Incidental Mutations

22 incidental mutations are currently displayed, and affect 21 genes.
1 are Possibly Damaging.
8 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 22 of 22] 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 90992 APN 4931417E11Rik 0.114 IGL01566 G1 6 73468690 T292I G A missense Het probably damaging 1.000 12/09/2013
2 90987 APN AB124611 0.000 IGL01566 G1 9 21535989 V149A T C missense Het possibly damaging 0.455 12/09/2013
3 90999 APN Casc3 0.946 IGL01566 G1 11 98823401 T C critical splice donor site 2 bp Het probably null phenotype 12/09/2013
4 90980 APN Dhdds 1.000 IGL01566 G1 4 133991337 I162V T C missense Het probably damaging 0.991 phenotype 12/09/2013
5 90994 APN Dsg1a 0.097 IGL01566 G1 18 20336783 T C splice site Het probably benign phenotype 12/09/2013
6 90981 APN E030025P04Rik 0.100 IGL01566 G1 11 109143888 D58V T A missense Het unknown 12/09/2013
7 90983 APN Gcn1l1 0.941 IGL01566 G1 5 115611058 N1883S A G missense Het probably damaging 0.996 12/09/2013
8 90982 APN Gucy1a2 0.336 IGL01566 G1 9 3634661 L235P T C missense Het probably damaging 1.000 phenotype 12/09/2013
9 90978 APN Kprp 0.168 IGL01566 G1 3 92823964 N593S T C missense Het probably benign 0.107 phenotype 12/09/2013
10 90995 APN Mme 0.000 IGL01566 G1 3 63361929 T C splice site Het probably benign phenotype 12/09/2013
11 90991 APN Nr6a1 1.000 IGL01566 G1 2 38727889 Q419K G T missense Het probably benign 0.058 phenotype 12/09/2013
12 90997 APN Pcolce 0.110 IGL01566 G1 5 137605160 A G utr 3 prime Het probably benign phenotype 12/09/2013
13 90993 APN Ppp2cb 0.000 IGL01566 G1 8 33611763 R110S C A missense Het probably benign 0.383 phenotype 12/09/2013
14 90990 APN Slc35f1 0.000 IGL01566 G1 10 53089455 Y322C A G missense Het probably damaging 1.000 phenotype 12/09/2013
15 90988 APN Slc5a3 1.000 IGL01566 G1 16 92077577 V174A T C missense Het probably damaging 0.993 phenotype 12/09/2013
16 90985 APN St8sia4 0.000 IGL01566 G1 1 95653757 R87S G T missense Het probably benign 0.190 phenotype 12/09/2013
17 90984 APN Tfdp2 0.920 IGL01566 G1 9 96295030 E5G A G missense Het probably damaging 1.000 phenotype 12/09/2013
18 90979 APN Tmem161b 1.000 IGL01566 G1 13 84294762 I267T T C missense Het probably benign 0.351 phenotype 12/09/2013
19 90986 APN Ttn 1.000 IGL01566 G1 2 76952021 L957P A G missense Het probably damaging 1.000 phenotype 12/09/2013
20 90998 APN Ttn 1.000 IGL01566 G1 2 76782101 A G splice site Het probably benign phenotype 12/09/2013
21 90989 APN Ubqln1 0.574 IGL01566 G1 13 58179667 A T splice site Het probably null phenotype 12/09/2013
22 90996 APN Wdfy3 0.926 IGL01566 G1 5 101896588 A C splice site Het probably benign phenotype 12/09/2013
[records 1 to 22 of 22]