Incidental Mutations

27 incidental mutations are currently displayed, and affect 27 genes.
3 are Possibly Damaging.
8 are Probably Damaging.
11 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 27 of 27] 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 8466 APN 4930503E14Rik 0.058 IGL00778 G1 14 44163934 H152Y G A missense Het probably benign 0.105 12/06/2012
2 8517 APN Abca1 1.000 IGL00778 G1 4 53086132 D457G T C missense Het probably benign 0.000 phenotype 12/06/2012
3 9142 APN Atp8a1 0.000 IGL00778 G1 5 67659903 K913N T G missense Het possibly damaging 0.576 phenotype 12/06/2012
4 9482 APN Cd180 0.000 IGL00778 G1 13 102705409 S321N G A missense Het probably benign 0.000 phenotype 12/06/2012
5 9516 APN Cdc14b 0.350 IGL00778 G1 13 64215656 N264D T C missense Het probably damaging 1.000 phenotype 12/06/2012
6 9606 APN Cenpf 0.572 IGL00778 G1 1 189654912 C1724S A T missense Het probably benign 0.007 phenotype 12/06/2012
7 9686 APN Chil4 0.000 IGL00778 G1 3 106201797 S397P A G missense Het probably benign 0.000 12/06/2012
8 277931 APN Clpb 0.913 IGL00778 G1 7 101778608 R387* C T nonsense Het probably null phenotype 04/16/2015
9 9910 APN Csgalnact2 0.230 IGL00778 G1 6 118126272 M1K A T start codon destroyed Het probably null 0.879 phenotype 12/06/2012
10 10480 APN Enpp3 0.149 IGL00778 G1 10 24798262 C380F C A missense Het probably damaging 1.000 phenotype 12/06/2012
11 11176 APN Gtf3c1 1.000 IGL00778 G1 7 125667374 R967W G A missense Het probably damaging 0.999 phenotype 12/06/2012
12 11314 APN Hnrnpr 0.000 IGL00778 G1 4 136339545 D472E T A missense Het unknown phenotype 12/06/2012
13 11658 APN Klhl28 0.255 IGL00778 G1 12 64950066 D500E A T missense Het probably damaging 1.000 12/06/2012
14 11782 APN Lmo7 0.286 IGL00778 G1 14 101910885 C T splice site Het probably benign phenotype 12/06/2012
15 12066 APN Mphosph8 0.526 IGL00778 G1 14 56674443 I308V A G missense Het probably benign 0.002 12/06/2012
16 12186 APN Myo6 0.000 IGL00778 G1 9 80283586 T A critical splice donor site 2 bp Het probably null phenotype 12/06/2012
17 12790 APN Nsmaf 0.147 IGL00778 G1 4 6435056 C T critical splice donor site 1 bp Het probably null phenotype 12/06/2012
18 12897 APN Padi6 0.000 IGL00778 G1 4 140727623 I668L T A missense Het possibly damaging 0.559 phenotype 12/06/2012
19 13010 APN Pigw 0.165 IGL00778 G1 11 84877324 I393T A G missense Het possibly damaging 0.638 phenotype 12/06/2012
20 10350 APN Prg3 0.000 IGL00778 G1 2 84993732 C212Y G A missense Het probably damaging 1.000 12/06/2012
21 13234 APN Pwp1 1.000 IGL00778 G1 10 85879888 V267A T C missense Het probably benign 0.047 phenotype 12/06/2012
22 13770 APN Raver2 0.097 IGL00778 G1 4 101096271 Q79K C A missense Het probably benign 0.001 12/06/2012
23 13943 APN Sdr9c7 0.070 IGL00778 G1 10 127909828 S270P T C missense Het probably damaging 0.998 phenotype 12/06/2012
24 13999 APN Sfmbt2 1.000 IGL00778 G1 2 10402007 E39G A G missense Het probably damaging 0.999 12/06/2012
25 14281 APN Strada 0.541 IGL00778 G1 11 106171150 A G splice site Het probably benign phenotype 12/06/2012
26 14891 APN Xrn1 0.900 IGL00778 G1 9 95973447 T C splice site Het probably benign phenotype 12/06/2012
27 15033 APN Zic3 IGL00778 G1 X 58034419 Y424C A G missense Het probably damaging 1.000 phenotype 12/06/2012
[records 1 to 27 of 27]