Incidental Mutations

23 incidental mutations are currently displayed, and affect 23 genes.
3 are Possibly Damaging.
10 are Probably Damaging.
7 are Probably Benign.
3 are Probably Null.
1 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 23 of 23] 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 8767 APN Aldh3a1 0.000 IGL00833 G1 11 61217180 E350G A G missense Het probably damaging 0.986 phenotype 12/06/2012
2 9000 APN Apob 0.896 IGL00833 G1 12 8010101 V2861A T C missense Het probably benign 0.144 phenotype 12/06/2012
3 9288 APN Bpifb9a 0.000 IGL00833 G1 2 154264275 Q358* C T nonsense Het probably null 12/06/2012
4 9416 APN Cbfa2t2 0.707 IGL00833 G1 2 154528875 Y423N T A missense Het probably damaging 0.999 phenotype 12/06/2012
5 9490 APN Cd209e 0.045 IGL00833 G1 8 3852800 M102R A C missense Het probably benign 0.052 phenotype 12/06/2012
6 10098 APN Ddx42 1.000 IGL00833 G1 11 106231178 V173D T A missense Het possibly damaging 0.524 phenotype 12/06/2012
7 10214 APN Dnah11 0.642 IGL00833 G1 12 118179580 F443L A G missense Het probably damaging 1.000 phenotype 12/06/2012
8 10578 APN Exoc4 1.000 IGL00833 G1 6 33971924 E901K G A missense Het probably damaging 1.000 phenotype 12/06/2012
9 11072 APN Gp5 0.000 IGL00833 G1 16 30309466 D130G T C missense Het possibly damaging 0.886 phenotype 12/06/2012
10 11200 APN H2-T3 0.000 IGL00833 G1 17 36187041 S327R T G missense Het probably benign 0.000 phenotype 12/06/2012
11 12170 APN Myo1e 0.000 IGL00833 G1 9 70338778 I417T T C missense Het probably damaging 0.991 phenotype 12/06/2012
12 12240 APN Nasp 1.000 IGL00833 G1 4 116602736 V377A A G missense Het probably damaging 0.996 phenotype 12/06/2012
13 12278 APN Nbn 1.000 IGL00833 G1 4 15964320 I132V A G missense Het probably benign 0.011 phenotype 12/06/2012
14 12298 APN Nckap5 0.000 IGL00833 G1 1 126027152 K622N C A missense Het probably damaging 0.993 12/06/2012
15 12386 APN Nlrp4e 0.000 IGL00833 G1 7 23340471 V740I G A missense Het probably benign 0.001 12/06/2012
16 13095 APN Polr3gl 0.128 IGL00833 G1 3 96578560 D130A T G missense Het probably damaging 0.998 12/06/2012
17 13219 APN Ptprc 0.000 IGL00833 G1 1 138078492 K784R T C missense Het possibly damaging 0.550 phenotype 12/06/2012
18 14314 APN Sycp1 0.473 IGL00833 G1 3 102876301 A G critical splice donor site 2 bp Het probably null phenotype 12/06/2012
19 14438 APN Tg 0.184 IGL00833 G1 15 66688801 T1004I C T missense Het probably benign 0.337 phenotype 12/06/2012
20 14483 APN Tmco5b 0.063 IGL00833 G1 2 113296849 I255N T A missense Het probably damaging 0.994 12/06/2012
21 14688 APN Ubr4 1.000 IGL00833 G1 4 139393159 G A critical splice donor site 1 bp Het probably null phenotype 12/06/2012
22 14923 APN Zeb1 0.924 IGL00833 G1 18 5767774 T762A A G missense Het probably benign 0.003 phenotype 12/06/2012
23 14969 APN Zfp345 0.117 IGL00833 G1 2 150472729 E296G T C missense Het probably damaging 0.997 12/06/2012
[records 1 to 23 of 23]