Incidental Mutations

37 incidental mutations are currently displayed, and affect 37 genes.
5 are Possibly Damaging.
17 are Probably Damaging.
13 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 37 of 37] 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 4051 APN Adamts20 0.158 IGL00433 G1 15 94394641 A196V G A missense Het probably benign 0.000 phenotype 04/20/2012
2 5830 APN BC024139 0.057 IGL00433 G1 15 76125100 V238A A G missense Het probably benign 0.062 04/20/2012
3 4008 APN Bfar 0.129 IGL00433 G1 16 13698963 D350N G A missense Het probably benign 0.034 04/20/2012
4 3864 APN C4b 0.000 IGL00433 G1 17 34742041 F217Y A T missense Het possibly damaging 0.754 phenotype 04/20/2012
5 9362 APN Camk1g 0.122 IGL00433 G1 1 193347349 T C unclassified Het probably benign phenotype 12/06/2012
6 5735 APN Camkmt 0.000 IGL00433 G1 17 85096666 A G splice site Het probably benign phenotype 04/20/2012
7 6952 APN Cass4 0.000 IGL00433 G1 2 172416250 L56P T C missense Het probably damaging 1.000 04/20/2012
8 332407 APN Ccs 0.297 IGL00433 G1 19 4825608 I243T A G missense Het possibly damaging 0.940 phenotype 08/05/2015
9 9576 APN Cds2 1.000 IGL00433 G1 2 132297293 V152A T C missense Het probably damaging 0.996 phenotype 12/06/2012
10 6812 APN Chd1l 0.157 IGL00433 G1 3 97590605 N307D T C missense Het probably damaging 1.000 phenotype 04/20/2012
11 4980 APN Cmtm2b 0.056 IGL00433 G1 8 104330446 I146T T C missense Het possibly damaging 0.954 phenotype 04/20/2012
12 5927 APN Cntnap3 0.072 IGL00433 G1 13 64772731 Y608C T C missense Het probably damaging 0.999 phenotype 04/20/2012
13 4426 APN Cog5 0.894 IGL00433 G1 12 31685704 R157G A G missense Het probably damaging 0.999 phenotype 04/20/2012
14 5061 APN Csmd1 0.000 IGL00433 G1 8 16231373 F713V A C missense Het probably damaging 0.997 phenotype 04/20/2012
15 5242 APN Csrp3 0.642 IGL00433 G1 7 48830692 N175D T C missense Het probably benign 0.242 phenotype 04/20/2012
16 5462 APN Exoc4 1.000 IGL00433 G1 6 33296788 D176G A G missense Het probably damaging 0.999 phenotype 04/20/2012
17 4540 APN Fam57a 0.132 IGL00433 G1 11 76207991 F164L T C missense Het probably damaging 1.000 phenotype 04/20/2012
18 6678 APN Fbxo10 0.000 IGL00433 G1 4 45058684 D351G T C missense Het probably damaging 0.982 phenotype 04/20/2012
19 6062 APN Gm12185 0.087 IGL00433 G1 11 48907222 S815T A T missense Het probably benign 0.008 04/20/2012
20 5948 APN Gpld1 0.000 IGL00433 G1 13 24986922 A G splice site Het probably benign phenotype 04/20/2012
21 4396 APN Hspa2 0.000 IGL00433 G1 12 76406349 C606R T C missense Het possibly damaging 0.939 phenotype 04/20/2012
22 4844 APN Leo1 1.000 IGL00433 G1 9 75450480 C T splice site Het probably benign phenotype 04/20/2012
23 277600 APN Mta3 0.482 IGL00433 G1 17 83708432 P21L C T missense Het probably damaging 1.000 04/16/2015
24 5009 APN Pkn1 0.000 IGL00433 G1 8 83681006 E471G T C missense Het probably damaging 0.963 phenotype 04/20/2012
25 6899 APN Postn 0.000 IGL00433 G1 3 54373728 R425C C T missense Het probably damaging 1.000 phenotype 04/20/2012
26 6477 APN Reln 0.950 IGL00433 G1 5 22045009 L676P A G missense Het probably damaging 0.999 phenotype 04/20/2012
27 4876 APN Sin3a 1.000 IGL00433 G1 9 57097901 V362M G A missense Het probably damaging 1.000 phenotype 04/20/2012
28 3313 APN Slc6a7 0.119 IGL00433 G1 18 61001291 C T critical splice donor site 1 bp Het probably null phenotype 04/20/2012
29 4438 APN Smc6 1.000 IGL00433 G1 12 11299263 D749V A T missense Het possibly damaging 0.478 phenotype 04/20/2012
30 6845 APN Smg5 1.000 IGL00433 G1 3 88351428 Q569* C T nonsense Het probably null phenotype 04/20/2012
31 332408 APN Sspo 0.000 IGL00433 G1 6 48490036 C4130Y G A missense Het probably damaging 1.000 08/05/2015
32 7342 APN Tnn 0.414 IGL00433 G1 1 160098206 A T splice site Het probably benign 04/20/2012
33 5194 APN Tomt IGL00433 G1 7 101902186 R29H C T missense Het probably benign 0.001 phenotype 04/20/2012
34 4137 APN Uggt2 0.153 IGL00433 G1 14 119013487 D1199E A T missense Het probably benign 0.000 phenotype 04/20/2012
35 6733 APN Usp33 0.793 IGL00433 G1 3 152373409 K433E A G missense Het probably benign 0.004 phenotype 04/20/2012
36 332409 APN Vmn2r89 0.114 IGL00433 G1 14 51454965 Y75C A G missense Het probably damaging 0.999 08/05/2015
37 5401 APN Wnt7a 0.637 IGL00433 G1 6 91365991 G303D C T missense Het probably damaging 0.990 phenotype 04/20/2012
[records 1 to 37 of 37]