Incidental Mutations

28 incidental mutations are currently displayed, and affect 28 genes.
5 are Possibly Damaging.
5 are Probably Damaging.
15 are Probably Benign.
3 are Probably Null.
1 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 28 of 28] 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 184515 APN 9530053A07Rik 0.152 IGL02036 G1 7 28137525 V290M G A missense Het possibly damaging 0.824 05/07/2014
2 184530 APN Cep290 0.937 IGL02036 G1 10 100558100 C2056* T A nonsense Het probably null phenotype 05/07/2014
3 184508 APN Cyp2c38 0.146 IGL02036 G1 19 39460316 D143V T A missense Het probably null 0.966 05/07/2014
4 184510 APN Ddx10 0.975 IGL02036 G1 9 53204183 K617R T C missense Het probably benign 0.001 phenotype 05/07/2014
5 184524 APN Dgat2l6 IGL02036 G1 X 100545593 I336N T A missense Het probably damaging 0.997 phenotype 05/07/2014
6 184511 APN Dopey1 0.333 IGL02036 G1 9 86531765 I1906M A G missense Het probably benign 0.180 05/07/2014
7 184526 APN Dpep3 0.127 IGL02036 G1 8 105973785 T430P T G missense Het probably benign 0.000 phenotype 05/07/2014
8 184532 APN Dph1 1.000 IGL02036 G1 11 75184165 T C splice site 3 bp Het probably null phenotype 05/07/2014
9 184520 APN Epha7 0.519 IGL02036 G1 4 28950509 S775P T C missense Het probably damaging 1.000 phenotype 05/07/2014
10 184535 APN F5 1.000 IGL02036 G1 1 164183002 A G splice site Het probably benign phenotype 05/07/2014
11 184519 APN Hdx 0.063 IGL02036 G1 X 111659867 T342S T A missense Het probably benign 0.004 phenotype 05/07/2014
12 184534 APN Inpp4a 0.362 IGL02036 G1 1 37377569 T C intron Het probably benign phenotype 05/07/2014
13 184514 APN Itgad 0.057 IGL02036 G1 7 128189821 T515A A G missense Het possibly damaging 0.493 phenotype 05/07/2014
14 184525 APN Kcnc2 0.189 IGL02036 G1 10 112455926 S340T T A missense Het possibly damaging 0.943 phenotype 05/07/2014
15 184516 APN Krba1 0.084 IGL02036 G1 6 48415642 T830I C T missense Het possibly damaging 0.947 05/07/2014
16 184533 APN Lrch1 0.218 IGL02036 G1 14 74795293 G A splice site Het probably benign phenotype 05/07/2014
17 184512 APN Mag 0.000 IGL02036 G1 7 30908452 V295M C T missense Het probably damaging 0.971 phenotype 05/07/2014
18 184523 APN Mmp16 0.000 IGL02036 G1 4 18093371 D375E T A missense Het probably benign 0.001 phenotype 05/07/2014
19 184509 APN Olfr1216 0.039 IGL02036 G1 2 89013479 V195A A G missense Het probably benign 0.005 phenotype 05/07/2014
20 184522 APN Olfr314 0.000 IGL02036 G1 11 58787097 Y288H T C missense Het probably damaging 1.000 phenotype 05/07/2014
21 184529 APN Olfr90 0.044 IGL02036 G1 17 37085667 F166S A G missense Het probably damaging 1.000 phenotype 05/07/2014
22 184531 APN Pcyox1l 0.189 IGL02036 G1 18 61707536 T C unclassified Het probably benign 05/07/2014
23 184518 APN Secisbp2l 0.422 IGL02036 G1 2 125758207 S403P A G missense Het probably benign 0.000 05/07/2014
24 184527 APN Sh3tc2 0.000 IGL02036 G1 18 62014907 H1229Q T A missense Het probably benign 0.175 phenotype 05/07/2014
25 184528 APN Svep1 0.728 IGL02036 G1 4 58088245 W1735G A C missense Het possibly damaging 0.847 phenotype 05/07/2014
26 184517 APN Tbxas1 0.062 IGL02036 G1 6 39021157 C220S T A missense Het probably benign 0.000 phenotype 05/07/2014
27 184521 APN Vmn1r173 0.539 IGL02036 G1 7 23702896 M185I G T missense Het probably benign 0.040 05/07/2014
28 184513 APN Ywhag 0.000 IGL02036 G1 5 135911494 V82A A G missense Het probably benign 0.075 phenotype 05/07/2014
[records 1 to 28 of 28]