Incidental Mutations

34 incidental mutations are currently displayed, and affect 33 genes.
1 are Possibly Damaging.
16 are Probably Damaging.
13 are Probably Benign.
4 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 34 of 34] 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 409923 APN Abcb1a 0.151 IGL03119 5 8714887 (GRCm38) T626A A G missense Het probably benign 0.002 phenotype 2016-08-02
2 409897 APN Adcy1 0.000 IGL03119 11 7109051 (GRCm38) T319I C T missense Het probably damaging 0.999 phenotype 2016-08-02
3 409906 APN Adgrv1 0.000 IGL03119 13 81382373 (GRCm38) S5861P A G missense Het probably damaging 0.998 phenotype 2016-08-02
4 409909 APN Adgrv1 0.000 IGL03119 13 81433700 (GRCm38) C4742G A C missense Het probably benign 0.018 phenotype 2016-08-02
5 409920 APN Arid5b 0.942 IGL03119 10 68243227 (GRCm38) D93E A T missense Het probably damaging 1.000 phenotype 2016-08-02
6 409904 APN Atp6v1h 1.000 IGL03119 1 5095669 (GRCm38) T121A A G missense Het probably benign 0.338 phenotype 2016-08-02
7 409915 APN Atxn7 0.000 IGL03119 14 14100734 (GRCm38) L807F C T missense Het probably damaging 1.000 phenotype 2016-08-02
8 409919 APN Cep104 0.369 IGL03119 4 153981724 (GRCm38) K126N A C missense Het probably damaging 0.996 phenotype 2016-08-02
9 409917 APN Dcaf6 0.000 IGL03119 1 165339976 (GRCm38) E708G T C missense Het probably damaging 0.999 2016-08-02
10 409925 APN Dst 0.231 IGL03119 1 34161062 (GRCm38) Y107C A G missense Het probably damaging 1.000 phenotype 2016-08-02
11 409914 APN E2f3 1.000 IGL03119 13 29985365 (GRCm38) S102P A G missense Het probably benign 0.208 phenotype 2016-08-02
12 409901 APN Eif3e 0.961 IGL03119 15 43265604 (GRCm38) S207A A C missense Het probably benign 0.000 2016-08-02
13 409912 APN Etl4 0.783 IGL03119 2 20713387 (GRCm38) Y313C A G missense Het probably damaging 1.000 0.468 phenotype 2016-08-02
14 409910 APN Fyttd1 0.144 IGL03119 16 32900695 (GRCm38) V121A T C missense Het probably benign 0.077 2016-08-02
15 409913 APN Gstk1 0.104 IGL03119 6 42249899 (GRCm38) S200P T C missense Het probably damaging 1.000 phenotype 2016-08-02
16 409898 APN Ifrd1 0.669 IGL03119 12 40212334 (GRCm38) F244L A T missense Het probably null 0.029 phenotype 2016-08-02
17 409922 APN Ints7 0.949 IGL03119 1 191610365 (GRCm38) V491A T C missense Het probably damaging 0.997 phenotype 2016-08-02
18 409911 APN Kcnd2 0.094 IGL03119 6 21216509 (GRCm38) E71* G T nonsense Het probably null phenotype 2016-08-02
19 409918 APN Ltbp3 0.190 IGL03119 19 5757443 (GRCm38) Q1123L A T missense Het probably damaging 0.978 phenotype 2016-08-02
20 409921 APN Myo5a 0.951 IGL03119 9 75174015 (GRCm38) T961A A G missense Het probably benign 0.012 0.060 phenotype 2016-08-02
21 409900 APN Naa25 1.000 IGL03119 5 121434978 (GRCm38) V720E T A missense Het probably null 0.999 phenotype 2016-08-02
22 409895 APN Olfr1480 0.065 IGL03119 19 13530435 (GRCm38) I298T T C missense Het probably benign 0.109 phenotype 2016-08-02
23 409903 APN Olfr599 0.056 IGL03119 7 103338722 (GRCm38) I223V A G missense Het probably damaging 0.997 phenotype 2016-08-02
24 409896 APN Pcdhb15 0.067 IGL03119 18 37475014 (GRCm38) T433N C A missense Het probably damaging 0.999 phenotype 2016-08-02
25 409928 APN Peli1 0.000 IGL03119 11 21140560 (GRCm38) T C splice site Het probably benign phenotype 2016-08-02
26 409924 APN Ptbp1 1.000 IGL03119 10 79859624 (GRCm38) V209A T C missense Het probably damaging 0.999 phenotype 2016-08-02
27 409908 APN Ranbp2 1.000 IGL03119 10 58452003 (GRCm38) Y31C A G missense Het probably damaging 0.998 phenotype 2016-08-02
28 409916 APN Smg1 1.000 IGL03119 7 118195113 (GRCm38) G A utr 3 prime Het probably benign phenotype 2016-08-02
29 409899 APN Stat2 0.395 IGL03119 10 128283517 (GRCm38) M457V A G missense Het probably benign 0.148 phenotype 2016-08-02
30 409907 APN Trpm6 1.000 IGL03119 19 18838017 (GRCm38) E1156* G T nonsense Het probably null phenotype 2016-08-02
31 409927 APN Usp53 0.230 IGL03119 3 122961415 (GRCm38) R130S T A missense Het possibly damaging 0.803 phenotype 2016-08-02
32 409926 APN Vwa5b1 0.000 IGL03119 4 138606541 (GRCm38) S193P A G missense Het probably benign 0.012 2016-08-02
33 409902 APN Xrn2 0.964 IGL03119 2 147042872 (GRCm38) I626V A G missense Het probably damaging 0.995 phenotype 2016-08-02
34 409905 APN Zfp574 0.959 IGL03119 7 25080473 (GRCm38) A307T G A missense Het probably benign 0.000 2016-08-02
[records 1 to 34 of 34]