Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
2 are Possibly Damaging.
12 are Probably Damaging.
15 are Probably Benign.
4 are Probably Null.
2 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 33 of 33] 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 183516 APN Acadl 0.678 IGL01983 G1 1 66841624 Q328* G A nonsense Het probably null phenotype 05/07/2014
2 183535 APN Alpk2 0.000 IGL01983 G1 18 65350682 Y85C T C missense Het probably damaging 1.000 05/07/2014
3 183529 APN Arhgap31 0.306 IGL01983 G1 16 38601765 R1313Q C T missense Het probably damaging 1.000 phenotype 05/07/2014
4 183522 APN Chrnb1 0.527 IGL01983 G1 11 69795729 R22S G T missense Het probably benign 0.272 phenotype 05/07/2014
5 183546 APN Clec7a 0.079 IGL01983 G1 6 129465576 G A splice site Het probably benign 05/07/2014
6 183544 APN Epb41l5 1.000 IGL01983 G1 1 119579084 A G splice site Het probably benign phenotype 05/07/2014
7 183534 APN Fam49b 0.000 IGL01983 G1 15 63937387 S251P A G missense Het probably benign 0.004 05/07/2014
8 183532 APN Gm10093 0.783 IGL01983 G1 17 78492853 D424E T A missense Het probably benign 0.000 05/07/2014
9 183519 APN Hydin 0.701 IGL01983 G1 8 110514895 I2106L A C missense Het probably benign 0.024 phenotype 05/07/2014
10 183515 APN Igkv3-5 0.252 IGL01983 G1 6 70663686 D50E T A missense Het probably benign 0.002 05/07/2014
11 183525 APN Irf2bp1 0.583 IGL01983 G1 7 19005295 A287S G T missense Het possibly damaging 0.705 05/07/2014
12 183539 APN Ldb3 1.000 IGL01983 G1 14 34577199 S156L G A missense Het probably benign 0.004 phenotype 05/07/2014
13 183518 APN Lnpep 0.000 IGL01983 G1 17 17531178 W942R A T missense Het probably damaging 1.000 phenotype 05/07/2014
14 183528 APN Mst1r 0.337 IGL01983 G1 9 107917276 V1218D T A missense Het probably damaging 0.993 phenotype 05/07/2014
15 183545 APN Naxd 0.330 IGL01983 G1 8 11510218 G T unclassified Het probably benign 05/07/2014
16 183543 APN Nol9 0.959 IGL01983 G1 4 152046037 T C critical splice donor site 2 bp Het probably null 05/07/2014
17 183517 APN Nus1 1.000 IGL01983 G1 10 52436657 L295Q T A missense Het probably damaging 0.979 phenotype 05/07/2014
18 183524 APN Nxph2 0.071 IGL01983 G1 2 23399934 I99M A G missense Het probably benign 0.319 05/07/2014
19 183523 APN Plekhg1 0.215 IGL01983 G1 10 3945904 I432N T A missense Het probably damaging 0.999 05/07/2014
20 183527 APN Pon3 1.000 IGL01983 G1 6 5240974 L69S A G missense Het probably damaging 1.000 phenotype 05/07/2014
21 183536 APN Pram1 0.000 IGL01983 G1 17 33640861 A134D C A missense Het probably damaging 0.976 phenotype 05/07/2014
22 183541 APN Serpinb6c 0.143 IGL01983 G1 13 33897334 T A splice site Het probably benign 05/07/2014
23 183526 APN Stk10 0.109 IGL01983 G1 11 32589460 E280V A T missense Het probably benign 0.055 0.594 phenotype 05/07/2014
24 183520 APN Tbc1d10c 0.119 IGL01983 G1 19 4190709 Q34L T A missense Het possibly damaging 0.873 phenotype 05/07/2014
25 183537 APN Tnr 0.000 IGL01983 G1 1 159863779 V500I G A missense Het probably benign 0.002 phenotype 05/07/2014
26 183533 APN Trim66 0.145 IGL01983 G1 7 109458251 R992* G A nonsense Het probably null 05/07/2014
27 183538 APN Unc45b 1.000 IGL01983 G1 11 82936861 D728G A G missense Het probably benign 0.000 phenotype 05/07/2014
28 183530 APN Usp13 0.000 IGL01983 G1 3 32917459 D696G A G missense Het probably damaging 1.000 05/07/2014
29 183531 APN Utrn 0.000 IGL01983 G1 10 12669781 V1707I C T missense Het probably benign 0.180 phenotype 05/07/2014
30 183514 APN Vmn2r96 0.162 IGL01983 G1 17 18597265 H368L A T missense Het probably damaging 0.988 05/07/2014
31 183542 APN Xrn1 0.849 IGL01983 G1 9 95973368 T C critical splice donor site 2 bp Het probably null phenotype 05/07/2014
32 183540 APN Zfhx3 0.939 IGL01983 G1 8 108947234 L1639M C A missense Het probably damaging 0.999 phenotype 05/07/2014
33 183521 APN Znfx1 0.000 IGL01983 G1 2 167056350 V218E A T missense Het probably damaging 0.999 05/07/2014
[records 1 to 33 of 33]