Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
2 are Possibly Damaging.
10 are Probably Damaging.
16 are Probably Benign.
3 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 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 79256 APN Acvr1 1.000 IGL01392 G1 2 58500546 V2A A G missense Het probably benign 0.013 phenotype 11/05/2013
2 79246 APN Adgrf5 0.000 IGL01392 G1 17 43450012 Q866L A T missense Het probably benign 0.003 phenotype 11/05/2013
3 79251 APN Ankrd13a 0.129 IGL01392 G1 5 114797853 E295G A G missense Het probably benign 0.000 11/05/2013
4 79243 APN Arid1a 1.000 IGL01392 G1 4 133681037 D2053G T C missense Het unknown phenotype 11/05/2013
5 79267 APN Calr4 0.130 IGL01392 G1 4 109253874 E272G A G missense Het probably benign 0.411 11/05/2013
6 79255 APN Cmya5 0.277 IGL01392 G1 13 93089206 S3125G T C missense Het probably damaging 0.993 11/05/2013
7 79254 APN Dnah7b 0.138 IGL01392 G1 1 46126788 Y538H T C missense Het probably damaging 1.000 11/05/2013
8 79270 APN Eri3 0.000 IGL01392 G1 4 117589159 T C critical splice donor site 2 bp Het probably null 11/05/2013
9 79265 APN Fmo6 0.079 IGL01392 G1 1 162930011 R63* T A nonsense Het probably null 11/05/2013
10 79242 APN Gm7168 0.098 IGL01392 G1 17 13948907 D179N G A missense Het probably benign 0.000 11/05/2013
11 79250 APN Gm8979 0.215 IGL01392 G1 7 106083755 I98V T C missense Het probably benign 0.007 11/05/2013
12 79253 APN Got1l1 0.056 IGL01392 G1 8 27197991 T337A T C missense Het probably damaging 0.999 11/05/2013
13 79248 APN Igf2r 0.926 IGL01392 G1 17 12704349 M1191T A G missense Het probably benign 0.000 phenotype 11/05/2013
14 79240 APN Ighv1-54 0.265 IGL01392 G1 12 115193937 L30P A G missense Het probably damaging 1.000 11/05/2013
15 79247 APN Igkv8-30 0.151 IGL01392 G1 6 70117347 S27P A G missense Het probably benign 0.146 11/05/2013
16 79258 APN Kcnab2 0.123 IGL01392 G1 4 152393797 V335E A T missense Het possibly damaging 0.941 phenotype 11/05/2013
17 79268 APN Klf12 0.376 IGL01392 G1 14 100149757 I3N A T missense Het probably damaging 0.986 phenotype 11/05/2013
18 79262 APN Megf8 0.939 IGL01392 G1 7 25363749 V2510A T C missense Het probably benign 0.032 phenotype 11/05/2013
19 79260 APN Mme 0.000 IGL01392 G1 3 63362046 D592G A G missense Het probably damaging 0.999 phenotype 11/05/2013
20 79261 APN Myh1 0.000 IGL01392 G1 11 67221301 N1727S A G missense Het probably benign 0.203 phenotype 11/05/2013
21 79257 APN Ncor1 1.000 IGL01392 G1 11 62340594 S796P A G missense Het probably damaging 0.988 phenotype 11/05/2013
22 79271 APN Nlrp14 0.203 IGL01392 G1 7 107197913 A G utr 3 prime Het probably benign phenotype 11/05/2013
23 79244 APN Olfr1443 0.050 IGL01392 G1 19 12680803 Y232N T A missense Het probably benign 0.424 phenotype 11/05/2013
24 79241 APN Olfr508 0.118 IGL01392 G1 7 108630678 R229C C T missense Het probably benign 0.007 phenotype 11/05/2013
25 79259 APN Olfr564 0.074 IGL01392 G1 7 102803854 Y125* T A nonsense Het probably null phenotype 11/05/2013
26 79249 APN Plekhm2 0.000 IGL01392 G1 4 141642426 V86A A G missense Het probably damaging 0.981 phenotype 11/05/2013
27 79252 APN Popdc2 0.000 IGL01392 G1 16 38374131 V305L G T missense Het probably benign 0.000 phenotype 11/05/2013
28 79239 APN Prpmp5 0.135 IGL01392 G1 6 132312420 N147S T C missense Het unknown 11/05/2013
29 79263 APN Rttn 1.000 IGL01392 G1 18 88995613 H469Y C T missense Het probably benign 0.027 phenotype 11/05/2013
30 79245 APN Slc2a12 0.000 IGL01392 G1 10 22664684 V146A T C missense Het probably damaging 0.969 phenotype 11/05/2013
31 79264 APN Sptlc3 0.117 IGL01392 G1 2 139546421 E111G A G missense Het possibly damaging 0.554 phenotype 11/05/2013
32 79269 APN Zfp108 0.066 IGL01392 G1 7 24258447 T C splice site Het probably benign 11/05/2013
33 79266 APN Zfp719 0.000 IGL01392 G1 7 43591130 F714Y T A missense Het probably damaging 0.999 11/05/2013
[records 1 to 33 of 33]