Incidental Mutations

26 incidental mutations are currently displayed, and affect 26 genes.
3 are Possibly Damaging.
8 are Probably Damaging.
11 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 26 of 26] 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 181798 APN 4930435E12Rik 0.078 IGL01979 G1 16 38827893 S285A A C missense Het possibly damaging 0.610 05/07/2014
2 279246 APN Adh4 0.089 IGL01979 G1 3 138429027 C T unclassified Het probably benign phenotype 04/16/2015
3 181800 APN Ap3b1 0.630 IGL01979 G1 13 94448463 L394* T A nonsense Het probably null phenotype 05/07/2014
4 181795 APN Cdk2ap1 1.000 IGL01979 G1 5 124348709 V57M C T missense Het probably damaging 1.000 phenotype 05/07/2014
5 181813 APN Csnk2b IGL01979 G1 17 35118016 N65I T A missense Het possibly damaging 0.919 phenotype 05/07/2014
6 181807 APN Dennd4a 0.437 IGL01979 G1 9 64894409 E945K G A missense Het probably benign 0.004 phenotype 05/07/2014
7 181803 APN Eif2b2 1.000 IGL01979 G1 12 85219834 D59G A G missense Het probably benign 0.001 phenotype 05/07/2014
8 181805 APN Ero1l 0.228 IGL01979 G1 14 45287744 N441K A T missense Het probably damaging 1.000 phenotype 05/07/2014
9 181793 APN Fam91a1 0.000 IGL01979 G1 15 58432584 D383G A G missense Het probably damaging 1.000 phenotype 05/07/2014
10 181808 APN Fbxl7 0.000 IGL01979 G1 15 26789563 S26I C A missense Het probably damaging 0.979 phenotype 05/07/2014
11 181812 APN Il20 0.000 IGL01979 G1 1 130911102 I42K A T missense Het probably damaging 0.981 phenotype 05/07/2014
12 181801 APN Nav3 0.000 IGL01979 G1 10 109704929 F1947L A G missense Het probably benign 0.013 phenotype 05/07/2014
13 181815 APN Ncapd3 0.962 IGL01979 G1 9 27071965 T A critical splice donor site 2 bp Het probably null phenotype 05/07/2014
14 181804 APN Numb 1.000 IGL01979 G1 12 83842277 H23N G T missense Het probably damaging 0.999 phenotype 05/07/2014
15 181816 APN Olfr1419 0.070 IGL01979 G1 19 11871223 G A splice site Het probably benign phenotype 05/07/2014
16 181792 APN Olfr507 0.110 IGL01979 G1 7 108622441 I210V A G missense Het probably benign 0.092 phenotype 05/07/2014
17 181810 APN Ppp1r1b 0.138 IGL01979 G1 11 98356840 T111I C T missense Het probably damaging 0.989 phenotype 05/07/2014
18 181796 APN Rad50 1.000 IGL01979 G1 11 53686178 Q528* G A nonsense Het probably null phenotype 05/07/2014
19 181799 APN Scara3 0.137 IGL01979 G1 14 65930963 S402T A T missense Het probably benign 0.006 phenotype 05/07/2014
20 181797 APN Sept3 0.127 IGL01979 G1 15 82284392 Y132C A G missense Het probably damaging 0.988 phenotype 05/07/2014
21 181811 APN Sim2 1.000 IGL01979 G1 16 94123482 N495K C A missense Het possibly damaging 0.810 phenotype 05/07/2014
22 181802 APN Slc9b1 0.117 IGL01979 G1 3 135371982 A G splice site 3 bp Het probably null phenotype 05/07/2014
23 181806 APN Tanc2 1.000 IGL01979 G1 11 105776920 D109G A G missense Het probably benign 0.000 phenotype 05/07/2014
24 181814 APN Traf1 0.119 IGL01979 G1 2 34943893 I404V T C missense Het probably benign 0.002 phenotype 05/07/2014
25 181794 APN Vmn2r68 0.083 IGL01979 G1 7 85222117 V653L C A missense Het probably benign 0.000 05/07/2014
26 181809 APN Wdr93 0.062 IGL01979 G1 7 79776652 Q555L A T missense Het probably benign 0.029 05/07/2014
[records 1 to 26 of 26]