Incidental Mutations

29 incidental mutations are currently displayed, and affect 29 genes.
4 are Possibly Damaging.
11 are Probably Damaging.
12 are Probably Benign.
2 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 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 5908 APN 4930452B06Rik 0.080 IGL00423 G1 14 8473370 P600S G A missense Het possibly damaging 0.572 04/20/2012
2 5224 APN Acan 1.000 IGL00423 G1 7 79097824 E781G A G missense Het probably benign 0.001 phenotype 04/20/2012
3 6295 APN Acp7 0.282 IGL00423 G1 7 28614697 T358A T C missense Het possibly damaging 0.790 phenotype 04/20/2012
4 8582 APN Adamtsl2 1.000 IGL00423 G1 2 27085088 T199K C A missense Het probably damaging 0.998 phenotype 12/06/2012
5 7046 APN Ap4e1 0.139 IGL00423 G1 2 127028289 S179T T A missense Het probably damaging 0.990 phenotype 04/20/2012
6 6344 APN BC048671 0.051 IGL00423 G1 6 90303218 T39A A G missense Het probably benign 0.019 04/20/2012
7 6696 APN Cnr1 0.191 IGL00423 G1 4 33944116 S168N G A missense Het probably damaging 1.000 phenotype 04/20/2012
8 6927 APN Cp 0.000 IGL00423 G1 3 19985662 V881A T C missense Het possibly damaging 0.948 phenotype 04/20/2012
9 6603 APN Cyp4x1 0.190 IGL00423 G1 4 115121948 T151A T C missense Het probably benign 0.002 phenotype 04/20/2012
10 4890 APN Drd2 0.427 IGL00423 G1 9 49395758 I48T T C missense Het probably damaging 0.999 phenotype 04/20/2012
11 6056 APN Gemin5 1.000 IGL00423 G1 11 58163817 I253N A T missense Het probably damaging 0.999 phenotype 04/20/2012
12 5439 APN Herc3 0.000 IGL00423 G1 6 58868715 I407K T A missense Het probably damaging 0.991 phenotype 04/20/2012
13 11422 APN Ighmbp2 1.000 IGL00423 G1 19 3268704 H457Q G T missense Het probably benign 0.019 phenotype 12/06/2012
14 4326 APN Mboat1 0.000 IGL00423 G1 13 30195793 A G splice site Het probably benign phenotype 04/20/2012
15 4578 APN Myh2 0.268 IGL00423 G1 11 67197345 V1929A T C missense Het probably benign 0.000 phenotype 04/20/2012
16 27733 APN Nucb2 0.156 IGL00423 G1 7 116521831 T A splice site Het probably benign phenotype 04/17/2013
17 12945 APN Pcsk5 1.000 IGL00423 G1 19 17642559 N383S T C missense Het probably benign 0.235 phenotype 12/06/2012
18 12953 APN Pde1a 0.000 IGL00423 G1 2 79865670 L443P A G missense Het probably damaging 1.000 phenotype 12/06/2012
19 3839 APN Prph2 0.000 IGL00423 G1 17 46919778 N199I A T missense Het probably damaging 0.973 phenotype 04/20/2012
20 5702 APN Rab27b 0.000 IGL00423 G1 18 69996067 A G critical splice donor site 2 bp Het probably null phenotype 04/20/2012
21 332380 APN Ranbp3 0.959 IGL00423 G1 17 56709238 D336N G A missense Het probably damaging 0.995 phenotype 08/05/2015
22 4069 APN Rangap1 1.000 IGL00423 G1 15 81721993 D49G T C missense Het probably benign 0.041 phenotype 04/20/2012
23 5065 APN Rasa3 1.000 IGL00423 G1 8 13595410 G A unclassified Het probably benign phenotype 04/20/2012
24 4370 APN Serpina6 0.058 IGL00423 G1 12 103651903 N217I T A missense Het probably damaging 0.997 phenotype 04/20/2012
25 332381 APN Sorbs2 0.000 IGL00423 G1 8 45799706 A G splice site Het probably null phenotype 08/05/2015
26 3304 APN Spire1 0.202 IGL00423 G1 18 67529015 V116A A G missense Het probably damaging 0.999 phenotype 04/20/2012
27 3152 APN Tdrd1 0.579 IGL00423 G1 19 56851464 V652A T C missense Het possibly damaging 0.514 phenotype 04/20/2012
28 6419 APN Tmprss11g 0.061 IGL00423 G1 5 86492191 E193G T C missense Het probably benign 0.001 04/20/2012
29 7515 APN Zfp451 0.000 IGL00423 G1 1 33777579 V213D A T missense Het probably benign 0.445 04/20/2012
[records 1 to 29 of 29]