Incidental Mutations

36 incidental mutations are currently displayed, and affect 36 genes.
3 are Possibly Damaging.
11 are Probably Damaging.
17 are Probably Benign.
5 are Probably Null.
1 create premature stop codons.
1 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 272783 UTSW 9130011E15Rik 1.000 R3796 G1 225 Y 19 45921610 (GRCm38) A G splice site Het probably benign 2015-03-25
2 272761 UTSW Adamts17 0.071 R3796 G1 225 Y 7 66839914 (GRCm38) A G splice site 3 bp Het probably null 0.976 phenotype 2015-03-25
3 272762 UTSW Alpk3 0.281 R3796 G1 225 Y 7 81092753 (GRCm38) P773T C A missense Het probably benign 0.017 0.090 phenotype 2015-03-25
4 272747 UTSW Alppl2 0.072 R3796 G1 225 Y 1 87088354 (GRCm38) A G critical splice donor site 2 bp Het probably null 0.938 phenotype 2015-03-25
5 272775 UTSW Basp1 1.000 R3796 G1 206 Y 15 25364312 (GRCm38) C A unclassified Het probably benign 0.151 phenotype 2015-03-25
6 272772 UTSW Clec14a 0.053 R3796 G1 225 Y 12 58267909 (GRCm38) A309V G A missense Het probably benign 0.335 0.076 phenotype 2015-03-25
7 272752 UTSW Clk2 0.240 R3796 G1 225 Y 3 89175689 (GRCm38) N424S A G missense Het probably benign 0.000 0.060 phenotype 2015-03-25
8 272760 UTSW Cops7a 0.000 R3796 G1 225 Y 6 124959832 (GRCm38) R252H C T missense Het probably damaging 0.996 0.120 phenotype 2015-03-25
9 473636 UTSW Csmd2 0.151 R3796 G1 225 N 4 128517595 (GRCm38) P2469S C T missense Het probably benign 0.204 2017-04-14
10 272782 UTSW Cwf19l1 0.822 R3796 G1 225 Y 19 44114567 (GRCm38) V403A A G missense Het probably damaging 0.966 0.475 phenotype 2015-03-25
11 272756 UTSW Dnajc16 0.605 R3796 G1 225 Y 4 141767737 (GRCm38) D521E G T missense Het probably benign 0.000 0.074 2015-03-25
12 272766 UTSW Dnm2 1.000 R3796 G1 225 Y 9 21505487 (GRCm38) V772A T C missense Het probably benign 0.000 0.060 phenotype 2015-03-25
13 473634 UTSW Dst 0.197 R3796 G1 225 N 1 34181915 (GRCm38) V2267F G T missense Het probably benign 0.146 phenotype 2017-04-14
14 272776 UTSW Eif3d 0.967 R3796 G1 206 Y 15 77968569 (GRCm38) F4S A G missense Het probably damaging 1.000 0.971 phenotype 2015-03-25
15 272765 UTSW Fgfr1 1.000 R3796 G1 225 Y 8 25572437 (GRCm38) D663N G A missense Het probably damaging 1.000 0.293 phenotype 2015-03-25
16 272748 UTSW Hmcn1 0.000 R3796 G1 225 Y 1 150586418 (GRCm38) Y5170H A G missense Het probably damaging 0.999 0.314 phenotype 2015-03-25
17 272755 UTSW Kcna2 1.000 R3796 G1 225 Y 3 107105590 (GRCm38) L496I T A missense Het probably benign 0.374 0.082 phenotype 2015-03-25
18 272777 UTSW Krt8 1.000 R3796 G1 225 Y 15 101999442 (GRCm38) I233V T C missense Het probably benign 0.001 0.090 phenotype 2015-03-25
19 272750 UTSW Mfap1b 0.898 R3796 G1 225 Y 2 121473905 (GRCm38) V3A A G missense Het probably benign 0.000 0.058 2015-03-25
20 272764 UTSW Phrf1 0.000 R3796 G1 225 Y 7 141259918 (GRCm38) R243* C T nonsense Het probably null 0.976 2015-03-25
21 272758 UTSW Plbd2 0.064 R3796 G1 225 Y 5 120492868 (GRCm38) I224N A T missense Het probably damaging 1.000 0.647 2015-03-25
22 272759 UTSW Rab19 0.000 R3796 G1 225 Y 6 39384041 (GRCm38) V41A T C missense Het probably benign 0.013 0.060 2015-03-25
23 272763 UTSW Rrm1 0.970 R3796 G1 225 Y 7 102465703 (GRCm38) T A splice site Het probably null 0.976 phenotype 2015-03-25
24 272774 UTSW Sacs 0.000 R3796 G1 225 Y 14 61206121 (GRCm38) V1872A T C missense Het possibly damaging 0.870 0.105 phenotype 2015-03-25
25 272767 UTSW Setd2 0.943 R3796 G1 225 Y 9 110549571 (GRCm38) V818A T C missense Het probably benign 0.004 0.090 phenotype 2015-03-25
26 272768 UTSW Shprh 0.000 R3796 G1 225 Y 10 11178757 (GRCm38) L1037F C T missense Het possibly damaging 0.895 0.179 Pcna. Neither homozygous truncation nor KO affect B cell somatic hypermutation or class switching. [provided by MGI curators] (source: MGI)">phenotype 2015-03-25
27 272751 UTSW Slc24a3 0.158 R3796 G1 225 Y 2 145616681 (GRCm38) D527G A G missense Het probably damaging 0.998 0.948 phenotype 2015-03-25
28 272780 UTSW Slc27a6 0.062 R3796 G1 225 Y 18 58598751 (GRCm38) T C splice site Het probably benign 0.090 phenotype 2015-03-25
29 272771 UTSW Slc35g3 0.071 R3796 G1 225 Y 11 69760917 (GRCm38) F103L A G missense Het probably benign 0.018 0.068 2015-03-25
30 272757 UTSW Slc5a1 0.138 R3796 G1 225 Y 5 33152652 (GRCm38) D408G A G missense Het probably damaging 1.000 0.912 phenotype 2015-03-25
31 272778 UTSW Spag6l 0.205 R3796 G1 225 Y 16 16763052 (GRCm38) I477N A T missense Het probably damaging 1.000 0.893 phenotype 2015-03-25
32 272769 UTSW Srgap1 0.261 R3796 G1 225 Y 10 122047132 (GRCm38) V21A A G missense Het probably benign 0.061 0.085 phenotype 2015-03-25
33 272770 UTSW Trim7 0.087 R3796 G1 159 Y 11 48845670 (GRCm38) A G splice site 4 bp Het probably null 0.976 phenotype 2015-03-25
34 272746 UTSW Trpa1 0.122 R3796 G1 225 Y 1 14893264 (GRCm38) N578S T C missense Het possibly damaging 0.736 0.664 phenotype 2015-03-25
35 272779 UTSW Xdh 0.326 R3796 G1 225 Y 17 73907658 (GRCm38) E764G T C missense Het probably damaging 1.000 0.630 phenotype 2015-03-25
36 272781 UTSW Zfp518a 0.924 R3796 G1 225 Y 19 40915310 (GRCm38) V1228F G T missense Het probably damaging 1.000 0.647 phenotype 2015-03-25
[records 1 to 36 of 36]