Incidental Mutations

26 incidental mutations are currently displayed, and affect 26 genes.
3 are Possibly Damaging.
16 are Probably Damaging.
7 are Probably Benign.
0 are Probably Null.
0 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 26 of 26] 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 183378 APN Ap5m1 0.000 IGL02011 G1 14 49081135 T A unclassified Het probably benign 05/07/2014
2 183357 APN Arg1 0.194 IGL02011 G1 10 24916377 T215A T C missense Het probably benign 0.001 phenotype 05/07/2014
3 183363 APN Arhgap15 0.424 IGL02011 G1 2 43780755 K50N A T missense Het probably damaging 1.000 phenotype 05/07/2014
4 279272 APN Ctdsp1 0.000 IGL02011 G1 1 74394016 C T splice site Het probably benign phenotype 04/16/2015
5 183353 APN Cwc22 1.000 IGL02011 G1 2 77921022 D363E A T missense Het possibly damaging 0.882 05/07/2014
6 183365 APN Drd2 0.225 IGL02011 G1 9 49406958 C400F G T missense Het probably damaging 1.000 phenotype 05/07/2014
7 183367 APN Eef1akmt1 0.000 IGL02011 G1 14 57558098 Y65N A T missense Het probably damaging 1.000 05/07/2014
8 183358 APN Gbp10 0.067 IGL02011 G1 5 105221101 G291W C A missense Het probably damaging 0.999 05/07/2014
9 183375 APN Lrit1 0.076 IGL02011 G1 14 37062323 V536E T A missense Het probably damaging 1.000 phenotype 05/07/2014
10 183355 APN Olfr1411 0.067 IGL02011 G1 1 92596899 Y127N T A missense Het probably damaging 1.000 phenotype 05/07/2014
11 183372 APN Olfr464 0.088 IGL02011 G1 11 87914882 W8L C A missense Het probably benign 0.011 phenotype 05/07/2014
12 183356 APN Olfr599 0.060 IGL02011 G1 7 103338849 R265L G T missense Het probably damaging 0.984 phenotype 05/07/2014
13 183361 APN Pcdh12 0.000 IGL02011 G1 18 38281420 G884D C T missense Het probably damaging 0.998 phenotype 05/07/2014
14 183376 APN Pih1d1 0.507 IGL02011 G1 7 45156732 A31S G T missense Het probably damaging 1.000 05/07/2014
15 183364 APN Plcxd2 0.208 IGL02011 G1 16 45965091 D317G T C missense Het probably damaging 0.960 05/07/2014
16 183370 APN Prkaca 0.576 IGL02011 G1 8 83990936 F231S T C missense Het probably damaging 1.000 phenotype 05/07/2014
17 183354 APN Raet1d 0.077 IGL02011 G1 10 22371574 I183K T A missense Het probably damaging 0.998 05/07/2014
18 183373 APN Scaper 0.622 IGL02011 G1 9 55580322 F752S A G missense Het probably damaging 1.000 05/07/2014
19 183366 APN Shisa9 0.077 IGL02011 G1 16 12244638 T241I C T missense Het possibly damaging 0.873 phenotype 05/07/2014
20 183362 APN Taar9 0.106 IGL02011 G1 10 24108579 R319H C T missense Het possibly damaging 0.930 0.179 phenotype 05/07/2014
21 183374 APN Unkl 0.264 IGL02011 G1 17 25218591 V365E T A missense Het probably damaging 0.996 phenotype 05/07/2014
22 183360 APN Usp34 0.626 IGL02011 G1 11 23471554 S3077F C T missense Het probably damaging 0.992 05/07/2014
23 183371 APN Vps16 0.965 IGL02011 G1 2 130441479 I566V A G missense Het probably benign 0.037 phenotype 05/07/2014
24 183368 APN Vrk2 0.183 IGL02011 G1 11 26471717 T414S T A missense Het probably benign 0.104 phenotype 05/07/2014
25 183377 APN Xpnpep1 1.000 IGL02011 G1 19 53002465 A T critical splice donor site 9 bp Het probably benign phenotype 05/07/2014
26 183359 APN Zfp804a 0.195 IGL02011 G1 2 82256691 Q288R A G missense Het probably damaging 0.997 phenotype 05/07/2014
[records 1 to 26 of 26]