Incidental Mutations

21 incidental mutations are currently displayed, and affect 21 genes.
5 are Possibly Damaging.
7 are Probably Damaging.
6 are Probably Benign.
3 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 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 2222 APN Flii 1.000 IGL00225 G1 11 60723415 N93D T C missense Het probably benign 0.031 phenotype 12/09/2011
2 306785 APN Gm8356 IGL00225 G1 14 6537141 K24E T C missense Het probably damaging 0.999 04/16/2015
3 2066 APN Hars 0.964 IGL00225 G1 18 36768172 T409M G A missense Het probably damaging 0.998 phenotype 12/09/2011
4 2523 APN Ivns1abp 0.395 IGL00225 G1 1 151351112 A G splice site 3 bp Het probably null phenotype 12/09/2011
5 306787 APN Kcnq4 0.371 IGL00225 G1 4 120698016 Q657* G A nonsense Het probably null phenotype 04/16/2015
6 2438 APN Kdm4c 0.000 IGL00225 G1 4 74345567 V696G T G missense Het probably benign 0.025 phenotype 12/09/2011
7 2369 APN Klrb1f 0.062 IGL00225 G1 6 129053175 T A intron Het probably benign 12/09/2011
8 2497 APN Lrp4 0.518 IGL00225 G1 2 91495026 V1399I G A missense Het probably benign 0.000 phenotype 12/09/2011
9 2326 APN Mki67 0.812 IGL00225 G1 7 135690120 V3168A A G missense Het probably benign 0.316 phenotype 12/09/2011
10 2215 APN Nf1 1.000 IGL00225 G1 11 79395905 I177K T A missense Het probably damaging 0.992 phenotype 12/09/2011
11 306786 APN Nnt 0.227 IGL00225 G1 13 119369997 N371K A T missense Het probably damaging 0.998 phenotype 04/16/2015
12 2333 APN Olfr472 0.089 IGL00225 G1 7 107903104 P129L C T missense Het probably damaging 1.000 phenotype 12/09/2011
13 2325 APN Olfr60 0.069 IGL00225 G1 7 140345210 Y260H A G missense Het probably damaging 1.000 phenotype 12/09/2011
14 2323 APN Oraov1 0.856 IGL00225 G1 7 144917668 G86D G A missense Het possibly damaging 0.943 12/09/2011
15 2111 APN Prkdc 0.954 IGL00225 G1 16 15809644 V3389L G T missense Het possibly damaging 0.638 phenotype 12/09/2011
16 2061 APN Prr16 0.067 IGL00225 G1 18 51303120 Y224N T A missense Het possibly damaging 0.818 12/09/2011
17 2507 APN Ptgs1 0.367 IGL00225 G1 2 36237219 C39Y G A missense Het probably damaging 1.000 phenotype 12/09/2011
18 2133 APN Sla 0.000 IGL00225 G1 15 66782630 D269G T C missense Het possibly damaging 0.587 phenotype 12/09/2011
19 2367 APN Stk38l 0.474 IGL00225 G1 6 146758473 M1K T A start codon destroyed Het probably null 0.048 phenotype 12/09/2011
20 2387 APN Trim24 0.000 IGL00225 G1 6 37903648 N160K T A missense Het possibly damaging 0.757 phenotype 12/09/2011
21 2540 APN Zfp451 0.000 IGL00225 G1 1 33786540 A G intron Het probably benign 12/09/2011
[records 1 to 21 of 21]