Incidental Mutations

28 incidental mutations are currently displayed, and affect 28 genes.
4 are Possibly Damaging.
7 are Probably Damaging.
11 are Probably Benign.
4 are Probably Null.
0 create premature stop codons.
2 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 332612 APN 1500035N22Rik IGL00562 G1 5 24997621 T C unclassified Het probably benign 08/05/2015
2 332614 APN AU016765 0.218 IGL00562 G1 17 64519882 C A exon Het noncoding transcript 08/05/2015
3 277770 APN Chaf1b 0.934 IGL00562 G1 16 93900191 T C unclassified Het probably benign phenotype 04/16/2015
4 277769 APN Clstn2 0.137 IGL00562 G1 9 97582452 A G splice site Het probably benign phenotype 04/16/2015
5 277767 APN Crip1 0.192 IGL00562 G1 12 113153612 T A splice site Het probably null phenotype 04/16/2015
6 332616 APN Cubn 1.000 IGL00562 G1 2 13294230 S3211P A G missense Het probably benign 0.012 phenotype 08/05/2015
7 277764 APN Dlx6 1.000 IGL00562 G1 6 6865143 R172W C T missense Het probably damaging 1.000 phenotype 04/16/2015
8 277766 APN Fktn 1.000 IGL00562 G1 4 53747007 A T critical splice acceptor site Het probably null phenotype 04/16/2015
9 277754 APN Focad 0.388 IGL00562 G1 4 88348809 M1019K T A missense Het unknown 04/16/2015
10 277758 APN Fuca2 0.169 IGL00562 G1 10 13505907 D188V A T missense Het probably damaging 0.988 0.280 phenotype 04/16/2015
11 6787 APN Kcna3 0.105 IGL00562 G1 3 107036730 D103G A G missense Het probably damaging 1.000 phenotype 04/20/2012
12 277750 APN Mrpl19 0.763 IGL00562 G1 6 81965872 V19A A G missense Het probably benign 0.019 phenotype 04/16/2015
13 277753 APN Ndufb3 0.350 IGL00562 G1 1 58595799 H103Q T A missense Het possibly damaging 0.947 phenotype 04/16/2015
14 277761 APN Pkd1l3 0.000 IGL00562 G1 8 109656147 V1675A T C missense Het possibly damaging 0.529 phenotype 04/16/2015
15 13209 APN Ptger4 0.239 IGL00562 G1 15 5243133 S2T A T missense Het probably benign 0.001 phenotype 12/06/2012
16 277757 APN Saxo1 0.059 IGL00562 G1 4 86445572 E225K C T missense Het probably damaging 0.997 04/16/2015
17 332615 APN Sftpb 0.592 IGL00562 G1 6 72309862 A228S G T missense Het probably benign 0.028 phenotype 08/05/2015
18 277752 APN Slc22a29 0.060 IGL00562 G1 19 8161629 T490S T A missense Het probably benign 0.029 04/16/2015
19 14077 APN Slc29a1 0.000 IGL00562 G1 17 45589992 N50S T C missense Het probably damaging 1.000 phenotype 12/06/2012
20 277751 APN Smc6 1.000 IGL00562 G1 12 11301531 S854T T A missense Het probably benign 0.017 phenotype 04/16/2015
21 277762 APN Smim23 0.040 IGL00562 G1 11 32821893 T58A T C missense Het probably benign 0.113 04/16/2015
22 277759 APN Tas2r134 0.033 IGL00562 G1 2 51628088 I193T T C missense Het possibly damaging 0.899 04/16/2015
23 277768 APN Thsd7a 0.168 IGL00562 G1 6 12379659 G T splice site Het probably null phenotype 04/16/2015
24 332613 APN Trav13n-4 0.046 IGL00562 G1 14 53363966 V64G T G missense Het possibly damaging 0.941 08/05/2015
25 277756 APN Trmt10a 0.000 IGL00562 G1 3 138147416 E13K G A missense Het probably damaging 0.966 phenotype 04/16/2015
26 277760 APN Txndc11 0.162 IGL00562 G1 16 11104632 S239G T C missense Het probably damaging 0.959 04/16/2015
27 277763 APN Vmn2r96 0.422 IGL00562 G1 17 18583815 N442K T A missense Het probably benign 0.003 04/16/2015
28 277765 APN Vps13a 0.000 IGL00562 G1 19 16734714 C T critical splice donor site 1 bp Het probably null phenotype 04/16/2015
[records 1 to 28 of 28]