Mutagenetix > Incidental Mutation

Incidental Mutation 'R1775:Csmd3'

204365

Institutional Source

Beutler Lab

Gene Symbol

Csmd3

Ensembl Gene

ENSMUSG00000022311

Gene Name

CUB and Sushi multiple domains 3

Synonyms

4930500N14Rik

MMRRC Submission

039806-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1775 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

47580637-48792063 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 47899739 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 1234 (T1234A)

Ref Sequence

ENSEMBL: ENSMUSP00000124753 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000100670
AA Change: T1338A

PolyPhen 2 Score 0.957 (Sensitivity: 0.78; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000098235
Gene: ENSMUSG00000022311
AA Change: T1338A

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 damaging
Transcript: ENSMUST00000160658
AA Change: T1234A

PolyPhen 2 Score 0.992 (Sensitivity: 0.70; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000124753
Gene: ENSMUSG00000022311
AA Change: T1234A

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

unknown
Transcript: ENSMUST00000161653
AA Change: T497A

SMART Domains

Protein: ENSMUSP00000124195
Gene: ENSMUSG00000022311
AA Change: T497A

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 damaging
Transcript: ENSMUST00000162830
AA Change: T1338A

PolyPhen 2 Score 0.957 (Sensitivity: 0.78; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000124775
Gene: ENSMUSG00000022311
AA Change: T1338A

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

Meta Mutation Damage Score

0.1156

Coding Region Coverage

1x: 97.5%
3x: 97.0%
10x: 95.5%
20x: 92.9%

Validation Efficiency

98% (95/97)

Allele List at MGI

Other mutations in this stock

Total: 93 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700034J04Rik	A	G	12: 11,222,142 (GRCm38)	S20P	unknown	Het
4921528I07Rik	G	A	9: 114,279,318 (GRCm38)		noncoding transcript	Het
4930562C15Rik	G	A	16: 4,851,558 (GRCm38)		probably null	Het
4933427I04Rik	A	G	4: 123,860,493 (GRCm38)	T67A	possibly damaging	Het
Abcc2	A	T	19: 43,798,419 (GRCm38)	N160Y	possibly damaging	Het
Acaca	A	G	11: 84,300,422 (GRCm38)	D155G	possibly damaging	Het
Afg3l1	G	A	8: 123,492,900 (GRCm38)	R389Q	possibly damaging	Het
Ank2	G	A	3: 126,934,547 (GRCm38)	T799M	probably benign	Het
Anxa2	T	C	9: 69,488,081 (GRCm38)	Y202H	possibly damaging	Het
Arhgef33	A	G	17: 80,373,743 (GRCm38)	T771A	probably benign	Het
Atp12a	T	C	14: 56,372,589 (GRCm38)	V182A	probably benign	Het
Birc6	T	C	17: 74,612,286 (GRCm38)	L210S	probably damaging	Het
Car3	A	G	3: 14,864,432 (GRCm38)	T73A	probably benign	Het
Cd5l	T	C	3: 87,368,659 (GRCm38)	L312P	probably damaging	Het
Celf5	A	G	10: 81,467,304 (GRCm38)		probably benign	Het
Cep290	T	A	10: 100,496,810 (GRCm38)	V257E	probably damaging	Het
Cntrob	T	C	11: 69,320,867 (GRCm38)	D177G	possibly damaging	Het
Copg2	A	T	6: 30,810,336 (GRCm38)	F658I	probably damaging	Het
Dhx35	A	G	2: 158,806,437 (GRCm38)	T72A	probably damaging	Het
Dmrtc2	A	T	7: 24,874,367 (GRCm38)	H209L	possibly damaging	Het
Eml5	G	T	12: 98,852,704 (GRCm38)		probably null	Het
Evpl	T	C	11: 116,223,660 (GRCm38)	E1068G	possibly damaging	Het
Ezh2	A	G	6: 47,576,660 (GRCm38)	M41T	probably damaging	Het
Fmo3	A	G	1: 162,968,725 (GRCm38)	S93P	possibly damaging	Het
Gdi2	A	G	13: 3,560,018 (GRCm38)	Y213C	possibly damaging	Het
Gpr15	A	T	16: 58,718,558 (GRCm38)	I56K	probably benign	Het
Gria2	G	T	3: 80,691,338 (GRCm38)	S796R	probably benign	Het
Hectd4	T	A	5: 121,291,191 (GRCm38)		probably benign	Het
Hgfac	T	C	5: 35,042,850 (GRCm38)		probably benign	Het
Hspg2	C	T	4: 137,520,156 (GRCm38)	R1200W	probably damaging	Het
Ift52	G	A	2: 163,025,355 (GRCm38)	D78N	possibly damaging	Het
Iqca1	C	A	1: 90,081,416 (GRCm38)	W415L	probably damaging	Het
Ism1	A	T	2: 139,746,043 (GRCm38)	K236N	probably damaging	Het
Itgb6	C	T	2: 60,672,644 (GRCm38)	W43*	probably null	Het
Kcnk18	T	A	19: 59,235,341 (GRCm38)	I306N	probably damaging	Het
Kctd8	T	C	5: 69,340,560 (GRCm38)	K248E	probably damaging	Het
Layn	T	A	9: 51,059,533 (GRCm38)	I237F	probably benign	Het
Lce3f	C	T	3: 92,992,941 (GRCm38)	P23L	unknown	Het
Lct	A	G	1: 128,300,301 (GRCm38)	F1152L	probably damaging	Het
Mettl25b	A	G	3: 87,923,817 (GRCm38)	S404P	probably damaging	Het
Mxra8	T	C	4: 155,843,074 (GRCm38)	I413T	probably damaging	Het
Nedd9	A	G	13: 41,317,962 (GRCm38)	V187A	probably benign	Het
Net1	A	G	13: 3,887,642 (GRCm38)	L207P	probably damaging	Het
Neurod1	G	T	2: 79,454,437 (GRCm38)	P201T	probably benign	Het
Nlrp1b	A	G	11: 71,161,821 (GRCm38)	F927S	probably damaging	Het
Ntrk3	T	A	7: 78,356,041 (GRCm38)	H524L	possibly damaging	Het
Nup98	A	C	7: 102,134,937 (GRCm38)	S1063A	probably benign	Het
Or10ak11	T	A	4: 118,829,868 (GRCm38)	M191L	probably benign	Het
Or11h4b	G	T	14: 50,681,166 (GRCm38)	P156Q	possibly damaging	Het
Or56b1	G	A	7: 104,636,159 (GRCm38)	V162I	probably benign	Het
Or5b97	C	A	19: 12,901,235 (GRCm38)	V182F	probably benign	Het
Or5m9b	G	A	2: 86,074,760 (GRCm38)	V7I	possibly damaging	Het
Or6d15	T	C	6: 116,582,964 (GRCm38)		probably benign	Het
Pdzd2	G	A	15: 12,592,460 (GRCm38)	R33W	probably damaging	Het
Phf21a	G	A	2: 92,330,515 (GRCm38)	V243I	probably damaging	Het
Ppp1r12b	A	G	1: 134,893,348 (GRCm38)		probably null	Het
Rexo5	T	C	7: 119,845,411 (GRCm38)	V703A	probably benign	Het
Rgs4	A	G	1: 169,745,278 (GRCm38)	S30P	probably benign	Het
Rxra	C	A	2: 27,756,244 (GRCm38)	D340E	probably damaging	Het
Samhd1	A	G	2: 157,107,547 (GRCm38)	V473A	probably benign	Het
Scn3a	T	A	2: 65,472,342 (GRCm38)	K1253N	probably damaging	Het
Scn7a	T	C	2: 66,680,955 (GRCm38)	N1207S	probably benign	Het
Sec24d	T	A	3: 123,336,517 (GRCm38)	I443N	probably damaging	Het
Sema4g	T	A	19: 44,999,242 (GRCm38)		probably null	Het
Sema5b	A	G	16: 35,660,324 (GRCm38)	K787R	probably benign	Het
Serpinc1	A	G	1: 160,989,647 (GRCm38)	N104D	probably benign	Het
Sfn	T	C	4: 133,601,231 (GRCm38)	H180R	probably damaging	Het
Slc22a6	G	T	19: 8,619,107 (GRCm38)		probably null	Het
Slc9a8	T	C	2: 167,457,358 (GRCm38)	S217P	probably benign	Het
Smc6	A	G	12: 11,309,269 (GRCm38)	N965D	probably benign	Het
Sod2	T	A	17: 13,015,032 (GRCm38)	I177N	probably damaging	Het
Sp4	A	T	12: 118,299,600 (GRCm38)	I237K	probably damaging	Het
Sulf2	T	C	2: 166,079,612 (GRCm38)	K697R	probably benign	Het
Svs4	A	T	2: 164,277,085 (GRCm38)	D110E	unknown	Het
Tas1r1	T	A	4: 152,038,218 (GRCm38)	R57*	probably null	Het
Tlr5	T	C	1: 182,973,722 (GRCm38)	I197T	probably damaging	Het
Tmc3	T	C	7: 83,612,532 (GRCm38)	V606A	probably benign	Het
Tmem241	T	A	18: 12,118,412 (GRCm38)	L37F	probably damaging	Het
Tmem59l	A	T	8: 70,486,253 (GRCm38)	N90K	probably damaging	Het
Tram1	A	C	1: 13,576,456 (GRCm38)		probably benign	Het
Trim15	T	A	17: 36,865,169 (GRCm38)	H162L	probably benign	Het
Ttc28	T	A	5: 111,276,811 (GRCm38)	Y1501N	probably benign	Het
Ttc34	T	C	4: 154,862,214 (GRCm38)	V857A	probably benign	Het
Tulp4	A	G	17: 6,139,046 (GRCm38)	T48A	probably damaging	Het
Usp9y	T	C	Y: 1,368,089 (GRCm38)	E939G	probably damaging	Het
Utp20	A	G	10: 88,770,808 (GRCm38)	I1634T	probably benign	Het
Vmn2r72	T	C	7: 85,738,170 (GRCm38)	M729V	probably benign	Het
Vps13c	C	T	9: 67,881,447 (GRCm38)	T334M	probably damaging	Het
Wnk4	C	G	11: 101,276,340 (GRCm38)		probably benign	Het
Xpo1	A	G	11: 23,271,193 (GRCm38)	N97D	probably benign	Het
Xpo4	A	T	14: 57,603,672 (GRCm38)	F518Y	probably benign	Het
Zfp668	C	T	7: 127,866,606 (GRCm38)	V469I	possibly damaging	Het
Zfp85	C	A	13: 67,749,704 (GRCm38)	C83F	probably damaging	Het

Other mutations in Csmd3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00158:Csmd3	APN	15	48,287,495 (GRCm38)	missense	possibly damaging	0.61
IGL00591:Csmd3	APN	15	48,004,883 (GRCm38)	missense	probably damaging	1.00
IGL00668:Csmd3	APN	15	47,913,945 (GRCm38)	missense	probably damaging	1.00
IGL00753:Csmd3	APN	15	47,644,235 (GRCm38)	missense	probably damaging	1.00
IGL00773:Csmd3	APN	15	47,590,719 (GRCm38)	missense	probably damaging	0.96
IGL00926:Csmd3	APN	15	47,710,964 (GRCm38)	missense	possibly damaging	0.87
IGL00942:Csmd3	APN	15	47,847,106 (GRCm38)	critical splice donor site	probably null
IGL01080:Csmd3	APN	15	47,881,403 (GRCm38)	missense	probably benign	0.12
IGL01314:Csmd3	APN	15	47,849,755 (GRCm38)	missense	probably damaging	1.00
IGL01326:Csmd3	APN	15	47,849,785 (GRCm38)	missense	probably benign	0.06
IGL01393:Csmd3	APN	15	48,457,599 (GRCm38)	missense	possibly damaging	0.88
IGL01432:Csmd3	APN	15	47,733,499 (GRCm38)	missense	probably damaging	1.00
IGL01519:Csmd3	APN	15	47,596,850 (GRCm38)	missense	probably benign	0.31
IGL01530:Csmd3	APN	15	47,669,617 (GRCm38)	missense	probably damaging	1.00
IGL01530:Csmd3	APN	15	47,838,437 (GRCm38)	missense	possibly damaging	0.95
IGL01547:Csmd3	APN	15	47,883,617 (GRCm38)	missense	probably benign	0.41
IGL01594:Csmd3	APN	15	47,629,239 (GRCm38)	missense	probably benign	0.01
IGL01618:Csmd3	APN	15	48,011,083 (GRCm38)	missense	probably benign	0.05
IGL01670:Csmd3	APN	15	47,611,829 (GRCm38)	missense	probably damaging	1.00
IGL01680:Csmd3	APN	15	47,970,030 (GRCm38)	missense	probably damaging	1.00
IGL01734:Csmd3	APN	15	48,185,304 (GRCm38)	missense	probably damaging	1.00
IGL01777:Csmd3	APN	15	47,698,198 (GRCm38)	missense	probably benign	0.06
IGL01779:Csmd3	APN	15	47,857,894 (GRCm38)	missense	probably benign	0.10
IGL01820:Csmd3	APN	15	47,607,142 (GRCm38)	nonsense	probably null
IGL01843:Csmd3	APN	15	47,658,999 (GRCm38)	splice site	probably benign
IGL01919:Csmd3	APN	15	47,675,772 (GRCm38)	missense	possibly damaging	0.62
IGL01986:Csmd3	APN	15	47,659,195 (GRCm38)	missense	possibly damaging	0.82
IGL02049:Csmd3	APN	15	48,001,474 (GRCm38)	missense	possibly damaging	0.91
IGL02065:Csmd3	APN	15	47,666,628 (GRCm38)	missense	probably damaging	1.00
IGL02112:Csmd3	APN	15	48,313,869 (GRCm38)	missense	possibly damaging	0.95
IGL02133:Csmd3	APN	15	47,857,942 (GRCm38)	missense	possibly damaging	0.86
IGL02203:Csmd3	APN	15	47,849,677 (GRCm38)	splice site	probably null
IGL02215:Csmd3	APN	15	47,585,688 (GRCm38)	missense	probably damaging	1.00
IGL02234:Csmd3	APN	15	47,948,116 (GRCm38)	missense	probably damaging	1.00
IGL02326:Csmd3	APN	15	47,755,963 (GRCm38)	splice site	probably benign
IGL02478:Csmd3	APN	15	47,838,398 (GRCm38)	splice site	probably benign
IGL02491:Csmd3	APN	15	47,914,115 (GRCm38)	splice site	probably benign
IGL02598:Csmd3	APN	15	47,669,690 (GRCm38)	missense	probably damaging	0.98
IGL02626:Csmd3	APN	15	47,704,107 (GRCm38)	splice site	probably benign
IGL02696:Csmd3	APN	15	47,669,669 (GRCm38)	missense	probably benign	0.33
IGL02876:Csmd3	APN	15	47,606,096 (GRCm38)	splice site	probably benign
IGL02971:Csmd3	APN	15	47,913,929 (GRCm38)	splice site	probably benign
IGL03068:Csmd3	APN	15	47,847,121 (GRCm38)	missense	possibly damaging	0.69
IGL03087:Csmd3	APN	15	47,977,033 (GRCm38)	missense	probably damaging	1.00
IGL03114:Csmd3	APN	15	47,820,451 (GRCm38)	missense	probably damaging	0.99
IGL03146:Csmd3	APN	15	47,881,477 (GRCm38)	missense	probably benign	0.25
IGL03193:Csmd3	APN	15	47,629,230 (GRCm38)	splice site	probably benign
IGL03274:Csmd3	APN	15	47,645,504 (GRCm38)	missense	probably damaging	1.00
R0040:Csmd3	UTSW	15	47,633,816 (GRCm38)	missense	probably damaging	1.00
R0071:Csmd3	UTSW	15	47,596,821 (GRCm38)	missense	probably benign	0.04
R0071:Csmd3	UTSW	15	47,596,821 (GRCm38)	missense	probably benign	0.04
R0119:Csmd3	UTSW	15	47,847,131 (GRCm38)	missense	probably benign	0.08
R0124:Csmd3	UTSW	15	47,590,716 (GRCm38)	missense	probably damaging	1.00
R0127:Csmd3	UTSW	15	47,981,930 (GRCm38)	missense	probably benign	0.45
R0136:Csmd3	UTSW	15	47,847,131 (GRCm38)	missense	probably benign	0.08
R0201:Csmd3	UTSW	15	47,619,729 (GRCm38)	splice site	probably benign
R0240:Csmd3	UTSW	15	47,629,239 (GRCm38)	missense	probably benign	0.05
R0240:Csmd3	UTSW	15	47,629,239 (GRCm38)	missense	probably benign	0.05
R0318:Csmd3	UTSW	15	47,659,153 (GRCm38)	missense	probably damaging	1.00
R0369:Csmd3	UTSW	15	47,970,147 (GRCm38)	missense	probably damaging	1.00
R0391:Csmd3	UTSW	15	47,657,573 (GRCm38)	missense	probably damaging	1.00
R0499:Csmd3	UTSW	15	47,847,131 (GRCm38)	missense	probably benign	0.08
R0506:Csmd3	UTSW	15	48,457,511 (GRCm38)	missense	probably benign	0.00
R0606:Csmd3	UTSW	15	48,457,662 (GRCm38)	missense	probably benign
R0639:Csmd3	UTSW	15	47,913,940 (GRCm38)	missense	probably damaging	1.00
R0658:Csmd3	UTSW	15	48,011,147 (GRCm38)	missense	possibly damaging	0.66
R0673:Csmd3	UTSW	15	47,913,940 (GRCm38)	missense	probably damaging	1.00
R0689:Csmd3	UTSW	15	47,756,025 (GRCm38)	missense	probably benign	0.19
R0696:Csmd3	UTSW	15	47,847,173 (GRCm38)	missense	probably benign	0.01
R0799:Csmd3	UTSW	15	48,185,384 (GRCm38)	splice site	probably benign
R0834:Csmd3	UTSW	15	47,883,677 (GRCm38)	intron	probably benign
R0894:Csmd3	UTSW	15	47,857,920 (GRCm38)	missense	possibly damaging	0.95
R0926:Csmd3	UTSW	15	47,977,033 (GRCm38)	missense	probably damaging	1.00
R0943:Csmd3	UTSW	15	47,675,739 (GRCm38)	missense	probably damaging	0.99
R0944:Csmd3	UTSW	15	47,611,831 (GRCm38)	missense	probably damaging	1.00
R0967:Csmd3	UTSW	15	47,857,831 (GRCm38)	missense	probably null	0.89
R0973:Csmd3	UTSW	15	47,659,089 (GRCm38)	missense	probably damaging	1.00
R1055:Csmd3	UTSW	15	47,881,537 (GRCm38)	missense	probably damaging	1.00
R1066:Csmd3	UTSW	15	47,913,965 (GRCm38)	missense	probably damaging	1.00
R1086:Csmd3	UTSW	15	47,695,755 (GRCm38)	missense	probably damaging	0.99
R1103:Csmd3	UTSW	15	47,948,006 (GRCm38)	missense	probably damaging	1.00
R1136:Csmd3	UTSW	15	47,675,817 (GRCm38)	missense	probably damaging	1.00
R1139:Csmd3	UTSW	15	47,695,836 (GRCm38)	missense	probably damaging	1.00
R1158:Csmd3	UTSW	15	48,292,774 (GRCm38)	splice site	probably null
R1215:Csmd3	UTSW	15	48,004,831 (GRCm38)	splice site	probably null
R1233:Csmd3	UTSW	15	48,673,531 (GRCm38)	missense	probably damaging	1.00
R1271:Csmd3	UTSW	15	48,011,059 (GRCm38)	missense	probably benign	0.11
R1469:Csmd3	UTSW	15	47,669,202 (GRCm38)	nonsense	probably null
R1469:Csmd3	UTSW	15	47,669,202 (GRCm38)	nonsense	probably null
R1479:Csmd3	UTSW	15	47,857,886 (GRCm38)	missense	probably damaging	1.00
R1480:Csmd3	UTSW	15	47,731,929 (GRCm38)	missense	possibly damaging	0.90
R1526:Csmd3	UTSW	15	47,585,632 (GRCm38)	critical splice donor site	probably null
R1527:Csmd3	UTSW	15	47,948,087 (GRCm38)	missense	probably benign	0.08
R1539:Csmd3	UTSW	15	47,820,398 (GRCm38)	missense	probably benign	0.24
R1544:Csmd3	UTSW	15	47,611,898 (GRCm38)	splice site	probably null
R1548:Csmd3	UTSW	15	47,981,975 (GRCm38)	missense	possibly damaging	0.91
R1574:Csmd3	UTSW	15	47,695,861 (GRCm38)	splice site	probably null
R1574:Csmd3	UTSW	15	47,695,861 (GRCm38)	splice site	probably null
R1619:Csmd3	UTSW	15	47,949,950 (GRCm38)	missense	probably damaging	1.00
R1630:Csmd3	UTSW	15	47,838,522 (GRCm38)	missense	possibly damaging	0.66
R1665:Csmd3	UTSW	15	47,696,789 (GRCm38)	missense	probably damaging	1.00
R1680:Csmd3	UTSW	15	47,741,170 (GRCm38)	missense	probably damaging	1.00
R1725:Csmd3	UTSW	15	47,596,807 (GRCm38)	missense	probably damaging	1.00
R1743:Csmd3	UTSW	15	48,622,089 (GRCm38)	missense	probably damaging	1.00
R1749:Csmd3	UTSW	15	47,585,660 (GRCm38)	missense	probably damaging	1.00
R1752:Csmd3	UTSW	15	47,660,273 (GRCm38)	missense	probably benign	0.15
R1769:Csmd3	UTSW	15	47,704,109 (GRCm38)	splice site	probably benign
R1795:Csmd3	UTSW	15	47,857,920 (GRCm38)	missense	possibly damaging	0.95
R1819:Csmd3	UTSW	15	47,753,735 (GRCm38)	missense	possibly damaging	0.56
R1840:Csmd3	UTSW	15	47,607,164 (GRCm38)	missense	probably damaging	1.00
R1860:Csmd3	UTSW	15	47,659,192 (GRCm38)	missense	probably damaging	1.00
R1861:Csmd3	UTSW	15	47,659,192 (GRCm38)	missense	probably damaging	1.00
R1879:Csmd3	UTSW	15	47,657,519 (GRCm38)	missense	possibly damaging	0.90
R1958:Csmd3	UTSW	15	48,004,639 (GRCm38)	critical splice donor site	probably null
R1965:Csmd3	UTSW	15	47,849,748 (GRCm38)	missense	probably benign	0.15
R1970:Csmd3	UTSW	15	48,673,531 (GRCm38)	missense	probably damaging	1.00
R2029:Csmd3	UTSW	15	47,838,579 (GRCm38)	missense	probably damaging	1.00
R2051:Csmd3	UTSW	15	48,621,993 (GRCm38)	critical splice donor site	probably null
R2108:Csmd3	UTSW	15	48,004,861 (GRCm38)	missense	possibly damaging	0.81
R2132:Csmd3	UTSW	15	48,457,503 (GRCm38)	missense	probably benign	0.06
R2146:Csmd3	UTSW	15	47,741,236 (GRCm38)	frame shift	probably null
R2147:Csmd3	UTSW	15	47,741,236 (GRCm38)	frame shift	probably null
R2148:Csmd3	UTSW	15	47,741,236 (GRCm38)	frame shift	probably null
R2157:Csmd3	UTSW	15	47,695,787 (GRCm38)	missense	probably damaging	0.99
R2159:Csmd3	UTSW	15	47,741,236 (GRCm38)	frame shift	probably null
R2160:Csmd3	UTSW	15	47,741,236 (GRCm38)	frame shift	probably null
R2161:Csmd3	UTSW	15	47,741,236 (GRCm38)	frame shift	probably null
R2162:Csmd3	UTSW	15	47,741,236 (GRCm38)	frame shift	probably null
R2164:Csmd3	UTSW	15	47,741,236 (GRCm38)	frame shift	probably null
R2213:Csmd3	UTSW	15	47,820,447 (GRCm38)	missense	possibly damaging	0.92
R2301:Csmd3	UTSW	15	47,731,998 (GRCm38)	missense	probably damaging	1.00
R2302:Csmd3	UTSW	15	48,314,051 (GRCm38)	missense	probably benign
R2355:Csmd3	UTSW	15	47,741,236 (GRCm38)	frame shift	probably null
R2497:Csmd3	UTSW	15	47,741,236 (GRCm38)	frame shift	probably null
R2509:Csmd3	UTSW	15	47,741,236 (GRCm38)	frame shift	probably null
R2566:Csmd3	UTSW	15	47,741,236 (GRCm38)	frame shift	probably null
R2567:Csmd3	UTSW	15	47,741,236 (GRCm38)	frame shift	probably null
R2568:Csmd3	UTSW	15	47,741,236 (GRCm38)	frame shift	probably null
R2570:Csmd3	UTSW	15	47,741,236 (GRCm38)	frame shift	probably null
R2571:Csmd3	UTSW	15	47,741,236 (GRCm38)	frame shift	probably null
R2870:Csmd3	UTSW	15	47,857,924 (GRCm38)	missense	probably damaging	1.00
R2870:Csmd3	UTSW	15	47,857,924 (GRCm38)	missense	probably damaging	1.00
R2907:Csmd3	UTSW	15	48,011,053 (GRCm38)	missense	probably damaging	0.99
R3116:Csmd3	UTSW	15	47,657,599 (GRCm38)	missense	probably damaging	1.00
R3423:Csmd3	UTSW	15	47,847,252 (GRCm38)	missense	probably damaging	0.98
R3425:Csmd3	UTSW	15	47,847,252 (GRCm38)	missense	probably damaging	0.98
R3508:Csmd3	UTSW	15	47,741,236 (GRCm38)	frame shift	probably null
R3746:Csmd3	UTSW	15	47,849,766 (GRCm38)	missense	probably benign	0.04
R3813:Csmd3	UTSW	15	48,791,813 (GRCm38)	missense	possibly damaging	0.82
R3832:Csmd3	UTSW	15	47,741,236 (GRCm38)	frame shift	probably null
R3959:Csmd3	UTSW	15	47,644,189 (GRCm38)	missense	probably benign	0.18
R4042:Csmd3	UTSW	15	47,614,084 (GRCm38)	missense	probably damaging	1.00
R4043:Csmd3	UTSW	15	47,755,966 (GRCm38)	critical splice donor site	probably null
R4191:Csmd3	UTSW	15	47,847,271 (GRCm38)	missense	probably damaging	0.99
R4192:Csmd3	UTSW	15	47,847,271 (GRCm38)	missense	probably damaging	0.99
R4419:Csmd3	UTSW	15	47,704,311 (GRCm38)	missense	probably damaging	1.00
R4426:Csmd3	UTSW	15	47,669,185 (GRCm38)	missense	possibly damaging	0.51
R4434:Csmd3	UTSW	15	47,899,795 (GRCm38)	missense	possibly damaging	0.68
R4438:Csmd3	UTSW	15	47,899,795 (GRCm38)	missense	possibly damaging	0.68
R4490:Csmd3	UTSW	15	48,314,033 (GRCm38)	missense	possibly damaging	0.83
R4562:Csmd3	UTSW	15	47,899,844 (GRCm38)	missense	probably benign	0.32
R4604:Csmd3	UTSW	15	48,004,815 (GRCm38)	missense	possibly damaging	0.90
R4620:Csmd3	UTSW	15	47,585,753 (GRCm38)	missense	probably benign	0.09
R4632:Csmd3	UTSW	15	48,011,209 (GRCm38)	missense	probably damaging	0.99
R4679:Csmd3	UTSW	15	48,161,083 (GRCm38)	nonsense	probably null
R4696:Csmd3	UTSW	15	47,913,968 (GRCm38)	missense	probably benign	0.24
R4718:Csmd3	UTSW	15	47,698,150 (GRCm38)	nonsense	probably null
R4723:Csmd3	UTSW	15	47,669,160 (GRCm38)	missense	probably benign	0.29
R4801:Csmd3	UTSW	15	47,621,292 (GRCm38)	missense	probably damaging	1.00
R4802:Csmd3	UTSW	15	47,621,292 (GRCm38)	missense	probably damaging	1.00
R4806:Csmd3	UTSW	15	48,314,068 (GRCm38)	missense	probably benign
R4816:Csmd3	UTSW	15	47,857,934 (GRCm38)	missense	possibly damaging	0.68
R4935:Csmd3	UTSW	15	48,161,084 (GRCm38)	missense	probably damaging	1.00
R4955:Csmd3	UTSW	15	48,673,518 (GRCm38)	missense	probably damaging	0.99
R4991:Csmd3	UTSW	15	48,001,478 (GRCm38)	missense	probably damaging	1.00
R5031:Csmd3	UTSW	15	47,659,192 (GRCm38)	missense	probably damaging	1.00
R5034:Csmd3	UTSW	15	47,629,287 (GRCm38)	missense	possibly damaging	0.94
R5035:Csmd3	UTSW	15	47,590,779 (GRCm38)	missense	probably damaging	1.00
R5120:Csmd3	UTSW	15	48,673,495 (GRCm38)	nonsense	probably null
R5224:Csmd3	UTSW	15	47,888,684 (GRCm38)	missense	possibly damaging	0.91
R5235:Csmd3	UTSW	15	47,629,278 (GRCm38)	missense	probably benign	0.20
R5279:Csmd3	UTSW	15	48,791,944 (GRCm38)	splice site	probably null
R5360:Csmd3	UTSW	15	47,669,203 (GRCm38)	missense	probably damaging	0.99
R5365:Csmd3	UTSW	15	48,004,749 (GRCm38)	missense	possibly damaging	0.68
R5379:Csmd3	UTSW	15	47,636,450 (GRCm38)	nonsense	probably null
R5381:Csmd3	UTSW	15	47,741,215 (GRCm38)	missense	probably benign	0.21
R5393:Csmd3	UTSW	15	47,633,703 (GRCm38)	missense	probably damaging	1.00
R5413:Csmd3	UTSW	15	47,838,435 (GRCm38)	missense	probably damaging	1.00
R5549:Csmd3	UTSW	15	48,185,357 (GRCm38)	missense	probably damaging	0.98
R5550:Csmd3	UTSW	15	48,185,357 (GRCm38)	missense	probably damaging	0.98
R5551:Csmd3	UTSW	15	48,314,096 (GRCm38)	missense	probably benign	0.13
R5567:Csmd3	UTSW	15	47,645,468 (GRCm38)	missense	possibly damaging	0.92
R5621:Csmd3	UTSW	15	48,313,978 (GRCm38)	missense	possibly damaging	0.84
R5668:Csmd3	UTSW	15	47,695,755 (GRCm38)	missense	possibly damaging	0.48
R5677:Csmd3	UTSW	15	48,622,051 (GRCm38)	missense	probably damaging	0.98
R5701:Csmd3	UTSW	15	48,540,333 (GRCm38)	missense	probably damaging	0.99
R5701:Csmd3	UTSW	15	47,650,221 (GRCm38)	missense	probably damaging	1.00
R5871:Csmd3	UTSW	15	47,888,716 (GRCm38)	missense	probably damaging	0.98
R5872:Csmd3	UTSW	15	47,582,527 (GRCm38)	missense	probably damaging	1.00
R5874:Csmd3	UTSW	15	47,644,270 (GRCm38)	missense	probably damaging	1.00
R5952:Csmd3	UTSW	15	47,733,505 (GRCm38)	missense	probably damaging	0.98
R5956:Csmd3	UTSW	15	48,791,882 (GRCm38)	missense	possibly damaging	0.84
R5966:Csmd3	UTSW	15	47,849,739 (GRCm38)	missense	probably damaging	0.96
R5969:Csmd3	UTSW	15	47,947,990 (GRCm38)	missense	probably damaging	1.00
R5989:Csmd3	UTSW	15	47,590,764 (GRCm38)	missense	possibly damaging	0.69
R6017:Csmd3	UTSW	15	48,314,012 (GRCm38)	missense	possibly damaging	0.95
R6057:Csmd3	UTSW	15	47,755,391 (GRCm38)	missense	probably damaging	1.00
R6127:Csmd3	UTSW	15	47,650,228 (GRCm38)	missense	probably damaging	1.00
R6178:Csmd3	UTSW	15	48,673,458 (GRCm38)	missense	probably damaging	1.00
R6198:Csmd3	UTSW	15	48,313,877 (GRCm38)	missense	probably benign	0.28
R6213:Csmd3	UTSW	15	47,629,260 (GRCm38)	missense	probably damaging	1.00
R6256:Csmd3	UTSW	15	47,669,729 (GRCm38)	missense	probably damaging	1.00
R6274:Csmd3	UTSW	15	47,621,437 (GRCm38)	missense	probably benign
R6327:Csmd3	UTSW	15	47,881,387 (GRCm38)	missense	probably damaging	1.00
R6354:Csmd3	UTSW	15	47,881,489 (GRCm38)	missense	probably damaging	1.00
R6405:Csmd3	UTSW	15	47,820,371 (GRCm38)	missense	probably damaging	0.99
R6410:Csmd3	UTSW	15	48,673,407 (GRCm38)	missense	probably damaging	1.00
R6416:Csmd3	UTSW	15	48,673,560 (GRCm38)	missense	probably damaging	1.00
R6463:Csmd3	UTSW	15	47,676,479 (GRCm38)	missense	probably damaging	1.00
R6536:Csmd3	UTSW	15	47,838,467 (GRCm38)	missense	probably damaging	1.00
R6625:Csmd3	UTSW	15	47,607,075 (GRCm38)	missense	probably benign	0.02
R6695:Csmd3	UTSW	15	47,857,834 (GRCm38)	missense	probably damaging	0.99
R6895:Csmd3	UTSW	15	47,666,514 (GRCm38)	splice site	probably null
R6906:Csmd3	UTSW	15	47,847,173 (GRCm38)	missense	probably benign	0.01
R6914:Csmd3	UTSW	15	48,011,138 (GRCm38)	missense	possibly damaging	0.53
R6920:Csmd3	UTSW	15	47,644,205 (GRCm38)	missense	probably damaging	1.00
R7024:Csmd3	UTSW	15	47,710,991 (GRCm38)	missense	probably damaging	1.00
R7178:Csmd3	UTSW	15	47,590,774 (GRCm38)	missense
R7192:Csmd3	UTSW	15	47,704,237 (GRCm38)	missense
R7220:Csmd3	UTSW	15	48,457,598 (GRCm38)	missense	probably damaging	0.99
R7362:Csmd3	UTSW	15	47,755,992 (GRCm38)	missense	possibly damaging	0.65
R7380:Csmd3	UTSW	15	47,586,965 (GRCm38)	missense
R7397:Csmd3	UTSW	15	47,695,734 (GRCm38)	missense
R7467:Csmd3	UTSW	15	47,629,244 (GRCm38)	missense
R7585:Csmd3	UTSW	15	48,622,075 (GRCm38)	missense	possibly damaging	0.76
R7623:Csmd3	UTSW	15	47,949,938 (GRCm38)	missense
R7649:Csmd3	UTSW	15	47,669,143 (GRCm38)	missense
R7691:Csmd3	UTSW	15	47,741,173 (GRCm38)	missense
R7695:Csmd3	UTSW	15	47,820,381 (GRCm38)	missense
R7759:Csmd3	UTSW	15	47,698,173 (GRCm38)	missense
R7817:Csmd3	UTSW	15	47,857,960 (GRCm38)	missense	probably damaging	0.99
R8052:Csmd3	UTSW	15	47,706,387 (GRCm38)	missense
R8089:Csmd3	UTSW	15	47,669,207 (GRCm38)	missense
R8110:Csmd3	UTSW	15	47,644,270 (GRCm38)	missense	probably damaging	1.00
R8152:Csmd3	UTSW	15	47,669,464 (GRCm38)	splice site	probably null
R8323:Csmd3	UTSW	15	47,698,151 (GRCm38)	missense
R8341:Csmd3	UTSW	15	47,698,151 (GRCm38)	missense
R8353:Csmd3	UTSW	15	47,949,953 (GRCm38)	missense	probably damaging	1.00
R8364:Csmd3	UTSW	15	48,673,441 (GRCm38)	missense	probably damaging	1.00
R8405:Csmd3	UTSW	15	47,755,983 (GRCm38)	missense	probably damaging	1.00
R8412:Csmd3	UTSW	15	47,636,398 (GRCm38)	missense
R8436:Csmd3	UTSW	15	48,004,822 (GRCm38)	missense	probably damaging	0.97
R8516:Csmd3	UTSW	15	47,629,365 (GRCm38)	nonsense	probably null
R8553:Csmd3	UTSW	15	47,621,328 (GRCm38)	missense	possibly damaging	0.52
R8554:Csmd3	UTSW	15	47,644,142 (GRCm38)	missense	probably benign	0.32
R8678:Csmd3	UTSW	15	47,636,453 (GRCm38)	missense
R8751:Csmd3	UTSW	15	47,982,006 (GRCm38)	missense
R8758:Csmd3	UTSW	15	47,606,197 (GRCm38)	missense
R8768:Csmd3	UTSW	15	47,698,176 (GRCm38)	missense
R8785:Csmd3	UTSW	15	48,314,086 (GRCm38)	missense	probably benign	0.00
R8788:Csmd3	UTSW	15	47,607,117 (GRCm38)	missense
R8798:Csmd3	UTSW	15	47,731,986 (GRCm38)	missense
R8801:Csmd3	UTSW	15	48,457,628 (GRCm38)	missense	possibly damaging	0.70
R8811:Csmd3	UTSW	15	47,696,743 (GRCm38)	missense
R8844:Csmd3	UTSW	15	48,673,419 (GRCm38)	missense	probably damaging	0.98
R8844:Csmd3	UTSW	15	47,741,194 (GRCm38)	missense	probably damaging	0.96
R8892:Csmd3	UTSW	15	47,741,238 (GRCm38)	missense
R8897:Csmd3	UTSW	15	48,359,343 (GRCm38)	missense	probably benign	0.06
R9001:Csmd3	UTSW	15	47,733,505 (GRCm38)	missense
R9007:Csmd3	UTSW	15	47,888,496 (GRCm38)	intron	probably benign
R9016:Csmd3	UTSW	15	47,659,042 (GRCm38)	missense
R9039:Csmd3	UTSW	15	47,619,912 (GRCm38)	splice site	probably benign
R9109:Csmd3	UTSW	15	47,753,791 (GRCm38)	missense
R9121:Csmd3	UTSW	15	47,820,378 (GRCm38)	missense
R9155:Csmd3	UTSW	15	47,585,655 (GRCm38)	missense
R9176:Csmd3	UTSW	15	48,001,541 (GRCm38)	missense
R9281:Csmd3	UTSW	15	47,596,876 (GRCm38)	missense
R9298:Csmd3	UTSW	15	47,753,791 (GRCm38)	missense
R9304:Csmd3	UTSW	15	47,706,409 (GRCm38)	missense
R9343:Csmd3	UTSW	15	48,151,605 (GRCm38)	missense	probably damaging	1.00
R9367:Csmd3	UTSW	15	47,704,168 (GRCm38)	missense
R9405:Csmd3	UTSW	15	47,675,791 (GRCm38)	missense
R9448:Csmd3	UTSW	15	47,596,919 (GRCm38)	missense
R9460:Csmd3	UTSW	15	47,753,734 (GRCm38)	missense
R9481:Csmd3	UTSW	15	47,607,063 (GRCm38)	missense
R9520:Csmd3	UTSW	15	47,698,212 (GRCm38)	missense
R9551:Csmd3	UTSW	15	48,791,960 (GRCm38)	start gained	probably benign
R9552:Csmd3	UTSW	15	48,791,960 (GRCm38)	start gained	probably benign
R9568:Csmd3	UTSW	15	48,287,546 (GRCm38)	missense	probably damaging	0.97
R9571:Csmd3	UTSW	15	48,792,002 (GRCm38)	start gained	probably benign
R9607:Csmd3	UTSW	15	47,755,415 (GRCm38)	missense	probably damaging	0.98
R9621:Csmd3	UTSW	15	47,849,720 (GRCm38)	missense
R9671:Csmd3	UTSW	15	47,981,903 (GRCm38)	missense
R9718:Csmd3	UTSW	15	47,696,687 (GRCm38)	missense
U24488:Csmd3	UTSW	15	47,710,399 (GRCm38)	missense	probably damaging	1.00
V8831:Csmd3	UTSW	15	48,457,696 (GRCm38)	missense	probably damaging	0.96
X0021:Csmd3	UTSW	15	47,970,093 (GRCm38)	nonsense	probably null
Z1088:Csmd3	UTSW	15	47,847,281 (GRCm38)	missense	probably damaging	0.98
Z1088:Csmd3	UTSW	15	47,636,393 (GRCm38)	missense	probably damaging	1.00
Z1177:Csmd3	UTSW	15	47,733,417 (GRCm38)	missense
Z1177:Csmd3	UTSW	15	47,675,734 (GRCm38)	missense

Predicted Primers

PCR Primer
(F):5'- ATCTAAGTGAAGACAGCACAGC -3'
(R):5'- CATATCCTTTATGACTGGCTGTTTG -3'

Sequencing Primer
(F):5'- AGCACAGCTGAAAAAGACTATATAAC -3'
(R):5'- CTGTTTGGCCTCACATATAGTAATTG -3'

Posted On

2014-06-23