Incidental Mutations

28 incidental mutations are currently displayed, and affect 28 genes.
5 are Possibly Damaging.
9 are Probably Damaging.
12 are Probably Benign.
2 are Probably Null.
0 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 28 of 28] 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 26834 APN 1500012F01Rik IGL00903 G1 2 167065486 G T critical splice donor site 6 bp Het probably benign 04/17/2013
2 28830 APN Arsk 0.103 IGL00903 G1 13 76098368 A G splice site 6 bp Het probably null phenotype 04/17/2013
3 29490 APN As3mt 0.165 IGL00903 G1 19 46712234 I159V A G missense Het probably benign 0.041 phenotype 04/17/2013
4 28828 APN Ctsll3 0.000 IGL00903 G1 13 60800261 V201L C A missense Het probably benign 0.177 04/17/2013
5 28826 APN Dapk1 0.275 IGL00903 G1 13 60761397 Y1275H T C missense Het probably damaging 0.992 phenotype 04/17/2013
6 28829 APN Erap1 0.219 IGL00903 G1 13 74673707 R727H G A missense Het probably benign 0.000 phenotype 04/17/2013
7 29034 APN Fam173b 0.164 IGL00903 G1 15 31606115 V73A T C missense Het possibly damaging 0.886 04/17/2013
8 26605 APN Fcrl6 0.028 IGL00903 G1 1 172599107 T91S T A missense Het probably benign 0.077 04/17/2013
9 27773 APN Gvin1 IGL00903 G1 7 106158170 E2364G T C missense Het probably benign 0.005 04/17/2013
10 28127 APN Hacd3 0.190 IGL00903 G1 9 65004253 T C splice site Het probably benign 04/17/2013
11 29132 APN Hcls1 0.383 IGL00903 G1 16 36956021 T A critical splice donor site 2 bp Het probably null phenotype 04/17/2013
12 29245 APN Igf2r 0.751 IGL00903 G1 17 12683867 R2432H C T missense Het possibly damaging 0.699 phenotype 04/17/2013
13 28827 APN Kif27 0.137 IGL00903 G1 13 58344672 V218F C A missense Het possibly damaging 0.695 phenotype 04/17/2013
14 26604 APN Klhl20 0.163 IGL00903 G1 1 161090506 Y70C T C missense Het probably benign 0.001 phenotype 04/17/2013
15 278056 APN Krt86 0.143 IGL00903 G1 15 101473860 H104Y C T missense Het probably benign 0.001 phenotype 04/16/2015
16 26833 APN Lcn12 IGL00903 G1 2 25493320 N15K G T missense Het possibly damaging 0.934 phenotype 04/17/2013
17 27774 APN Mrgpra1 0.049 IGL00903 G1 7 47335578 M118V T C missense Het probably benign 0.001 04/17/2013
18 28489 APN Nacad 0.381 IGL00903 G1 11 6600632 T853K G T missense Het probably damaging 0.987 04/17/2013
19 27383 APN Nos3 0.711 IGL00903 G1 5 24369862 Q293L A T missense Het probably damaging 0.999 phenotype 04/17/2013
20 28490 APN Prkca 0.382 IGL00903 G1 11 107983974 V381M C T missense Het probably damaging 0.998 phenotype 04/17/2013
21 27587 APN Ptcd3 0.926 IGL00903 G1 6 71907844 F37S A G missense Het possibly damaging 0.933 04/17/2013
22 26603 APN Ptgs2 0.515 IGL00903 G1 1 150104424 Y371C A G missense Het probably damaging 1.000 phenotype 04/17/2013
23 28699 APN Pygl 0.411 IGL00903 G1 12 70207742 Y143C T C missense Het probably damaging 1.000 phenotype 04/17/2013
24 26835 APN Samhd1 0.000 IGL00903 G1 2 157107423 A G splice site Het probably benign phenotype 04/17/2013
25 29035 APN Scube1 0.156 IGL00903 G1 15 83703501 H89L T A missense Het probably damaging 0.984 phenotype 04/17/2013
26 27987 APN Tmem59l 0.048 IGL00903 G1 8 70485665 G A splice site Het probably benign phenotype 04/17/2013
27 29246 APN Vmn2r108 0.093 IGL00903 G1 17 20462512 V810A A G missense Het probably damaging 0.980 04/17/2013
28 27772 APN Vmn2r61 0.105 IGL00903 G1 7 42300511 F785C T G missense Het probably damaging 1.000 04/17/2013
[records 1 to 28 of 28]