Incidental Mutations

41 incidental mutations are currently displayed, and affect 41 genes.
5 are Possibly Damaging.
20 are Probably Damaging.
12 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 41 of 41] 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 364946 APN 4933415F23Rik 0.026 IGL02952 1 23101990 I81N A T missense Het probably damaging 0.999 12/18/2015
2 364957 APN A2m 0.000 IGL02952 6 121678025 D1436V A T missense Het probably damaging 0.993 phenotype 12/18/2015
3 364947 APN Abca7 0.000 IGL02952 10 80007408 R1239L G T missense Het probably damaging 0.999 phenotype 12/18/2015
4 364981 APN Acp2 0.403 IGL02952 2 91208443 T C unclassified Het probably benign phenotype 12/18/2015
5 364952 APN Adamts4 0.000 IGL02952 1 171251348 N179S A G missense Het probably damaging 0.997 phenotype 12/18/2015
6 364944 APN Adgrv1 0.000 IGL02952 13 81433636 D4763G T C missense Het probably benign 0.005 phenotype 12/18/2015
7 364962 APN Atp11b 0.288 IGL02952 3 35828695 V633A T C missense Het probably damaging 0.998 phenotype 12/18/2015
8 364955 APN Cadm2 0.418 IGL02952 16 66664452 I342K A T missense Het probably damaging 0.990 phenotype 12/18/2015
9 364964 APN Capn10 0.142 IGL02952 1 92945174 S541P T C missense Het probably damaging 0.974 phenotype 12/18/2015
10 364975 APN Ccnf 1.000 IGL02952 17 24231325 L462P A G missense Het possibly damaging 0.930 phenotype 12/18/2015
11 364968 APN Cdc27 0.969 IGL02952 11 104517464 Y546C T C missense Het probably damaging 1.000 phenotype 12/18/2015
12 364979 APN Cep120 0.624 IGL02952 18 53683228 G T utr 3 prime Het probably benign phenotype 12/18/2015
13 364978 APN Cetn2 IGL02952 X 72914202 T C unclassified 706 bp Het probably null phenotype 12/18/2015
14 364971 APN Cyp1a1 0.138 IGL02952 9 57702710 S469L C T missense Het probably benign 0.000 phenotype 12/18/2015
15 364958 APN Dnah17 0.370 IGL02952 11 118088268 T1766I G A missense Het probably benign 0.032 phenotype 12/18/2015
16 364951 APN Doc2g 0.266 IGL02952 19 4006719 G345D G A missense Het possibly damaging 0.826 12/18/2015
17 364977 APN Dock4 0.257 IGL02952 12 40710903 T C critical splice donor site 2 bp Het probably null phenotype 12/18/2015
18 364980 APN Dopey1 0.321 IGL02952 9 86532922 T A splice site Het probably benign 12/18/2015
19 364965 APN Emilin2 0.242 IGL02952 17 71280821 V99F C A missense Het probably damaging 0.993 phenotype 12/18/2015
20 364960 APN Exoc8 0.591 IGL02952 8 124897536 S31P A G missense Het probably benign 0.017 phenotype 12/18/2015
21 364954 APN Fam198b 0.075 IGL02952 3 79886339 L38P T C missense Het probably damaging 1.000 12/18/2015
22 364976 APN Gm3115 IGL02952 14 4084302 T C splice site Het probably benign 12/18/2015
23 364974 APN Gm9742 IGL02952 13 8029894 T A exon Het noncoding transcript 12/18/2015
24 364949 APN Gpr160 0.248 IGL02952 3 30896294 Y172H T C missense Het probably benign 0.004 12/18/2015
25 364956 APN Ifnk 0.061 IGL02952 4 35152495 L141Q T A missense Het probably damaging 1.000 phenotype 12/18/2015
26 364963 APN Klhl36 0.231 IGL02952 8 119870484 E308G A G missense Het probably benign 0.007 12/18/2015
27 364970 APN Lrp1b 0.000 IGL02952 2 41506703 I450M T C missense Het probably benign 0.334 phenotype 12/18/2015
28 364950 APN Noxa1 0.000 IGL02952 2 25091761 Y110C T C missense Het probably damaging 1.000 phenotype 12/18/2015
29 364948 APN Olfr287 0.079 IGL02952 15 98207589 Y265C T C missense Het probably damaging 0.999 phenotype 12/18/2015
30 364972 APN Pkd2 1.000 IGL02952 5 104480160 T367S A T missense Het possibly damaging 0.482 phenotype 12/18/2015
31 364961 APN Polg2 1.000 IGL02952 11 106772713 I385V T C missense Het possibly damaging 0.782 phenotype 12/18/2015
32 364969 APN Prr14l 0.191 IGL02952 5 32835670 S17P A G missense Het unknown 12/18/2015
33 364967 APN Prss22 0.172 IGL02952 17 23996723 C75F C A missense Het probably damaging 1.000 phenotype 12/18/2015
34 364953 APN Ptgs1 0.569 IGL02952 2 36251241 K567E A G missense Het probably benign 0.001 phenotype 12/18/2015
35 364959 APN Ptprz1 0.342 IGL02952 6 23036926 I1141M A G missense Het probably damaging 0.998 phenotype 12/18/2015
36 364966 APN R3hcc1l 0.126 IGL02952 19 42563994 K477E A G missense Het probably damaging 0.973 12/18/2015
37 364973 APN Riok1 0.937 IGL02952 13 38048890 Y194C A G missense Het probably damaging 1.000 phenotype 12/18/2015
38 364941 APN Smr2 0.052 IGL02952 5 88088236 C16S T A missense Het possibly damaging 0.711 12/18/2015
39 364945 APN Stk25 0.000 IGL02952 1 93626076 I187N A T missense Het probably damaging 1.000 phenotype 12/18/2015
40 364943 APN Trhde 0.094 IGL02952 10 114800573 E243G T C missense Het probably damaging 0.987 phenotype 12/18/2015
41 364942 APN Vmn2r3 0.000 IGL02952 3 64278835 E143G T C missense Het probably damaging 0.998 12/18/2015
[records 1 to 41 of 41]