Incidental Mutations

28 incidental mutations are currently displayed, and affect 28 genes.

7 are Possibly Damaging.

12 are Probably Damaging.

6 are Probably Benign.

3 are Probably Null.

1 create premature stop codons.

1 are critical splice junction mutations.

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

[records 1 to 28 of 28] 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	75911		Adgre5	0.000	IGL01365	G1				8	83723889 (GRCm38)		G	T	splice site		Het	probably null			phenotype	2013-10-07
2	75895		Agtr1a	0.000	IGL01365	G1				13	30381828 (GRCm38)	Y292C	A	G	missense		Het	probably damaging	1.000		phenotype	2013-10-07
3	75919		Btbd11	0.174	IGL01365	G1				10	85633816 (GRCm38)	V867A	T	C	missense		Het	possibly damaging	0.745			2013-10-07
4	75901		CK137956	0.116	IGL01365	G1				4	127951342 (GRCm38)	S203P	A	G	missense		Het	probably benign	0.008			2013-10-07
5	75917		Cnbd1	0.000	IGL01365	G1				4	18860576 (GRCm38)	G390D	C	T	missense		Het	probably damaging	1.000			2013-10-07
6	75913		Cttnbp2nl	0.306	IGL01365	G1				3	105005030 (GRCm38)	T513A	T	C	missense		Het	probably damaging	0.998			2013-10-07
7	75906		Dppa2	0.102	IGL01365	G1				16	48313913 (GRCm38)	K67R	A	G	missense		Het	possibly damaging	0.828			2013-10-07
8	75916		Kif3a	1.000	IGL01365	G1				11	53593523 (GRCm38)	K486E	A	G	missense		Het	possibly damaging	0.528		phenotype	2013-10-07
9	75903		Lmnb2	1.000	IGL01365	G1				10	80904984 (GRCm38)	Q151K	G	T	missense		Het	probably benign	0.067		phenotype	2013-10-07
10	75896		Lmtk3	0.452	IGL01365	G1				7	45790907 (GRCm38)	L223Q	T	A	missense		Het	probably damaging	1.000		phenotype	2013-10-07
11	75908		Lrrk1	1.000	IGL01365	G1				7	66287701 (GRCm38)	I901T	A	G	missense		Het	probably damaging	1.000		phenotype	2013-10-07
12	75918		Macf1	1.000	IGL01365	G1				4	123391169 (GRCm38)	Y3624C	T	C	missense		Het	probably damaging	1.000		phenotype	2013-10-07
13	75909		Mios	0.947	IGL01365	G1				6	8216089 (GRCm38)	Y428*	T	A	nonsense		Het	probably null				2013-10-07
14	75899		Myb	1.000	IGL01365	G1				10	21152502 (GRCm38)	I154T	A	G	missense		Het	probably benign	0.305		phenotype	2013-10-07
15	75900		Olfr294	0.123	IGL01365	G1				7	86615997 (GRCm38)	Y216C	T	C	missense		Het	probably damaging	1.000		phenotype	2013-10-07
16	75904		Parp9	0.187	IGL01365	G1				16	35947954 (GRCm38)	T168I	C	T	missense		Het	possibly damaging	0.713			2013-10-07
17	75920		Pramel7	0.070	IGL01365	G1				2	87491413 (GRCm38)		T	C	splice site		Het	probably benign				2013-10-07
18	75910		Ptar1	0.934	IGL01365	G1				19	23705801 (GRCm38)	W140R	T	A	missense		Het	probably damaging	1.000			2013-10-07
19	75898		Sec14l2	0.121	IGL01365	G1				11	4098317 (GRCm38)	D400E	G	T	missense		Het	probably benign	0.000		phenotype	2013-10-07
20	75915		Setd3	0.000	IGL01365	G1				12	108157906 (GRCm38)	Y175N	A	T	missense		Het	probably damaging	1.000			2013-10-07
21	75921		Slc5a8	0.000	IGL01365	G1				10	88892097 (GRCm38)		C	T	splice site		Het	probably benign			phenotype	2013-10-07
22	75912		Slc8a3	0.000	IGL01365	G1				12	81315376 (GRCm38)	V223A	A	G	missense		Het	probably damaging	0.986		phenotype	2013-10-07
23	75914		Srsf1	1.000	IGL01365	G1				11	88049181 (GRCm38)	R173L	G	T	missense		Het	possibly damaging	0.881		phenotype	2013-10-07
24	75922		Svep1	1.000	IGL01365	G1				4	58100878 (GRCm38)		T	A	critical splice acceptor site		Het	probably null			phenotype	2013-10-07
25	75905		Tead2	0.000	IGL01365	G1				7	45217251 (GRCm38)	D11E	T	A	missense		Het	probably damaging	0.964		phenotype	2013-10-07
26	75897		Trappc12	0.440	IGL01365	G1				12	28747402 (GRCm38)	I44F	T	A	missense		Het	probably damaging	1.000			2013-10-07
27	75907		Ttll9	0.059	IGL01365	G1				2	153000134 (GRCm38)	Y303H	T	C	missense		Het	possibly damaging	0.870			2013-10-07
28	75902		Vmn1r28	0.125	IGL01365	G1				6	58265191 (GRCm38)	N6K	T	A	missense		Het	possibly damaging	0.757			2013-10-07
[records 1 to 28 of 28]