Incidental Mutations

23 incidental mutations are currently displayed, and affect 22 genes.
5 are Possibly Damaging.
7 are Probably Damaging.
8 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 23 of 23] 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 238308 UTSW Cdh2 1.000 R2194 G1 225 N 18 16640448 T275A T C missense Het probably damaging 0.997 phenotype 10/02/2014
2 238288 UTSW Col1a2 0.000 R2194 G1 225 N 6 4518822 G A unclassified Het probably benign 0.118 phenotype 10/02/2014
3 238286 UTSW Dab1 0.924 R2194 G1 180 N 4 104731751 A524V C T missense Het probably benign 0.289 0.223 phenotype 10/02/2014
4 238307 UTSW Fkbp5 0.000 R2194 G1 225 N 17 28438027 D72G T C missense Het probably benign 0.322 phenotype 10/02/2014
5 238305 UTSW Gm8104 0.135 R2194 G1 83 N 14 43101560 M69T T C missense Het possibly damaging 0.879 10/02/2014
6 238300 UTSW Greb1 0.000 R2194 G1 224 N 12 16690908 E1391G T C missense Het probably benign 0.076 phenotype 10/02/2014
7 238302 UTSW Hif1a 1.000 R2194 G1 225 N 12 73930747 N183S A G missense Het probably damaging 0.983 phenotype 10/02/2014
8 238291 UTSW Hnrnpul1 0.578 R2194 G1 225 N 7 25725922 A G critical splice donor site 2 bp Het probably null phenotype 10/02/2014
9 238303 UTSW Hsp90aa1 0.000 R2194 G1 225 N 12 110695680 M1L T A start codon destroyed Het possibly damaging 0.588 0.568 phenotype 10/02/2014
10 238304 UTSW Hsp90aa1 0.000 R2194 G1 225 N 12 110695681 C A critical splice acceptor site Het probably null 0.949 phenotype 10/02/2014
11 238310 UTSW Ighmbp2 1.000 R2194 G1 215 N 19 3265116 D768G T C missense Het probably benign 0.003 phenotype 10/02/2014
12 238296 UTSW Kitl 0.292 R2194 G1 225 N 10 100016037 T G critical splice donor site 2 bp Het probably null phenotype 10/02/2014
13 238295 UTSW Mfsd4b4 0.098 R2194 G1 225 N 10 39892923 N104I T A missense Het probably damaging 0.993 10/02/2014
14 238299 UTSW Nsf 1.000 R2194 G1 225 N 11 103930752 E26K C T missense Het possibly damaging 0.586 0.089 10/02/2014
15 238298 UTSW Obscn 0.804 R2194 G1 214 N 11 59131646 R758G T C missense Het possibly damaging 0.896 0.179 phenotype 10/02/2014
16 238297 UTSW Olfr331 0.056 R2194 G1 225 N 11 58501642 K305E T C missense Het probably damaging 0.970 phenotype 10/02/2014
17 238309 UTSW Pcdhb4 0.067 R2194 G1 225 N 18 37308735 V366A T C missense Het probably damaging 0.996 10/02/2014
18 238294 UTSW Polb 1.000 R2194 G1 225 N 8 22647467 R89H C T missense Het probably benign 0.047 phenotype 10/02/2014
19 238306 UTSW Rfc4 0.967 R2194 G1 217 N 16 23114152 TTTGTTGTTGTTG TTTGTTGTTG unclassified Het probably benign phenotype 10/02/2014
20 238293 UTSW Rnf40 0.968 R2194 G1 171 N 7 127597235 A785D C A missense Het probably damaging 1.000 phenotype 10/02/2014
21 238289 UTSW St7 0.268 R2194 G1 225 N 6 17942719 E494G A G missense Het probably damaging 0.996 phenotype 10/02/2014
22 238285 UTSW Tnks1bp1 0.000 R2194 G1 225 N 2 85063065 E1112G A G missense Het probably benign 0.056 10/02/2014
23 238292 UTSW Zfp607a 0.068 R2194 G1 225 N 7 27879380 E625G A G missense Het possibly damaging 0.730 10/02/2014
[records 1 to 23 of 23]