Incidental Mutations

22 incidental mutations are currently displayed, and affect 22 genes.
6 are Possibly Damaging.
4 are Probably Damaging.
10 are Probably Benign.
1 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 22 of 22] 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 179213 APN A730049H05Rik 1.000 IGL01889 G1 6 92828000 G A intron Het probably benign phenotype 05/07/2014
2 179212 APN Brap 1.000 IGL01889 G1 5 121660818 V18I G A missense Het probably benign 0.002 phenotype 05/07/2014
3 179215 APN Csmd1 0.000 IGL01889 G1 8 15998857 V2282M C T missense Het probably damaging 0.998 phenotype 05/07/2014
4 179204 APN Flnb 1.000 IGL01889 G1 14 7935967 E2269G A G missense Het possibly damaging 0.850 phenotype 05/07/2014
5 179201 APN Gaa 0.531 IGL01889 G1 11 119278297 I557V A G missense Het probably benign 0.026 phenotype 05/07/2014
6 179203 APN Gapt 0.000 IGL01889 G1 13 110353967 Q54L T A missense Het probably benign 0.001 phenotype 05/07/2014
7 179202 APN Gsdmc 0.053 IGL01889 G1 15 63780003 I253N A T missense Het possibly damaging 0.892 05/07/2014
8 179207 APN Kcnj3 0.000 IGL01889 G1 2 55437204 S2T T A missense Het possibly damaging 0.685 phenotype 05/07/2014
9 179218 APN Mindy2 0.144 IGL01889 G1 9 70631162 T C splice site Het probably benign 05/07/2014
10 179206 APN Ncor1 1.000 IGL01889 G1 11 62334601 V1048A A G missense Het possibly damaging 0.689 phenotype 05/07/2014
11 179209 APN Nlrp4d 0.000 IGL01889 G1 7 10378334 V636D A T missense Het unknown 0.000 05/07/2014
12 179211 APN Nphs1 1.000 IGL01889 G1 7 30460511 R82S G T missense Het probably damaging 0.998 phenotype 05/07/2014
13 179198 APN Olfr1269 0.208 IGL01889 G1 2 90118965 V211A A G missense Het possibly damaging 0.840 phenotype 05/07/2014
14 179216 APN Olfr1336 0.078 IGL01889 G1 7 6460503 G A splice site Het probably benign phenotype 05/07/2014
15 179199 APN Olfr512 0.108 IGL01889 G1 7 108713882 F164L T A missense Het probably benign 0.017 phenotype 05/07/2014
16 179210 APN Papln 0.000 IGL01889 G1 12 83786835 L1175Q T A missense Het probably benign 0.251 05/07/2014
17 179219 APN Rab22a 0.000 IGL01889 G1 2 173688238 T C intron Het probably benign phenotype 05/07/2014
18 179205 APN Rel 0.000 IGL01889 G1 11 23757035 Y56H A G missense Het probably damaging 0.958 phenotype 05/07/2014
19 179208 APN Sdc4 0.000 IGL01889 G1 2 164431207 L61P A G missense Het probably damaging 0.998 phenotype 05/07/2014
20 179217 APN Slc1a4 0.000 IGL01889 G1 11 20314089 A G splice site Het probably benign phenotype 05/07/2014
21 179214 APN Ubr4 1.000 IGL01889 G1 4 139462472 C3989* T A nonsense Het probably null phenotype 05/07/2014
22 179200 APN Zfyve16 0.214 IGL01889 G1 13 92522569 V278A A G missense Het possibly damaging 0.871 phenotype 05/07/2014
[records 1 to 22 of 22]