Incidental Mutations

62 incidental mutations are currently displayed, and affect 62 genes.
14 are Possibly Damaging.
22 are Probably Damaging.
12 are Probably Benign.
12 are Probably Null.
4 create premature stop codons.
3 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 62 of 62] 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 427943 UTSW 2610507B11Rik 0.961 R5419 G1 225 N 11 78272090 L926* T A nonsense Het probably null 09/01/2016
2 427931 UTSW 4931429L15Rik 0.000 R5419 G1 225 N 9 46309326 C T critical splice donor site 1 bp Het probably null 09/01/2016
3 427940 UTSW Abca13 0.000 R5419 G1 225 N 11 9193533 T A critical splice donor site 2 bp Het probably null phenotype 09/01/2016
4 427908 UTSW AI481877 0.127 R5419 G1 225 N 4 59049017 M1116K A T missense Het probably benign 0.041 09/01/2016
5 427925 UTSW Akap13 1.000 R5419 G1 225 N 7 75610243 T69S A T missense Het probably benign 0.013 phenotype 09/01/2016
6 427938 UTSW Arl1 0.776 R5419 G1 225 N 10 88737104 C80S T A missense Het probably damaging 1.000 phenotype 09/01/2016
7 427919 UTSW Brsk1 0.000 R5419 G1 225 N 7 4709004 T618A A G missense Het possibly damaging 0.528 phenotype 09/01/2016
8 427929 UTSW Cep295 0.938 R5419 G1 225 N 9 15324237 H1982R T C missense Het probably damaging 0.983 09/01/2016
9 427927 UTSW Ces5a 0.109 R5419 G1 225 N 8 93499431 S559T A T missense Het unknown phenotype 09/01/2016
10 427960 UTSW Clcf1 1.000 R5419 G1 225 N 19 4222159 N90S A G missense Het possibly damaging 0.462 phenotype 09/01/2016
11 427952 UTSW Clec16a 0.150 R5419 G1 225 N 16 10731679 C872Y G A missense Het probably damaging 0.994 0.122 phenotype 09/01/2016
12 427905 UTSW Cobll1 0.261 R5419 G1 225 N 2 65103357 D430E A T missense Het possibly damaging 0.568 09/01/2016
13 427932 UTSW Cyp1a2 0.289 R5419 G1 225 N 9 57682511 I7F T A missense Het probably benign 0.175 phenotype 09/01/2016
14 427920 UTSW Cyp2b23 0.112 R5419 G1 225 N 7 26681423 R126* G A nonsense Het probably null 09/01/2016
15 427957 UTSW Daam2 0.000 R5419 G1 225 N 17 49480754 W444R A G missense Het possibly damaging 0.952 Daam1 conditional KO increases the severity of the heart phenotype (abnormal ventricular morphology and pressure) of the Daam1 single KO. [provided by MGI curators] (source: MGI)">phenotype 09/01/2016
16 427953 UTSW Dcbld2 0.000 R5419 G1 225 N 16 58455258 C446S T A missense Het probably damaging 0.993 phenotype 09/01/2016
17 427961 UTSW Dnase1l1 0.061 R5419 G1 222 N X 74277038 C T critical splice donor site 1 bp Het probably null 0.971 phenotype 09/01/2016
18 501043 UTSW Eif2d 0.000 R5419 G1 160 N 1 131158298 *177R T C makesense Het probably null phenotype 12/01/2017
19 427909 UTSW Fkbp15 0.000 R5419 G1 185 N 4 62327877 A438V G A missense Het probably damaging 0.975 09/01/2016
20 427911 UTSW Gjb5 0.087 R5419 G1 225 N 4 127355859 A164V G A missense Het probably benign 0.000 phenotype 09/01/2016
21 427930 UTSW Gm17727 0.062 R5419 G1 225 N 9 35778111 T A splice site Het probably null 09/01/2016
22 427918 UTSW Gm5724 0.059 R5419 G1 225 N 6 141736100 C T splice site 5 bp Het probably null 09/01/2016
23 427901 UTSW Grin1 1.000 R5419 G1 225 N 2 25298273 A T splice site Het probably null phenotype 09/01/2016
24 427914 UTSW Grm3 0.000 R5419 G1 225 N 5 9570233 F337S A G missense Het probably damaging 1.000 phenotype 09/01/2016
25 427936 UTSW Hey2 0.910 R5419 G1 225 N 10 30834023 T245S T A missense Het probably benign 0.000 phenotype 09/01/2016
26 427899 UTSW Ifi206 0.137 R5419 G1 225 N 1 173481231 T400A T C missense Het probably benign 0.051 09/01/2016
27 427939 UTSW Itga7 0.658 R5419 G1 225 N 10 128944033 E480K G A missense Het probably null 0.057 phenotype 09/01/2016
28 427917 UTSW Itpr1 0.809 R5419 G1 225 N 6 108493794 Y2227H T C missense Het possibly damaging 0.948 phenotype 09/01/2016
29 427950 UTSW Krt8 1.000 R5419 G1 225 N 15 102003902 D113G T C missense Het probably damaging 0.979 phenotype 09/01/2016
30 427898 UTSW Lgr6 0.000 R5419 G1 225 N 1 134994010 A199T C T missense Het probably damaging 1.000 0.165 phenotype 09/01/2016
31 427922 UTSW Lins1 0.089 R5419 G1 225 N 7 66708095 A G unclassified Het probably benign phenotype 09/01/2016
32 427956 UTSW Lmf1 1.000 R5419 G1 225 N 17 25662636 D553V A T missense Het possibly damaging 0.938 phenotype 09/01/2016
33 427955 UTSW Lnpep 0.000 R5419 G1 225 N 17 17566730 S536P A G missense Het probably damaging 0.998 phenotype 09/01/2016
34 427903 UTSW Lrp1b 0.000 R5419 G1 225 N 2 40730704 C3587* A T nonsense Het probably null phenotype 09/01/2016
35 427910 UTSW Macf1 1.000 R5419 G1 225 N 4 123397124 D3435E A T missense Het possibly damaging 0.705 phenotype 09/01/2016
36 427928 UTSW Mmp1b 0.075 R5419 G1 225 N 9 7384897 I251V T C missense Het possibly damaging 0.606 0.082 phenotype 09/01/2016
37 427951 UTSW Myg1 0.253 R5419 G1 225 N 15 102336962 N206I A T missense Het probably damaging 0.990 phenotype 09/01/2016
38 427958 UTSW Myl12a 0.241 R5419 G1 225 N 17 70994699 R144S T G missense Het probably benign 0.025 phenotype 09/01/2016
39 427933 UTSW Myo5a 0.955 R5419 G1 225 N 9 75147897 I454K T A missense Het probably damaging 1.000 phenotype 09/01/2016
40 427915 UTSW Nwd2 0.130 R5419 G1 225 N 5 63807708 D1545G A G missense Het probably benign 0.107 09/01/2016
41 427947 UTSW Ogdhl 0.000 R5419 G1 225 N 14 32339224 D457E T G missense Het probably damaging 0.998 phenotype 09/01/2016
42 427954 UTSW Olfr202 0.058 R5419 G1 225 N 16 59284341 D52V T A missense Het probably damaging 0.991 phenotype 09/01/2016
43 427946 UTSW Olfr466 0.060 R5419 G1 225 N 13 65152774 L183F A C missense Het probably damaging 1.000 phenotype 09/01/2016
44 427921 UTSW Paf1 1.000 R5419 G1 225 N 7 28395670 I112V A G missense Het possibly damaging 0.684 phenotype 09/01/2016
45 427959 UTSW Pcdhga4 0.114 R5419 G1 225 N 18 37686745 P449L C T missense Het probably damaging 1.000 phenotype 09/01/2016
46 427949 UTSW Pla2g6 0.000 R5419 G1 225 N 15 79299142 I495N A T missense Het possibly damaging 0.819 0.923 phenotype 09/01/2016
47 427902 UTSW Ptgs1 0.342 R5419 G1 225 N 2 36237222 Y40C A G missense Het probably damaging 0.997 phenotype 09/01/2016
48 427945 UTSW Ptprn2 0.274 R5419 G1 225 N 12 117184647 I676F A T missense Het probably damaging 0.988 phenotype 09/01/2016
49 427937 UTSW Rev3l 1.000 R5419 G1 225 N 10 39824931 L1808P T C missense Het possibly damaging 0.947 phenotype 09/01/2016
50 427948 UTSW Sall2 0.000 R5419 G1 225 N 14 52313129 S868P A G missense Het probably damaging 0.998 phenotype 09/01/2016
51 427942 UTSW Slc47a2 0.000 R5419 G1 225 N 11 61307586 F428L A G missense Het probably benign 0.000 09/01/2016
52 427924 UTSW Slco3a1 0.213 R5419 G1 225 N 7 74284615 F603Y A T missense Het possibly damaging 0.766 09/01/2016
53 427900 UTSW Smyd2 0.000 R5419 G1 225 N 1 189909893 C65* A T nonsense Het probably null phenotype 09/01/2016
54 427913 UTSW Ssu72 0.957 R5419 G1 225 N 4 155715550 F57L T C missense Het probably damaging 1.000 09/01/2016
55 427944 UTSW Tanc2 1.000 R5419 G1 225 N 11 105922883 T1718A A G missense Het probably benign 0.001 phenotype 09/01/2016
56 427926 UTSW Tnks 0.000 R5419 G1 108 N 8 34965566 P34A G C missense Het unknown phenotype 09/01/2016
57 427941 UTSW Top3a 1.000 R5419 G1 225 N 11 60762522 T42I G A missense Het probably damaging 1.000 phenotype 09/01/2016
58 427934 UTSW Trank1 0.000 R5419 G1 225 N 9 111391301 S2369P T C missense Het probably damaging 1.000 09/01/2016
59 427906 UTSW Ttn 1.000 R5419 G1 225 N 2 76811243 L5176Q A T missense Het possibly damaging 0.943 0.071 phenotype 09/01/2016
60 501044 UTSW Ubqln1 0.612 R5419 G1 225 N 13 58183183 Q410R T C missense Het probably damaging 0.993 phenotype 12/01/2017
61 427916 UTSW Vmn2r11 0.099 R5419 G1 225 N 5 109059358 I32T A G missense Het possibly damaging 0.545 09/01/2016
62 427935 UTSW Xcr1 0.075 R5419 G1 225 N 9 123856310 F129S A G missense Het probably benign 0.059 phenotype 09/01/2016
[records 1 to 62 of 62]