Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
5 are Possibly Damaging.
10 are Probably Damaging.
11 are Probably Benign.
5 are Probably Null.
0 create premature stop codons.
3 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 301517 APN Alms1 0.000 IGL02636 6 85628654 Q1960K C A missense Het probably benign 0.281 phenotype 04/16/2015
2 301518 APN Arhgef40 0.284 IGL02636 14 51997408 V1056E T A missense Het probably damaging 1.000 phenotype 04/16/2015
3 301520 APN Cdh26 0.000 IGL02636 2 178449962 F105I T A missense Het probably damaging 0.998 phenotype 04/16/2015
4 301510 APN Cep162 0.179 IGL02636 9 87248379 D59E A T missense Het possibly damaging 0.901 04/16/2015
5 301506 APN Cngb3 0.101 IGL02636 4 19396690 T348S A T missense Het probably damaging 1.000 phenotype 04/16/2015
6 301523 APN Eci3 0.000 IGL02636 13 34946980 A T unclassified 1104 bp Het probably null 04/16/2015
7 301515 APN Gapvd1 1.000 IGL02636 2 34725404 I409T A G missense Het probably benign 0.015 04/16/2015
8 301531 APN Golga2 0.838 IGL02636 2 32296723 T C critical splice donor site 2 bp Het probably null phenotype 04/16/2015
9 301509 APN Hoxd3 0.818 IGL02636 2 74746954 A393T G A missense Het probably benign 0.319 phenotype 04/16/2015
10 301507 APN Htr5a 0.128 IGL02636 5 27842660 F71S T C missense Het probably damaging 0.995 phenotype 04/16/2015
11 301532 APN Hyou1 1.000 IGL02636 9 44381410 T C critical splice donor site 2 bp Het probably null phenotype 04/16/2015
12 301536 APN Igsf6 0.098 IGL02636 7 121067280 C A intron Het probably benign 04/16/2015
13 301529 APN Klrb1c 0.054 IGL02636 6 128788552 C25F C A missense Het probably benign 0.015 phenotype 04/16/2015
14 301528 APN Lrguk 0.093 IGL02636 6 34090188 T483K C A missense Het probably damaging 1.000 04/16/2015
15 301534 APN Lrpprc 1.000 IGL02636 17 84753104 A T unclassified Het probably benign phenotype 04/16/2015
16 301537 APN Lrrk1 1.000 IGL02636 7 66308659 A T critical splice donor site 2 bp Het probably null phenotype 04/16/2015
17 301516 APN Megf8 0.916 IGL02636 7 25358432 G2098D G A missense Het probably damaging 0.991 phenotype 04/16/2015
18 301526 APN Nfkbia 1.000 IGL02636 12 55491173 Q165R T C missense Het possibly damaging 0.482 phenotype 04/16/2015
19 301535 APN Nipsnap2 0.000 IGL02636 5 129745290 A G intron Het probably benign phenotype 04/16/2015
20 301521 APN Phykpl 0.560 IGL02636 11 51598713 T382I C T missense Het probably damaging 1.000 phenotype 04/16/2015
21 301514 APN Prdm10 1.000 IGL02636 9 31329681 D206G A G missense Het possibly damaging 0.675 phenotype 04/16/2015
22 301513 APN Rab26 0.117 IGL02636 17 24533559 S9G T C missense Het probably benign 0.009 phenotype 04/16/2015
23 301530 APN Sema3e 0.387 IGL02636 5 14225656 N258K C A missense Het probably benign 0.000 phenotype 04/16/2015
24 301512 APN Slfn10-ps 0.074 IGL02636 11 83030145 T A unclassified Het noncoding transcript 04/16/2015
25 301527 APN Tgm5 0.131 IGL02636 2 121076796 C149S A T missense Het probably damaging 0.994 phenotype 04/16/2015
26 301533 APN Timp4 0.219 IGL02636 6 115249824 C T splice site 5 bp Het probably null phenotype 04/16/2015
27 301519 APN Traf7 0.777 IGL02636 17 24512990 K251E T C missense Het probably benign 0.000 phenotype 04/16/2015
28 301524 APN Ugcg 1.000 IGL02636 4 59207763 R34L G T missense Het possibly damaging 0.731 phenotype 04/16/2015
29 301522 APN Unc13d 0.247 IGL02636 11 116073618 H300R T C missense Het probably damaging 1.000 phenotype 04/16/2015
30 301525 APN Vmn1r20 0.495 IGL02636 6 57431761 C24F G T missense Het probably benign 0.000 04/16/2015
31 301505 APN Vmn2r13 0.072 IGL02636 5 109192017 R31G T C missense Het probably damaging 0.981 04/16/2015
32 301511 APN Vsig10l 0.151 IGL02636 7 43463578 T87A A G missense Het possibly damaging 0.528 04/16/2015
33 301508 APN Zfp353-ps 0.081 IGL02636 8 42082440 T A exon Het noncoding transcript 04/16/2015
[records 1 to 33 of 33]