Incidental Mutations

26 incidental mutations are currently displayed, and affect 26 genes.
2 are Possibly Damaging.
9 are Probably Damaging.
13 are Probably Benign.
1 are Probably Null.
0 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 26 of 26] 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 5042 APN Adam26a 0.000 IGL00519 G1 8 43569525 N309K A T missense Het probably damaging 0.997 phenotype 04/20/2012
2 362022 APN Asap1 0.167 IGL00519 G1 15 64110942 P846S G A missense Het probably damaging 1.000 phenotype 12/18/2015
3 9106 APN Atg10 0.076 IGL00519 G1 13 91154211 A G splice site Het probably benign phenotype 12/06/2012
4 9570 APN Cdk18 0.368 IGL00519 G1 1 132115488 R433L C A missense Het probably benign 0.363 12/06/2012
5 4058 APN Celsr1 0.844 IGL00519 G1 15 86030836 Y979H A G missense Het probably damaging 1.000 phenotype 04/20/2012
6 5092 APN Cracr2b 0.075 IGL00519 G1 7 141465757 T C unclassified Het probably benign 04/20/2012
7 362024 APN Csmd2 0.124 IGL00519 G1 4 128483473 F2049L T C missense Het probably benign 0.027 12/18/2015
8 7280 APN Cubn 1.000 IGL00519 G1 2 13282919 N3450D T C missense Het probably benign 0.003 phenotype 04/20/2012
9 5677 APN Dmrt1 0.735 IGL00519 G1 19 25603274 L350P T C missense Het probably damaging 0.981 phenotype 04/20/2012
10 362023 APN Dnah5 0.868 IGL00519 G1 15 28444218 D4054V A T missense Het probably benign 0.105 phenotype 12/18/2015
11 6165 APN Dpp8 0.221 IGL00519 G1 9 65078008 T783S A T missense Het probably damaging 0.996 phenotype 04/20/2012
12 4751 APN Enpp3 0.149 IGL00519 G1 10 24787772 T564A T C missense Het probably benign 0.001 phenotype 04/20/2012
13 5416 APN Exoc6b 0.663 IGL00519 G1 6 84989453 K180E T C missense Het probably benign 0.081 phenotype 04/20/2012
14 6609 APN Faf1 1.000 IGL00519 G1 4 109840381 F301L T A missense Het probably benign 0.096 phenotype 04/20/2012
15 6096 APN Fbxo7 0.000 IGL00519 G1 10 86029064 E77V A T missense Het probably damaging 0.975 phenotype 04/20/2012
16 3952 APN Gabpa 1.000 IGL00519 G1 16 84860601 *455G T G makesense Het probably null phenotype 04/20/2012
17 6015 APN Hexim2 0.259 IGL00519 G1 11 103134079 M1L A T start codon destroyed Het probably benign 0.135 phenotype 04/20/2012
18 5826 APN Lrrc24 0.092 IGL00519 G1 15 76718063 N164I T A missense Het probably damaging 1.000 04/20/2012
19 5568 APN Lrrc8b 0.146 IGL00519 G1 5 105481725 A646T G A missense Het possibly damaging 0.825 04/20/2012
20 6330 APN Mansc1 0.069 IGL00519 G1 6 134610806 Q136L T A missense Het possibly damaging 0.877 04/20/2012
21 5541 APN Mlxip 0.337 IGL00519 G1 5 123447205 V592E T A missense Het probably benign 0.348 phenotype 04/20/2012
22 5535 APN Ncor2 1.000 IGL00519 G1 5 125084924 T429A T C missense Het unknown phenotype 04/20/2012
23 5997 APN Tbcd 0.959 IGL00519 G1 11 121575321 N591S A G missense Het probably damaging 0.957 phenotype 04/20/2012
24 5207 APN Tenm4 1.000 IGL00519 G1 7 96805138 T C splice site Het probably benign phenotype 04/20/2012
25 5272 APN Uri1 0.000 IGL00519 G1 7 37961553 S522P A G missense Het probably damaging 1.000 phenotype 04/20/2012
26 7300 APN Ush2a 0.615 IGL00519 G1 1 188444668 S1343L C T missense Het probably benign 0.027 phenotype 04/20/2012
[records 1 to 26 of 26]