Incidental Mutations

36 incidental mutations are currently displayed, and affect 35 genes.
6 are Possibly Damaging.
10 are Probably Damaging.
16 are Probably Benign.
4 are Probably Null.
3 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 36 of 36] 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 306639 APN 0610009L18Rik IGL00978 G1 11 120350947 (GRCm38) T C unclassified Het probably benign 2015-04-16
2 29465 APN Alpk2 0.000 IGL00978 G1 18 65291534 (GRCm38) A T splice site Het probably benign 2013-04-17
3 28260 APN Angptl8 0.000 IGL00978 G1 9 21837053 (GRCm38) T C intron Het probably benign phenotype 2013-04-17
4 27344 APN AU040320 0.000 IGL00978 G1 4 126828839 (GRCm38) D383E T A missense Het probably benign 0.003 phenotype 2013-04-17
5 29201 APN Cep97 1.000 IGL00978 G1 16 55924960 (GRCm38) C T splice site Het probably benign 2013-04-17
6 27936 APN Clcn4 0.000 IGL00978 G1 7 7287673 (GRCm38) L649H A T missense Het probably damaging 0.992 phenotype 2013-04-17
7 26762 APN Col5a2 1.000 IGL00978 G1 1 45376739 (GRCm38) N1416S T C missense Het probably benign 0.013 phenotype 2013-04-17
8 28656 APN Erbb2 1.000 IGL00978 G1 11 98435630 (GRCm38) P1027S C T missense Het probably damaging 1.000 phenotype 2013-04-17
9 306640 APN Eya1 0.859 IGL00978 G1 1 14270701 (GRCm38) A G splice site Het probably benign phenotype 2015-04-16
10 28900 APN Gfm2 0.660 IGL00978 G1 13 97162977 (GRCm38) I402T T C missense Het probably benign 0.201 phenotype 2013-04-17
11 27021 APN Gmeb2 0.168 IGL00978 G1 2 181259043 (GRCm38) V187E A T missense Het probably benign 0.184 phenotype 2013-04-17
12 28788 APN Hectd1 1.000 IGL00978 G1 12 51791390 (GRCm38) H662R T C missense Het possibly damaging 0.948 phenotype 2013-04-17
13 27346 APN Ifne 0.000 IGL00978 G1 4 88880031 (GRCm38) Q50R T C missense Het probably benign 0.170 phenotype 2013-04-17
14 28790 APN Kidins220 1.000 IGL00978 G1 12 25057474 (GRCm38) D1642G A G missense Het probably damaging 1.000 phenotype 2013-04-17
15 27345 APN Klhl32 0.075 IGL00978 G1 4 24682245 (GRCm38) D146V T A missense Het probably damaging 0.999 2013-04-17
16 28655 APN Krt36 0.058 IGL00978 G1 11 100102948 (GRCm38) I355V T C missense Het probably damaging 0.975 phenotype 2013-04-17
17 27160 APN Lrrcc1 0.000 IGL00978 G1 3 14536128 (GRCm38) S73R T A missense Het possibly damaging 0.910 2013-04-17
18 29550 APN Ltbp3 0.212 IGL00978 G1 19 5754019 (GRCm38) H853L A T missense Het probably benign 0.262 phenotype 2013-04-17
19 28427 APN Map3k5 0.000 IGL00978 G1 10 20141567 (GRCm38) R1369Q G A missense Het probably damaging 1.000 phenotype 2013-04-17
20 27020 APN Mcm8 0.639 IGL00978 G1 2 132821406 (GRCm38) N148S A G missense Het probably benign 0.000 phenotype 2013-04-17
21 28084 APN Mylk3 0.238 IGL00978 G1 8 85355526 (GRCm38) L211* A T nonsense Het probably null phenotype 2013-04-17
22 27161 APN Nras 0.472 IGL00978 G1 3 103058916 (GRCm38) T C utr 5 prime Het probably benign phenotype 2013-04-17
23 29353 APN Olfr135 0.059 IGL00978 G1 17 38208982 (GRCm38) I246F A T missense Het probably damaging 0.991 phenotype 2013-04-17
24 27935 APN Olfr670 0.089 IGL00978 G1 7 104960716 (GRCm38) N5K A T missense Het probably damaging 0.957 0.647 phenotype 2013-04-17
25 28426 APN Os9 0.000 IGL00978 G1 10 127120509 (GRCm38) Y66N A T missense Het probably damaging 0.997 phenotype 2013-04-17
26 29549 APN Pitpnm1 0.000 IGL00978 G1 19 4101228 (GRCm38) D15G A G missense Het possibly damaging 0.606 phenotype 2013-04-17
27 27709 APN Reg3a 0.049 IGL00978 G1 6 78382301 (GRCm38) R95* A T nonsense Het probably null 2013-04-17
28 28999 APN Rnf17 0.540 IGL00978 G1 14 56512271 (GRCm38) P1425S C T missense Het probably damaging 1.000 phenotype 2013-04-17
29 29464 APN Smad2 1.000 IGL00978 G1 18 76299775 (GRCm38) T C splice site Het probably benign phenotype 2013-04-17
30 28789 APN Ttll5 0.458 IGL00978 G1 12 85933482 (GRCm38) Q76* C T nonsense Het probably null phenotype 2013-04-17
31 27937 APN Uri1 0.000 IGL00978 G1 7 37996731 (GRCm38) A T splice site Het probably benign phenotype 2013-04-17
32 29355 APN Vmn2r102 0.000 IGL00978 G1 17 19678923 (GRCm38) G T splice site 5 bp Het probably null 2013-04-17
33 27934 APN Vmn2r70 0.160 IGL00978 G1 7 85563799 (GRCm38) M467L T G missense Het probably benign 0.001 2013-04-17
34 29354 APN Zfp318 0.000 IGL00978 G1 17 46413726 (GRCm38) D2218E T A missense Het possibly damaging 0.638 phenotype 2013-04-17
35 28653 APN Zfp692 0.000 IGL00978 G1 11 58314029 (GRCm38) I405T T C missense Het possibly damaging 0.945 2013-04-17
36 28654 APN Zfp692 0.000 IGL00978 G1 11 58309998 (GRCm38) H235R A G missense Het possibly damaging 0.917 2013-04-17
[records 1 to 36 of 36]