Incidental Mutations

55 incidental mutations are currently displayed, and affect 54 genes.
15 are Possibly Damaging.
20 are Probably Damaging.
14 are Probably Benign.
5 are Probably Null.
3 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 55 of 55] 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 84527 APN 1700020A23Rik IGL01448 G1 2 130405847 E75D A T missense Het possibly damaging 0.587 11/11/2013
2 84510 APN 1700084J12Rik IGL01448 G1 15 33405633 A G intron Het probably benign 11/11/2013
3 84525 APN 2610303G11Rik 0.164 IGL01448 G1 9 98186709 T A exon Het noncoding transcript 11/11/2013
4 84488 APN 4931414P19Rik 0.082 IGL01448 G1 14 54585960 D320G T C missense Het possibly damaging 0.775 11/11/2013
5 84496 APN Adamts6 0.740 IGL01448 G1 13 104297164 E34K G A missense Het probably damaging 1.000 phenotype 11/11/2013
6 84535 APN Alms1 0.000 IGL01448 G1 6 85677899 N3142K T A missense Het possibly damaging 0.934 phenotype 11/11/2013
7 84491 APN Anapc7 0.913 IGL01448 G1 5 122428213 A62T G A missense Het probably damaging 0.999 phenotype 11/11/2013
8 84495 APN Atp8b3 0.194 IGL01448 G1 10 80520422 P1152L G A missense Het probably benign 0.018 phenotype 11/11/2013
9 84526 APN Cc2d2a 0.632 IGL01448 G1 5 43684185 T181I C T missense Het possibly damaging 0.652 phenotype 11/11/2013
10 84528 APN Celsr2 0.000 IGL01448 G1 3 108393239 L2835P A G missense Het probably damaging 0.986 phenotype 11/11/2013
11 84509 APN Ctns 0.103 IGL01448 G1 11 73188722 V99D A T missense Het possibly damaging 0.880 phenotype 11/11/2013
12 84524 APN Dchs1 1.000 IGL01448 G1 7 105771927 R429G T C missense Het probably damaging 0.982 phenotype 11/11/2013
13 84502 APN Ddx11 1.000 IGL01448 G1 17 66134137 V218A T C missense Het probably damaging 0.999 phenotype 11/11/2013
14 84540 APN Eftud2 0.948 IGL01448 G1 11 102865563 G A splice site Het probably benign phenotype 11/11/2013
15 84503 APN Erich1 0.093 IGL01448 G1 8 14078853 T29N G T missense Het possibly damaging 0.953 11/11/2013
16 84508 APN Exosc8 0.932 IGL01448 G1 3 54729265 E215G T C missense Het probably damaging 0.967 phenotype 11/11/2013
17 84492 APN Fam184a 0.296 IGL01448 G1 10 53698949 A188E G T missense Het probably benign 0.194 11/11/2013
18 84520 APN Fign 1.000 IGL01448 G1 2 63979688 S413P A G missense Het probably damaging 0.972 phenotype 11/11/2013
19 84529 APN Fkbp6 0.000 IGL01448 G1 5 135349696 S33P A G missense Het probably damaging 0.968 phenotype 11/11/2013
20 84541 APN Glb1 0.000 IGL01448 G1 9 114450677 A G splice site Het probably benign phenotype 11/11/2013
21 84537 APN H2-Q1 0.087 IGL01448 G1 17 35323461 T C splice site Het probably benign 11/11/2013
22 84516 APN Helz2 0.000 IGL01448 G1 2 181233977 T1575A T C missense Het probably damaging 1.000 phenotype 11/11/2013
23 84513 APN Il18r1 0.043 IGL01448 G1 1 40474730 E32G A G missense Het probably damaging 1.000 phenotype 11/11/2013
24 84493 APN Ints5 0.319 IGL01448 G1 19 8895487 P270L C T missense Het possibly damaging 0.930 phenotype 11/11/2013
25 84517 APN Itga7 0.667 IGL01448 G1 10 128949468 E847* G T nonsense Het probably null phenotype 11/11/2013
26 84523 APN Kcns3 0.261 IGL01448 G1 12 11091643 S352A A C missense Het possibly damaging 0.910 phenotype 11/11/2013
27 84521 APN Kiz 0.000 IGL01448 G1 2 146863801 K94E A G missense Het probably benign 0.218 phenotype 11/11/2013
28 84498 APN Lin7b 0.324 IGL01448 G1 7 45369200 V12M C T missense Het probably damaging 0.995 phenotype 11/11/2013
29 84515 APN Myo18b 1.000 IGL01448 G1 5 112811704 I1409N A T missense Het probably damaging 0.999 phenotype 11/11/2013
30 84501 APN Myo5b 0.486 IGL01448 G1 18 74644090 H407R A G missense Het probably damaging 0.974 phenotype 11/11/2013
31 84519 APN Nelfa 0.965 IGL01448 G1 5 33898802 T506A T C missense Het probably damaging 0.982 phenotype 11/11/2013
32 84490 APN Olfr497 0.121 IGL01448 G1 7 108423028 Y152* T A nonsense Het probably null phenotype 11/11/2013
33 84504 APN Olfr763 0.144 IGL01448 G1 10 129011860 T192A A G missense Het probably damaging 0.996 phenotype 11/11/2013
34 84494 APN Olfr816 0.066 IGL01448 G1 10 129912245 I11T A G missense Het possibly damaging 0.888 phenotype 11/11/2013
35 84530 APN Olfr984 0.181 IGL01448 G1 9 40101082 M136K A T missense Het probably damaging 0.973 phenotype 11/11/2013
36 84533 APN Pclo 0.000 IGL01448 G1 5 14676394 A C unclassified Het probably benign phenotype 11/11/2013
37 84534 APN Pes1 1.000 IGL01448 G1 11 3977979 E544K G A missense Het possibly damaging 0.889 phenotype 11/11/2013
38 84538 APN Rabgap1l 0.000 IGL01448 G1 1 160740745 A G splice site Het probably benign phenotype 11/11/2013
39 84539 APN Rapgef2 1.000 IGL01448 G1 3 79103962 C T critical splice donor site 1 bp Het probably null phenotype 11/11/2013
40 84500 APN Rapgef2 1.000 IGL01448 G1 3 79068937 M1521V T C missense Het probably benign 0.000 phenotype 11/11/2013
41 84507 APN Reln 0.943 IGL01448 G1 5 22040405 V735A A G missense Het probably benign 0.397 phenotype 11/11/2013
42 84497 APN Slc2a4 0.363 IGL01448 G1 11 69945076 S316P A G missense Het possibly damaging 0.802 phenotype 11/11/2013
43 84531 APN Smarce1 1.000 IGL01448 G1 11 99210187 G373E C T missense Het possibly damaging 0.685 phenotype 11/11/2013
44 84518 APN Spata31d1a 0.071 IGL01448 G1 13 59701559 R918S T A missense Het probably benign 0.057 11/11/2013
45 84505 APN St3gal4 0.333 IGL01448 G1 9 35052331 K227R T C missense Het probably benign 0.001 phenotype 11/11/2013
46 84542 APN Stra6l 0.238 IGL01448 G1 4 45864864 T A splice site Het probably null 11/11/2013
47 84532 APN Stxbp5l 0.000 IGL01448 G1 16 37215979 I425V T C missense Het probably damaging 0.993 phenotype 11/11/2013
48 84506 APN Tcaf2 0.136 IGL01448 G1 6 42630328 T231A T C missense Het probably benign 0.050 11/11/2013
49 84499 APN Tiparp 0.439 IGL01448 G1 3 65552609 G442* G T nonsense Het probably null phenotype 11/11/2013
50 84512 APN Tnks 0.000 IGL01448 G1 8 34839982 Y1138H A G missense Het probably damaging 1.000 phenotype 11/11/2013
51 84522 APN Vezt 1.000 IGL01448 G1 10 93996857 I231F T A missense Het probably damaging 1.000 phenotype 11/11/2013
52 84489 APN Vmn2r4 0.047 IGL01448 G1 3 64406395 N388K A T missense Het probably damaging 0.988 11/11/2013
53 84536 APN Zbed3 IGL01448 G1 13 95336634 K189E A G missense Het possibly damaging 0.659 phenotype 11/11/2013
54 84514 APN Zfp512b 0.000 IGL01448 G1 2 181587785 T625A T C missense Het possibly damaging 0.615 11/11/2013
55 84511 APN Zfp827 0.353 IGL01448 G1 8 79060733 Q176L A T missense Het possibly damaging 0.816 11/11/2013
[records 1 to 55 of 55]