Incidental Mutations

34 incidental mutations are currently displayed, and affect 34 genes.
7 are Possibly Damaging.
10 are Probably Damaging.
12 are Probably Benign.
5 are Probably Null.
1 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 34 of 34] 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 103220 APN Acaca 1.000 IGL01663 G1 11 84277802 I1085V A G missense Het possibly damaging 0.849 phenotype 01/21/2014
2 103234 APN Adamts16 0.000 IGL01663 G1 13 70793141 T376A T C missense Het probably benign 0.012 phenotype 01/21/2014
3 103247 APN Aifm3 0.111 IGL01663 G1 16 17502786 T A critical splice donor site 2 bp Het probably null 01/21/2014
4 103239 APN Ankrd16 0.123 IGL01663 G1 2 11778662 E25G A G missense Het probably damaging 0.996 01/21/2014
5 103252 APN Ano6 0.586 IGL01663 G1 15 95967614 T A splice site Het probably null phenotype 01/21/2014
6 103240 APN Cdh18 0.099 IGL01663 G1 15 23445991 I509T T C missense Het possibly damaging 0.921 phenotype 01/21/2014
7 103245 APN Cdon 0.415 IGL01663 G1 9 35483214 T919A A G missense Het possibly damaging 0.575 phenotype 01/21/2014
8 103225 APN Clca3a2 0.174 IGL01663 G1 3 144817155 P148L G A missense Het probably damaging 0.972 01/21/2014
9 103221 APN Dnph1 0.297 IGL01663 G1 17 46498482 R74L G T missense Het probably benign 0.007 phenotype 01/21/2014
10 103237 APN Epha6 0.000 IGL01663 G1 16 59775644 A895T C T missense Het probably damaging 1.000 phenotype 01/21/2014
11 103250 APN Exoc3l4 0.111 IGL01663 G1 12 111429411 T A splice site Het probably benign 01/21/2014
12 103231 APN Fbll1 0.185 IGL01663 G1 11 35797821 I205T A G missense Het probably damaging 0.999 01/21/2014
13 103226 APN Frem2 1.000 IGL01663 G1 3 53517013 H3001L T A missense Het probably damaging 1.000 phenotype 01/21/2014
14 103241 APN Galk2 0.000 IGL01663 G1 2 125983179 N432D A G missense Het probably benign 0.000 phenotype 01/21/2014
15 103243 APN Gm7535 0.207 IGL01663 G1 17 17911357 A C intron Het probably benign 01/21/2014
16 103229 APN Il10 0.823 IGL01663 G1 1 131021414 E104G A G missense Het probably benign 0.001 phenotype 01/21/2014
17 103238 APN Il1a 0.000 IGL01663 G1 2 129304717 K152R T C missense Het probably benign 0.000 phenotype 01/21/2014
18 103227 APN Kdm1b 0.544 IGL01663 G1 13 47073737 N568K T A missense Het probably damaging 0.994 phenotype 01/21/2014
19 103233 APN Kmt2c 1.000 IGL01663 G1 5 25310670 L2725R A C missense Het probably damaging 1.000 phenotype 01/21/2014
20 103246 APN Krba1 0.067 IGL01663 G1 6 48411754 L527F G T missense Het probably damaging 0.994 01/21/2014
21 103232 APN Lrp2 1.000 IGL01663 G1 2 69428706 S4547P A G missense Het probably benign 0.000 phenotype 01/21/2014
22 103224 APN Nin 0.000 IGL01663 G1 12 70043665 A992E G T missense Het possibly damaging 0.723 phenotype 01/21/2014
23 103222 APN Olfr510 0.067 IGL01663 G1 7 108667891 H158Q T A missense Het probably benign 0.013 phenotype 01/21/2014
24 103219 APN Olfr740 0.104 IGL01663 G1 14 50453150 V33M G A missense Het probably benign 0.043 phenotype 01/21/2014
25 103230 APN Pcdhb1 0.113 IGL01663 G1 18 37267133 I712M A G missense Het possibly damaging 0.826 phenotype 01/21/2014
26 103251 APN Prmt2 0.000 IGL01663 G1 10 76217309 C T splice site 5 bp Het probably null phenotype 01/21/2014
27 103235 APN Rbm20 0.133 IGL01663 G1 19 53840995 V608G T G missense Het probably damaging 1.000 phenotype 01/21/2014
28 103248 APN Smarcc2 0.916 IGL01663 G1 10 128488977 C T unclassified Het probably benign phenotype 01/21/2014
29 103242 APN Speer3 0.054 IGL01663 G1 5 13793222 R48* A T nonsense Het probably null 01/21/2014
30 103223 APN Tlr1 0.000 IGL01663 G1 5 64925073 N720K A T missense Het possibly damaging 0.478 phenotype 01/21/2014
31 103244 APN Tnfrsf21 0.133 IGL01663 G1 17 43087811 M603L A T missense Het probably benign 0.127 phenotype 01/21/2014
32 103249 APN Ttc3 0.714 IGL01663 G1 16 94409731 T A critical splice donor site 2 bp Het probably null 01/21/2014
33 103228 APN Usp4 0.139 IGL01663 G1 9 108365880 A249E C A missense Het possibly damaging 0.798 phenotype 01/21/2014
34 103236 APN Wdr20 0.908 IGL01663 G1 12 110793514 V278E T A missense Het probably damaging 0.997 phenotype 01/21/2014
[records 1 to 34 of 34]