Incidental Mutations

28 incidental mutations are currently displayed, and affect 28 genes.
3 are Possibly Damaging.
10 are Probably Damaging.
13 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 28 of 28] 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 88519 APN 4930590J08Rik 0.000 IGL01478 G1 6 91934609 T613A A G missense Het probably benign 0.013 11/18/2013
2 88534 APN Cdh16 0.071 IGL01478 G1 8 104614488 G T splice site Het probably benign phenotype 11/18/2013
3 88520 APN Epn2 0.000 IGL01478 G1 11 61523086 S419P A G missense Het probably benign 0.001 0.061 phenotype 11/18/2013
4 88515 APN Eral1 1.000 IGL01478 G1 11 78075732 V234D A T missense Het probably damaging 1.000 phenotype 11/18/2013
5 88528 APN Fhad1 0.063 IGL01478 G1 4 141951638 K576E T C missense Het possibly damaging 0.841 11/18/2013
6 88509 APN Frmd4b 0.000 IGL01478 G1 6 97328293 D170V T A missense Het probably damaging 0.998 phenotype 11/18/2013
7 88510 APN Gm4353 0.142 IGL01478 G1 7 116083740 V202A A G missense Het possibly damaging 0.817 11/18/2013
8 88529 APN Ighmbp2 1.000 IGL01478 G1 19 3274531 I245T A G missense Het probably benign 0.035 phenotype 11/18/2013
9 88531 APN Igsf23 0.115 IGL01478 G1 7 19938236 G A utr 3 prime Het probably benign phenotype 11/18/2013
10 88533 APN Krt1 0.391 IGL01478 G1 15 101846286 A G splice site Het probably benign phenotype 11/18/2013
11 88514 APN Mapk8 0.722 IGL01478 G1 14 33383900 V371A A G missense Het probably benign 0.006 phenotype 11/18/2013
12 88532 APN Mtrf1 0.101 IGL01478 G1 14 79402920 T G splice site Het probably benign phenotype 11/18/2013
13 88530 APN Myzap 0.152 IGL01478 G1 9 71515067 A G critical splice donor site 2 bp Het probably null phenotype 11/18/2013
14 88525 APN Nsrp1 1.000 IGL01478 G1 11 77050652 V73I C T missense Het probably benign 0.001 phenotype 11/18/2013
15 88511 APN Olfr1089 0.282 IGL01478 G1 2 86733329 Y94* A T nonsense Het probably null phenotype 11/18/2013
16 278522 APN Olfr344 0.086 IGL01478 G1 2 36568742 L48H T A missense Het probably damaging 1.000 phenotype 04/16/2015
17 88517 APN Olfr670 0.065 IGL01478 G1 7 104960348 I128T A G missense Het probably damaging 0.974 phenotype 11/18/2013
18 88518 APN Pex6 0.716 IGL01478 G1 17 46725304 R976C C T missense Het probably benign 0.002 phenotype 11/18/2013
19 88523 APN Ranbp9 0.943 IGL01478 G1 13 43414084 T546I G A missense Het probably benign 0.315 phenotype 11/18/2013
20 88522 APN Rfx5 0.183 IGL01478 G1 3 94958440 V350A T C missense Het possibly damaging 0.883 phenotype 11/18/2013
21 88524 APN Rnf19b 0.131 IGL01478 G1 4 129058830 E187G A G missense Het probably damaging 0.999 phenotype 11/18/2013
22 88526 APN Sbf1 0.476 IGL01478 G1 15 89299743 V1217A A G missense Het probably damaging 0.969 phenotype 11/18/2013
23 88516 APN Sfmbt1 0.599 IGL01478 G1 14 30811521 D618E T A missense Het probably damaging 0.998 phenotype 11/18/2013
24 88521 APN Sipa1l1 0.000 IGL01478 G1 12 82446898 E1697G A G missense Het probably benign 0.005 11/18/2013
25 88512 APN Syk 1.000 IGL01478 G1 13 52624748 Y290C A G missense Het probably benign 0.002 phenotype 11/18/2013
26 88508 APN Trim69 0.068 IGL01478 G1 2 122178443 L328P T C missense Het probably damaging 0.980 phenotype 11/18/2013
27 88513 APN Unc5c 1.000 IGL01478 G1 3 141828451 I911N T A missense Het probably damaging 1.000 phenotype 11/18/2013
28 88527 APN Wdr5 0.966 IGL01478 G1 2 27533832 V294A T C missense Het probably damaging 0.997 phenotype 11/18/2013
[records 1 to 28 of 28]