Incidental Mutations

28 incidental mutations are currently displayed, and affect 28 genes.
2 are Possibly Damaging.
11 are Probably Damaging.
9 are Probably Benign.
4 are Probably Null.
2 create premature stop codons.
2 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 290992 APN Adamtsl1 0.155 IGL02373 4 86249805 L462F C T missense Het probably damaging 1.000 phenotype 04/16/2015
2 291006 APN Adgrv1 0.000 IGL02373 13 81459713 D4080G T C missense Het possibly damaging 0.899 phenotype 04/16/2015
3 291001 APN Apc 0.968 IGL02373 18 34316159 D2002A A C missense Het probably damaging 1.000 phenotype 04/16/2015
4 290994 APN Apobr 0.063 IGL02373 7 126585391 F25I T A missense Het probably damaging 1.000 phenotype 04/16/2015
5 290987 APN Cyp4a10 0.062 IGL02373 4 115521077 L120* T A nonsense Het probably null phenotype 04/16/2015
6 290991 APN Daam2 0.000 IGL02373 17 49473380 S704P A G missense Het probably damaging 0.998 Daam1 conditional KO increases the severity of the heart phenotype (abnormal ventricular morphology and pressure) of the Daam1 single KO. [provided by MGI curators] (source: MGI)">phenotype 04/16/2015
7 291004 APN Dcst1 0.070 IGL02373 3 89357891 N217K G T missense Het probably damaging 0.979 phenotype 04/16/2015
8 290998 APN Efr3b 0.000 IGL02373 12 3983391 V139I C T missense Het probably benign 0.402 04/16/2015
9 291005 APN Fmn1 0.246 IGL02373 2 113364126 P57Q C A missense Het unknown phenotype 04/16/2015
10 290996 APN Galnt1 0.290 IGL02373 18 24280035 G464D G A missense Het possibly damaging 0.684 phenotype 04/16/2015
11 291008 APN Ggcx 0.436 IGL02373 6 72427919 W437R T A missense Het probably damaging 1.000 phenotype 04/16/2015
12 290986 APN Gm11487 0.253 IGL02373 4 73403643 M52V T C missense Het probably benign 0.013 phenotype 04/16/2015
13 291009 APN Igkv13-54-1 0.099 IGL02373 6 69617320 T C exon Het noncoding transcript 04/16/2015
14 291002 APN Iglon5 0.073 IGL02373 7 43479219 E58G T C missense Het probably benign 0.085 04/16/2015
15 290995 APN Met 1.000 IGL02373 6 17491529 P97S C T missense Het probably damaging 1.000 phenotype 04/16/2015
16 291000 APN Myg1 0.304 IGL02373 15 102336833 M158K T A missense Het probably damaging 0.985 phenotype 04/16/2015
17 290999 APN Ncald 0.000 IGL02373 15 37372209 M131L T A missense Het probably benign 0.050 phenotype 04/16/2015
18 290997 APN Nipa2 0.870 IGL02373 7 55933128 I290V T C missense Het probably benign 0.012 phenotype 04/16/2015
19 290984 APN Olfr1307 0.161 IGL02373 2 111944833 V208L C A missense Het probably benign 0.009 phenotype 04/16/2015
20 290985 APN Olfr507 0.093 IGL02373 7 108622103 Y97F A T missense Het probably benign 0.110 phenotype 04/16/2015
21 290988 APN Olfr818 0.054 IGL02373 10 129945465 L84S A G missense Het probably benign 0.107 phenotype 04/16/2015
22 290993 APN Ppfia3 0.727 IGL02373 7 45358849 R48Q C T missense Het probably damaging 0.983 phenotype 04/16/2015
23 290990 APN Rab12 0.000 IGL02373 17 66498065 L156P A G missense Het probably damaging 1.000 04/16/2015
24 291010 APN Slc28a3 0.000 IGL02373 13 58578404 C T critical splice donor site 1 bp Het probably null phenotype 04/16/2015
25 291007 APN Slc4a11 0.153 IGL02373 2 130684898 N770S T C missense Het probably benign 0.069 phenotype 04/16/2015
26 291011 APN Tanc1 0.000 IGL02373 2 59796028 T C critical splice donor site 2 bp Het probably null phenotype 04/16/2015
27 290989 APN Vmn2r-ps130 0.122 IGL02373 17 23076892 R679* A T nonsense Het probably null 04/16/2015
28 291003 APN Vwa5b2 0.129 IGL02373 16 20604844 R1169H G A missense Het probably damaging 0.988 04/16/2015
[records 1 to 28 of 28]