Incidental Mutations

23 incidental mutations are currently displayed, and affect 23 genes.
4 are Possibly Damaging.
7 are Probably Damaging.
11 are Probably Benign.
1 are Probably Null.
0 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 23 of 23] 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 90360 APN 1700013G24Rik 0.056 IGL01547 G1 4 137455262 G243R G A missense Het possibly damaging 0.822 12/03/2013
2 90367 APN Afg3l1 0.088 IGL01547 G1 8 123501351 V625A T C missense Het probably benign 0.172 phenotype 12/03/2013
3 90374 APN Arhgap39 0.209 IGL01547 G1 15 76737815 T C splice site Het probably benign 12/03/2013
4 90356 APN Bag1 1.000 IGL01547 G1 4 40936661 C332R A G missense Het probably damaging 1.000 phenotype 12/03/2013
5 90364 APN Bcas2 0.962 IGL01547 G1 3 103171999 Y49H T C missense Het probably damaging 1.000 phenotype 12/03/2013
6 90373 APN Cacna1b 0.000 IGL01547 G1 2 24632035 C A unclassified Het probably benign phenotype 12/03/2013
7 90357 APN Cdyl 0.441 IGL01547 G1 13 35790162 D53G A G missense Het possibly damaging 0.904 phenotype 12/03/2013
8 90369 APN Csmd3 0.000 IGL01547 G1 15 47883617 I1322V T C missense Het probably benign 0.406 12/03/2013
9 90366 APN Evc2 1.000 IGL01547 G1 5 37393087 A815E C A missense Het probably benign 0.093 phenotype 12/03/2013
10 90361 APN Gm6309 0.052 IGL01547 G1 5 146168411 D231N C T missense Het probably benign 0.018 12/03/2013
11 90368 APN Mtfr2 0.096 IGL01547 G1 10 20357599 P305S C T missense Het probably damaging 0.998 12/03/2013
12 90353 APN Olfr301 0.058 IGL01547 G1 7 86412871 N170D A G missense Het possibly damaging 0.943 phenotype 12/03/2013
13 90370 APN Olfr639 0.119 IGL01547 G1 7 104012660 I14N A T missense Het probably benign 0.425 phenotype 12/03/2013
14 90362 APN Olfr77 0.068 IGL01547 G1 9 19920901 I231F A T missense Het probably benign 0.003 phenotype 12/03/2013
15 90371 APN Pcdhb1 0.132 IGL01547 G1 18 37267342 H782R A G missense Het probably benign 0.061 phenotype 12/03/2013
16 90358 APN Polr2a 0.965 IGL01547 G1 11 69744942 S480P A G missense Het probably damaging 0.988 phenotype 12/03/2013
17 90363 APN Scaf11 0.000 IGL01547 G1 15 96418429 T1085A T C missense Het probably benign 0.136 12/03/2013
18 90365 APN Sema6c 0.401 IGL01547 G1 3 95172398 R668C C T missense Het probably damaging 0.997 phenotype 12/03/2013
19 90359 APN Tas2r123 0.050 IGL01547 G1 6 132847458 T106I C T missense Het probably damaging 1.000 12/03/2013
20 90375 APN Tgm5 0.247 IGL01547 G1 2 121049202 A G splice site Het probably benign phenotype 12/03/2013
21 90355 APN Vmn2r23 0.056 IGL01547 G1 6 123704424 I97N T A missense Het possibly damaging 0.879 12/03/2013
22 90354 APN Vmn2r6 0.188 IGL01547 G1 3 64538104 K644N T A missense Het probably damaging 1.000 12/03/2013
23 90372 APN Zfp608 0.918 IGL01547 G1 18 54894449 A G critical splice donor site 2 bp Het probably null 12/03/2013
[records 1 to 23 of 23]