Incidental Mutations

35 incidental mutations are currently displayed, and affect 35 genes.
5 are Possibly Damaging.
13 are Probably Damaging.
14 are Probably Benign.
2 are Probably Null.
0 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 35 of 35] 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 90453 APN Adamts6 0.876 IGL01517 G1 13 104390192 A T splice site Het probably benign phenotype 12/09/2013
2 90452 APN Arpc1b 0.000 IGL01517 G1 5 145127869 A G utr 3 prime Het probably benign phenotype 12/09/2013
3 90437 APN Ccdc54 0.060 IGL01517 G1 16 50589917 L329F G A missense Het possibly damaging 0.915 12/09/2013
4 90444 APN Cdc42bpg 0.356 IGL01517 G1 19 6318437 R1055H G A missense Het probably damaging 0.999 12/09/2013
5 90435 APN Cylc1 IGL01517 G1 X 111119030 T29A A G missense Het possibly damaging 0.707 12/09/2013
6 90426 APN Ddx50 0.223 IGL01517 G1 10 62647132 T53A T C missense Het probably benign 0.000 phenotype 12/09/2013
7 90425 APN Dmap1 1.000 IGL01517 G1 4 117676009 R283C G A missense Het probably damaging 1.000 phenotype 12/09/2013
8 90434 APN Extl3 1.000 IGL01517 G1 14 65076707 L342H A T missense Het probably damaging 1.000 phenotype 12/09/2013
9 90436 APN Gjb3 1.000 IGL01517 G1 4 127326121 I206S A C missense Het probably damaging 0.992 phenotype 12/09/2013
10 90447 APN Gphn 1.000 IGL01517 G1 12 78376374 I53K T A missense Het probably damaging 0.996 phenotype 12/09/2013
11 278568 APN Gpr22 0.000 IGL01517 G1 12 31708710 C T unclassified Het probably benign phenotype 04/16/2015
12 90423 APN Inpp5b 0.233 IGL01517 G1 4 124782436 C362S T A missense Het probably benign 0.002 phenotype 12/09/2013
13 90448 APN Iqgap3 0.352 IGL01517 G1 3 88109396 Q1062K C A missense Het probably benign 0.091 12/09/2013
14 90450 APN Kdm2a 0.962 IGL01517 G1 19 4362061 A G splice site Het probably benign phenotype 12/09/2013
15 90445 APN Ltbp3 0.191 IGL01517 G1 19 5757732 D1167G A G missense Het possibly damaging 0.567 phenotype 12/09/2013
16 90440 APN Mpo 0.000 IGL01517 G1 11 87795821 N65D A G missense Het possibly damaging 0.831 phenotype 12/09/2013
17 90446 APN Mrpl2 0.932 IGL01517 G1 17 46649983 R268G A G missense Het probably damaging 0.999 phenotype 12/09/2013
18 90424 APN Nfkbia 1.000 IGL01517 G1 12 55490645 A220T C T missense Het probably damaging 0.994 phenotype 12/09/2013
19 90441 APN Nlrc3 0.123 IGL01517 G1 16 3947487 I1091F T A missense Het probably damaging 0.994 phenotype 12/09/2013
20 90439 APN Notch2 1.000 IGL01517 G1 3 98138655 S1674R T A missense Het probably benign 0.159 phenotype 12/09/2013
21 90449 APN Olfr298 0.109 IGL01517 G1 7 86489557 T C utr 5 prime Het probably benign phenotype 12/09/2013
22 90430 APN Olfr63 0.098 IGL01517 G1 17 33269655 N310K T A missense Het probably benign 0.001 phenotype 12/09/2013
23 90451 APN Pde8b 0.204 IGL01517 G1 13 95100887 A G critical splice donor site 2 bp Het probably null phenotype 12/09/2013
24 90432 APN Pla2r1 0.000 IGL01517 G1 2 60504253 Y392H A G missense Het probably damaging 1.000 phenotype 12/09/2013
25 90431 APN Plekhm1 0.000 IGL01517 G1 11 103394783 N275K A T missense Het possibly damaging 0.539 phenotype 12/09/2013
26 90443 APN Prdm16 0.706 IGL01517 G1 4 154328425 H1041R T C missense Het probably damaging 1.000 phenotype 12/09/2013
27 90427 APN Rapsn 1.000 IGL01517 G1 2 91036618 N88K C A missense Het probably damaging 1.000 phenotype 12/09/2013
28 90421 APN Rasef 0.097 IGL01517 G1 4 73769822 Q31H T A missense Het probably benign 0.031 phenotype 12/09/2013
29 90442 APN Rpl28-ps4 0.713 IGL01517 G1 6 117213852 T C exon Het noncoding transcript 12/09/2013
30 90428 APN Trpc7 0.137 IGL01517 G1 13 56861065 Y263C T C missense Het probably damaging 1.000 phenotype 12/09/2013
31 90429 APN Ttn 1.000 IGL01517 G1 2 76747596 T24318A T C missense Het probably damaging 0.998 phenotype 12/09/2013
32 90422 APN Vmn1r35 0.060 IGL01517 G1 6 66679450 T79A T C missense Het probably benign 0.006 12/09/2013
33 90420 APN Vmn2r100 0.078 IGL01517 G1 17 19521963 S200T T A missense Het probably benign 0.373 12/09/2013
34 90433 APN Wnt9b 1.000 IGL01517 G1 11 103731081 V250A A G missense Het probably benign 0.132 phenotype 12/09/2013
35 90438 APN Zyg11a 0.177 IGL01517 G1 4 108201194 K383M T A missense Het probably null 1.000 12/09/2013
[records 1 to 35 of 35]