Incidental Mutations

32 incidental mutations are currently displayed, and affect 32 genes.
6 are Possibly Damaging.
9 are Probably Damaging.
17 are Probably Benign.
0 are Probably Null.
0 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 32 of 32] 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 76162 APN 1300017J02Rik 0.263 IGL01371 G1 9 103254776 E504G T C missense Het possibly damaging 0.480 10/07/2013
2 76143 APN Abcc9 0.104 IGL01371 G1 6 142656614 R691Q C T missense Het probably benign 0.035 phenotype 10/07/2013
3 76150 APN AI314180 0.366 IGL01371 G1 4 58809718 L1583P A G missense Het probably damaging 1.000 10/07/2013
4 76140 APN Ambra1 0.877 IGL01371 G1 2 91825286 G700W G T missense Het probably damaging 1.000 phenotype 10/07/2013
5 76155 APN Atp6v1c1 1.000 IGL01371 G1 15 38682960 I198V A G missense Het probably benign 0.000 phenotype 10/07/2013
6 76158 APN Bptf 1.000 IGL01371 G1 11 107055907 N2353S T C missense Het probably benign 0.002 phenotype 10/07/2013
7 76161 APN Cd84 0.000 IGL01371 G1 1 171886370 T312S A T missense Het probably benign 0.357 phenotype 10/07/2013
8 76146 APN Chl1 0.525 IGL01371 G1 6 103715364 C1064F G T missense Het probably damaging 1.000 phenotype 10/07/2013
9 76137 APN Clca4a 0.297 IGL01371 G1 3 144960672 D473G T C missense Het probably damaging 1.000 10/07/2013
10 76151 APN Dsp 1.000 IGL01371 G1 13 38193617 R1793G A G missense Het probably benign 0.130 phenotype 10/07/2013
11 76148 APN Dync1h1 1.000 IGL01371 G1 12 110638851 N2374S A G missense Het probably benign 0.047 phenotype 10/07/2013
12 76142 APN Gm43191 IGL01371 G1 3 116645463 I130N A T missense Het probably damaging 0.988 10/07/2013
13 76147 APN Gm5134 0.141 IGL01371 G1 10 76004747 L475R T G missense Het probably damaging 0.988 10/07/2013
14 76160 APN Grm1 0.187 IGL01371 G1 10 10720039 V615A A G missense Het probably benign 0.013 phenotype 10/07/2013
15 76145 APN Loxl1 0.000 IGL01371 G1 9 58294422 Q462L T A missense Het possibly damaging 0.893 phenotype 10/07/2013
16 76153 APN Nwd1 0.249 IGL01371 G1 8 72675115 W755R T C missense Het probably damaging 1.000 phenotype 10/07/2013
17 76159 APN Olfr1102 0.160 IGL01371 G1 2 87002923 K318M A T missense Het probably benign 0.311 phenotype 10/07/2013
18 76138 APN Olfr1408 0.068 IGL01371 G1 1 173130531 S229P A G missense Het possibly damaging 0.671 phenotype 10/07/2013
19 76133 APN Olfr1459 0.083 IGL01371 G1 19 13145828 T277I G A missense Het possibly damaging 0.822 phenotype 10/07/2013
20 76154 APN Otud4 0.147 IGL01371 G1 8 79673761 F1034L T C missense Het probably damaging 0.999 phenotype 10/07/2013
21 76134 APN Pakap IGL01371 G1 4 57856325 D551E C A missense Het probably benign 0.025 phenotype 10/07/2013
22 76144 APN Panx3 0.000 IGL01371 G1 9 37661475 T260P T G missense Het probably benign 0.025 phenotype 10/07/2013
23 76135 APN Ppfia4 0.101 IGL01371 G1 1 134328086 S194T A T missense Het probably benign 0.001 10/07/2013
24 76157 APN Rnf135 0.000 IGL01371 G1 11 80189255 I124N T A missense Het probably benign 0.131 phenotype 10/07/2013
25 76149 APN Rpf1 0.918 IGL01371 G1 3 146507547 N283S T C missense Het probably damaging 1.000 10/07/2013
26 76163 APN Smg5 1.000 IGL01371 G1 3 88359644 A G unclassified Het probably benign phenotype 10/07/2013
27 76152 APN Stard9 0.193 IGL01371 G1 2 120701368 E2702G A G missense Het probably benign 0.041 10/07/2013
28 76141 APN Tbk1 1.000 IGL01371 G1 10 121559871 M439K A T missense Het probably benign 0.088 phenotype 10/07/2013
29 76139 APN Tmem235 0.062 IGL01371 G1 11 117862306 L85P T C missense Het possibly damaging 0.952 10/07/2013
30 76136 APN Trhde 0.100 IGL01371 G1 10 114588500 V460E A T missense Het possibly damaging 0.567 0.919 phenotype 10/07/2013
31 76164 APN Ttn 1.000 IGL01371 G1 2 76790264 T C splice site Het probably benign phenotype 10/07/2013
32 76156 APN Vmn1r83 0.058 IGL01371 G1 7 12321233 F299S A G missense Het probably benign 0.103 10/07/2013
[records 1 to 32 of 32]