Incidental Mutations

42 incidental mutations are currently displayed, and affect 42 genes.
5 are Possibly Damaging.
20 are Probably Damaging.
15 are Probably Benign.
2 are Probably Null.
1 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 42 of 42] 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 84427 APN Abca13 0.000 IGL01446 G1 11 9403834 T3719A A G missense Het probably damaging 0.974 phenotype 11/11/2013
2 84430 APN Acaca 1.000 IGL01446 G1 11 84260631 K785R A G missense Het probably damaging 1.000 phenotype 11/11/2013
3 84432 APN Acsm3 0.000 IGL01446 G1 7 119778454 V401M G A missense Het probably damaging 0.997 phenotype 11/11/2013
4 84414 APN Aff4 1.000 IGL01446 G1 11 53415469 R1146L G T missense Het probably damaging 0.988 phenotype 11/11/2013
5 84434 APN Alms1 0.000 IGL01446 G1 6 85696701 P3562T C A missense Het probably damaging 1.000 phenotype 11/11/2013
6 84422 APN Arsj 0.055 IGL01446 G1 3 126438814 E403G A G missense Het probably benign 0.015 phenotype 11/11/2013
7 84438 APN Baiap2l1 0.000 IGL01446 G1 5 144275913 V431I C T missense Het probably benign 0.096 phenotype 11/11/2013
8 84437 APN Cecr2 1.000 IGL01446 G1 6 120758599 M904K T A missense Het probably benign 0.000 phenotype 11/11/2013
9 84431 APN Cenpe 1.000 IGL01446 G1 3 135237539 T775S A T missense Het probably benign 0.006 phenotype 11/11/2013
10 84429 APN Dennd1b 0.000 IGL01446 G1 1 139023110 E30K G A missense Het possibly damaging 0.608 phenotype 11/11/2013
11 84421 APN Dnah5 0.799 IGL01446 G1 15 28326669 D2008G A G missense Het probably damaging 1.000 phenotype 11/11/2013
12 84424 APN Dnm2 1.000 IGL01446 G1 9 21481376 V460A T C missense Het probably damaging 0.999 phenotype 11/11/2013
13 84415 APN Ell2 0.000 IGL01446 G1 13 75761991 L285F G T missense Het probably benign 0.019 11/11/2013
14 84418 APN Erg 1.000 IGL01446 G1 16 95361282 S322P A G missense Het probably damaging 1.000 phenotype 11/11/2013
15 84416 APN Extl3 1.000 IGL01446 G1 14 65077080 F218L A G missense Het probably benign 0.000 phenotype 11/11/2013
16 84413 APN Fam84a 0.124 IGL01446 G1 12 14149928 I266N A T missense Het probably damaging 0.998 11/11/2013
17 84409 APN Fzd9 0.347 IGL01446 G1 5 135250566 E155G T C missense Het probably damaging 0.999 phenotype 11/11/2013
18 84433 APN Ghr 0.000 IGL01446 G1 15 3333355 W212R A G missense Het probably damaging 1.000 phenotype 11/11/2013
19 84444 APN Gulp1 0.147 IGL01446 G1 1 44744548 A G splice site Het probably benign phenotype 11/11/2013
20 84436 APN Hdgfl2 0.229 IGL01446 G1 17 56097281 R332C C T missense Het possibly damaging 0.944 phenotype 11/11/2013
21 84442 APN Nsd2 0.858 IGL01446 G1 5 33861186 T C splice site Het probably benign phenotype 11/11/2013
22 84405 APN Olfr1259 0.597 IGL01446 G1 2 89943938 F59S A G missense Het probably damaging 0.991 phenotype 11/11/2013
23 84410 APN Olfr1441 0.086 IGL01446 G1 19 12422801 I164T T C missense Het possibly damaging 0.907 phenotype 11/11/2013
24 84404 APN Olfr1480 0.054 IGL01446 G1 19 13530252 T237I C T missense Het probably benign 0.002 phenotype 11/11/2013
25 84408 APN Phf11b 0.120 IGL01446 G1 14 59341291 S9A A C missense Het probably benign 0.016 11/11/2013
26 84425 APN Psd4 0.000 IGL01446 G1 2 24405395 S854P T C missense Het probably damaging 1.000 11/11/2013
27 84423 APN Reln 0.949 IGL01446 G1 5 21969317 D1963N C T missense Het probably damaging 0.987 phenotype 11/11/2013
28 84441 APN Rpe65 0.192 IGL01446 G1 3 159600405 T A splice site Het probably benign phenotype 11/11/2013
29 84417 APN Sdccag8 1.000 IGL01446 G1 1 176845245 S235P T C missense Het probably damaging 0.999 phenotype 11/11/2013
30 84440 APN Sgip1 0.000 IGL01446 G1 4 102928913 G T critical splice donor site 1 bp Het probably null phenotype 11/11/2013
31 84411 APN Skint5 0.073 IGL01446 G1 4 113942822 P36L G A missense Het probably damaging 1.000 11/11/2013
32 84443 APN Slc26a3 0.634 IGL01446 G1 12 31452491 G T splice site Het probably benign phenotype 11/11/2013
33 84412 APN Snx13 1.000 IGL01446 G1 12 35124480 C669* T A nonsense Het probably null phenotype 11/11/2013
34 84439 APN Svil 0.183 IGL01446 G1 18 5062385 T902S A T missense Het probably damaging 1.000 phenotype 11/11/2013
35 84435 APN Syne2 0.292 IGL01446 G1 12 76041375 S4989P T C missense Het probably damaging 1.000 phenotype 11/11/2013
36 84426 APN Ttn 1.000 IGL01446 G1 2 76809939 T13775M G A missense Het probably damaging 0.991 phenotype 11/11/2013
37 84445 APN Ubr4 1.000 IGL01446 G1 4 139438040 T C splice site Het probably benign phenotype 11/11/2013
38 84420 APN Ush1c 0.000 IGL01446 G1 7 46208956 R636H C T missense Het possibly damaging 0.864 phenotype 11/11/2013
39 84406 APN Usp17lc 1.000 IGL01446 G1 7 103418444 R315S A T missense Het probably benign 0.001 phenotype 11/11/2013
40 84428 APN Vmn1r236 0.073 IGL01446 G1 17 21286656 V12D T A missense Het probably benign 0.005 11/11/2013
41 84407 APN Wsb2 0.000 IGL01446 G1 5 117371164 I170S T G missense Het probably damaging 0.969 phenotype 11/11/2013
42 84419 APN Zfp800 0.506 IGL01446 G1 6 28242984 L661F G A missense Het possibly damaging 0.874 11/11/2013
[records 1 to 42 of 42]