Incidental Mutations

29 incidental mutations are currently displayed, and affect 29 genes.
3 are Possibly Damaging.
11 are Probably Damaging.
11 are Probably Benign.
3 are Probably Null.
1 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 29 of 29] per page Full List
 
ID question?
Source question?
Gene question?
E-score question?
 
Stock # question?
Gen question?
Quality
-
Vld question?
Strain question?
Chr question?
Position question?
 
Mutation question?
Ref
Var
Type question?
Exon Dist question?
 
Zygosity question?
Predicted Effect question?
PPH Score question?
-
Meta Score question?
 
MGI Phenotype question?
Posted question?
 
1 104170 APN 3830406C13Rik 0.000 IGL01693 G1 14 12287380 L55P T C missense Het probably damaging 0.999 01/21/2014
2 104173 APN Akr1b8 0.000 IGL01693 G1 6 34363336 M145K T A missense Het possibly damaging 0.899 phenotype 01/21/2014
3 104182 APN Arhgap39 0.193 IGL01693 G1 15 76725967 D943G T C missense Het probably null 1.000 01/21/2014
4 104181 APN Arhgap42 0.906 IGL01693 G1 9 9006506 W630R A T missense Het probably damaging 0.997 phenotype 01/21/2014
5 104190 APN Bbs5 0.000 IGL01693 G1 2 69663080 S225T T A missense Het probably benign 0.000 phenotype 01/21/2014
6 104174 APN Cacna1f 0.000 IGL01693 G1 X 7625367 N1159Y A T missense Het probably damaging 0.999 phenotype 01/21/2014
7 104194 APN Catsperg1 0.068 IGL01693 G1 7 29185098 A G unclassified Het probably benign 01/21/2014
8 104184 APN Cep97 1.000 IGL01693 G1 16 55930594 W20R A T missense Het probably damaging 0.998 01/21/2014
9 104185 APN Cmtm8 0.101 IGL01693 G1 9 114789705 T160M G A missense Het probably damaging 1.000 phenotype 01/21/2014
10 104186 APN Csf2ra 0.073 IGL01693 G1 19 61225996 S244P A G missense Het possibly damaging 0.567 phenotype 01/21/2014
11 104178 APN Dnah7b 0.186 IGL01693 G1 1 46358147 P3913S C T missense Het probably benign 0.292 01/21/2014
12 104180 APN Ezh1 0.000 IGL01693 G1 11 101215258 M100I C T missense Het probably benign 0.000 phenotype 01/21/2014
13 104177 APN Gadl1 0.091 IGL01693 G1 9 115949585 P189Q C A missense Het probably damaging 1.000 01/21/2014
14 104168 APN Gcnt2 0.153 IGL01693 G1 13 40888073 S236N G A missense Het probably benign 0.000 phenotype 01/21/2014
15 104191 APN Gm17689 0.050 IGL01693 G1 9 36581366 T81I G A missense Het probably benign 0.306 01/21/2014
16 104171 APN H1fnt 0.242 IGL01693 G1 15 98256381 Y296D A C missense Het unknown phenotype 01/21/2014
17 104187 APN Hmcn1 0.000 IGL01693 G1 1 150583280 D5191V T A missense Het probably damaging 0.999 phenotype 01/21/2014
18 104176 APN Mycbp2 1.000 IGL01693 G1 14 103127979 D4194E A T missense Het probably damaging 0.988 phenotype 01/21/2014
19 104192 APN Ncf2 0.088 IGL01693 G1 1 152824323 T203K C A missense Het probably benign 0.001 phenotype 01/21/2014
20 104183 APN Olfr76 0.174 IGL01693 G1 19 12120557 V40L C A missense Het probably benign 0.000 phenotype 01/21/2014
21 104179 APN Phf8 0.518 IGL01693 G1 X 151550875 V113E T A missense Het probably damaging 1.000 phenotype 01/21/2014
22 104193 APN Pkm 1.000 IGL01693 G1 9 59670522 K207N G T missense Het probably damaging 1.000 phenotype 01/21/2014
23 104169 APN Slco1a6 0.070 IGL01693 G1 6 142133209 S120* G T nonsense Het probably null 01/21/2014
24 104175 APN Sox10 1.000 IGL01693 G1 15 79156273 V195M C T missense Het possibly damaging 0.854 phenotype 01/21/2014
25 104189 APN Swt1 0.255 IGL01693 G1 1 151422104 I24T A G missense Het probably benign 0.024 01/21/2014
26 104172 APN Thada 0.000 IGL01693 G1 17 84446644 T300A T C missense Het probably benign 0.000 phenotype 01/21/2014
27 104188 APN Tmem2 0.770 IGL01693 G1 19 21801887 I354L A C missense Het probably benign 0.003 01/21/2014
28 104167 APN Vmn2r17 0.113 IGL01693 G1 5 109452518 Y561H T C missense Het probably damaging 1.000 01/21/2014
29 104195 APN Wdr78 0.108 IGL01693 G1 4 103087330 T C splice site 3 bp Het probably null 01/21/2014
[records 1 to 29 of 29]