Incidental Mutations

37 incidental mutations are currently displayed, and affect 37 genes.
2 are Possibly Damaging.
16 are Probably Damaging.
13 are Probably Benign.
5 are Probably Null.
1 create premature stop codons.
3 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 37 of 37] 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 418404 APN 1700006A11Rik 0.091 IGL03092 3 124406470 (GRCm38) L491P A G missense Het probably damaging 0.999 2016-08-02
2 418431 APN 5430419D17Rik 0.000 IGL03092 7 131201798 (GRCm38) G T critical splice donor site 1 bp Het probably null 2016-08-02
3 418425 APN Abcc6 0.785 IGL03092 7 45986470 (GRCm38) D1051V T A missense Het probably damaging 1.000 phenotype 2016-08-02
4 418423 APN Aqr 1.000 IGL03092 2 114158943 (GRCm38) E133V T A missense Het probably benign 0.385 phenotype 2016-08-02
5 418412 APN Bag6 1.000 IGL03092 17 35145627 (GRCm38) N911D A G missense Het probably damaging 0.998 phenotype 2016-08-02
6 418420 APN BC024978 0.259 IGL03092 7 27201136 (GRCm38) M180T T C missense Het probably damaging 1.000 2016-08-02
7 418433 APN Ces4a 0.000 IGL03092 8 105148204 (GRCm38) C T splice site Het probably benign phenotype 2016-08-02
8 418435 APN Clec3b 0.000 IGL03092 9 123151035 (GRCm38) A T start gained Het probably benign phenotype 2016-08-02
9 418429 APN Cnot1 0.000 IGL03092 8 95769615 (GRCm38) T C intron Het probably benign phenotype 2016-08-02
10 418416 APN Ctsg 0.049 IGL03092 14 56099960 (GRCm38) *262L T A makesense Het probably null phenotype 2016-08-02
11 418419 APN Cyp17a1 0.243 IGL03092 19 46672611 (GRCm38) H78L T A missense Het possibly damaging 0.792 phenotype 2016-08-02
12 418428 APN Dcaf13 0.962 IGL03092 15 39127976 (GRCm38) C A splice site Het probably benign 2016-08-02
13 418411 APN Dcun1d1 0.719 IGL03092 3 35920992 (GRCm38) Q52K G T missense Het possibly damaging 0.883 2016-08-02
14 418410 APN Ddb1 1.000 IGL03092 19 10612945 (GRCm38) R279W C T missense Het probably damaging 0.999 phenotype 2016-08-02
15 418432 APN Dock1 1.000 IGL03092 7 134765216 (GRCm38) A G splice site Het probably benign phenotype 2016-08-02
16 418405 APN Dsel 0.111 IGL03092 1 111860063 (GRCm38) L914P A G missense Het probably damaging 0.999 phenotype 2016-08-02
17 418421 APN Fbxo31 0.000 IGL03092 8 121560018 (GRCm38) F174L A G missense Het probably benign 0.000 phenotype 2016-08-02
18 418422 APN Gm9116 0.311 IGL03092 3 93910206 (GRCm38) A G unclassified Het noncoding transcript 2016-08-02
19 418407 APN Gspt1 0.966 IGL03092 16 11238899 (GRCm38) V211I C T missense Het probably benign 0.107 2016-08-02
20 418418 APN Hmgb1 0.942 IGL03092 5 149050698 (GRCm38) S14T A T missense Het probably benign 0.245 phenotype 2016-08-02
21 418437 APN Igsf8 0.000 IGL03092 1 172312529 (GRCm38) A G intron Het probably benign phenotype 2016-08-02
22 418424 APN Klf13 0.167 IGL03092 7 63891669 (GRCm38) F237L A G missense Het probably damaging 0.999 phenotype 2016-08-02
23 418408 APN Mon2 0.938 IGL03092 10 123018100 (GRCm38) I962N A T missense Het probably damaging 1.000 2016-08-02
24 418414 APN Nfx1 0.542 IGL03092 4 41024851 (GRCm38) D1108G A G missense Het probably damaging 1.000 phenotype 2016-08-02
25 418413 APN Nr2e1 0.841 IGL03092 10 42571482 (GRCm38) Y178C T C missense Het probably damaging 0.999 phenotype 2016-08-02
26 418403 APN Olfr1426 0.110 IGL03092 19 12087866 (GRCm38) E309* C A nonsense Het probably null phenotype 2016-08-02
27 418402 APN Olfr646 0.182 IGL03092 7 104106647 (GRCm38) I123F A T missense Het probably damaging 0.991 phenotype 2016-08-02
28 418401 APN Pde3b 0.000 IGL03092 7 114523348 (GRCm38) H717L A T missense Het probably damaging 1.000 phenotype 2016-08-02
29 418417 APN Polr1b 1.000 IGL03092 2 129123129 (GRCm38) Y712H T C missense Het probably damaging 1.000 phenotype 2016-08-02
30 418426 APN Pramef25 0.053 IGL03092 4 143950197 (GRCm38) K112N C A missense Het probably damaging 0.967 2016-08-02
31 418436 APN Rnf157 0.000 IGL03092 11 116347969 (GRCm38) T A critical splice acceptor site Het probably null phenotype 2016-08-02
32 418415 APN Ros1 0.186 IGL03092 10 52098806 (GRCm38) E1561G T C missense Het probably damaging 0.988 phenotype 2016-08-02
33 418430 APN Serpina6 0.066 IGL03092 12 103653895 (GRCm38) A G critical splice donor site 2 bp Het probably null phenotype 2016-08-02
34 418427 APN St18 0.000 IGL03092 1 6768894 (GRCm38) A G splice site Het probably benign 2016-08-02
35 418434 APN Ugp2 0.000 IGL03092 11 21329722 (GRCm38) A G splice site Het probably benign phenotype 2016-08-02
36 418406 APN Vmn1r70 0.078 IGL03092 7 10634259 (GRCm38) S225P T C missense Het probably benign 0.229 2016-08-02
37 418409 APN Zfp641 0.000 IGL03092 15 98290516 (GRCm38) D161G T C missense Het probably damaging 0.997 2016-08-02
[records 1 to 37 of 37]