Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
5 are Possibly Damaging.
11 are Probably Damaging.
13 are Probably Benign.
2 are Probably Null.
1 create premature stop codons.
0 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 363492 APN Adamtsl5 0.048 IGL02898 10 80342231 A G unclassified Het probably benign 12/18/2015
2 363476 APN Brd3 0.529 IGL02898 2 27459741 S267P A G missense Het possibly damaging 0.808 phenotype 12/18/2015
3 363489 APN Btaf1 0.947 IGL02898 19 36969068 T425A A G missense Het probably benign 0.000 phenotype 12/18/2015
4 363475 APN Caskin1 0.223 IGL02898 17 24502409 E544D A T missense Het probably benign 0.003 12/18/2015
5 363486 APN Col20a1 0.164 IGL02898 2 180989112 Q58* C T nonsense Het probably null 12/18/2015
6 363487 APN Eif2ak1 0.227 IGL02898 5 143889452 V428I G A missense Het probably damaging 1.000 phenotype 12/18/2015
7 363478 APN Fez2 0.220 IGL02898 17 78384755 I345T A G missense Het probably benign 0.030 phenotype 12/18/2015
8 363477 APN Focad 0.385 IGL02898 4 88391997 M1388L A T missense Het probably benign 0.017 12/18/2015
9 363485 APN Gfer 0.907 IGL02898 17 24695947 R41G T C missense Het probably benign 0.000 phenotype 12/18/2015
10 363466 APN Gm6614 0.093 IGL02898 6 141994297 Y140F T A missense Het probably benign 0.006 12/18/2015
11 363479 APN Gm9956 IGL02898 10 56745254 S4L C T missense Het unknown 12/18/2015
12 363473 APN Krtap6-1 0.087 IGL02898 16 89031755 G13D G A missense Het unknown 12/18/2015
13 363470 APN Megf8 0.913 IGL02898 7 25346508 E1492G A G missense Het possibly damaging 0.791 phenotype 12/18/2015
14 363467 APN Myh7 0.794 IGL02898 14 54983740 I909V T C missense Het probably damaging 0.999 phenotype 12/18/2015
15 363464 APN Olfr380 0.132 IGL02898 11 73453735 H159L T A missense Het probably damaging 0.999 phenotype 12/18/2015
16 363462 APN Olfr741 0.087 IGL02898 14 50486186 S243T T A missense Het probably damaging 0.996 phenotype 12/18/2015
17 363468 APN Otog 0.568 IGL02898 7 46310138 E717G A G missense Het probably damaging 1.000 phenotype 12/18/2015
18 363474 APN Pik3r4 1.000 IGL02898 9 105650406 I319M A G missense Het probably benign 0.212 phenotype 12/18/2015
19 363493 APN Piwil4 0.587 IGL02898 9 14706287 A T unclassified Het probably benign phenotype 12/18/2015
20 363471 APN Plekho1 0.109 IGL02898 3 95992181 H100L T A missense Het probably damaging 0.998 phenotype 12/18/2015
21 363481 APN Prr30 0.029 IGL02898 14 101198481 D215A T G missense Het probably benign 0.000 12/18/2015
22 363488 APN Prss52 0.026 IGL02898 14 64113666 A300V C T missense Het possibly damaging 0.838 12/18/2015
23 363490 APN Ralgps2 0.349 IGL02898 1 156817744 K514N C A missense Het probably benign 0.132 12/18/2015
24 363483 APN Robo4 0.345 IGL02898 9 37408176 I463T T C missense Het probably damaging 0.985 phenotype 12/18/2015
25 363480 APN Sars 0.977 IGL02898 3 108429263 F268Y A T missense Het probably damaging 1.000 phenotype 12/18/2015
26 363472 APN Sidt1 0.143 IGL02898 16 44282495 R289Q C T missense Het possibly damaging 0.865 12/18/2015
27 363463 APN Slco2a1 1.000 IGL02898 9 103079606 V539A T C missense Het probably damaging 1.000 phenotype 12/18/2015
28 363494 APN Snrnp200 1.000 IGL02898 2 127216756 A G splice site Het probably benign phenotype 12/18/2015
29 363484 APN Spag17 0.490 IGL02898 3 100101386 D1944G A G missense Het probably benign 0.003 phenotype 12/18/2015
30 363491 APN Spata1 0.177 IGL02898 3 146475339 R288Q C T missense Het possibly damaging 0.711 12/18/2015
31 363482 APN Tatdn3 0.162 IGL02898 1 191046310 *233W T C makesense Het probably null 12/18/2015
32 363469 APN Ttc3 0.809 IGL02898 16 94419426 V536E T A missense Het probably damaging 1.000 12/18/2015
33 363465 APN V1rd19 0.047 IGL02898 7 24003429 T107P A C missense Het probably damaging 1.000 12/18/2015
[records 1 to 33 of 33]