Incidental Mutations

35 incidental mutations are currently displayed, and affect 35 genes.
8 are Possibly Damaging.
12 are Probably Damaging.
12 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 35 of 35] 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 93430 APN 1600012H06Rik 0.165 IGL01606 G1 17 14943863 D84G A G missense Het probably damaging 1.000 phenotype 12/09/2013
2 93420 APN Adat3 0.085 IGL01606 G1 10 80607338 I337F A T missense Het probably damaging 0.965 phenotype 12/09/2013
3 93427 APN Carmil3 0.270 IGL01606 G1 14 55493849 N128K T A missense Het possibly damaging 0.828 12/09/2013
4 93413 APN Ceacam2 0.127 IGL01606 G1 7 25530707 E158G T C missense Het possibly damaging 0.949 phenotype 12/09/2013
5 93422 APN Cel 0.189 IGL01606 G1 2 28560564 I150V T C missense Het probably benign 0.038 phenotype 12/09/2013
6 93438 APN Chd5 0.000 IGL01606 G1 4 152360975 H441R A G missense Het probably damaging 0.994 phenotype 12/09/2013
7 93418 APN Clic5 0.000 IGL01606 G1 17 44248746 R109L G T missense Het probably benign 0.001 phenotype 12/09/2013
8 93424 APN Cpd 0.924 IGL01606 G1 11 76812640 M466V T C missense Het probably benign 0.000 phenotype 12/09/2013
9 93439 APN Cyp39a1 0.064 IGL01606 G1 17 43746618 T A splice site Het probably benign phenotype 12/09/2013
10 93408 APN Dnah11 0.611 IGL01606 G1 12 117983032 A3106S C A missense Het probably benign 0.151 phenotype 12/09/2013
11 93440 APN Fasn 1.000 IGL01606 G1 11 120809023 A C critical splice donor site 2 bp Het probably null phenotype 12/09/2013
12 93417 APN Fat1 1.000 IGL01606 G1 8 45023049 V1688I G A missense Het probably benign 0.259 phenotype 12/09/2013
13 93436 APN Fibcd1 0.057 IGL01606 G1 2 31833853 I258T A G missense Het probably benign 0.209 phenotype 12/09/2013
14 93415 APN Frem2 1.000 IGL01606 G1 3 53653591 R1165I C A missense Het possibly damaging 0.692 phenotype 12/09/2013
15 93433 APN Gm5627 IGL01606 G1 9 102749486 C T exon Het noncoding transcript 12/09/2013
16 93410 APN Gm5862 0.175 IGL01606 G1 5 26019516 T152S T A missense Het probably benign 0.000 12/09/2013
17 93425 APN Gnb3 0.000 IGL01606 G1 6 124837255 D154V T A missense Het probably damaging 0.977 phenotype 12/09/2013
18 93406 APN Ighv1-14 IGL01606 G1 12 114646837 T C exon Het noncoding transcript 12/09/2013
19 93412 APN Klrb1 0.000 IGL01606 G1 6 128723005 E14D C A missense Het probably benign 0.007 phenotype 12/09/2013
20 93429 APN Osbpl1a 0.145 IGL01606 G1 18 12756214 D556E A T missense Het possibly damaging 0.787 phenotype 12/09/2013
21 93435 APN Pkd1 1.000 IGL01606 G1 17 24576523 V2330A T C missense Het probably damaging 0.969 phenotype 12/09/2013
22 93416 APN Pkdrej 0.072 IGL01606 G1 15 85817700 K1345R T C missense Het possibly damaging 0.670 phenotype 12/09/2013
23 93431 APN Plxna4 0.557 IGL01606 G1 6 32158001 F1756L A G missense Het probably damaging 0.999 phenotype 12/09/2013
24 93421 APN Psg28 0.072 IGL01606 G1 7 18430371 S139A A C missense Het probably benign 0.010 12/09/2013
25 93437 APN Ptpru 0.000 IGL01606 G1 4 131808481 I395N A T missense Het possibly damaging 0.691 phenotype 12/09/2013
26 93407 APN Reps1 0.518 IGL01606 G1 10 18107687 E426G A G missense Het probably damaging 0.999 phenotype 12/09/2013
27 93409 APN Rtp4 0.114 IGL01606 G1 16 23613254 S179T T A missense Het probably benign 0.177 12/09/2013
28 93428 APN Sh3pxd2a 1.000 IGL01606 G1 19 47268596 R561L C A missense Het probably benign 0.000 phenotype 12/09/2013
29 93414 APN Slc29a2 0.248 IGL01606 G1 19 5027439 L215Q T A missense Het possibly damaging 0.724 phenotype 12/09/2013
30 93411 APN Slc44a4 0.000 IGL01606 G1 17 34929018 F653L T C missense Het probably damaging 1.000 phenotype 12/09/2013
31 93434 APN Sulf1 0.614 IGL01606 G1 1 12836204 R490L G T missense Het possibly damaging 0.872 phenotype 12/09/2013
32 93432 APN Ttll4 0.244 IGL01606 G1 1 74685893 L602P T C missense Het probably damaging 1.000 12/09/2013
33 93426 APN Ttn 1.000 IGL01606 G1 2 76776790 V17963A A G missense Het probably damaging 0.998 phenotype 12/09/2013
34 93423 APN Urb1 1.000 IGL01606 G1 16 90760459 S1760P A G missense Het probably damaging 0.999 12/09/2013
35 93419 APN Zmynd11 0.734 IGL01606 G1 13 9697688 R149W G A missense Het probably damaging 0.999 phenotype 12/09/2013
[records 1 to 35 of 35]