Incidental Mutations

40 incidental mutations are currently displayed, and affect 40 genes.
5 are Possibly Damaging.
16 are Probably Damaging.
14 are Probably Benign.
4 are Probably Null.
1 create premature stop codons.
3 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 40 of 40] 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 406640 APN 1700020D05Rik 0.085 IGL02983 19 5503181 (GRCm38) F191L A G missense Het possibly damaging 0.461 2016-08-02
2 406633 APN Abca13 0.000 IGL02983 11 9290663 (GRCm38) N842S A G missense Het probably benign 0.402 phenotype 2016-08-02
3 406630 APN Acvr1b 1.000 IGL02983 15 101203078 (GRCm38) R374G A G missense Het probably damaging 0.980 0.747 phenotype 2016-08-02
4 406634 APN Brip1 0.000 IGL02983 11 86139124 (GRCm38) I565V T C missense Het probably benign 0.029 phenotype 2016-08-02
5 406628 APN Camta2 0.603 IGL02983 11 70672022 (GRCm38) R959Q C T missense Het probably damaging 0.988 phenotype 2016-08-02
6 406644 APN Cbln2 0.083 IGL02983 18 86713379 (GRCm38) E104G A G missense Het probably benign 0.066 phenotype 2016-08-02
7 406641 APN Cdc42ep4 0.116 IGL02983 11 113729169 (GRCm38) K132R T C missense Het probably benign 0.132 phenotype 2016-08-02
8 406645 APN Clcnka 0.000 IGL02983 4 141390131 (GRCm38) I452F T A missense Het probably damaging 0.994 phenotype 2016-08-02
9 406648 APN Clec4a3 0.000 IGL02983 6 122967567 (GRCm38) T A critical splice donor site 2 bp Het probably null 2016-08-02
10 406647 APN Crat 0.212 IGL02983 2 30404526 (GRCm38) A C critical splice donor site 2 bp Het probably null phenotype 2016-08-02
11 406627 APN Cspp1 0.354 IGL02983 1 10127525 (GRCm38) K227R A G missense Het probably benign 0.337 phenotype 2016-08-02
12 406616 APN Ddx1 1.000 IGL02983 12 13223862 (GRCm38) I588N A T missense Het probably damaging 1.000 phenotype 2016-08-02
13 406620 APN Dip2b 0.651 IGL02983 15 100132022 (GRCm38) R98L G T missense Het possibly damaging 0.810 phenotype 2016-08-02
14 406625 APN Dock5 0.354 IGL02983 14 67764670 (GRCm38) P1617L G A missense Het probably damaging 0.995 phenotype 2016-08-02
15 406649 APN Fa2h 0.342 IGL02983 8 111346522 (GRCm38) C T critical splice acceptor site Het probably null phenotype 2016-08-02
16 406612 APN Fezf1 1.000 IGL02983 6 23247872 (GRCm38) N68I T A missense Het probably damaging 0.988 phenotype 2016-08-02
17 406619 APN Gabrb2 0.462 IGL02983 11 42421400 (GRCm38) L17F A T missense Het probably benign 0.004 phenotype 2016-08-02
18 406615 APN Gm17078 0.282 IGL02983 14 51611190 (GRCm38) K30R T C missense Het probably benign 0.002 2016-08-02
19 406610 APN Gramd4 0.000 IGL02983 15 86127018 (GRCm38) V249M G A missense Het probably damaging 0.970 phenotype 2016-08-02
20 406639 APN Kcnd2 0.094 IGL02983 6 21216555 (GRCm38) D86A A C missense Het probably damaging 1.000 phenotype 2016-08-02
21 406646 APN Lrp1 1.000 IGL02983 10 127550199 (GRCm38) E3486G T C missense Het probably damaging 1.000 phenotype 2016-08-02
22 406613 APN Ltb 0.116 IGL02983 17 35194670 (GRCm38) D50G A G missense Het probably benign 0.146 phenotype 2016-08-02
23 406618 APN Med18 0.953 IGL02983 4 132459686 (GRCm38) Y167* A T nonsense Het probably null phenotype 2016-08-02
24 406636 APN Nat14 0.119 IGL02983 7 4924128 (GRCm38) A100T G A missense Het probably damaging 0.998 2016-08-02
25 406635 APN Nxph2 0.054 IGL02983 2 23400362 (GRCm38) V242A T C missense Het probably damaging 1.000 2016-08-02
26 406617 APN Olfr338 0.054 IGL02983 2 36377637 (GRCm38) I287N T A missense Het probably damaging 1.000 phenotype 2016-08-02
27 406626 APN Olfr443-ps1 0.169 IGL02983 6 43094648 (GRCm38) T C exon Het noncoding transcript 2016-08-02
28 406631 APN Olfr54 0.065 IGL02983 11 51027380 (GRCm38) V126A T C missense Het probably damaging 0.998 phenotype 2016-08-02
29 406611 APN Olfr818 0.052 IGL02983 10 129945189 (GRCm38) N291I T A missense Het probably damaging 1.000 phenotype 2016-08-02
30 406643 APN Pramef20 0.000 IGL02983 4 144373127 (GRCm38) E356G T C missense Het probably benign 0.239 2016-08-02
31 406624 APN Rad21l 0.000 IGL02983 2 151655120 (GRCm38) L358S A G missense Het probably damaging 1.000 phenotype 2016-08-02
32 406637 APN Rasgef1c 0.080 IGL02983 11 49957049 (GRCm38) T4A A G missense Het possibly damaging 0.954 2016-08-02
33 406629 APN Spata31d1a 0.052 IGL02983 13 59703694 (GRCm38) S207P A G missense Het possibly damaging 0.655 2016-08-02
34 406622 APN Stxbp2 1.000 IGL02983 8 3641971 (GRCm38) I538F A T missense Het probably benign 0.439 phenotype 2016-08-02
35 406638 APN Szt2 0.581 IGL02983 4 118365779 (GRCm38) T C unclassified Het probably benign phenotype 2016-08-02
36 406623 APN Taf6 1.000 IGL02983 5 138178880 (GRCm38) T642A T C missense Het probably benign 0.000 phenotype 2016-08-02
37 406621 APN Tmem30a 1.000 IGL02983 9 79771443 (GRCm38) M277K A T missense Het possibly damaging 0.903 phenotype 2016-08-02
38 406632 APN Vmn1r86 0.051 IGL02983 7 13102814 (GRCm38) D45G T C missense Het probably damaging 1.000 2016-08-02
39 406614 APN Xkr5 0.000 IGL02983 8 18933832 (GRCm38) I565V T C missense Het probably benign 0.001 2016-08-02
40 406642 APN Zfp526 0.225 IGL02983 7 25224415 (GRCm38) A33V C T missense Het probably benign 0.272 2016-08-02
[records 1 to 40 of 40]