Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
7 are Possibly Damaging.
8 are Probably Damaging.
10 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 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 342937 UTSW 1700017G19Rik 0.075 R4558 G1 225 Y 3 40513091 A G unclassified Het noncoding transcript 09/24/2015
2 342930 UTSW A830018L16Rik 0.155 R4558 G1 225 Y 1 11972076 S440* C A nonsense Het probably null 0.618 phenotype 09/24/2015
3 342939 UTSW Acot11 0.239 R4558 G1 225 Y 4 106748366 N583S T C missense Het probably damaging 0.999 0.106 phenotype 09/24/2015
4 342948 UTSW Alox12 0.126 R4558 G1 225 Y 11 70253063 M164L T G missense Het probably benign 0.027 0.064 phenotype 09/24/2015
5 342950 UTSW Atad2b 0.000 R4558 G1 225 Y 12 4943223 I247M A G missense Het probably benign 0.103 0.116 phenotype 09/24/2015
6 342931 UTSW Bmpr2 1.000 R4558 G1 225 Y 1 59845692 M279K T A missense Het probably damaging 0.989 0.252 phenotype 09/24/2015
7 342957 UTSW Cacna2d3 0.000 R4558 G1 225 Y 14 29103713 T502A T C missense Het possibly damaging 0.700 0.100 phenotype 09/24/2015
8 342945 UTSW Casp12 0.000 R4558 G1 225 Y 9 5352742 Y188F A T missense Het probably damaging 0.999 0.200 phenotype 09/24/2015
9 342951 UTSW Catsperb 0.111 R4558 G1 225 Y 12 101591540 Y790C A G missense Het possibly damaging 0.940 0.096 09/24/2015
10 342938 UTSW Cnbd1 0.087 R4558 G1 225 Y 4 19055095 N110K G T missense Het possibly damaging 0.869 0.055 09/24/2015
11 342962 UTSW Fam122b 0.053 R4558 G1 222 Y X 53260677 G A splice site Het probably benign 0.066 phenotype 09/24/2015
12 397271 UTSW Fam189a2 0.156 R4558 G1 200 Y 19 24030549 S130L G A missense Het probably damaging 0.993 0.032 07/05/2016
13 342936 UTSW Fam227b 0.078 R4558 G1 225 Y 2 126127043 S37N C T missense Het probably benign 0.004 0.117 phenotype 09/24/2015
14 342935 UTSW Fsip2 0.264 R4558 G1 225 Y 2 82984953 S3677P T C missense Het possibly damaging 0.734 0.124 phenotype 09/24/2015
15 342946 UTSW Gm10764 0.232 R4558 G1 217 Y 10 87290820 A G exon Het noncoding transcript 0.050 09/24/2015
16 342960 UTSW H2-Q6 0.357 R4558 G1 193 Y 17 35428315 V312A T C missense Het probably benign 0.003 0.244 phenotype 09/24/2015
17 342953 UTSW Hecw1 0.137 R4558 G1 225 Y 13 14247605 D972V T A missense Het probably damaging 0.994 0.434 09/24/2015
18 342959 UTSW Kalrn 0.868 R4558 G1 225 Y 16 33987208 T2597I G A missense Het possibly damaging 0.462 0.096 phenotype 09/24/2015
19 342958 UTSW Kng1 0.000 R4558 G1 225 Y 16 23077418 C A intron 37 bp Het probably null 0.638 phenotype 09/24/2015
20 342949 UTSW Med13 0.942 R4558 G1 225 Y 11 86299054 T1010A T C missense Het probably damaging 0.999 0.296 phenotype 09/24/2015
21 342932 UTSW Nbeal1 0.438 R4558 G1 225 Y 1 60281310 R2021* C T nonsense Het probably null 0.602 09/24/2015
22 342941 UTSW Ncapg 0.879 R4558 G1 225 Y 5 45676644 T341S A T missense Het probably benign 0.001 0.056 phenotype 09/24/2015
23 342947 UTSW Obscn 0.693 R4558 G1 225 Y 11 59131646 R758G T C missense Het possibly damaging 0.896 0.062 phenotype 09/24/2015
24 342961 UTSW Pcdhb4 0.058 R4558 G1 225 Y 18 37309964 I776V A G missense Het probably benign 0.000 0.084 09/24/2015
25 342952 UTSW Ppp4r4 0.119 R4558 G1 225 Y 12 103606933 V697A T C missense Het probably benign 0.002 0.022 phenotype 09/24/2015
26 342940 UTSW Pramef12 0.076 R4558 G1 225 Y 4 144395972 M1V T C start codon destroyed Het probably null 1.000 0.282 09/24/2015
27 342934 UTSW Psd4 0.000 R4558 G1 225 Y 2 24404794 V789M G A missense Het probably damaging 0.998 0.218 09/24/2015
28 342944 UTSW Rasa3 1.000 R4558 G1 225 Y 8 13598259 E135G T C missense Het probably damaging 0.957 0.222 phenotype 09/24/2015
29 342955 UTSW Serpinb9c 0.043 R4558 G1 225 N 13 33154499 E139V T A missense Het probably benign 0.124 09/24/2015
30 342942 UTSW Sgsm1 0.251 R4558 G1 225 Y 5 113258111 G A intron Het probably benign 09/24/2015
31 342956 UTSW Tmem161b 1.000 R4558 G1 225 Y 13 84251244 I6M A G missense Het possibly damaging 0.497 0.206 phenotype 09/24/2015
32 342933 UTSW Upf2 1.000 R4558 G1 225 Y 2 5973593 M423V A G missense Het unknown 0.166 phenotype 09/24/2015
33 342954 UTSW Vmn1r207-ps 0.326 R4558 G1 225 Y 13 22726411 A G exon Het noncoding transcript 0.105 09/24/2015
[records 1 to 33 of 33]