Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
4 are Possibly Damaging.
12 are Probably Damaging.
13 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 33 of 33] 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 290965 APN 1700001P01Rik 0.274 IGL02372 11 97775699 Y54N A T missense Het probably damaging 1.000 04/16/2015
2 290981 APN Alyref 0.949 IGL02372 11 120594875 A G unclassified Het probably benign 04/16/2015
3 290968 APN Ankrd27 0.000 IGL02372 7 35633036 A G splice site 4587 bp Het probably null 04/16/2015
4 290956 APN Arc 1.000 IGL02372 15 74672105 S90P A G missense Het probably damaging 0.999 phenotype 04/16/2015
5 290972 APN Atp6v1e1 1.000 IGL02372 6 120801123 K150N T A missense Het probably benign 0.002 phenotype 04/16/2015
6 290983 APN Atrn 0.000 IGL02372 2 131002754 T C splice site Het probably benign phenotype 04/16/2015
7 290975 APN Ccnb1 1.000 IGL02372 13 100781316 Y259H A G missense Het probably damaging 1.000 phenotype 04/16/2015
8 290964 APN Celsr1 0.638 IGL02372 15 85929907 V1938A A G missense Het probably benign 0.006 phenotype 04/16/2015
9 290973 APN Ckmt2 0.416 IGL02372 13 91865224 V37A A G missense Het probably benign 0.021 phenotype 04/16/2015
10 290958 APN Dpys 0.158 IGL02372 15 39793271 P467T G T missense Het probably benign 0.167 phenotype 04/16/2015
11 290955 APN Ehbp1l1 1.000 IGL02372 19 5710834 T1535A T C missense Het possibly damaging 0.528 phenotype 04/16/2015
12 290977 APN Eif4enif1 0.327 IGL02372 11 3229986 L302P T C missense Het probably benign 0.090 phenotype 04/16/2015
13 290957 APN Faf1 1.000 IGL02372 4 109935582 F584V T G missense Het probably benign 0.174 phenotype 04/16/2015
14 290978 APN Glb1l2 0.055 IGL02372 9 26796476 R72C G A missense Het probably damaging 1.000 phenotype 04/16/2015
15 290951 APN Gm9892 0.162 IGL02372 8 52196836 T C exon Het noncoding transcript 04/16/2015
16 290976 APN Hecw1 0.000 IGL02372 13 14264121 D892E G T missense Het probably damaging 1.000 04/16/2015
17 290970 APN Hr 0.000 IGL02372 14 70558350 E474G A G missense Het possibly damaging 0.936 phenotype 04/16/2015
18 290963 APN Ltbp1 1.000 IGL02372 17 75252406 F297V T G missense Het probably damaging 0.988 phenotype 04/16/2015
19 290961 APN Myc 1.000 IGL02372 15 61987858 N127D A G missense Het probably damaging 0.996 phenotype 04/16/2015
20 290971 APN Nbn 1.000 IGL02372 4 15986613 N671K T A missense Het probably benign 0.002 phenotype 04/16/2015
21 290953 APN Nup210l 0.424 IGL02372 3 90201971 T1607N C A missense Het possibly damaging 0.795 phenotype 04/16/2015
22 290952 APN Olfr281 0.071 IGL02372 15 98456828 T173S A T missense Het probably damaging 1.000 phenotype 04/16/2015
23 290962 APN Osbpl1a 0.145 IGL02372 18 12841313 K22* T A nonsense Het probably null phenotype 04/16/2015
24 290966 APN Phf20l1 0.308 IGL02372 15 66641801 L942P T C missense Het probably damaging 1.000 04/16/2015
25 290954 APN Plekhg5 0.152 IGL02372 4 152102080 R40W C T missense Het probably damaging 0.959 phenotype 04/16/2015
26 290982 APN Pomt2 1.000 IGL02372 12 87122835 C T splice site Het probably benign phenotype 04/16/2015
27 290980 APN Rab3gap1 0.295 IGL02372 1 127919561 A G splice site Het probably benign phenotype 04/16/2015
28 290974 APN Sbk1 0.395 IGL02372 7 126291058 L81P T C missense Het probably damaging 1.000 04/16/2015
29 290959 APN Scrib 1.000 IGL02372 15 76048255 P1524S G A missense Het probably damaging 0.987 phenotype 04/16/2015
30 290969 APN Smpdl3a 0.000 IGL02372 10 57807515 N240K T A missense Het probably benign 0.053 04/16/2015
31 290960 APN Smyd4 0.000 IGL02372 11 75390285 K195* A T nonsense Het probably null phenotype 04/16/2015
32 290967 APN Tulp3 1.000 IGL02372 6 128327598 M231K A T missense Het possibly damaging 0.923 phenotype 04/16/2015
33 290979 APN Zfp87 0.087 IGL02372 13 67520620 A G splice site Het probably benign 04/16/2015
[records 1 to 33 of 33]