Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
3 are Possibly Damaging.
12 are Probably Damaging.
12 are Probably Benign.
5 are Probably Null.
2 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 33 of 33] 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 93132 APN 4932438A13Rik 1.000 IGL01638 G1 3 36974311 N2377D A G missense Het probably damaging 0.999 phenotype 12/09/2013
2 93147 APN Adamts9 1.000 IGL01638 G1 6 92872428 T436A T C missense Het probably benign 0.193 phenotype 12/09/2013
3 93152 APN Adgrb3 0.493 IGL01638 G1 1 25559751 T A splice site Het probably benign phenotype 12/09/2013
4 93150 APN Ajap1 0.000 IGL01638 G1 4 153432236 V216A A G missense Het possibly damaging 0.927 12/09/2013
5 93135 APN Akap7 0.000 IGL01638 G1 10 25267425 I124F T A missense Het probably damaging 0.997 phenotype 12/09/2013
6 93146 APN Arfgef2 0.522 IGL01638 G1 2 166873945 V1385M G A missense Het probably damaging 0.967 phenotype 12/09/2013
7 93145 APN Arhgap30 0.000 IGL01638 G1 1 171397570 K65E A G missense Het probably damaging 1.000 12/09/2013
8 93129 APN Cacna1a 0.931 IGL01638 G1 8 84571827 F1260S T C missense Het probably damaging 0.978 phenotype 12/09/2013
9 93124 APN Cad 0.967 IGL01638 G1 5 31067614 C954S T A missense Het probably damaging 1.000 phenotype 12/09/2013
10 93144 APN Fcmr 0.000 IGL01638 G1 1 130875122 E157D A T missense Het probably benign 0.057 phenotype 12/09/2013
11 93142 APN Gm4204 0.127 IGL01638 G1 1 135233135 A T exon Het noncoding transcript 12/09/2013
12 93133 APN Gzmn 0.054 IGL01638 G1 14 56169019 D16E A T missense Het probably benign 0.031 12/09/2013
13 93151 APN Krt86 0.065 IGL01638 G1 15 101475472 A C splice site Het probably benign phenotype 12/09/2013
14 93128 APN Macc1 0.066 IGL01638 G1 12 119446511 L338P T C missense Het probably benign 0.003 phenotype 12/09/2013
15 93139 APN Ms4a6d 0.074 IGL01638 G1 19 11587168 L113Q A T missense Het probably damaging 0.990 phenotype 12/09/2013
16 93131 APN Myh15 0.183 IGL01638 G1 16 49069480 S145P T C missense Het probably damaging 1.000 12/09/2013
17 93125 APN Nav3 0.000 IGL01638 G1 10 109852863 K518E T C missense Het probably damaging 0.995 phenotype 12/09/2013
18 93123 APN Olfr974 0.075 IGL01638 G1 9 39942520 S87P T C missense Het probably benign 0.029 phenotype 12/09/2013
19 93137 APN Parp11 0.000 IGL01638 G1 6 127491529 F181I T A missense Het probably benign 0.134 phenotype 12/09/2013
20 93136 APN Ppil1 0.874 IGL01638 G1 17 29261792 K52N C A missense Het probably benign 0.085 phenotype 12/09/2013
21 93143 APN Prl5a1 0.056 IGL01638 G1 13 28145439 C34S T A missense Het possibly damaging 0.770 12/09/2013
22 93127 APN Prss55 0.069 IGL01638 G1 14 64077187 V178A A G missense Het probably benign 0.023 phenotype 12/09/2013
23 93141 APN S100a7a 0.068 IGL01638 G1 3 90655530 D8G A G missense Het probably benign 0.181 12/09/2013
24 93149 APN Sh3glb2 0.223 IGL01638 G1 2 30345850 V310A A G missense Het possibly damaging 0.725 12/09/2013
25 93155 APN Slc22a7 0.088 IGL01638 G1 17 46437994 T C splice site 3 bp Het probably null phenotype 12/09/2013
26 93134 APN Slc27a6 0.055 IGL01638 G1 18 58607813 D482G A G missense Het probably damaging 1.000 phenotype 12/09/2013
27 93138 APN Smarcc2 0.871 IGL01638 G1 10 128488074 T A unclassified Het probably benign phenotype 12/09/2013
28 93140 APN Specc1l 0.566 IGL01638 G1 10 75246205 Y478* T A nonsense Het probably null phenotype 12/09/2013
29 93153 APN Spryd3 0.000 IGL01638 G1 15 102130276 A G critical splice donor site 2 bp Het probably null 12/09/2013
30 93126 APN Tcerg1l 0.000 IGL01638 G1 7 138280076 R295C G A missense Het probably damaging 0.998 12/09/2013
31 93148 APN Trpv1 0.414 IGL01638 G1 11 73253329 I637T T C missense Het probably damaging 0.980 phenotype 12/09/2013
32 93154 APN Ttc7 0.742 IGL01638 G1 17 87359112 A C critical splice acceptor site Het probably null phenotype 12/09/2013
33 93130 APN Vmn1r6 0.111 IGL01638 G1 6 57003192 Q280* C T nonsense Het probably null 12/09/2013
[records 1 to 33 of 33]