Incidental Mutations

21 incidental mutations are currently displayed, and affect 21 genes.
2 are Possibly Damaging.
12 are Probably Damaging.
7 are Probably Benign.
0 are Probably Null.
0 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 21 of 21] 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 88980 APN Abcc12 0.082 IGL01504 G1 8 86557602 I326N A T missense Het probably damaging 1.000 phenotype 12/03/2013
2 88978 APN Acot6 0.194 IGL01504 G1 12 84109402 V375M G A missense Het probably benign 0.047 phenotype 12/03/2013
3 88987 APN Als2cl 0.077 IGL01504 G1 9 110889283 R364Q G A missense Het probably benign 0.045 12/03/2013
4 88979 APN Cpa1 0.000 IGL01504 G1 6 30640721 T121S A T missense Het probably benign 0.002 phenotype 12/03/2013
5 88993 APN Ctnnbl1 0.953 IGL01504 G1 2 157818116 A G splice site Het probably benign phenotype 12/03/2013
6 88986 APN Fam196a 1.000 IGL01504 G1 7 134917940 Q287L T A missense Het probably benign 0.148 phenotype 12/03/2013
7 88983 APN Frrs1 0.164 IGL01504 G1 3 116900658 Q76K C A missense Het probably damaging 0.998 phenotype 12/03/2013
8 88985 APN Gja10 0.000 IGL01504 G1 4 32602375 D3V T A missense Het probably damaging 1.000 phenotype 12/03/2013
9 88990 APN Krt76 0.000 IGL01504 G1 15 101888173 E400G T C missense Het probably damaging 1.000 phenotype 12/03/2013
10 88989 APN Mdm1 0.135 IGL01504 G1 10 118146600 T47A A G missense Het probably damaging 0.996 phenotype 12/03/2013
11 88988 APN Ncf2 0.157 IGL01504 G1 1 152833329 K336R A G missense Het probably benign 0.001 phenotype 12/03/2013
12 88984 APN Ndrg4 0.000 IGL01504 G1 8 95706266 L34I C A missense Het probably damaging 0.997 phenotype 12/03/2013
13 88981 APN Phf20l1 0.182 IGL01504 G1 15 66597691 H148Q T A missense Het possibly damaging 0.726 12/03/2013
14 88977 APN Rhobtb1 0.164 IGL01504 G1 10 69249698 H89R A G missense Het probably damaging 0.999 phenotype 12/03/2013
15 88974 APN Sult1e1 0.051 IGL01504 G1 5 87576301 N266D T C missense Het probably damaging 0.997 phenotype 12/03/2013
16 88976 APN Sult2a2 0.086 IGL01504 G1 7 13738264 S129P T C missense Het probably damaging 1.000 phenotype 12/03/2013
17 88973 APN Trank1 0.000 IGL01504 G1 9 111373544 E1659G A G missense Het probably damaging 1.000 12/03/2013
18 88991 APN Trpa1 0.119 IGL01504 G1 1 14882219 I863L T G missense Het possibly damaging 0.790 phenotype 12/03/2013
19 88992 APN Vmn1r177 0.408 IGL01504 G1 7 23866410 V14M C T missense Het probably damaging 0.981 12/03/2013
20 88975 APN Vmn2r14 0.341 IGL01504 G1 5 109221419 M96K A T missense Het probably benign 0.008 12/03/2013
21 88982 APN Zp1 0.118 IGL01504 G1 19 10919011 V117M C T missense Het probably damaging 0.990 phenotype 12/03/2013
[records 1 to 21 of 21]