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 (GRCm38) E246G T C missense Het probably damaging 1.000 phenotype 2013-12-03
2 89474 APN B3galt5 0.000 IGL01523 G1 16 96315891 (GRCm38) D241E T A missense Het probably damaging 1.000 phenotype 2013-12-03
3 89463 APN Camta1 0.698 IGL01523 G1 4 151145050 (GRCm38) F442L A G missense Het possibly damaging 0.730 phenotype 2013-12-03
4 89468 APN Cntnap5b 0.120 IGL01523 G1 1 100431779 (GRCm38) E709V A T missense Het probably benign 0.022 2013-12-03
5 89469 APN Ctnnal1 0.248 IGL01523 G1 4 56835243 (GRCm38) I345V T C missense Het probably damaging 0.997 phenotype 2013-12-03
6 89483 APN Evpl 0.000 IGL01523 G1 11 116233444 (GRCm38) N183S T C missense Het probably damaging 0.999 phenotype 2013-12-03
7 89478 APN Fam90a1b 0.031 IGL01523 G1 X 94356759 (GRCm38) D155G T C missense Het probably benign 0.020 phenotype 2013-12-03
8 89480 APN Fsip2 0.101 IGL01523 G1 2 82977519 (GRCm38) S1394N G A missense Het probably benign 0.000 phenotype 2013-12-03
9 89473 APN Gcnt2 0.087 IGL01523 G1 13 40887863 (GRCm38) Q166L A T missense Het probably benign 0.064 phenotype 2013-12-03
10 89486 APN Gpatch1 1.000 IGL01523 G1 7 35308338 (GRCm38) D99G T C missense Het probably null 1.000 2013-12-03
11 89484 APN Grin2b 1.000 IGL01523 G1 6 136044265 (GRCm38) W13R A T missense Het probably null 0.991 phenotype 2013-12-03
12 89479 APN Hbb-bh1 0.000 IGL01523 G1 7 103841817 (GRCm38) V127M C T missense Het probably benign 0.027 phenotype 2013-12-03
13 89462 APN Hc 0.555 IGL01523 G1 2 35039238 (GRCm38) M282I C T missense Het probably benign 0.042 phenotype 2013-12-03
14 89485 APN Hirip3 0.000 IGL01523 G1 7 126862704 (GRCm38) E57G A G missense Het probably damaging 0.996 phenotype 2013-12-03
15 89489 APN Inpp5j 0.382 IGL01523 G1 11 3495932 (GRCm38) C T splice site 1766 bp Het probably null phenotype 2013-12-03
16 89464 APN Krt84 0.109 IGL01523 G1 15 101528744 (GRCm38) V328E A T missense Het probably damaging 1.000 phenotype 2013-12-03
17 89465 APN Lrriq1 0.088 IGL01523 G1 10 103218116 (GRCm38) E247* C A nonsense Het probably null 2013-12-03
18 89470 APN Mmrn2 0.051 IGL01523 G1 14 34403217 (GRCm38) F918L T A missense Het probably damaging 1.000 phenotype 2013-12-03
19 89476 APN Myh13 0.110 IGL01523 G1 11 67347943 (GRCm38) E704G A G missense Het possibly damaging 0.726 2013-12-03
20 89481 APN Myo16 0.491 IGL01523 G1 8 10370908 (GRCm38) N249K T A missense Het probably damaging 0.998 phenotype 2013-12-03
21 89466 APN Nobox 0.334 IGL01523 G1 6 43304123 (GRCm38) K472N C A missense Het probably damaging 0.959 phenotype 2013-12-03
22 89487 APN Olfr3 0.341 IGL01523 G1 2 36812403 (GRCm38) T230S T A missense Het probably benign 0.000 phenotype 2013-12-03
23 89477 APN Orc4 0.967 IGL01523 G1 2 48917224 (GRCm38) S232T A T missense Het probably benign 0.004 phenotype 2013-12-03
24 89471 APN Pign 0.819 IGL01523 G1 1 105653178 (GRCm38) Y159N A T missense Het probably damaging 0.981 phenotype 2013-12-03
25 89488 APN Rere 1.000 IGL01523 G1 4 150615555 (GRCm38) V1032E T A missense Het possibly damaging 0.931 phenotype 2013-12-03
26 89482 APN Ror2 1.000 IGL01523 G1 13 53118963 (GRCm38) Q210R T C missense Het probably benign 0.021 phenotype 2013-12-03
27 89475 APN Sh3tc2 0.000 IGL01523 G1 18 61990883 (GRCm38) R905Q G A missense Het probably benign 0.001 phenotype 2013-12-03
28 89467 APN Ttn 1.000 IGL01523 G1 2 76954983 (GRCm38) S683P A G missense Het possibly damaging 0.779 phenotype 2013-12-03
[records 1 to 28 of 28]