Incidental Mutations

28 incidental mutations are currently displayed, and affect 28 genes.
2 are Possibly Damaging.
13 are Probably Damaging.
8 are Probably Benign.
3 are Probably Null.
0 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 179560 APN 4931406B18Rik 0.049 IGL01902 G1 7 43497843 S228P A G missense Het probably damaging 0.958 05/07/2014
2 179550 APN Adamtsl2 1.000 IGL01902 G1 2 27087252 I242F A T missense Het probably damaging 1.000 phenotype 05/07/2014
3 179567 APN Bicdl1 0.640 IGL01902 G1 5 115651874 L284P A G missense Het probably damaging 1.000 05/07/2014
4 179554 APN Bnc2 1.000 IGL01902 G1 4 84390944 I138T A G missense Het probably damaging 1.000 phenotype 05/07/2014
5 179561 APN Cep350 0.957 IGL01902 G1 1 155861985 L2704S A G missense Het probably damaging 1.000 phenotype 05/07/2014
6 179548 APN Col7a1 1.000 IGL01902 G1 9 108977827 P2442T C A missense Het unknown phenotype 05/07/2014
7 179556 APN Cpne6 0.227 IGL01902 G1 14 55512750 T113S A T missense Het possibly damaging 0.796 phenotype 05/07/2014
8 179572 APN Crnkl1 0.952 IGL01902 G1 2 145924712 T C splice site 3 bp Het probably null phenotype 05/07/2014
9 179549 APN Cyp2c67 0.097 IGL01902 G1 19 39649026 D2V T A missense Het probably damaging 1.000 05/07/2014
10 179557 APN Frzb 0.445 IGL01902 G1 2 80413367 S323C T A missense Het probably damaging 0.967 phenotype 05/07/2014
11 279052 APN Gm21738 0.861 IGL01902 G1 14 19416979 S144L G A missense Het probably benign 0.011 04/16/2015
12 279053 APN Gm5862 0.175 IGL01902 G1 5 26022771 W41G A C missense Het probably benign 0.000 04/16/2015
13 179568 APN Ins2 0.422 IGL01902 G1 7 142679442 C31Y C T missense Het probably damaging 1.000 phenotype 05/07/2014
14 179555 APN Lipf 0.153 IGL01902 G1 19 33970779 N234Y A T missense Het probably benign 0.330 phenotype 05/07/2014
15 179566 APN Mtf1 1.000 IGL01902 G1 4 124804927 F73L T C missense Het probably damaging 0.989 phenotype 05/07/2014
16 179571 APN Nrxn1 0.000 IGL01902 G1 17 91088491 A G splice site Het probably null phenotype 05/07/2014
17 179564 APN Pcnx 0.000 IGL01902 G1 12 81979094 T1538A A G missense Het probably damaging 0.997 phenotype 05/07/2014
18 179559 APN Polr1a 1.000 IGL01902 G1 6 71963748 V47D T A missense Het probably damaging 0.999 phenotype 05/07/2014
19 179563 APN Prune2 0.000 IGL01902 G1 19 17118638 E502G A G missense Het probably benign 0.001 phenotype 05/07/2014
20 179565 APN Ralgapa2 0.218 IGL01902 G1 2 146315014 V1886M C T missense Het probably damaging 0.999 phenotype 05/07/2014
21 179551 APN Rapgef3 0.168 IGL01902 G1 15 97750300 H676L T A missense Het probably benign 0.317 phenotype 05/07/2014
22 179553 APN Rbm20 0.153 IGL01902 G1 19 53840991 N607Y A T missense Het probably damaging 0.992 phenotype 05/07/2014
23 179552 APN Smc5 1.000 IGL01902 G1 19 23259768 T233I G A missense Het possibly damaging 0.845 phenotype 05/07/2014
24 179569 APN Snx13 1.000 IGL01902 G1 12 35133307 A T critical splice acceptor site Het probably null phenotype 05/07/2014
25 179558 APN Suz12 1.000 IGL01902 G1 11 80025950 C510S T A missense Het probably benign 0.039 phenotype 05/07/2014
26 179562 APN Tab2 1.000 IGL01902 G1 10 7919992 M242K A T missense Het probably benign 0.121 phenotype 05/07/2014
27 179570 APN Tep1 0.000 IGL01902 G1 14 50866091 A G splice site Het probably benign phenotype 05/07/2014
28 279054 APN Vmn2r-ps159 0.728 IGL01902 G1 4 156338254 C T exon Het noncoding transcript 04/16/2015
[records 1 to 28 of 28]