Incidental Mutations

38 incidental mutations are currently displayed, and affect 38 genes.
6 are Possibly Damaging.
12 are Probably Damaging.
14 are Probably Benign.
6 are Probably Null.
2 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 38 of 38] 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 416949 APN 9930111J21Rik1 0.130 IGL03334 11 48947475 F762L A G missense Het probably benign 0.085 08/02/2016
2 416976 APN A430078G23Rik 0.025 IGL03334 8 3388023 I286F A T missense Het probably benign 0.038 08/02/2016
3 416959 APN Angpt1 1.000 IGL03334 15 42496412 E208V T A missense Het possibly damaging 0.938 phenotype 08/02/2016
4 416961 APN Arhgef5 0.000 IGL03334 6 43274000 S562P T C missense Het possibly damaging 0.465 phenotype 08/02/2016
5 416972 APN Asb6 0.345 IGL03334 2 30824484 T205A T C missense Het probably benign 0.026 phenotype 08/02/2016
6 416982 APN B4galnt4 0.492 IGL03334 7 141067441 G A splice site 5 bp Het probably null 08/02/2016
7 416956 APN Clca4a 0.260 IGL03334 3 144953866 M743K A T missense Het probably benign 0.283 08/02/2016
8 416954 APN Col14a1 0.000 IGL03334 15 55448821 T C unclassified Het probably benign phenotype 08/02/2016
9 416960 APN Col27a1 1.000 IGL03334 4 63314722 Y359F A T missense Het probably damaging 1.000 phenotype 08/02/2016
10 416971 APN Dhcr7 1.000 IGL03334 7 143840497 V125D T A missense Het possibly damaging 0.795 phenotype 08/02/2016
11 416984 APN Ercc3 1.000 IGL03334 18 32240837 T C critical splice donor site 2 bp Het probably null phenotype 08/02/2016
12 416977 APN Fnbp1l 0.453 IGL03334 3 122557949 V315A A G missense Het probably benign 0.002 08/02/2016
13 416953 APN Gm17174 IGL03334 14 51591963 R48* T A nonsense Het probably null 08/02/2016
14 416979 APN Golga4 0.000 IGL03334 9 118537233 C T splice site Het probably benign phenotype 08/02/2016
15 416981 APN Grin1 1.000 IGL03334 2 25298393 C T critical splice donor site 1 bp Het probably null phenotype 08/02/2016
16 416957 APN Ifi203 0.096 IGL03334 1 173937835 K58* T A nonsense Het probably null 08/02/2016
17 416950 APN Ighv2-9-1 IGL03334 12 113769923 S93P A G missense Het probably benign 0.038 08/02/2016
18 416974 APN Il27ra 0.078 IGL03334 8 84031122 V594A A G missense Het probably benign 0.081 phenotype 08/02/2016
19 416970 APN Krr1 0.864 IGL03334 10 111980054 S275R T G missense Het probably benign 0.446 08/02/2016
20 416965 APN Lars 0.931 IGL03334 18 42221506 D792G T C missense Het probably benign 0.000 phenotype 08/02/2016
21 416966 APN Myo1f 0.261 IGL03334 17 33598194 R737H G A missense Het probably damaging 1.000 phenotype 08/02/2016
22 416969 APN Nebl 0.289 IGL03334 2 17413711 H292L T A missense Het probably damaging 0.980 08/02/2016
23 416980 APN Nell1 1.000 IGL03334 7 50062611 C A splice site Het probably null phenotype 08/02/2016
24 416968 APN Nktr 0.340 IGL03334 9 121748176 F412L T C missense Het probably benign 0.177 phenotype 08/02/2016
25 416958 APN Nlrp3 0.059 IGL03334 11 59549016 I473N T A missense Het probably damaging 0.999 phenotype 08/02/2016
26 416948 APN Olfr338 0.038 IGL03334 2 36377051 Y92H T C missense Het possibly damaging 0.656 phenotype 08/02/2016
27 416964 APN Phf3 0.245 IGL03334 1 30805729 V1383A A G missense Het probably damaging 0.986 phenotype 08/02/2016
28 416962 APN Prss48 0.074 IGL03334 3 85997318 E191G T C missense Het probably damaging 0.999 08/02/2016
29 416951 APN Psg25 0.020 IGL03334 7 18529774 L41F T A missense Het probably benign 0.015 08/02/2016
30 416973 APN Sema3b 0.512 IGL03334 9 107604077 L78P A G missense Het probably damaging 1.000 phenotype 08/02/2016
31 416975 APN Spen 1.000 IGL03334 4 141469969 N3496K G T missense Het probably damaging 0.999 phenotype 08/02/2016
32 416967 APN Tbk1 1.000 IGL03334 10 121584199 H28Q A T missense Het possibly damaging 0.790 phenotype 08/02/2016
33 416983 APN Trpv3 0.137 IGL03334 11 73281665 T A splice site Het probably benign phenotype 08/02/2016
34 416952 APN Vmn1r218 0.079 IGL03334 13 23136618 L45P T C missense Het probably damaging 1.000 08/02/2016
35 416947 APN Vmn2r35 IGL03334 7 7786494 Y748F T A missense Het probably damaging 1.000 08/02/2016
36 416978 APN Vps18 1.000 IGL03334 2 119297482 R929W C T missense Het probably damaging 0.999 phenotype 08/02/2016
37 416963 APN Xpnpep1 1.000 IGL03334 19 53010146 K224E T C missense Het probably damaging 1.000 phenotype 08/02/2016
38 416955 APN Zbed5 0.305 IGL03334 5 129902355 F382I T A missense Het possibly damaging 0.663 phenotype 08/02/2016
[records 1 to 38 of 38]