Incidental Mutations

28 incidental mutations are currently displayed, and affect 28 genes.
3 are Possibly Damaging.
13 are Probably Damaging.
8 are Probably Benign.
4 are Probably Null.
2 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 28 of 28] 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 410233 APN A930011G23Rik 0.156 IGL03129 5 99229379 V403A A G missense Het probably damaging 0.978 08/02/2016
2 410241 APN Adpgk 0.229 IGL03129 9 59313805 L298P T C missense Het probably damaging 1.000 phenotype 08/02/2016
3 410253 APN Akap6 0.322 IGL03129 12 53140306 D1501V A T missense Het probably damaging 1.000 phenotype 08/02/2016
4 410247 APN Ank2 1.000 IGL03129 3 126955870 E503D C A missense Het probably damaging 0.998 phenotype 08/02/2016
5 410243 APN Ankhd1 0.341 IGL03129 18 36658008 Y2478* T A nonsense Het probably null 0.618 08/02/2016
6 410237 APN Col6a3 0.000 IGL03129 1 90821862 Y417H A G missense Het probably damaging 0.995 phenotype 08/02/2016
7 410249 APN Csmd1 0.291 IGL03129 8 15961521 F2511L A G missense Het probably damaging 0.993 phenotype 08/02/2016
8 410250 APN Dzip3 1.000 IGL03129 16 48942083 M602V T C missense Het possibly damaging 0.507 phenotype 08/02/2016
9 410259 APN Efna2 0.000 IGL03129 10 80188512 G A splice site 5 bp Het probably null phenotype 08/02/2016
10 410246 APN Fzd8 0.000 IGL03129 18 9214270 S451P T C missense Het probably damaging 1.000 phenotype 08/02/2016
11 410240 APN Galntl6 0.125 IGL03129 8 58427716 D134E A T missense Het probably damaging 1.000 08/02/2016
12 410239 APN Gm10334 0.115 IGL03129 6 41443498 N98S T C missense Het probably benign 0.000 08/02/2016
13 410244 APN Grid2 0.000 IGL03129 6 64063904 S277P T C missense Het probably damaging 0.978 phenotype 08/02/2016
14 410251 APN Lcn2 0.000 IGL03129 2 32387704 V91A A G missense Het possibly damaging 0.699 phenotype 08/02/2016
15 410260 APN Lrp1b 0.000 IGL03129 2 41312466 G A splice site Het probably benign phenotype 08/02/2016
16 410236 APN Lrrc7 0.740 IGL03129 3 158161059 Y1015F T A missense Het probably benign 0.021 phenotype 08/02/2016
17 410248 APN Mdn1 0.969 IGL03129 4 32729994 C2779S T A missense Het possibly damaging 0.466 08/02/2016
18 410254 APN Nlrp10 0.000 IGL03129 7 108924911 F454Y A T missense Het probably damaging 1.000 phenotype 08/02/2016
19 410234 APN Obox5 0.128 IGL03129 7 15758759 L213Q T A missense Het probably damaging 0.992 08/02/2016
20 410238 APN Olfr97 0.069 IGL03129 17 37232196 Y58F T A missense Het probably damaging 1.000 phenotype 08/02/2016
21 410255 APN Piezo2 1.000 IGL03129 18 63114972 M486V T C missense Het probably benign 0.000 phenotype 08/02/2016
22 410257 APN Plcg1 1.000 IGL03129 2 160774526 A C critical splice acceptor site Het probably null phenotype 08/02/2016
23 410242 APN Polr1b 1.000 IGL03129 2 129115707 V561I G A missense Het probably benign 0.001 phenotype 08/02/2016
24 410256 APN Polr3c 0.950 IGL03129 3 96719454 A T splice site Het probably benign 08/02/2016
25 410245 APN Prkg1 0.650 IGL03129 19 30585281 K523* T A nonsense Het probably null phenotype 08/02/2016
26 410258 APN Sema3b 0.512 IGL03129 9 107599796 T A unclassified Het probably benign phenotype 08/02/2016
27 410252 APN Sp9 0.598 IGL03129 2 73273521 T140A A G missense Het probably benign 0.005 08/02/2016
28 410235 APN Zfp507 0.245 IGL03129 7 35794206 R471G T C missense Het probably damaging 1.000 08/02/2016
[records 1 to 28 of 28]