Incidental Mutations

27 incidental mutations are currently displayed, and affect 27 genes.
4 are Possibly Damaging.
12 are Probably Damaging.
5 are Probably Benign.
6 are Probably Null.
2 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 27 of 27] 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 100391 UTSW Bcl10 0.000 R1161 G1 225 N 3 145930425 V26G T G missense Het probably damaging 0.988 phenotype 01/15/2014
2 100429 UTSW C4b 0.000 R1161 G1 225 N 17 34729593 V1581A A G missense Het probably damaging 0.999 phenotype 01/15/2014
3 100385 UTSW Camk1g 0.153 R1161 G1 225 N 1 193348354 D349G T C missense Het probably benign 0.000 phenotype 01/15/2014
4 100403 UTSW Ccdc106 0.088 R1161 G1 225 N 7 5059540 D11N G A missense Het possibly damaging 0.922 01/15/2014
5 100387 UTSW Ckap5 1.000 R1161 G1 225 N 2 91599375 L1464R T G missense Het probably null 0.999 phenotype 01/15/2014
6 100427 UTSW Def6 0.000 R1161 G1 213 N 17 28217619 V86I G A missense Het probably benign 0.002 phenotype 01/15/2014
7 100381 UTSW Dnm3 0.000 R1161 G1 225 N 1 162353574 T179S T A missense Het probably benign 0.059 phenotype 01/15/2014
8 100421 UTSW Dync1h1 1.000 R1161 G1 225 N 12 110636509 E2195K G A missense Het probably benign 0.044 0.065 phenotype 01/15/2014
9 100419 UTSW Eme1 0.000 R1161 G1 225 N 11 94645542 R534C G A missense Het probably damaging 1.000 phenotype 01/15/2014
10 100389 UTSW Fam160a1 1.000 R1161 G1 225 N 3 85672468 I810T A G missense Het probably damaging 0.957 01/15/2014
11 100425 UTSW Fzd3 1.000 R1161 G1 225 N 14 65212088 R514C G A missense Het probably damaging 0.998 phenotype 01/15/2014
12 100431 UTSW H2-T24 0.000 R1161 G1 225 N 17 36014996 Y234* G T nonsense Het probably null 01/15/2014
13 100433 UTSW Ifit1bl1 0.000 R1161 G1 176 N 19 34593696 S454P A G missense Het possibly damaging 0.802 01/15/2014
14 100417 UTSW Ipcef1 0.127 R1161 G1 225 N 10 6980288 T A critical splice acceptor site Het probably null 01/15/2014
15 100399 UTSW Mmel1 0.249 R1161 G1 167 N 4 154895214 R764C C T missense Het probably damaging 1.000 phenotype 01/15/2014
16 100413 UTSW Olfr857 0.079 R1161 G1 225 N 9 19713180 M118V A G missense Het probably damaging 0.998 phenotype 01/15/2014
17 100409 UTSW Pde4c 0.000 R1161 G1 225 N 8 70749923 D592G A G missense Het possibly damaging 0.903 phenotype 01/15/2014
18 100407 UTSW Prx 0.000 R1161 G1 225 N 7 27519677 F1340S T C missense Het probably damaging 1.000 phenotype 01/15/2014
19 100383 UTSW Rgs7 0.583 R1161 G1 225 N 1 175079455 T90A T C missense Het probably damaging 1.000 phenotype 01/15/2014
20 100415 UTSW Scn11a 0.100 R1161 G1 225 N 9 119755057 W1497* C T nonsense Het probably null phenotype 01/15/2014
21 100395 UTSW Snrnp40 1.000 R1161 G1 196 N 4 130378043 C G splice site Het probably null 0.976 phenotype 01/15/2014
22 100401 UTSW Srrm3 0.313 R1161 G1 106 N 5 135854392 CAAGAAGAAGAAGAA CAAGAAGAAGAA small deletion Het probably benign 01/15/2014
23 100393 UTSW Svep1 1.000 R1161 G1 225 N 4 58069416 Y2790F T A missense Het possibly damaging 0.707 phenotype 01/15/2014
24 100379 UTSW Tmeff2 1.000 R1161 G1 225 N 1 51181787 V307A T C missense Het probably damaging 0.997 phenotype 01/15/2014
25 100411 UTSW Tmem38a 0.000 R1161 G1 225 N 8 72579970 F98I T A missense Het probably damaging 1.000 phenotype 01/15/2014
26 100397 UTSW Trp73 0.452 R1161 G1 225 N 4 154081323 A G splice site 6 bp Het probably null phenotype 01/15/2014
27 100405 UTSW Usp29 0.000 R1161 G1 225 N 7 6961530 E124G A G missense Het probably damaging 0.999 01/15/2014
[records 1 to 27 of 27]