Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
3 are Possibly Damaging.
11 are Probably Damaging.
15 are Probably Benign.
3 are Probably Null.
1 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 33 of 33] 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 278207 APN 1110038F14Rik IGL01135 G1 15 76950275 V124I G A missense Het probably damaging 0.999 04/16/2015
2 52491 APN 5730507C01Rik 0.243 IGL01135 G1 12 18533374 R145H G A missense Het possibly damaging 0.906 06/21/2013
3 51173 APN Acox3 0.000 IGL01135 G1 5 35588752 V93E T A missense Het probably benign 0.019 phenotype 06/21/2013
4 50332 APN Ankar 0.057 IGL01135 G1 1 72665219 N848S T C missense Het probably benign 0.277 06/21/2013
5 50330 APN Blzf1 0.209 IGL01135 G1 1 164303930 A G unclassified Het probably benign 0.072 06/21/2013
6 278206 APN Cc2d1a 0.821 IGL01135 G1 8 84143404 H161N G T missense Het probably benign 0.112 phenotype 04/16/2015
7 278208 APN Cfap206 0.313 IGL01135 G1 4 34721562 S162N C T missense Het probably damaging 1.000 04/16/2015
8 50598 APN Ckmt1 0.288 IGL01135 G1 2 121361150 D267A A C missense Het probably damaging 1.000 phenotype 06/21/2013
9 50329 APN Dtl 1.000 IGL01135 G1 1 191548330 T364K G T missense Het probably damaging 1.000 phenotype 06/21/2013
10 51984 APN Fam46a 0.368 IGL01135 G1 9 85326599 V57A A G missense Het probably damaging 0.972 phenotype 06/21/2013
11 51812 APN Fat1 1.000 IGL01135 G1 8 45024840 F2308I T A missense Het probably damaging 1.000 phenotype 06/21/2013
12 51368 APN Fbxo41 0.371 IGL01135 G1 6 85477908 S673T A T missense Het probably benign 0.415 phenotype 06/21/2013
13 52721 APN Flnb 1.000 IGL01135 G1 14 7909736 V1397I G A missense Het probably benign 0.000 phenotype 06/21/2013
14 52602 APN Gdi2 1.000 IGL01135 G1 13 3548855 A G splice site Het probably benign phenotype 06/21/2013
15 51631 APN Gm5155 0.000 IGL01135 G1 7 17902471 A T exon Het noncoding transcript 06/21/2013
16 50963 APN Grik3 0.260 IGL01135 G1 4 125632415 T147I C T missense Het probably benign 0.000 phenotype 06/21/2013
17 52603 APN Htr1a 0.000 IGL01135 G1 13 105445284 V344A T C missense Het possibly damaging 0.877 phenotype 06/21/2013
18 50781 APN Isg20l2 0.945 IGL01135 G1 3 87931761 D93V A T missense Het probably damaging 0.985 phenotype 06/21/2013
19 50331 APN Kcnt2 0.137 IGL01135 G1 1 140354555 T C critical splice donor site 2 bp Het probably null phenotype 06/21/2013
20 52148 APN Mfsd4b3 0.095 IGL01135 G1 10 39948072 M64T A G missense Het probably benign 0.304 06/21/2013
21 53107 APN Nox3 0.362 IGL01135 G1 17 3696252 T A utr 5 prime Het probably benign phenotype 06/21/2013
22 51632 APN Olfr693 0.088 IGL01135 G1 7 106678193 A98T C T missense Het probably benign 0.411 phenotype 06/21/2013
23 50328 APN Pikfyve 1.000 IGL01135 G1 1 65251635 N1204K T A missense Het probably damaging 0.959 phenotype 06/21/2013
24 53197 APN Pou4f3 0.724 IGL01135 G1 18 42395966 Q325* C T nonsense Het probably null phenotype 06/21/2013
25 50780 APN Rap1a 0.534 IGL01135 G1 3 105732035 T103S T A missense Het probably benign 0.007 phenotype 06/21/2013
26 52962 APN Rfc4 0.959 IGL01135 G1 16 23115776 R165C G A missense Het probably damaging 1.000 phenotype 06/21/2013
27 50597 APN Smtnl1 0.000 IGL01135 G1 2 84818887 S8P A G missense Het probably benign 0.000 phenotype 06/21/2013
28 51633 APN Syt17 0.000 IGL01135 G1 7 118382047 G351S C T missense Het possibly damaging 0.920 06/21/2013
29 52847 APN Tcf20 0.645 IGL01135 G1 15 82853900 M1117L T A missense Het probably benign 0.000 phenotype 06/21/2013
30 51172 APN Tgfbr3 1.000 IGL01135 G1 5 107215028 H39Q A T missense Het probably damaging 1.000 phenotype 06/21/2013
31 50599 APN Trdmt1 0.320 IGL01135 G1 2 13521260 T C splice site 3 bp Het probably null phenotype 06/21/2013
32 51986 APN Twf2 0.000 IGL01135 G1 9 106212828 I127V A G missense Het probably benign 0.006 phenotype 06/21/2013
33 51985 APN Unc13c 0.000 IGL01135 G1 9 73484893 V2059A A G missense Het probably damaging 0.997 phenotype 06/21/2013
[records 1 to 33 of 33]