Incidental Mutations

36 incidental mutations are currently displayed, and affect 35 genes.
4 are Possibly Damaging.
17 are Probably Damaging.
12 are Probably Benign.
2 are Probably Null.
1 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 36 of 36] 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 51505 APN Arhgap33 0.192 IGL01092 G1 7 30529946 (GRCm38) R335G T C missense Het probably damaging 0.994 phenotype 2013-06-21
2 52444 APN Atad2b 0.000 IGL01092 G1 12 5017987 (GRCm38) S995L C T missense Het probably damaging 0.980 phenotype 2013-06-21
3 50476 APN Atrn 0.000 IGL01092 G1 2 130947636 (GRCm38) R340* A T nonsense Het probably null phenotype 2013-06-21
4 51502 APN Ccdc83 0.000 IGL01092 G1 7 90247105 (GRCm38) D85E A T missense Het probably benign 0.114 2013-06-21
5 51506 APN Chd2 0.659 IGL01092 G1 7 73441686 (GRCm38) H1602Q A T missense Het possibly damaging 0.691 phenotype 2013-06-21
6 51749 APN Cog2 1.000 IGL01092 G1 8 124545280 (GRCm38) D511G A G missense Het probably damaging 1.000 phenotype 2013-06-21
7 278171 APN Col4a4 0.076 IGL01092 G1 1 82466545 (GRCm38) P1334T G T missense Het unknown phenotype 2015-04-16
8 50728 APN Creb3l4 0.796 IGL01092 G1 3 90237738 (GRCm38) E369G T C missense Het probably damaging 1.000 phenotype 2013-06-21
9 50477 APN Crnkl1 0.966 IGL01092 G1 2 145919948 (GRCm38) K563R T C missense Het probably benign 0.001 phenotype 2013-06-21
10 50242 APN Dbi 0.236 IGL01092 G1 1 120113477 (GRCm38) K131E T C missense Het probably benign 0.064 phenotype 2013-06-21
11 52558 APN Edn1 1.000 IGL01092 G1 13 42303671 (GRCm38) D60G A G missense Het probably damaging 1.000 phenotype 2013-06-21
12 52557 APN Erbin 0.000 IGL01092 G1 13 103834012 (GRCm38) N1032S T C missense Het probably damaging 0.999 phenotype 2013-06-21
13 52672 APN Ero1l 0.318 IGL01092 G1 14 45303586 (GRCm38) D107G T C missense Het probably benign 0.192 phenotype 2013-06-21
14 51087 APN Glmn 1.000 IGL01092 G1 5 107578512 (GRCm38) A T critical splice acceptor site Het probably null phenotype 2013-06-21
15 51086 APN Grxcr1 0.169 IGL01092 G1 5 68110562 (GRCm38) T C splice site Het probably benign phenotype 2013-06-21
16 52671 APN Itih3 0.061 IGL01092 G1 14 30909781 (GRCm38) K593I T A missense Het probably damaging 0.979 phenotype 2013-06-21
17 51504 APN Kmt2b 1.000 IGL01092 G1 7 30580507 (GRCm38) Y1356C T C missense Het probably damaging 1.000 phenotype 2013-06-21
18 50474 APN Lrp1b 0.000 IGL01092 G1 2 40750947 (GRCm38) C3495Y C T missense Het probably damaging 0.970 phenotype 2013-06-21
19 52910 APN Map3k13 0.000 IGL01092 G1 16 21928016 (GRCm38) T950S A T missense Het probably damaging 0.974 phenotype 2013-06-21
20 51899 APN Me1 0.000 IGL01092 G1 9 86598748 (GRCm38) V348D A T missense Het probably damaging 1.000 phenotype 2013-06-21
21 52268 APN Morc2a 1.000 IGL01092 G1 11 3684042 (GRCm38) V718A T C missense Het probably benign 0.001 phenotype 2013-06-21
22 52670 APN Myh7 0.868 IGL01092 G1 14 54971632 (GRCm38) E1883G T C missense Het possibly damaging 0.907 phenotype 2013-06-21
23 50883 APN Olfr1338 0.728 IGL01092 G1 4 118753762 (GRCm38) I259F T A missense Het possibly damaging 0.780 phenotype 2013-06-21
24 51900 APN Olfr913 0.051 IGL01092 G1 9 38594905 (GRCm38) I228R T G missense Het probably damaging 0.983 phenotype 2013-06-21
25 51901 APN Pdcd6ip 0.000 IGL01092 G1 9 113680181 (GRCm38) A G splice site Het probably benign phenotype 2013-06-21
26 53241 APN Plcb3 0.551 IGL01092 G1 19 6955322 (GRCm38) E1025V T A missense Het probably benign 0.267 phenotype 2013-06-21
27 50478 APN Ppp1r26 0.000 IGL01092 G1 2 28453860 (GRCm38) C T utr 3 prime Het probably benign 2013-06-21
28 52443 APN Prkd1 1.000 IGL01092 G1 12 50383515 (GRCm38) T C splice site Het probably benign phenotype 2013-06-21
29 51748 APN Rwdd4a 0.132 IGL01092 G1 8 47544112 (GRCm38) T122M C T missense Het possibly damaging 0.956 2013-06-21
30 50884 APN Sdhb 1.000 IGL01092 G1 4 140977480 (GRCm38) C251G T G missense Het probably damaging 1.000 phenotype 2013-06-21
31 50475 APN Siglec1 0.071 IGL01092 G1 2 131079217 (GRCm38) I678N A T missense Het probably damaging 1.000 phenotype 2013-06-21
32 51503 APN Snrnp70 0.961 IGL01092 G1 7 45377377 (GRCm38) D215G T C missense Het probably damaging 0.984 phenotype 2013-06-21
33 53047 APN Ston1 0.219 IGL01092 G1 17 88644443 (GRCm38) E674G A G missense Het probably benign 0.002 phenotype 2013-06-21
34 53048 APN Tbl3 0.964 IGL01092 G1 17 24705252 (GRCm38) I177N A T missense Het probably damaging 1.000 phenotype 2013-06-21
35 53046 APN Tbl3 0.964 IGL01092 G1 17 24701905 (GRCm38) T C splice site Het probably benign phenotype 2013-06-21
36 52269 APN Tnrc6c 0.000 IGL01092 G1 11 117721985 (GRCm38) V483A T C missense Het probably damaging 0.992 phenotype 2013-06-21
[records 1 to 36 of 36]