Incidental Mutations

42 incidental mutations are currently displayed, and affect 41 genes.
4 are Possibly Damaging.
16 are Probably Damaging.
18 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 42 of 42] 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 298378 APN 1700109H08Rik 0.175 IGL02558 5 3582194 *25C A C makesense Het probably null 04/16/2015
2 298374 APN Abca13 0.000 IGL02558 11 9399387 Y3654H T C missense Het probably damaging 1.000 phenotype 04/16/2015
3 298401 APN Ankle1 0.430 IGL02558 8 71408992 F438S T C missense Het probably damaging 1.000 phenotype 04/16/2015
4 298380 APN Atp10a 0.319 IGL02558 7 58819642 R1080S A T missense Het probably damaging 0.984 p23DFiOD deletion may be responsible for the obesity phenotypes associated with that deletion. [provided by MGI curators] (source: MGI)">phenotype 04/16/2015
5 298382 APN Ccdc51 0.672 IGL02558 9 109092184 N380Y A T missense Het probably damaging 0.999 04/16/2015
6 298389 APN Ccr8 0.000 IGL02558 9 120094658 I280F A T missense Het probably benign 0.012 phenotype 04/16/2015
7 298372 APN Cdc45 1.000 IGL02558 16 18798729 M200I C T missense Het probably benign 0.059 0.115 phenotype 04/16/2015
8 298379 APN Cep162 0.157 IGL02558 9 87225726 T537N G T missense Het probably benign 0.000 04/16/2015
9 298377 APN Cep162 0.157 IGL02558 9 87225733 T535A T C missense Het probably benign 0.042 04/16/2015
10 298398 APN Cfap52 0.349 IGL02558 11 67954138 D35G T C missense Het probably benign 0.315 phenotype 04/16/2015
11 298388 APN Cmip 1.000 IGL02558 8 117449088 S530N G A missense Het probably damaging 0.985 phenotype 04/16/2015
12 298404 APN Col9a3 0.258 IGL02558 2 180606806 A T critical splice acceptor site Het probably null phenotype 04/16/2015
13 298407 APN Csf3r 0.305 IGL02558 4 126038135 T C splice site Het probably benign phenotype 04/16/2015
14 298402 APN Csk 1.000 IGL02558 9 57630263 E123K C T missense Het probably benign 0.000 phenotype 04/16/2015
15 298393 APN Csrnp3 0.162 IGL02558 2 66022229 E322K G A missense Het probably damaging 0.997 phenotype 04/16/2015
16 298384 APN Ddx11 1.000 IGL02558 17 66148672 I663F A T missense Het probably damaging 0.993 phenotype 04/16/2015
17 298394 APN Dnah1 0.000 IGL02558 14 31274379 M2667L T A missense Het possibly damaging 0.956 phenotype 04/16/2015
18 298391 APN Foxred1 1.000 IGL02558 9 35210133 K40E T C missense Het probably damaging 1.000 phenotype 04/16/2015
19 298385 APN Gata2 1.000 IGL02558 6 88199780 P74S C T missense Het probably benign 0.041 phenotype 04/16/2015
20 298387 APN Gdf10 0.000 IGL02558 14 33923980 C29G T G missense Het probably benign 0.000 phenotype 04/16/2015
21 298381 APN Hectd4 0.914 IGL02558 5 121344785 E3133G A G missense Het probably benign 0.278 04/16/2015
22 298400 APN Ints8 0.954 IGL02558 4 11218771 R784W G A missense Het probably damaging 1.000 phenotype 04/16/2015
23 298369 APN Lrriq1 0.076 IGL02558 10 103146283 E1392G T C missense Het probably damaging 1.000 04/16/2015
24 298399 APN Muc19 0.132 IGL02558 15 91897622 T C exon Het noncoding transcript phenotype 04/16/2015
25 298386 APN Myom2 0.124 IGL02558 8 15114237 D1044V A T missense Het probably benign 0.306 phenotype 04/16/2015
26 298375 APN Nphp4 0.144 IGL02558 4 152555531 R958L G T missense Het probably damaging 0.996 phenotype 04/16/2015
27 298383 APN Nup205 0.956 IGL02558 6 35189924 P293S C T missense Het probably damaging 0.999 phenotype 04/16/2015
28 298395 APN Olfr1130 0.147 IGL02558 2 87607559 I57T T C missense Het probably benign 0.002 phenotype 04/16/2015
29 298366 APN Olfr23 0.151 IGL02558 11 73940825 H193L A T missense Het probably benign 0.007 phenotype 04/16/2015
30 298406 APN Plxdc2 0.000 IGL02558 2 16669598 A G splice site Het probably benign phenotype 04/16/2015
31 298390 APN Pwp2 0.427 IGL02558 10 78179065 S362G T C missense Het probably damaging 1.000 04/16/2015
32 298403 APN Siglec1 0.132 IGL02558 2 131074995 S1113R G T missense Het possibly damaging 0.885 phenotype 04/16/2015
33 298396 APN Sirpa 0.000 IGL02558 2 129630069 E472G A G missense Het probably damaging 1.000 phenotype 04/16/2015
34 298392 APN Slc39a4 1.000 IGL02558 15 76614203 L345M G T missense Het probably damaging 0.999 phenotype 04/16/2015
35 298367 APN Snx27 1.000 IGL02558 3 94502881 R496Q C T missense Het probably damaging 0.994 phenotype 04/16/2015
36 298376 APN Stard9 0.146 IGL02558 2 120696907 H1215R A G missense Het possibly damaging 0.947 04/16/2015
37 298373 APN Stau1 0.000 IGL02558 2 166950848 Y371H A G missense Het probably benign 0.100 phenotype 04/16/2015
38 298371 APN Sult2a1 0.083 IGL02558 7 13832595 W152G A C missense Het probably benign 0.027 phenotype 04/16/2015
39 298397 APN Syt16 0.000 IGL02558 12 74235058 K319* A T nonsense Het probably null 04/16/2015
40 298405 APN Tcf7 0.748 IGL02558 11 52253970 T A splice site Het probably benign phenotype 04/16/2015
41 298368 APN Tfdp1 1.000 IGL02558 8 13369546 N92D A G missense Het possibly damaging 0.955 phenotype 04/16/2015
42 298370 APN Zfp13 0.115 IGL02558 17 23576098 A493T C T missense Het probably benign 0.053 04/16/2015
[records 1 to 42 of 42]