Incidental Mutations

43 incidental mutations are currently displayed, and affect 43 genes.
7 are Possibly Damaging.
14 are Probably Damaging.
16 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 43 of 43] 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 365230 APN Aars2 1.000 IGL02958 17 45518172 V755L G T missense Het probably benign 0.001 phenotype 12/18/2015
2 365221 APN Abhd15 0.000 IGL02958 11 77515965 V256A T C missense Het possibly damaging 0.941 12/18/2015
3 365202 APN Agtr1b 0.000 IGL02958 3 20316094 V116E A T missense Het possibly damaging 0.910 phenotype 12/18/2015
4 365215 APN Ahi1 0.768 IGL02958 10 20963799 D203V A T missense Het probably damaging 1.000 phenotype 12/18/2015
5 365244 APN Aplp2 0.000 IGL02958 9 31164676 G T splice site Het probably benign phenotype 12/18/2015
6 365213 APN Arid4a 0.000 IGL02958 12 71097563 S1249P T C missense Het probably benign 0.012 phenotype 12/18/2015
7 365219 APN Asz1 0.343 IGL02958 6 18073814 K298M T A missense Het possibly damaging 0.921 phenotype 12/18/2015
8 365217 APN C4bp 0.000 IGL02958 1 130636795 I384T A G missense Het probably damaging 0.999 12/18/2015
9 365207 APN Cacna1e 0.147 IGL02958 1 154465741 A1236S C A missense Het probably damaging 1.000 phenotype 12/18/2015
10 365224 APN Cdh13 0.000 IGL02958 8 119312721 I634T T C missense Het possibly damaging 0.905 phenotype 12/18/2015
11 365227 APN Cemip 0.094 IGL02958 7 83975055 F524L A T missense Het probably damaging 0.987 phenotype 12/18/2015
12 365204 APN Dnah7c 0.142 IGL02958 1 46657111 R2051H G A missense Het probably damaging 0.999 12/18/2015
13 365222 APN Dnajc17 1.000 IGL02958 2 119185762 K77E T C missense Het probably benign 0.026 phenotype 12/18/2015
14 365242 APN Efhc2 0.244 IGL02958 X 17161246 C T splice site Het probably benign phenotype 12/18/2015
15 365203 APN Ergic2 0.323 IGL02958 6 148181943 *50K A T makesense Het probably null phenotype 12/18/2015
16 365214 APN Fam83g 0.223 IGL02958 11 61707722 P812S C T missense Het probably damaging 1.000 phenotype 12/18/2015
17 365212 APN Flg2 0.108 IGL02958 3 93203613 R983W C T missense Het unknown 0.087 12/18/2015
18 365231 APN Gm7102 0.216 IGL02958 19 61175680 Q106K G T missense Het possibly damaging 0.833 12/18/2015
19 365225 APN Gm9047 0.154 IGL02958 6 29471626 G34R G A missense Het probably damaging 0.999 12/18/2015
20 365236 APN Itih3 0.067 IGL02958 14 30913182 T73A T C missense Het probably benign 0.002 phenotype 12/18/2015
21 365216 APN Kcnj1 0.076 IGL02958 9 32396555 S72G A G missense Het probably damaging 1.000 phenotype 12/18/2015
22 365211 APN Kcnn4 0.199 IGL02958 7 24374745 V78A T C missense Het probably benign 0.001 phenotype 12/18/2015
23 365235 APN Lrp1b 0.000 IGL02958 2 41302916 D1353V T A missense Het probably damaging 0.999 phenotype 12/18/2015
24 365241 APN Lrrc2 0.000 IGL02958 9 110962673 T A critical splice donor site 2 bp Het probably null phenotype 12/18/2015
25 365234 APN Ndufs8 1.000 IGL02958 19 3911232 E45G T C missense Het probably benign 0.095 phenotype 12/18/2015
26 365240 APN Nell1 1.000 IGL02958 7 50220337 G A critical splice donor site 1 bp Het probably null phenotype 12/18/2015
27 365243 APN Nxt1 0.886 IGL02958 2 148675772 A G utr 3 prime Het probably benign phenotype 12/18/2015
28 365208 APN Olfr1039 0.089 IGL02958 2 86131007 I219F T A missense Het probably benign 0.002 phenotype 12/18/2015
29 365209 APN Olfr1390 0.068 IGL02958 11 49341300 Y256C A G missense Het probably benign 0.444 phenotype 12/18/2015
30 365223 APN Pdzd8 0.000 IGL02958 19 59300372 C865* A T nonsense Het probably null 12/18/2015
31 365232 APN Pop1 0.952 IGL02958 15 34530363 C969F G T missense Het probably damaging 0.994 phenotype 12/18/2015
32 365237 APN Rc3h2 0.000 IGL02958 2 37414700 I16S A C missense Het probably damaging 1.000 phenotype 12/18/2015
33 365226 APN Shank1 0.439 IGL02958 7 44354473 V1863A T C missense Het possibly damaging 0.588 phenotype 12/18/2015
34 365228 APN Slc15a4 0.073 IGL02958 5 127604665 L296Q A T missense Het possibly damaging 0.930 phenotype 12/18/2015
35 365210 APN Ssr4 IGL02958 X 73787250 T C unclassified Het probably benign phenotype 12/18/2015
36 365238 APN Supt20 0.940 IGL02958 3 54713723 T A intron Het probably benign phenotype 12/18/2015
37 365229 APN Ttc8 0.504 IGL02958 12 98964544 K282N A T missense Het probably benign 0.027 phenotype 12/18/2015
38 365220 APN Usp40 0.000 IGL02958 1 87978485 V676E A T missense Het probably damaging 0.994 phenotype 12/18/2015
39 365205 APN Vmn1r43 0.054 IGL02958 6 89870049 I152V T C missense Het probably benign 0.085 12/18/2015
40 365206 APN Vmn2r61 0.119 IGL02958 7 42299937 I594F A T missense Het probably benign 0.000 12/18/2015
41 365233 APN Vps53 1.000 IGL02958 11 76117711 I261S A C missense Het probably damaging 0.996 phenotype 12/18/2015
42 365239 APN Wdr19 1.000 IGL02958 5 65212807 T A splice site Het probably null phenotype 12/18/2015
43 365218 APN Zc3hav1 0.088 IGL02958 6 38332984 D301V T A missense Het probably damaging 0.999 phenotype 12/18/2015
[records 1 to 43 of 43]