2
|
APN |
9 |
110,458,302 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01571:Nbeal2
|
APN |
9 |
110,461,826 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL01612:Nbeal2
|
APN |
9 |
110,473,746 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01924:Nbeal2
|
APN |
9 |
110,460,482 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02056:Nbeal2
|
APN |
9 |
110,456,392 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02481:Nbeal2
|
APN |
9 |
110,455,063 (GRCm39) |
nonsense |
probably null |
|
IGL02483:Nbeal2
|
APN |
9 |
110,455,063 (GRCm39) |
nonsense |
probably null |
|
IGL02502:Nbeal2
|
APN |
9 |
110,462,836 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02631:Nbeal2
|
APN |
9 |
110,459,276 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02637:Nbeal2
|
APN |
9 |
110,455,045 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL02727:Nbeal2
|
APN |
9 |
110,468,353 (GRCm39) |
splice site |
probably benign |
|
IGL02887:Nbeal2
|
APN |
9 |
110,457,344 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02896:Nbeal2
|
APN |
9 |
110,468,360 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03110:Nbeal2
|
APN |
9 |
110,460,501 (GRCm39) |
missense |
probably damaging |
1.00 |
Antonym
|
UTSW |
9 |
110,459,320 (GRCm39) |
missense |
probably damaging |
1.00 |
Beowulf
|
UTSW |
9 |
110,467,005 (GRCm39) |
missense |
possibly damaging |
0.65 |
Blackmail
|
UTSW |
9 |
110,458,707 (GRCm39) |
missense |
probably damaging |
1.00 |
dog
|
UTSW |
9 |
110,464,409 (GRCm39) |
missense |
possibly damaging |
0.89 |
extortion
|
UTSW |
9 |
110,459,311 (GRCm39) |
missense |
probably damaging |
1.00 |
legion
|
UTSW |
9 |
110,458,247 (GRCm39) |
missense |
probably damaging |
1.00 |
litigious
|
UTSW |
9 |
110,457,263 (GRCm39) |
missense |
probably damaging |
1.00 |
mall
|
UTSW |
9 |
110,461,954 (GRCm39) |
missense |
probably damaging |
1.00 |
Mollusca
|
UTSW |
9 |
110,474,506 (GRCm39) |
splice site |
probably null |
|
Schleuter
|
UTSW |
9 |
110,457,812 (GRCm39) |
missense |
possibly damaging |
0.69 |
shellfish
|
UTSW |
9 |
110,457,788 (GRCm39) |
missense |
probably damaging |
1.00 |
Sophomoric
|
UTSW |
9 |
110,462,115 (GRCm39) |
missense |
probably damaging |
1.00 |
F5770:Nbeal2
|
UTSW |
9 |
110,467,005 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0032:Nbeal2
|
UTSW |
9 |
110,466,936 (GRCm39) |
splice site |
probably benign |
|
R0084:Nbeal2
|
UTSW |
9 |
110,472,778 (GRCm39) |
critical splice donor site |
probably null |
|
R0147:Nbeal2
|
UTSW |
9 |
110,471,211 (GRCm39) |
nonsense |
probably null |
|
R0294:Nbeal2
|
UTSW |
9 |
110,461,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R0310:Nbeal2
|
UTSW |
9 |
110,467,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R0494:Nbeal2
|
UTSW |
9 |
110,456,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R0550:Nbeal2
|
UTSW |
9 |
110,471,226 (GRCm39) |
missense |
probably benign |
0.01 |
R0630:Nbeal2
|
UTSW |
9 |
110,465,102 (GRCm39) |
splice site |
probably benign |
|
R0762:Nbeal2
|
UTSW |
9 |
110,472,876 (GRCm39) |
splice site |
probably benign |
|
R0862:Nbeal2
|
UTSW |
9 |
110,457,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R0864:Nbeal2
|
UTSW |
9 |
110,457,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R1225:Nbeal2
|
UTSW |
9 |
110,461,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R1240:Nbeal2
|
UTSW |
9 |
110,456,176 (GRCm39) |
missense |
probably damaging |
0.98 |
R1450:Nbeal2
|
UTSW |
9 |
110,462,740 (GRCm39) |
splice site |
probably benign |
|
R1519:Nbeal2
|
UTSW |
9 |
110,465,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R1655:Nbeal2
|
UTSW |
9 |
110,461,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R1668:Nbeal2
|
UTSW |
9 |
110,467,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R1705:Nbeal2
|
UTSW |
9 |
110,454,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R1784:Nbeal2
|
UTSW |
9 |
110,459,925 (GRCm39) |
nonsense |
probably null |
|
R1834:Nbeal2
|
UTSW |
9 |
110,456,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R1997:Nbeal2
|
UTSW |
9 |
110,461,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R2013:Nbeal2
|
UTSW |
9 |
110,463,139 (GRCm39) |
missense |
probably benign |
0.09 |
R2014:Nbeal2
|
UTSW |
9 |
110,463,139 (GRCm39) |
missense |
probably benign |
0.09 |
R2055:Nbeal2
|
UTSW |
9 |
110,464,375 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2086:Nbeal2
|
UTSW |
9 |
110,463,139 (GRCm39) |
missense |
probably benign |
0.09 |
R2113:Nbeal2
|
UTSW |
9 |
110,454,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R2167:Nbeal2
|
UTSW |
9 |
110,467,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R2201:Nbeal2
|
UTSW |
9 |
110,459,318 (GRCm39) |
missense |
probably benign |
0.16 |
R2309:Nbeal2
|
UTSW |
9 |
110,455,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R2378:Nbeal2
|
UTSW |
9 |
110,459,876 (GRCm39) |
missense |
probably damaging |
0.99 |
R2945:Nbeal2
|
UTSW |
9 |
110,457,136 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3052:Nbeal2
|
UTSW |
9 |
110,462,153 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3076:Nbeal2
|
UTSW |
9 |
110,460,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R3176:Nbeal2
|
UTSW |
9 |
110,465,955 (GRCm39) |
splice site |
probably benign |
|
R3974:Nbeal2
|
UTSW |
9 |
110,462,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R4183:Nbeal2
|
UTSW |
9 |
110,465,743 (GRCm39) |
missense |
probably benign |
|
R4342:Nbeal2
|
UTSW |
9 |
110,460,861 (GRCm39) |
intron |
probably benign |
|
R4654:Nbeal2
|
UTSW |
9 |
110,461,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R4707:Nbeal2
|
UTSW |
9 |
110,461,123 (GRCm39) |
missense |
probably benign |
0.10 |
R4822:Nbeal2
|
UTSW |
9 |
110,465,383 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4854:Nbeal2
|
UTSW |
9 |
110,460,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R4860:Nbeal2
|
UTSW |
9 |
110,464,262 (GRCm39) |
missense |
probably benign |
0.00 |
R4860:Nbeal2
|
UTSW |
9 |
110,464,262 (GRCm39) |
missense |
probably benign |
0.00 |
R4990:Nbeal2
|
UTSW |
9 |
110,463,871 (GRCm39) |
missense |
probably benign |
0.10 |
R4991:Nbeal2
|
UTSW |
9 |
110,467,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R5021:Nbeal2
|
UTSW |
9 |
110,466,531 (GRCm39) |
missense |
probably damaging |
0.99 |
R5057:Nbeal2
|
UTSW |
9 |
110,460,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R5092:Nbeal2
|
UTSW |
9 |
110,455,796 (GRCm39) |
splice site |
probably null |
|
R5161:Nbeal2
|
UTSW |
9 |
110,458,936 (GRCm39) |
missense |
probably benign |
|
R5202:Nbeal2
|
UTSW |
9 |
110,473,734 (GRCm39) |
missense |
probably damaging |
0.99 |
R5217:Nbeal2
|
UTSW |
9 |
110,461,158 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5408:Nbeal2
|
UTSW |
9 |
110,466,588 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5540:Nbeal2
|
UTSW |
9 |
110,460,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R5866:Nbeal2
|
UTSW |
9 |
110,460,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R5925:Nbeal2
|
UTSW |
9 |
110,458,948 (GRCm39) |
missense |
probably benign |
0.00 |
R6057:Nbeal2
|
UTSW |
9 |
110,470,945 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6191:Nbeal2
|
UTSW |
9 |
110,457,058 (GRCm39) |
critical splice donor site |
probably null |
|
R6232:Nbeal2
|
UTSW |
9 |
110,467,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R6372:Nbeal2
|
UTSW |
9 |
110,457,812 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6423:Nbeal2
|
UTSW |
9 |
110,455,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R6543:Nbeal2
|
UTSW |
9 |
110,473,526 (GRCm39) |
missense |
probably benign |
|
R6648:Nbeal2
|
UTSW |
9 |
110,466,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R6722:Nbeal2
|
UTSW |
9 |
110,462,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R6738:Nbeal2
|
UTSW |
9 |
110,465,973 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6916:Nbeal2
|
UTSW |
9 |
110,455,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R6935:Nbeal2
|
UTSW |
9 |
110,468,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R7022:Nbeal2
|
UTSW |
9 |
110,467,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R7023:Nbeal2
|
UTSW |
9 |
110,467,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R7050:Nbeal2
|
UTSW |
9 |
110,457,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R7072:Nbeal2
|
UTSW |
9 |
110,455,119 (GRCm39) |
missense |
probably benign |
0.01 |
R7073:Nbeal2
|
UTSW |
9 |
110,455,177 (GRCm39) |
missense |
probably damaging |
0.99 |
R7099:Nbeal2
|
UTSW |
9 |
110,474,506 (GRCm39) |
splice site |
probably null |
|
R7354:Nbeal2
|
UTSW |
9 |
110,458,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R7394:Nbeal2
|
UTSW |
9 |
110,459,257 (GRCm39) |
critical splice donor site |
probably null |
|
R7397:Nbeal2
|
UTSW |
9 |
110,457,100 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7552:Nbeal2
|
UTSW |
9 |
110,482,985 (GRCm39) |
missense |
probably benign |
0.16 |
R7619:Nbeal2
|
UTSW |
9 |
110,454,886 (GRCm39) |
missense |
probably benign |
0.19 |
R7821:Nbeal2
|
UTSW |
9 |
110,459,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R7902:Nbeal2
|
UTSW |
9 |
110,466,615 (GRCm39) |
missense |
probably benign |
|
R7923:Nbeal2
|
UTSW |
9 |
110,460,514 (GRCm39) |
nonsense |
probably null |
|
R8018:Nbeal2
|
UTSW |
9 |
110,458,225 (GRCm39) |
unclassified |
probably benign |
|
R8190:Nbeal2
|
UTSW |
9 |
110,455,158 (GRCm39) |
missense |
probably benign |
0.04 |
R8297:Nbeal2
|
UTSW |
9 |
110,464,409 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8404:Nbeal2
|
UTSW |
9 |
110,463,457 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8502:Nbeal2
|
UTSW |
9 |
110,463,457 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8737:Nbeal2
|
UTSW |
9 |
110,456,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R8782:Nbeal2
|
UTSW |
9 |
110,459,873 (GRCm39) |
missense |
probably benign |
0.04 |
R8807:Nbeal2
|
UTSW |
9 |
110,458,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R8877:Nbeal2
|
UTSW |
9 |
110,459,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R9057:Nbeal2
|
UTSW |
9 |
110,456,218 (GRCm39) |
missense |
probably benign |
|
R9267:Nbeal2
|
UTSW |
9 |
110,462,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R9313:Nbeal2
|
UTSW |
9 |
110,463,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R9352:Nbeal2
|
UTSW |
9 |
110,456,916 (GRCm39) |
missense |
probably benign |
0.03 |
R9482:Nbeal2
|
UTSW |
9 |
110,463,066 (GRCm39) |
missense |
probably benign |
0.25 |
R9533:Nbeal2
|
UTSW |
9 |
110,473,729 (GRCm39) |
missense |
probably benign |
0.01 |
R9566:Nbeal2
|
UTSW |
9 |
110,457,989 (GRCm39) |
missense |
probably benign |
0.00 |
R9769:Nbeal2
|
UTSW |
9 |
110,455,347 (GRCm39) |
missense |
probably benign |
0.01 |
V7583:Nbeal2
|
UTSW |
9 |
110,467,005 (GRCm39) |
missense |
possibly damaging |
0.65 |
X0017:Nbeal2
|
UTSW |
9 |
110,473,346 (GRCm39) |
missense |
probably benign |
0.02 |
X0065:Nbeal2
|
UTSW |
9 |
110,473,481 (GRCm39) |
splice site |
probably benign |
|
Z1088:Nbeal2
|
UTSW |
9 |
110,461,440 (GRCm39) |
missense |
possibly damaging |
0.51 |
Z1176:Nbeal2
|
UTSW |
9 |
110,467,903 (GRCm39) |
missense |
probably benign |
|
Z1176:Nbeal2
|
UTSW |
9 |
110,454,884 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Nbeal2
|
UTSW |
9 |
110,458,922 (GRCm39) |
missense |
probably benign |
0.03 |
|