Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
6 are Possibly Damaging.
13 are Probably Damaging.
10 are Probably Benign.
3 are Probably Null.
0 create premature stop codons.
2 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 415371 APN 1700037H04Rik IGL03274 2 131153592 A T critical splice donor site 2 bp Het probably null 08/02/2016
2 415365 APN Anln 0.958 IGL03274 9 22382269 R26M C A missense Het probably damaging 1.000 phenotype 08/02/2016
3 415360 APN Capn15 0.176 IGL03274 17 25961838 S753T A T missense Het probably damaging 0.998 phenotype 08/02/2016
4 415350 APN Ccdc62 0.000 IGL03274 5 123954680 N576S A G missense Het probably benign 0.001 phenotype 08/02/2016
5 415345 APN Csmd3 0.848 IGL03274 15 47645504 D2895G T C missense Het probably damaging 1.000 08/02/2016
6 415356 APN Dspp 0.000 IGL03274 5 104174948 V37E T A missense Het probably damaging 0.988 phenotype 08/02/2016
7 415349 APN Efcab6 0.447 IGL03274 15 83868249 D1473G T C missense Het probably damaging 0.997 phenotype 08/02/2016
8 415372 APN Ehhadh 0.000 IGL03274 16 21763340 T C splice site Het probably benign phenotype 08/02/2016
9 415370 APN Fbln1 0.652 IGL03274 15 85232678 T C critical splice donor site 2 bp Het probably null phenotype 08/02/2016
10 415342 APN Gbp9 0.136 IGL03274 5 105082786 V424A A G missense Het possibly damaging 0.579 08/02/2016
11 415347 APN Gda 0.367 IGL03274 19 21417007 Y236C T C missense Het possibly damaging 0.879 phenotype 08/02/2016
12 415341 APN Gm11639 0.182 IGL03274 11 104721093 D587V A T missense Het probably benign 0.026 08/02/2016
13 415346 APN Gm4884 0.111 IGL03274 7 41044545 E646G A G missense Het probably damaging 0.999 08/02/2016
14 415369 APN Gm4952 0.023 IGL03274 19 12623596 C A splice site Het probably benign 08/02/2016
15 415353 APN Gm5422 0.793 IGL03274 10 31250352 G T exon Het noncoding transcript 08/02/2016
16 415352 APN Grin2b 1.000 IGL03274 6 135780255 D403N C T missense Het possibly damaging 0.904 phenotype 08/02/2016
17 415361 APN Hsf2bp 0.122 IGL03274 17 32007770 R204C G A missense Het probably damaging 1.000 phenotype 08/02/2016
18 415354 APN Il16 0.216 IGL03274 7 83661234 E488G T C missense Het probably damaging 0.999 phenotype 08/02/2016
19 415357 APN Kat6b 0.792 IGL03274 14 21609763 D212Y G T missense Het possibly damaging 0.953 phenotype 08/02/2016
20 415351 APN Kctd2 0.282 IGL03274 11 115429382 I247L A C missense Het possibly damaging 0.682 08/02/2016
21 415359 APN Kel 0.339 IGL03274 6 41687995 T A unclassified 2278 bp Het probably null phenotype 08/02/2016
22 415368 APN Krt20 0.077 IGL03274 11 99430029 A T splice site Het probably benign phenotype 08/02/2016
23 415355 APN Litaf 0.351 IGL03274 16 10966569 T26A T C missense Het probably damaging 0.997 phenotype 08/02/2016
24 415343 APN N4bp2l2 0.357 IGL03274 5 150661466 Q350K G T missense Het probably damaging 0.987 08/02/2016
25 415362 APN Nav2 0.749 IGL03274 7 49362099 I26S T G missense Het probably damaging 0.999 phenotype 08/02/2016
26 415363 APN Nfya 1.000 IGL03274 17 48391347 Y162H A G missense Het probably damaging 1.000 phenotype 08/02/2016
27 415348 APN Olfr117 0.091 IGL03274 17 37659755 A193T C T missense Het probably benign 0.350 phenotype 08/02/2016
28 415364 APN Pbx4 0.368 IGL03274 8 69866550 S244C A T missense Het probably damaging 1.000 phenotype 08/02/2016
29 415344 APN Pcdhb16 0.133 IGL03274 18 37479232 V415A T C missense Het probably benign 0.044 phenotype 08/02/2016
30 415373 APN Rbbp8 1.000 IGL03274 18 11741076 A G splice site Het probably benign phenotype 08/02/2016
31 415366 APN Sp100 0.168 IGL03274 1 85707304 T C intron Het probably benign 08/02/2016
32 415367 APN Spag16 0.220 IGL03274 1 69844381 A G splice site Het probably benign phenotype 08/02/2016
33 415358 APN Star 1.000 IGL03274 8 25811054 D138G A G missense Het possibly damaging 0.716 phenotype 08/02/2016
[records 1 to 33 of 33]