Incidental Mutations

26 incidental mutations are currently displayed, and affect 26 genes.
3 are Possibly Damaging.
15 are Probably Damaging.
7 are Probably Benign.
1 are Probably Null.
0 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 26 of 26] 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 90348 APN 1700016D06Rik 0.101 IGL01546 G1 8 11656136 M133L T A missense Het probably benign 0.001 12/03/2013
2 90343 APN Amdhd2 0.617 IGL01546 G1 17 24163600 R22L C A missense Het probably benign 0.375 12/03/2013
3 90352 APN Arg2 0.000 IGL01546 G1 12 79149859 T C splice site Het probably benign phenotype 12/03/2013
4 90344 APN Catip 0.000 IGL01546 G1 1 74362795 L43P T C missense Het probably damaging 0.997 12/03/2013
5 90349 APN Ccdc30 0.000 IGL01546 G1 4 119398188 L123R A C missense Het probably damaging 0.988 12/03/2013
6 90347 APN Cep89 0.135 IGL01546 G1 7 35420900 L369P T C missense Het probably damaging 1.000 12/03/2013
7 90341 APN Dolpp1 0.914 IGL01546 G1 2 30397095 F180L T C missense Het probably damaging 1.000 phenotype 12/03/2013
8 90333 APN Kctd19 0.058 IGL01546 G1 8 105386962 H670R T C missense Het probably benign 0.000 12/03/2013
9 90338 APN Kntc1 0.953 IGL01546 G1 5 123765005 I315N T A missense Het probably benign 0.023 phenotype 12/03/2013
10 90328 APN Mfsd4b2 0.091 IGL01546 G1 10 39921475 W295R A T missense Het probably damaging 1.000 12/03/2013
11 90330 APN Mgam 0.121 IGL01546 G1 6 40654693 T116A A G missense Het probably damaging 0.976 phenotype 12/03/2013
12 90346 APN Mn1 1.000 IGL01546 G1 5 111421248 D1028V A T missense Het probably damaging 0.996 phenotype 12/03/2013
13 90331 APN Olfr19 0.303 IGL01546 G1 16 16673265 S239P A G missense Het probably damaging 1.000 phenotype 12/03/2013
14 90334 APN Olfr23 0.259 IGL01546 G1 11 73941194 G316D G A missense Het probably benign 0.000 phenotype 12/03/2013
15 90327 APN Olfr592 0.111 IGL01546 G1 7 103187410 I270F A T missense Het probably damaging 0.989 phenotype 12/03/2013
16 90337 APN Olfr690 0.066 IGL01546 G1 7 105329692 R167G T C missense Het probably damaging 1.000 phenotype 12/03/2013
17 90329 APN Olfr694 0.113 IGL01546 G1 7 106689531 S67P A G missense Het probably damaging 0.999 phenotype 12/03/2013
18 90340 APN Olfr845 0.161 IGL01546 G1 9 19338772 V104G T G missense Het possibly damaging 0.562 phenotype 12/03/2013
19 90342 APN Phc3 0.000 IGL01546 G1 3 30961739 A108S C A missense Het probably damaging 0.997 12/03/2013
20 90345 APN Pkhd1l1 0.000 IGL01546 G1 15 44566316 Y3310C A G missense Het probably damaging 0.997 12/03/2013
21 90351 APN Ppp4r3b 0.000 IGL01546 G1 11 29209488 T C unclassified 2 bp Het probably null 12/03/2013
22 90332 APN Slx4ip 0.000 IGL01546 G1 2 137066199 T159A A G missense Het probably benign 0.000 12/03/2013
23 90335 APN Sos1 1.000 IGL01546 G1 17 80408611 Y974F T A missense Het probably damaging 1.000 phenotype 12/03/2013
24 90336 APN Taar8a 0.079 IGL01546 G1 10 24076915 Y139F A T missense Het possibly damaging 0.946 12/03/2013
25 90339 APN Vcam1 0.578 IGL01546 G1 3 116115942 C579R A G missense Het possibly damaging 0.856 phenotype 12/03/2013
26 90350 APN Zdhhc17 0.000 IGL01546 G1 10 110946193 V547M C T missense Het probably damaging 0.997 phenotype 12/03/2013
[records 1 to 26 of 26]