Incidental Mutations

39 incidental mutations are currently displayed, and affect 39 genes.
9 are Possibly Damaging.
15 are Probably Damaging.
11 are Probably Benign.
3 are Probably Null.
2 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 39 of 39] 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 1673 APN 4933402N22Rik IGL00155 G1 5 11921410 S110G A G missense Het possibly damaging 0.845 07/12/2011
2 1621 APN Aacs 0.557 IGL00155 G1 5 125513171 F498S T C missense Het probably damaging 0.995 07/12/2011
3 1857 APN Arhgap11a 0.000 IGL00155 G1 2 113834256 S561P A G missense Het probably benign 0.005 phenotype 07/12/2011
4 1217 APN Best3 0.141 IGL00155 G1 10 116988727 Y33H T C missense Het probably damaging 1.000 phenotype 07/12/2011
5 1422 APN Cd209b 0.058 IGL00155 G1 8 3919945 T A splice site Het probably benign phenotype 07/12/2011
6 1847 APN Cep152 1.000 IGL00155 G1 2 125563888 S1575P A G missense Het probably benign 0.008 phenotype 07/12/2011
7 1781 APN Crabp2 0.688 IGL00155 G1 3 87952199 Y52C A G missense Het probably damaging 1.000 phenotype 07/12/2011
8 1248 APN Crybg1 1.000 IGL00155 G1 10 43992509 D1017G T C missense Het probably damaging 1.000 07/12/2011
9 1571 APN Ctnna2 0.923 IGL00155 G1 6 76980761 W137R A T missense Het probably damaging 1.000 phenotype 07/12/2011
10 1645 APN Cxcl9 0.000 IGL00155 G1 5 92323869 H104L T A missense Het possibly damaging 0.533 phenotype 07/12/2011
11 1944 APN Ddr2 0.000 IGL00155 G1 1 169984427 I742T A G missense Het possibly damaging 0.947 phenotype 07/12/2011
12 1726 APN Frem1 0.647 IGL00155 G1 4 82959389 V223A A G missense Het possibly damaging 0.460 phenotype 07/12/2011
13 1618 APN Fzd10 0.000 IGL00155 G1 5 128601528 I104N T A missense Het probably damaging 0.997 phenotype 07/12/2011
14 1092 APN Greb1 0.000 IGL00155 G1 12 16711961 S473P A G missense Het probably damaging 1.000 phenotype 07/12/2011
15 1616 APN Gtf2i 1.000 IGL00155 G1 5 134242748 Y873C T C missense Het probably damaging 1.000 phenotype 07/12/2011
16 1443 APN Igsf6 0.064 IGL00155 G1 7 121070653 K89* T A nonsense Het probably null 07/12/2011
17 1776 APN Ints3 0.969 IGL00155 G1 3 90406329 F331L A G missense Het probably damaging 0.999 phenotype 07/12/2011
18 886 APN Kcnh3 0.000 IGL00155 G1 15 99242473 H1080L A T missense Het possibly damaging 0.848 phenotype 07/12/2011
19 1863 APN Mettl15 0.172 IGL00155 G1 2 109093176 Y300* A T nonsense Het probably null 07/12/2011
20 697 APN Mms19 0.966 IGL00155 G1 19 41948233 F654L A G missense Het probably benign 0.124 07/12/2011
21 920 APN Myc 1.000 IGL00155 G1 15 61989820 H425R A G missense Het probably benign 0.031 phenotype 07/12/2011
22 1167 APN Ntn1 0.521 IGL00155 G1 11 68226619 G T splice site Het probably benign phenotype 07/12/2011
23 1208 APN Ormdl2 0.347 IGL00155 G1 10 128820075 G69W C A missense Het probably damaging 1.000 07/12/2011
24 1364 APN Pdpr 0.301 IGL00155 G1 8 111102072 V69A T C missense Het possibly damaging 0.690 phenotype 07/12/2011
25 1441 APN Rbbp6 1.000 IGL00155 G1 7 122988685 I254T T C missense Het probably damaging 1.000 phenotype 07/12/2011
26 1850 APN Sema6d 0.000 IGL00155 G1 2 124659865 R543G A G missense Het possibly damaging 0.907 phenotype 07/12/2011
27 1398 APN Slc18a1 0.000 IGL00155 G1 8 69051346 A314T C T missense Het probably damaging 1.000 phenotype 07/12/2011
28 718 APN Slc22a26 0.050 IGL00155 G1 19 7782836 L514P A G missense Het probably damaging 0.990 07/12/2011
29 717 APN Slc22a28 0.318 IGL00155 G1 19 8130203 S167A A C missense Het possibly damaging 0.888 07/12/2011
30 1774 APN Tchh 0.058 IGL00155 G1 3 93445299 E682G A G missense Het unknown 07/12/2011
31 831 APN Thbs2 0.131 IGL00155 G1 17 14668835 M1134K A T missense Het probably damaging 1.000 phenotype 07/12/2011
32 1240 APN Tmem26 0.088 IGL00155 G1 10 68775354 S218G A G missense Het probably damaging 1.000 phenotype 07/12/2011
33 1647 APN Tmprss11c 0.000 IGL00155 G1 5 86239395 S208R A T missense Het probably benign 0.001 07/12/2011
34 1688 APN Tnfrsf8 0.056 IGL00155 G1 4 145292591 T C splice site 3 bp Het probably null phenotype 07/12/2011
35 1929 APN Ush2a 0.605 IGL00155 G1 1 188864678 S3872P T C missense Het probably benign 0.004 phenotype 07/12/2011
36 1535 APN Vmn1r69 0.057 IGL00155 G1 7 10579952 N205S T C missense Het probably benign 0.001 07/12/2011
37 1534 APN Vmn2r54 0.116 IGL00155 G1 7 12631913 T A splice site Het probably benign 07/12/2011
38 1790 APN Wwtr1 0.896 IGL00155 G1 3 57463521 M328K A T missense Het possibly damaging 0.461 phenotype 07/12/2011
39 1814 APN Zfp64 0.890 IGL00155 G1 2 168926681 S337L G A missense Het probably benign 0.060 07/12/2011
[records 1 to 39 of 39]