Incidental Mutations

13 incidental mutations are currently displayed, and affect 13 genes.

3 are Possibly Damaging.

6 are Probably Damaging.

3 are Probably Benign.

1 are Probably Null.

0 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 13 of 13] 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	246006		Ces1a	0.000	R2347	G1	225	N		8	93025319 (GRCm38)	V396M	C	T	missense		Het	probably benign	0.066	0.090		2014-10-30
2	246009		Ddx6	1.000	R2347	G1	225	N		9	44607591 (GRCm38)	K67E	A	G	missense		Het	probably benign	0.002		phenotype	2014-10-30
3	246004		Fut2	0.000	R2347	G1	225	N		7	45650328 (GRCm38)	D340G	T	C	missense		Het	probably damaging	0.994		phenotype	2014-10-30
4	246002		Gm128	0.000	R2347	G1	225	N		3	95240930 (GRCm38)	Y18H	A	G	missense		Het	probably benign	0.022		phenotype	2014-10-30
5	246001		Gon4l	0.759	R2347	G1	225	N		3	88863517 (GRCm38)	D502G	A	G	missense		Het	probably damaging	0.999		phenotype	2014-10-30
6	246013		Lman2	0.239	R2347	G1	225	N		13	55352999 (GRCm38)	N129I	T	A	missense		Het	possibly damaging	0.910		phenotype	2014-10-30
7	246012		Nsf	1.000	R2347	G1	225	N		11	103930752 (GRCm38)	E26K	C	T	missense		Het	possibly damaging	0.586	0.089		2014-10-30
8	245999		Olfr1263	0.070	R2347	G1	225	N		2	90015614 (GRCm38)	R228L	G	T	missense		Het	possibly damaging	0.822		phenotype	2014-10-30
9	246005		Olfr527	0.053	R2347	G1	225	N		7	140336147 (GRCm38)	M95K	T	A	missense		Het	probably damaging	0.983		phenotype	2014-10-30
10	246008		Olfr935	0.057	R2347	G1	225	N		9	38994509 (GRCm38)	*309K	A	T	makesense		Het	probably null			phenotype	2014-10-30
11	245998		Pappa2	0.000	R2347	G1	225	N		1	158765043 (GRCm38)	C1588F	C	A	missense		Het	probably damaging	1.000		phenotype	2014-10-30
12	246014		Piwil2	0.000	R2347	G1	127	N		14	70408917 (GRCm38)	D390G	T	C	missense		Het	probably damaging	0.979		phenotype	2014-10-30
13	246003		Rest	1.000	R2347	G1	225	N		5	77268593 (GRCm38)	Y218C	A	G	missense		Het	probably damaging	1.000		phenotype	2014-10-30
[records 1 to 13 of 13]