Mutagenetix > Incidental Mutation

Incidental Mutation 'R0391:Csmd3'

31725

Institutional Source

Beutler Lab

Gene Symbol

Csmd3

Ensembl Gene

ENSMUSG00000022311

Gene Name

CUB and Sushi multiple domains 3

Synonyms

4930500N14Rik

MMRRC Submission

038597-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0391 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

47580637-48792063 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 47657573 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Leucine at position 1881 (V1881L)

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: V2792L

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000098235
Gene: ENSMUSG00000022311
AA Change: V2792L

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

possibly damaging
Transcript: ENSMUST00000160658
AA Change: V2623L

PolyPhen 2 Score 0.692 (Sensitivity: 0.86; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000124753
Gene: ENSMUSG00000022311
AA Change: V2623L

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 damaging
Transcript: ENSMUST00000161653
AA Change: V1881L

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000124195
Gene: ENSMUSG00000022311
AA Change: V1881L

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: V2792L

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000124775
Gene: ENSMUSG00000022311
AA Change: V2792L

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

0.1050

Coding Region Coverage

1x: 99.1%
3x: 98.2%
10x: 95.9%
20x: 91.8%

Validation Efficiency

97% (97/100)

Allele List at MGI

Other mutations in this stock

Total: 97 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
9530002B09Rik	T	A	4: 122,701,177 (GRCm38)		probably benign	Het
Abcc2	G	A	19: 43,821,605 (GRCm38)		probably benign	Het
Abcc8	C	G	7: 46,122,173 (GRCm38)	G838A	probably damaging	Het
Akr1c21	G	A	13: 4,581,200 (GRCm38)	A245T	probably damaging	Het
Anapc15-ps	T	C	10: 95,673,277 (GRCm38)	E47G	probably damaging	Het
Apoa1	A	G	9: 46,229,842 (GRCm38)	T79A	probably benign	Het
Atp6v1b1	A	G	6: 83,756,921 (GRCm38)	H378R	possibly damaging	Het
C4b	A	G	17: 34,735,614 (GRCm38)		probably benign	Het
Catsperd	A	T	17: 56,662,821 (GRCm38)	E638D	probably benign	Het
Cckar	C	T	5: 53,706,253 (GRCm38)		probably null	Het
Cfap100	C	T	6: 90,405,339 (GRCm38)		probably benign	Het
Chd1	G	T	17: 15,749,894 (GRCm38)	G970C	probably damaging	Het
Col14a1	A	G	15: 55,446,259 (GRCm38)		probably benign	Het
Col17a1	C	T	19: 47,663,824 (GRCm38)	V698M	probably damaging	Het
Cpeb1	T	C	7: 81,361,725 (GRCm38)	D156G	possibly damaging	Het
Cryl1	A	G	14: 57,303,775 (GRCm38)	Y151H	possibly damaging	Het
Ctnnal1	C	T	4: 56,847,921 (GRCm38)	A73T	probably damaging	Het
Cyp2c37	T	C	19: 39,994,506 (GRCm38)	S180P	probably damaging	Het
Cyp2c54	T	C	19: 40,072,169 (GRCm38)	T123A	possibly damaging	Het
Dennd6b	T	C	15: 89,187,214 (GRCm38)	D304G	probably damaging	Het
Dnmt3l	T	C	10: 78,051,916 (GRCm38)		probably benign	Het
Eci1	G	A	17: 24,433,260 (GRCm38)		probably null	Het
Efhc1	A	G	1: 20,960,188 (GRCm38)	Y115C	probably damaging	Het
Ern1	T	A	11: 106,407,178 (GRCm38)	K706*	probably null	Het
Ghrl	T	C	6: 113,719,338 (GRCm38)	E31G	probably damaging	Het
Gpr108	A	C	17: 57,243,101 (GRCm38)	V179G	probably benign	Het
Henmt1	A	G	3: 108,958,535 (GRCm38)		probably benign	Het
Ift172	A	G	5: 31,286,667 (GRCm38)	V69A	probably damaging	Het
Il17ra	T	C	6: 120,476,979 (GRCm38)		probably benign	Het
Il17rb	G	T	14: 30,006,155 (GRCm38)		probably null	Het
Il17rb	T	C	14: 30,004,347 (GRCm38)	N95D	probably benign	Het
Iqub	G	A	6: 24,446,155 (GRCm38)	L757F	probably benign	Het
Itpr1	T	C	6: 108,378,167 (GRCm38)	V473A	probably benign	Het
Itpr2	T	G	6: 146,229,773 (GRCm38)	N1978H	probably damaging	Het
Klk1b26	T	A	7: 44,012,727 (GRCm38)	F3Y	probably damaging	Het
Lars1	A	G	18: 42,251,363 (GRCm38)	V50A	probably benign	Het
Lax1	G	T	1: 133,680,066 (GRCm38)	H312Q	probably benign	Het
Lctl	T	C	9: 64,122,314 (GRCm38)		probably benign	Het
Lrp2	G	A	2: 69,460,337 (GRCm38)		probably benign	Het
Lrp2	T	A	2: 69,456,858 (GRCm38)	D3745V	probably damaging	Het
Lvrn	A	T	18: 46,850,466 (GRCm38)	H92L	probably benign	Het
Marchf1	A	G	8: 66,418,973 (GRCm38)	T385A	probably damaging	Het
Marf1	C	T	16: 14,142,534 (GRCm38)	A549T	probably damaging	Het
Mbd5	T	C	2: 49,272,416 (GRCm38)	V970A	possibly damaging	Het
Mccc1	A	G	3: 35,963,570 (GRCm38)		probably benign	Het
Mpp4	A	T	1: 59,143,829 (GRCm38)		probably benign	Het
Mrnip	G	A	11: 50,199,920 (GRCm38)	A304T	probably damaging	Het
Muc5b	T	C	7: 141,865,082 (GRCm38)	S3922P	possibly damaging	Het
Myh3	T	A	11: 67,096,507 (GRCm38)		probably benign	Het
Nbea	A	T	3: 56,037,277 (GRCm38)	H555Q	probably damaging	Het
Niban3	T	A	8: 71,602,499 (GRCm38)		probably benign	Het
Nlrp9c	A	T	7: 26,371,476 (GRCm38)		probably benign	Het
Nmur1	A	T	1: 86,387,678 (GRCm38)	V178E	probably damaging	Het
Nod2	T	G	8: 88,663,778 (GRCm38)	S238A	probably benign	Het
Ogfod1	A	T	8: 94,063,023 (GRCm38)	T451S	probably damaging	Het
Or1e17	T	C	11: 73,941,109 (GRCm38)	F288L	probably damaging	Het
Or2d36	T	A	7: 107,148,187 (GRCm38)	Y290*	probably null	Het
Or2z8	C	T	8: 72,058,400 (GRCm38)	T240M	probably damaging	Het
Or8b8	G	A	9: 37,897,842 (GRCm38)	G146D	probably benign	Het
Pcdh20	T	C	14: 88,468,668 (GRCm38)	I399V	probably benign	Het
Pdlim1	G	T	19: 40,243,573 (GRCm38)	H120Q	probably damaging	Het
Plg	T	C	17: 12,419,081 (GRCm38)	V798A	probably damaging	Het
Polr2c	A	G	8: 94,857,775 (GRCm38)	I39V	possibly damaging	Het
Ppfia2	C	A	10: 106,830,714 (GRCm38)		probably benign	Het
Ppp1r3a	A	T	6: 14,719,697 (GRCm38)	I406N	probably benign	Het
Psg28	A	T	7: 18,426,173 (GRCm38)	M366K	probably benign	Het
Rad54b	T	C	4: 11,601,702 (GRCm38)	I419T	probably damaging	Het
Rnf43	A	G	11: 87,731,282 (GRCm38)	Q403R	possibly damaging	Het
Sema6a	G	A	18: 47,290,045 (GRCm38)		probably null	Het
Slc28a3	A	G	13: 58,569,415 (GRCm38)		probably benign	Het
Smad2	A	T	18: 76,289,037 (GRCm38)		probably null	Het
Smad4	G	A	18: 73,658,649 (GRCm38)	P274S	probably benign	Het
Smchd1	A	T	17: 71,403,154 (GRCm38)	V906D	probably damaging	Het
Soat2	C	A	15: 102,158,753 (GRCm38)	R320S	possibly damaging	Het
Spata33	C	T	8: 123,221,887 (GRCm38)	A57V	probably damaging	Het
Stab1	A	G	14: 31,143,418 (GRCm38)	L1814P	probably benign	Het
Stab2	T	C	10: 86,947,144 (GRCm38)	K680R	probably benign	Het
Stil	A	G	4: 115,041,172 (GRCm38)		probably null	Het
Sympk	T	A	7: 19,046,849 (GRCm38)	L759H	probably benign	Het
Tet1	A	T	10: 62,814,546 (GRCm38)		probably null	Het
Tfpi2	A	T	6: 3,965,460 (GRCm38)	N117K	probably benign	Het
Tle3	A	G	9: 61,416,661 (GRCm38)	Y766C	probably damaging	Het
Trpt1	C	A	19: 6,997,930 (GRCm38)		probably null	Het
Tshz1	A	G	18: 84,016,049 (GRCm38)	F78S	possibly damaging	Het
Ttc1	T	C	11: 43,738,808 (GRCm38)	D177G	probably damaging	Het
Ttc13	T	A	8: 124,674,401 (GRCm38)	Y741F	probably damaging	Het
Ulk3	C	T	9: 57,594,832 (GRCm38)	S462L	probably benign	Het
Utrn	C	T	10: 12,525,333 (GRCm38)		probably benign	Het
V1rd19	A	C	7: 24,003,585 (GRCm38)	T159P	probably damaging	Het
Vars1	T	C	17: 35,011,486 (GRCm38)	V515A	possibly damaging	Het
Vmn1r85	A	G	7: 13,084,588 (GRCm38)	Y210H	probably benign	Het
Vmn2r89	A	G	14: 51,455,978 (GRCm38)	T262A	probably damaging	Het
Vps53	G	A	11: 76,121,579 (GRCm38)	T209I	probably benign	Het
Wdfy2	T	C	14: 62,925,133 (GRCm38)	F95L	possibly damaging	Het
Wwp1	G	T	4: 19,627,911 (GRCm38)	S694Y	probably damaging	Het
Zbtb8b	T	A	4: 129,432,670 (GRCm38)	D201V	probably damaging	Het
Zmym5	A	C	14: 56,804,451 (GRCm38)	N123K	possibly 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
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
R1775:Csmd3	UTSW	15	47,899,739 (GRCm38)	missense	probably damaging	0.99
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'- GCCACCTCATATCAGGGAATAGGGTCA -3'
(R):5'- GCACAATGTTTTCAATAACAGTGCCGT -3'

Sequencing Primer
(F):5'- ATCAGGGAATAGGGTCACTTTC -3'
(R):5'- TTGACCAGTGACACAAGATAATAAG -3'

Posted On

2013-04-24