Incidental Mutations

36 incidental mutations are currently displayed, and affect 36 genes.
5 are Possibly Damaging.
12 are Probably Damaging.
15 are Probably Benign.
3 are Probably Null.
1 create premature stop codons.
2 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 28532 APN 2310033P09Rik 0.207 IGL00927 G1 11 59208848 T92A A G missense Het probably damaging 0.986 04/17/2013
2 29412 APN Ankhd1 0.000 IGL00927 G1 18 36632072 S1007G A G missense Het probably benign 0.013 04/17/2013
3 29509 APN Cabp4 0.000 IGL00927 G1 19 4139407 S50R A T missense Het possibly damaging 0.878 phenotype 04/17/2013
4 28166 APN Camp 0.058 IGL00927 G1 9 109849268 L56Q A T missense Het probably damaging 0.999 phenotype 04/17/2013
5 29146 APN Cblb 0.226 IGL00927 G1 16 52166098 N568S A G missense Het probably benign 0.000 phenotype 04/17/2013
6 29273 APN Ccr6 0.000 IGL00927 G1 17 8255993 T10K C A missense Het probably benign 0.074 phenotype 04/17/2013
7 26646 APN Chit1 0.306 IGL00927 G1 1 134145254 F106S T C missense Het probably damaging 1.000 phenotype 04/17/2013
8 27100 APN Cyb561d1 0.078 IGL00927 G1 3 108199627 L34P A G missense Het probably damaging 0.999 04/17/2013
9 27102 APN Dcun1d1 0.536 IGL00927 G1 3 35920965 A T splice site Het probably benign 04/17/2013
10 28167 APN Deup1 0.000 IGL00927 G1 9 15610671 A G splice site Het probably benign 04/17/2013
11 28027 APN Erich1 0.108 IGL00927 G1 8 14033518 F184S A G missense Het probably damaging 1.000 04/17/2013
12 29065 APN Fmnl3 0.755 IGL00927 G1 15 99337628 A G critical splice donor site 2 bp Het probably null phenotype 04/17/2013
13 29510 APN Grk2 1.000 IGL00927 G1 19 4287954 N508S T C missense Het probably benign 0.095 phenotype 04/17/2013
14 28335 APN Herc4 0.791 IGL00927 G1 10 63273537 I184V A G missense Het probably benign 0.008 phenotype 04/17/2013
15 278079 APN Hnrnpm 1.000 IGL00927 G1 17 33649902 R517L C A missense Het probably damaging 0.988 phenotype 04/16/2015
16 26896 APN Kif3b 1.000 IGL00927 G1 2 153316461 A61T G A missense Het possibly damaging 0.889 phenotype 04/17/2013
17 29064 APN Kmt2d 1.000 IGL00927 G1 15 98845009 G A unclassified Het probably benign phenotype 04/17/2013
18 27101 APN Lrrc7 0.771 IGL00927 G1 3 158161090 V1005L C A missense Het possibly damaging 0.945 phenotype 04/17/2013
19 27629 APN Lrrtm1 0.000 IGL00927 G1 6 77244063 M168L A T missense Het probably benign 0.002 phenotype 04/17/2013
20 27249 APN Ndc1 0.955 IGL00927 G1 4 107384780 C T splice site Het probably benign phenotype 04/17/2013
21 27821 APN Nphs1 1.000 IGL00927 G1 7 30460739 A G unclassified Het probably benign phenotype 04/17/2013
22 27819 APN Olfr692 0.135 IGL00927 G1 7 105369247 Y298F A T missense Het probably damaging 1.000 phenotype 04/17/2013
23 28336 APN Pbld2 0.000 IGL00927 G1 10 63071955 V200A T C missense Het probably benign 0.006 04/17/2013
24 29413 APN Pcdhb21 0.062 IGL00927 G1 18 37514553 Y245C A G missense Het probably damaging 1.000 phenotype 04/17/2013
25 28028 APN Pcm1 0.000 IGL00927 G1 8 41287881 T1055A A G missense Het probably damaging 0.999 phenotype 04/17/2013
26 29274 APN Plcl2 0.235 IGL00927 G1 17 50606920 S319L C T missense Het probably benign 0.012 phenotype 04/17/2013
27 27628 APN Plekha8 0.000 IGL00927 G1 6 54629837 Y372* C A nonsense Het probably null 04/17/2013
28 26648 APN Ralb 0.000 IGL00927 G1 1 119471776 N184I T A missense Het probably benign 0.003 phenotype 04/17/2013
29 28168 APN Robo3 1.000 IGL00927 G1 9 37427754 C T critical splice donor site 1 bp Het probably null phenotype 04/17/2013
30 26647 APN Slc41a1 0.000 IGL00927 G1 1 131839176 L144H T A missense Het probably damaging 1.000 04/17/2013
31 27820 APN Smg1 1.000 IGL00927 G1 7 118140632 G3364D C T missense Het probably damaging 0.996 phenotype 04/17/2013
32 28337 APN Theg 0.000 IGL00927 G1 10 79576599 S329P A G missense Het probably damaging 0.989 phenotype 04/17/2013
33 27630 APN Ttc26 0.593 IGL00927 G1 6 38382220 T C splice site Het probably benign phenotype 04/17/2013
34 27818 APN Vmn1r123 IGL00927 G1 7 21162291 V36D T A missense Het possibly damaging 0.927 04/17/2013
35 29411 APN Zbtb7c 0.266 IGL00927 G1 18 76145850 S460P T C missense Het possibly damaging 0.919 phenotype 04/17/2013
36 29414 APN Zscan30 0.127 IGL00927 G1 18 23971777 T C exon Het noncoding transcript 04/17/2013
[records 1 to 36 of 36]