Incidental Mutations

12 incidental mutations are currently displayed, and affect 10 genes.
0 are Possibly Damaging.
5 are Probably Damaging.
2 are Probably Benign.
4 are Probably Null.
1 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 12 of 12] 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 164807 UTSW 4921517D22Rik 0.079 R1207 G1 217 N 13 59691598 GCC GC frame shift Het probably null 0.646 03/28/2014
2 500175 UTSW Camsap3 0.932 R1207 G1 198 N 8 3604708 R782C C T missense Het probably damaging 1.000 0.198 phenotype 12/01/2017
3 164810 UTSW Creld2 0.000 R1207 G1 225 N 15 88820631 W103* G A nonsense Het probably null 0.616 03/28/2014
4 164808 UTSW Parp4 0.167 R1207 G1 205 N 14 56647882 I1473L A C missense Het unknown 0.056 phenotype 03/28/2014
5 500176 UTSW Pdlim2 0.085 R1207 G1 133 N 14 70164779 R296H C T missense Het probably damaging 1.000 0.212 phenotype 12/01/2017
6 100481 UTSW Sfi1 0.243 R1207 G1 217 N 11 3146254 TCGC TC frame shift Het probably null 01/15/2014
7 100483 UTSW Sfi1 0.243 R1207 G1 114 N 11 3146255 C CT frame shift Het probably null 01/15/2014
8 100485 UTSW Sfi1 0.243 R1207 G1 214 N 11 3177419 CCTCTC CCTCTCTC critical splice donor site Het probably benign 01/15/2014
9 164806 UTSW Tepp 0.064 R1207 G1 225 N 8 95320509 R94L G T missense Het probably damaging 1.000 03/28/2014
10 164804 UTSW Ttn 1.000 R1207 G1 225 N 2 76757060 K13236M T A missense Het probably damaging 0.989 phenotype 03/28/2014
11 100475 UTSW Ugt1a10 0.157 R1207 G1 92 N 1 88216254 A199T G A missense Het probably damaging 1.000 01/15/2014
12 100492 UTSW Vmn2r115 0.136 R1207 G1 191 N 17 23359988 ATCTTCT ATCT small deletion Het probably benign 0.145 01/15/2014
[records 1 to 12 of 12]