Incidental Mutations

31 incidental mutations are currently displayed, and affect 30 genes.
1 are Possibly Damaging.
15 are Probably Damaging.
9 are Probably Benign.
4 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 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 50805 APN 4632415L05Rik 0.442 IGL01149 G1 3 19895112 A G exon Het noncoding transcript 06/21/2013
2 52395 APN Adcy1 0.000 IGL01149 G1 11 7137385 N420H A C missense Het probably damaging 0.994 phenotype 06/21/2013
3 278216 APN Avp 1.000 IGL01149 G1 2 130580673 T C utr 3 prime Het probably benign phenotype 04/16/2015
4 52620 APN B3galnt2 0.690 IGL01149 G1 13 13980685 I216F A T missense Het probably benign 0.070 phenotype 06/21/2013
5 50354 APN Cdc42bpa 0.403 IGL01149 G1 1 180074572 S465P T C missense Het probably damaging 0.985 phenotype 06/21/2013
6 53305 APN Cdc42bpg 0.806 IGL01149 G1 19 6312205 T A splice site Het probably benign 06/21/2013
7 50989 APN Cdcp2 0.115 IGL01149 G1 4 107107111 F386S T C missense Het probably benign 0.000 06/21/2013
8 50641 APN Cdh4 0.000 IGL01149 G1 2 179874144 T372A A G missense Het probably damaging 0.995 phenotype 06/21/2013
9 50991 APN Clspn 0.976 IGL01149 G1 4 126573178 M612R T G missense Het probably damaging 0.998 phenotype 06/21/2013
10 50639 APN Dll4 1.000 IGL01149 G1 2 119331109 C391R T C missense Het probably damaging 1.000 phenotype 06/21/2013
11 50640 APN Dll4 1.000 IGL01149 G1 2 119332745 Y616H T C missense Het probably damaging 1.000 phenotype 06/21/2013
12 51200 APN Exoc1 0.944 IGL01149 G1 5 76542244 A G splice site Het probably benign phenotype 06/21/2013
13 50646 APN F830045P16Rik 0.124 IGL01149 G1 2 129460312 A G critical splice donor site 2 bp Het probably null 06/21/2013
14 51839 APN Fhod1 0.343 IGL01149 G1 8 105347807 A G unclassified Het probably benign 06/21/2013
15 50645 APN Fign 1.000 IGL01149 G1 2 63979760 R389G T C missense Het possibly damaging 0.919 phenotype 06/21/2013
16 50642 APN Gm13941 0.215 IGL01149 G1 2 111101137 E50V T A missense Het unknown 06/21/2013
17 50990 APN Gm436 0.072 IGL01149 G1 4 144673779 D143G T C missense Het probably benign 0.122 06/21/2013
18 51199 APN Kit 0.852 IGL01149 G1 5 75610876 T231M C T missense Het probably damaging 0.972 phenotype 06/21/2013
19 51671 APN Neu3 0.102 IGL01149 G1 7 99813880 H212R T C missense Het probably benign 0.004 phenotype 06/21/2013
20 50638 APN Nup214 1.000 IGL01149 G1 2 32034700 S1747I G T missense Het probably damaging 0.995 phenotype 06/21/2013
21 50643 APN Olfr1289 0.109 IGL01149 G1 2 111484101 S224P T C missense Het probably damaging 0.999 phenotype 06/21/2013
22 52735 APN Olfr735 0.114 IGL01149 G1 14 50345614 A276E G T missense Het probably damaging 0.988 phenotype 06/21/2013
23 52015 APN Olfr870 0.050 IGL01149 G1 9 20171530 L14I G T missense Het probably damaging 0.998 phenotype 06/21/2013
24 52623 APN Secisbp2 0.142 IGL01149 G1 13 51676455 T C critical splice donor site 2 bp Het probably null phenotype 06/21/2013
25 52169 APN Slc26a10 0.610 IGL01149 G1 10 127174177 G A splice site Het probably benign 06/21/2013
26 51838 APN Slc7a6 0.134 IGL01149 G1 8 106179600 S155P T C missense Het probably damaging 0.963 06/21/2013
27 52621 APN Slf1 0.000 IGL01149 G1 13 77112648 I173N A T missense Het probably damaging 0.994 phenotype 06/21/2013
28 278217 APN Tedc1 0.554 IGL01149 G1 12 113163188 R357* C T nonsense Het probably null 04/16/2015
29 53306 APN Tkfc 0.085 IGL01149 G1 19 10600651 L38P A G missense Het probably damaging 0.999 phenotype 06/21/2013
30 50644 APN Tubgcp4 0.962 IGL01149 G1 2 121184783 D324G A G missense Het probably null 0.002 phenotype 06/21/2013
31 52622 APN Zfyve16 0.323 IGL01149 G1 13 92508283 H1137R T C missense Het probably damaging 1.000 phenotype 06/21/2013
[records 1 to 31 of 31]