Incidental Mutations

27 incidental mutations are currently displayed, and affect 27 genes.
2 are Possibly Damaging.
15 are Probably Damaging.
6 are Probably Benign.
3 are Probably Null.
0 create premature stop codons.
3 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 27 of 27] 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 45847 UTSW 0610009O20Rik 0.201 R0560 G1 225 Y 18 38254498 L230Q T A missense Het probably damaging 1.000 0.040 06/11/2013
2 45823 UTSW AI464131 0.246 R0560 G1 225 Y 4 41498167 R488W G A missense Het probably damaging 0.991 0.026 06/11/2013
3 45839 UTSW Apob 0.772 R0560 G1 223 Y 12 8005101 Y1334H T C missense Het probably damaging 1.000 0.206 phenotype 06/11/2013
4 45841 UTSW Arsb 0.257 R0560 G1 225 Y 13 93790198 T159A A G missense Het possibly damaging 0.659 0.154 phenotype 06/11/2013
5 45814 UTSW Asb18 0.123 R0560 G1 225 Y 1 90014528 V17G A C missense Het probably damaging 1.000 0.078 phenotype 06/11/2013
6 45828 UTSW Bicd1 0.430 R0560 G1 225 Y 6 149511962 K284E A G missense Het probably benign 0.345 0.086 phenotype 06/11/2013
7 45824 UTSW Bspry 0.182 R0560 G1 225 Y 4 62486449 R161G A G missense Het probably damaging 0.998 0.034 06/11/2013
8 45837 UTSW Ccdc138 0.085 R0560 G1 225 Y 10 58575717 T636A A G missense Het probably damaging 0.999 0.120 06/11/2013
9 45816 UTSW Cubn 1.000 R0560 G1 225 Y 2 13428680 W1140R A T missense Het probably damaging 1.000 0.178 phenotype 06/11/2013
10 45829 UTSW Cyp2t4 0.065 R0560 G1 225 Y 7 27158511 T479A A G missense Het probably damaging 0.985 0.035 06/11/2013
11 45845 UTSW Dtx3l 0.265 R0560 G1 225 Y 16 35932935 S434P A G missense Het probably damaging 1.000 0.122 phenotype 06/11/2013
12 45818 UTSW Duox2 0.000 R0560 G1 225 Y 2 122291554 V611A A G missense Het probably benign 0.038 0.220 phenotype 06/11/2013
13 45846 UTSW Epb41l3 0.000 R0560 G1 225 Y 17 69274897 T G critical splice donor site 2 bp Het probably null 0.488 phenotype 06/11/2013
14 45840 UTSW Fam161b 0.107 R0560 G1 189 Y 12 84357718 D63N C T missense Het probably damaging 0.959 0.090 06/11/2013
15 45836 UTSW Gm5422 0.793 R0560 G1 225 N 10 31249244 G A exon Het noncoding transcript 06/11/2013
16 45817 UTSW Gpr158 0.073 R0560 G1 225 Y 2 21825274 D710V A T missense Het probably damaging 1.000 0.446 06/11/2013
17 45821 UTSW Krtcap2 0.144 R0560 G1 225 Y 3 89249142 T C critical splice donor site 2 bp Het probably null 0.550 06/11/2013
18 45844 UTSW Mtrf1 0.159 R0560 G1 225 Y 14 79406850 D199E T A missense Het probably damaging 1.000 0.038 phenotype 06/11/2013
19 45842 UTSW Naip6 0.115 R0560 G1 121 Y 13 100300600 A472T C T missense Het probably benign 0.077 0.044 phenotype 06/11/2013
20 45815 UTSW Ncf2 0.133 R0560 G1 189 Y 1 152821522 Y47N T A missense Het probably damaging 1.000 0.212 phenotype 06/11/2013
21 45822 UTSW Ovgp1 0.000 R0560 G1 225 Y 3 105986410 T C unclassified Het probably benign 0.048 phenotype 06/11/2013
22 45819 UTSW Siglec1 0.078 R0560 G1 170 Y 2 131070346 T1692N G T missense Het probably benign 0.016 0.180 phenotype 06/11/2013
23 45833 UTSW Slc10a2 0.000 R0560 G1 225 Y 8 5089092 N284S T C missense Het probably benign 0.019 0.068 phenotype 06/11/2013
24 45838 UTSW Slfn3 0.000 R0560 G1 225 Y 11 83213152 F283S T C missense Het probably damaging 0.993 0.038 phenotype 06/11/2013
25 45834 UTSW Trank1 0.000 R0560 G1 225 Y 9 111391086 F2297S T C missense Het possibly damaging 0.879 0.050 06/11/2013
26 45830 UTSW Vmn2r69 0.165 R0560 G1 225 Y 7 85409714 A G critical splice donor site 2 bp Het probably null 0.618 06/11/2013
27 45825 UTSW Vps13d 1.000 R0560 G1 225 Y 4 145054190 E3957G T C missense Het probably damaging 0.997 0.214 phenotype 06/11/2013
[records 1 to 27 of 27]