Incidental Mutations

29 incidental mutations are currently displayed, and affect 29 genes.
7 are Possibly Damaging.
7 are Probably Damaging.
9 are Probably Benign.
4 are Probably Null.
1 create premature stop codons.
3 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 29 of 29] 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 156909 UTSW 5730522E02Rik 0.124 R1337 G1 225 N 11 25769033 S37P A G missense Het unknown 02/11/2014
2 156890 UTSW Abca12 1.000 R1337 G1 225 N 1 71294819 I1175V T C missense Het probably benign 0.032 phenotype 02/11/2014
3 156919 UTSW Ager 0.241 R1337 G1 225 N 17 34600622 G T critical splice donor site 1 bp Het probably null phenotype 02/11/2014
4 156915 UTSW Amph 0.515 R1337 G1 225 N 13 19142028 V643M G A missense Het probably damaging 0.974 0.076 phenotype 02/11/2014
5 156902 UTSW Cacna1c 0.788 R1337 G1 225 N 6 118627455 I1278T A G missense Het probably damaging 1.000 phenotype 02/11/2014
6 156895 UTSW Casp8ap2 1.000 R1337 G1 225 N 4 32645721 V1598A T C missense Het possibly damaging 0.638 phenotype 02/11/2014
7 156911 UTSW Cdk12 1.000 R1337 G1 225 N 11 98245671 T C critical splice donor site 2 bp Het probably null phenotype 02/11/2014
8 156907 UTSW Ces2g 0.043 R1337 G1 225 N 8 104963965 Y126F A T missense Het possibly damaging 0.633 02/11/2014
9 156923 UTSW Ehbp1l1 0.520 R1337 G1 225 N 19 5718230 M1015K A T missense Het probably benign 0.003 phenotype 02/11/2014
10 156914 UTSW Engase 0.143 R1337 G1 225 N 11 118482574 T248A A G missense Het possibly damaging 0.458 phenotype 02/11/2014
11 156912 UTSW Gsdma 0.042 R1337 G1 225 N 11 98669707 Q162* C T nonsense Het probably null 02/11/2014
12 156904 UTSW Hapln3 0.084 R1337 G1 225 N 7 79118076 E190G T C missense Het probably benign 0.057 phenotype 02/11/2014
13 156893 UTSW Hdc 0.286 R1337 G1 225 N 2 126616276 Q42R T C missense Het probably benign 0.000 phenotype 02/11/2014
14 156894 UTSW Larp1b 0.262 R1337 G1 225 N 3 41033402 P20S C T missense Het probably damaging 1.000 02/11/2014
15 156898 UTSW Macf1 1.000 R1337 G1 225 N 4 123476275 R1564S T G missense Het probably benign 0.342 phenotype 02/11/2014
16 156906 UTSW Muc5b 0.113 R1337 G1 185 N 7 141858624 Y1769C A G missense Het unknown phenotype 02/11/2014
17 156910 UTSW Nup88 0.956 R1337 G1 225 N 11 70944890 Q576L T A missense Het probably damaging 0.998 phenotype 02/11/2014
18 156905 UTSW Olfr566 0.095 R1337 G1 225 N 7 102856871 N137S T C missense Het probably benign 0.025 phenotype 02/11/2014
19 156908 UTSW Olfr836 0.186 R1337 G1 225 N 9 19121803 I280V A G missense Het probably benign 0.000 phenotype 02/11/2014
20 156924 UTSW Prune2 0.085 R1337 G1 225 N 19 17119607 S825L C T missense Het possibly damaging 0.699 phenotype 02/11/2014
21 156892 UTSW Ryr3 0.378 R1337 G1 225 N 2 112779963 M2301I C A missense Het possibly damaging 0.462 phenotype 02/11/2014
22 156913 UTSW Sdk2 0.165 R1337 G1 225 N 11 113832331 V1278G A C missense Het possibly damaging 0.794 phenotype 02/11/2014
23 156903 UTSW Sertad3 0.375 R1337 G1 225 N 7 27476441 L100P T C missense Het probably damaging 0.996 phenotype 02/11/2014
24 156888 UTSW Slco5a1 0.159 R1337 G1 225 N 1 12939142 T370A T C missense Het probably benign 0.006 phenotype 02/11/2014
25 156899 UTSW Srrm1 1.000 R1337 G1 225 N 4 135346733 A G critical splice donor site 2 bp Het probably null 02/11/2014
26 156922 UTSW Stk32a 0.180 R1337 G1 225 N 18 43261349 D121G A G missense Het probably benign 0.002 02/11/2014
27 156921 UTSW Ttc7 0.768 R1337 G1 225 N 17 87290296 R99W A T missense Het probably damaging 0.999 phenotype 02/11/2014
28 156889 UTSW Xkr9 0.098 R1337 G1 225 N 1 13701124 S288Y C A missense Het possibly damaging 0.936 02/11/2014
29 156900 UTSW Zfp644 0.213 R1337 G1 225 N 5 106637554 S376P A G missense Het probably damaging 0.992 phenotype 02/11/2014
[records 1 to 29 of 29]