Incidental Mutations

28 incidental mutations are currently displayed, and affect 28 genes.
2 are Possibly Damaging.
15 are Probably Damaging.
8 are Probably Benign.
3 are Probably Null.
1 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 28 of 28] 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 8419 APN 1700011I03Rik 0.060 IGL00863 G1 18 57594086 E136V A T missense Het probably damaging 0.976 12/06/2012
2 9310 APN Bsn 0.344 IGL00863 G1 9 108115322 I1077T A G missense Het probably damaging 0.999 phenotype 12/06/2012
3 9380 APN Car8 0.078 IGL00863 G1 4 8183251 A G critical splice donor site 2 bp Het probably null phenotype 12/06/2012
4 9472 APN Ccny 0.149 IGL00863 G1 18 9345444 D143E A T missense Het probably benign 0.183 phenotype 12/06/2012
5 9544 APN Cdh19 0.000 IGL00863 G1 1 110949144 V155A A G missense Het probably damaging 0.997 phenotype 12/06/2012
6 9892 APN Cript IGL00863 G1 17 87027723 I14N T A missense Het probably damaging 0.990 phenotype 12/06/2012
7 278038 APN Crygd 0.269 IGL00863 G1 1 65062091 R115Q C T missense Het probably benign 0.321 phenotype 04/16/2015
8 278039 APN Eef1b2 0.000 IGL00863 G1 1 63178506 G91R G A missense Het probably damaging 1.000 phenotype 04/16/2015
9 10660 APN Fam49a 0.432 IGL00863 G1 12 12359234 I72F A T missense Het probably benign 0.000 12/06/2012
10 10704 APN Fbln5 0.144 IGL00863 G1 12 101809916 V60A A G missense Het probably damaging 0.983 phenotype 12/06/2012
11 10708 APN Fbn1 0.879 IGL00863 G1 2 125403219 E249D T A missense Het possibly damaging 0.837 phenotype 12/06/2012
12 10864 APN G6pc 1.000 IGL00863 G1 11 101370723 R83L G T missense Het probably damaging 1.000 phenotype 12/06/2012
13 11148 APN Grik2 0.000 IGL00863 G1 10 49355928 V502A A G missense Het possibly damaging 0.947 phenotype 12/06/2012
14 11226 APN Heatr1 0.968 IGL00863 G1 13 12435128 V2001A T C missense Het probably benign 0.022 12/06/2012
15 11450 APN Il4i1 0.000 IGL00863 G1 7 44838046 Y148* T A nonsense Het probably null phenotype 12/06/2012
16 11528 APN Jmjd4 0.118 IGL00863 G1 11 59450743 S113P T C missense Het probably benign 0.000 phenotype 12/06/2012
17 12068 APN Mpp5 0.618 IGL00863 G1 12 78809821 D146G A G missense Het probably damaging 0.998 phenotype 12/06/2012
18 12292 APN Nceh1 0.117 IGL00863 G1 3 27241313 P241L C T missense Het probably damaging 1.000 phenotype 12/06/2012
19 12924 APN Pcdh10 0.292 IGL00863 G1 3 45380302 D350E T A missense Het probably damaging 0.997 phenotype 12/06/2012
20 12965 APN Pdgfrl 0.137 IGL00863 G1 8 40985534 E169G A G missense Het probably damaging 0.999 phenotype 12/06/2012
21 13120 APN Ppm1l 0.174 IGL00863 G1 3 69317950 D128E T A missense Het probably damaging 1.000 phenotype 12/06/2012
22 13756 APN Rasa1 1.000 IGL00863 G1 13 85288429 V160A A G missense Het probably benign 0.022 phenotype 12/06/2012
23 11384 APN Serf2 1.000 IGL00863 G1 2 121457703 T C critical splice donor site 2 bp Het probably null 12/06/2012
24 14141 APN Slitrk1 0.000 IGL00863 G1 14 108911837 N481Y T A missense Het probably damaging 1.000 phenotype 12/06/2012
25 14376 APN Tas2r139 0.000 IGL00863 G1 6 42141121 S62R T G missense Het probably damaging 1.000 phenotype 12/06/2012
26 14417 APN Tdpoz4 0.744 IGL00863 G1 3 93797073 T226S A T missense Het probably benign 0.221 12/06/2012
27 10650 APN Tvp23b 0.000 IGL00863 G1 11 62883638 A36E C A missense Het probably damaging 0.974 12/06/2012
28 14724 APN Upp2 0.098 IGL00863 G1 2 58790064 E301K G A missense Het probably benign 0.432 0.090 12/06/2012
[records 1 to 28 of 28]