Incidental Mutations

20 incidental mutations are currently displayed, and affect 20 genes.
2 are Possibly Damaging.
10 are Probably Damaging.
6 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 20 of 20] 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 260097 UTSW Adgrl3 0.000 R2891 G1 225 N 5 81693519 Y816H T C missense Het probably damaging 1.000 phenotype 01/23/2015
2 260094 UTSW Clcn6 0.145 R2891 G1 225 N 4 148012616 C T critical splice donor site 1 bp Het probably null phenotype 01/23/2015
3 260107 UTSW Farp1 0.000 R2891 G1 224 N 14 121256736 A543V C T missense Het probably damaging 1.000 phenotype 01/23/2015
4 260088 UTSW Hhat 1.000 R2891 G1 215 N 1 192595086 Y355C T C missense Het probably damaging 1.000 phenotype 01/23/2015
5 260100 UTSW Ireb2 0.000 R2891 G1 225 N 9 54899990 H612L A T missense Het probably benign 0.007 phenotype 01/23/2015
6 260090 UTSW Kcnj3 0.000 R2891 G1 225 N 2 55447015 I298F A T missense Het probably damaging 1.000 phenotype 01/23/2015
7 260096 UTSW Kdr 1.000 R2891 G1 225 N 5 75946836 F1016L A G missense Het probably damaging 1.000 phenotype 01/23/2015
8 260086 UTSW Klf7 1.000 R2891 G1 225 N 1 64042362 Y269C T C missense Het probably damaging 1.000 phenotype 01/23/2015
9 260093 UTSW Klhl9 0.000 R2891 G1 225 N 4 88720970 I345V T C missense Het probably benign 0.021 phenotype 01/23/2015
10 477027 UTSW Miga2 0.000 R2891 G1 225 N 2 30378294 A T splice site Het probably null 05/15/2017
11 260095 UTSW Nadk 0.921 R2891 G1 200 N 4 155587360 N232S A G missense Het possibly damaging 0.458 phenotype 01/23/2015
12 260092 UTSW Ncoa6 1.000 R2891 G1 225 N 2 155437961 D45V T A missense Het possibly damaging 0.859 phenotype 01/23/2015
13 260099 UTSW Pcnx2 0.000 R2891 G1 225 N 8 125891058 S153P A G missense Het probably damaging 0.999 phenotype 01/23/2015
14 260087 UTSW Per2 0.199 R2891 G1 225 N 1 91445603 Q154H C A missense Het probably damaging 1.000 phenotype 01/23/2015
15 260110 UTSW Pik3ap1 0.000 R2891 G1 173 N 19 41376061 A73V G A missense Het probably benign 0.002 phenotype 01/23/2015
16 260098 UTSW Plod3 1.000 R2891 G1 225 N 5 136988146 A50P G C missense Het probably benign 0.382 0.104 phenotype 01/23/2015
17 260091 UTSW Rapsn 1.000 R2891 G1 225 N 2 91036824 D157V A T missense Het probably damaging 0.981 phenotype 01/23/2015
18 260101 UTSW Shprh 0.000 R2891 G1 225 N 10 11164356 S4R T G missense Het probably damaging 1.000 Pcna. Neither homozygous truncation nor KO affect B cell somatic hypermutation or class switching. [provided by MGI curators] (source: MGI)">phenotype 01/23/2015
19 260102 UTSW Taar8a 0.107 R2891 G1 225 N 10 24077130 V211I G A missense Het probably benign 0.023 01/23/2015
20 260103 UTSW Vpreb3 0.000 R2891 G1 225 N 10 75943222 C T unclassified Het probably benign 0.090 phenotype 01/23/2015
[records 1 to 20 of 20]