Incidental Mutations

32 incidental mutations are currently displayed, and affect 31 genes.
6 are Possibly Damaging.
12 are Probably Damaging.
10 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 32 of 32] 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 91739 APN 2410124H12Rik IGL01598 G1 16 92478929 T A exon Het noncoding transcript 12/09/2013
2 91756 APN Apc2 0.263 IGL01598 G1 10 80313048 L1283Q T A missense Het probably damaging 1.000 phenotype 12/09/2013
3 91746 APN Apol6 0.052 IGL01598 G1 15 77050716 A62T G A missense Het probably damaging 1.000 phenotype 12/09/2013
4 91753 APN AU018091 0.216 IGL01598 G1 7 3162270 I204N A T missense Het possibly damaging 0.713 12/09/2013
5 91758 APN B4galnt4 0.124 IGL01598 G1 7 141070515 R765L G T missense Het probably benign 0.148 12/09/2013
6 91731 APN Brca1 1.000 IGL01598 G1 11 101524330 T993A T C missense Het probably benign 0.042 phenotype 12/09/2013
7 91759 APN Cadps 1.000 IGL01598 G1 14 12522202 C T critical splice donor site 1 bp Het probably null phenotype 12/09/2013
8 91748 APN Ccdc177 0.117 IGL01598 G1 12 80758745 S252P A G missense Het unknown 12/09/2013
9 91757 APN Cdc73 1.000 IGL01598 G1 1 143699279 S59P A G missense Het probably damaging 0.999 phenotype 12/09/2013
10 91754 APN Cep63 0.749 IGL01598 G1 9 102590458 Q570K G T missense Het possibly damaging 0.880 phenotype 12/09/2013
11 91735 APN Ces1c 0.056 IGL01598 G1 8 93118413 I120K A T missense Het probably benign 0.000 phenotype 12/09/2013
12 91755 APN Cpeb1 0.000 IGL01598 G1 7 81361801 M131V T C missense Het probably benign 0.000 phenotype 12/09/2013
13 91741 APN Dync1h1 1.000 IGL01598 G1 12 110658128 V3701I G A missense Het probably damaging 0.992 phenotype 12/09/2013
14 91734 APN Fxr1 1.000 IGL01598 G1 3 34064232 S535P T C missense Het possibly damaging 0.606 0.097 phenotype 12/09/2013
15 91744 APN Gldc 1.000 IGL01598 G1 19 30133756 V540D A T missense Het probably damaging 0.997 phenotype 12/09/2013
16 91750 APN Iqcf6 0.380 IGL01598 G1 9 106627508 T124A A G missense Het probably benign 0.000 12/09/2013
17 91738 APN Itih4 0.000 IGL01598 G1 14 30887817 I35V A G missense Het possibly damaging 0.915 phenotype 12/09/2013
18 91733 APN Kmt2c 1.000 IGL01598 G1 5 25273666 *1525W T C makesense Het probably null phenotype 12/09/2013
19 91736 APN Kmt2c 1.000 IGL01598 G1 5 25354771 V963E A T missense Het probably damaging 1.000 phenotype 12/09/2013
20 91749 APN Lmnb2 1.000 IGL01598 G1 10 80907165 S202G T C missense Het probably benign 0.004 phenotype 12/09/2013
21 91751 APN Med23 1.000 IGL01598 G1 10 24903798 S924R T G missense Het probably benign 0.344 phenotype 12/09/2013
22 91730 APN Olfr1454 0.057 IGL01598 G1 19 13064149 V246A T C missense Het probably damaging 1.000 phenotype 12/09/2013
23 91745 APN Pcif1 0.172 IGL01598 G1 2 164886611 F263L T C missense Het possibly damaging 0.863 12/09/2013
24 91752 APN Pon2 0.000 IGL01598 G1 6 5272331 L163H A T missense Het probably damaging 1.000 phenotype 12/09/2013
25 91747 APN Scn1a 1.000 IGL01598 G1 2 66302485 V165M C T missense Het possibly damaging 0.630 phenotype 12/09/2013
26 91740 APN Sema6d 0.000 IGL01598 G1 2 124665098 P961Q C A missense Het probably damaging 0.998 phenotype 12/09/2013
27 91732 APN Snx27 1.000 IGL01598 G1 3 94561843 Y64H A G missense Het probably damaging 1.000 phenotype 12/09/2013
28 91729 APN Srsf11 1.000 IGL01598 G1 3 158012035 C T unclassified Het probably benign phenotype 12/09/2013
29 91737 APN Taok1 0.587 IGL01598 G1 11 77571684 V193A A G missense Het probably damaging 0.999 12/09/2013
30 91742 APN Vps13d 1.000 IGL01598 G1 4 145016901 T4137A T C missense Het probably benign 0.209 phenotype 12/09/2013
31 91743 APN Zbtb26 0.249 IGL01598 G1 2 37436271 Y251C T C missense Het probably damaging 0.997 12/09/2013
32 91760 APN Zcchc11 0.000 IGL01598 G1 4 108550820 A G unclassified Het probably benign phenotype 12/09/2013
[records 1 to 32 of 32]