Incidental Mutations

29 incidental mutations are currently displayed, and affect 29 genes.
3 are Possibly Damaging.
9 are Probably Damaging.
13 are Probably Benign.
4 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 29 of 29] 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 88536 APN Akr1c12 0.085 IGL01479 G1 13 4272935 K225R T C missense Het probably benign 0.010 11/18/2013
2 88543 APN Amn 1.000 IGL01479 G1 12 111271793 A47E C A missense Het probably damaging 0.969 phenotype 11/18/2013
3 88542 APN Arhgef1 0.254 IGL01479 G1 7 24912603 I137T T C missense Het probably benign 0.010 phenotype 11/18/2013
4 88541 APN Cep57l1 0.290 IGL01479 G1 10 41728639 K165E T C missense Het possibly damaging 0.952 11/18/2013
5 88562 APN Chfr 0.248 IGL01479 G1 5 110144993 A G unclassified Het probably benign phenotype 11/18/2013
6 88556 APN Dnah9 0.659 IGL01479 G1 11 65955717 V2923A A G missense Het probably benign 0.140 phenotype 11/18/2013
7 88537 APN Dnaja2 0.508 IGL01479 G1 8 85553951 Y35C T C missense Het probably damaging 1.000 phenotype 11/18/2013
8 88540 APN Dnajc2 0.914 IGL01479 G1 5 21757893 T481A T C missense Het probably damaging 0.996 phenotype 11/18/2013
9 88561 APN Foxred2 0.186 IGL01479 G1 15 77952289 A G splice site 6 bp Het probably null 11/18/2013
10 88550 APN Gin1 0.225 IGL01479 G1 1 97792372 T364I C T missense Het possibly damaging 0.953 11/18/2013
11 88552 APN Glt8d2 0.147 IGL01479 G1 10 82660736 V163I C T missense Het probably damaging 1.000 phenotype 11/18/2013
12 88545 APN Gm10118 0.100 IGL01479 G1 10 63926820 T C intron Het probably benign 11/18/2013
13 88563 APN Hps5 0.227 IGL01479 G1 7 46762942 C T critical splice donor site 1 bp Het probably null phenotype 11/18/2013
14 88548 APN Kdm4c 0.426 IGL01479 G1 4 74343501 K638E A G missense Het probably benign 0.177 phenotype 11/18/2013
15 88551 APN L3mbtl2 0.316 IGL01479 G1 15 81676392 T285A A G missense Het probably benign 0.052 phenotype 11/18/2013
16 88549 APN Mab21l1 0.000 IGL01479 G1 3 55783832 Y280C A G missense Het probably damaging 0.999 phenotype 11/18/2013
17 88559 APN Mcoln2 0.202 IGL01479 G1 3 146175652 T A splice site Het probably benign phenotype 11/18/2013
18 88554 APN Myo9b 0.485 IGL01479 G1 8 71359342 R1926L G T missense Het probably damaging 1.000 phenotype 11/18/2013
19 88544 APN Rrp12 0.884 IGL01479 G1 19 41865202 V1251A A G missense Het probably benign 0.051 11/18/2013
20 88547 APN Rtn4rl1 0.240 IGL01479 G1 11 75265342 D200G A G missense Het probably damaging 1.000 phenotype 11/18/2013
21 88535 APN Sbsn 0.026 IGL01479 G1 7 30752357 A266T G A missense Het possibly damaging 0.904 11/18/2013
22 88555 APN Sgca 0.410 IGL01479 G1 11 94963378 C335* A T nonsense Het probably null phenotype 11/18/2013
23 88560 APN Spag1 0.471 IGL01479 G1 15 36233199 T C splice site Het probably benign phenotype 11/18/2013
24 88546 APN Sult6b1 0.204 IGL01479 G1 17 78905576 V82D A T missense Het probably benign 0.004 11/18/2013
25 88553 APN Tigit 0.051 IGL01479 G1 16 43659522 T137A T C missense Het probably benign 0.001 phenotype 11/18/2013
26 88557 APN Tmem125 0.094 IGL01479 G1 4 118541623 Q204* G A nonsense Het probably null 11/18/2013
27 88539 APN Tmem59l 0.074 IGL01479 G1 8 70486098 R111Q C T missense Het probably benign 0.003 phenotype 11/18/2013
28 88538 APN Vmn2r95 0.311 IGL01479 G1 17 18443862 G448R G A missense Het probably damaging 1.000 11/18/2013
29 88558 APN Zfp64 0.566 IGL01479 G1 2 168951679 H49R T C missense Het probably damaging 0.998 11/18/2013
[records 1 to 29 of 29]