Incidental Mutations

29 incidental mutations are currently displayed, and affect 29 genes.
5 are Possibly Damaging.
11 are Probably Damaging.
11 are Probably Benign.
2 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 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 293265 APN AI314180 0.371 IGL02435 4 58830325 A G splice site Het probably benign 04/16/2015
2 293263 APN Amph 0.256 IGL02435 13 19139163 A G splice site Het probably benign phenotype 04/16/2015
3 293259 APN Ankrd12 0.177 IGL02435 17 65987156 S427R G T missense Het probably damaging 0.999 phenotype 04/16/2015
4 293242 APN Atp4a 0.099 IGL02435 7 30717057 T420A A G missense Het probably benign 0.000 phenotype 04/16/2015
5 293260 APN Braf 1.000 IGL02435 6 39646766 S414N C T missense Het probably benign 0.003 phenotype 04/16/2015
6 293251 APN C1rl 0.000 IGL02435 6 124508873 L401P T C missense Het probably damaging 1.000 04/16/2015
7 293261 APN Elmo1 0.000 IGL02435 13 20589656 D612V A T missense Het probably damaging 0.999 phenotype 04/16/2015
8 293255 APN Fbxo15 0.000 IGL02435 18 84959226 S88P T C missense Het probably damaging 0.968 phenotype 04/16/2015
9 293252 APN Glrx3 1.000 IGL02435 7 137461396 N132S A G missense Het possibly damaging 0.605 phenotype 04/16/2015
10 293257 APN Hamp 0.034 IGL02435 7 30943899 Q29K G T missense Het probably benign 0.254 phenotype 04/16/2015
11 293248 APN Igfbp2 0.286 IGL02435 1 72852086 R281Q G A missense Het probably damaging 1.000 phenotype 04/16/2015
12 293249 APN Itih3 0.066 IGL02435 14 30915754 A483T C T missense Het probably damaging 0.994 phenotype 04/16/2015
13 293250 APN Mrc1 0.084 IGL02435 2 14248860 Q231* C T nonsense Het probably null phenotype 04/16/2015
14 293246 APN Nif3l1 0.399 IGL02435 1 58447861 T69A A G missense Het possibly damaging 0.906 phenotype 04/16/2015
15 293262 APN Ntrk1 1.000 IGL02435 3 87788732 F157S A G missense Het probably benign 0.012 phenotype 04/16/2015
16 293240 APN Olfr1245 0.195 IGL02435 2 89575546 F60S A G missense Het probably damaging 0.988 phenotype 04/16/2015
17 293243 APN Olfr1447 0.062 IGL02435 19 12901027 I251N A T missense Het probably damaging 0.998 phenotype 04/16/2015
18 293239 APN Olfr694 0.113 IGL02435 7 106689503 V76A A G missense Het probably benign 0.259 phenotype 04/16/2015
19 293266 APN Pck2 0.253 IGL02435 14 55544390 T C splice site Het probably benign phenotype 04/16/2015
20 293264 APN Pdgfrb 1.000 IGL02435 18 61064926 T C critical splice donor site 2 bp Het probably null phenotype 04/16/2015
21 293245 APN Ric8b 1.000 IGL02435 10 84980076 N194S A G missense Het probably benign 0.064 04/16/2015
22 293244 APN Rlbp1 0.000 IGL02435 7 79381666 F105L A G missense Het probably damaging 0.996 phenotype 04/16/2015
23 293241 APN Sde2 0.938 IGL02435 1 180866152 K402N G T missense Het probably damaging 1.000 04/16/2015
24 293253 APN Slc13a3 0.000 IGL02435 2 165408940 H461R T C missense Het possibly damaging 0.951 phenotype 04/16/2015
25 293256 APN Spag17 0.000 IGL02435 3 99982444 I210F A T missense Het possibly damaging 0.533 phenotype 04/16/2015
26 293258 APN Szt2 0.739 IGL02435 4 118390823 R735W G A missense Het probably damaging 0.995 phenotype 04/16/2015
27 293247 APN Tspan6 IGL02435 X 133892744 Y186C T C missense Het probably benign 0.000 phenotype 04/16/2015
28 293254 APN Ugt8a 0.717 IGL02435 3 125867320 S508P A G missense Het probably benign 0.004 phenotype 04/16/2015
29 293238 APN Zfp217 0.926 IGL02435 2 170119453 D318G T C missense Het possibly damaging 0.558 04/16/2015
[records 1 to 29 of 29]