Incidental Mutations

30 incidental mutations are currently displayed, and affect 30 genes.
2 are Possibly Damaging.
10 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 30 of 30] 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 416545 APN Acod1 0.000 IGL03323 14 103055294 D418V A T missense Het probably damaging 0.999 phenotype 08/02/2016
2 416563 APN Ahdc1 0.263 IGL03323 4 133065428 G1327S G A missense Het probably benign 0.000 phenotype 08/02/2016
3 416558 APN Bcl2l15 0.056 IGL03323 3 103833403 I62L A T missense Het probably benign 0.001 08/02/2016
4 416542 APN Ccdc7a 0.055 IGL03323 8 129058763 D105E A T missense Het probably benign 0.024 08/02/2016
5 416559 APN Cldn12 0.000 IGL03323 5 5508421 G2V C A missense Het probably damaging 0.996 phenotype 08/02/2016
6 416550 APN Eapp 0.908 IGL03323 12 54673615 H272N G T missense Het probably damaging 1.000 phenotype 08/02/2016
7 416564 APN Fcrla 0.000 IGL03323 1 170927545 A G utr 5 prime Het probably benign phenotype 08/02/2016
8 416551 APN Fmnl3 0.737 IGL03323 15 99321281 G787S C T missense Het probably damaging 1.000 phenotype 08/02/2016
9 416566 APN Fmo5 0.098 IGL03323 3 97639007 G T splice site 5 bp Het probably null phenotype 08/02/2016
10 416554 APN Golgb1 0.885 IGL03323 16 36913453 E1021* G T nonsense Het probably null phenotype 08/02/2016
11 416547 APN Hspa4 0.936 IGL03323 11 53265133 N648K A T missense Het probably benign 0.046 phenotype 08/02/2016
12 416549 APN Iigp1 0.059 IGL03323 18 60389824 F5L T C missense Het probably benign 0.039 phenotype 08/02/2016
13 416567 APN Lad1 0.058 IGL03323 1 135830974 T A critical splice donor site 2 bp Het probably null phenotype 08/02/2016
14 416557 APN Man2b2 0.000 IGL03323 5 36818514 D399G T C missense Het probably benign 0.071 08/02/2016
15 416546 APN Mc5r 0.140 IGL03323 18 68339215 T215I C T missense Het probably benign 0.005 phenotype 08/02/2016
16 416561 APN Mx2 0.173 IGL03323 16 97546375 S156G A G missense Het probably damaging 0.988 08/02/2016
17 416560 APN Necap2 0.100 IGL03323 4 141068222 I242N A T missense Het possibly damaging 0.893 phenotype 08/02/2016
18 416556 APN Nme8 0.129 IGL03323 13 19688950 E175K C T missense Het probably benign 0.056 phenotype 08/02/2016
19 416562 APN Notch4 0.000 IGL03323 17 34582471 C1098S T A missense Het probably damaging 1.000 phenotype 08/02/2016
20 416540 APN Olfr345 0.073 IGL03323 2 36640141 M34K T A missense Het possibly damaging 0.950 phenotype 08/02/2016
21 416539 APN Olfr8 0.198 IGL03323 10 78955600 Y132H T C missense Het probably benign 0.000 phenotype 08/02/2016
22 416565 APN Osbpl9 0.000 IGL03323 4 109062459 A G splice site Het probably benign phenotype 08/02/2016
23 416555 APN Prag1 0.000 IGL03323 8 36140008 S968P T C missense Het probably damaging 0.999 phenotype 08/02/2016
24 416552 APN Qsox2 0.103 IGL03323 2 26220979 S125P A G missense Het probably benign 0.000 phenotype 08/02/2016
25 416541 APN Rptn 0.074 IGL03323 3 93397153 T598A A G missense Het probably benign 0.000 08/02/2016
26 416544 APN Slc2a2 1.000 IGL03323 3 28726290 M375I G A missense Het probably damaging 0.995 phenotype 08/02/2016
27 416548 APN Tmed9 0.261 IGL03323 13 55596878 T173I C T missense Het probably damaging 0.976 phenotype 08/02/2016
28 416553 APN Trank1 0.000 IGL03323 9 111352116 D402G A G missense Het probably damaging 1.000 08/02/2016
29 416568 APN Ttc21a 0.414 IGL03323 9 119940536 G T intron Het probably benign 08/02/2016
30 416543 APN Vmn2r58 0.430 IGL03323 7 41861871 M503V T C missense Het probably benign 0.056 08/02/2016
[records 1 to 30 of 30]