Incidental Mutations

41 incidental mutations are currently displayed, and affect 41 genes.
4 are Possibly Damaging.
14 are Probably Damaging.
22 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 41 of 41] 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 93310 APN AB124611 0.000 IGL01571 G1 9 21539081 (GRCm38) T A splice site Het probably benign 2013-12-09
2 93294 APN Cep164 1.000 IGL01571 G1 9 45794338 (GRCm38) Q127R T C missense Het possibly damaging 0.816 phenotype 2013-12-09
3 93298 APN Ces1f 0.089 IGL01571 G1 8 93258368 (GRCm38) M444L T A missense Het probably benign 0.002 2013-12-09
4 93319 APN Chd5 0.000 IGL01571 G1 4 152384115 (GRCm38) T A splice site Het probably benign phenotype 2013-12-09
5 93301 APN Cpd 0.937 IGL01571 G1 11 76782296 (GRCm38) Y1341F T A missense Het probably damaging 0.999 phenotype 2013-12-09
6 93297 APN Cryz 0.231 IGL01571 G1 3 154621743 (GRCm38) I268T T C missense Het probably damaging 0.995 phenotype 2013-12-09
7 93295 APN Csnk2a1 1.000 IGL01571 G1 2 152275406 (GRCm38) R278H G A missense Het probably damaging 0.999 phenotype 2013-12-09
8 93304 APN Cyp4a12b 0.067 IGL01571 G1 4 115438157 (GRCm38) I487V A G missense Het probably benign 0.001 2013-12-09
9 93315 APN Dnajb5 0.130 IGL01571 G1 4 42956516 (GRCm38) T C splice site Het probably benign phenotype 2013-12-09
10 93281 APN Dxo 0.101 IGL01571 G1 17 34839040 (GRCm38) H214L A T missense Het probably damaging 0.999 phenotype 2013-12-09
11 93314 APN Etfb 0.640 IGL01571 G1 7 43452959 (GRCm38) T C critical splice donor site 2 bp Het probably null phenotype 2013-12-09
12 93302 APN G6pc2 0.067 IGL01571 G1 2 69222967 (GRCm38) V122I G A missense Het probably damaging 1.000 phenotype 2013-12-09
13 93309 APN Gm5431 0.065 IGL01571 G1 11 48894713 (GRCm38) D278E A T missense Het probably benign 0.003 2013-12-09
14 93313 APN Gstt2 0.000 IGL01571 G1 10 75834171 (GRCm38) C T splice site Het probably benign phenotype 2013-12-09
15 93312 APN Hnf4g 0.139 IGL01571 G1 3 3651266 (GRCm38) A C splice site Het probably benign phenotype 2013-12-09
16 93299 APN Ifi44 0.000 IGL01571 G1 3 151745537 (GRCm38) D259G T C missense Het probably damaging 0.972 2013-12-09
17 93287 APN Klk1 0.055 IGL01571 G1 7 44228596 (GRCm38) V92A T C missense Het probably damaging 0.979 phenotype 2013-12-09
18 93280 APN Lypla1 0.000 IGL01571 G1 1 4844988 (GRCm38) I222T T C missense Het probably benign 0.153 phenotype 2013-12-09
19 93303 APN Nbeal2 0.261 IGL01571 G1 9 110632758 (GRCm38) N1510D T C missense Het possibly damaging 0.630 phenotype 2013-12-09
20 93290 APN Ndufaf7 1.000 IGL01571 G1 17 78943852 (GRCm38) R229G A G missense Het probably damaging 0.961 phenotype 2013-12-09
21 93296 APN Nphp4 0.106 IGL01571 G1 4 152556382 (GRCm38) V1069M G A missense Het probably benign 0.211 phenotype 2013-12-09
22 93308 APN Nsd2 0.829 IGL01571 G1 5 33864687 (GRCm38) H528R A G missense Het probably benign 0.320 phenotype 2013-12-09
23 93288 APN Olfr1298 0.131 IGL01571 G1 2 111645380 (GRCm38) V206L C A missense Het probably benign phenotype 2013-12-09
24 93285 APN Olfr1355 0.069 IGL01571 G1 10 78879837 (GRCm38) I222V A G missense Het possibly damaging 0.947 phenotype 2013-12-09
25 93306 APN Olfr763 0.072 IGL01571 G1 10 129011827 (GRCm38) I181F A T missense Het probably damaging 0.991 phenotype 2013-12-09
26 93316 APN Pigh 1.000 IGL01571 G1 12 79085860 (GRCm38) A C splice site Het probably benign phenotype 2013-12-09
27 93291 APN Prr14l 0.140 IGL01571 G1 5 32828806 (GRCm38) M1115K A T missense Het probably benign 0.009 2013-12-09
28 93282 APN Psg21 0.048 IGL01571 G1 7 18654825 (GRCm38) D114G T C missense Het probably damaging 1.000 2013-12-09
29 278724 APN Psmg2 0.953 IGL01571 G1 18 67653223 (GRCm38) V218I G A missense Het probably benign 0.000 2015-04-16
30 93293 APN Pygb 0.186 IGL01571 G1 2 150830473 (GRCm38) S831P T C missense Het probably benign 0.005 phenotype 2013-12-09
31 93289 APN Ryr2 1.000 IGL01571 G1 13 11721761 (GRCm38) D2260V T A missense Het probably damaging 1.000 phenotype 2013-12-09
32 93305 APN Sgo2a 0.000 IGL01571 G1 1 58017974 (GRCm38) S1106P T C missense Het probably damaging 0.993 phenotype 2013-12-09
33 93317 APN Slc5a5 0.000 IGL01571 G1 8 70891332 (GRCm38) G A unclassified Het probably benign phenotype 2013-12-09
34 93300 APN Tekt4 0.123 IGL01571 G1 17 25476384 (GRCm38) D397G A G missense Het probably benign 0.311 phenotype 2013-12-09
35 93311 APN Trrap 1.000 IGL01571 G1 5 144833287 (GRCm38) T A splice site Het probably benign phenotype 2013-12-09
36 93307 APN Upf2 1.000 IGL01571 G1 2 6018939 (GRCm38) T C unclassified Het probably benign phenotype 2013-12-09
37 93286 APN Usp17lb 0.105 IGL01571 G1 7 104840381 (GRCm38) N445K A T missense Het possibly damaging 0.590 2013-12-09
38 93283 APN Vmn2r111 0.087 IGL01571 G1 17 22571392 (GRCm38) V211A A G missense Het probably damaging 0.989 2013-12-09
39 93284 APN Vmn2r23 0.055 IGL01571 G1 6 123704407 (GRCm38) I91M A G missense Het probably damaging 0.999 2013-12-09
40 93318 APN Vps13b 0.000 IGL01571 G1 15 35877489 (GRCm38) C T splice site Het probably benign phenotype 2013-12-09
41 93292 APN Zc3hc1 0.607 IGL01571 G1 6 30390863 (GRCm38) T47I G A missense Het probably benign 0.425 phenotype 2013-12-09
[records 1 to 41 of 41]