Incidental Mutations

22 incidental mutations are currently displayed, and affect 22 genes.
3 are Possibly Damaging.
7 are Probably Damaging.
9 are Probably Benign.
3 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 22 of 22] 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 27443 APN Cc2d2a 0.881 IGL00937 G1 5 43688122 A T critical splice acceptor site Het probably null phenotype 04/17/2013
2 26661 APN Cd34 0.068 IGL00937 G1 1 194960114 E381G A G missense Het probably damaging 1.000 phenotype 04/17/2013
3 29516 APN Chka 1.000 IGL00937 G1 19 3892189 E381G A G missense Het probably benign 0.159 phenotype 04/17/2013
4 26660 APN Dennd1b 0.000 IGL00937 G1 1 139170239 C673S T A missense Het probably benign 0.012 phenotype 04/17/2013
5 27262 APN E130308A19Rik 0.145 IGL00937 G1 4 59690846 A227T G A missense Het probably benign 0.009 04/17/2013
6 26663 APN F13b 0.000 IGL00937 G1 1 139517360 T A splice site Het probably benign phenotype 04/17/2013
7 26920 APN Hipk3 0.000 IGL00937 G1 2 104433172 N933D T C missense Het possibly damaging 0.820 phenotype 04/17/2013
8 28186 APN Mmp27 0.063 IGL00937 G1 9 7578899 T C critical splice acceptor site Het probably benign phenotype 04/17/2013
9 27640 APN Nod1 0.000 IGL00937 G1 6 54937364 V815I C T missense Het probably benign 0.079 phenotype 04/17/2013
10 28544 APN Olfr411 0.059 IGL00937 G1 11 74347429 V52I C T missense Het probably benign 0.001 phenotype 04/17/2013
11 27638 APN Olfr448 0.112 IGL00937 G1 6 42896634 F61Y T A missense Het probably damaging 0.999 phenotype 04/17/2013
12 27834 APN Olfr552 0.112 IGL00937 G1 7 102604357 M1K T A start codon destroyed Het probably null 0.987 phenotype 04/17/2013
13 27835 APN Olfr555 0.144 IGL00937 G1 7 102659348 S176T T A missense Het probably damaging 0.982 phenotype 04/17/2013
14 27833 APN Olfr613 0.051 IGL00937 G1 7 103551857 A24E C A missense Het probably damaging 0.988 phenotype 04/17/2013
15 27836 APN Olfr697 0.085 IGL00937 G1 7 106741157 Y259F T A missense Het probably damaging 1.000 phenotype 04/17/2013
16 26662 APN Pms1 0.000 IGL00937 G1 1 53275251 E45V T A missense Het possibly damaging 0.742 phenotype 04/17/2013
17 28185 APN Prkcsh 1.000 IGL00937 G1 9 22006565 S126P T C missense Het possibly damaging 0.946 phenotype 04/17/2013
18 29154 APN Pros1 1.000 IGL00937 G1 16 62910045 L299F A T missense Het probably damaging 0.988 phenotype 04/17/2013
19 27639 APN Scrn1 0.145 IGL00937 G1 6 54520733 I291T A G missense Het probably benign 0.020 phenotype 04/17/2013
20 29155 APN Slc15a2 0.102 IGL00937 G1 16 36751880 Y676* A T nonsense Het probably null phenotype 04/17/2013
21 28545 APN Tenm2 0.471 IGL00937 G1 11 36024623 V2028G A C missense Het probably damaging 0.999 phenotype 04/17/2013
22 26664 APN Trpa1 0.110 IGL00937 G1 1 14880277 T C splice site Het probably benign phenotype 04/17/2013
[records 1 to 22 of 22]