Incidental Mutations

49 incidental mutations are currently displayed, and affect 49 genes.
7 are Possibly Damaging.
13 are Probably Damaging.
21 are Probably Benign.
5 are Probably Null.
3 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 49 of 49] 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 291637 APN 4930597O21Rik IGL02388 6 66896113 A T unclassified Het probably benign 04/16/2015
2 291634 APN 9230019H11Rik 0.227 IGL02388 10 3125050 A T unclassified Het noncoding transcript 0.087 04/16/2015
3 291657 APN Abca8a 0.073 IGL02388 11 110078815 A G unclassified Het probably benign 04/16/2015
4 291653 APN Asphd1 0.156 IGL02388 7 126946712 A T unclassified Het probably benign 04/16/2015
5 291626 APN Ccdc77 0.000 IGL02388 6 120331897 A301V G A missense Het probably benign 0.000 04/16/2015
6 291644 APN Cep350 0.959 IGL02388 1 155953753 T135K G T missense Het probably benign 0.277 phenotype 04/16/2015
7 291622 APN Chrna7 0.000 IGL02388 7 63107691 D153E A T missense Het probably damaging 0.997 phenotype 04/16/2015
8 291655 APN Clec4b2 0.059 IGL02388 6 123202228 G T splice site 3 bp Het probably null 04/16/2015
9 291609 APN Cyp2c67 0.085 IGL02388 19 39643355 N133D T C missense Het probably benign 0.202 04/16/2015
10 291630 APN Dglucy 0.124 IGL02388 12 100856998 I484T T C missense Het probably damaging 0.997 phenotype 04/16/2015
11 291643 APN Dtna 0.366 IGL02388 18 23597514 M319I G T missense Het probably benign 0.002 phenotype 04/16/2015
12 291648 APN E2f5 0.719 IGL02388 3 14588280 M152K T A missense Het probably benign 0.002 phenotype 04/16/2015
13 291649 APN Emsy 0.422 IGL02388 7 98641666 M58K A T missense Het probably damaging 0.988 04/16/2015
14 291646 APN Epha1 0.160 IGL02388 6 42365016 Y367H A G missense Het probably damaging 1.000 phenotype 04/16/2015
15 291621 APN Etv1 0.426 IGL02388 12 38781799 S32G A G missense Het possibly damaging 0.617 phenotype 04/16/2015
16 291654 APN Fam114a1 0.000 IGL02388 5 65008980 A T unclassified Het probably benign 04/16/2015
17 291623 APN Fbxo30 0.192 IGL02388 10 11290378 N281K T A missense Het probably benign 0.011 phenotype 04/16/2015
18 291636 APN Galnt12 0.000 IGL02388 4 47117941 R412L G T missense Het probably damaging 0.999 phenotype 04/16/2015
19 291629 APN Gm5786 IGL02388 12 59081596 T A exon Het noncoding transcript 04/16/2015
20 291632 APN Gm9845 0.498 IGL02388 3 39358467 T C exon Het noncoding transcript 04/16/2015
21 291616 APN Hecw2 0.608 IGL02388 1 53925699 V656A A G missense Het probably benign 0.166 phenotype 04/16/2015
22 291627 APN Hpse2 0.216 IGL02388 19 43294253 V187D A T missense Het probably damaging 1.000 phenotype 04/16/2015
23 291620 APN Itsn2 0.000 IGL02388 12 4629557 M122K T A missense Het possibly damaging 0.912 phenotype 04/16/2015
24 291614 APN Kcnj11 0.000 IGL02388 7 46099789 S37P A G missense Het probably benign 0.223 phenotype 04/16/2015
25 291635 APN Kif13b 0.000 IGL02388 14 64800358 I1491T T C missense Het probably damaging 1.000 phenotype 04/16/2015
26 291618 APN Krt36 0.066 IGL02388 11 100105164 K145* T A nonsense Het probably null phenotype 04/16/2015
27 291625 APN Loxhd1 0.185 IGL02388 18 77369137 I499V A G missense Het probably benign 0.176 phenotype 04/16/2015
28 291645 APN Map3k4 0.949 IGL02388 17 12271610 N311K G T missense Het probably damaging 0.989 0.647 phenotype 04/16/2015
29 291641 APN Mical2 0.322 IGL02388 7 112335413 H880N C A missense Het probably benign 0.000 phenotype 04/16/2015
30 291642 APN Myo1d 0.000 IGL02388 11 80637997 C666* A T nonsense Het probably null 04/16/2015
31 291628 APN Nlrx1 0.163 IGL02388 9 44264005 R158H C T missense Het probably benign 0.090 phenotype 04/16/2015
32 291617 APN Olfr1115 0.065 IGL02388 2 87251951 Y5N T A missense Het probably benign 0.000 phenotype 04/16/2015
33 291611 APN Olfr1251 0.318 IGL02388 2 89666972 S305G T C missense Het probably benign 0.004 phenotype 04/16/2015
34 291612 APN Olfr1494 0.073 IGL02388 19 13749630 H175N C A missense Het possibly damaging 0.907 phenotype 04/16/2015
35 291619 APN Olfr380 0.000 IGL02388 11 73453280 L311I A T missense Het probably benign 0.185 phenotype 04/16/2015
36 291613 APN Olfr45 0.064 IGL02388 7 140691111 T69A A G missense Het probably benign 0.002 phenotype 04/16/2015
37 291650 APN Pdgfrl 0.137 IGL02388 8 40977057 R154G A G missense Het probably benign 0.000 phenotype 04/16/2015
38 291610 APN Pitpnb 1.000 IGL02388 5 111330833 F7S T C missense Het possibly damaging 0.582 phenotype 04/16/2015
39 291647 APN Ppm1n 0.133 IGL02388 7 19279172 R285C G A missense Het probably damaging 1.000 04/16/2015
40 291615 APN Prdm11 0.496 IGL02388 2 92975612 I331N A T missense Het possibly damaging 0.897 04/16/2015
41 291638 APN Ptprb 1.000 IGL02388 10 116367521 P2066L C T missense Het probably damaging 1.000 phenotype 04/16/2015
42 291656 APN Ric8b 1.000 IGL02388 10 84992271 T C unclassified Het probably benign 04/16/2015
43 291651 APN Setx 0.000 IGL02388 2 29173653 I2320M A G missense Het probably damaging 0.998 phenotype 04/16/2015
44 291631 APN Skil 0.000 IGL02388 3 31111638 S368* C A nonsense Het probably null phenotype 04/16/2015
45 291652 APN Slc1a5 0.231 IGL02388 7 16785719 G T critical splice donor site 1 bp Het probably null phenotype 04/16/2015
46 291639 APN Trpm7 1.000 IGL02388 2 126819891 V1079G A C missense Het possibly damaging 0.799 phenotype 04/16/2015
47 291624 APN Tulp1 0.522 IGL02388 17 28358659 F2L A G missense Het probably damaging 0.999 phenotype 04/16/2015
48 291633 APN Zbtb17 1.000 IGL02388 4 141461913 Y48C A G missense Het probably damaging 1.000 phenotype 04/16/2015
49 291640 APN Zfp605 0.094 IGL02388 5 110127640 I208N T A missense Het possibly damaging 0.950 04/16/2015
[records 1 to 49 of 49]