Incidental Mutations

35 incidental mutations are currently displayed, and affect 35 genes.
7 are Possibly Damaging.
7 are Probably Damaging.
14 are Probably Benign.
7 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 35 of 35] 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 360659 APN Adcy1 0.000 IGL02813 11 7146591 Q660K C A missense Het possibly damaging 0.830 phenotype 12/18/2015
2 360675 APN Arhgap5 1.000 IGL02813 12 52516965 T240P A C missense Het probably benign 0.202 phenotype 12/18/2015
3 360682 APN Arhgef7 1.000 IGL02813 8 11800767 C T unclassified Het probably benign phenotype 12/18/2015
4 360667 APN Cttnbp2 0.000 IGL02813 6 18367538 V1594F C A missense Het possibly damaging 0.945 phenotype 12/18/2015
5 360655 APN Cyp2a22 0.087 IGL02813 7 26936434 Q235K G T missense Het probably benign 0.186 12/18/2015
6 360678 APN E330009J07Rik 0.122 IGL02813 6 40418539 V212I C T missense Het probably benign 0.002 12/18/2015
7 360664 APN Ecm1 0.245 IGL02813 3 95736786 P169S G A missense Het probably damaging 0.993 phenotype 12/18/2015
8 360680 APN Emilin3 0.000 IGL02813 2 160908729 Q320* G A nonsense Het probably null 0.976 12/18/2015
9 360662 APN Ern1 1.000 IGL02813 11 106423425 D183G T C missense Het probably damaging 1.000 phenotype 12/18/2015
10 360658 APN Gpat2 0.000 IGL02813 2 127434455 V635A T C missense Het possibly damaging 0.902 12/18/2015
11 360670 APN Gria1 0.000 IGL02813 11 57283584 N564S A G missense Het probably damaging 0.999 phenotype 12/18/2015
12 360671 APN Grtp1 0.000 IGL02813 8 13186945 I173S A C missense Het possibly damaging 0.932 12/18/2015
13 360683 APN Hsd17b4 0.689 IGL02813 18 50128348 A G utr 5 prime Het probably benign phenotype 12/18/2015
14 360686 APN Lrp1b 0.000 IGL02813 2 40679217 T C critical splice acceptor site Het probably null phenotype 12/18/2015
15 360681 APN Mark4 0.000 IGL02813 7 19447256 A T splice site Het probably null phenotype 12/18/2015
16 360673 APN Mphosph9 0.000 IGL02813 5 124315628 D207G T C missense Het probably benign 0.368 12/18/2015
17 360663 APN Mrgprd 0.000 IGL02813 7 145321514 M41V A G missense Het probably benign 0.001 phenotype 12/18/2015
18 360661 APN Myo1g 0.000 IGL02813 11 6518743 *66W T C makesense Het probably null phenotype 12/18/2015
19 360660 APN Neto2 0.182 IGL02813 8 85690886 D30Y C A missense Het probably benign 0.000 phenotype 12/18/2015
20 360679 APN Nlrp6 0.077 IGL02813 7 140923420 I450F A T missense Het possibly damaging 0.861 phenotype 12/18/2015
21 360688 APN Nup155 1.000 IGL02813 15 8130121 T A splice site Het probably benign phenotype 12/18/2015
22 360657 APN Olfr1205 0.055 IGL02813 2 88831151 I11M A G missense Het probably benign 0.345 phenotype 12/18/2015
23 360654 APN Pcdhb10 0.082 IGL02813 18 37413762 S630R T G missense Het possibly damaging 0.942 phenotype 12/18/2015
24 360687 APN Rwdd4a 0.125 IGL02813 8 47537361 T C critical splice donor site 2 bp Het probably null 12/18/2015
25 360684 APN Slc12a7 0.000 IGL02813 13 73813676 T A unclassified Het probably benign phenotype 12/18/2015
26 360677 APN Slc22a20 0.341 IGL02813 19 5984858 V192I C T missense Het probably benign 0.003 12/18/2015
27 360668 APN Slc9a2 0.070 IGL02813 1 40742669 S353T T A missense Het probably damaging 0.998 phenotype 12/18/2015
28 360676 APN Srgap3 0.262 IGL02813 6 112731480 F753L A G missense Het probably damaging 0.995 phenotype 12/18/2015
29 360669 APN Tcea1 1.000 IGL02813 1 4886756 T93I C T missense Het probably benign 0.058 phenotype 12/18/2015
30 360665 APN Tctex1d1 0.104 IGL02813 4 102992572 N64S A G missense Het probably damaging 1.000 12/18/2015
31 360672 APN Tecpr2 0.000 IGL02813 12 110933192 S665C A T missense Het probably damaging 0.996 phenotype 12/18/2015
32 360666 APN Tor4a 0.220 IGL02813 2 25194749 E381* C A nonsense Het probably null 12/18/2015
33 360674 APN Vdr 0.000 IGL02813 15 97869681 Y143H A G missense Het probably benign 0.450 phenotype 12/18/2015
34 360656 APN Vmn2r91 0.072 IGL02813 17 18136086 T672P A C missense Het possibly damaging 0.907 12/18/2015
35 360685 APN Wdr41 0.000 IGL02813 13 94995245 A G splice site Het probably null phenotype 12/18/2015
[records 1 to 35 of 35]