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Incidental Mutations

39 incidental mutations are currently displayed, and affect 38 genes.

8 are Possibly Damaging.

16 are Probably Damaging.

11 are Probably Benign.

4 are Probably Null.

1 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 39 of 39] 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	84375		0610010F05Rik	0.214	IGL01444	G1				11	23620225		T	G	splice site		Het	probably benign				11/11/2013
2	84348		Adad1	0.242	IGL01444	G1				3	37092034	N517I	A	T	missense		Het	probably damaging	1.000		phenotype	11/11/2013
3	84347		Adam25	0.073	IGL01444	G1				8	40754921	R408H	G	A	missense		Het	probably benign	0.000		phenotype	11/11/2013
4	84344		Ang	0.195	IGL01444	G1				14	51101667	Y88*	C	A	nonsense		Het	probably null			phenotype	11/11/2013
5	84353		Ankrd42	0.071	IGL01444	G1				7	92610585	T327A	T	C	missense		Het	probably damaging	0.957			11/11/2013
6	84354		Birc6	1.000	IGL01444	G1				17	74631687	D2696G	A	G	missense		Het	probably damaging	0.998		phenotype	11/11/2013
7	84339		Chd3	0.000	IGL01444	G1				11	69348742	T1717M	G	A	missense		Het	probably benign	0.285		phenotype	11/11/2013
8	84362		Csmd1	0.000	IGL01444	G1				8	16200055	M970L	T	A	missense		Het	probably benign	0.001		phenotype	11/11/2013
9	84351		Dhx32	0.092	IGL01444	G1				7	133748977	I121M	T	C	missense		Het	possibly damaging	0.759		phenotype	11/11/2013
10	84356		Dnah11	0.690	IGL01444	G1				12	118020232	S2506F	G	A	missense		Het	possibly damaging	0.907		phenotype	11/11/2013
11	84361		Dscam	1.000	IGL01444	G1				16	96673709	I1218F	T	A	missense		Het	possibly damaging	0.951		phenotype	11/11/2013
12	84343		Duox1	0.000	IGL01444	G1				2	122340090	L1197P	T	C	missense		Het	probably damaging	0.980		phenotype	11/11/2013
13	84376		Eps8l2	0.000	IGL01444	G1				7	141361375		T	C	splice site		Het	probably benign			phenotype	11/11/2013
14	84340		Exoc3	0.968	IGL01444	G1				13	74206935	K49R	T	C	missense		Het	probably damaging	1.000		phenotype	11/11/2013
15	84349		Exoc8	1.000	IGL01444	G1				8	124895841	T596S	T	A	missense		Het	possibly damaging	0.842		phenotype	11/11/2013
16	84355		F13a1	0.000	IGL01444	G1				13	36918577	G391R	C	T	missense		Het	probably null	1.000		phenotype	11/11/2013
17	84371		Fam35a	0.135	IGL01444	G1				14	34237557	V823F	C	A	missense		Het	probably damaging	1.000			11/11/2013
18	84365		Fat3	0.568	IGL01444	G1				9	15998848	S1953T	A	T	missense		Het	probably damaging	0.997		phenotype	11/11/2013
19	84366		Gls2	0.000	IGL01444	G1				10	128201347	N252K	C	A	missense		Het	probably damaging	0.999		phenotype	11/11/2013
20	84345		Gm5346	0.054	IGL01444	G1				8	43626433	D251E	A	T	missense		Het	probably benign	0.058			11/11/2013
21	84373		Haus2	0.942	IGL01444	G1				2	120615942	R115K	G	A	missense		Het	probably benign	0.002		phenotype	11/11/2013
22	84369		Ift122	1.000	IGL01444	G1				6	115884379	K262E	A	G	missense		Het	probably benign	0.083		phenotype	11/11/2013
23	84358		Islr2	1.000	IGL01444	G1				9	58198378	C533Y	C	T	missense		Het	probably damaging	1.000		phenotype	11/11/2013
24	84367		Lrp2	1.000	IGL01444	G1				2	69443716	F3997I	A	T	missense		Het	possibly damaging	0.936		phenotype	11/11/2013
25	84357		Nt5c1a	0.124	IGL01444	G1				4	123216169	R354W	C	T	missense		Het	probably damaging	0.997		phenotype	11/11/2013
26	84341		Olfr776	0.055	IGL01444	G1				10	129261335	C125S	T	A	missense		Het	probably damaging	1.000		phenotype	11/11/2013
27	84364		Pcolce	0.196	IGL01444	G1				5	137607476	S200R	A	T	missense		Het	probably damaging	0.980		phenotype	11/11/2013
28	84346		Plec	0.879	IGL01444	G1				15	76179297	V2213A	A	G	missense		Het	possibly damaging	0.455		phenotype	11/11/2013
29	84350		Prmt3	0.647	IGL01444	G1				7	49780372	D74E	T	A	missense		Het	probably benign	0.001		phenotype	11/11/2013
30	84372		Ptk7	1.000	IGL01444	G1				17	46565387	F1046S	A	G	missense		Het	probably damaging	1.000		phenotype	11/11/2013
31	84342		Ranbp2	1.000	IGL01444	G1				10	58475300	Y887H	T	C	missense		Het	possibly damaging	0.790		phenotype	11/11/2013
32	84360		Sez6l2	0.000	IGL01444	G1				7	126961883	E447K	G	A	missense		Het	possibly damaging	0.912		phenotype	11/11/2013
33	84374		Snrnp70	0.969	IGL01444	G1				7	45387236		C	T	unclassified	154 bp	Het	probably null			phenotype	11/11/2013
34	84368		Timm10	0.973	IGL01444	G1				2	84829864	V49E	T	A	missense		Het	probably damaging	1.000		phenotype	11/11/2013
35	84377		Tox2	0.000	IGL01444	G1				2	163225466		T	C	utr 5 prime		Het	probably benign				11/11/2013
36	84363		Usp20	0.000	IGL01444	G1				2	30998789	M1K	T	A	start codon destroyed		Het	probably null	1.000		phenotype	11/11/2013
37	84370		Usp32	1.000	IGL01444	G1				11	85059164	L223V	A	C	missense		Het	probably damaging	0.966			11/11/2013
38	84359		Zeb1	0.907	IGL01444	G1				18	5767138	S550P	T	C	missense		Het	probably benign	0.000	0.061	phenotype	11/11/2013
39	84352		Zeb1	0.907	IGL01444	G1				18	5767906	A806S	G	T	missense		Het	probably damaging	0.997		phenotype	11/11/2013
[records 1 to 39 of 39]