Incidental Mutations

35 incidental mutations are currently displayed, and affect 35 genes.
5 are Possibly Damaging.
10 are Probably Damaging.
16 are Probably Benign.
4 are Probably Null.
1 create premature stop codons.
3 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 5654 APN 9130011E15Rik 1.000 IGL00392 G1 19 45940488 H389P T G missense Het probably benign 0.195 04/20/2012
2 5217 APN Alpk3 0.484 IGL00392 G1 7 81078009 Y296H T C missense Het possibly damaging 0.952 phenotype 04/20/2012
3 5493 APN Brca2 1.000 IGL00392 G1 5 150541240 T1490A A G missense Het probably benign 0.017 phenotype 04/20/2012
4 3195 APN Btaf1 0.961 IGL00392 G1 19 37009702 D1732V A T missense Het probably damaging 1.000 phenotype 04/20/2012
5 6547 APN Capzb 1.000 IGL00392 G1 4 139288947 I273T T C missense Het probably benign 0.002 phenotype 04/20/2012
6 4331 APN Carmil1 0.000 IGL00392 G1 13 24094491 T165I G A missense Het probably damaging 0.998 phenotype 04/20/2012
7 5632 APN Cc2d2a 0.747 IGL00392 G1 5 43724380 A G splice site Het probably benign phenotype 04/20/2012
8 7170 APN Ccdc173 0.095 IGL00392 G1 2 69771984 H361R T C missense Het probably benign 0.000 04/20/2012
9 6968 APN Cdh22 0.164 IGL00392 G1 2 165112601 Y667H A G missense Het possibly damaging 0.543 phenotype 04/20/2012
10 4059 APN Celsr1 0.735 IGL00392 G1 15 85931345 Q1823L T A missense Het probably benign 0.043 phenotype 04/20/2012
11 332364 APN Cntrl 0.889 IGL00392 G1 2 35137814 T C splice site Het probably benign phenotype 08/05/2015
12 5627 APN Dhx15 0.938 IGL00392 G1 5 52157582 A T splice site Het probably benign phenotype 04/20/2012
13 5958 APN Dip2c 0.569 IGL00392 G1 13 9493108 D30V A T missense Het probably damaging 0.974 phenotype 04/20/2012
14 6088 APN Dyrk2 0.507 IGL00392 G1 10 118859844 D503G T C missense Het probably damaging 0.999 phenotype 04/20/2012
15 4752 APN Enpp1 0.346 IGL00392 G1 10 24645427 I801F T A missense Het possibly damaging 0.929 phenotype 04/20/2012
16 7124 APN Fnbp4 0.907 IGL00392 G1 2 90751622 A C splice site Het probably benign 04/20/2012
17 5261 APN Klk1b5 0.043 IGL00392 G1 7 44216504 W2R T A missense Het probably benign 0.001 phenotype 04/20/2012
18 4748 APN Lama2 0.335 IGL00392 G1 10 27188265 K1240R T C missense Het probably benign 0.006 phenotype 04/20/2012
19 4107 APN Matn2 0.000 IGL00392 G1 15 34402856 N409S A G missense Het probably benign 0.003 phenotype 04/20/2012
20 3380 APN Mep1b 0.108 IGL00392 G1 18 21084186 K121* A T nonsense Het probably null phenotype 04/20/2012
21 5766 APN Mettl26 0.105 IGL00392 G1 17 25876124 T C critical splice donor site 2 bp Het probably null 04/20/2012
22 332362 APN Myh7 0.812 IGL00392 G1 14 54987388 E574G T C missense Het probably damaging 1.000 phenotype 08/05/2015
23 5757 APN Nfkbie 0.364 IGL00392 G1 17 45560213 G A critical splice donor site 1 bp Het probably null phenotype 04/20/2012
24 3423 APN Nlrc4 0.143 IGL00392 G1 17 74446534 R285G T C missense Het probably benign 0.016 phenotype 04/20/2012
25 7266 APN Pax8 1.000 IGL00392 G1 2 24443132 Y66C T C missense Het probably damaging 1.000 phenotype 04/20/2012
26 7287 APN Plxna2 0.000 IGL00392 G1 1 194800568 D1523G A G missense Het probably damaging 1.000 phenotype 04/20/2012
27 7334 APN Pou2f1 1.000 IGL00392 G1 1 165896590 A G splice site Het probably benign phenotype 04/20/2012
28 5631 APN Prom1 0.309 IGL00392 G1 5 44007021 A G critical splice donor site 2 bp Het probably null phenotype 04/20/2012
29 6937 APN Ptk6 0.000 IGL00392 G1 2 181195818 D436G T C missense Het probably benign 0.001 phenotype 04/20/2012
30 4914 APN Robo4 0.216 IGL00392 G1 9 37408229 F592I T A missense Het probably damaging 1.000 phenotype 04/20/2012
31 5903 APN Sec24c 1.000 IGL00392 G1 14 20693203 S964R C A missense Het probably benign 0.028 phenotype 04/20/2012
32 332363 APN Sgcb 0.207 IGL00392 G1 5 73635678 N260K G T missense Het possibly damaging 0.919 phenotype 08/05/2015
33 4479 APN Smarcd2 0.944 IGL00392 G1 11 106265904 D221G T C missense Het probably damaging 1.000 phenotype 04/20/2012
34 6685 APN Unc13b 0.586 IGL00392 G1 4 43240285 R3569W C T missense Het probably damaging 0.998 0.068 phenotype 04/20/2012
35 5692 APN Zfpl1 0.000 IGL00392 G1 19 6081107 R285L C A missense Het possibly damaging 0.870 04/20/2012
[records 1 to 35 of 35]