Incidental Mutations

32 incidental mutations are currently displayed, and affect 32 genes.

6 are Possibly Damaging.

12 are Probably Damaging.

9 are Probably Benign.

4 are Probably Null.

3 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 32 of 32] 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	102872		4933421I07Rik	0.054	IGL01653	G1				7	42446974 (GRCm38)	D119G	T	C	missense		Het	probably damaging	1.000			2014-01-21
2	102896		5430403G16Rik	0.111	IGL01653	G1				5	109677316 (GRCm38)	Y89*	A	C	nonsense		Het	probably null				2014-01-21
3	102881		Apol7c	0.050	IGL01653	G1				15	77526300 (GRCm38)	C149R	A	G	missense		Het	probably damaging	1.000			2014-01-21
4	102877		Arfgef1	1.000	IGL01653	G1				1	10159908 (GRCm38)	R1235*	G	A	nonsense		Het	probably null			phenotype	2014-01-21
5	102882		Bpifb4	0.050	IGL01653	G1				2	153944783 (GRCm38)	D285G	A	G	missense		Het	probably damaging	0.998			2014-01-21
6	102878		Cep192	0.000	IGL01653	G1				18	67852972 (GRCm38)	H1682Q	T	A	missense		Het	possibly damaging	0.569			2014-01-21
7	102874		Cerk	0.073	IGL01653	G1				15	86149351 (GRCm38)	Y290*	G	T	nonsense		Het	probably null			phenotype	2014-01-21
8	102897		Cyld	0.000	IGL01653	G1				8	88741370 (GRCm38)	I544F	A	T	missense		Het	probably damaging	0.997		phenotype	2014-01-21
9	102893		Dcp1a	0.293	IGL01653	G1				14	30505571 (GRCm38)	S134P	T	C	missense		Het	possibly damaging	0.521		phenotype	2014-01-21
10	332105		Epha6	0.000	IGL01653	G1				16	59839303 (GRCm38)	N817K	A	C	missense		Het	probably benign	0.047		phenotype	2015-08-05
11	102900		Ephb4	1.000	IGL01653	G1				5	137365741 (GRCm38)		A	G	splice site		Het	probably benign			phenotype	2014-01-21
12	102876		Fcgr3	0.000	IGL01653	G1				1	171059280 (GRCm38)	L25Q	A	T	missense		Het	probably damaging	1.000		phenotype	2014-01-21
13	102885		Heatr3	0.929	IGL01653	G1				8	88144617 (GRCm38)	I83V	A	G	missense		Het	probably benign	0.000		phenotype	2014-01-21
14	102895		Hormad1	0.000	IGL01653	G1				3	95578297 (GRCm38)	N265K	T	A	missense		Het	possibly damaging	0.489		phenotype	2014-01-21
15	102880		Kpna1	0.516	IGL01653	G1				16	36020192 (GRCm38)	T201A	A	G	missense		Het	probably benign	0.000		phenotype	2014-01-21
16	102894		Krt6b	0.147	IGL01653	G1				15	101679114 (GRCm38)	T182S	T	A	missense		Het	probably damaging	0.999			2014-01-21
17	102890		Macc1	0.070	IGL01653	G1				12	119450353 (GRCm38)	K755E	A	G	missense		Het	probably damaging	0.995		phenotype	2014-01-21
18	102884		Med12l	0.271	IGL01653	G1				3	59261893 (GRCm38)	T1568M	C	T	missense		Het	probably damaging	1.000		phenotype	2014-01-21
19	102899		Muc4	0.099	IGL01653	G1				16	32761348 (GRCm38)		G	T	splice site	5 bp	Het	probably null			phenotype	2014-01-21
20	102883		Myt1l	0.000	IGL01653	G1				12	29910771 (GRCm38)	S1028P	T	C	missense		Het	unknown			phenotype	2014-01-21
21	102887		Nhlrc2	1.000	IGL01653	G1				19	56570850 (GRCm38)	R256C	C	T	missense		Het	probably benign	0.255			2014-01-21
22	102886		Olfr1230	0.072	IGL01653	G1				2	89297127 (GRCm38)	T48S	T	A	missense		Het	probably benign	0.084		phenotype	2014-01-21
23	102875		Olfr1441	0.121	IGL01653	G1				19	12422372 (GRCm38)	R21H	G	A	missense		Het	probably benign	0.000		phenotype	2014-01-21
24	102879		Pfkfb4	0.000	IGL01653	G1				9	108999134 (GRCm38)	R79H	G	A	missense		Het	probably damaging	1.000		phenotype	2014-01-21
25	102898		Piezo2	1.000	IGL01653	G1				18	63182833 (GRCm38)		T	C	splice site		Het	probably benign			phenotype	2014-01-21
26	102871		Pramel5	0.104	IGL01653	G1				4	144273859 (GRCm38)	R49H	C	T	missense		Het	probably benign	0.015			2014-01-21
27	102889		Ralgapb	1.000	IGL01653	G1				2	158462159 (GRCm38)	S613T	T	A	missense		Het	possibly damaging	0.942			2014-01-21
28	102888		Ryr1	1.000	IGL01653	G1				7	29078597 (GRCm38)	E2158G	T	C	missense		Het	probably damaging	0.989		phenotype	2014-01-21
29	102873		Scgb2b19	0.033	IGL01653	G1				7	33279728 (GRCm38)	Y43F	T	A	missense		Het	probably damaging	0.987			2014-01-21
30	102892		Slc17a6	1.000	IGL01653	G1				7	51668022 (GRCm38)	T468A	A	G	missense		Het	possibly damaging	0.922		phenotype	2014-01-21
31	102870		Slc36a1	0.633	IGL01653	G1				11	55228321 (GRCm38)	D374G	A	G	missense		Het	possibly damaging	0.734		phenotype	2014-01-21
32	102891		Wdtc1	0.000	IGL01653	G1				4	133295232 (GRCm38)	D601G	T	C	missense		Het	probably damaging	1.000		phenotype	2014-01-21
[records 1 to 32 of 32]