Incidental Mutations

26 incidental mutations are currently displayed, and affect 26 genes.
5 are Possibly Damaging.
11 are Probably Damaging.
7 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 26 of 26] 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 28568 APN Ccl2 0.075 IGL00948 G1 11 82035732 Q24L A T missense Het possibly damaging 0.828 phenotype 04/17/2013
2 27856 APN Cd33 0.000 IGL00948 G1 7 43529558 G A intron Het probably benign phenotype 04/17/2013
3 28870 APN Cmya5 0.345 IGL00948 G1 13 93091036 I2515V T C missense Het probably benign 0.000 04/17/2013
4 26681 APN Cntnap5b 0.145 IGL00948 G1 1 100141357 T101A A G missense Het probably benign 0.001 04/17/2013
5 27287 APN Cyp4a12a 0.084 IGL00948 G1 4 115301962 M143K T A missense Het probably damaging 0.983 04/17/2013
6 27459 APN Ephb4 1.000 IGL00948 G1 5 137366659 S663R C A missense Het probably damaging 1.000 phenotype 04/17/2013
7 26683 APN Gm4847 0.108 IGL00948 G1 1 166630338 D482G T C missense Het probably benign 0.008 04/17/2013
8 28760 APN Gskip 0.149 IGL00948 G1 12 105698844 N47K C A missense Het probably damaging 0.999 phenotype 04/17/2013
9 27461 APN Kmt2c 1.000 IGL00948 G1 5 25377161 Y473C T C missense Het probably benign 0.077 phenotype 04/17/2013
10 27122 APN Lrrc7 0.567 IGL00948 G1 3 158161557 N849I T A missense Het probably damaging 1.000 phenotype 04/17/2013
11 27855 APN Magel2 1.000 IGL00948 G1 7 62379322 V658E T A missense Het unknown phenotype 04/17/2013
12 29169 APN Nmral1 0.000 IGL00948 G1 16 4716406 G57E C T missense Het probably damaging 1.000 phenotype 04/17/2013
13 28364 APN Olfr801 0.052 IGL00948 G1 10 129669887 L211I A T missense Het probably damaging 1.000 phenotype 04/17/2013
14 28203 APN Olfr921 0.060 IGL00948 G1 9 38775812 Q186* C T nonsense Het probably null phenotype 04/17/2013
15 278104 APN Padi3 0.000 IGL00948 G1 4 140788943 R542L C A missense Het possibly damaging 0.915 phenotype 04/16/2015
16 27123 APN Plrg1 1.000 IGL00948 G1 3 83068119 V260A T C missense Het probably damaging 1.000 phenotype 04/17/2013
17 26682 APN Prex2 0.264 IGL00948 G1 1 11170614 H982R A G missense Het probably damaging 0.983 phenotype 04/17/2013
18 28960 APN Rbm26 0.576 IGL00948 G1 14 105150343 T448S T A missense Het probably damaging 0.999 04/17/2013
19 27854 APN Ryr1 1.000 IGL00948 G1 7 29020195 M4262I C T missense Het possibly damaging 0.780 phenotype 04/17/2013
20 27658 APN Slc41a3 0.000 IGL00948 G1 6 90645714 D441V A T missense Het probably damaging 1.000 phenotype 04/17/2013
21 28038 APN Slc7a2 0.000 IGL00948 G1 8 40912524 E448G A G missense Het probably benign 0.044 phenotype 04/17/2013
22 28569 APN Smtnl2 0.169 IGL00948 G1 11 72411241 C A splice site 3 bp Het probably null 04/17/2013
23 28037 APN Tox3 0.929 IGL00948 G1 8 90270434 P66L G A missense Het probably damaging 1.000 phenotype 04/17/2013
24 27657 APN Vmn1r19 0.110 IGL00948 G1 6 57405262 F267L T C missense Het probably benign 0.030 04/17/2013
25 27460 APN Vmn2r12 0.091 IGL00948 G1 5 109097675 S64P A G missense Het possibly damaging 0.473 04/17/2013
26 27853 APN Zfp764 0.056 IGL00948 G1 7 127405204 S252G T C missense Het possibly damaging 0.927 04/17/2013
[records 1 to 26 of 26]