Incidental Mutations

34 incidental mutations are currently displayed, and affect 34 genes.
5 are Possibly Damaging.
12 are Probably Damaging.
14 are Probably Benign.
3 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 34 of 34] 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 388005 UTSW 4930407I10Rik 0.066 R5094 G1 225 Y 15 82062682 (GRCm38) G260V G T missense Het possibly damaging 0.720 0.179 2016-06-06
2 387981 UTSW Agap3 0.128 R5094 G1 182 Y 5 24451321 (GRCm38) T C unclassified Het probably benign 0.090 2016-06-06
3 387986 UTSW Bicra 0.127 R5094 G1 225 Y 7 15975371 (GRCm38) S1173P A G missense Het probably damaging 1.000 0.119 2016-06-06
4 452817 UTSW C3 0.000 R5094 G1 225 Y 17 57225033 (GRCm38) A T critical splice donor site 2 bp Het probably null 0.949 phenotype 2017-01-10
5 452816 UTSW Cdh18 0.096 R5094 G1 73 Y 15 22714539 (GRCm38) G A intron Het probably benign 0.090 phenotype 2017-01-10
6 387995 UTSW Cep290 0.902 R5094 G1 225 Y 10 100567030 (GRCm38) K2274E A G missense Het probably damaging 0.968 0.066 phenotype 2016-06-06
7 387994 UTSW Cfap54 0.072 R5094 G1 225 Y 10 92898999 (GRCm38) T C utr 3 prime Het probably benign 0.072 phenotype 2016-06-06
8 388004 UTSW Chat 0.849 R5094 G1 225 Y 14 32408939 (GRCm38) I582F T A missense Het probably damaging 0.998 0.612 phenotype 2016-06-06
9 387990 UTSW Chrnb4 0.082 R5094 G1 225 Y 9 55035313 (GRCm38) I226V T C missense Het probably benign 0.001 0.075 phenotype 2016-06-06
10 387980 UTSW Dnajc2 0.957 R5094 G1 225 Y 5 21776732 (GRCm38) T139A T C missense Het probably damaging 0.997 0.337 phenotype 2016-06-06
11 388001 UTSW Eml1 0.233 R5094 G1 225 Y 12 108536311 (GRCm38) F712S T C missense Het probably benign 0.112 0.500 phenotype 2016-06-06
12 387988 UTSW Fgfr1 1.000 R5094 G1 225 Y 8 25570165 (GRCm38) S524L C T missense Het probably damaging 1.000 0.117 phenotype 2016-06-06
13 387985 UTSW Gimap3 0.000 R5094 G1 225 Y 6 48765372 (GRCm38) E208G T C missense Het probably damaging 0.998 0.647 phenotype 2016-06-06
14 387997 UTSW Gm12185 0.079 R5094 G1 225 Y 11 48907548 (GRCm38) D706V T A missense Het probably benign 0.348 0.090 2016-06-06
15 387989 UTSW Gucy1a2 0.459 R5094 G1 225 Y 9 3865443 (GRCm38) V639D T A missense Het probably damaging 1.000 0.951 phenotype 2016-06-06
16 387992 UTSW Hivep2 0.869 R5094 G1 225 N 10 14132149 (GRCm38) F1497S T C missense Het probably benign 0.000 phenotype 2016-06-06
17 388007 UTSW Hunk 0.000 R5094 G1 225 Y 16 90496666 (GRCm38) D612G A G missense Het probably benign 0.013 0.090 phenotype 2016-06-06
18 388009 UTSW Ifit3b 0.069 R5094 G1 225 N 19 34612548 (GRCm38) S375T T A missense Het possibly damaging 0.925 2016-06-06
19 388006 UTSW Mucl1 0.055 R5094 G1 225 Y 15 103755403 (GRCm38) S13P A G missense Het possibly damaging 0.827 0.209 2016-06-06
20 387977 UTSW Olfr1051 0.053 R5094 G1 225 Y 2 86276040 (GRCm38) Y149F T A missense Het probably damaging 1.000 0.647 phenotype 2016-06-06
21 387978 UTSW Olfr1135 0.074 R5094 G1 225 Y 2 87671830 (GRCm38) C179Y C T missense Het possibly damaging 0.896 0.446 phenotype 2016-06-06
22 387993 UTSW Pah 0.000 R5094 G1 225 Y 10 87538219 (GRCm38) Y78* T A nonsense Het probably null 0.976 phenotype 2016-06-06
23 387996 UTSW Pex13 1.000 R5094 G1 225 Y 11 23655441 (GRCm38) V263A A G missense Het probably benign 0.003 0.060 phenotype 2016-06-06
24 387975 UTSW Pfdn2 1.000 R5094 G1 225 Y 1 171356499 (GRCm38) T A intron Het probably benign 0.090 phenotype 2016-06-06
25 387991 UTSW Phip 1.000 R5094 G1 225 Y 9 82871844 (GRCm38) V1616I C T missense Het probably benign 0.000 0.090 phenotype 2016-06-06
26 387984 UTSW Pigg 0.065 R5094 G1 225 Y 5 108336257 (GRCm38) S457G A G missense Het possibly damaging 0.904 0.072 phenotype 2016-06-06
27 388002 UTSW Ppp1r13b 0.849 R5094 G1 225 Y 12 111843610 (GRCm38) S97P A G missense Het probably benign 0.003 0.059 phenotype 2016-06-06
28 388008 UTSW Slc22a6 0.054 R5094 G1 221 Y 19 8626177 (GRCm38) L535P T C missense Het probably damaging 1.000 0.238 phenotype 2016-06-06
29 387982 UTSW Slc5a1 0.186 R5094 G1 225 Y 5 33158280 (GRCm38) T548A A G missense Het probably damaging 1.000 0.235 phenotype 2016-06-06
30 387998 UTSW Smtnl2 0.174 R5094 G1 225 Y 11 72400385 (GRCm38) S346C T A missense Het probably damaging 0.999 0.156 2016-06-06
31 388003 UTSW Spata31d1a 0.052 R5094 G1 225 Y 13 59705044 (GRCm38) A G critical splice donor site 2 bp Het probably null 0.919 2016-06-06
32 387999 UTSW Tlcd2 0.074 R5094 G1 225 Y 11 75469814 (GRCm38) S228P T C missense Het probably benign 0.003 0.072 2016-06-06
33 387987 UTSW Tmem135 0.172 R5094 G1 225 Y 7 89143793 (GRCm38) L411P A G missense Het probably damaging 0.999 0.751 2016-06-06
34 388000 UTSW Tnrc6c 0.000 R5094 G1 225 Y 11 117721046 (GRCm38) V170A T C missense Het probably benign 0.002 0.063 phenotype 2016-06-06
[records 1 to 34 of 34]