Mutagenetix > Incidental Mutations

Incidental Mutation 'R8516:Csmd3'

656175

Institutional Source

Beutler Lab

Gene Symbol

Csmd3

Ensembl Gene

ENSMUSG00000022311

Gene Name

CUB and Sushi multiple domains 3

Synonyms

4930500N14Rik

MMRRC Submission

Accession Numbers

Is this an essential gene?

Non essential (E-score: 0.000) question?

Stock #

R8516 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

47580637-48792063 bp(-) (GRCm38)

Type of Mutation

nonsense

DNA Base Change (assembly)

G to A at 47629365 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Stop codon at position 2216 (R2216*)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

probably null
Transcript: ENSMUST00000100670
AA Change: R3127*

SMART Domains

Protein: ENSMUSP00000098235
Gene: ENSMUSG00000022311
AA Change: R3127*

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

probably null
Transcript: ENSMUST00000160658
AA Change: R2958*

SMART Domains

Protein: ENSMUSP00000124753
Gene: ENSMUSG00000022311
AA Change: R2958*

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

probably null
Transcript: ENSMUST00000161653
AA Change: R2216*

SMART Domains

Protein: ENSMUSP00000124195
Gene: ENSMUSG00000022311
AA Change: R2216*

Domain	Start	End	E-Value	Type
CCP	1	51	6.59e-1	SMART
CUB	55	163	3.23e-37	SMART
CCP	170	223	1.82e-13	SMART
CUB	227	337	4.87e-23	SMART
CCP	342	397	1.82e-13	SMART
CUB	401	509	5.02e-25	SMART
CCP	514	570	2.5e-11	SMART
CUB	574	683	6.27e-26	SMART
CCP	688	744	4.41e-12	SMART
CUB	748	856	5.37e-34	SMART
CCP	861	918	1.18e-12	SMART
Pfam:CUB	922	964	9.7e-8	PFAM
CCP	968	1025	1.84e-9	SMART
CUB	1029	1137	1.8e-35	SMART
CCP	1142	1197	4.48e-13	SMART
CUB	1201	1309	3.95e-32	SMART
CCP	1314	1369	4.02e-15	SMART
CUB	1373	1480	1.74e-33	SMART
CCP	1485	1542	5.82e-12	SMART
CUB	1547	1657	5.3e-24	SMART
CCP	1659	1717	2.11e-9	SMART
CCP	1722	1779	8.23e-12	SMART
CCP	1784	1844	8.56e-10	SMART
CCP	1849	1902	1.14e-14	SMART
CCP	1907	1960	4.76e-17	SMART
CCP	1965	2018	1.85e-14	SMART
CCP	2023	2080	9.9e-15	SMART
CCP	2085	2138	1.79e-12	SMART
CCP	2146	2199	1.72e-14	SMART
CCP	2204	2258	3.17e-13	SMART
CCP	2263	2318	1.25e-11	SMART
CCP	2323	2376	1.25e-11	SMART
CCP	2381	2434	8.23e-12	SMART
CCP	2442	2496	5.6e-14	SMART
CCP	2501	2556	1.89e-11	SMART
transmembrane domain	2720	2742	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000162830
AA Change: R3127*

SMART Domains

Protein: ENSMUSP00000124775
Gene: ENSMUSG00000022311
AA Change: R3127*

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: 100.0%
3x: 99.9%
10x: 99.5%
20x: 98.6%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aasdhppt	A	T	9: 4,309,373	S22T	probably benign	Het
Actr8	G	T	14: 29,990,899	A500S	probably benign	Het
Adamtsl1	A	G	4: 86,342,543	Y1005C	probably damaging	Het
Ank3	T	A	10: 69,927,729	Y884*	probably null	Het
Arhgap28	T	C	17: 67,873,073	R306G	probably benign	Het
Atp8a2	A	C	14: 59,691,472	I1044M	probably benign	Het
Bahd1	A	G	2: 118,916,971	Y357C	probably benign	Het
Btd	A	T	14: 31,666,867	T182S	probably damaging	Het
Casc3	C	T	11: 98,822,781	R280C	probably damaging	Het
Cisd2	T	C	3: 135,411,013	T106A	probably damaging	Het
Cldn15	G	T	5: 136,974,696	C184F	probably damaging	Het
Clk4	G	A	11: 51,275,261	R198Q	probably damaging	Het
Coprs	G	T	8: 13,885,065	F163L	probably damaging	Het
Defb7	A	T	8: 19,497,607	I43F	possibly damaging	Het
Dpp8	C	A	9: 65,078,009	T783K	probably damaging	Het
Eif2s1	G	A	12: 78,881,162	G204D	probably damaging	Het
Elavl4	T	C	4: 110,251,379	N56S	probably damaging	Het
Emilin1	G	A	5: 30,917,171	R252H	probably damaging	Het
Exd1	A	T	2: 119,520,073	L569Q	probably damaging	Het
Gm498	T	A	7: 143,897,274	I342N	probably damaging	Het
Gpn2	C	T	4: 133,584,831	R125C	probably damaging	Het
Gria2	T	C	3: 80,706,987	E582G	probably benign	Het
Hadha	A	T	5: 30,126,584	V458E	probably damaging	Het
Hap1	T	C	11: 100,356,067	K4R	possibly damaging	Het
Hectd4	A	T	5: 121,349,010	H3356L	possibly damaging	Het
Herc2	G	A	7: 56,206,570	V3919I	probably benign	Het
Lgr6	G	T	1: 135,075,283	N76K	probably damaging	Het
Olfr692	A	G	7: 105,368,769	I148V	probably benign	Het
P4ha3	A	G	7: 100,314,662	M462V	probably damaging	Het
Pde3b	A	T	7: 114,526,849	M773L	probably benign	Het
Peak1	T	C	9: 56,260,000	S215G	probably damaging	Het
Pgm5	T	A	19: 24,815,710	M331L	probably benign	Het
Piwil2	A	G	14: 70,420,739	V213A	probably benign	Het
Plch2	T	C	4: 154,986,307	H1205R	probably benign	Het
Pop4	A	T	7: 38,267,402	M85K	probably benign	Het
Ppp3ca	T	A	3: 136,877,768	I212N	probably damaging	Het
Prom1	T	C	5: 44,007,099	K714R	probably benign	Het
Psip1	C	T	4: 83,466,715	G207S	probably benign	Het
Rgs22	A	G	15: 36,010,335	*1259Q	probably null	Het
Scn1a	C	T	2: 66,326,134	G477D	possibly damaging	Het
Sf3b1	T	C	1: 55,012,103	E222G	probably null	Het
Snrpa1	G	A	7: 66,070,633	G195R	probably benign	Het
Spem2	T	C	11: 69,816,895	R415G	possibly damaging	Het
Tmem167	T	A	13: 90,098,396	V13E	probably damaging	Het
Trim2	C	T	3: 84,208,320	A102T	probably damaging	Het
Trim30b	A	G	7: 104,357,404	S82P	probably benign	Het
Uba6	A	C	5: 86,127,748	S760R	possibly damaging	Het
Upf2	T	C	2: 6,018,971	F711L	unknown	Het
Utrn	T	A	10: 12,486,510	D2693V	probably damaging	Het
Vmn1r30	T	G	6: 58,435,124	Y241S	probably damaging	Het
Vmn2r110	A	G	17: 20,574,613	L598P	probably damaging	Het
Wfdc18	T	A	11: 83,709,158	F14Y	probably benign	Het
Wnt10b	A	T	15: 98,772,880	C256S	probably damaging	Het
Xrn1	T	A	9: 96,048,391	Y1554*	probably null	Het
Zc3h12a	T	A	4: 125,119,839	S411C	probably damaging	Het
Zfp112	G	A	7: 24,123,964	G63E	probably benign	Het
Zfp786	A	T	6: 47,820,543	L487Q	probably damaging	Het
Zfp953	T	A	13: 67,345,355	Y75F	possibly 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	splice site	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
R1743:Csmd3	UTSW	15	48622089	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	splice site	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
R7691:Csmd3	UTSW	15	47741173	missense
R7695:Csmd3	UTSW	15	47820381	missense
R7759:Csmd3	UTSW	15	47698173	missense
R7817:Csmd3	UTSW	15	47857960	missense	probably damaging	0.99
R8052:Csmd3	UTSW	15	47706387	missense
R8089:Csmd3	UTSW	15	47669207	missense
R8110:Csmd3	UTSW	15	47644270	missense	probably damaging	1.00
R8152:Csmd3	UTSW	15	47669464	splice site	probably null
R8323:Csmd3	UTSW	15	47698151	missense
R8341:Csmd3	UTSW	15	47698151	missense
R8353:Csmd3	UTSW	15	47949953	missense	probably damaging	1.00
R8364:Csmd3	UTSW	15	48673441	missense	probably damaging	1.00
R8405:Csmd3	UTSW	15	47755983	missense	probably damaging	1.00
R8412:Csmd3	UTSW	15	47636398	missense
R8436:Csmd3	UTSW	15	48004822	missense	probably damaging	0.97
R8553:Csmd3	UTSW	15	47621328	missense	possibly damaging	0.52
R8554:Csmd3	UTSW	15	47644142	missense	probably benign	0.32
R8678:Csmd3	UTSW	15	47636453	missense
R8751:Csmd3	UTSW	15	47982006	missense
R8758:Csmd3	UTSW	15	47606197	missense
R8768:Csmd3	UTSW	15	47698176	missense
R8785:Csmd3	UTSW	15	48314086	missense	probably benign	0.00
R8788:Csmd3	UTSW	15	47607117	missense
R8798:Csmd3	UTSW	15	47731986	missense
R8801:Csmd3	UTSW	15	48457628	missense	possibly damaging	0.70
R8811:Csmd3	UTSW	15	47696743	missense
R8844:Csmd3	UTSW	15	47741194	missense	probably damaging	0.96
R8844:Csmd3	UTSW	15	48673419	missense	probably damaging	0.98
R8892:Csmd3	UTSW	15	47741238	missense
R8897:Csmd3	UTSW	15	48359343	missense	probably benign	0.06
R9001:Csmd3	UTSW	15	47733505	missense
R9016:Csmd3	UTSW	15	47659042	missense
R9109:Csmd3	UTSW	15	47753791	missense
R9121:Csmd3	UTSW	15	47820378	missense
R9155:Csmd3	UTSW	15	47585655	missense
R9176:Csmd3	UTSW	15	48001541	missense
R9281:Csmd3	UTSW	15	47596876	missense
R9298:Csmd3	UTSW	15	47753791	missense
R9304:Csmd3	UTSW	15	47706409	missense
R9367:Csmd3	UTSW	15	47704168	missense
R9405:Csmd3	UTSW	15	47675791	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
Z1177:Csmd3	UTSW	15	47675734	missense
Z1177:Csmd3	UTSW	15	47733417	missense

Predicted Primers

PCR Primer
(F):5'- GGCTTCGAATTCTTGAAATCATCAGTG -3'
(R):5'- CAAGGTGTTTCACTGCTAAATTTGG -3'

Sequencing Primer
(F):5'- CACACATAGTCTTTTAATCGCAAAG -3'
(R):5'- GTGTTTCACTGCTAAATTTGGAGAAG -3'

Posted On

2020-10-20