Incidental Mutations

27 incidental mutations are currently displayed, and affect 27 genes.
6 are Possibly Damaging.
7 are Probably Damaging.
12 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 27 of 27] 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 278740 APN Brip1 0.000 IGL01605 G1 11 86062004 T984S T A missense Het possibly damaging 0.528 phenotype 04/16/2015
2 278734 APN Cdh17 0.089 IGL01605 G1 4 11795670 Y417H T C missense Het probably damaging 1.000 phenotype 04/16/2015
3 278747 APN Chd7 0.951 IGL01605 G1 4 8833834 I1196N T A missense Het probably damaging 1.000 phenotype 04/16/2015
4 278727 APN Cyp3a57 0.075 IGL01605 G1 5 145387044 F447S T C missense Het probably damaging 1.000 04/16/2015
5 278750 APN Dock8 0.096 IGL01605 G1 19 25089888 C T splice site Het probably benign phenotype 04/16/2015
6 278739 APN Fam163b 0.058 IGL01605 G1 2 27112676 F103S A G missense Het probably damaging 0.988 04/16/2015
7 278744 APN G0s2 0.075 IGL01605 G1 1 193272656 L40P A G missense Het probably damaging 0.998 phenotype 04/16/2015
8 278749 APN Gm2046 IGL01605 G1 12 87973760 A T unclassified Het noncoding transcript 04/16/2015
9 278731 APN Gucy1b1 0.909 IGL01605 G1 3 82035353 R494Q C T missense Het probably benign 0.174 phenotype 04/16/2015
10 278735 APN Hsd17b1 0.000 IGL01605 G1 11 101078929 V89A T C missense Het probably damaging 1.000 phenotype 04/16/2015
11 278743 APN Iqcg 0.000 IGL01605 G1 16 33016978 T C unclassified Het probably benign phenotype 04/16/2015
12 278752 APN Lmo7 0.265 IGL01605 G1 14 101910756 T C splice site Het probably benign phenotype 04/16/2015
13 278748 APN Mmp17 0.074 IGL01605 G1 5 129601944 D331G A G missense Het probably benign 0.001 phenotype 04/16/2015
14 278746 APN Mnx1 1.000 IGL01605 G1 5 29477593 D228G T C missense Het unknown phenotype 04/16/2015
15 278751 APN Msh2 0.875 IGL01605 G1 17 87696489 T C unclassified Het probably benign phenotype 04/16/2015
16 278733 APN Pabpc1 0.767 IGL01605 G1 15 36599306 Y382H A G missense Het probably benign 0.363 phenotype 04/16/2015
17 278738 APN Prl7b1 0.000 IGL01605 G1 13 27602044 S214P A G missense Het possibly damaging 0.698 phenotype 04/16/2015
18 93405 APN Ptk2 1.000 IGL01605 G1 15 73264339 C T splice site Het probably benign phenotype 12/09/2013
19 278730 APN Rbpj-ps3 IGL01605 G1 6 46530091 T C intron Het probably benign 04/16/2015
20 278745 APN Sgsm1 0.000 IGL01605 G1 5 113285665 M162K A T missense Het possibly damaging 0.923 04/16/2015
21 278728 APN Skint2 0.059 IGL01605 G1 4 112625994 T199A A G missense Het probably benign 0.438 04/16/2015
22 278737 APN Stim1 1.000 IGL01605 G1 7 102386115 D100G A G missense Het possibly damaging 0.857 phenotype 04/16/2015
23 278736 APN Taar5 0.076 IGL01605 G1 10 23971064 T120I C T missense Het probably benign 0.065 phenotype 04/16/2015
24 278742 APN Trhde 0.086 IGL01605 G1 10 114787943 V352A A G missense Het probably benign 0.000 phenotype 04/16/2015
25 278729 APN Ubap2 0.230 IGL01605 G1 4 41227237 D160V T A missense Het probably damaging 0.999 phenotype 04/16/2015
26 278732 APN Vmn2r18 0.100 IGL01605 G1 5 151586641 V89A A G missense Het possibly damaging 0.642 04/16/2015
27 278741 APN Wbp1l 0.000 IGL01605 G1 19 46654400 D264G A G missense Het possibly damaging 0.921 04/16/2015
[records 1 to 27 of 27]