Incidental Mutations

29 incidental mutations are currently displayed, and affect 29 genes.
5 are Possibly Damaging.
13 are Probably Damaging.
6 are Probably Benign.
4 are Probably Null.
2 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 29 of 29] 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 87976 APN 2210408I21Rik 0.000 IGL01461 G1 13 77281095 F767S T C missense Het probably benign 0.255 11/18/2013
2 87999 APN 2810474O19Rik 0.000 IGL01461 G1 6 149331515 T C unclassified Het probably benign 11/18/2013
3 278496 APN Abca13 0.000 IGL01461 G1 11 9403834 T3719A A G missense Het probably damaging 0.974 phenotype 04/16/2015
4 87978 APN Apob 0.896 IGL01461 G1 12 8001884 M1137L A T missense Het probably benign 0.129 phenotype 11/18/2013
5 87987 APN Brd9 1.000 IGL01461 G1 13 73951598 Q445* C T nonsense Het probably null 11/18/2013
6 87990 APN Cdh23 0.598 IGL01461 G1 10 60409147 T990A T C missense Het possibly damaging 0.528 phenotype 11/18/2013
7 87995 APN Cenpf 0.572 IGL01461 G1 1 189657096 L1513S A G missense Het probably damaging 1.000 phenotype 11/18/2013
8 87984 APN Col27a1 1.000 IGL01461 G1 4 63224243 K56R A G missense Het probably damaging 0.998 phenotype 11/18/2013
9 87983 APN Cryaa 0.000 IGL01461 G1 17 31681026 Y118C A G missense Het probably damaging 1.000 phenotype 11/18/2013
10 87985 APN Dtl 1.000 IGL01461 G1 1 191546617 T378A T C missense Het possibly damaging 0.879 phenotype 11/18/2013
11 87996 APN E330020D12Rik 0.085 IGL01461 G1 1 153408359 A G exon Het noncoding transcript 11/18/2013
12 87981 APN F7 0.092 IGL01461 G1 8 13032245 D145G A G missense Het possibly damaging 0.941 phenotype 11/18/2013
13 87998 APN Flvcr2 0.895 IGL01461 G1 12 85803131 A G splice site Het probably benign phenotype 11/18/2013
14 87973 APN Hltf 1.000 IGL01461 G1 3 20099939 K680* A T nonsense Het probably null phenotype 11/18/2013
15 87989 APN Ing1 0.961 IGL01461 G1 8 11561453 F22V T G missense Het probably benign 0.332 phenotype 11/18/2013
16 87979 APN Ipo5 0.925 IGL01461 G1 14 120928533 D330G A G missense Het probably damaging 0.978 phenotype 11/18/2013
17 87988 APN Itgax 0.071 IGL01461 G1 7 128135018 D321Y G T missense Het probably damaging 0.996 phenotype 11/18/2013
18 87994 APN Kdelc1 0.308 IGL01461 G1 1 44110934 Q365R T C missense Het probably damaging 1.000 phenotype 11/18/2013
19 87997 APN Kel 0.088 IGL01461 G1 6 41701911 A C critical splice donor site 2 bp Het probably null phenotype 11/18/2013
20 278495 APN March10 0.056 IGL01461 G1 11 105389605 K618R T C missense Het probably damaging 1.000 phenotype 04/16/2015
21 87992 APN Mast4 0.282 IGL01461 G1 13 102754068 M925L T A missense Het probably damaging 1.000 phenotype 11/18/2013
22 87982 APN Miga1 0.000 IGL01461 G1 3 152335297 E78K C T missense Het probably damaging 1.000 11/18/2013
23 87975 APN Olfr1204 0.059 IGL01461 G1 2 88852325 C125F G T missense Het probably damaging 0.994 phenotype 11/18/2013
24 87974 APN Olfr58 0.054 IGL01461 G1 9 19783949 T A splice site 557 bp Het probably null phenotype 11/18/2013
25 87980 APN Pkdrej 0.098 IGL01461 G1 15 85820374 I454V T C missense Het possibly damaging 0.771 phenotype 11/18/2013
26 87986 APN Prpf6 1.000 IGL01461 G1 2 181631511 T283N C A missense Het probably benign 0.000 phenotype 11/18/2013
27 87991 APN R3hdm1 0.000 IGL01461 G1 1 128178906 H197R A G missense Het probably damaging 0.999 11/18/2013
28 87977 APN Smpd4 0.123 IGL01461 G1 16 17621506 Q7P A C missense Het probably damaging 0.999 phenotype 11/18/2013
29 87993 APN Vmn2r84 0.077 IGL01461 G1 10 130391225 I248K A T missense Het possibly damaging 0.655 11/18/2013
[records 1 to 29 of 29]