Incidental Mutations

34 incidental mutations are currently displayed, and affect 33 genes.

1 are Possibly Damaging.

16 are Probably Damaging.

13 are Probably Benign.

4 are Probably Null.

2 create premature stop codons.

0 are critical splice junction mutations.

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Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing

[records 1 to 34 of 34] 10 25 50 100 500 1000 per page Full List
	ID	Source UTSW APN	Gene	E-score	Stock #	Gen G0 G0' G1 G2 G3 G3R F1 F2 F3 C0 C1 C2 C3 D1 HES IPS A3 ABI	Quality -	Vld Y N ?	Strain	Chr 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 X Y	Position	Mutation A R N D C E Q G H I L K M F P S T W Y V * A R N D C E Q G H I L K M F P S T W Y V *	Ref A C G T -	Var A C G T -	Type makesense missense nonsense start codon destroyed start gained synonymous splice acceptor site splice donor site critical splice acceptor site critical splice donor site splice site large deletion large insertion rearrangement small deletion small insertion exon frame shift intragenic intron utr 3 prime utr 5 prime unclassified	Exon Dist	Zygosity Homo Het Hemi Null	Predicted Effect unknown probably benign probably null possibly damaging probably damaging noncoding transcript silent not run no transcript	PPH Score -	Meta Score	MGI Phenotype available none listed	Posted
1	409923		Abcb1a	0.151	IGL03119					5	8714887 (GRCm38)	T626A	A	G	missense		Het	probably benign	0.002		phenotype	2016-08-02
2	409897		Adcy1	0.000	IGL03119					11	7109051 (GRCm38)	T319I	C	T	missense		Het	probably damaging	0.999		phenotype	2016-08-02
3	409906		Adgrv1	0.000	IGL03119					13	81382373 (GRCm38)	S5861P	A	G	missense		Het	probably damaging	0.998		phenotype	2016-08-02
4	409909		Adgrv1	0.000	IGL03119					13	81433700 (GRCm38)	C4742G	A	C	missense		Het	probably benign	0.018		phenotype	2016-08-02
5	409920		Arid5b	0.942	IGL03119					10	68243227 (GRCm38)	D93E	A	T	missense		Het	probably damaging	1.000		phenotype	2016-08-02
6	409904		Atp6v1h	1.000	IGL03119					1	5095669 (GRCm38)	T121A	A	G	missense		Het	probably benign	0.338		phenotype	2016-08-02
7	409915		Atxn7	0.000	IGL03119					14	14100734 (GRCm38)	L807F	C	T	missense		Het	probably damaging	1.000		phenotype	2016-08-02
8	409919		Cep104	0.369	IGL03119					4	153981724 (GRCm38)	K126N	A	C	missense		Het	probably damaging	0.996		phenotype	2016-08-02
9	409917		Dcaf6	0.000	IGL03119					1	165339976 (GRCm38)	E708G	T	C	missense		Het	probably damaging	0.999			2016-08-02
10	409925		Dst	0.231	IGL03119					1	34161062 (GRCm38)	Y107C	A	G	missense		Het	probably damaging	1.000		phenotype	2016-08-02
11	409914		E2f3	1.000	IGL03119					13	29985365 (GRCm38)	S102P	A	G	missense		Het	probably benign	0.208		phenotype	2016-08-02
12	409901		Eif3e	0.961	IGL03119					15	43265604 (GRCm38)	S207A	A	C	missense		Het	probably benign	0.000			2016-08-02
13	409912		Etl4	0.783	IGL03119					2	20713387 (GRCm38)	Y313C	A	G	missense		Het	probably damaging	1.000	0.468	phenotype	2016-08-02
14	409910		Fyttd1	0.144	IGL03119					16	32900695 (GRCm38)	V121A	T	C	missense		Het	probably benign	0.077			2016-08-02
15	409913		Gstk1	0.104	IGL03119					6	42249899 (GRCm38)	S200P	T	C	missense		Het	probably damaging	1.000		phenotype	2016-08-02
16	409898		Ifrd1	0.669	IGL03119					12	40212334 (GRCm38)	F244L	A	T	missense		Het	probably null	0.029		phenotype	2016-08-02
17	409922		Ints7	0.949	IGL03119					1	191610365 (GRCm38)	V491A	T	C	missense		Het	probably damaging	0.997		phenotype	2016-08-02
18	409911		Kcnd2	0.094	IGL03119					6	21216509 (GRCm38)	E71*	G	T	nonsense		Het	probably null			phenotype	2016-08-02
19	409918		Ltbp3	0.190	IGL03119					19	5757443 (GRCm38)	Q1123L	A	T	missense		Het	probably damaging	0.978		phenotype	2016-08-02
20	409921		Myo5a	0.951	IGL03119					9	75174015 (GRCm38)	T961A	A	G	missense		Het	probably benign	0.012	0.060	phenotype	2016-08-02
21	409900		Naa25	1.000	IGL03119					5	121434978 (GRCm38)	V720E	T	A	missense		Het	probably null	0.999		phenotype	2016-08-02
22	409895		Olfr1480	0.065	IGL03119					19	13530435 (GRCm38)	I298T	T	C	missense		Het	probably benign	0.109		phenotype	2016-08-02
23	409903		Olfr599	0.056	IGL03119					7	103338722 (GRCm38)	I223V	A	G	missense		Het	probably damaging	0.997		phenotype	2016-08-02
24	409896		Pcdhb15	0.067	IGL03119					18	37475014 (GRCm38)	T433N	C	A	missense		Het	probably damaging	0.999		phenotype	2016-08-02
25	409928		Peli1	0.000	IGL03119					11	21140560 (GRCm38)		T	C	splice site		Het	probably benign			phenotype	2016-08-02
26	409924		Ptbp1	1.000	IGL03119					10	79859624 (GRCm38)	V209A	T	C	missense		Het	probably damaging	0.999		phenotype	2016-08-02
27	409908		Ranbp2	1.000	IGL03119					10	58452003 (GRCm38)	Y31C	A	G	missense		Het	probably damaging	0.998		phenotype	2016-08-02
28	409916		Smg1	1.000	IGL03119					7	118195113 (GRCm38)		G	A	utr 3 prime		Het	probably benign			phenotype	2016-08-02
29	409899		Stat2	0.395	IGL03119					10	128283517 (GRCm38)	M457V	A	G	missense		Het	probably benign	0.148		phenotype	2016-08-02
30	409907		Trpm6	1.000	IGL03119					19	18838017 (GRCm38)	E1156*	G	T	nonsense		Het	probably null			phenotype	2016-08-02
31	409927		Usp53	0.230	IGL03119					3	122961415 (GRCm38)	R130S	T	A	missense		Het	possibly damaging	0.803		phenotype	2016-08-02
32	409926		Vwa5b1	0.000	IGL03119					4	138606541 (GRCm38)	S193P	A	G	missense		Het	probably benign	0.012			2016-08-02
33	409902		Xrn2	0.964	IGL03119					2	147042872 (GRCm38)	I626V	A	G	missense		Het	probably damaging	0.995		phenotype	2016-08-02
34	409905		Zfp574	0.959	IGL03119					7	25080473 (GRCm38)	A307T	G	A	missense		Het	probably benign	0.000			2016-08-02
[records 1 to 34 of 34]