Incidental Mutations

26 incidental mutations are currently displayed, and affect 26 genes.
5 are Possibly Damaging.
12 are Probably Damaging.
7 are Probably Benign.
2 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 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 4278 APN Adgrv1 0.000 IGL00471 G1 13 81509542 V2793A A G missense Het probably damaging 0.991 phenotype 04/20/2012
2 7122 APN Agbl2 0.000 IGL00471 G1 2 90801045 Y249C A G missense Het probably damaging 0.997 phenotype 04/20/2012
3 3889 APN Anks1 0.513 IGL00471 G1 17 28058416 S1082P T C missense Het possibly damaging 0.937 phenotype 04/20/2012
4 277545 APN Barhl2 1.000 IGL00471 G1 5 106455499 A265T C T missense Het possibly damaging 0.922 phenotype 04/16/2015
5 3865 APN C4b 0.000 IGL00471 G1 17 34734429 T1027P T G missense Het probably damaging 1.000 phenotype 04/20/2012
6 5375 APN Clec4d 0.000 IGL00471 G1 6 123274773 I205F A T missense Het probably damaging 1.000 phenotype 04/20/2012
7 6434 APN Cpeb2 0.238 IGL00471 G1 5 43285831 Y955F A T missense Het probably damaging 0.984 phenotype 04/20/2012
8 7004 APN Cst13 0.035 IGL00471 G1 2 148830304 M133K T A missense Het probably damaging 0.957 04/20/2012
9 5537 APN Dnah10 0.510 IGL00471 G1 5 124794341 L2418P T C missense Het probably damaging 0.996 phenotype 04/20/2012
10 4337 APN Gli3 1.000 IGL00471 G1 13 15723769 T C critical splice donor site 2 bp Het probably null phenotype 04/20/2012
11 6446 APN Hgfac 0.090 IGL00471 G1 5 35046526 H463N C A missense Het probably damaging 1.000 phenotype 04/20/2012
12 7306 APN Hlx 1.000 IGL00471 G1 1 184731595 F183I A T missense Het probably damaging 1.000 phenotype 04/20/2012
13 332432 APN Ighv1-5 IGL00471 G1 12 114513473 I70L T G missense Het probably benign 0.446 08/05/2015
14 28683 APN Ltbp2 0.541 IGL00471 G1 12 84791064 T1181A T C missense Het probably damaging 0.999 phenotype 04/17/2013
15 6514 APN Morn1 0.306 IGL00471 G1 4 155092328 K140Q A C missense Het possibly damaging 0.811 04/20/2012
16 5035 APN Nek1 0.766 IGL00471 G1 8 61043284 M358L A T missense Het probably benign 0.001 phenotype 04/20/2012
17 4303 APN Pcbd2 0.167 IGL00471 G1 13 55776600 C T splice site Het probably benign 04/20/2012
18 7128 APN Pramel7 0.108 IGL00471 G1 2 87491085 L202Q A T missense Het probably damaging 0.997 04/20/2012
19 5398 APN Shq1 0.931 IGL00471 G1 6 100664483 S146P A G missense Het probably benign 0.001 phenotype 04/20/2012
20 5990 APN Slc25a21 0.335 IGL00471 G1 12 56718137 T C splice site 3 bp Het probably null phenotype 04/20/2012
21 6710 APN Slc26a7 0.063 IGL00471 G1 4 14548403 A T splice site Het probably benign phenotype 04/20/2012
22 332433 APN Sspo 0.000 IGL00471 G1 6 48498213 G A splice site Het probably benign 08/05/2015
23 7209 APN Stam2 0.000 IGL00471 G1 2 52720935 D25G T C missense Het probably damaging 1.000 phenotype 04/20/2012
24 6144 APN Tbx18 1.000 IGL00471 G1 9 87705623 D480E A T missense Het possibly damaging 0.897 phenotype 04/20/2012
25 4712 APN Tmem26 0.425 IGL00471 G1 10 68778681 I309F A T missense Het possibly damaging 0.784 phenotype 04/20/2012
26 6973 APN Ube2c 0.205 IGL00471 G1 2 164771293 T44A A G missense Het probably benign 0.002 phenotype 04/20/2012
[records 1 to 26 of 26]