Incidental Mutations

15 incidental mutations are currently displayed, and affect 15 genes.
3 are Possibly Damaging.
3 are Probably Damaging.
7 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 15 of 15] 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 151621 UTSW Aak1 0.416 R1262 G1 225 N 6 86935488 (GRCm38) V114A T C missense Het probably benign 0.092 phenotype 2014-01-29
2 151624 UTSW BC048679 0.056 R1262 G1 152 N 7 81495341 (GRCm38) F85L A G missense Het probably benign 0.000 2014-01-29
3 151628 UTSW Btbd7 0.447 R1262 G1 225 N 12 102787951 (GRCm38) I852T A G missense Het probably benign 0.000 2014-01-29
4 151629 UTSW Cenpk 0.817 R1262 G1 225 N 13 104230785 (GRCm38) V43E T A missense Het possibly damaging 0.896 phenotype 2014-01-29
5 151631 UTSW Chmp7 1.000 R1262 G1 225 N 14 69719450 (GRCm38) M336I C T missense Het probably benign 0.380 0.114 2014-01-29
6 151622 UTSW Cyp2b10 0.134 R1262 G1 225 N 7 25915411 (GRCm38) T281M C T missense Het probably benign 0.155 phenotype 2014-01-29
7 151627 UTSW Lrriq1 0.088 R1262 G1 225 N 10 103234137 (GRCm38) D6G T C missense Het possibly damaging 0.871 2014-01-29
8 151632 UTSW Ltbp1 1.000 R1262 G1 225 N 17 75225285 (GRCm38) Q118R A G missense Het possibly damaging 0.752 0.110 phenotype 2014-01-29
9 151616 UTSW Nipsnap3b 0.072 R1262 G1 225 N 4 53015166 (GRCm38) G71V G T missense Het probably damaging 1.000 phenotype 2014-01-29
10 151625 UTSW Olfr623 0.154 R1262 G1 225 N 7 103660441 (GRCm38) P270S G A missense Het probably benign 0.333 phenotype 2014-01-29
11 262744 UTSW Olfr648 0.460 R1262 G1 141 N 7 104179416 (GRCm38) A G splice site 40 bp Het probably null phenotype 2015-02-04
12 151626 UTSW Snx25 1.000 R1262 G1 225 N 8 46105291 (GRCm38) R80S T A missense Het probably damaging 0.983 2014-01-29
13 151615 UTSW Syt6 0.102 R1262 G1 220 N 3 103585340 (GRCm38) A T critical splice acceptor site Het probably null phenotype 2014-01-29
14 151617 UTSW Tas1r2 0.090 R1262 G1 225 N 4 139655288 (GRCm38) R79Q G A missense Het probably damaging 0.993 phenotype 2014-01-29
15 151633 UTSW Ttc7 0.812 R1262 G1 225 N 17 87340936 (GRCm38) T521I C T missense Het probably benign 0.086 phenotype 2014-01-29
[records 1 to 15 of 15]