Incidental Mutations

29 incidental mutations are currently displayed, and affect 29 genes.
3 are Possibly Damaging.
14 are Probably Damaging.
10 are Probably Benign.
2 are Probably Null.
0 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 29 of 29] 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 399029 UTSW Afap1 0.369 R5251 G1 225 N 5 35950892 E194V A T missense Het probably damaging 1.000 phenotype 07/06/2016
2 399009 UTSW Ankrd16 0.137 R5251 G1 225 N 2 11778741 D51E T A missense Het probably damaging 0.997 07/06/2016
3 399034 UTSW Arhgef5 0.000 R5251 G1 225 N 6 43272881 T189A A G missense Het possibly damaging 0.765 phenotype 07/06/2016
4 399067 UTSW Camk4 0.107 R5251 G1 225 N 18 33184879 D363G A G missense Het probably benign 0.312 phenotype 07/06/2016
5 399025 UTSW Camta1 0.645 R5251 G1 225 N 4 151163884 I199T A G missense Het probably damaging 0.995 phenotype 07/06/2016
6 486784 UTSW Ccdc141 0.000 R5251 G1 225 N 2 77027774 C1021Y C T missense Het probably damaging 1.000 phenotype 08/17/2017
7 399047 UTSW Cdc34 0.366 R5251 G1 225 N 10 79685256 S129L C T missense Het probably damaging 0.990 phenotype 07/06/2016
8 399059 UTSW Cenph 1.000 R5251 G1 225 N 13 100761840 N185I T A missense Het possibly damaging 0.793 phenotype 07/06/2016
9 399061 UTSW Colq 0.074 R5251 G1 217 N 14 31539819 A G critical splice donor site 2 bp Het probably null phenotype 07/06/2016
10 399021 UTSW Dph2 1.000 R5251 G1 225 N 4 117890346 D280E A T missense Het probably damaging 0.998 phenotype 07/06/2016
11 399038 UTSW Exosc5 0.954 R5251 G1 225 N 7 25667755 Y224C A G missense Het probably damaging 0.999 07/06/2016
12 399027 UTSW Fgfr3 0.407 R5251 G1 225 N 5 33735556 C T unclassified Het probably benign phenotype 07/06/2016
13 399066 UTSW Hs3st6 0.218 R5251 G1 225 N 17 24757985 D146E T A missense Het probably benign 0.000 07/06/2016
14 399036 UTSW Igkv13-84 0.127 R5251 G1 225 N 6 68939788 Q23L A T missense Het probably benign 0.276 07/06/2016
15 399022 UTSW Macf1 1.000 R5251 G1 225 N 4 123449967 V2154A A G missense Het probably benign 0.205 phenotype 07/06/2016
16 399019 UTSW Man1a2 1.000 R5251 G1 225 N 3 100620099 E225G T C missense Het probably damaging 1.000 phenotype 07/06/2016
17 399012 UTSW Mertk 0.142 R5251 G1 225 N 2 128729455 S110P T C missense Het probably damaging 1.000 phenotype 07/06/2016
18 399051 UTSW Nav3 0.000 R5251 G1 225 N 10 109853253 F388L A G missense Het probably damaging 0.991 phenotype 07/06/2016
19 399053 UTSW Nme8 0.121 R5251 G1 225 N 13 19660625 N98S T C missense Het probably benign 0.333 phenotype 07/06/2016
20 399031 UTSW Nup205 0.959 R5251 G1 225 N 6 35196482 A G intron 4523 bp Het probably null phenotype 07/06/2016
21 399055 UTSW Prl7d1 0.000 R5251 G1 225 N 13 27709244 N228S T C missense Het probably benign 0.331 07/06/2016
22 399040 UTSW Prss23 0.060 R5251 G1 225 N 7 89510322 K180E T C missense Het probably damaging 0.996 phenotype 07/06/2016
23 399045 UTSW Psap 1.000 R5251 G1 101 N 10 60301700 D549N G A missense Het probably damaging 0.991 phenotype 07/06/2016
24 399011 UTSW Sec16a 0.954 R5251 G1 225 N 2 26439345 V886A A G missense Het probably benign 0.002 phenotype 07/06/2016
25 399007 UTSW Sh2d1b2 R5251 G1 225 N 1 170250073 E81D A T missense Het probably benign 0.192 phenotype 07/06/2016
26 399041 UTSW Tbx6 1.000 R5251 G1 225 N 7 126783344 N254I A T missense Het probably damaging 1.000 phenotype 07/06/2016
27 399017 UTSW Tchhl1 0.000 R5251 G1 225 N 3 93470553 V188A T C missense Het possibly damaging 0.701 phenotype 07/06/2016
28 399014 UTSW Trpc3 1.000 R5251 G1 225 N 3 36670954 L291Q A T missense Het probably damaging 1.000 phenotype 07/06/2016
29 399043 UTSW Zbtb38 0.479 R5251 G1 225 N 9 96687108 T641N G T missense Het probably benign 0.430 phenotype 07/06/2016
[records 1 to 29 of 29]