Incidental Mutations

43 incidental mutations are currently displayed, and affect 43 genes.
6 are Possibly Damaging.
17 are Probably Damaging.
11 are Probably Benign.
8 are Probably Null.
5 create premature stop codons.
1 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 306604 APN AI606181 0.218 IGL00963 G1 19 41593789 A C utr 3 prime Het probably benign 04/16/2015
2 26728 APN Alyref2 0.810 IGL00963 G1 1 171504248 Q198* C T nonsense Het probably null 04/17/2013
3 27494 APN Ankrd13a 0.106 IGL00963 G1 5 114801802 S497P T C missense Het probably damaging 0.994 04/17/2013
4 27310 APN Chd5 0.000 IGL00963 G1 4 152382938 N1644K C A missense Het probably damaging 0.995 phenotype 04/17/2013
5 28398 APN Col13a1 0.000 IGL00963 G1 10 61838697 T C utr 3 prime Het probably benign phenotype 04/17/2013
6 28397 APN Ctnna3 0.264 IGL00963 G1 10 64945949 D730E T A missense Het probably damaging 0.996 phenotype 04/17/2013
7 29594 APN Dock11 0.262 IGL00963 G1 X 36032382 Q1197R A G missense Het possibly damaging 0.629 04/17/2013
8 29088 APN Drosha 0.957 IGL00963 G1 15 12925997 I1224N T A missense Het probably damaging 0.994 phenotype 04/17/2013
9 29439 APN Dsc1 0.070 IGL00963 G1 18 20111986 K42R T C missense Het probably null 0.007 phenotype 04/17/2013
10 28605 APN Engase 0.087 IGL00963 G1 11 118482998 D322G A G missense Het probably damaging 1.000 phenotype 04/17/2013
11 27308 APN Ephb2 0.851 IGL00963 G1 4 136658951 D829G T C missense Het probably benign 0.035 phenotype 04/17/2013
12 27889 APN Fgfr2 1.000 IGL00963 G1 7 130228761 M47I C T missense Het probably damaging 0.994 phenotype 04/17/2013
13 306602 APN Gad1-ps 0.148 IGL00963 G1 10 99445448 G T exon Het noncoding transcript 04/16/2015
14 27147 APN Gatb 0.958 IGL00963 G1 3 85618948 S378G A G missense Het probably benign 0.005 04/17/2013
15 28395 APN Hivep2 0.853 IGL00963 G1 10 14129347 S563N G A missense Het probably damaging 0.999 phenotype 04/17/2013
16 28056 APN Irs2 0.613 IGL00963 G1 8 11005867 A855V G A missense Het probably benign 0.001 phenotype 04/17/2013
17 27686 APN Jagn1 IGL00963 G1 6 113447475 S103P T C missense Het probably damaging 0.999 phenotype 04/17/2013
18 29595 APN Kdm6a 1.000 IGL00963 G1 X 18246426 T A splice site Het probably benign phenotype 04/17/2013
19 27685 APN Lmcd1 0.000 IGL00963 G1 6 112329934 C356R T C missense Het probably damaging 1.000 phenotype 04/17/2013
20 29184 APN Mefv 0.098 IGL00963 G1 16 3715720 Y229F T A missense Het possibly damaging 0.828 phenotype 04/17/2013
21 26974 APN Myef2 0.312 IGL00963 G1 2 125115475 Y120C T C missense Het probably damaging 1.000 04/17/2013
22 28231 APN Myo9a 0.000 IGL00963 G1 9 59900372 I2074S T G missense Het probably damaging 0.976 phenotype 04/17/2013
23 29593 APN Nhs 0.000 IGL00963 G1 X 161847049 S337P A G missense Het probably damaging 0.999 phenotype 04/17/2013
24 27307 APN Nphp4 0.169 IGL00963 G1 4 152537861 H566Q T G missense Het probably benign 0.010 phenotype 04/17/2013
25 27888 APN Olfr618 0.059 IGL00963 G1 7 103597637 T A unclassified Het probably null phenotype 04/17/2013
26 27890 APN Olfr715 0.175 IGL00963 G1 7 107129065 C109* A T nonsense Het probably null phenotype 04/17/2013
27 29440 APN Pabpc2 0.142 IGL00963 G1 18 39775337 Q552K C A missense Het possibly damaging 0.784 04/17/2013
28 27309 APN Podn 0.000 IGL00963 G1 4 108022174 N104I T A missense Het probably damaging 1.000 phenotype 04/17/2013
29 27146 APN Rit1 0.125 IGL00963 G1 3 88726431 V94A T C missense Het probably damaging 1.000 phenotype 04/17/2013
30 26976 APN Scn7a 0.113 IGL00963 G1 2 66703945 A T splice site Het probably benign phenotype 04/17/2013
31 28606 APN Sept4 0.673 IGL00963 G1 11 87583373 K29M A T missense Het possibly damaging 0.893 phenotype 04/17/2013
32 27495 APN Sowahb 0.237 IGL00963 G1 5 93044011 Y283C T C missense Het probably damaging 0.982 phenotype 04/17/2013
33 29327 APN Srbd1 0.958 IGL00963 G1 17 86115209 W460R A T missense Het probably damaging 0.997 04/17/2013
34 27306 APN Svep1 1.000 IGL00963 G1 4 58072791 K2173* T A nonsense Het probably null phenotype 04/17/2013
35 27493 APN Tlr6 0.098 IGL00963 G1 5 64954676 N296S T C missense Het possibly damaging 0.894 phenotype 04/17/2013
36 26727 APN Trpm8 0.275 IGL00963 G1 1 88379827 D1073G A G missense Het possibly damaging 0.820 phenotype 04/17/2013
37 306603 APN Ttc28 0.000 IGL00963 G1 5 111286389 K2399* A T nonsense Het probably null 04/16/2015
38 26975 APN Ttn 1.000 IGL00963 G1 2 76887283 A G intron Het probably benign phenotype 04/17/2013
39 27687 APN Uroc1 0.000 IGL00963 G1 6 90338828 T189I C T missense Het probably benign 0.000 phenotype 04/17/2013
40 27688 APN Usp18 0.167 IGL00963 G1 6 121255382 Q122* C T nonsense Het probably null phenotype 04/17/2013
41 306600 APN Zfp420 0.000 IGL00963 G1 7 29875093 I246T T C missense Het probably damaging 0.997 phenotype 04/16/2015
42 27496 APN Zfp644 0.176 IGL00963 G1 5 106638637 T C critical splice acceptor site Het probably null phenotype 04/17/2013
43 29328 APN Zfp871 1.000 IGL00963 G1 17 32774752 V483E A T missense Het probably benign 0.253 04/17/2013
[records 1 to 43 of 43]