Incidental Mutations

36 incidental mutations are currently displayed, and affect 36 genes.
3 are Possibly Damaging.
15 are Probably Damaging.
10 are Probably Benign.
6 are Probably Null.
4 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 88140 APN Adam1a 0.073 IGL01467 G1 5 121519728 C501R A G missense Het probably damaging 1.000 phenotype 11/18/2013
2 88126 APN Atxn1 0.000 IGL01467 G1 13 45567193 V409I C T missense Het probably damaging 0.998 phenotype 11/18/2013
3 88122 APN Cdkn2aip 0.640 IGL01467 G1 8 47711212 R489G T C missense Het probably damaging 0.975 phenotype 11/18/2013
4 88138 APN Cgn 1.000 IGL01467 G1 3 94779588 S135P A G missense Het probably damaging 1.000 phenotype 11/18/2013
5 88142 APN Cpne3 0.152 IGL01467 G1 4 19553737 C98F C A missense Het probably benign 0.000 phenotype 11/18/2013
6 88132 APN Cyp2c23 0.000 IGL01467 G1 19 44015073 N221S T C missense Het possibly damaging 0.945 phenotype 11/18/2013
7 88143 APN Dnah8 0.295 IGL01467 G1 17 30779916 N3525S A G missense Het probably damaging 1.000 phenotype 11/18/2013
8 88141 APN Efr3b 0.000 IGL01467 G1 12 3969597 E560G T C missense Het probably damaging 0.979 11/18/2013
9 88127 APN Eif2b5 0.965 IGL01467 G1 16 20508964 C154* C A nonsense Het probably null phenotype 11/18/2013
10 88136 APN Eps8l2 0.000 IGL01467 G1 7 141361601 E595G A G missense Het probably damaging 0.995 phenotype 11/18/2013
11 88131 APN Gm8394 0.842 IGL01467 G1 10 85314122 A G exon Het noncoding transcript 11/18/2013
12 88124 APN Gm9839 0.193 IGL01467 G1 1 32519951 I350N A T missense Het probably damaging 1.000 11/18/2013
13 88153 APN Hdlbp 0.946 IGL01467 G1 1 93417698 A T splice site Het probably benign phenotype 11/18/2013
14 88150 APN Il18rap 0.000 IGL01467 G1 1 40548639 I466F A T missense Het probably damaging 1.000 phenotype 11/18/2013
15 88151 APN Itpr1 0.874 IGL01467 G1 6 108488496 I2123N T A missense Het probably damaging 0.964 phenotype 11/18/2013
16 88133 APN Jakmip2 0.312 IGL01467 G1 18 43582287 I58T A G missense Het probably benign 0.342 phenotype 11/18/2013
17 88145 APN Kdm2a 0.964 IGL01467 G1 19 4324407 S899P A G missense Het probably damaging 0.987 phenotype 11/18/2013
18 88149 APN Mmp15 0.000 IGL01467 G1 8 95366331 F113I T A missense Het probably benign 0.305 phenotype 11/18/2013
19 88137 APN Neb 0.784 IGL01467 G1 2 52159487 H6448R T C missense Het possibly damaging 0.545 phenotype 11/18/2013
20 88130 APN Olfr165 0.069 IGL01467 G1 16 19407789 T77A T C missense Het probably benign 0.238 phenotype 11/18/2013
21 88123 APN Olfr340 0.091 IGL01467 G1 2 36452644 R20* C T nonsense Het probably null phenotype 11/18/2013
22 88147 APN Pdgfc 1.000 IGL01467 G1 3 81209091 T251A A G missense Het probably damaging 0.996 phenotype 11/18/2013
23 88155 APN Pdgfra 1.000 IGL01467 G1 5 75185631 T C critical splice donor site 2 bp Het probably null phenotype 11/18/2013
24 88148 APN Pdpk1 1.000 IGL01467 G1 17 24088170 S269P A G missense Het probably damaging 0.984 phenotype 11/18/2013
25 88144 APN Pip4k2c 0.000 IGL01467 G1 10 127199629 F347L A T missense Het probably benign 0.241 phenotype 11/18/2013
26 88152 APN Platr26 0.167 IGL01467 G1 2 71723312 T C exon Het noncoding transcript 11/18/2013
27 88139 APN Pnisr 0.955 IGL01467 G1 4 21874650 C T unclassified Het probably benign 11/18/2013
28 88154 APN Rab3gap1 0.462 IGL01467 G1 1 127930384 T A splice site Het probably null phenotype 11/18/2013
29 88129 APN Scn10a 0.180 IGL01467 G1 9 119658412 V619I C T missense Het probably benign 0.329 phenotype 11/18/2013
30 88146 APN Slc38a11 0.000 IGL01467 G1 2 65316856 T426S T A missense Het probably benign 0.003 11/18/2013
31 88135 APN Son 0.955 IGL01467 G1 16 91657277 S971P T C missense Het possibly damaging 0.930 phenotype 11/18/2013
32 88128 APN Stk33 0.077 IGL01467 G1 7 109329589 I239L T A missense Het probably damaging 0.993 11/18/2013
33 278505 APN Tiparp 0.843 IGL01467 G1 3 65552609 G442* G T nonsense Het probably null phenotype 04/16/2015
34 88134 APN Tmem270 0.050 IGL01467 G1 5 134901961 G T intron Het probably benign 11/18/2013
35 278504 APN Vmn2r4 0.063 IGL01467 G1 3 64406395 N388K A T missense Het probably damaging 0.988 04/16/2015
36 88125 APN Zfp750 0.513 IGL01467 G1 11 121512941 C369* A T nonsense Het probably null phenotype 11/18/2013
[records 1 to 36 of 36]