Incidental Mutations

19 incidental mutations are currently displayed, and affect 19 genes.
3 are Possibly Damaging.
4 are Probably Damaging.
10 are Probably Benign.
2 are Probably Null.
0 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 19 of 19] 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 8514 APN Aars 0.967 IGL00731 G1 8 111044869 A G splice site Het probably benign phenotype 12/06/2012
2 8586 APN Adcy10 0.188 IGL00731 G1 1 165572614 F1531L T C missense Het probably benign 0.000 phenotype 12/06/2012
3 10048 APN Dab2 0.920 IGL00731 G1 15 6435710 S463P T C missense Het possibly damaging 0.953 phenotype 12/06/2012
4 10454 APN Ehf 0.738 IGL00731 G1 2 103266840 C T splice site 236 bp Het probably null phenotype 12/06/2012
5 10792 APN Fnbp4 0.923 IGL00731 G1 2 90768643 V704L G T missense Het probably benign 0.000 12/06/2012
6 10928 APN Gbp7 0.088 IGL00731 G1 3 142546428 S591P T C missense Het probably benign 0.012 phenotype 12/06/2012
7 11102 APN Gpr155 0.000 IGL00731 G1 2 73362613 L498P A G missense Het probably damaging 1.000 12/06/2012
8 11424 APN Igll1 0.076 IGL00731 G1 16 16860919 T176A T C missense Het probably benign 0.036 phenotype 12/06/2012
9 11662 APN Klk1b21 0.048 IGL00731 G1 7 44105923 E182G A G missense Het possibly damaging 0.813 phenotype 12/06/2012
10 277862 APN Mb21d1 0.158 IGL00731 G1 9 78435488 P344L G A missense Het probably damaging 0.988 phenotype 04/16/2015
11 12769 APN Npat 1.000 IGL00731 G1 9 53562086 E393K G A missense Het probably damaging 0.987 12/06/2012
12 12772 APN Npnt 0.134 IGL00731 G1 3 132904657 C T critical splice donor site 1 bp Het probably null phenotype 12/06/2012
13 12956 APN Pde2a 0.715 IGL00731 G1 7 101508099 Y693C A G missense Het probably benign 0.040 phenotype 12/06/2012
14 13738 APN Ralgapa1 0.856 IGL00731 G1 12 55702452 S1269P A G missense Het possibly damaging 0.936 phenotype 12/06/2012
15 13760 APN Rasal2 0.000 IGL00731 G1 1 157157764 D804E A C missense Het probably benign 0.006 phenotype 12/06/2012
16 13791 APN Rdh10 0.920 IGL00731 G1 1 16107875 N124D A G missense Het probably benign 0.000 phenotype 12/06/2012
17 14140 APN Slit3 0.855 IGL00731 G1 11 35622154 D536Y G T missense Het probably damaging 1.000 phenotype 12/06/2012
18 14179 APN Snx24 0.072 IGL00731 G1 18 53384609 C T splice site Het probably benign 12/06/2012
19 29385 APN Spink12 0.000 IGL00731 G1 18 44108110 G A utr 3 prime Het probably benign 04/17/2013
[records 1 to 19 of 19]