Incidental Mutations

31 incidental mutations are currently displayed, and affect 31 genes.

6 are Possibly Damaging.

8 are Probably Damaging.

14 are Probably Benign.

2 are Probably Null.

1 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 31 of 31] 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	97432		Aldh1l2	0.000	R1117	G1	225	N		10	83508623 (GRCm38)	T353I	G	A	missense		Het	probably benign	0.012		phenotype	2014-01-05
2	97408		Arpc1b	0.000	R1117	G1	225	N		5	145125754 (GRCm38)	V226A	T	C	missense		Het	possibly damaging	0.950		phenotype	2014-01-05
3	97400		Casz1	1.000	R1117	G1	225	N		4	148934595 (GRCm38)	T451K	C	A	missense		Het	probably damaging	0.996		phenotype	2014-01-05
4	97430		Ccr4	0.000	R1117	G1	225	N		9	114492017 (GRCm38)	V327M	C	T	missense		Het	probably benign	0.004		phenotype	2014-01-05
5	97386		Cntrl	0.864	R1117	G1	225	N		2	35127973 (GRCm38)	E465G	A	G	missense		Het	probably damaging	1.000		phenotype	2014-01-05
6	97410		Cpa1	0.000	R1117	G1	225	N		6	30645261 (GRCm38)	D412G	A	G	missense		Het	probably benign	0.164		phenotype	2014-01-05
7	97368		Crispld1	0.079	R1117	G1	225	N		1	17749622 (GRCm38)	N281K	T	A	missense		Het	probably benign	0.028			2014-01-05
8	97376		Cul3	1.000	R1117	G1	225	N		1	80280924 (GRCm38)	Q465R	T	C	missense		Het	probably damaging	0.999		phenotype	2014-01-05
9	97468		Cyp2c68	0.000	R1117	G1	225	N		19	39712459 (GRCm38)	T305M	G	A	missense		Het	probably damaging	1.000			2014-01-05
10	97390		Elp4	0.965	R1117	G1	225	N		2	105842311 (GRCm38)	D143G	T	C	missense		Het	probably benign	0.003		phenotype	2014-01-05
11	97394		Etnppl	0.088	R1117	G1	225	N		3	130634563 (GRCm38)	I462M	A	G	missense		Het	probably benign	0.005			2014-01-05
12	97380		Fmo4	0.101	R1117	G1	225	N		1	162803663 (GRCm38)	V245A	A	G	missense		Het	probably benign	0.033		phenotype	2014-01-05
13	97443		Gm4076	0.286	R1117	G1	225	N		13	85127318 (GRCm38)		A	G	exon		Het	noncoding transcript				2014-01-05
14	97460		Gm9573	0.076	R1117	G1	221	N		17	35620028 (GRCm38)		T	C	intron		Het	probably benign				2014-01-05
15	97374		Gtf3c3	0.965	R1117	G1	225	N		1	54417778 (GRCm38)	A488T	C	T	missense		Het	probably damaging	0.998	0.654	phenotype	2014-01-05
16	97456		Kcnj15	0.000	R1117	G1	225	N		16	95295625 (GRCm38)	M8I	G	A	missense		Het	probably benign	0.282		phenotype	2014-01-05
17	97414		Klk1b22	0.052	R1117	G1	225	N		7	44116859 (GRCm38)	M255L	A	T	missense		Het	probably benign	0.004		phenotype	2014-01-05
18	97412		Mmrn1	0.000	R1117	G1	225	N		6	60976325 (GRCm38)	I530K	T	A	missense		Het	possibly damaging	0.513		phenotype	2014-01-05
19	97444		Nid2	0.188	R1117	G1	225	N		14	19763664 (GRCm38)		A	C	critical splice acceptor site		Het	probably null			phenotype	2014-01-05
20	97438		Olfr311	0.088	R1117	G1	225	N		11	58841815 (GRCm38)	K234E	A	G	missense		Het	possibly damaging	0.643		phenotype	2014-01-05
21	97458		Olfr63	0.085	R1117	G1	225	N		17	33268966 (GRCm38)	R81*	C	T	nonsense		Het	probably null		0.976	phenotype	2014-01-05
22	97420		Olfr981	0.132	R1117	G1	225	N		9	40022762 (GRCm38)	F123S	T	C	missense		Het	probably damaging	0.994		phenotype	2014-01-05
23	97422		Peak1	0.336	R1117	G1	225	N		9	56258418 (GRCm38)	T742M	G	A	missense		Het	probably benign	0.045		phenotype	2014-01-05
24	97402		Sel1l3	0.000	R1117	G1	225	N		5	53172607 (GRCm38)	T469S	T	A	missense		Het	probably benign	0.004			2014-01-05
25	97440		Sez6	0.000	R1117	G1	225	N		11	77974514 (GRCm38)	Y659C	A	G	missense		Het	probably damaging	1.000		phenotype	2014-01-05
26	97382		Slc19a2	0.160	R1117	G1	219	N		1	164263456 (GRCm38)	I278F	A	T	missense		Het	possibly damaging	0.858		phenotype	2014-01-05
27	97436		Slc36a3	0.096	R1117	G1	221	N		11	55146180 (GRCm38)	I100V	T	C	missense		Het	possibly damaging	0.778			2014-01-05
28	97464		Tcerg1	1.000	R1117	G1	225	N		18	42574652 (GRCm38)	D1079G	A	G	missense		Het	probably damaging	0.991		phenotype	2014-01-05
29	97426		Trim43c	0.081	R1117	G1	225	N		9	88844977 (GRCm38)	S286P	T	C	missense		Het	probably benign	0.204	0.090		2014-01-05
30	97416		Umod	0.117	R1117	G1	191	N		7	119477306 (GRCm38)	N79S	T	C	missense		Het	possibly damaging	0.707		phenotype	2014-01-05
31	97462		Wdr43	0.964	R1117	G1	148	N		17	71616387 (GRCm38)	T43A	A	G	missense		Het	probably benign	0.353			2014-01-05
[records 1 to 31 of 31]