Incidental Mutations

25 incidental mutations are currently displayed, and affect 25 genes.
5 are Possibly Damaging.
6 are Probably Damaging.
10 are Probably Benign.
3 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 25 of 25] 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 303629 APN Adam39 0.073 IGL02688 8 40826320 R583S C A missense Het probably benign 0.001 04/16/2015
2 303630 APN Bcl9l 0.000 IGL02688 9 44505263 T211I C T missense Het possibly damaging 0.861 phenotype 04/16/2015
3 303639 APN C6 0.118 IGL02688 15 4798320 I724V A G missense Het probably benign 0.004 phenotype 04/16/2015
4 303645 APN Cacna2d4 0.000 IGL02688 6 119270749 T A splice site Het probably null phenotype 04/16/2015
5 303637 APN Casp4 0.000 IGL02688 9 5322844 E40G A G missense Het possibly damaging 0.763 phenotype 04/16/2015
6 303627 APN Cdc45 1.000 IGL02688 16 18798729 M200I C T missense Het probably benign 0.059 0.196 phenotype 04/16/2015
7 303626 APN Dnah7a 0.117 IGL02688 1 53444472 M3382R A C missense Het possibly damaging 0.928 04/16/2015
8 303632 APN Dst 0.392 IGL02688 1 34195952 L3526P T C missense Het probably damaging 0.998 phenotype 04/16/2015
9 303640 APN Eya4 1.000 IGL02688 10 23159110 S116P A G missense Het probably benign 0.006 phenotype 04/16/2015
10 303636 APN Gabra4 0.000 IGL02688 5 71572167 E423D T A missense Het probably benign 0.000 phenotype 04/16/2015
11 303622 APN Ighv1-67 IGL02688 12 115604023 T90P T G missense Het probably damaging 1.000 04/16/2015
12 303638 APN Kcnh8 0.000 IGL02688 17 52959443 T828A A G missense Het probably benign 0.001 phenotype 04/16/2015
13 303644 APN Nr5a2 1.000 IGL02688 1 136940407 A G critical splice donor site 2 bp Het probably null phenotype 04/16/2015
14 303621 APN Nup214 1.000 IGL02688 2 32031275 P1237S C T missense Het probably benign 0.000 phenotype 04/16/2015
15 303634 APN Phactr3 0.150 IGL02688 2 178278999 D215G A G missense Het probably damaging 0.962 phenotype 04/16/2015
16 303623 APN Phf2 0.547 IGL02688 13 48805839 P897Q G T missense Het unknown phenotype 04/16/2015
17 303628 APN Pla2r1 0.000 IGL02688 2 60455201 R690G T C missense Het probably damaging 1.000 phenotype 04/16/2015
18 303642 APN Ppargc1b 0.395 IGL02688 18 61312243 S181P A G missense Het possibly damaging 0.937 phenotype 04/16/2015
19 303631 APN Sele 0.103 IGL02688 1 164050130 I165F A T missense Het probably damaging 0.999 phenotype 04/16/2015
20 303625 APN Srcap 0.956 IGL02688 7 127542453 S1626P T C missense Het probably benign 0.044 phenotype 04/16/2015
21 303635 APN Tenm2 0.763 IGL02688 11 36068458 I1088T A G missense Het probably benign 0.051 phenotype 04/16/2015
22 303641 APN Tnrc18 0.582 IGL02688 5 142790172 S69G T C missense Het probably damaging 0.961 04/16/2015
23 303624 APN Trmt5 0.962 IGL02688 12 73281458 E324* C A nonsense Het probably null phenotype 04/16/2015
24 303643 APN Ttll3 0.000 IGL02688 6 113399739 I360T T C missense Het probably benign 0.004 phenotype 04/16/2015
25 303633 APN Zfp277 0.089 IGL02688 12 40328688 V390A A G missense Het possibly damaging 0.952 0.262 phenotype 04/16/2015
[records 1 to 25 of 25]