Incidental Mutations

27 incidental mutations are currently displayed, and affect 27 genes.
3 are Possibly Damaging.
12 are Probably Damaging.
8 are Probably Benign.
3 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 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 529017 UTSW Adam20 0.000 R6708 G1 225.01 N 8 40796494 L547P T C missense Het probably damaging 0.996 07/24/2018
2 529009 UTSW Atp8b5 0.081 R6708 G1 225.01 N 4 43334249 H338Q T G missense Het probably benign 0.000 07/24/2018
3 529007 UTSW Btbd3 0.463 R6708 G1 225.01 N 2 138283571 E225G A G missense Het possibly damaging 0.621 07/24/2018
4 529012 UTSW Cd163 0.000 R6708 G1 225.01 N 6 124309208 H239R A G missense Het probably damaging 1.000 0.275 phenotype 07/24/2018
5 529018 UTSW Cdh15 0.000 R6708 G1 205.01 N 8 122863555 I409T T C missense Het probably benign 0.317 phenotype 07/24/2018
6 529030 UTSW Cep55 0.955 R6708 G1 225.01 N 19 38060261 S122T T A missense Het probably benign 0.226 07/24/2018
7 529020 UTSW Col5a3 0.230 R6708 G1 225.01 N 9 20775035 P1382L G A missense Het unknown phenotype 07/24/2018
8 529025 UTSW Ehmt2 1.000 R6708 G1 115.01 N 17 34899899 K186* A T nonsense Het probably null phenotype 07/24/2018
9 529010 UTSW Elavl2 0.411 R6708 G1 225.01 N 4 91253397 I295N A T missense Het probably damaging 1.000 phenotype 07/24/2018
10 529006 UTSW Elf5 1.000 R6708 G1 225.01 N 2 103448989 D185G A G missense Het probably damaging 0.966 phenotype 07/24/2018
11 529011 UTSW Emx1 0.000 R6708 G1 136.01 N 6 85194140 E175G A G missense Het probably damaging 0.992 phenotype 07/24/2018
12 529014 UTSW Fan1 0.000 R6708 G1 225.01 N 7 64372806 N233T T G missense Het probably benign 0.001 phenotype 07/24/2018
13 529008 UTSW Frem2 1.000 R6708 G1 225.01 N 3 53585501 I1865F T A missense Het probably benign 0.001 phenotype 07/24/2018
14 529016 UTSW Kcnu1 0.000 R6708 G1 225.01 N 8 25937711 D352G A G missense Het probably benign 0.000 phenotype 07/24/2018
15 529022 UTSW Klhdc1 0.000 R6708 G1 225.01 N 12 69259530 H247L A T missense Het possibly damaging 0.752 07/24/2018
16 529026 UTSW L3mbtl4 0.000 R6708 G1 225.01 N 17 68630258 T425S A T missense Het probably benign 0.188 07/24/2018
17 529027 UTSW Mrpl21 0.936 R6708 G1 191.01 N 19 3286890 V87A T C missense Het probably damaging 1.000 phenotype 07/24/2018
18 529029 UTSW Olfr1423 0.285 R6708 G1 225.01 N 19 12036739 M1K A T start codon destroyed Het probably null 0.998 phenotype 07/24/2018
19 529024 UTSW Olfr203 0.108 R6708 G1 225.01 N 16 59304053 L301Q T A missense Het probably damaging 0.998 phenotype 07/24/2018
20 529021 UTSW Olfr811 0.060 R6708 G1 225.01 N 10 129801820 A235D G T missense Het probably damaging 1.000 0.647 phenotype 07/24/2018
21 529005 UTSW Orc4 0.965 R6708 G1 225.01 N 2 48937493 H29Q A T missense Het probably benign 0.001 phenotype 07/24/2018
22 529019 UTSW Pcnx2 0.000 R6708 G1 216.01 N 8 125860953 C T critical splice donor site 1 bp Het probably null phenotype 07/24/2018
23 529004 UTSW Pogk 0.292 R6708 G1 225.01 N 1 166403509 V83A A G missense Het probably damaging 0.998 phenotype 07/24/2018
24 529015 UTSW Synm 0.000 R6708 G1 225.01 N 7 67733246 E1556G T C missense Het possibly damaging 0.719 phenotype 07/24/2018
25 529028 UTSW Tmem109 0.000 R6708 G1 225.01 N 19 10872031 L153F C A missense Het probably damaging 1.000 phenotype 07/24/2018
26 529023 UTSW Ttc8 0.452 R6708 G1 225.01 N 12 98943532 T74A A G missense Het probably damaging 0.991 phenotype 07/24/2018
27 529013 UTSW Zfp180 0.407 R6708 G1 179.01 N 7 24106096 T647S A T missense Het probably damaging 0.984 phenotype 07/24/2018
[records 1 to 27 of 27]