Incidental Mutations

15 incidental mutations are currently displayed, and affect 15 genes.

3 are Possibly Damaging.

3 are Probably Damaging.

7 are Probably Benign.

2 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 15 of 15] 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	151621		Aak1	0.416	R1262	G1	225	N		6	86935488 (GRCm38)	V114A	T	C	missense		Het	probably benign	0.092		phenotype	2014-01-29
2	151624		BC048679	0.056	R1262	G1	152	N		7	81495341 (GRCm38)	F85L	A	G	missense		Het	probably benign	0.000			2014-01-29
3	151628		Btbd7	0.447	R1262	G1	225	N		12	102787951 (GRCm38)	I852T	A	G	missense		Het	probably benign	0.000			2014-01-29
4	151629		Cenpk	0.817	R1262	G1	225	N		13	104230785 (GRCm38)	V43E	T	A	missense		Het	possibly damaging	0.896		phenotype	2014-01-29
5	151631		Chmp7	1.000	R1262	G1	225	N		14	69719450 (GRCm38)	M336I	C	T	missense		Het	probably benign	0.380	0.114		2014-01-29
6	151622		Cyp2b10	0.134	R1262	G1	225	N		7	25915411 (GRCm38)	T281M	C	T	missense		Het	probably benign	0.155		phenotype	2014-01-29
7	151627		Lrriq1	0.088	R1262	G1	225	N		10	103234137 (GRCm38)	D6G	T	C	missense		Het	possibly damaging	0.871			2014-01-29
8	151632		Ltbp1	1.000	R1262	G1	225	N		17	75225285 (GRCm38)	Q118R	A	G	missense		Het	possibly damaging	0.752	0.110	phenotype	2014-01-29
9	151616		Nipsnap3b	0.072	R1262	G1	225	N		4	53015166 (GRCm38)	G71V	G	T	missense		Het	probably damaging	1.000		phenotype	2014-01-29
10	151625		Olfr623	0.154	R1262	G1	225	N		7	103660441 (GRCm38)	P270S	G	A	missense		Het	probably benign	0.333		phenotype	2014-01-29
11	262744		Olfr648	0.460	R1262	G1	141	N		7	104179416 (GRCm38)		A	G	splice site	40 bp	Het	probably null			phenotype	2015-02-04
12	151626		Snx25	1.000	R1262	G1	225	N		8	46105291 (GRCm38)	R80S	T	A	missense		Het	probably damaging	0.983			2014-01-29
13	151615		Syt6	0.102	R1262	G1	220	N		3	103585340 (GRCm38)		A	T	critical splice acceptor site		Het	probably null			phenotype	2014-01-29
14	151617		Tas1r2	0.090	R1262	G1	225	N		4	139655288 (GRCm38)	R79Q	G	A	missense		Het	probably damaging	0.993		phenotype	2014-01-29
15	151633		Ttc7	0.812	R1262	G1	225	N		17	87340936 (GRCm38)	T521I	C	T	missense		Het	probably benign	0.086		phenotype	2014-01-29
[records 1 to 15 of 15]