Mutagenetix > Incidental Mutation

Incidental Mutation 'R6057:Csmd3'

483005

Institutional Source

Beutler Lab

Gene Symbol

Csmd3

Ensembl Gene

ENSMUSG00000022311

Gene Name

CUB and Sushi multiple domains 3

Synonyms

4930500N14Rik

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R6057 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

47444033-48655459 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 47618787 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Cysteine at position 1867 (Y1867C)

Ref Sequence

ENSEMBL: ENSMUSP00000124775 (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: Y1867C

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

SMART Domains

Protein: ENSMUSP00000098235
Gene: ENSMUSG00000022311
AA Change: Y1867C

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: Y1763C

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

SMART Domains

Protein: ENSMUSP00000124753
Gene: ENSMUSG00000022311
AA Change: Y1763C

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 benign
Transcript: ENSMUST00000161653

SMART Domains

Protein: ENSMUSP00000124195
Gene: ENSMUSG00000022311

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: Y1867C

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

SMART Domains

Protein: ENSMUSP00000124775
Gene: ENSMUSG00000022311
AA Change: Y1867C

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: 99.9%
3x: 99.6%
10x: 97.9%
20x: 93.6%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 87 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
5730596B20Rik	A	G	6: 52,156,500 (GRCm39)		probably benign	Het
Acan	A	G	7: 78,749,530 (GRCm39)	S11G	probably null	Het
Ankrd13d	A	C	19: 4,332,256 (GRCm39)	V56G	probably damaging	Het
Arl15	A	G	13: 114,104,151 (GRCm39)	Y76C	probably damaging	Het
Aspg	G	A	12: 112,087,432 (GRCm39)	C296Y	probably damaging	Het
Astl	T	A	2: 127,187,889 (GRCm39)	D101E	probably benign	Het
Bmpr2	A	G	1: 59,881,977 (GRCm39)	N202S	probably benign	Het
Borcs7	T	C	19: 46,690,003 (GRCm39)	*106Q	probably null	Het
Brip1	A	G	11: 85,955,865 (GRCm39)	S883P	possibly damaging	Het
Cacng2	A	T	15: 78,002,991 (GRCm39)	L34Q	probably damaging	Het
Catip	A	C	1: 74,402,077 (GRCm39)	D84A	probably damaging	Het
Ccdc162	A	G	10: 41,510,037 (GRCm39)	L856S	possibly damaging	Het
Ccdc38	A	G	10: 93,417,608 (GRCm39)	K500E	probably damaging	Het
Ccser2	T	C	14: 36,663,122 (GRCm39)	K21E	probably damaging	Het
Cd93	A	T	2: 148,283,439 (GRCm39)	Y636N	probably damaging	Het
Cep128	A	T	12: 91,262,998 (GRCm39)	N300K	possibly damaging	Het
Cfap44	A	G	16: 44,269,460 (GRCm39)	T1155A	probably benign	Het
Clec16a	T	C	16: 10,447,951 (GRCm39)	L550P	probably damaging	Het
Cul3	A	T	1: 80,249,249 (GRCm39)	I674N	probably damaging	Het
Cybb	C	G	X: 9,316,989 (GRCm39)	D246H	probably benign	Het
Cyp2d34	T	C	15: 82,500,552 (GRCm39)	H429R	probably benign	Het
Dab2ip	T	A	2: 35,582,267 (GRCm39)	C4*	probably null	Het
Dcaf1	A	G	9: 106,731,446 (GRCm39)	E641G	probably damaging	Het
Dda1	T	A	8: 71,927,276 (GRCm39)		probably benign	Het
Dmgdh	C	T	13: 93,888,960 (GRCm39)	T866I	probably benign	Het
Ect2l	T	C	10: 18,037,250 (GRCm39)	T383A	probably benign	Het
Ets2	A	G	16: 95,515,416 (GRCm39)	N181D	probably benign	Het
Ezh2	A	G	6: 47,529,357 (GRCm39)	F222L	probably damaging	Het
Frem3	T	C	8: 81,342,216 (GRCm39)	L1503P	probably damaging	Het
Fsip2	C	A	2: 82,809,777 (GRCm39)	A2032E	probably damaging	Het
Gm1818	C	T	12: 48,602,346 (GRCm39)		noncoding transcript	Het
Gm9493	A	G	19: 23,597,106 (GRCm39)	S1G	probably damaging	Het
Grin2b	A	G	6: 135,710,942 (GRCm39)	I868T	possibly damaging	Het
Ift22	A	T	5: 136,939,987 (GRCm39)	T17S	possibly damaging	Het
Il4ra	T	C	7: 125,170,735 (GRCm39)	W216R	probably damaging	Het
Kcnj6	A	T	16: 94,633,236 (GRCm39)	W274R	probably damaging	Het
Kctd19	G	A	8: 106,123,082 (GRCm39)	H111Y	probably damaging	Het
Kremen2	A	G	17: 23,961,679 (GRCm39)	V276A	probably benign	Het
Lig1	C	A	7: 13,022,598 (GRCm39)	Q143K	probably damaging	Het
Lrp1	A	T	10: 127,403,359 (GRCm39)	D2071E	probably damaging	Het
Macf1	C	T	4: 123,404,536 (GRCm39)	M475I	probably damaging	Het
Mbtd1	G	A	11: 93,820,485 (GRCm39)	A427T	probably damaging	Het
Myof	A	G	19: 37,915,429 (GRCm39)		probably null	Het
Nbeal2	T	C	9: 110,470,945 (GRCm39)	D308G	possibly damaging	Het
Ncdn	T	C	4: 126,638,824 (GRCm39)	Q665R	probably benign	Het
Nkd1	T	C	8: 89,316,442 (GRCm39)		probably null	Het
Nktr	G	A	9: 121,577,455 (GRCm39)		probably benign	Het
Npc1l1	A	T	11: 6,167,806 (GRCm39)	M995K	possibly damaging	Het
Or10ag59	C	A	2: 87,406,363 (GRCm39)	R312S	probably benign	Het
Or11g7	A	T	14: 50,691,201 (GRCm39)	R231*	probably null	Het
Or14n1-ps1	T	A	7: 86,092,397 (GRCm39)	C69*	probably null	Het
Padi4	T	C	4: 140,487,351 (GRCm39)	T184A	probably damaging	Het
Pgm2l1	C	T	7: 99,915,881 (GRCm39)	P409S	probably benign	Het
Pgpep1	G	A	8: 71,105,101 (GRCm39)	T53M	probably damaging	Het
Pgr	T	C	9: 8,902,006 (GRCm39)	L513P	probably damaging	Het
Pikfyve	T	A	1: 65,311,730 (GRCm39)	I1989N	probably damaging	Het
Prrc2a	T	C	17: 35,371,716 (GRCm39)	T1806A	probably benign	Het
Psd	T	C	19: 46,311,753 (GRCm39)	E309G	possibly damaging	Het
Qtrt1	C	T	9: 21,323,299 (GRCm39)	T50I	probably damaging	Het
Rims2	A	C	15: 39,538,416 (GRCm39)	T1320P	probably damaging	Het
Scn11a	T	G	9: 119,594,514 (GRCm39)	N1293T	probably damaging	Het
Scn8a	T	C	15: 100,872,548 (GRCm39)	F529S	possibly damaging	Het
Sec14l4	A	T	11: 3,985,142 (GRCm39)	D25V	possibly damaging	Het
Sema3a	C	T	5: 13,615,832 (GRCm39)	R419C	probably damaging	Het
Slc12a1	T	C	2: 125,032,133 (GRCm39)	Y595H	probably damaging	Het
Slc25a28	A	T	19: 43,655,364 (GRCm39)	H170Q	possibly damaging	Het
Slc26a1	T	A	5: 108,821,631 (GRCm39)	Q86L	probably damaging	Het
Slc48a1	T	A	15: 97,687,798 (GRCm39)	W51R	probably damaging	Het
Sptlc3	T	A	2: 139,423,533 (GRCm39)	V309D	probably damaging	Het
Srcap	G	A	7: 127,140,528 (GRCm39)	S1375N	probably damaging	Het
Tanc1	C	A	2: 59,647,837 (GRCm39)	H986Q	possibly damaging	Het
Tbc1d4	A	G	14: 101,727,353 (GRCm39)	V486A	probably damaging	Het
Tceanc2	T	C	4: 107,004,776 (GRCm39)	D124G	probably damaging	Het
Tdrd9	A	G	12: 111,979,720 (GRCm39)	M402V	possibly damaging	Het
Tmem132d	T	C	5: 127,861,934 (GRCm39)	D729G	probably damaging	Het
Tmem62	T	A	2: 120,807,943 (GRCm39)	I55N	probably damaging	Het
Tnfrsf21	A	T	17: 43,350,606 (GRCm39)	N257Y	possibly damaging	Het
Trappc3	T	C	4: 126,167,834 (GRCm39)	L131P	probably damaging	Het
Vmn2r25	A	T	6: 123,799,900 (GRCm39)	M814K	possibly damaging	Het
Vmn2r87	T	C	10: 130,308,226 (GRCm39)	I671V	probably benign	Het
Vwa8	A	T	14: 79,320,313 (GRCm39)	D1108V	probably benign	Het
Xrcc4	C	G	13: 90,139,198 (GRCm39)	A241P	possibly damaging	Het
Xylt1	T	A	7: 117,191,135 (GRCm39)	D310E	probably benign	Het
Zfp27	T	G	7: 29,594,444 (GRCm39)	H507P	possibly damaging	Het
Zfp341	C	T	2: 154,466,954 (GRCm39)	P108S	probably benign	Het
Zfp641	T	C	15: 98,190,816 (GRCm39)	N76S	probably benign	Het
Zfp936	T	C	7: 42,839,787 (GRCm39)	V418A	probably benign	Het

Other mutations in Csmd3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00158:Csmd3	APN	15	48,150,891 (GRCm39)	missense	possibly damaging	0.61
IGL00591:Csmd3	APN	15	47,868,279 (GRCm39)	missense	probably damaging	1.00
IGL00668:Csmd3	APN	15	47,777,341 (GRCm39)	missense	probably damaging	1.00
IGL00753:Csmd3	APN	15	47,507,631 (GRCm39)	missense	probably damaging	1.00
IGL00773:Csmd3	APN	15	47,454,115 (GRCm39)	missense	probably damaging	0.96
IGL00926:Csmd3	APN	15	47,574,360 (GRCm39)	missense	possibly damaging	0.87
IGL00942:Csmd3	APN	15	47,710,502 (GRCm39)	critical splice donor site	probably null
IGL01080:Csmd3	APN	15	47,744,799 (GRCm39)	missense	probably benign	0.12
IGL01314:Csmd3	APN	15	47,713,151 (GRCm39)	missense	probably damaging	1.00
IGL01326:Csmd3	APN	15	47,713,181 (GRCm39)	missense	probably benign	0.06
IGL01393:Csmd3	APN	15	48,320,995 (GRCm39)	missense	possibly damaging	0.88
IGL01432:Csmd3	APN	15	47,596,895 (GRCm39)	missense	probably damaging	1.00
IGL01519:Csmd3	APN	15	47,460,246 (GRCm39)	missense	probably benign	0.31
IGL01530:Csmd3	APN	15	47,533,013 (GRCm39)	missense	probably damaging	1.00
IGL01530:Csmd3	APN	15	47,701,833 (GRCm39)	missense	possibly damaging	0.95
IGL01547:Csmd3	APN	15	47,747,013 (GRCm39)	missense	probably benign	0.41
IGL01594:Csmd3	APN	15	47,492,635 (GRCm39)	missense	probably benign	0.01
IGL01618:Csmd3	APN	15	47,874,479 (GRCm39)	missense	probably benign	0.05
IGL01670:Csmd3	APN	15	47,475,225 (GRCm39)	missense	probably damaging	1.00
IGL01680:Csmd3	APN	15	47,833,426 (GRCm39)	missense	probably damaging	1.00
IGL01734:Csmd3	APN	15	48,048,700 (GRCm39)	missense	probably damaging	1.00
IGL01777:Csmd3	APN	15	47,561,594 (GRCm39)	missense	probably benign	0.06
IGL01779:Csmd3	APN	15	47,721,290 (GRCm39)	missense	probably benign	0.10
IGL01820:Csmd3	APN	15	47,470,538 (GRCm39)	nonsense	probably null
IGL01843:Csmd3	APN	15	47,522,395 (GRCm39)	splice site	probably benign
IGL01919:Csmd3	APN	15	47,539,168 (GRCm39)	missense	possibly damaging	0.62
IGL01986:Csmd3	APN	15	47,522,591 (GRCm39)	missense	possibly damaging	0.82
IGL02049:Csmd3	APN	15	47,864,870 (GRCm39)	missense	possibly damaging	0.91
IGL02065:Csmd3	APN	15	47,530,024 (GRCm39)	missense	probably damaging	1.00
IGL02112:Csmd3	APN	15	48,177,265 (GRCm39)	missense	possibly damaging	0.95
IGL02133:Csmd3	APN	15	47,721,338 (GRCm39)	missense	possibly damaging	0.86
IGL02203:Csmd3	APN	15	47,713,073 (GRCm39)	splice site	probably null
IGL02215:Csmd3	APN	15	47,449,084 (GRCm39)	missense	probably damaging	1.00
IGL02234:Csmd3	APN	15	47,811,512 (GRCm39)	missense	probably damaging	1.00
IGL02326:Csmd3	APN	15	47,619,359 (GRCm39)	splice site	probably benign
IGL02478:Csmd3	APN	15	47,701,794 (GRCm39)	splice site	probably benign
IGL02491:Csmd3	APN	15	47,777,511 (GRCm39)	splice site	probably benign
IGL02598:Csmd3	APN	15	47,533,086 (GRCm39)	missense	probably damaging	0.98
IGL02626:Csmd3	APN	15	47,567,503 (GRCm39)	splice site	probably benign
IGL02696:Csmd3	APN	15	47,533,065 (GRCm39)	missense	probably benign	0.33
IGL02876:Csmd3	APN	15	47,469,492 (GRCm39)	splice site	probably benign
IGL02971:Csmd3	APN	15	47,777,325 (GRCm39)	splice site	probably benign
IGL03068:Csmd3	APN	15	47,710,517 (GRCm39)	missense	possibly damaging	0.69
IGL03087:Csmd3	APN	15	47,840,429 (GRCm39)	missense	probably damaging	1.00
IGL03114:Csmd3	APN	15	47,683,847 (GRCm39)	missense	probably damaging	0.99
IGL03146:Csmd3	APN	15	47,744,873 (GRCm39)	missense	probably benign	0.25
IGL03193:Csmd3	APN	15	47,492,626 (GRCm39)	splice site	probably benign
IGL03274:Csmd3	APN	15	47,508,900 (GRCm39)	missense	probably damaging	1.00
R0040:Csmd3	UTSW	15	47,497,212 (GRCm39)	missense	probably damaging	1.00
R0071:Csmd3	UTSW	15	47,460,217 (GRCm39)	missense	probably benign	0.04
R0071:Csmd3	UTSW	15	47,460,217 (GRCm39)	missense	probably benign	0.04
R0119:Csmd3	UTSW	15	47,710,527 (GRCm39)	missense	probably benign	0.08
R0124:Csmd3	UTSW	15	47,454,112 (GRCm39)	missense	probably damaging	1.00
R0127:Csmd3	UTSW	15	47,845,326 (GRCm39)	missense	probably benign	0.45
R0136:Csmd3	UTSW	15	47,710,527 (GRCm39)	missense	probably benign	0.08
R0201:Csmd3	UTSW	15	47,483,125 (GRCm39)	splice site	probably benign
R0240:Csmd3	UTSW	15	47,492,635 (GRCm39)	missense	probably benign	0.05
R0240:Csmd3	UTSW	15	47,492,635 (GRCm39)	missense	probably benign	0.05
R0318:Csmd3	UTSW	15	47,522,549 (GRCm39)	missense	probably damaging	1.00
R0369:Csmd3	UTSW	15	47,833,543 (GRCm39)	missense	probably damaging	1.00
R0391:Csmd3	UTSW	15	47,520,969 (GRCm39)	missense	probably damaging	1.00
R0499:Csmd3	UTSW	15	47,710,527 (GRCm39)	missense	probably benign	0.08
R0506:Csmd3	UTSW	15	48,320,907 (GRCm39)	missense	probably benign	0.00
R0606:Csmd3	UTSW	15	48,321,058 (GRCm39)	missense	probably benign
R0639:Csmd3	UTSW	15	47,777,336 (GRCm39)	missense	probably damaging	1.00
R0658:Csmd3	UTSW	15	47,874,543 (GRCm39)	missense	possibly damaging	0.66
R0673:Csmd3	UTSW	15	47,777,336 (GRCm39)	missense	probably damaging	1.00
R0689:Csmd3	UTSW	15	47,619,421 (GRCm39)	missense	probably benign	0.19
R0696:Csmd3	UTSW	15	47,710,569 (GRCm39)	missense	probably benign	0.01
R0799:Csmd3	UTSW	15	48,048,780 (GRCm39)	splice site	probably benign
R0834:Csmd3	UTSW	15	47,747,073 (GRCm39)	intron	probably benign
R0894:Csmd3	UTSW	15	47,721,316 (GRCm39)	missense	possibly damaging	0.95
R0926:Csmd3	UTSW	15	47,840,429 (GRCm39)	missense	probably damaging	1.00
R0943:Csmd3	UTSW	15	47,539,135 (GRCm39)	missense	probably damaging	0.99
R0944:Csmd3	UTSW	15	47,475,227 (GRCm39)	missense	probably damaging	1.00
R0967:Csmd3	UTSW	15	47,721,227 (GRCm39)	missense	probably null	0.89
R0973:Csmd3	UTSW	15	47,522,485 (GRCm39)	missense	probably damaging	1.00
R1055:Csmd3	UTSW	15	47,744,933 (GRCm39)	missense	probably damaging	1.00
R1066:Csmd3	UTSW	15	47,777,361 (GRCm39)	missense	probably damaging	1.00
R1086:Csmd3	UTSW	15	47,559,151 (GRCm39)	missense	probably damaging	0.99
R1103:Csmd3	UTSW	15	47,811,402 (GRCm39)	missense	probably damaging	1.00
R1136:Csmd3	UTSW	15	47,539,213 (GRCm39)	missense	probably damaging	1.00
R1139:Csmd3	UTSW	15	47,559,232 (GRCm39)	missense	probably damaging	1.00
R1158:Csmd3	UTSW	15	48,156,170 (GRCm39)	splice site	probably null
R1215:Csmd3	UTSW	15	47,868,227 (GRCm39)	splice site	probably null
R1233:Csmd3	UTSW	15	48,536,927 (GRCm39)	missense	probably damaging	1.00
R1271:Csmd3	UTSW	15	47,874,455 (GRCm39)	missense	probably benign	0.11
R1469:Csmd3	UTSW	15	47,532,598 (GRCm39)	nonsense	probably null
R1469:Csmd3	UTSW	15	47,532,598 (GRCm39)	nonsense	probably null
R1479:Csmd3	UTSW	15	47,721,282 (GRCm39)	missense	probably damaging	1.00
R1480:Csmd3	UTSW	15	47,595,325 (GRCm39)	missense	possibly damaging	0.90
R1526:Csmd3	UTSW	15	47,449,028 (GRCm39)	critical splice donor site	probably null
R1527:Csmd3	UTSW	15	47,811,483 (GRCm39)	missense	probably benign	0.08
R1539:Csmd3	UTSW	15	47,683,794 (GRCm39)	missense	probably benign	0.24
R1544:Csmd3	UTSW	15	47,475,294 (GRCm39)	splice site	probably null
R1548:Csmd3	UTSW	15	47,845,371 (GRCm39)	missense	possibly damaging	0.91
R1574:Csmd3	UTSW	15	47,559,257 (GRCm39)	splice site	probably null
R1574:Csmd3	UTSW	15	47,559,257 (GRCm39)	splice site	probably null
R1619:Csmd3	UTSW	15	47,813,346 (GRCm39)	missense	probably damaging	1.00
R1630:Csmd3	UTSW	15	47,701,918 (GRCm39)	missense	possibly damaging	0.66
R1665:Csmd3	UTSW	15	47,560,185 (GRCm39)	missense	probably damaging	1.00
R1680:Csmd3	UTSW	15	47,604,566 (GRCm39)	missense	probably damaging	1.00
R1725:Csmd3	UTSW	15	47,460,203 (GRCm39)	missense	probably damaging	1.00
R1743:Csmd3	UTSW	15	48,485,485 (GRCm39)	missense	probably damaging	1.00
R1749:Csmd3	UTSW	15	47,449,056 (GRCm39)	missense	probably damaging	1.00
R1752:Csmd3	UTSW	15	47,523,669 (GRCm39)	missense	probably benign	0.15
R1769:Csmd3	UTSW	15	47,567,505 (GRCm39)	splice site	probably benign
R1775:Csmd3	UTSW	15	47,763,135 (GRCm39)	missense	probably damaging	0.99
R1795:Csmd3	UTSW	15	47,721,316 (GRCm39)	missense	possibly damaging	0.95
R1819:Csmd3	UTSW	15	47,617,131 (GRCm39)	missense	possibly damaging	0.56
R1840:Csmd3	UTSW	15	47,470,560 (GRCm39)	missense	probably damaging	1.00
R1860:Csmd3	UTSW	15	47,522,588 (GRCm39)	missense	probably damaging	1.00
R1861:Csmd3	UTSW	15	47,522,588 (GRCm39)	missense	probably damaging	1.00
R1879:Csmd3	UTSW	15	47,520,915 (GRCm39)	missense	possibly damaging	0.90
R1958:Csmd3	UTSW	15	47,868,035 (GRCm39)	critical splice donor site	probably null
R1965:Csmd3	UTSW	15	47,713,144 (GRCm39)	missense	probably benign	0.15
R1970:Csmd3	UTSW	15	48,536,927 (GRCm39)	missense	probably damaging	1.00
R2029:Csmd3	UTSW	15	47,701,975 (GRCm39)	missense	probably damaging	1.00
R2051:Csmd3	UTSW	15	48,485,389 (GRCm39)	critical splice donor site	probably null
R2108:Csmd3	UTSW	15	47,868,257 (GRCm39)	missense	possibly damaging	0.81
R2132:Csmd3	UTSW	15	48,320,899 (GRCm39)	missense	probably benign	0.06
R2146:Csmd3	UTSW	15	47,604,632 (GRCm39)	frame shift	probably null
R2147:Csmd3	UTSW	15	47,604,632 (GRCm39)	frame shift	probably null
R2148:Csmd3	UTSW	15	47,604,632 (GRCm39)	frame shift	probably null
R2157:Csmd3	UTSW	15	47,559,183 (GRCm39)	missense	probably damaging	0.99
R2159:Csmd3	UTSW	15	47,604,632 (GRCm39)	frame shift	probably null
R2160:Csmd3	UTSW	15	47,604,632 (GRCm39)	frame shift	probably null
R2161:Csmd3	UTSW	15	47,604,632 (GRCm39)	frame shift	probably null
R2162:Csmd3	UTSW	15	47,604,632 (GRCm39)	frame shift	probably null
R2164:Csmd3	UTSW	15	47,604,632 (GRCm39)	frame shift	probably null
R2213:Csmd3	UTSW	15	47,683,843 (GRCm39)	missense	possibly damaging	0.92
R2301:Csmd3	UTSW	15	47,595,394 (GRCm39)	missense	probably damaging	1.00
R2302:Csmd3	UTSW	15	48,177,447 (GRCm39)	missense	probably benign
R2355:Csmd3	UTSW	15	47,604,632 (GRCm39)	frame shift	probably null
R2497:Csmd3	UTSW	15	47,604,632 (GRCm39)	frame shift	probably null
R2509:Csmd3	UTSW	15	47,604,632 (GRCm39)	frame shift	probably null
R2566:Csmd3	UTSW	15	47,604,632 (GRCm39)	frame shift	probably null
R2567:Csmd3	UTSW	15	47,604,632 (GRCm39)	frame shift	probably null
R2568:Csmd3	UTSW	15	47,604,632 (GRCm39)	frame shift	probably null
R2570:Csmd3	UTSW	15	47,604,632 (GRCm39)	frame shift	probably null
R2571:Csmd3	UTSW	15	47,604,632 (GRCm39)	frame shift	probably null
R2870:Csmd3	UTSW	15	47,721,320 (GRCm39)	missense	probably damaging	1.00
R2870:Csmd3	UTSW	15	47,721,320 (GRCm39)	missense	probably damaging	1.00
R2907:Csmd3	UTSW	15	47,874,449 (GRCm39)	missense	probably damaging	0.99
R3116:Csmd3	UTSW	15	47,520,995 (GRCm39)	missense	probably damaging	1.00
R3423:Csmd3	UTSW	15	47,710,648 (GRCm39)	missense	probably damaging	0.98
R3425:Csmd3	UTSW	15	47,710,648 (GRCm39)	missense	probably damaging	0.98
R3508:Csmd3	UTSW	15	47,604,632 (GRCm39)	frame shift	probably null
R3746:Csmd3	UTSW	15	47,713,162 (GRCm39)	missense	probably benign	0.04
R3813:Csmd3	UTSW	15	48,655,209 (GRCm39)	missense	possibly damaging	0.82
R3832:Csmd3	UTSW	15	47,604,632 (GRCm39)	frame shift	probably null
R3959:Csmd3	UTSW	15	47,507,585 (GRCm39)	missense	probably benign	0.18
R4042:Csmd3	UTSW	15	47,477,480 (GRCm39)	missense	probably damaging	1.00
R4043:Csmd3	UTSW	15	47,619,362 (GRCm39)	critical splice donor site	probably null
R4191:Csmd3	UTSW	15	47,710,667 (GRCm39)	missense	probably damaging	0.99
R4192:Csmd3	UTSW	15	47,710,667 (GRCm39)	missense	probably damaging	0.99
R4419:Csmd3	UTSW	15	47,567,707 (GRCm39)	missense	probably damaging	1.00
R4426:Csmd3	UTSW	15	47,532,581 (GRCm39)	missense	possibly damaging	0.51
R4434:Csmd3	UTSW	15	47,763,191 (GRCm39)	missense	possibly damaging	0.68
R4438:Csmd3	UTSW	15	47,763,191 (GRCm39)	missense	possibly damaging	0.68
R4490:Csmd3	UTSW	15	48,177,429 (GRCm39)	missense	possibly damaging	0.83
R4562:Csmd3	UTSW	15	47,763,240 (GRCm39)	missense	probably benign	0.32
R4604:Csmd3	UTSW	15	47,868,211 (GRCm39)	missense	possibly damaging	0.90
R4620:Csmd3	UTSW	15	47,449,149 (GRCm39)	missense	probably benign	0.09
R4632:Csmd3	UTSW	15	47,874,605 (GRCm39)	missense	probably damaging	0.99
R4679:Csmd3	UTSW	15	48,024,479 (GRCm39)	nonsense	probably null
R4696:Csmd3	UTSW	15	47,777,364 (GRCm39)	missense	probably benign	0.24
R4718:Csmd3	UTSW	15	47,561,546 (GRCm39)	nonsense	probably null
R4723:Csmd3	UTSW	15	47,532,556 (GRCm39)	missense	probably benign	0.29
R4801:Csmd3	UTSW	15	47,484,688 (GRCm39)	missense	probably damaging	1.00
R4802:Csmd3	UTSW	15	47,484,688 (GRCm39)	missense	probably damaging	1.00
R4806:Csmd3	UTSW	15	48,177,464 (GRCm39)	missense	probably benign
R4816:Csmd3	UTSW	15	47,721,330 (GRCm39)	missense	possibly damaging	0.68
R4935:Csmd3	UTSW	15	48,024,480 (GRCm39)	missense	probably damaging	1.00
R4955:Csmd3	UTSW	15	48,536,914 (GRCm39)	missense	probably damaging	0.99
R4991:Csmd3	UTSW	15	47,864,874 (GRCm39)	missense	probably damaging	1.00
R5031:Csmd3	UTSW	15	47,522,588 (GRCm39)	missense	probably damaging	1.00
R5034:Csmd3	UTSW	15	47,492,683 (GRCm39)	missense	possibly damaging	0.94
R5035:Csmd3	UTSW	15	47,454,175 (GRCm39)	missense	probably damaging	1.00
R5120:Csmd3	UTSW	15	48,536,891 (GRCm39)	nonsense	probably null
R5224:Csmd3	UTSW	15	47,752,080 (GRCm39)	missense	possibly damaging	0.91
R5235:Csmd3	UTSW	15	47,492,674 (GRCm39)	missense	probably benign	0.20
R5279:Csmd3	UTSW	15	48,655,340 (GRCm39)	splice site	probably null
R5360:Csmd3	UTSW	15	47,532,599 (GRCm39)	missense	probably damaging	0.99
R5365:Csmd3	UTSW	15	47,868,145 (GRCm39)	missense	possibly damaging	0.68
R5379:Csmd3	UTSW	15	47,499,846 (GRCm39)	nonsense	probably null
R5381:Csmd3	UTSW	15	47,604,611 (GRCm39)	missense	probably benign	0.21
R5393:Csmd3	UTSW	15	47,497,099 (GRCm39)	missense	probably damaging	1.00
R5413:Csmd3	UTSW	15	47,701,831 (GRCm39)	missense	probably damaging	1.00
R5549:Csmd3	UTSW	15	48,048,753 (GRCm39)	missense	probably damaging	0.98
R5550:Csmd3	UTSW	15	48,048,753 (GRCm39)	missense	probably damaging	0.98
R5551:Csmd3	UTSW	15	48,177,492 (GRCm39)	missense	probably benign	0.13
R5567:Csmd3	UTSW	15	47,508,864 (GRCm39)	missense	possibly damaging	0.92
R5621:Csmd3	UTSW	15	48,177,374 (GRCm39)	missense	possibly damaging	0.84
R5668:Csmd3	UTSW	15	47,559,151 (GRCm39)	missense	possibly damaging	0.48
R5677:Csmd3	UTSW	15	48,485,447 (GRCm39)	missense	probably damaging	0.98
R5701:Csmd3	UTSW	15	48,403,729 (GRCm39)	missense	probably damaging	0.99
R5701:Csmd3	UTSW	15	47,513,617 (GRCm39)	missense	probably damaging	1.00
R5871:Csmd3	UTSW	15	47,752,112 (GRCm39)	missense	probably damaging	0.98
R5872:Csmd3	UTSW	15	47,445,923 (GRCm39)	missense	probably damaging	1.00
R5874:Csmd3	UTSW	15	47,507,666 (GRCm39)	missense	probably damaging	1.00
R5952:Csmd3	UTSW	15	47,596,901 (GRCm39)	missense	probably damaging	0.98
R5956:Csmd3	UTSW	15	48,655,278 (GRCm39)	missense	possibly damaging	0.84
R5966:Csmd3	UTSW	15	47,713,135 (GRCm39)	missense	probably damaging	0.96
R5969:Csmd3	UTSW	15	47,811,386 (GRCm39)	missense	probably damaging	1.00
R5989:Csmd3	UTSW	15	47,454,160 (GRCm39)	missense	possibly damaging	0.69
R6017:Csmd3	UTSW	15	48,177,408 (GRCm39)	missense	possibly damaging	0.95
R6127:Csmd3	UTSW	15	47,513,624 (GRCm39)	missense	probably damaging	1.00
R6178:Csmd3	UTSW	15	48,536,854 (GRCm39)	missense	probably damaging	1.00
R6198:Csmd3	UTSW	15	48,177,273 (GRCm39)	missense	probably benign	0.28
R6213:Csmd3	UTSW	15	47,492,656 (GRCm39)	missense	probably damaging	1.00
R6256:Csmd3	UTSW	15	47,533,125 (GRCm39)	missense	probably damaging	1.00
R6274:Csmd3	UTSW	15	47,484,833 (GRCm39)	missense	probably benign
R6327:Csmd3	UTSW	15	47,744,783 (GRCm39)	missense	probably damaging	1.00
R6354:Csmd3	UTSW	15	47,744,885 (GRCm39)	missense	probably damaging	1.00
R6405:Csmd3	UTSW	15	47,683,767 (GRCm39)	missense	probably damaging	0.99
R6410:Csmd3	UTSW	15	48,536,803 (GRCm39)	missense	probably damaging	1.00
R6416:Csmd3	UTSW	15	48,536,956 (GRCm39)	missense	probably damaging	1.00
R6463:Csmd3	UTSW	15	47,539,875 (GRCm39)	missense	probably damaging	1.00
R6536:Csmd3	UTSW	15	47,701,863 (GRCm39)	missense	probably damaging	1.00
R6625:Csmd3	UTSW	15	47,470,471 (GRCm39)	missense	probably benign	0.02
R6695:Csmd3	UTSW	15	47,721,230 (GRCm39)	missense	probably damaging	0.99
R6895:Csmd3	UTSW	15	47,529,910 (GRCm39)	splice site	probably null
R6906:Csmd3	UTSW	15	47,710,569 (GRCm39)	missense	probably benign	0.01
R6914:Csmd3	UTSW	15	47,874,534 (GRCm39)	missense	possibly damaging	0.53
R6920:Csmd3	UTSW	15	47,507,601 (GRCm39)	missense	probably damaging	1.00
R7024:Csmd3	UTSW	15	47,574,387 (GRCm39)	missense	probably damaging	1.00
R7178:Csmd3	UTSW	15	47,454,170 (GRCm39)	missense
R7192:Csmd3	UTSW	15	47,567,633 (GRCm39)	missense
R7220:Csmd3	UTSW	15	48,320,994 (GRCm39)	missense	probably damaging	0.99
R7362:Csmd3	UTSW	15	47,619,388 (GRCm39)	missense	possibly damaging	0.65
R7380:Csmd3	UTSW	15	47,450,361 (GRCm39)	missense
R7397:Csmd3	UTSW	15	47,559,130 (GRCm39)	missense
R7467:Csmd3	UTSW	15	47,492,640 (GRCm39)	missense
R7585:Csmd3	UTSW	15	48,485,471 (GRCm39)	missense	possibly damaging	0.76
R7623:Csmd3	UTSW	15	47,813,334 (GRCm39)	missense
R7649:Csmd3	UTSW	15	47,532,539 (GRCm39)	missense
R7691:Csmd3	UTSW	15	47,604,569 (GRCm39)	missense
R7695:Csmd3	UTSW	15	47,683,777 (GRCm39)	missense
R7759:Csmd3	UTSW	15	47,561,569 (GRCm39)	missense
R7817:Csmd3	UTSW	15	47,721,356 (GRCm39)	missense	probably damaging	0.99
R8052:Csmd3	UTSW	15	47,569,783 (GRCm39)	missense
R8089:Csmd3	UTSW	15	47,532,603 (GRCm39)	missense
R8110:Csmd3	UTSW	15	47,507,666 (GRCm39)	missense	probably damaging	1.00
R8152:Csmd3	UTSW	15	47,532,860 (GRCm39)	splice site	probably null
R8323:Csmd3	UTSW	15	47,561,547 (GRCm39)	missense
R8341:Csmd3	UTSW	15	47,561,547 (GRCm39)	missense
R8353:Csmd3	UTSW	15	47,813,349 (GRCm39)	missense	probably damaging	1.00
R8364:Csmd3	UTSW	15	48,536,837 (GRCm39)	missense	probably damaging	1.00
R8405:Csmd3	UTSW	15	47,619,379 (GRCm39)	missense	probably damaging	1.00
R8412:Csmd3	UTSW	15	47,499,794 (GRCm39)	missense
R8436:Csmd3	UTSW	15	47,868,218 (GRCm39)	missense	probably damaging	0.97
R8516:Csmd3	UTSW	15	47,492,761 (GRCm39)	nonsense	probably null
R8553:Csmd3	UTSW	15	47,484,724 (GRCm39)	missense	possibly damaging	0.52
R8554:Csmd3	UTSW	15	47,507,538 (GRCm39)	missense	probably benign	0.32
R8678:Csmd3	UTSW	15	47,499,849 (GRCm39)	missense
R8751:Csmd3	UTSW	15	47,845,402 (GRCm39)	missense
R8758:Csmd3	UTSW	15	47,469,593 (GRCm39)	missense
R8768:Csmd3	UTSW	15	47,561,572 (GRCm39)	missense
R8785:Csmd3	UTSW	15	48,177,482 (GRCm39)	missense	probably benign	0.00
R8788:Csmd3	UTSW	15	47,470,513 (GRCm39)	missense
R8798:Csmd3	UTSW	15	47,595,382 (GRCm39)	missense
R8801:Csmd3	UTSW	15	48,321,024 (GRCm39)	missense	possibly damaging	0.70
R8811:Csmd3	UTSW	15	47,560,139 (GRCm39)	missense
R8844:Csmd3	UTSW	15	48,536,815 (GRCm39)	missense	probably damaging	0.98
R8844:Csmd3	UTSW	15	47,604,590 (GRCm39)	missense	probably damaging	0.96
R8892:Csmd3	UTSW	15	47,604,634 (GRCm39)	missense
R8897:Csmd3	UTSW	15	48,222,739 (GRCm39)	missense	probably benign	0.06
R9001:Csmd3	UTSW	15	47,596,901 (GRCm39)	missense
R9007:Csmd3	UTSW	15	47,751,892 (GRCm39)	intron	probably benign
R9016:Csmd3	UTSW	15	47,522,438 (GRCm39)	missense
R9039:Csmd3	UTSW	15	47,483,308 (GRCm39)	splice site	probably benign
R9109:Csmd3	UTSW	15	47,617,187 (GRCm39)	missense
R9121:Csmd3	UTSW	15	47,683,774 (GRCm39)	missense
R9155:Csmd3	UTSW	15	47,449,051 (GRCm39)	missense
R9176:Csmd3	UTSW	15	47,864,937 (GRCm39)	missense
R9281:Csmd3	UTSW	15	47,460,272 (GRCm39)	missense
R9298:Csmd3	UTSW	15	47,617,187 (GRCm39)	missense
R9304:Csmd3	UTSW	15	47,569,805 (GRCm39)	missense
R9343:Csmd3	UTSW	15	48,015,001 (GRCm39)	missense	probably damaging	1.00
R9367:Csmd3	UTSW	15	47,567,564 (GRCm39)	missense
R9405:Csmd3	UTSW	15	47,539,187 (GRCm39)	missense
R9448:Csmd3	UTSW	15	47,460,315 (GRCm39)	missense
R9460:Csmd3	UTSW	15	47,617,130 (GRCm39)	missense
R9481:Csmd3	UTSW	15	47,470,459 (GRCm39)	missense
R9520:Csmd3	UTSW	15	47,561,608 (GRCm39)	missense
R9551:Csmd3	UTSW	15	48,655,356 (GRCm39)	start gained	probably benign
R9552:Csmd3	UTSW	15	48,655,356 (GRCm39)	start gained	probably benign
R9568:Csmd3	UTSW	15	48,150,942 (GRCm39)	missense	probably damaging	0.97
R9571:Csmd3	UTSW	15	48,655,398 (GRCm39)	start gained	probably benign
R9607:Csmd3	UTSW	15	47,618,811 (GRCm39)	missense	probably damaging	0.98
R9621:Csmd3	UTSW	15	47,713,116 (GRCm39)	missense
R9671:Csmd3	UTSW	15	47,845,299 (GRCm39)	missense
R9718:Csmd3	UTSW	15	47,560,083 (GRCm39)	missense
U24488:Csmd3	UTSW	15	47,573,795 (GRCm39)	missense	probably damaging	1.00
V8831:Csmd3	UTSW	15	48,321,092 (GRCm39)	missense	probably damaging	0.96
X0021:Csmd3	UTSW	15	47,833,489 (GRCm39)	nonsense	probably null
Z1088:Csmd3	UTSW	15	47,710,677 (GRCm39)	missense	probably damaging	0.98
Z1088:Csmd3	UTSW	15	47,499,789 (GRCm39)	missense	probably damaging	1.00
Z1177:Csmd3	UTSW	15	47,596,813 (GRCm39)	missense
Z1177:Csmd3	UTSW	15	47,539,130 (GRCm39)	missense

Predicted Primers

PCR Primer
(F):5'- TTGGATAAAGCACCAGTGTTCCAG -3'
(R):5'- CCCAAGGAAAATATATTGCTAGCAG -3'

Posted On

2017-07-14