Incidental Mutations

25 incidental mutations are currently displayed, and affect 25 genes.
4 are Possibly Damaging.
4 are Probably Damaging.
11 are Probably Benign.
4 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 25 of 25] 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 96460 UTSW Adrm1 0.612 R1129 G1 225 N 2 180172919 G C unclassified Het probably benign phenotype 01/05/2014
2 96456 UTSW Bub1b 1.000 R1129 G1 225 N 2 118615006 D269V A T missense Het probably damaging 1.000 phenotype 01/05/2014
3 96452 UTSW Ccdc73 0.086 R1129 G1 225 N 2 104992190 N828S A G missense Het possibly damaging 0.507 01/05/2014
4 96497 UTSW Cdk12 1.000 R1129 G1 156 N 11 98245375 S1152P T C missense Het unknown phenotype 01/05/2014
5 96446 UTSW Cnnm3 0.115 R1129 G1 190 N 1 36513016 L369P T C missense Het probably damaging 1.000 01/05/2014
6 96517 UTSW Cxadr 1.000 R1129 G1 225 N 16 78336433 K360R A G missense Het probably benign 0.267 phenotype 01/05/2014
7 96483 UTSW Dlg2 0.000 R1129 G1 225 N 7 92431174 G A splice site 5 bp Het probably null phenotype 01/05/2014
8 96444 UTSW Dst 0.343 R1129 G1 225 N 1 34199554 V3779A T C missense Het probably benign 0.285 phenotype 01/05/2014
9 96509 UTSW Fbxo16 0.059 R1129 G1 102 N 14 65295532 R161K G A missense Het probably benign 0.000 phenotype 01/05/2014
10 96499 UTSW Gm9726 R1129 G1 225 N 12 93928526 T A unclassified Het noncoding transcript 01/05/2014
11 96475 UTSW Hectd4 0.442 R1129 G1 225 N 5 121310599 T337A A G missense Het possibly damaging 0.659 01/05/2014
12 96501 UTSW Hist1h1t 0.000 R1129 G1 225 N 13 23696324 K153N G T missense Het possibly damaging 0.921 0.151 phenotype 01/05/2014
13 262420 UTSW Ints1 1.000 R1129 G1 81 N 5 139758471 L1510S A G missense Het probably benign 0.004 phenotype 02/04/2015
14 96515 UTSW Kansl2 0.934 R1129 G1 225 N 15 98533581 Y63C T C missense Het probably damaging 1.000 01/05/2014
15 96507 UTSW Lats2 1.000 R1129 G1 225 N 14 57700333 E233G T C missense Het possibly damaging 0.714 phenotype 01/05/2014
16 96493 UTSW Naca 0.802 R1129 G1 225 N 10 128040202 T C intron Het probably benign phenotype 01/05/2014
17 96522 UTSW Pprc1 1.000 R1129 G1 225 N 19 46063806 A591S G T missense Het probably benign 0.354 phenotype 01/05/2014
18 96479 UTSW Sbsn 0.061 R1129 G1 225 N 7 30753440 P627S C T missense Het probably benign 0.000 01/05/2014
19 262421 UTSW Sema6b 0.139 R1129 G1 90 N 17 56124347 E772G T C missense Het probably benign 0.000 phenotype 02/04/2015
20 96473 UTSW Tmem33 0.114 R1129 G1 225 N 5 67264460 A G splice site 3 bp Het probably null 01/05/2014
21 96513 UTSW Tmtc4 0.000 R1129 G1 225 N 14 122943153 A G critical splice donor site 2 bp Het probably null 01/05/2014
22 96485 UTSW Ubqlnl 0.101 R1129 G1 225 N 7 104149650 H213Q A T missense Het probably damaging 0.981 phenotype 01/05/2014
23 96448 UTSW Ugt1a10 0.133 R1129 G1 225 N 1 88055609 M43T T C missense Het probably benign 0.000 01/05/2014
24 96481 UTSW Vmn2r68 0.089 R1129 G1 225 N 7 85237504 T C splice site 4 bp Het probably null 01/05/2014
25 96491 UTSW Zcchc14 0.000 R1129 G1 225 N 8 121608415 A G unclassified Het probably benign 01/05/2014
[records 1 to 25 of 25]