Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
5 are Possibly Damaging.
14 are Probably Damaging.
13 are Probably Benign.
1 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 33 of 33] 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 27611 APN Aass 0.000 IGL00916 G1 6 23075852 Q762L T A missense Het probably benign 0.096 phenotype 04/17/2013
2 29498 APN Aldh1a1 0.847 IGL00916 G1 19 20619997 V114A T C missense Het probably benign 0.129 phenotype 04/17/2013
3 28322 APN Ano4 0.000 IGL00916 G1 10 88998098 I459V T C missense Het probably benign 0.014 04/17/2013
4 28515 APN Atad5 1.000 IGL00916 G1 11 80119000 P1199S C T missense Het probably damaging 1.000 phenotype 04/17/2013
5 27610 APN Bmp10 1.000 IGL00916 G1 6 87429160 F43S T C missense Het possibly damaging 0.865 phenotype 04/17/2013
6 29138 APN Cd96 0.000 IGL00916 G1 16 46041312 E505G T C missense Het probably benign 0.069 phenotype 04/17/2013
7 29265 APN D17Wsu92e 0.000 IGL00916 G1 17 27767919 Y278H A G missense Het probably damaging 0.996 04/17/2013
8 28721 APN Eapp 0.906 IGL00916 G1 12 54692808 T75A T C missense Het possibly damaging 0.778 phenotype 04/17/2013
9 27408 APN Emilin1 0.143 IGL00916 G1 5 30913902 Y10H T C missense Het probably damaging 0.972 phenotype 04/17/2013
10 28937 APN Ercc6 0.495 IGL00916 G1 14 32562655 A G intron Het probably benign phenotype 04/17/2013
11 28513 APN Gucy2e 0.550 IGL00916 G1 11 69223097 I1089V T C missense Het possibly damaging 0.882 phenotype 04/17/2013
12 27232 APN H6pd 0.115 IGL00916 G1 4 149994468 C A critical splice donor site 1 bp Het probably null phenotype 04/17/2013
13 27086 APN Igsf10 0.255 IGL00916 G1 3 59331127 F544L A T missense Het probably damaging 0.970 04/17/2013
14 27609 APN Il23r 0.000 IGL00916 G1 6 67473931 Y188C T C missense Het probably damaging 1.000 phenotype 04/17/2013
15 28514 APN Inpp5j 0.341 IGL00916 G1 11 3502389 E287G T C missense Het probably damaging 0.999 phenotype 04/17/2013
16 27608 APN Lrp6 0.965 IGL00916 G1 6 134484289 D735G T C missense Het probably damaging 0.999 phenotype 04/17/2013
17 27231 APN Mast2 0.000 IGL00916 G1 4 116327633 M240K A T missense Het possibly damaging 0.885 phenotype 04/17/2013
18 26629 APN Mreg 0.000 IGL00916 G1 1 72164132 T96S T A missense Het probably benign 0.033 phenotype 04/17/2013
19 29499 APN Mta2 1.000 IGL00916 G1 19 8947101 M220L A T missense Het probably benign 0.231 phenotype 04/17/2013
20 28938 APN Mycbp2 1.000 IGL00916 G1 14 103291283 A G splice site Het probably benign phenotype 04/17/2013
21 28840 APN Naip2 0.074 IGL00916 G1 13 100161431 N699I T A missense Het probably damaging 0.969 phenotype 04/17/2013
22 27409 APN Ncapg 0.949 IGL00916 G1 5 45671192 I95S T G missense Het probably benign 0.366 phenotype 04/17/2013
23 28011 APN Ndufa13 1.000 IGL00916 G1 8 69894419 A G intron Het probably benign phenotype 04/17/2013
24 28722 APN Nol10 0.962 IGL00916 G1 12 17361129 T A splice site Het probably benign 04/17/2013
25 28841 APN Parp8 0.000 IGL00916 G1 13 116927323 I85F T A missense Het probably damaging 0.999 04/17/2013
26 26630 APN Rgs2 0.203 IGL00916 G1 1 144002229 I78F T A missense Het probably damaging 1.000 phenotype 04/17/2013
27 27612 APN Rpia 1.000 IGL00916 G1 6 70775102 C T splice site Het probably benign phenotype 04/17/2013
28 28323 APN Sec63 1.000 IGL00916 G1 10 42812457 S488P T C missense Het possibly damaging 0.565 phenotype 04/17/2013
29 29050 APN Tfcp2 0.000 IGL00916 G1 15 100520678 H201P T G missense Het probably damaging 1.000 phenotype 04/17/2013
30 28720 APN Tnfaip2 0.000 IGL00916 G1 12 111453549 I705R T G missense Het probably damaging 1.000 phenotype 04/17/2013
31 26868 APN Ttf1 0.895 IGL00916 G1 2 29070042 N554S A G missense Het probably benign 0.051 04/17/2013
32 27410 APN Ulk1 0.000 IGL00916 G1 5 110793011 S351P A G missense Het probably damaging 0.999 phenotype 04/17/2013
33 27794 APN Zp2 0.060 IGL00916 G1 7 120138174 N264Y T A missense Het probably damaging 1.000 phenotype 04/17/2013
[records 1 to 33 of 33]