Incidental Mutations

31 incidental mutations are currently displayed, and affect 31 genes.
6 are Possibly Damaging.
10 are Probably Damaging.
9 are Probably Benign.
5 are Probably Null.
3 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 31 of 31] 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 6761 APN Arhgap29 0.628 IGL00492 G1 3 122003312 E108* G T nonsense Het probably null phenotype 04/20/2012
2 9296 APN Braf 1.000 IGL00492 G1 6 39660999 A T splice site Het probably null phenotype 12/06/2012
3 5020 APN Calr3 0.308 IGL00492 G1 8 72431396 Q112* G A nonsense Het probably null phenotype 04/20/2012
4 5860 APN Dis3 0.974 IGL00492 G1 14 99082674 I649T A G missense Het probably damaging 0.998 04/20/2012
5 3944 APN Dopey2 0.346 IGL00492 G1 16 93780782 V65A T C missense Het probably benign 0.005 04/20/2012
6 7187 APN Dpp4 0.000 IGL00492 G1 2 62379302 Y126H A G missense Het probably damaging 1.000 phenotype 04/20/2012
7 5713 APN Dtwd2 0.144 IGL00492 G1 18 49723709 Y170* A T nonsense Het probably null 04/20/2012
8 332217 APN Efcab7 0.125 IGL00492 G1 4 99831463 T61A A G missense Het probably benign 0.122 08/05/2015
9 4140 APN Fbxl3 0.266 IGL00492 G1 14 103095294 L83M G T missense Het probably damaging 1.000 phenotype 04/20/2012
10 10728 APN Fbxo17 0.107 IGL00492 G1 7 28735341 S184R A C missense Het probably damaging 0.999 phenotype 12/06/2012
11 10748 APN Fcf1 0.915 IGL00492 G1 12 84982332 T C critical splice donor site 2 bp Het probably null 12/06/2012
12 6650 APN Gm428 IGL00492 G1 4 73687333 T327I C T missense Het probably damaging 0.993 phenotype 04/20/2012
13 4842 APN Hcrtr2 0.171 IGL00492 G1 9 76246441 Y223C T C missense Het probably damaging 0.999 phenotype 04/20/2012
14 332220 APN Kcnn1 0.000 IGL00492 G1 8 70848062 F432S A G missense Het probably benign 0.000 phenotype 08/05/2015
15 4898 APN Kmt2a 1.000 IGL00492 G1 9 44807934 C T unclassified Het probably benign phenotype 04/20/2012
16 332216 APN Lce1j 0.089 IGL00492 G1 3 92789406 T22A T C missense Het unknown 08/05/2015
17 5989 APN Lrfn5 0.273 IGL00492 G1 12 61844126 S734T T A missense Het probably benign 0.000 phenotype 04/20/2012
18 4344 APN Lyst 0.385 IGL00492 G1 13 13678175 S2253R T A missense Het possibly damaging 0.538 phenotype 04/20/2012
19 11000 APN Myrfl 0.314 IGL00492 G1 10 116796106 L645F G A missense Het possibly damaging 0.463 12/06/2012
20 12800 APN Nudt9 0.171 IGL00492 G1 5 104061762 A G unclassified Het probably benign phenotype 12/06/2012
21 3985 APN Ostn 0.487 IGL00492 G1 16 27321382 M15K T A missense Het possibly damaging 0.665 phenotype 04/20/2012
22 332219 APN Psg20 0.104 IGL00492 G1 7 18674611 T395A T C missense Het possibly damaging 0.724 08/05/2015
23 6737 APN Rpf1 0.820 IGL00492 G1 3 146512247 H171Y G A missense Het probably benign 0.104 04/20/2012
24 14010 APN Shprh 0.436 IGL00492 G1 10 11188158 E1325G A G missense Het probably damaging 1.000 Pcna. Neither homozygous truncation nor KO affect B cell somatic hypermutation or class switching. [provided by MGI curators] (source: MGI)">phenotype 12/06/2012
25 3257 APN Slc22a8 0.000 IGL00492 G1 19 8594135 V77L G T missense Het probably benign 0.373 phenotype 04/20/2012
26 332218 APN Tbck 0.286 IGL00492 G1 3 132722740 K285N A C missense Het probably benign 0.005 phenotype 08/05/2015
27 6313 APN Vmn1r86 0.061 IGL00492 G1 7 13102541 C86Y C T missense Het possibly damaging 0.906 04/20/2012
28 4180 APN Zdhhc20 0.068 IGL00492 G1 14 57873924 I73T A G missense Het probably damaging 0.993 04/20/2012
29 15044 APN Zfp512b 0.000 IGL00492 G1 2 181587069 D701G T C missense Het probably damaging 0.976 12/06/2012
30 6043 APN Zfp735 0.091 IGL00492 G1 11 73711366 Y379N T A missense Het possibly damaging 0.861 04/20/2012
31 6961 APN Znfx1 0.000 IGL00492 G1 2 167036923 H980Q G T missense Het probably damaging 1.000 04/20/2012
[records 1 to 31 of 31]