Mutagenetix > Incidental Mutations

Incidental Mutation 'R1743:Csmd3'

200544

Institutional Source

Beutler Lab

Gene Symbol

Csmd3

Ensembl Gene

ENSMUSG00000022311

Gene Name

CUB and Sushi multiple domains 3

Synonyms

4930500N14Rik

MMRRC Submission

039775-MU

Accession Numbers

Is this an essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1743 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

47580637-48792063 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 48622089 bp

Zygosity

Heterozygous

Amino Acid Change

Leucine to Proline at position 140 (L140P)

Ref Sequence

ENSEMBL: ENSMUSP00000124775 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000100670] [ENSMUST00000160658] [ENSMUST00000162830]

Predicted Effect

probably damaging
Transcript: ENSMUST00000100670
AA Change: L140P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000098235
Gene: ENSMUSG00000022311
AA Change: L140P

Domain	Start	End	E-Value	Type
CUB	65	173	8.79e-30	SMART
CCP	178	235	1.77e-11	SMART
CUB	241	345	2.29e-28	SMART
low complexity region	370	387	N/A	INTRINSIC
CCP	486	543	6.9e-14	SMART
CUB	548	659	9.22e-24	SMART
CCP	664	717	1.29e-13	SMART
CUB	721	829	6.87e-32	SMART
CCP	834	891	5.19e-9	SMART
CUB	895	1003	3.23e-37	SMART
CCP	1010	1063	1.82e-13	SMART
CUB	1067	1177	4.87e-23	SMART
CCP	1182	1237	1.82e-13	SMART
CUB	1241	1349	5.02e-25	SMART
CCP	1354	1410	2.5e-11	SMART
CUB	1414	1523	6.27e-26	SMART
CCP	1528	1584	4.41e-12	SMART
CUB	1588	1696	5.37e-34	SMART
CCP	1701	1758	1.18e-12	SMART
CUB	1762	1870	2.27e-23	SMART
CCP	1878	1935	1.84e-9	SMART
CUB	1939	2047	1.8e-35	SMART
CCP	2052	2107	4.48e-13	SMART
CUB	2111	2219	3.95e-32	SMART
CCP	2224	2279	4.02e-15	SMART
CUB	2283	2390	1.74e-33	SMART
CCP	2395	2452	5.82e-12	SMART
CUB	2457	2567	5.3e-24	SMART
CCP	2569	2627	2.11e-9	SMART
CCP	2632	2689	8.23e-12	SMART
CCP	2694	2754	8.56e-10	SMART
CCP	2759	2812	1.14e-14	SMART
CCP	2817	2870	4.76e-17	SMART
CCP	2875	2928	1.85e-14	SMART
CCP	2933	2990	9.9e-15	SMART
CCP	2995	3048	1.79e-12	SMART
CCP	3056	3109	1.72e-14	SMART
CCP	3114	3168	3.17e-13	SMART
CCP	3173	3228	1.25e-11	SMART
CCP	3233	3286	1.25e-11	SMART
CCP	3291	3344	8.23e-12	SMART
CCP	3352	3406	5.6e-14	SMART
CCP	3411	3466	1.89e-11	SMART
transmembrane domain	3630	3652	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000160655

Predicted Effect

probably benign
Transcript: ENSMUST00000160658
AA Change: L140P

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000124753
Gene: ENSMUSG00000022311
AA Change: L140P

Domain	Start	End	E-Value	Type
CUB	65	173	8.79e-30	SMART
CCP	178	235	1.77e-11	SMART
CUB	241	345	2.29e-28	SMART
CCP	382	439	6.9e-14	SMART
CUB	444	555	9.22e-24	SMART
CCP	560	613	1.29e-13	SMART
CUB	617	725	6.87e-32	SMART
CCP	730	787	5.19e-9	SMART
CUB	791	899	3.23e-37	SMART
CCP	906	959	1.82e-13	SMART
CUB	963	1073	4.87e-23	SMART
CCP	1078	1133	1.82e-13	SMART
CUB	1137	1245	5.02e-25	SMART
CCP	1250	1306	2.5e-11	SMART
CUB	1310	1419	6.27e-26	SMART
CCP	1424	1480	4.41e-12	SMART
CUB	1484	1592	5.37e-34	SMART
CCP	1597	1654	1.18e-12	SMART
CUB	1658	1766	2.27e-23	SMART
CCP	1774	1831	1.84e-9	SMART
CUB	1835	1943	1.8e-35	SMART
CCP	1948	2003	4.48e-13	SMART
CUB	2007	2115	3.95e-32	SMART
CCP	2120	2175	4.02e-15	SMART
CUB	2179	2286	1.74e-33	SMART
CCP	2291	2348	5.82e-12	SMART
CUB	2353	2463	5.3e-24	SMART
CCP	2465	2523	2.11e-9	SMART
CCP	2528	2585	8.23e-12	SMART
CCP	2590	2643	1.14e-14	SMART
CCP	2648	2701	4.76e-17	SMART
CCP	2706	2759	1.85e-14	SMART
CCP	2764	2821	9.9e-15	SMART
CCP	2826	2879	1.79e-12	SMART
CCP	2887	2940	1.72e-14	SMART
CCP	2945	2999	3.17e-13	SMART
CCP	3004	3059	1.25e-11	SMART
CCP	3064	3117	1.25e-11	SMART
CCP	3122	3175	8.23e-12	SMART
CCP	3183	3237	5.6e-14	SMART
CCP	3242	3297	1.89e-11	SMART
transmembrane domain	3461	3483	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000160716

Predicted Effect

probably damaging
Transcript: ENSMUST00000162830
AA Change: L140P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000124775
Gene: ENSMUSG00000022311
AA Change: L140P

Domain	Start	End	E-Value	Type
CUB	65	173	8.79e-30	SMART
CCP	178	235	1.77e-11	SMART
CUB	241	345	2.29e-28	SMART
low complexity region	370	387	N/A	INTRINSIC
CCP	486	543	6.9e-14	SMART
CUB	548	659	9.22e-24	SMART
CCP	664	717	1.29e-13	SMART
CUB	721	829	6.87e-32	SMART
CCP	834	891	5.19e-9	SMART
CUB	895	1003	3.23e-37	SMART
CCP	1010	1063	1.82e-13	SMART
CUB	1067	1177	4.87e-23	SMART
CCP	1182	1237	1.82e-13	SMART
CUB	1241	1349	5.02e-25	SMART
CCP	1354	1410	2.5e-11	SMART
CUB	1414	1523	6.27e-26	SMART
CCP	1528	1584	4.41e-12	SMART
CUB	1588	1696	5.37e-34	SMART
CCP	1701	1758	1.18e-12	SMART
CUB	1762	1870	2.27e-23	SMART
CCP	1878	1935	1.84e-9	SMART
CUB	1939	2047	1.8e-35	SMART
CCP	2052	2107	4.48e-13	SMART
CUB	2111	2219	3.95e-32	SMART
CCP	2224	2279	4.02e-15	SMART
CUB	2283	2390	1.74e-33	SMART
CCP	2395	2452	5.82e-12	SMART
CUB	2457	2567	5.3e-24	SMART
CCP	2569	2627	2.11e-9	SMART
CCP	2632	2689	8.23e-12	SMART
CCP	2694	2754	8.56e-10	SMART
CCP	2759	2812	1.14e-14	SMART
CCP	2817	2870	4.76e-17	SMART
CCP	2875	2928	1.85e-14	SMART
CCP	2933	2990	9.9e-15	SMART
CCP	2995	3048	1.79e-12	SMART
CCP	3056	3109	1.72e-14	SMART
CCP	3114	3168	3.17e-13	SMART
CCP	3173	3228	1.25e-11	SMART
CCP	3233	3286	1.25e-11	SMART
CCP	3291	3344	8.23e-12	SMART
CCP	3352	3406	5.6e-14	SMART
CCP	3411	3466	1.89e-11	SMART
transmembrane domain	3630	3652	N/A	INTRINSIC

Coding Region Coverage

1x: 97.4%
3x: 96.8%
10x: 95.1%
20x: 91.7%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 72 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aff4	T	A	11: 53,368,695	M11K	possibly damaging	Het
Ank2	T	C	3: 126,928,675	D88G	probably damaging	Het
Arhgap32	A	G	9: 32,259,431	E1169G	probably benign	Het
Atp7b	A	T	8: 22,006,387	V865E	probably damaging	Het
Bcl2l13	T	A	6: 120,848,543	Y13*	probably null	Het
Birc6	A	G	17: 74,579,756	Q693R	possibly damaging	Het
Bub1	T	C	2: 127,813,850	D520G	probably damaging	Het
Ccdc15	A	T	9: 37,277,477	Y770*	probably null	Het
Cenpf	T	C	1: 189,654,263	E1940G	probably benign	Het
Cep295	C	T	9: 15,340,883	E397K	probably damaging	Het
Cmya5	A	G	13: 93,097,317	V421A	probably benign	Het
Cnnm1	A	T	19: 43,471,913	Y698F	possibly damaging	Het
Cnst	C	T	1: 179,610,392	T507I	probably benign	Het
Coq8a	T	C	1: 180,182,229	M4V	probably benign	Het
Cul2	A	T	18: 3,426,851	I431F	probably damaging	Het
Dnah8	G	T	17: 30,769,651	E3198D	probably benign	Het
Epn2	T	A	11: 61,546,411	I112F	possibly damaging	Het
Ext2	T	C	2: 93,730,225	E532G	probably damaging	Het
Fndc3a	A	T	14: 72,652,081	V37E	probably damaging	Het
Gabbr2	A	G	4: 46,677,603	F759S	possibly damaging	Het
Ghr	G	A	15: 3,320,241	P485L	probably benign	Het
Glipr1l2	G	T	10: 112,092,565	V122L	probably benign	Het
Gm10608	CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	9: 119,160,716		probably benign	Het
Gm13128	T	C	4: 144,333,005	S429P	probably benign	Het
Gm6871	G	T	7: 41,546,452	T287K	probably damaging	Het
Gm7275	A	G	16: 48,073,757		noncoding transcript	Het
Hephl1	C	T	9: 15,090,068	V254I	probably damaging	Het
Hnf4a	C	A	2: 163,566,339	Q362K	possibly damaging	Het
Kcne3	C	T	7: 100,184,424	R83C	probably damaging	Het
Klb	C	A	5: 65,375,861	N504K	probably damaging	Het
Loxl2	T	A	14: 69,692,402	I743N	possibly damaging	Het
Lrrc9	A	T	12: 72,456,117	L287F	probably damaging	Het
Mcm3ap	C	T	10: 76,484,674	P822L	possibly damaging	Het
Nacc2	T	C	2: 26,060,143	N527S	probably benign	Het
Ncam1	G	T	9: 49,557,145	P338H	probably damaging	Het
Nfkbiz	G	T	16: 55,816,394	Q515K	possibly damaging	Het
Nipsnap2	T	C	5: 129,757,085	L263P	probably damaging	Het
Nlrp1a	A	T	11: 71,124,206	S73T	probably benign	Het
Nomo1	G	A	7: 46,070,037		probably null	Het
Nos3	G	A	5: 24,377,312	G594D	probably benign	Het
Olfr1330	A	G	4: 118,893,526	T148A	probably benign	Het
Olfr1359	A	G	13: 21,703,450	I150V	probably benign	Het
Olfr148	A	T	9: 39,613,620	T18S	possibly damaging	Het
Oprm1	A	G	10: 6,830,105	I256V	probably damaging	Het
Oxct2a	A	T	4: 123,323,516	L24Q	possibly damaging	Het
Pcdhb14	T	G	18: 37,448,178	S112R	probably benign	Het
Polr2a	A	G	11: 69,739,503	I1246T	probably damaging	Het
Ppil4	A	T	10: 7,807,381	K327N	probably damaging	Het
Pstpip1	T	C	9: 56,125,930	Y249H	probably damaging	Het
Qrsl1	A	T	10: 43,881,515	V369E	probably damaging	Het
Ranbp10	G	T	8: 105,779,978	P237T	probably damaging	Het
Rapgef6	A	G	11: 54,676,284	N1097S	probably damaging	Het
Repin1	T	A	6: 48,597,750	S538T	probably damaging	Het
Rims2	A	T	15: 39,679,650	M1151L	probably benign	Het
Rin3	T	A	12: 102,390,096	D965E	possibly damaging	Het
Sdc2	A	G	15: 33,028,078	D114G	probably benign	Het
Slc25a30	C	A	14: 75,775,083	A42S	probably benign	Het
Sphkap	G	A	1: 83,277,515	R838*	probably null	Het
Ssh2	T	A	11: 77,437,756	F383I	probably damaging	Het
St8sia1	A	T	6: 142,829,016	V279E	probably damaging	Het
Tacc2	C	A	7: 130,626,598	S1690*	probably null	Het
Taf1b	A	G	12: 24,547,178	D372G	possibly damaging	Het
Timm21	G	C	18: 84,949,262	L130V	probably damaging	Het
Tmem165	G	T	5: 76,207,826	G272C	probably damaging	Het
Tsc22d2	TCAGTTAACACCTATGAACAGT	TCAGT	3: 58,417,539		probably null	Het
Tssk4	C	A	14: 55,651,031	A119D	probably damaging	Het
Usp9y	A	G	Y: 1,316,727	Y1941H	probably damaging	Het
Vmn2r42	A	T	7: 8,184,265	M786K	probably benign	Het
Wdfy3	G	T	5: 101,844,065	T3470K	probably benign	Het
Wdr63	C	A	3: 146,097,262	R58L	possibly damaging	Het
Zc3h14	T	C	12: 98,779,189	V479A	probably benign	Het
Zfp821	G	A	8: 109,724,164	R263Q	probably damaging	Het

Other mutations in Csmd3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00158:Csmd3	APN	15	48287495	missense	possibly damaging	0.61
IGL00591:Csmd3	APN	15	48004883	missense	probably damaging	1.00
IGL00668:Csmd3	APN	15	47913945	missense	probably damaging	1.00
IGL00753:Csmd3	APN	15	47644235	missense	probably damaging	1.00
IGL00773:Csmd3	APN	15	47590719	missense	probably damaging	0.96
IGL00926:Csmd3	APN	15	47710964	missense	possibly damaging	0.87
IGL00942:Csmd3	APN	15	47847106	critical splice donor site	probably null
IGL01080:Csmd3	APN	15	47881403	missense	probably benign	0.12
IGL01314:Csmd3	APN	15	47849755	missense	probably damaging	1.00
IGL01326:Csmd3	APN	15	47849785	missense	probably benign	0.06
IGL01393:Csmd3	APN	15	48457599	missense	possibly damaging	0.88
IGL01432:Csmd3	APN	15	47733499	missense	probably damaging	1.00
IGL01519:Csmd3	APN	15	47596850	missense	probably benign	0.31
IGL01530:Csmd3	APN	15	47838437	missense	possibly damaging	0.95
IGL01530:Csmd3	APN	15	47669617	missense	probably damaging	1.00
IGL01547:Csmd3	APN	15	47883617	missense	probably benign	0.41
IGL01594:Csmd3	APN	15	47629239	missense	probably benign	0.01
IGL01618:Csmd3	APN	15	48011083	missense	probably benign	0.05
IGL01670:Csmd3	APN	15	47611829	missense	probably damaging	1.00
IGL01680:Csmd3	APN	15	47970030	missense	probably damaging	1.00
IGL01734:Csmd3	APN	15	48185304	missense	probably damaging	1.00
IGL01777:Csmd3	APN	15	47698198	missense	probably benign	0.06
IGL01779:Csmd3	APN	15	47857894	missense	probably benign	0.10
IGL01820:Csmd3	APN	15	47607142	nonsense	probably null
IGL01843:Csmd3	APN	15	47658999	splice site	probably benign
IGL01919:Csmd3	APN	15	47675772	missense	possibly damaging	0.62
IGL01986:Csmd3	APN	15	47659195	missense	possibly damaging	0.82
IGL02049:Csmd3	APN	15	48001474	missense	possibly damaging	0.91
IGL02065:Csmd3	APN	15	47666628	missense	probably damaging	1.00
IGL02112:Csmd3	APN	15	48313869	missense	possibly damaging	0.95
IGL02133:Csmd3	APN	15	47857942	missense	possibly damaging	0.86
IGL02203:Csmd3	APN	15	47849677	splice site	probably null
IGL02215:Csmd3	APN	15	47585688	missense	probably damaging	1.00
IGL02234:Csmd3	APN	15	47948116	missense	probably damaging	1.00
IGL02326:Csmd3	APN	15	47755963	splice site	probably benign
IGL02478:Csmd3	APN	15	47838398	splice site	probably benign
IGL02491:Csmd3	APN	15	47914115	splice site	probably benign
IGL02598:Csmd3	APN	15	47669690	missense	probably damaging	0.98
IGL02626:Csmd3	APN	15	47704107	splice site	probably benign
IGL02696:Csmd3	APN	15	47669669	missense	probably benign	0.33
IGL02876:Csmd3	APN	15	47606096	splice site	probably benign
IGL02971:Csmd3	APN	15	47913929	splice site	probably benign
IGL03068:Csmd3	APN	15	47847121	missense	possibly damaging	0.69
IGL03087:Csmd3	APN	15	47977033	missense	probably damaging	1.00
IGL03114:Csmd3	APN	15	47820451	missense	probably damaging	0.99
IGL03146:Csmd3	APN	15	47881477	missense	probably benign	0.25
IGL03193:Csmd3	APN	15	47629230	splice site	probably benign
IGL03274:Csmd3	APN	15	47645504	missense	probably damaging	1.00
R0040:Csmd3	UTSW	15	47633816	missense	probably damaging	1.00
R0071:Csmd3	UTSW	15	47596821	missense	probably benign	0.04
R0071:Csmd3	UTSW	15	47596821	missense	probably benign	0.04
R0119:Csmd3	UTSW	15	47847131	missense	probably benign	0.08
R0124:Csmd3	UTSW	15	47590716	missense	probably damaging	1.00
R0127:Csmd3	UTSW	15	47981930	missense	probably benign	0.45
R0136:Csmd3	UTSW	15	47847131	missense	probably benign	0.08
R0201:Csmd3	UTSW	15	47619729	splice site	probably benign
R0240:Csmd3	UTSW	15	47629239	missense	probably benign	0.05
R0240:Csmd3	UTSW	15	47629239	missense	probably benign	0.05
R0318:Csmd3	UTSW	15	47659153	missense	probably damaging	1.00
R0369:Csmd3	UTSW	15	47970147	missense	probably damaging	1.00
R0391:Csmd3	UTSW	15	47657573	missense	probably damaging	1.00
R0499:Csmd3	UTSW	15	47847131	missense	probably benign	0.08
R0506:Csmd3	UTSW	15	48457511	missense	probably benign	0.00
R0606:Csmd3	UTSW	15	48457662	missense	probably benign
R0639:Csmd3	UTSW	15	47913940	missense	probably damaging	1.00
R0658:Csmd3	UTSW	15	48011147	missense	possibly damaging	0.66
R0673:Csmd3	UTSW	15	47913940	missense	probably damaging	1.00
R0689:Csmd3	UTSW	15	47756025	missense	probably benign	0.19
R0696:Csmd3	UTSW	15	47847173	missense	probably benign	0.01
R0799:Csmd3	UTSW	15	48185384	splice site	probably benign
R0834:Csmd3	UTSW	15	47883677	intron	probably benign
R0894:Csmd3	UTSW	15	47857920	missense	possibly damaging	0.95
R0926:Csmd3	UTSW	15	47977033	missense	probably damaging	1.00
R0943:Csmd3	UTSW	15	47675739	missense	probably damaging	0.99
R0944:Csmd3	UTSW	15	47611831	missense	probably damaging	1.00
R0967:Csmd3	UTSW	15	47857831	missense	probably null	0.89
R0973:Csmd3	UTSW	15	47659089	missense	probably damaging	1.00
R1055:Csmd3	UTSW	15	47881537	missense	probably damaging	1.00
R1066:Csmd3	UTSW	15	47913965	missense	probably damaging	1.00
R1086:Csmd3	UTSW	15	47695755	missense	probably damaging	0.99
R1103:Csmd3	UTSW	15	47948006	missense	probably damaging	1.00
R1136:Csmd3	UTSW	15	47675817	missense	probably damaging	1.00
R1139:Csmd3	UTSW	15	47695836	missense	probably damaging	1.00
R1158:Csmd3	UTSW	15	48292774	splice site	probably null
R1215:Csmd3	UTSW	15	48004831	unclassified	probably null
R1233:Csmd3	UTSW	15	48673531	missense	probably damaging	1.00
R1271:Csmd3	UTSW	15	48011059	missense	probably benign	0.11
R1469:Csmd3	UTSW	15	47669202	nonsense	probably null
R1469:Csmd3	UTSW	15	47669202	nonsense	probably null
R1479:Csmd3	UTSW	15	47857886	missense	probably damaging	1.00
R1480:Csmd3	UTSW	15	47731929	missense	possibly damaging	0.90
R1526:Csmd3	UTSW	15	47585632	critical splice donor site	probably null
R1527:Csmd3	UTSW	15	47948087	missense	probably benign	0.08
R1539:Csmd3	UTSW	15	47820398	missense	probably benign	0.24
R1544:Csmd3	UTSW	15	47611898	splice site	probably null
R1548:Csmd3	UTSW	15	47981975	missense	possibly damaging	0.91
R1574:Csmd3	UTSW	15	47695861	splice site	probably null
R1574:Csmd3	UTSW	15	47695861	splice site	probably null
R1619:Csmd3	UTSW	15	47949950	missense	probably damaging	1.00
R1630:Csmd3	UTSW	15	47838522	missense	possibly damaging	0.66
R1665:Csmd3	UTSW	15	47696789	missense	probably damaging	1.00
R1680:Csmd3	UTSW	15	47741170	missense	probably damaging	1.00
R1725:Csmd3	UTSW	15	47596807	missense	probably damaging	1.00
R1749:Csmd3	UTSW	15	47585660	missense	probably damaging	1.00
R1752:Csmd3	UTSW	15	47660273	missense	probably benign	0.15
R1769:Csmd3	UTSW	15	47704109	splice site	probably benign
R1775:Csmd3	UTSW	15	47899739	missense	probably damaging	0.99
R1795:Csmd3	UTSW	15	47857920	missense	possibly damaging	0.95
R1819:Csmd3	UTSW	15	47753735	missense	possibly damaging	0.56
R1840:Csmd3	UTSW	15	47607164	missense	probably damaging	1.00
R1860:Csmd3	UTSW	15	47659192	missense	probably damaging	1.00
R1861:Csmd3	UTSW	15	47659192	missense	probably damaging	1.00
R1879:Csmd3	UTSW	15	47657519	missense	possibly damaging	0.90
R1958:Csmd3	UTSW	15	48004639	critical splice donor site	probably null
R1965:Csmd3	UTSW	15	47849748	missense	probably benign	0.15
R1970:Csmd3	UTSW	15	48673531	missense	probably damaging	1.00
R2029:Csmd3	UTSW	15	47838579	missense	probably damaging	1.00
R2051:Csmd3	UTSW	15	48621993	critical splice donor site	probably null
R2108:Csmd3	UTSW	15	48004861	missense	possibly damaging	0.81
R2132:Csmd3	UTSW	15	48457503	missense	probably benign	0.06
R2146:Csmd3	UTSW	15	47741236	frame shift	probably null
R2147:Csmd3	UTSW	15	47741236	frame shift	probably null
R2148:Csmd3	UTSW	15	47741236	frame shift	probably null
R2157:Csmd3	UTSW	15	47695787	missense	probably damaging	0.99
R2159:Csmd3	UTSW	15	47741236	frame shift	probably null
R2160:Csmd3	UTSW	15	47741236	frame shift	probably null
R2161:Csmd3	UTSW	15	47741236	frame shift	probably null
R2162:Csmd3	UTSW	15	47741236	frame shift	probably null
R2164:Csmd3	UTSW	15	47741236	frame shift	probably null
R2213:Csmd3	UTSW	15	47820447	missense	possibly damaging	0.92
R2301:Csmd3	UTSW	15	47731998	missense	probably damaging	1.00
R2302:Csmd3	UTSW	15	48314051	missense	probably benign
R2355:Csmd3	UTSW	15	47741236	frame shift	probably null
R2497:Csmd3	UTSW	15	47741236	frame shift	probably null
R2509:Csmd3	UTSW	15	47741236	frame shift	probably null
R2566:Csmd3	UTSW	15	47741236	frame shift	probably null
R2567:Csmd3	UTSW	15	47741236	frame shift	probably null
R2568:Csmd3	UTSW	15	47741236	frame shift	probably null
R2570:Csmd3	UTSW	15	47741236	frame shift	probably null
R2571:Csmd3	UTSW	15	47741236	frame shift	probably null
R2870:Csmd3	UTSW	15	47857924	missense	probably damaging	1.00
R2870:Csmd3	UTSW	15	47857924	missense	probably damaging	1.00
R2907:Csmd3	UTSW	15	48011053	missense	probably damaging	0.99
R3116:Csmd3	UTSW	15	47657599	missense	probably damaging	1.00
R3423:Csmd3	UTSW	15	47847252	missense	probably damaging	0.98
R3425:Csmd3	UTSW	15	47847252	missense	probably damaging	0.98
R3508:Csmd3	UTSW	15	47741236	frame shift	probably null
R3746:Csmd3	UTSW	15	47849766	missense	probably benign	0.04
R3813:Csmd3	UTSW	15	48791813	missense	possibly damaging	0.82
R3832:Csmd3	UTSW	15	47741236	frame shift	probably null
R3959:Csmd3	UTSW	15	47644189	missense	probably benign	0.18
R4042:Csmd3	UTSW	15	47614084	missense	probably damaging	1.00
R4043:Csmd3	UTSW	15	47755966	critical splice donor site	probably null
R4191:Csmd3	UTSW	15	47847271	missense	probably damaging	0.99
R4192:Csmd3	UTSW	15	47847271	missense	probably damaging	0.99
R4419:Csmd3	UTSW	15	47704311	missense	probably damaging	1.00
R4426:Csmd3	UTSW	15	47669185	missense	possibly damaging	0.51
R4434:Csmd3	UTSW	15	47899795	missense	possibly damaging	0.68
R4438:Csmd3	UTSW	15	47899795	missense	possibly damaging	0.68
R4490:Csmd3	UTSW	15	48314033	missense	possibly damaging	0.83
R4562:Csmd3	UTSW	15	47899844	missense	probably benign	0.32
R4604:Csmd3	UTSW	15	48004815	missense	possibly damaging	0.90
R4620:Csmd3	UTSW	15	47585753	missense	probably benign	0.09
R4632:Csmd3	UTSW	15	48011209	missense	probably damaging	0.99
R4679:Csmd3	UTSW	15	48161083	nonsense	probably null
R4696:Csmd3	UTSW	15	47913968	missense	probably benign	0.24
R4718:Csmd3	UTSW	15	47698150	nonsense	probably null
R4723:Csmd3	UTSW	15	47669160	missense	probably benign	0.29
R4801:Csmd3	UTSW	15	47621292	missense	probably damaging	1.00
R4802:Csmd3	UTSW	15	47621292	missense	probably damaging	1.00
R4806:Csmd3	UTSW	15	48314068	missense	probably benign
R4816:Csmd3	UTSW	15	47857934	missense	possibly damaging	0.68
R4935:Csmd3	UTSW	15	48161084	missense	probably damaging	1.00
R4955:Csmd3	UTSW	15	48673518	missense	probably damaging	0.99
R4991:Csmd3	UTSW	15	48001478	missense	probably damaging	1.00
R5031:Csmd3	UTSW	15	47659192	missense	probably damaging	1.00
R5034:Csmd3	UTSW	15	47629287	missense	possibly damaging	0.94
R5035:Csmd3	UTSW	15	47590779	missense	probably damaging	1.00
R5120:Csmd3	UTSW	15	48673495	nonsense	probably null
R5224:Csmd3	UTSW	15	47888684	missense	possibly damaging	0.91
R5235:Csmd3	UTSW	15	47629278	missense	probably benign	0.20
R5279:Csmd3	UTSW	15	48791944	unclassified	probably null
R5360:Csmd3	UTSW	15	47669203	missense	probably damaging	0.99
R5365:Csmd3	UTSW	15	48004749	missense	possibly damaging	0.68
R5379:Csmd3	UTSW	15	47636450	nonsense	probably null
R5381:Csmd3	UTSW	15	47741215	missense	probably benign	0.21
R5393:Csmd3	UTSW	15	47633703	missense	probably damaging	1.00
R5413:Csmd3	UTSW	15	47838435	missense	probably damaging	1.00
R5549:Csmd3	UTSW	15	48185357	missense	probably damaging	0.98
R5550:Csmd3	UTSW	15	48185357	missense	probably damaging	0.98
R5551:Csmd3	UTSW	15	48314096	missense	probably benign	0.13
R5567:Csmd3	UTSW	15	47645468	missense	possibly damaging	0.92
R5621:Csmd3	UTSW	15	48313978	missense	possibly damaging	0.84
R5668:Csmd3	UTSW	15	47695755	missense	possibly damaging	0.48
R5677:Csmd3	UTSW	15	48622051	missense	probably damaging	0.98
R5701:Csmd3	UTSW	15	47650221	missense	probably damaging	1.00
R5701:Csmd3	UTSW	15	48540333	missense	probably damaging	0.99
R5871:Csmd3	UTSW	15	47888716	missense	probably damaging	0.98
R5872:Csmd3	UTSW	15	47582527	missense	probably damaging	1.00
R5874:Csmd3	UTSW	15	47644270	missense	probably damaging	1.00
R5952:Csmd3	UTSW	15	47733505	missense	probably damaging	0.98
R5956:Csmd3	UTSW	15	48791882	missense	possibly damaging	0.84
R5966:Csmd3	UTSW	15	47849739	missense	probably damaging	0.96
R5969:Csmd3	UTSW	15	47947990	missense	probably damaging	1.00
R5989:Csmd3	UTSW	15	47590764	missense	possibly damaging	0.69
R6017:Csmd3	UTSW	15	48314012	missense	possibly damaging	0.95
R6057:Csmd3	UTSW	15	47755391	missense	probably damaging	1.00
R6127:Csmd3	UTSW	15	47650228	missense	probably damaging	1.00
R6178:Csmd3	UTSW	15	48673458	missense	probably damaging	1.00
R6198:Csmd3	UTSW	15	48313877	missense	probably benign	0.28
R6213:Csmd3	UTSW	15	47629260	missense	probably damaging	1.00
R6256:Csmd3	UTSW	15	47669729	missense	probably damaging	1.00
R6274:Csmd3	UTSW	15	47621437	missense	probably benign
R6327:Csmd3	UTSW	15	47881387	missense	probably damaging	1.00
R6354:Csmd3	UTSW	15	47881489	missense	probably damaging	1.00
R6405:Csmd3	UTSW	15	47820371	missense	probably damaging	0.99
R6410:Csmd3	UTSW	15	48673407	missense	probably damaging	1.00
R6416:Csmd3	UTSW	15	48673560	missense	probably damaging	1.00
R6463:Csmd3	UTSW	15	47676479	missense	probably damaging	1.00
R6536:Csmd3	UTSW	15	47838467	missense	probably damaging	1.00
R6625:Csmd3	UTSW	15	47607075	missense	probably benign	0.02
R6695:Csmd3	UTSW	15	47857834	missense	probably damaging	0.99
R6895:Csmd3	UTSW	15	47666514	splice site	probably null
R6906:Csmd3	UTSW	15	47847173	missense	probably benign	0.01
R6914:Csmd3	UTSW	15	48011138	missense	possibly damaging	0.53
R6920:Csmd3	UTSW	15	47644205	missense	probably damaging	1.00
R7024:Csmd3	UTSW	15	47710991	missense	probably damaging	1.00
R7178:Csmd3	UTSW	15	47590774	missense
R7192:Csmd3	UTSW	15	47704237	missense
R7220:Csmd3	UTSW	15	48457598	missense	probably damaging	0.99
R7362:Csmd3	UTSW	15	47755992	missense	possibly damaging	0.65
R7380:Csmd3	UTSW	15	47586965	missense
R7397:Csmd3	UTSW	15	47695734	missense
R7467:Csmd3	UTSW	15	47629244	missense
R7585:Csmd3	UTSW	15	48622075	missense	possibly damaging	0.76
R7623:Csmd3	UTSW	15	47949938	missense
R7649:Csmd3	UTSW	15	47669143	missense
U24488:Csmd3	UTSW	15	47710399	missense	probably damaging	1.00
V8831:Csmd3	UTSW	15	48457696	missense	probably damaging	0.96
X0021:Csmd3	UTSW	15	47970093	nonsense	probably null
Z1088:Csmd3	UTSW	15	47636393	missense	probably damaging	1.00
Z1088:Csmd3	UTSW	15	47847281	missense	probably damaging	0.98

Predicted Primers

PCR Primer
(F):5'- AAGATTTGGGACCAATAGGTAAATACTGACAC -3'
(R):5'- AGGACATTGATCTACACACCCATTATAACCAT -3'

Sequencing Primer
(F):5'- ACTGACACTATACTCCTATGGTACG -3'
(R):5'- CCATCACACGAATCATGTATTTAATG -3'

Posted On

2014-05-23