Incidental Mutations

29 incidental mutations are currently displayed, and affect 29 genes.
6 are Possibly Damaging.
11 are Probably Damaging.
9 are Probably Benign.
3 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 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 29562 APN 2610002M06Rik IGL00476 G1 X 107816160 A C unclassified Het probably benign 04/17/2013
2 12421 APN 4931414P19Rik 0.075 IGL00476 G1 14 54595578 T47A T C missense Het possibly damaging 0.559 12/06/2012
3 12649 APN Adgrv1 0.000 IGL00476 G1 13 81489074 F3416S A G missense Het probably damaging 0.978 phenotype 12/06/2012
4 6192 APN Arhgap42 0.916 IGL00476 G1 9 9006343 D684G T C missense Het probably damaging 0.998 phenotype 04/20/2012
5 5030 APN Atp13a1 1.000 IGL00476 G1 8 69796897 L270P T C missense Het probably damaging 1.000 04/20/2012
6 7195 APN Baz2b 0.242 IGL00476 G1 2 59913739 N1474S T C missense Het probably benign 0.058 phenotype 04/20/2012
7 5049 APN Chrna6 0.084 IGL00476 G1 8 27406532 I439T A G missense Het probably damaging 0.999 phenotype 04/20/2012
8 332174 APN Cylc2 0.057 IGL00476 G1 4 51228157 M76T T C missense Het probably damaging 1.000 08/05/2015
9 12572 APN Ddx19a 0.953 IGL00476 G1 8 110976470 K445R T C missense Het probably benign 0.000 12/06/2012
10 4863 APN Dennd4a 0.417 IGL00476 G1 9 64911762 Y1733F A T missense Het probably damaging 1.000 phenotype 04/20/2012
11 12590 APN Dopey2 0.000 IGL00476 G1 16 93800026 G A unclassified Het probably benign 12/06/2012
12 3857 APN Dpcr1 0.052 IGL00476 G1 17 35638102 H202N G T missense Het possibly damaging 0.462 04/20/2012
13 3994 APN Ephb3 0.888 IGL00476 G1 16 21220415 T A splice site Het probably null phenotype 04/20/2012
14 27366 APN Gpc2 0.000 IGL00476 G1 5 138274309 G A utr 3 prime Het probably benign phenotype 04/17/2013
15 6457 APN Ift172 1.000 IGL00476 G1 5 31275896 Y550H A G missense Het probably damaging 1.000 phenotype 04/20/2012
16 277558 APN Kat2a 1.000 IGL00476 G1 11 100705384 R782W G A missense Het probably damaging 0.995 phenotype 04/16/2015
17 12705 APN Ldhd 0.264 IGL00476 G1 8 111628638 R238S G T missense Het possibly damaging 0.614 phenotype 12/06/2012
18 332176 APN Men1 1.000 IGL00476 G1 19 6337207 G A intron 1593 bp Het probably null phenotype 08/05/2015
19 4177 APN Mipep 0.955 IGL00476 G1 14 60827361 L388R T G missense Het probably damaging 0.996 phenotype 04/20/2012
20 12750 APN Naa35 0.966 IGL00476 G1 13 59630055 D610G A G missense Het probably damaging 1.000 12/06/2012
21 4978 APN Nae1 1.000 IGL00476 G1 8 104526381 L137Q A T missense Het possibly damaging 0.700 phenotype 04/20/2012
22 4682 APN Nt5dc3 0.000 IGL00476 G1 10 86833974 T C unclassified 2 bp Het probably null 04/20/2012
23 12820 APN Nyx 0.000 IGL00476 G1 X 13487025 F373L T C missense Het possibly damaging 0.533 phenotype 12/06/2012
24 4048 APN Scaf11 0.000 IGL00476 G1 15 96418580 D1034E A T missense Het possibly damaging 0.938 04/20/2012
25 332175 APN Sp2 1.000 IGL00476 G1 11 96954561 R578H C T missense Het probably damaging 0.999 phenotype 08/05/2015
26 28282 APN Taar7a 0.091 IGL00476 G1 10 23992396 A T unclassified Het probably benign 04/17/2013
27 6461 APN Tcf23 0.000 IGL00476 G1 5 30973525 C169F G T missense Het probably benign 0.355 phenotype 04/20/2012
28 4613 APN Trim7 0.077 IGL00476 G1 11 48848078 N308I A T missense Het probably benign 0.389 phenotype 04/20/2012
29 14696 APN Ubxn8 0.081 IGL00476 G1 8 33635305 E89G T C missense Het probably benign 0.116 phenotype 12/06/2012
[records 1 to 29 of 29]