Incidental Mutations

32 incidental mutations are currently displayed, and affect 32 genes.
7 are Possibly Damaging.
10 are Probably Damaging.
11 are Probably Benign.
3 are Probably Null.
0 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 32 of 32] 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 104568 APN Adamts19 0.000 IGL01705 G1 18 59032966 T1077A A G missense Het possibly damaging 0.911 phenotype 01/21/2014
2 104552 APN Akap13 1.000 IGL01705 G1 7 75746767 V2504A T C missense Het possibly damaging 0.860 phenotype 01/21/2014
3 104560 APN Anks3 1.000 IGL01705 G1 16 4947723 W172R A T missense Het probably benign 0.001 01/21/2014
4 104567 APN Asap2 0.117 IGL01705 G1 12 21249368 N633K T A missense Het possibly damaging 0.853 phenotype 01/21/2014
5 104564 APN Astn1 0.089 IGL01705 G1 1 158504313 S326C A T missense Het probably damaging 0.995 phenotype 01/21/2014
6 104569 APN Cachd1 0.298 IGL01705 G1 4 100983539 K900E A G missense Het possibly damaging 0.459 01/21/2014
7 104580 APN Cd5 0.000 IGL01705 G1 19 10726295 A T critical splice donor site 2 bp Het probably null phenotype 01/21/2014
8 104553 APN D130043K22Rik 0.000 IGL01705 G1 13 24857941 N284K T A missense Het probably benign 0.005 phenotype 01/21/2014
9 104557 APN Dtna 0.359 IGL01705 G1 18 23545731 A38V C T missense Het probably damaging 0.997 phenotype 01/21/2014
10 104577 APN Eny2 0.907 IGL01705 G1 15 44432435 C A splice site Het probably null 01/21/2014
11 104572 APN Grm5 0.192 IGL01705 G1 7 88130046 Q930R A G missense Het possibly damaging 0.587 phenotype 01/21/2014
12 104550 APN Igkv4-73 0.239 IGL01705 G1 6 69197725 A T exon Het noncoding transcript 01/21/2014
13 104578 APN Lama2 0.294 IGL01705 G1 10 27189274 A T splice site Het probably benign phenotype 01/21/2014
14 104579 APN Lipg 0.097 IGL01705 G1 18 74947971 A G critical splice donor site 2 bp Het probably null phenotype 01/21/2014
15 104570 APN Mettl7b 0.053 IGL01705 G1 10 128958862 I198F T A missense Het probably benign 0.001 01/21/2014
16 104571 APN Neto2 0.192 IGL01705 G1 8 85641003 K371E T C missense Het probably damaging 1.000 phenotype 01/21/2014
17 104551 APN Olfr965 0.105 IGL01705 G1 9 39719581 M118T T C missense Het possibly damaging 0.946 phenotype 01/21/2014
18 104573 APN Paxbp1 0.956 IGL01705 G1 16 91016988 F834L A G missense Het probably benign 0.008 phenotype 01/21/2014
19 104574 APN Paxip1 1.000 IGL01705 G1 5 27748859 S946R A T missense Het probably damaging 1.000 phenotype 01/21/2014
20 104562 APN Pclo 0.000 IGL01705 G1 5 14677865 A G unclassified Het probably benign phenotype 01/21/2014
21 104555 APN Plcg2 0.000 IGL01705 G1 8 117581662 L331P T C missense Het probably damaging 1.000 phenotype 01/21/2014
22 104566 APN Reep1 0.000 IGL01705 G1 6 71773288 T95A A G missense Het probably damaging 0.999 phenotype 01/21/2014
23 104575 APN Rfx2 0.706 IGL01705 G1 17 56785303 Y332H A G missense Het possibly damaging 0.879 phenotype 01/21/2014
24 104576 APN Smchd1 0.754 IGL01705 G1 17 71381398 D1288E A T missense Het probably damaging 1.000 phenotype 01/21/2014
25 104556 APN Spag17 0.000 IGL01705 G1 3 100022730 M582V A G missense Het probably benign 0.008 phenotype 01/21/2014
26 104581 APN Susd1 0.074 IGL01705 G1 4 59332931 A G splice site Het probably benign 01/21/2014
27 104559 APN Syt9 0.000 IGL01705 G1 7 107436352 L192R T G missense Het probably damaging 0.959 phenotype 01/21/2014
28 104558 APN Tlr6 0.111 IGL01705 G1 5 64954130 K478R T C missense Het probably benign 0.027 phenotype 01/21/2014
29 104565 APN Tmem115 0.207 IGL01705 G1 9 107535204 L242F G T missense Het probably benign 0.442 01/21/2014
30 104563 APN Tnfaip1 0.543 IGL01705 G1 11 78525468 D263G T C missense Het probably benign 0.161 phenotype 01/21/2014
31 104561 APN Ubqln3 0.142 IGL01705 G1 7 104142677 I69F T A missense Het probably damaging 1.000 phenotype 01/21/2014
32 104554 APN Vps52 1.000 IGL01705 G1 17 33966068 L712P T C missense Het probably damaging 0.996 phenotype 01/21/2014
[records 1 to 32 of 32]