Incidental Mutations

27 incidental mutations are currently displayed, and affect 27 genes.

1 are Possibly Damaging.

13 are Probably Damaging.

12 are Probably Benign.

1 are Probably Null.

0 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 27 of 27] 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	157622		1700021F07Rik	0.053	R1319	G1	225	N		2	173527923 (GRCm38)	S77C	A	T	missense		Het	probably damaging	0.981			2014-02-18
2	157644		Adam28	0.159	R1319	G1	225	N		14	68609129 (GRCm38)	E745G	T	C	missense		Het	probably benign	0.278		phenotype	2014-02-18
3	157645		Adamts12	0.095	R1319	G1	225	N		15	11286791 (GRCm38)	K827N	G	T	missense		Het	probably benign	0.021		phenotype	2014-02-18
4	157643		Ang2	0.062	R1319	G1	225	N		14	51195707 (GRCm38)	T73A	T	C	missense		Het	probably benign	0.024			2014-02-18
5	157638		Bbs10	1.000	R1319	G1	155	N		10	111298874 (GRCm38)	L51P	T	C	missense		Het	probably damaging	1.000		phenotype	2014-02-18
6	157633		Bean1	0.000	R1319	G1	225	N		8	104217224 (GRCm38)	I137T	T	C	missense		Het	probably benign	0.000		phenotype	2014-02-18
7	157628		Cttnbp2	0.000	R1319	G1	225	N		6	18434630 (GRCm38)	T410A	T	C	missense		Het	probably benign	0.001		phenotype	2014-02-18
8	157626		Cyp4a10	0.082	R1319	G1	225	N		4	115521145 (GRCm38)	I143L	A	C	missense		Het	probably damaging	0.978		phenotype	2014-02-18
9	157631		Dlg2	0.000	R1319	G1	225	N		7	92438023 (GRCm38)	Q788L	A	T	missense		Het	probably damaging	0.977		phenotype	2014-02-18
10	157627		Epha10	0.000	R1319	G1	225	N		4	124881914 (GRCm38)	V14I	G	A	missense		Het	probably benign	0.000		phenotype	2014-02-18
11	157620		Eprs	1.000	R1319	G1	225	N		1	185384962 (GRCm38)	D401N	G	A	missense		Het	probably damaging	1.000		phenotype	2014-02-18
12	157642		Fam169a	0.077	R1319	G1	225	N		13	97097562 (GRCm38)	V114A	T	C	missense		Het	probably damaging	0.996			2014-02-18
13	157649		Fbn2	0.902	R1319	G1	225	N		18	58200610 (GRCm38)	P178S	G	A	missense		Het	possibly damaging	0.880		phenotype	2014-02-18
14	157624		Fcrls	0.053	R1319	G1	124	N		3	87262177 (GRCm38)		A	C	critical splice donor site	2 bp	Het	probably null			phenotype	2014-02-18
15	157635		Grm1	0.389	R1319	G1	119	N		10	10689398 (GRCm38)	H1055Q	G	T	missense		Het	probably benign	0.047		phenotype	2014-02-18
16	157619		Mcm6	1.000	R1319	G1	215	N		1	128349052 (GRCm38)	N267S	T	C	missense		Het	probably benign	0.000		phenotype	2014-02-18
17	157650		Olfr262	0.100	R1319	G1	225	N		19	12241502 (GRCm38)	D53G	T	C	missense		Het	probably damaging	0.997		phenotype	2014-02-18
18	157623		Phc3	0.000	R1319	G1	225	N		3	30929869 (GRCm38)	I699V	T	C	missense		Het	probably damaging	0.971			2014-02-18
19	157641		Prl2c2	0.148	R1319	G1	156	N		13	13002201 (GRCm38)	T47R	G	C	missense		Het	probably damaging	0.983	0.647		2014-02-18
20	157629		Pyroxd1	1.000	R1319	G1	210	N		6	142359148 (GRCm38)	V367A	T	C	missense		Het	probably benign	0.331			2014-02-18
21	157618		R3hdm1	0.000	R1319	G1	225	N		1	128231405 (GRCm38)	R939H	G	A	missense		Het	probably benign	0.009			2014-02-18
22	157621		Rag1	0.509	R1319	G1	225	N		2	101643192 (GRCm38)	I535N	A	T	missense		Het	probably damaging	0.997		phenotype	2014-02-18
23	157640		Rhot1	1.000	R1319	G1	225	N		11	80246021 (GRCm38)	C310R	T	C	missense		Het	probably damaging	0.982		phenotype	2014-02-18
24	157632		Tnrc6a	0.821	R1319	G1	225	N		7	123184251 (GRCm38)	V1481M	G	A	missense		Het	probably benign	0.017		phenotype	2014-02-18
25	157646		Vmn1r234	0.051	R1319	G1	225	N		17	21228910 (GRCm38)	M29L	A	T	missense		Het	probably benign	0.011			2014-02-18
26	157630		Vmn2r68	0.073	R1319	G1	225	N		7	85232492 (GRCm38)	I460T	A	G	missense		Het	probably damaging	0.959			2014-02-18
27	157634		Zfhx3	0.924	R1319	G1	202	N		8	108933833 (GRCm38)	Y1240N	T	A	missense		Het	probably damaging	0.993		phenotype	2014-02-18
[records 1 to 27 of 27]