Incidental Mutations

30 incidental mutations are currently displayed, and affect 30 genes.
4 are Possibly Damaging.
7 are Probably Damaging.
14 are Probably Benign.
3 are Probably Null.
3 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 30 of 30] 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 8988 APN Ap5m1 0.000 IGL00323 G1 14 49073790 Y106H T C missense Het probably damaging 1.000 12/06/2012
2 9154 APN Atrnl1 0.167 IGL00323 G1 19 57691817 N716K C A missense Het probably benign 0.019 phenotype 12/06/2012
3 9564 APN Cdk13 1.000 IGL00323 G1 13 17721098 N1075K A T missense Het possibly damaging 0.876 phenotype 12/06/2012
4 10044 APN Daam1 1.000 IGL00323 G1 12 71958743 G A splice site Het probably benign phenotype 12/06/2012
5 10566 APN Exd2 0.121 IGL00323 G1 12 80476166 V133A T C missense Het probably damaging 0.999 12/06/2012
6 10666 APN Fam58b 1.000 IGL00323 G1 11 78750956 V236A A G missense Het probably benign 0.444 phenotype 12/06/2012
7 10974 APN Glrb 1.000 IGL00323 G1 3 80861955 D155G T C missense Het probably damaging 0.999 phenotype 12/06/2012
8 332247 APN Gm13941 0.120 IGL00323 G1 2 111104853 M11L T A missense Het unknown 08/05/2015
9 332250 APN Gm4553 IGL00323 G1 7 142165227 S155G T C missense Het unknown 08/05/2015
10 11466 APN Inpp5d 0.926 IGL00323 G1 1 87683815 V329F G T missense Het probably benign 0.001 phenotype 12/06/2012
11 11070 APN Lilr4b 0.290 IGL00323 G1 10 51481251 D61V A T missense Het probably benign 0.002 12/06/2012
12 11888 APN Malt1 0.497 IGL00323 G1 18 65448963 C299* T A nonsense Het probably null phenotype 12/06/2012
13 12843 APN Olfr1306 0.137 IGL00323 G1 2 111912036 M298K A T missense Het possibly damaging 0.950 phenotype 12/06/2012
14 12844 APN Olfr1408 0.082 IGL00323 G1 1 173130411 Q269* G A nonsense Het probably null phenotype 12/06/2012
15 13005 APN Pigk 0.851 IGL00323 G1 3 152747632 S282* C A nonsense Het probably null phenotype 12/06/2012
16 13014 APN Pik3r1 0.000 IGL00323 G1 13 101690536 M1L T A start codon destroyed Het probably benign 0.000 phenotype 12/06/2012
17 13078 APN Pnpla1 0.107 IGL00323 G1 17 28877442 Y165C A G missense Het probably damaging 1.000 phenotype 12/06/2012
18 13812 APN Rfx7 0.804 IGL00323 G1 9 72617420 N631D A G missense Het probably damaging 0.968 phenotype 12/06/2012
19 13855 APN Rp1 0.098 IGL00323 G1 1 4346746 D1381V T A missense Het probably damaging 0.981 phenotype 12/06/2012
20 27737 APN Rrp8 0.294 IGL00323 G1 7 105733016 T C unclassified Het probably benign 04/17/2013
21 13935 APN Scn4a 1.000 IGL00323 G1 11 106319919 D1757E A T missense Het probably benign 0.000 phenotype 12/06/2012
22 332252 APN Sec62 0.871 IGL00323 G1 3 30810442 T C splice site Het probably benign phenotype 08/05/2015
23 14149 APN Smarca5 1.000 IGL00323 G1 8 80714041 T598M G A missense Het probably benign 0.099 phenotype 12/06/2012
24 332248 APN Sptbn5 0.367 IGL00323 G1 2 120054467 T C unclassified Het probably benign 08/05/2015
25 332251 APN Srcap 0.960 IGL00323 G1 7 127542713 T C splice site Het probably benign phenotype 08/05/2015
26 14251 APN Stab1 0.000 IGL00323 G1 14 31139306 E71D T A missense Het probably benign 0.041 phenotype 12/06/2012
27 332249 APN Trhde 0.138 IGL00323 G1 10 114486747 S716R A T missense Het possibly damaging 0.773 phenotype 08/05/2015
28 10378 APN Ttn 1.000 IGL00323 G1 2 76896515 T C intron Het probably benign phenotype 12/06/2012
29 14874 APN Wscd2 0.000 IGL00323 G1 5 113551175 T81P A C missense Het possibly damaging 0.560 12/06/2012
30 14967 APN Zfp335 1.000 IGL00323 G1 2 164892382 T1295I G A missense Het probably damaging 0.999 phenotype 12/06/2012
[records 1 to 30 of 30]