Incidental Mutations

29 incidental mutations are currently displayed, and affect 29 genes.
6 are Possibly Damaging.
9 are Probably Damaging.
10 are Probably Benign.
2 are Probably Null.
1 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 29 of 29] 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 5527 APN Abhd11 0.000 IGL00338 G1 5 135011985 D217G A G missense Het probably benign 0.213 phenotype 04/20/2012
2 8865 APN Ankar 0.065 IGL00338 G1 1 72690131 Y285F T A missense Het probably damaging 1.000 12/06/2012
3 5024 APN Ano8 0.000 IGL00338 G1 8 71484258 C A splice site Het probably benign 04/20/2012
4 332330 APN Bche 0.000 IGL00338 G1 3 73701307 V262A A G missense Het probably benign 0.001 phenotype 08/05/2015
5 6929 APN Car13 0.000 IGL00338 G1 3 14656904 T C splice site Het probably benign phenotype 04/20/2012
6 332331 APN Cd244 0.054 IGL00338 G1 1 171574370 T A critical splice donor site 2 bp Het probably null phenotype 08/05/2015
7 7233 APN Cfap157 0.091 IGL00338 G1 2 32781383 D137G T C missense Het probably damaging 1.000 phenotype 04/20/2012
8 6078 APN Cobl 0.000 IGL00338 G1 11 12375813 R119G T C missense Het possibly damaging 0.895 phenotype 04/20/2012
9 332328 APN Gm4553 IGL00338 G1 7 142165227 S155G T C missense Het unknown 08/05/2015
10 6263 APN Gp2 0.000 IGL00338 G1 7 119454390 M116T A G missense Het probably damaging 0.960 phenotype 04/20/2012
11 332329 APN Gp5 0.000 IGL00338 G1 16 30308822 A345S C A missense Het probably benign 0.013 phenotype 08/05/2015
12 4395 APN Gphn 1.000 IGL00338 G1 12 78504632 I285F A T missense Het probably damaging 0.999 phenotype 04/20/2012
13 5741 APN Heatr5b 0.284 IGL00338 G1 17 78803434 V995A A G missense Het probably damaging 1.000 0.330 04/20/2012
14 7480 APN Hecw2 0.657 IGL00338 G1 1 53827881 T C splice site Het probably benign phenotype 04/20/2012
15 4964 APN Hydin 0.701 IGL00338 G1 8 110569802 N3654K C A missense Het possibly damaging 0.688 phenotype 04/20/2012
16 6580 APN Inpp5b 0.186 IGL00338 G1 4 124784375 Y440C A G missense Het possibly damaging 0.944 phenotype 04/20/2012
17 7125 APN Olfr1256 0.098 IGL00338 G1 2 89835458 Y162* A T nonsense Het probably null phenotype 04/20/2012
18 4053 APN Pphln1 1.000 IGL00338 G1 15 93465210 K306E A G missense Het probably damaging 0.999 phenotype 04/20/2012
19 28111 APN Rnf26 0.144 IGL00338 G1 9 44112859 S31A A C missense Het probably benign 0.335 phenotype 04/17/2013
20 4726 APN Ros1 0.146 IGL00338 G1 10 52125811 S1072T A T missense Het probably benign 0.000 phenotype 04/20/2012
21 277838 APN Skiv2l 1.000 IGL00338 G1 17 34846667 W304R A G missense Het probably damaging 0.988 phenotype 04/16/2015
22 4793 APN Slc22a14 0.079 IGL00338 G1 9 119178513 F277L A G missense Het possibly damaging 0.580 phenotype 04/20/2012
23 3260 APN Slc22a26 0.052 IGL00338 G1 19 7782975 L468I A T missense Het probably benign 0.252 04/20/2012
24 6826 APN Tchh 0.068 IGL00338 G1 3 93447644 L1464F C T missense Het unknown 04/20/2012
25 5886 APN Tmem260 0.000 IGL00338 G1 14 48477636 T249M C T missense Het probably damaging 0.972 0.647 04/20/2012
26 7145 APN Ttn 1.000 IGL00338 G1 2 76974065 S288P A G missense Het probably damaging 0.999 phenotype 04/20/2012
27 5188 APN Usp17lc 1.000 IGL00338 G1 7 103418941 H481R A G missense Het possibly damaging 0.743 0.301 phenotype 04/20/2012
28 6379 APN Vps50 0.870 IGL00338 G1 6 3602670 T929M C T missense Het probably benign 0.003 04/20/2012
29 3997 APN Zdhhc8 0.673 IGL00338 G1 16 18225196 L380P A G missense Het possibly damaging 0.656 phenotype 04/20/2012
[records 1 to 29 of 29]