Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd17a |
A |
G |
10: 80,419,737 (GRCm39) |
Y290H |
probably benign |
Het |
Aco2 |
T |
C |
15: 81,788,142 (GRCm39) |
V257A |
probably damaging |
Het |
Adam26a |
C |
A |
8: 44,023,007 (GRCm39) |
C161F |
possibly damaging |
Het |
Adam9 |
G |
A |
8: 25,445,988 (GRCm39) |
P820S |
unknown |
Het |
Adcy4 |
G |
A |
14: 56,010,922 (GRCm39) |
T665M |
probably benign |
Het |
Ahnak |
T |
A |
19: 8,984,188 (GRCm39) |
M1824K |
probably benign |
Het |
Alpi |
T |
C |
1: 87,026,795 (GRCm39) |
N428D |
probably benign |
Het |
Ano5 |
C |
T |
7: 51,196,528 (GRCm39) |
P153L |
probably benign |
Het |
Atp1a1 |
A |
T |
3: 101,489,437 (GRCm39) |
L725* |
probably null |
Het |
Atp8b2 |
G |
A |
3: 89,854,071 (GRCm39) |
T595I |
probably damaging |
Het |
Ccdc66 |
T |
C |
14: 27,220,820 (GRCm39) |
I35V |
possibly damaging |
Het |
Cd163 |
A |
G |
6: 124,284,187 (GRCm39) |
T120A |
probably benign |
Het |
Cmah |
A |
T |
13: 24,640,938 (GRCm39) |
T396S |
possibly damaging |
Het |
Cmya5 |
C |
T |
13: 93,205,820 (GRCm39) |
V3350I |
probably benign |
Het |
Commd9 |
A |
C |
2: 101,731,410 (GRCm39) |
K198N |
probably damaging |
Het |
Cxcr1 |
A |
G |
1: 74,231,773 (GRCm39) |
V83A |
probably benign |
Het |
D630045J12Rik |
A |
G |
6: 38,125,383 (GRCm39) |
S1544P |
probably damaging |
Het |
Ddt |
A |
T |
10: 75,609,048 (GRCm39) |
|
probably null |
Het |
Depdc7 |
A |
G |
2: 104,557,585 (GRCm39) |
S222P |
possibly damaging |
Het |
Ehd2 |
A |
G |
7: 15,684,431 (GRCm39) |
I456T |
probably damaging |
Het |
Epas1 |
A |
T |
17: 87,136,471 (GRCm39) |
M748L |
probably benign |
Het |
Esr1 |
G |
A |
10: 4,806,903 (GRCm39) |
R273H |
probably damaging |
Het |
Fras1 |
G |
A |
5: 96,916,297 (GRCm39) |
D3444N |
probably damaging |
Het |
Hand2 |
A |
G |
8: 57,775,272 (GRCm39) |
R111G |
probably damaging |
Het |
Hecw1 |
A |
T |
13: 14,490,835 (GRCm39) |
V306E |
probably damaging |
Het |
Ift140 |
T |
C |
17: 25,252,089 (GRCm39) |
I312T |
probably benign |
Het |
Ikbke |
A |
T |
1: 131,199,887 (GRCm39) |
L257* |
probably null |
Het |
Kcnk5 |
G |
A |
14: 20,192,349 (GRCm39) |
P271S |
probably benign |
Het |
Lama1 |
T |
C |
17: 68,044,662 (GRCm39) |
V187A |
|
Het |
Lemd2 |
A |
T |
17: 27,412,810 (GRCm39) |
|
probably null |
Het |
Lig3 |
T |
A |
11: 82,679,717 (GRCm39) |
D341E |
probably benign |
Het |
Lpcat1 |
C |
T |
13: 73,643,014 (GRCm39) |
S196L |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 40,567,582 (GRCm39) |
D4048E |
|
Het |
Lrrfip1 |
G |
A |
1: 91,033,005 (GRCm39) |
E158K |
probably damaging |
Het |
Mcm5 |
T |
C |
8: 75,848,220 (GRCm39) |
S490P |
probably damaging |
Het |
Mia3 |
A |
C |
1: 183,147,036 (GRCm39) |
Y73* |
probably null |
Het |
Minar1 |
T |
A |
9: 89,483,888 (GRCm39) |
H503L |
probably benign |
Het |
Msr1 |
A |
T |
8: 40,077,003 (GRCm39) |
N202K |
probably benign |
Het |
N4bp2l2 |
A |
T |
5: 150,585,286 (GRCm39) |
Y231* |
probably null |
Het |
Ncor1 |
T |
C |
11: 62,264,250 (GRCm39) |
E384G |
possibly damaging |
Het |
Neb |
A |
G |
2: 52,137,202 (GRCm39) |
V254A |
|
Het |
Nlrp9b |
T |
C |
7: 19,779,691 (GRCm39) |
S785P |
probably benign |
Het |
Oprd1 |
T |
G |
4: 131,841,092 (GRCm39) |
I289L |
possibly damaging |
Het |
Or4c10 |
G |
T |
2: 89,761,064 (GRCm39) |
D304Y |
probably benign |
Het |
Or4s2 |
A |
G |
2: 88,473,752 (GRCm39) |
I214V |
probably benign |
Het |
Or5m12 |
A |
G |
2: 85,734,447 (GRCm39) |
V317A |
probably benign |
Het |
Or6a2 |
T |
C |
7: 106,600,534 (GRCm39) |
T178A |
probably benign |
Het |
Or6c2 |
T |
A |
10: 129,362,429 (GRCm39) |
F111Y |
possibly damaging |
Het |
Orc1 |
A |
G |
4: 108,445,951 (GRCm39) |
N23S |
probably benign |
Het |
Paip1 |
A |
T |
13: 119,577,356 (GRCm39) |
H149L |
possibly damaging |
Het |
Pdhx |
A |
T |
2: 102,877,099 (GRCm39) |
D103E |
probably benign |
Het |
Pi4ka |
T |
C |
16: 17,109,080 (GRCm39) |
Y1614C |
|
Het |
Pias3 |
ACC |
AC |
3: 96,608,701 (GRCm39) |
|
probably null |
Het |
Pigb |
A |
G |
9: 72,941,770 (GRCm39) |
V163A |
probably benign |
Het |
Pla2g4d |
A |
G |
2: 120,114,620 (GRCm39) |
I37T |
possibly damaging |
Het |
Ppfia1 |
A |
T |
7: 144,059,982 (GRCm39) |
V610D |
probably damaging |
Het |
Pramel41 |
G |
A |
5: 94,596,394 (GRCm39) |
C477Y |
probably damaging |
Het |
Prss1 |
T |
C |
6: 41,439,507 (GRCm39) |
V80A |
probably benign |
Het |
Psph |
G |
A |
5: 129,847,800 (GRCm39) |
R49W |
probably benign |
Het |
Qrich2 |
T |
C |
11: 116,347,080 (GRCm39) |
Y1248C |
possibly damaging |
Het |
Rlbp1 |
T |
A |
7: 79,029,861 (GRCm39) |
Y124F |
probably damaging |
Het |
Scn4a |
T |
A |
11: 106,239,995 (GRCm39) |
E74V |
probably benign |
Het |
Sdk2 |
A |
T |
11: 113,764,039 (GRCm39) |
I249N |
possibly damaging |
Het |
Sgsh |
A |
T |
11: 119,237,378 (GRCm39) |
L412Q |
probably damaging |
Het |
Shank1 |
C |
A |
7: 44,002,452 (GRCm39) |
D1390E |
probably benign |
Het |
Slc12a6 |
A |
G |
2: 112,172,319 (GRCm39) |
D421G |
probably damaging |
Het |
Snx29 |
T |
A |
16: 11,238,649 (GRCm39) |
|
probably null |
Het |
Spata31d1c |
A |
G |
13: 65,183,937 (GRCm39) |
Y493C |
probably damaging |
Het |
Stmn4 |
G |
A |
14: 66,593,727 (GRCm39) |
G40E |
probably damaging |
Het |
Stox2 |
A |
G |
8: 47,656,154 (GRCm39) |
|
probably null |
Het |
Strada |
T |
C |
11: 106,077,830 (GRCm39) |
S45G |
unknown |
Het |
Taco1 |
G |
A |
11: 105,962,774 (GRCm39) |
G154S |
probably benign |
Het |
Tas2r121 |
T |
C |
6: 132,677,505 (GRCm39) |
M156V |
probably benign |
Het |
Tbc1d31 |
A |
G |
15: 57,804,136 (GRCm39) |
S384G |
probably benign |
Het |
Tbc1d9 |
A |
T |
8: 83,966,560 (GRCm39) |
D387V |
probably damaging |
Het |
Tet3 |
A |
G |
6: 83,345,289 (GRCm39) |
L1716P |
probably damaging |
Het |
Thbs1 |
A |
G |
2: 117,943,843 (GRCm39) |
K154E |
possibly damaging |
Het |
Ush2a |
T |
C |
1: 187,999,241 (GRCm39) |
Y184H |
possibly damaging |
Het |
Vmn1r235 |
C |
A |
17: 21,481,713 (GRCm39) |
Q13K |
probably benign |
Het |
Vmn2r15 |
A |
T |
5: 109,440,774 (GRCm39) |
Y361* |
probably null |
Het |
Vmn2r88 |
A |
T |
14: 51,648,315 (GRCm39) |
|
probably null |
Het |
Vps54 |
T |
C |
11: 21,248,831 (GRCm39) |
V460A |
probably benign |
Het |
Wdr64 |
A |
G |
1: 175,613,147 (GRCm39) |
N674S |
possibly damaging |
Het |
Zfp592 |
A |
G |
7: 80,673,390 (GRCm39) |
D118G |
probably benign |
Het |
Zfp763 |
A |
G |
17: 33,237,625 (GRCm39) |
Y507H |
probably benign |
Het |
Zfp934 |
T |
C |
13: 62,640,705 (GRCm39) |
E16G |
probably damaging |
Het |
Zfyve26 |
G |
A |
12: 79,337,731 (GRCm39) |
L94F |
probably damaging |
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 |
R6180:Nbeal2
|
UTSW |
9 |
110,454,215 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|