Incidental Mutations

30 incidental mutations are currently displayed, and affect 30 genes.
5 are Possibly Damaging.
9 are Probably Damaging.
9 are Probably Benign.
5 are Probably Null.
2 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 30 of 30] 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 3425 APN Alk 0.176 IGL00401 G1 17 71895748 D1164V T A missense Het probably damaging 0.997 phenotype 04/20/2012
2 3897 APN Baiap3 0.000 IGL00401 G1 17 25244328 L964F T G missense Het probably damaging 0.999 phenotype 04/20/2012
3 4819 APN Cacna2d2 0.915 IGL00401 G1 9 107514873 V471E T A missense Het probably damaging 1.000 phenotype 04/20/2012
4 5875 APN Carmil3 0.663 IGL00401 G1 14 55498298 T569M C T missense Het probably damaging 0.989 04/20/2012
5 6162 APN Dapk2 0.000 IGL00401 G1 9 66268778 G T splice site Het probably benign phenotype 04/20/2012
6 5021 APN Eps15l1 0.265 IGL00401 G1 8 72384838 Y291* A T nonsense Het probably null 04/20/2012
7 6340 APN Fancd2 1.000 IGL00401 G1 6 113564396 T C critical splice donor site 2 bp Het probably null phenotype 04/20/2012
8 7208 APN Fmnl2 0.000 IGL00401 G1 2 53114917 D674E T G missense Het probably damaging 0.996 phenotype 04/20/2012
9 4325 APN Foxq1 0.389 IGL00401 G1 13 31559277 I121F A T missense Het probably damaging 1.000 phenotype 04/20/2012
10 26797 APN Galnt13 0.089 IGL00401 G1 2 54516535 C T utr 5 prime Het probably benign phenotype 04/17/2013
11 4538 APN Git1 1.000 IGL00401 G1 11 77498956 T C splice site Het probably benign phenotype 04/20/2012
12 6468 APN Gm10220 0.437 IGL00401 G1 5 26118611 F146Y A T missense Het possibly damaging 0.942 04/20/2012
13 306588 APN Gm7353 0.877 IGL00401 G1 7 3110630 A G exon Het noncoding transcript 04/16/2015
14 3364 APN Hspa9 0.966 IGL00401 G1 18 34938580 G A splice site Het probably benign phenotype 04/20/2012
15 5327 APN Kptn 0.000 IGL00401 G1 7 16120125 D56G A G missense Het possibly damaging 0.928 phenotype 04/20/2012
16 6026 APN Krtap4-13 0.195 IGL00401 G1 11 99809717 C39S A T missense Het unknown 04/20/2012
17 7517 APN Lgsn 0.192 IGL00401 G1 1 31203566 K243R A G missense Het possibly damaging 0.754 phenotype 04/20/2012
18 4659 APN Lyz2 0.100 IGL00401 G1 10 117282185 V20I C T missense Het probably benign 0.000 phenotype 04/20/2012
19 4193 APN Mettl3 1.000 IGL00401 G1 14 52296967 T A unclassified Het probably benign phenotype 04/20/2012
20 4189 APN Myh6 1.000 IGL00401 G1 14 54953417 M934L T A missense Het probably benign 0.001 phenotype 04/20/2012
21 7347 APN Nmnat2 1.000 IGL00401 G1 1 153094117 A G splice site 4 bp Het probably null phenotype 04/20/2012
22 3289 APN Pias2 0.000 IGL00401 G1 18 77133211 C381S T A missense Het probably damaging 1.000 phenotype 04/20/2012
23 4622 APN Psme4 0.000 IGL00401 G1 11 30821079 T C splice site Het probably benign phenotype 04/20/2012
24 6879 APN Smc4 0.969 IGL00401 G1 3 69030379 D887E T A missense Het probably damaging 0.979 phenotype 04/20/2012
25 6443 APN Sorcs2 0.000 IGL00401 G1 5 36037401 C A splice site 5 bp Het probably null phenotype 04/20/2012
26 6751 APN Tet2 1.000 IGL00401 G1 3 133466882 E1873G T C missense Het possibly damaging 0.719 phenotype 04/20/2012
27 306589 APN Txlng IGL00401 G1 X 162782309 K341* T A nonsense Het probably null phenotype 04/16/2015
28 6412 APN Ugt2b37 0.068 IGL00401 G1 5 87242481 T369S T A missense Het possibly damaging 0.905 04/20/2012
29 5615 APN Usp46 0.203 IGL00401 G1 5 74003171 V302F C A missense Het probably damaging 1.000 phenotype 04/20/2012
30 6693 APN Zfp292 0.829 IGL00401 G1 4 34808683 C1454R A G missense Het probably benign 0.153 04/20/2012
[records 1 to 30 of 30]