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Incidental Mutations

46 incidental mutations are currently displayed, and affect 45 genes.

7 are Possibly Damaging.

19 are Probably Damaging.

14 are Probably Benign.

5 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 46 of 46] 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	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	485158		Agbl1	0.000	R6117	G1	225.01	N		7	76698786	Y625C	A	G	missense		Het	probably damaging	1.000		phenotype	08/16/2017
2	485144		Ankmy1	0.076	R6117	G1	225.01	N		1	92861274		A	G	unclassified		Het	probably benign				08/16/2017
3	485150		Apmap	0.000	R6117	G1	225.01	N		2	150600332	T41A	T	C	missense		Het	probably benign	0.131			08/16/2017
4	485161		Cacna1a	0.921	R6117	G1	225.01	N		8	84614721	Y1804C	A	G	missense		Het	probably damaging	1.000		phenotype	08/16/2017
5	485145		Cacna1e	0.130	R6117	G1	225.01	N		1	154561791	I333N	A	T	missense		Het	possibly damaging	0.675		phenotype	08/16/2017
6	485186		Cdsn	1.000	R6117	G1	181.01	N		17	35555034	S153R	C	A	missense		Het	unknown			phenotype	08/16/2017
7	485182		Celsr1	0.782	R6117	G1	225.01	N		15	85932411	M1777K	A	T	missense		Het	probably benign	0.043		phenotype	08/16/2017
8	485185		Cmtr1	0.966	R6117	G1	225.01	N		17	29682165	M249V	A	G	missense		Het	probably benign	0.431			08/16/2017
9	485176		Cmya5	0.324	R6117	G1	225.01	N		13	93095166	L1138P	A	G	missense		Het	probably damaging	0.976			08/16/2017
10	485187		Crim1	1.000	R6117	G1	225.01	N		17	78303088	D324A	A	C	missense		Het	probably damaging	1.000		phenotype	08/16/2017
11	485151		Dmap1	1.000	R6117	G1	178.01	N		4	117675535		T	A	intron		Het	probably null			phenotype	08/16/2017
12	485174		Dnah17	0.000	R6117	G1	215.01	N		11	118119571	Y307C	T	C	missense		Het	probably benign	0.002		phenotype	08/16/2017
13	485181		Dnah5	0.808	R6117	G1	225.01	N		15	28270420	L956H	T	A	missense		Het	probably damaging	0.989		phenotype	08/16/2017
14	485167		Enpp3	0.220	R6117	G1	225.01	N		10	24787852	S537N	C	T	missense		Het	probably damaging	0.998		phenotype	08/16/2017
15	485153		Eya3	0.810	R6117	G1	225.01	N		4	132711862	L323Q	T	A	missense		Het	probably damaging	1.000		phenotype	08/16/2017
16	485190		Fads3	0.000	R6117	G1	225.01	N		19	10054267	H226L	A	T	missense		Het	probably damaging	1.000		phenotype	08/16/2017
17	485149		Flrt3	1.000	R6117	G1	225.01	N		2	140660445	D421V	T	A	missense		Het	possibly damaging	0.461		phenotype	08/16/2017
18	485146		Frmd4a	0.156	R6117	G1	225.01	N		2	4602249	V370A	T	C	missense		Het	possibly damaging	0.660		phenotype	08/16/2017
19	485147		Gapvd1	1.000	R6117	G1	225.01	N		2	34690459		T	C	splice site	3 bp	Het	probably null				08/16/2017
20	485178		Gm2178		R6117	G1	225.01	N		14	26514840		T	C	intron		Het	probably benign				08/16/2017
21	485156		Gm5592	0.061	R6117	G1	225.01	N		7	41288464	N390S	A	G	missense		Het	probably benign	0.002			08/16/2017
22	485155		Hoxa10	0.000	R6117	G1	225.01	N		6	52234820	R39*	T	A	nonsense		Het	probably null			phenotype	08/16/2017
23	485165		Kcnj1	0.074	R6117	G1	225.01	N		9	32397182	T281A	A	G	missense		Het	probably damaging	0.999		phenotype	08/16/2017
24	485180		Myo10	0.000	R6117	G1	225.01	N		15	25805659	Y1709H	T	C	missense		Het	probably benign	0.005		phenotype	08/16/2017
25	485171		Nacad	0.000	R6117	G1	225.01	N		11	6599810	D1127G	T	C	missense		Het	probably benign	0.002	0.090		08/16/2017
26	485177		Naip1	0.000	R6117	G1	225.01	N		13	100444737	M1L	T	A	start codon destroyed		Het	probably damaging	0.989		phenotype	08/16/2017
27	485152		Olfr1331	0.055	R6117	G1	225.01	N		4	118869144	Y121F	A	T	missense		Het	probably benign	0.394		phenotype	08/16/2017
28	485169		Olfr811	0.056	R6117	G1	225.01	N		10	129801820	A235V	G	A	missense		Het	probably damaging	1.000	0.302	phenotype	08/16/2017
29	485170		Olfr811	0.056	R6117	G1	225.01	N		10	129801821	A235S	C	A	missense		Het	probably damaging	1.000	0.163	phenotype	08/16/2017
30	485189		Pcdhb12	0.061	R6117	G1	112.01	N		18	37435642		G	A	intron		Het	probably benign				08/16/2017
31	485184		Pde1b	0.000	R6117	G1	225.01	N		15	103521482	V134A	T	C	missense		Het	probably damaging	0.994		phenotype	08/16/2017
32	485183		Plxnb2	0.943	R6117	G1	225.01	N		15	89158000	D1600E	A	T	missense		Het	probably benign	0.043		phenotype	08/16/2017
33	485163		Prss54	0.055	R6117	G1	225.01	N		8	95565458		T	A	splice site		Het	probably null			phenotype	08/16/2017
34	485148		Ryr3	0.385	R6117	G1	225.01	N		2	112635396	I4757N	A	T	missense		Het	probably damaging	1.000		phenotype	08/16/2017
35	485168		Slc1a6	0.092	R6117	G1	225.01	N		10	78788988	Y76H	T	C	missense		Het	possibly damaging	0.723		phenotype	08/16/2017
36	485157		Slco3a1	0.234	R6117	G1	225.01	N		7	74318506	D489N	C	T	missense		Het	probably benign	0.019	0.084		08/16/2017
37	485172		Sox15	0.000	R6117	G1	225.01	N		11	69655890	G173V	G	T	missense		Het	possibly damaging	0.903		phenotype	08/16/2017
38	485173		Stard3	0.000	R6117	G1	225.01	N		11	98372262	S48P	T	C	missense		Het	probably damaging	1.000		phenotype	08/16/2017
39	485160		Stk32c	0.000	R6117	G1	225.01	N		7	139122923	Q67*	G	A	nonsense		Het	probably null			phenotype	08/16/2017
40	485188		Svil	0.217	R6117	G1	225.01	N		18	5116016	W2101R	T	A	missense		Het	probably damaging	1.000		phenotype	08/16/2017
41	485166		Taar7e	0.105	R6117	G1	225.01	N		10	24038529	Y306N	T	A	missense		Het	probably damaging	0.976			08/16/2017
42	485164		Tarbp1	0.000	R6117	G1	225.01	N		8	126427541	M1485L	T	A	missense		Het	probably benign	0.002		phenotype	08/16/2017
43	485175		Togaram1	0.563	R6117	G1	225.01	N		12	64967487	D504G	A	G	missense		Het	probably damaging	0.999			08/16/2017
44	485154		Trrap	1.000	R6117	G1	225.01	N		5	144802961	L1091S	T	C	missense		Het	possibly damaging	0.777		phenotype	08/16/2017
45	485143		Unc80	0.891	R6117	G1	225.01	N		1	66675067	E2856G	A	G	missense		Het	possibly damaging	0.719		phenotype	08/16/2017
46	485159		Usp47	0.688	R6117	G1	225.01	N		7	112087932	T699M	C	T	missense		Het	probably damaging	0.976		phenotype	08/16/2017
[records 1 to 46 of 46]