Incidental Mutations

28 incidental mutations are currently displayed, and affect 28 genes.
4 are Possibly Damaging.
10 are Probably Damaging.
10 are Probably Benign.
4 are Probably Null.
1 create premature stop codons.
0 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 89472 APN Abca8b 0.000 IGL01523 G1 11 109976494 E246G T C missense Het probably damaging 1.000 phenotype 12/03/2013
2 89474 APN B3galt5 0.000 IGL01523 G1 16 96315891 D241E T A missense Het probably damaging 1.000 phenotype 12/03/2013
3 89463 APN Camta1 0.649 IGL01523 G1 4 151145050 F442L A G missense Het possibly damaging 0.730 phenotype 12/03/2013
4 89468 APN Cntnap5b 0.123 IGL01523 G1 1 100431779 E709V A T missense Het probably benign 0.022 12/03/2013
5 89469 APN Ctnnal1 0.271 IGL01523 G1 4 56835243 I345V T C missense Het probably damaging 0.997 phenotype 12/03/2013
6 89483 APN Evpl 0.000 IGL01523 G1 11 116233444 N183S T C missense Het probably damaging 0.999 phenotype 12/03/2013
7 89478 APN Fam90a1b 0.031 IGL01523 G1 X 94356759 D155G T C missense Het probably benign 0.020 phenotype 12/03/2013
8 89480 APN Fsip2 0.108 IGL01523 G1 2 82977519 S1394N G A missense Het probably benign 0.000 phenotype 12/03/2013
9 89473 APN Gcnt2 0.096 IGL01523 G1 13 40887863 Q166L A T missense Het probably benign 0.064 phenotype 12/03/2013
10 89486 APN Gpatch1 1.000 IGL01523 G1 7 35308338 D99G T C missense Het probably null 1.000 12/03/2013
11 89484 APN Grin2b 1.000 IGL01523 G1 6 136044265 W13R A T missense Het probably null 0.991 phenotype 12/03/2013
12 89479 APN Hbb-bh1 0.000 IGL01523 G1 7 103841817 V127M C T missense Het probably benign 0.027 phenotype 12/03/2013
13 89462 APN Hc 0.668 IGL01523 G1 2 35039238 M282I C T missense Het probably benign 0.042 phenotype 12/03/2013
14 89485 APN Hirip3 0.000 IGL01523 G1 7 126862704 E57G A G missense Het probably damaging 0.996 phenotype 12/03/2013
15 89489 APN Inpp5j 0.533 IGL01523 G1 11 3495932 C T splice site 1766 bp Het probably null phenotype 12/03/2013
16 89464 APN Krt84 0.122 IGL01523 G1 15 101528744 V328E A T missense Het probably damaging 1.000 phenotype 12/03/2013
17 89465 APN Lrriq1 0.073 IGL01523 G1 10 103218116 E247* C A nonsense Het probably null 12/03/2013
18 89470 APN Mmrn2 0.054 IGL01523 G1 14 34403217 F918L T A missense Het probably damaging 1.000 phenotype 12/03/2013
19 89476 APN Myh13 0.111 IGL01523 G1 11 67347943 E704G A G missense Het possibly damaging 0.726 12/03/2013
20 89481 APN Myo16 0.399 IGL01523 G1 8 10370908 N249K T A missense Het probably damaging 0.998 phenotype 12/03/2013
21 89466 APN Nobox 0.481 IGL01523 G1 6 43304123 K472N C A missense Het probably damaging 0.959 phenotype 12/03/2013
22 89487 APN Olfr3 0.194 IGL01523 G1 2 36812403 T230S T A missense Het probably benign 0.000 phenotype 12/03/2013
23 89477 APN Orc4 0.965 IGL01523 G1 2 48917224 S232T A T missense Het probably benign 0.004 phenotype 12/03/2013
24 89471 APN Pign 0.787 IGL01523 G1 1 105653178 Y159N A T missense Het probably damaging 0.981 phenotype 12/03/2013
25 89488 APN Rere 1.000 IGL01523 G1 4 150615555 V1032E T A missense Het possibly damaging 0.931 phenotype 12/03/2013
26 89482 APN Ror2 1.000 IGL01523 G1 13 53118963 Q210R T C missense Het probably benign 0.021 phenotype 12/03/2013
27 89475 APN Sh3tc2 0.000 IGL01523 G1 18 61990883 R905Q G A missense Het probably benign 0.001 phenotype 12/03/2013
28 89467 APN Ttn 1.000 IGL01523 G1 2 76954983 S683P A G missense Het possibly damaging 0.779 phenotype 12/03/2013
[records 1 to 28 of 28]