Incidental Mutations

27 incidental mutations are currently displayed, and affect 27 genes.
5 are Possibly Damaging.
11 are Probably Damaging.
6 are Probably Benign.
5 are Probably Null.
1 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 27 of 27] 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 257551 UTSW Aldh18a1 1.000 R3012 G1 225 N 19 40557691 Y585* G T nonsense Het probably null phenotype 01/11/2015
2 257530 UTSW Ankrd17 1.000 R3012 G1 225 N 5 90230868 P2563S G A missense Het probably damaging 0.996 phenotype 01/11/2015
3 257545 UTSW Atg10 0.078 R3012 G1 225 N 13 91154278 F47Y A T missense Het probably damaging 0.994 phenotype 01/11/2015
4 257526 UTSW Ccdc39 0.324 R3012 G1 225 N 3 33814668 R798Q C T missense Het probably damaging 1.000 0.647 phenotype 01/11/2015
5 257527 UTSW Cfi 0.000 R3012 G1 225 N 3 129874930 D535G A G missense Het probably damaging 1.000 phenotype 01/11/2015
6 257549 UTSW Dgat1 0.757 R3012 G1 225 N 15 76503393 Q308H T A missense Het possibly damaging 0.900 phenotype 01/11/2015
7 257544 UTSW Dsp 1.000 R3012 G1 225 N 13 38193342 I1701T T C missense Het possibly damaging 0.605 phenotype 01/11/2015
8 257531 UTSW E330009J07Rik 0.146 R3012 G1 160 N 6 40435992 E45G T C missense Het probably benign 0.000 01/11/2015
9 257541 UTSW Egr2 1.000 R3012 G1 217 N 10 67539903 GAA GA frame shift Het probably null 0.976 phenotype 01/11/2015
10 257534 UTSW Fes 0.000 R3012 G1 225 N 7 80387167 S56R G C missense Het possibly damaging 0.806 phenotype 01/11/2015
11 257543 UTSW Gria1 0.000 R3012 G1 225 N 11 57289434 V737M G A missense Het probably damaging 0.999 phenotype 01/11/2015
12 257533 UTSW Gtf2h1 0.966 R3012 G1 225 N 7 46803895 H84R A G missense Het probably damaging 1.000 01/11/2015
13 257525 UTSW Ifi208 0.000 R3012 G1 225 N 1 173695570 A G critical splice acceptor site Het probably null 01/11/2015
14 257537 UTSW Il15 0.000 R3012 G1 225 N 8 82344420 N22I T A missense Het probably damaging 0.999 phenotype 01/11/2015
15 257539 UTSW Me1 0.000 R3012 G1 225 N 9 86611912 S323P A G missense Het probably benign 0.001 phenotype 01/11/2015
16 257535 UTSW Olfr713 0.060 R3012 G1 225 N 7 107036362 F69S T C missense Het possibly damaging 0.787 phenotype 01/11/2015
17 257546 UTSW Parp4 0.165 R3012 G1 225 N 14 56595416 T C critical splice donor site 2 bp Het probably null phenotype 01/11/2015
18 477403 UTSW Pcdhga7 0.292 R3012 G1 225 N 18 37715638 T233A A G missense Het probably benign 0.010 phenotype 05/15/2017
19 257542 UTSW Rab36 0.000 R3012 G1 225 N 10 75044496 V63I G A missense Het probably damaging 1.000 0.209 01/11/2015
20 257528 UTSW Rpe65 0.201 R3012 G1 225 N 3 159604563 V128F G T missense Het possibly damaging 0.612 phenotype 01/11/2015
21 257536 UTSW Slc5a11 0.075 R3012 G1 217 N 7 123239372 GGTGC G frame shift Het probably null phenotype 01/11/2015
22 257540 UTSW Tbc1d32 0.868 R3012 G1 225 N 10 56173915 V509A A G missense Het probably benign 0.081 phenotype 01/11/2015
23 257529 UTSW Tln1 1.000 R3012 G1 225 N 4 43542525 T1428S T A missense Het probably benign 0.000 phenotype 01/11/2015
24 257550 UTSW Ttc27 0.960 R3012 G1 225 N 17 74840459 I669F A T missense Het probably benign 0.170 01/11/2015
25 257538 UTSW Tubb3 1.000 R3012 G1 225 N 8 123421236 C303G T G missense Het probably damaging 0.997 phenotype 01/11/2015
26 257532 UTSW Tulp2 0.086 R3012 G1 225 N 7 45518763 V188L G T missense Het probably damaging 0.998 phenotype 01/11/2015
27 257547 UTSW Zfr 1.000 R3012 G1 225 N 15 12166163 Y840H T C missense Het probably damaging 1.000 phenotype 01/11/2015
[records 1 to 27 of 27]