Incidental Mutations

26 incidental mutations are currently displayed, and affect 26 genes.
5 are Possibly Damaging.
9 are Probably Damaging.
8 are Probably Benign.
4 are Probably Null.
1 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 26 of 26] 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 100186 UTSW 9430007A20Rik 0.056 R1202 G1 225 N 4 144523666 F137L T C missense Het probably benign 0.070 01/15/2014
2 100182 UTSW Cct3 1.000 R1202 G1 225 N 3 88318528 T C critical splice donor site 2 bp Het probably null phenotype 01/15/2014
3 100229 UTSW Fermt3 1.000 R1202 G1 225 N 19 7003482 F294L A G missense Het probably damaging 1.000 phenotype 01/15/2014
4 100172 UTSW Fmn2 0.743 R1202 G1 225 N 1 174612535 K58* A T nonsense Het probably null phenotype 01/15/2014
5 100184 UTSW Fndc5 0.148 R1202 G1 220 N 4 129139445 V102M G A missense Het probably damaging 0.969 phenotype 01/15/2014
6 100174 UTSW Gle1 1.000 R1202 G1 225 N 2 29949265 A523V C T missense Het probably damaging 1.000 phenotype 01/15/2014
7 100178 UTSW Hoxd11 0.664 R1202 G1 81 N 2 74682577 A62V C T missense Het possibly damaging 0.922 phenotype 01/15/2014
8 100196 UTSW Il23r 0.000 R1202 G1 225 N 6 67478953 V177A A G missense Het possibly damaging 0.950 phenotype 01/15/2014
9 100211 UTSW Impdh2 1.000 R1202 G1 225 N 9 108563187 R224Q G A missense Het probably damaging 0.999 phenotype 01/15/2014
10 100219 UTSW Larp4b 0.489 R1202 G1 225 N 13 9166326 T516A A G missense Het possibly damaging 0.842 phenotype 01/15/2014
11 100209 UTSW Mtmr2 0.322 R1202 G1 225 N 9 13803452 Y431H T C missense Het probably benign 0.000 phenotype 01/15/2014
12 100207 UTSW N4bp1 0.000 R1202 G1 225 N 8 86844887 T828A T C missense Het probably benign 0.017 01/15/2014
13 100188 UTSW Nphp4 0.174 R1202 G1 225 N 4 152488729 G A splice site Het probably null phenotype 01/15/2014
14 100223 UTSW Nup155 1.000 R1202 G1 225 N 15 8157760 H1391L A T missense Het probably damaging 0.998 0.088 phenotype 01/15/2014
15 100180 UTSW Pabpc1l 0.000 R1202 G1 225 N 2 164037171 V313F G T missense Het possibly damaging 0.736 0.179 phenotype 01/15/2014
16 100227 UTSW Pacs1 0.000 R1202 G1 225 N 19 5135237 P885S G A missense Het probably damaging 1.000 phenotype 01/15/2014
17 100176 UTSW Scn3a 1.000 R1202 G1 225 N 2 65506147 N705S T C missense Het probably benign 0.072 phenotype 01/15/2014
18 100231 UTSW Sema4g 0.000 R1202 G1 225 N 19 44998257 R383L G T missense Het probably benign 0.311 phenotype 01/15/2014
19 100213 UTSW Slc26a10 0.000 R1202 G1 225 N 10 127173348 L648P A G missense Het probably damaging 0.994 01/15/2014
20 100200 UTSW St8sia2 0.152 R1202 G1 225 N 7 73972035 V37E A T missense Het probably benign 0.425 phenotype 01/15/2014
21 100194 UTSW Tmem209 0.722 R1202 G1 225 N 6 30508790 V6L C G missense Het probably benign 0.010 01/15/2014
22 100192 UTSW Tmprss11a 0.000 R1202 G1 225 N 5 86411925 T A critical splice acceptor site Het probably null phenotype 01/15/2014
23 100217 UTSW Ube2o 0.590 R1202 G1 225 N 11 116541582 D853N C T missense Het probably damaging 0.998 phenotype 01/15/2014
24 100203 UTSW Usp17lb 0.194 R1202 G1 225 N 7 104842488 S6F G A missense Het probably damaging 0.984 01/15/2014
25 100201 UTSW Vmn2r74 0.140 R1202 G1 225 N 7 85961337 T49I G A missense Het possibly damaging 0.833 01/15/2014
26 100225 UTSW Zfp236 1.000 R1202 G1 225 N 18 82628166 T1041S T A missense Het probably benign 0.002 01/15/2014
[records 1 to 26 of 26]