Incidental Mutations

50 incidental mutations are currently displayed, and affect 50 genes.
7 are Possibly Damaging.
24 are Probably Damaging.
13 are Probably Benign.
5 are Probably Null.
2 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 50 of 50] 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 284962 APN 2700062C07Rik 0.761 IGL02217 18 24470898 C A utr 5 prime Het probably benign 04/16/2015
2 284950 APN Actn1 0.427 IGL02217 12 80174094 Q647* G A nonsense Het probably null phenotype 04/16/2015
3 284965 APN Adamts6 0.660 IGL02217 13 104462365 T A splice site Het probably benign phenotype 04/16/2015
4 284935 APN Brd8 0.939 IGL02217 18 34602727 S899N C T missense Het probably damaging 0.997 phenotype 04/16/2015
5 284928 APN Cabin1 1.000 IGL02217 10 75700047 T1389I G A missense Het possibly damaging 0.955 phenotype 04/16/2015
6 284963 APN Cenpc1 1.000 IGL02217 5 86029200 A G splice site Het probably benign phenotype 04/16/2015
7 284925 APN Clca4a 0.293 IGL02217 3 144961996 T405S T A missense Het possibly damaging 0.605 04/16/2015
8 284959 APN Cntln 0.273 IGL02217 4 85100258 V1168M G A missense Het probably damaging 0.998 04/16/2015
9 284934 APN Col18a1 0.000 IGL02217 10 77053298 S1494P A G missense Het probably damaging 0.962 phenotype 04/16/2015
10 284958 APN Cps1 1.000 IGL02217 1 67174382 T758S A T missense Het probably benign 0.058 phenotype 04/16/2015
11 284949 APN Cul3 1.000 IGL02217 1 80283767 M247K A T missense Het probably damaging 0.970 phenotype 04/16/2015
12 284964 APN Cyp3a57 0.047 IGL02217 5 145369143 A G splice site 4 bp Het probably null 04/16/2015
13 284937 APN Dennd4c 0.315 IGL02217 4 86813799 C917S T A missense Het probably benign 0.000 04/16/2015
14 284960 APN Dhrs11 0.151 IGL02217 11 84822395 Y166* A T nonsense Het probably null 04/16/2015
15 284926 APN Dtl 1.000 IGL02217 1 191568314 V146A A G missense Het probably damaging 1.000 phenotype 04/16/2015
16 284951 APN Exosc9 0.975 IGL02217 3 36552744 E20G A G missense Het probably damaging 0.994 phenotype 04/16/2015
17 284931 APN Fer 0.464 IGL02217 17 64138965 K437R A G missense Het probably benign 0.001 phenotype 04/16/2015
18 284948 APN Fkbp6 0.000 IGL02217 5 135337630 V284E A T missense Het probably benign 0.004 phenotype 04/16/2015
19 284956 APN Foxq1 0.412 IGL02217 13 31559169 S85C A T missense Het probably damaging 0.976 phenotype 04/16/2015
20 284929 APN Galnt12 0.367 IGL02217 4 47113832 S83R T A missense Het probably damaging 1.000 phenotype 04/16/2015
21 284968 APN Gm5244 IGL02217 19 12846863 A T exon Het noncoding transcript 04/16/2015
22 284940 APN Gm765 0.101 IGL02217 6 98248072 E83D T A missense Het possibly damaging 0.927 04/16/2015
23 284969 APN Gm884 0.234 IGL02217 11 103612871 T C splice site Het probably benign 04/16/2015
24 284930 APN Gpr156 0.463 IGL02217 16 38005311 D630G A G missense Het probably benign 0.185 phenotype 04/16/2015
25 284966 APN Hace1 0.383 IGL02217 10 45590375 A T splice site 3 bp Het probably null phenotype 04/16/2015
26 284942 APN Hemgn 0.357 IGL02217 4 46396420 T272K G T missense Het probably damaging 0.976 04/16/2015
27 284954 APN Ifi213 0.022 IGL02217 1 173595032 E89A T G missense Het possibly damaging 0.907 04/16/2015
28 284941 APN Jarid2 1.000 IGL02217 13 44913201 E954G A G missense Het probably damaging 0.999 phenotype 04/16/2015
29 284923 APN Kcnu1 0.000 IGL02217 8 25858184 D126G A G missense Het probably damaging 0.997 phenotype 04/16/2015
30 284932 APN Lbh 0.437 IGL02217 17 72921252 I31F A T missense Het possibly damaging 0.742 phenotype 04/16/2015
31 284924 APN Muc6 0.496 IGL02217 7 141649624 E490G T C missense Het probably damaging 1.000 phenotype 04/16/2015
32 284947 APN Ncoa3 0.910 IGL02217 2 166055346 S686P T C missense Het probably damaging 1.000 phenotype 04/16/2015
33 284927 APN Nme4 0.189 IGL02217 17 26093860 M108T A G missense Het probably damaging 0.993 phenotype 04/16/2015
34 284952 APN Nod1 0.000 IGL02217 6 54943419 V638G A C missense Het possibly damaging 0.629 phenotype 04/16/2015
35 284945 APN Nrip2 0.132 IGL02217 6 128406539 N70S A G missense Het probably damaging 0.999 04/16/2015
36 284953 APN Olfr1111 0.283 IGL02217 2 87149887 M258T A G missense Het probably benign 0.005 phenotype 04/16/2015
37 284957 APN Olfr1344 0.096 IGL02217 7 6440245 I115N T A missense Het probably damaging 0.961 phenotype 04/16/2015
38 284970 APN Pitrm1 0.928 IGL02217 13 6567341 G A splice site Het probably benign phenotype 04/16/2015
39 284943 APN Proser1 0.000 IGL02217 3 53471491 K115E A G missense Het probably damaging 0.964 phenotype 04/16/2015
40 284946 APN Ptov1 0.208 IGL02217 7 44867476 G70R C T missense Het probably damaging 0.999 phenotype 04/16/2015
41 284967 APN Qtrt1 0.361 IGL02217 9 21417389 T G critical splice donor site 2 bp Het probably null phenotype 04/16/2015
42 284961 APN Rbbp8nl 0.027 IGL02217 2 180278188 A G unclassified Het probably benign 04/16/2015
43 284944 APN Rtn3 0.184 IGL02217 19 7435084 T794I G A missense Het probably damaging 0.990 phenotype 04/16/2015
44 284955 APN Setd4 0.186 IGL02217 16 93593295 L82P A G missense Het probably damaging 0.999 04/16/2015
45 284938 APN Shank2 0.000 IGL02217 7 144285047 L27F C T missense Het possibly damaging 0.592 phenotype 04/16/2015
46 284922 APN Srpk2 0.000 IGL02217 5 23545570 V45G A C missense Het probably damaging 0.998 phenotype 04/16/2015
47 284936 APN Utrn 0.000 IGL02217 10 12751559 F57S A G missense Het probably damaging 1.000 phenotype 04/16/2015
48 284939 APN Vcan 1.000 IGL02217 13 89703077 T1255P T G missense Het probably damaging 1.000 phenotype 04/16/2015
49 284921 APN Vmn2r16 0.132 IGL02217 5 109339810 H183P A C missense Het probably damaging 0.978 04/16/2015
50 284933 APN Wdr48 1.000 IGL02217 9 119909535 I286T T C missense Het probably benign 0.010 phenotype 04/16/2015
[records 1 to 50 of 50]