Incidental Mutations

24 incidental mutations are currently displayed, and affect 24 genes.
3 are Possibly Damaging.
6 are Probably Damaging.
10 are Probably Benign.
5 are Probably Null.
2 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 24 of 24] 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 12433 APN Ablim1 0.430 IGL00847 G1 19 57152290 E142G T C missense Het possibly damaging 0.586 phenotype 12/06/2012
2 12474 APN Arid4a 0.000 IGL00847 G1 12 71075718 P958S C T missense Het probably damaging 1.000 phenotype 12/06/2012
3 12491 APN BC049730 0.037 IGL00847 G1 7 24714248 T230A A G missense Het probably benign 0.010 12/06/2012
4 29015 APN Cct5 0.963 IGL00847 G1 15 31590927 T C unclassified Het probably benign phenotype 04/17/2013
5 12540 APN Cntnap4 0.162 IGL00847 G1 8 112767619 C T splice site Het probably benign phenotype 12/06/2012
6 12542 APN Col4a3 0.000 IGL00847 G1 1 82717869 L1597F C T missense Het probably damaging 1.000 phenotype 12/06/2012
7 12632 APN Gla IGL00847 G1 X 134595198 V179L C A missense Het probably benign 0.000 phenotype 12/06/2012
8 15007 APN Gm20422 IGL00847 G1 8 69742992 C212* A T nonsense Het probably null 12/06/2012
9 12657 APN Hace1 0.393 IGL00847 G1 10 45672357 Y14* T A nonsense Het probably null phenotype 12/06/2012
10 12659 APN Hcfc2 0.197 IGL00847 G1 10 82741278 T A splice site Het probably null phenotype 12/06/2012
11 12489 APN Helz2 0.000 IGL00847 G1 2 181232245 D2152G T C missense Het possibly damaging 0.725 phenotype 12/06/2012
12 12724 APN Mcm8 0.783 IGL00847 G1 2 132819674 L74V T G missense Het probably benign 0.289 phenotype 12/06/2012
13 12744 APN Myo18b 1.000 IGL00847 G1 5 112830389 A G splice site Het probably benign phenotype 12/06/2012
14 13221 APN Ptprg 0.000 IGL00847 G1 14 12215265 N1084I A T missense Het probably damaging 0.999 phenotype 12/06/2012
15 13728 APN Rad21l 0.000 IGL00847 G1 2 151660715 A192S C A missense Het probably benign 0.001 phenotype 12/06/2012
16 13931 APN Scn2a 1.000 IGL00847 G1 2 65670734 D80G A G missense Het probably damaging 1.000 phenotype 12/06/2012
17 13979 APN Serpinb3c 0.092 IGL00847 G1 1 107276260 A G critical splice donor site 2 bp Het probably null 12/06/2012
18 14004 APN Sgip1 0.156 IGL00847 G1 4 102928921 A G splice site Het probably benign phenotype 12/06/2012
19 14073 APN Slc25a41 0.074 IGL00847 G1 17 57034957 G T splice site Het probably null phenotype 12/06/2012
20 14174 APN Snx14 1.000 IGL00847 G1 9 88420329 R140S C A missense Het probably damaging 0.999 phenotype 12/06/2012
21 278005 APN Svs6 0.056 IGL00847 G1 2 164317587 K90T A C missense Het possibly damaging 0.847 04/16/2015
22 14465 APN Tlcd1 0.315 IGL00847 G1 11 78180088 Y168N T A missense Het probably damaging 1.000 12/06/2012
23 12635 APN Vps13d 1.000 IGL00847 G1 4 145085408 I3312T A G missense Het probably benign 0.261 phenotype 12/06/2012
24 14941 APN Zfp11 0.241 IGL00847 G1 5 129657914 V161A A G missense Het probably benign 0.165 12/06/2012
[records 1 to 24 of 24]