Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
3 are Possibly Damaging.
8 are Probably Damaging.
17 are Probably Benign.
5 are Probably Null.
2 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 33 of 33] 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 290827 APN 4930546C10Rik IGL02368 18 68949989 A G splice site Het probably benign 04/16/2015
2 290819 APN Abca17 0.381 IGL02368 17 24287793 V1196L C A missense Het probably benign 0.007 04/16/2015
3 290810 APN Aldh4a1 0.256 IGL02368 4 139648200 W540* G A nonsense Het probably null phenotype 04/16/2015
4 290808 APN Antxr2 0.117 IGL02368 5 97949198 P352L G A missense Het probably damaging 1.000 phenotype 04/16/2015
5 290828 APN Atic 0.965 IGL02368 1 71564565 C T splice site Het probably benign phenotype 04/16/2015
6 290800 APN Cfhr1 0.034 IGL02368 1 139547813 A G unclassified Het probably benign phenotype 04/16/2015
7 290801 APN Clspn 0.969 IGL02368 4 126566107 S207P T C missense Het probably benign 0.000 phenotype 04/16/2015
8 290816 APN Depdc1b 0.169 IGL02368 13 108363579 T209P A C missense Het probably benign 0.000 04/16/2015
9 290814 APN Exosc3 0.947 IGL02368 4 45319671 I117T A G missense Het probably damaging 0.999 phenotype 04/16/2015
10 290803 APN Eya2 0.629 IGL02368 2 165763718 D347E T A missense Het probably damaging 0.998 phenotype 04/16/2015
11 290822 APN Gm10748 IGL02368 3 5215001 G T unclassified Het probably benign 04/16/2015
12 290807 APN Gm17079 IGL02368 14 51693067 N107S T C missense Het possibly damaging 0.954 04/16/2015
13 290813 APN Gpr68 0.000 IGL02368 12 100878767 F173L A G missense Het probably damaging 1.000 phenotype 04/16/2015
14 290806 APN Hgf 1.000 IGL02368 5 16564794 V89F G T missense Het possibly damaging 0.950 phenotype 04/16/2015
15 290809 APN Igsf10 0.372 IGL02368 3 59328231 S1510T A T missense Het probably benign 0.000 04/16/2015
16 290818 APN Il4 IGL02368 11 53612636 N22K A T missense Het probably damaging 0.997 phenotype 04/16/2015
17 290820 APN Izumo2 0.155 IGL02368 7 44708837 L32R T G missense Het probably damaging 0.998 04/16/2015
18 290821 APN Mark2 0.819 IGL02368 19 7284490 L359P A G missense Het probably damaging 1.000 phenotype 04/16/2015
19 290796 APN Myo15b 0.058 IGL02368 11 115877002 K1376R A G missense Het probably benign 0.132 04/16/2015
20 290823 APN Ncam1 0.851 IGL02368 9 49543083 R543* G A nonsense Het probably null phenotype 04/16/2015
21 290797 APN Pax2 1.000 IGL02368 19 44835409 N347S A G missense Het possibly damaging 0.548 phenotype 04/16/2015
22 290815 APN Ppargc1a 0.736 IGL02368 5 51474156 L377P A G missense Het probably benign 0.053 phenotype 04/16/2015
23 290804 APN Pum3 0.646 IGL02368 19 27425957 V48A A G missense Het probably benign 0.001 phenotype 04/16/2015
24 290802 APN Rad1 0.921 IGL02368 15 10493251 Y255H T C missense Het probably benign 0.188 phenotype 04/16/2015
25 290824 APN Rimbp2 0.000 IGL02368 5 128788154 C T splice site 5 bp Het probably null phenotype 04/16/2015
26 290805 APN Rpn2 0.964 IGL02368 2 157302408 N330S A G missense Het probably benign 0.000 phenotype 04/16/2015
27 290798 APN Rptn 0.049 IGL02368 3 93397171 S604G A G missense Het probably benign 0.177 04/16/2015
28 290811 APN Rragc 0.335 IGL02368 4 123921111 D200G A G missense Het probably benign 0.114 phenotype 04/16/2015
29 290817 APN Slco4a1 0.169 IGL02368 2 180473128 F615V T G missense Het probably damaging 0.978 04/16/2015
30 290799 APN Snx2 0.000 IGL02368 18 53189721 S59P T C missense Het probably benign 0.000 phenotype 04/16/2015
31 290812 APN Timp4 0.221 IGL02368 6 115246399 A T intron Het probably null phenotype 04/16/2015
32 290826 APN Tln2 0.400 IGL02368 9 67240810 A G splice site Het probably benign phenotype 04/16/2015
33 290825 APN Txnrd1 1.000 IGL02368 10 82895974 C A splice site Het probably null phenotype 04/16/2015
[records 1 to 33 of 33]