Incidental Mutations

36 incidental mutations are currently displayed, and affect 36 genes.
4 are Possibly Damaging.
8 are Probably Damaging.
17 are Probably Benign.
6 are Probably Null.
3 create premature stop codons.
2 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 88175 APN Abca7 0.000 IGL01468 G1 10 80003877 V781I G A missense Het probably benign 0.210 phenotype 11/18/2013
2 88188 APN Aldh5a1 0.359 IGL01468 G1 13 24911553 G T utr 3 prime Het probably benign phenotype 11/18/2013
3 88170 APN Arhgap12 0.000 IGL01468 G1 18 6057576 T435A T C missense Het probably benign 0.010 phenotype 11/18/2013
4 88177 APN Atrnl1 0.263 IGL01468 G1 19 57699712 V870I G A missense Het probably benign 0.023 phenotype 11/18/2013
5 88181 APN Cerkl 0.293 IGL01468 G1 2 79343215 A T critical splice donor site 2 bp Het probably null phenotype 11/18/2013
6 88169 APN Cntnap2 0.266 IGL01468 G1 6 47271371 L13* T A nonsense Het probably null phenotype 11/18/2013
7 88165 APN Cr2 0.165 IGL01468 G1 1 195168535 P208S G A missense Het probably damaging 0.999 phenotype 11/18/2013
8 88180 APN Dapk1 0.310 IGL01468 G1 13 60760798 D1075G A G missense Het probably benign 0.000 phenotype 11/18/2013
9 88168 APN Dhx57 0.211 IGL01468 G1 17 80255610 K863* T A nonsense Het probably null 11/18/2013
10 88182 APN Dnaaf5 0.182 IGL01468 G1 5 139151480 C A splice site Het probably null phenotype 11/18/2013
11 88161 APN Fbxw7 1.000 IGL01468 G1 3 84972499 I336K T A missense Het probably benign 0.207 phenotype 11/18/2013
12 88162 APN Ftcd 0.306 IGL01468 G1 10 76584587 D385G A G missense Het probably benign 0.033 phenotype 11/18/2013
13 278508 APN Gm10153 IGL01468 G1 7 142190041 S117G T C missense Het unknown 04/16/2015
14 88158 APN Gzmb 0.052 IGL01468 G1 14 56260315 Y156C T C missense Het probably benign 0.030 phenotype 11/18/2013
15 88171 APN Herc3 0.000 IGL01468 G1 6 58854895 D83E T A missense Het probably benign 0.001 phenotype 11/18/2013
16 88164 APN Kif2b 0.592 IGL01468 G1 11 91576365 V364A A G missense Het probably damaging 0.998 11/18/2013
17 88187 APN Mknk2 0.000 IGL01468 G1 10 80667664 A G splice site Het probably benign phenotype 11/18/2013
18 88167 APN Olfr1352 0.442 IGL01468 G1 10 78983862 Q24L A T missense Het probably damaging 0.961 phenotype 11/18/2013
19 88178 APN Pgm2 0.718 IGL01468 G1 4 99962170 N197I A T missense Het possibly damaging 0.817 phenotype 11/18/2013
20 88186 APN Prss39 0.016 IGL01468 G1 1 34499400 C T splice site Het probably benign 11/18/2013
21 88179 APN Shroom3 1.000 IGL01468 G1 5 92940342 V236A T C missense Het probably damaging 0.998 phenotype 11/18/2013
22 88184 APN Slc17a8 0.172 IGL01468 G1 10 89592021 C T critical splice donor site 1 bp Het probably null phenotype 11/18/2013
23 88163 APN Slc24a3 0.137 IGL01468 G1 2 145613580 Y463C A G missense Het probably benign 0.158 phenotype 11/18/2013
24 88174 APN Slc4a7 0.803 IGL01468 G1 14 14737480 E149G A G missense Het probably damaging 0.996 phenotype 11/18/2013
25 88183 APN Synj1 1.000 IGL01468 G1 16 91010172 G A splice site Het probably benign phenotype 11/18/2013
26 88160 APN Tas2r138 0.107 IGL01468 G1 6 40612476 M279L T A missense Het probably benign 0.225 phenotype 11/18/2013
27 88185 APN Terb1 0.000 IGL01468 G1 8 104482167 A G intron Het probably benign phenotype 11/18/2013
28 278507 APN Tiparp 0.439 IGL01468 G1 3 65552609 G442* G T nonsense Het probably null phenotype 04/16/2015
29 88176 APN Trmt5 0.975 IGL01468 G1 12 73281104 V442I C T missense Het probably benign 0.076 phenotype 11/18/2013
30 88172 APN Tsc2 1.000 IGL01468 G1 17 24621097 I383V T C missense Het possibly damaging 0.903 phenotype 11/18/2013
31 88159 APN Uchl4 1.000 IGL01468 G1 9 64235716 T160A A G missense Het possibly damaging 0.816 phenotype 11/18/2013
32 88156 APN Vmn2r3 0.000 IGL01468 G1 3 64274961 M439K A T missense Het possibly damaging 0.571 11/18/2013
33 278506 APN Vmn2r4 0.047 IGL01468 G1 3 64406395 N388K A T missense Het probably damaging 0.988 04/16/2015
34 88157 APN Vmn2r52 0.087 IGL01468 G1 7 10158941 L757Q A T missense Het probably damaging 1.000 11/18/2013
35 88173 APN Zfp518a 0.732 IGL01468 G1 19 40916031 V1468A T C missense Het probably benign 0.255 phenotype 11/18/2013
36 88166 APN Zxdc 0.257 IGL01468 G1 6 90373779 E404V A T missense Het probably damaging 1.000 11/18/2013
[records 1 to 36 of 36]