Mutagenetix > Incidental Mutation

Incidental Mutation 'PIT4453001:Srcap'

555322

Institutional Source

Beutler Lab

Gene Symbol

Srcap

Ensembl Gene

ENSMUSG00000053877

Gene Name

Snf2-related CREBBP activator protein

Synonyms

D030022P06Rik, F630004O05Rik, B930091H02Rik

Accession Numbers

Essential gene?

Probably essential (E-score: 0.962) question?

Stock #

PIT4453001 (G1)

Quality Score

182.009

Status

Not validated

Chromosome

Chromosomal Location

127511983-127561219 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 127549320 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Phenylalanine at position 1947 (I1947F)

Ref Sequence

ENSEMBL: ENSMUSP00000140036 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000186954] [ENSMUST00000187040] [ENSMUST00000189629] [ENSMUST00000190390]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000186954
AA Change: I1790F

PolyPhen 2 Score 0.029 (Sensitivity: 0.95; Specificity: 0.82)

SMART Domains

Protein: ENSMUSP00000139536
Gene: ENSMUSG00000053877
AA Change: I1790F

Domain	Start	End	E-Value	Type
low complexity region	26	48	N/A	INTRINSIC
HSA	125	196	5.4e-25	SMART
low complexity region	257	280	N/A	INTRINSIC
low complexity region	283	310	N/A	INTRINSIC
low complexity region	322	347	N/A	INTRINSIC
low complexity region	396	420	N/A	INTRINSIC
low complexity region	480	558	N/A	INTRINSIC
low complexity region	577	592	N/A	INTRINSIC
DEXDc	626	818	5e-37	SMART
low complexity region	993	1001	N/A	INTRINSIC
low complexity region	1027	1042	N/A	INTRINSIC
low complexity region	1046	1063	N/A	INTRINSIC
low complexity region	1175	1194	N/A	INTRINSIC
internal_repeat_1	1202	1245	2.24e-5	PROSPERO
low complexity region	1274	1302	N/A	INTRINSIC
low complexity region	1304	1318	N/A	INTRINSIC
low complexity region	1335	1353	N/A	INTRINSIC
low complexity region	1355	1370	N/A	INTRINSIC
low complexity region	1414	1441	N/A	INTRINSIC
low complexity region	1452	1466	N/A	INTRINSIC
low complexity region	1504	1533	N/A	INTRINSIC
internal_repeat_1	1536	1579	2.24e-5	PROSPERO
internal_repeat_2	1537	1559	5.66e-5	PROSPERO
internal_repeat_2	1569	1589	5.66e-5	PROSPERO
low complexity region	1590	1607	N/A	INTRINSIC
low complexity region	1609	1627	N/A	INTRINSIC
low complexity region	1644	1678	N/A	INTRINSIC
low complexity region	1713	1726	N/A	INTRINSIC
low complexity region	1828	1840	N/A	INTRINSIC
HELICc	1916	1999	1.2e-28	SMART
low complexity region	2058	2078	N/A	INTRINSIC
coiled coil region	2166	2201	N/A	INTRINSIC
low complexity region	2282	2348	N/A	INTRINSIC
low complexity region	2374	2409	N/A	INTRINSIC
low complexity region	2588	2600	N/A	INTRINSIC
low complexity region	2642	2657	N/A	INTRINSIC
low complexity region	2685	2712	N/A	INTRINSIC
AT_hook	2745	2757	2.4e-2	SMART
low complexity region	2797	2817	N/A	INTRINSIC
AT_hook	2825	2837	2.6e-3	SMART
low complexity region	2838	2849	N/A	INTRINSIC
low complexity region	2858	2885	N/A	INTRINSIC
AT_hook	2889	2901	2.4e-3	SMART
low complexity region	2934	2945	N/A	INTRINSIC
low complexity region	2946	2956	N/A	INTRINSIC
low complexity region	3043	3079	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000187040
AA Change: I1947F

PolyPhen 2 Score 0.516 (Sensitivity: 0.88; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000140036
Gene: ENSMUSG00000053877
AA Change: I1947F

Domain	Start	End	E-Value	Type
low complexity region	26	48	N/A	INTRINSIC
HSA	125	196	5.4e-25	SMART
low complexity region	257	280	N/A	INTRINSIC
low complexity region	283	310	N/A	INTRINSIC
low complexity region	322	347	N/A	INTRINSIC
low complexity region	396	420	N/A	INTRINSIC
low complexity region	480	558	N/A	INTRINSIC
low complexity region	577	592	N/A	INTRINSIC
DEXDc	626	818	5e-37	SMART
low complexity region	993	1001	N/A	INTRINSIC
low complexity region	1027	1042	N/A	INTRINSIC
low complexity region	1046	1063	N/A	INTRINSIC
low complexity region	1120	1143	N/A	INTRINSIC
low complexity region	1150	1178	N/A	INTRINSIC
low complexity region	1277	1305	N/A	INTRINSIC
low complexity region	1332	1351	N/A	INTRINSIC
internal_repeat_1	1359	1402	1.78e-5	PROSPERO
low complexity region	1431	1459	N/A	INTRINSIC
low complexity region	1461	1475	N/A	INTRINSIC
low complexity region	1492	1510	N/A	INTRINSIC
low complexity region	1512	1527	N/A	INTRINSIC
low complexity region	1571	1598	N/A	INTRINSIC
low complexity region	1609	1623	N/A	INTRINSIC
low complexity region	1661	1690	N/A	INTRINSIC
internal_repeat_1	1693	1736	1.78e-5	PROSPERO
internal_repeat_2	1694	1716	4.56e-5	PROSPERO
internal_repeat_2	1726	1746	4.56e-5	PROSPERO
low complexity region	1747	1764	N/A	INTRINSIC
low complexity region	1766	1784	N/A	INTRINSIC
low complexity region	1801	1835	N/A	INTRINSIC
low complexity region	1870	1883	N/A	INTRINSIC
low complexity region	1985	1997	N/A	INTRINSIC
HELICc	2073	2156	1.2e-28	SMART
low complexity region	2215	2235	N/A	INTRINSIC
coiled coil region	2323	2358	N/A	INTRINSIC
low complexity region	2439	2505	N/A	INTRINSIC
low complexity region	2531	2566	N/A	INTRINSIC
low complexity region	2745	2757	N/A	INTRINSIC
low complexity region	2799	2814	N/A	INTRINSIC
low complexity region	2842	2869	N/A	INTRINSIC
AT_hook	2902	2914	2.4e-2	SMART
low complexity region	2954	2974	N/A	INTRINSIC
AT_hook	2982	2994	2.6e-3	SMART
low complexity region	2995	3006	N/A	INTRINSIC
low complexity region	3015	3042	N/A	INTRINSIC
AT_hook	3046	3058	2.4e-3	SMART
low complexity region	3091	3102	N/A	INTRINSIC
low complexity region	3103	3113	N/A	INTRINSIC
low complexity region	3200	3236	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000189629
AA Change: I1771F

PolyPhen 2 Score 0.029 (Sensitivity: 0.95; Specificity: 0.82)

SMART Domains

Protein: ENSMUSP00000139644
Gene: ENSMUSG00000107023
AA Change: I1771F

Domain	Start	End	E-Value	Type
low complexity region	7	29	N/A	INTRINSIC
HSA	106	177	5.4e-25	SMART
low complexity region	238	261	N/A	INTRINSIC
low complexity region	264	291	N/A	INTRINSIC
low complexity region	303	328	N/A	INTRINSIC
low complexity region	377	401	N/A	INTRINSIC
low complexity region	461	539	N/A	INTRINSIC
low complexity region	558	573	N/A	INTRINSIC
DEXDc	607	799	5e-37	SMART
low complexity region	974	982	N/A	INTRINSIC
low complexity region	1008	1023	N/A	INTRINSIC
low complexity region	1027	1044	N/A	INTRINSIC
low complexity region	1156	1175	N/A	INTRINSIC
internal_repeat_1	1183	1226	2e-5	PROSPERO
low complexity region	1255	1283	N/A	INTRINSIC
low complexity region	1285	1299	N/A	INTRINSIC
low complexity region	1316	1334	N/A	INTRINSIC
low complexity region	1336	1351	N/A	INTRINSIC
low complexity region	1395	1422	N/A	INTRINSIC
low complexity region	1433	1447	N/A	INTRINSIC
low complexity region	1485	1514	N/A	INTRINSIC
internal_repeat_1	1517	1560	2e-5	PROSPERO
internal_repeat_2	1518	1540	5.08e-5	PROSPERO
internal_repeat_2	1550	1570	5.08e-5	PROSPERO
low complexity region	1571	1588	N/A	INTRINSIC
low complexity region	1590	1608	N/A	INTRINSIC
low complexity region	1625	1659	N/A	INTRINSIC
low complexity region	1694	1707	N/A	INTRINSIC
low complexity region	1809	1821	N/A	INTRINSIC
HELICc	1897	1980	1.2e-28	SMART
low complexity region	2039	2059	N/A	INTRINSIC
coiled coil region	2147	2182	N/A	INTRINSIC
low complexity region	2263	2329	N/A	INTRINSIC
low complexity region	2355	2390	N/A	INTRINSIC
low complexity region	2569	2581	N/A	INTRINSIC
low complexity region	2623	2638	N/A	INTRINSIC
low complexity region	2666	2693	N/A	INTRINSIC
AT_hook	2726	2738	2.4e-2	SMART
low complexity region	2778	2798	N/A	INTRINSIC
AT_hook	2806	2818	2.6e-3	SMART
low complexity region	2819	2830	N/A	INTRINSIC
low complexity region	2839	2866	N/A	INTRINSIC
AT_hook	2870	2882	2.4e-3	SMART
low complexity region	2915	2926	N/A	INTRINSIC
low complexity region	2927	2937	N/A	INTRINSIC
low complexity region	3024	3060	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000190390
AA Change: I1886F

PolyPhen 2 Score 0.516 (Sensitivity: 0.88; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000139399
Gene: ENSMUSG00000053877
AA Change: I1886F

Domain	Start	End	E-Value	Type
low complexity region	26	48	N/A	INTRINSIC
HSA	125	196	5.4e-25	SMART
low complexity region	257	280	N/A	INTRINSIC
low complexity region	283	310	N/A	INTRINSIC
low complexity region	322	347	N/A	INTRINSIC
low complexity region	396	420	N/A	INTRINSIC
low complexity region	480	558	N/A	INTRINSIC
low complexity region	577	592	N/A	INTRINSIC
DEXDc	626	818	5e-37	SMART
low complexity region	993	1001	N/A	INTRINSIC
low complexity region	1027	1042	N/A	INTRINSIC
low complexity region	1046	1063	N/A	INTRINSIC
low complexity region	1120	1143	N/A	INTRINSIC
low complexity region	1150	1178	N/A	INTRINSIC
low complexity region	1271	1290	N/A	INTRINSIC
internal_repeat_1	1298	1341	2.01e-5	PROSPERO
low complexity region	1370	1398	N/A	INTRINSIC
low complexity region	1400	1414	N/A	INTRINSIC
low complexity region	1431	1449	N/A	INTRINSIC
low complexity region	1451	1466	N/A	INTRINSIC
low complexity region	1510	1537	N/A	INTRINSIC
low complexity region	1548	1562	N/A	INTRINSIC
low complexity region	1600	1629	N/A	INTRINSIC
internal_repeat_1	1632	1675	2.01e-5	PROSPERO
internal_repeat_2	1633	1655	5.11e-5	PROSPERO
internal_repeat_2	1665	1685	5.11e-5	PROSPERO
low complexity region	1686	1703	N/A	INTRINSIC
low complexity region	1705	1723	N/A	INTRINSIC
low complexity region	1740	1774	N/A	INTRINSIC
low complexity region	1809	1822	N/A	INTRINSIC
low complexity region	1924	1936	N/A	INTRINSIC
HELICc	2012	2095	1.2e-28	SMART
low complexity region	2154	2174	N/A	INTRINSIC
coiled coil region	2262	2297	N/A	INTRINSIC
low complexity region	2378	2444	N/A	INTRINSIC
low complexity region	2470	2505	N/A	INTRINSIC
low complexity region	2684	2696	N/A	INTRINSIC
low complexity region	2738	2753	N/A	INTRINSIC
low complexity region	2781	2808	N/A	INTRINSIC
AT_hook	2841	2853	2.4e-2	SMART
low complexity region	2893	2913	N/A	INTRINSIC
AT_hook	2921	2933	2.6e-3	SMART
low complexity region	2934	2945	N/A	INTRINSIC
low complexity region	2954	2981	N/A	INTRINSIC
AT_hook	2985	2997	2.4e-3	SMART
low complexity region	3030	3041	N/A	INTRINSIC
low complexity region	3042	3052	N/A	INTRINSIC
low complexity region	3139	3175	N/A	INTRINSIC

Coding Region Coverage

1x: 93.3%
3x: 90.9%
10x: 85.6%
20x: 74.1%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes the core catalytic component of the multiprotein chromatin-remodeling SRCAP complex. The encoded protein is an ATPase that is necessary for the incorporation of the histone variant H2A.Z into nucleosomes. It can function as a transcriptional activator in Notch-mediated, CREB-mediated and steroid receptor-mediated transcription. Mutations in this gene cause Floating-Harbor syndrome, a rare disorder characterized by short stature, language deficits and dysmorphic facial features. [provided by RefSeq, Feb 2012]

Allele List at MGI

Other mutations in this stock

Total: 82 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca4	T	G	3: 122,105,316	I649S	probably damaging	Het
Abcc2	T	A	19: 43,803,782	L334*	probably null	Het
Adam28	A	T	14: 68,634,876	S306T	probably benign	Het
Adam34	T	A	8: 43,651,312	D432V	probably damaging	Het
Adcy7	A	G	8: 88,323,636	Y723C	probably benign	Het
Adgre5	T	A	8: 83,724,460	M713L	probably benign	Het
Aebp2	C	A	6: 140,637,686	C295*	probably null	Het
Amn1	G	T	6: 149,170,859	Q127K	probably benign	Het
Atcay	C	T	10: 81,210,549	V314M	probably damaging	Het
Atp1a1	T	C	3: 101,581,179	E847G	probably benign	Het
Atp2b1	A	G	10: 99,016,978	E1039G	probably benign	Het
Caskin1	A	G	17: 24,499,292	Y292C	probably damaging	Het
Cftr	A	G	6: 18,214,106	T94A	probably damaging	Het
Ciart	T	A	3: 95,880,476	K182M	probably damaging	Het
Col1a2	A	C	6: 4,527,079	S603R	possibly damaging	Het
Cspp1	C	A	1: 10,074,872	S298R	possibly damaging	Het
Cul7	T	A	17: 46,651,820	C126S	probably damaging	Het
Cyp2c55	A	T	19: 39,011,791	I145F	probably damaging	Het
Cypt4	G	C	9: 24,625,474	A87P	probably damaging	Het
Disp2	G	A	2: 118,787,644	V224M	probably benign	Het
Dlgap5	TTC	T	14: 47,401,522		probably null	Het
Dock1	A	G	7: 135,152,300	K1602R	probably benign	Het
Ears2	T	C	7: 122,048,339	I241V	probably benign	Het
Eml6	T	C	11: 29,802,489	T975A	probably damaging	Het
Ephb2	T	C	4: 136,660,810	T660A	probably benign	Het
Fbxw7	G	A	3: 84,965,314	V268M		Het
Gart	A	G	16: 91,636,538	F289S	probably damaging	Het
Gmcl1	G	T	6: 86,704,538	N391K	probably benign	Het
Greb1l	A	C	18: 10,533,031	Q975P	probably damaging	Het
Greb1l	G	T	18: 10,533,032	Q975H	probably benign	Het
Grik5	C	A	7: 25,010,694	R872L	probably damaging	Het
Hmox2	T	A	16: 4,765,057	I218N	probably damaging	Het
Hook1	A	T	4: 96,014,852	D526V	probably damaging	Het
Ifna4	A	T	4: 88,841,954	N32Y	probably damaging	Het
Ighg2b	T	A	12: 113,306,872	N213Y	unknown	Het
Itih4	G	A	14: 30,901,170	V900I	probably benign	Het
Itpr2	A	T	6: 146,373,173	F837Y	probably damaging	Het
Kif3a	T	C	11: 53,579,114	V147A	probably benign	Het
Klra9	T	A	6: 130,191,321		probably benign	Het
Lamp3	G	T	16: 19,673,460	Q345K	probably benign	Het
Ltbp3	G	A	19: 5,757,794	E1188K	probably damaging	Het
Med1	T	A	11: 98,158,417	I518L	probably benign	Het
Mis18bp1	T	C	12: 65,158,673	T242A	probably damaging	Het
Nemp1	T	A	10: 127,696,254	F392Y	probably benign	Het
Obscn	C	A	11: 59,060,976	G3984W	probably damaging	Het
Obscn	T	A	11: 59,069,834	H3217L	possibly damaging	Het
Olfr1157	C	T	2: 87,962,458	V145M	possibly damaging	Het
Olfr1328	A	G	4: 118,934,626	M74T	probably benign	Het
Olfr1532-ps1	C	T	7: 106,914,929	H244Y	probably damaging	Het
Olfr709-ps1	T	C	7: 106,926,842	I206V	probably benign	Het
Olfr71	A	G	4: 43,706,464	Y35H	probably damaging	Het
P4ha1	G	T	10: 59,350,472	A258S	probably benign	Het
Parn	T	C	16: 13,607,281	I423V	probably benign	Het
Pcdh20	C	A	14: 88,467,308	S852I	probably damaging	Het
Pcnx3	A	G	19: 5,672,756		probably null	Het
Pcsk1	A	T	13: 75,112,650	I331F	probably damaging	Het
Pkd1l2	G	T	8: 117,022,022	S1803R	probably benign	Het
Pkd1l3	C	A	8: 109,660,801	N1792K	probably damaging	Het
Plekhg1	C	A	10: 3,963,469	Q1119K		Het
Prr30	T	A	14: 101,198,935	T64S	probably benign	Het
Rec114	T	C	9: 58,660,370	N111S	probably benign	Het
Reck	G	A	4: 43,895,850	V79I	probably benign	Het
Rexo1	A	G	10: 80,550,397	F276L	probably damaging	Het
Rgs6	T	C	12: 83,091,779	Y296H	probably damaging	Het
Sdk1	A	G	5: 142,212,038	R2149G	probably benign	Het
Slc20a2	C	A	8: 22,535,382	F33L	probably damaging	Het
Spopl	T	A	2: 23,545,449	T25S	probably damaging	Het
Srek1	A	C	13: 103,744,783		probably null	Het
St8sia1	C	T	6: 142,829,252	W200*	probably null	Het
Tas2r106	A	T	6: 131,678,502	F129I	possibly damaging	Het
Tbrg4	A	T	11: 6,620,857	L205Q	probably damaging	Het
Tchh	C	A	3: 93,445,880	R876S	unknown	Het
Thap12	G	T	7: 98,715,038	A138S	probably benign	Het
Tjp1	C	T	7: 65,343,614		probably null	Het
Traf4	G	A	11: 78,161,534	P95L	probably benign	Het
Trappc9	ATCTC	ATCTCTC	15: 73,031,598		probably null	Het
Usp20	G	A	2: 31,017,486	V677M	possibly damaging	Het
Usp50	C	A	2: 126,783,316		probably benign	Het
Vmn1r21	T	C	6: 57,844,322	T46A	probably benign	Het
Vmn2r54	T	A	7: 12,629,742	H408L	probably benign	Het
Zfp266	T	C	9: 20,506,003	T30A	probably benign	Het
Zfp536	T	C	7: 37,479,757	H1141R	probably benign	Het

Other mutations in Srcap

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00323:Srcap	APN	7	127542713	splice site	probably benign
IGL00475:Srcap	APN	7	127552921	missense	possibly damaging	0.92
IGL01064:Srcap	APN	7	127559892	unclassified	probably benign
IGL01129:Srcap	APN	7	127521651	missense	probably damaging	1.00
IGL01670:Srcap	APN	7	127528432	missense	probably damaging	1.00
IGL01861:Srcap	APN	7	127525285	splice site	probably benign
IGL02237:Srcap	APN	7	127534692	splice site	probably benign
IGL02665:Srcap	APN	7	127540903	missense	probably damaging	1.00
IGL02688:Srcap	APN	7	127542453	missense	probably benign	0.04
IGL02744:Srcap	APN	7	127534666	missense	probably damaging	1.00
IGL02810:Srcap	APN	7	127521663	critical splice donor site	probably null
IGL03184:Srcap	APN	7	127530502	unclassified	probably benign
IGL03309:Srcap	APN	7	127530793	missense	probably damaging	0.99
R1340:Srcap	UTSW	7	127560738	intron	probably benign
R1401:Srcap	UTSW	7	127559952	unclassified	probably benign
R1455:Srcap	UTSW	7	127530650	missense	probably damaging	0.99
R1470:Srcap	UTSW	7	127559727	unclassified	probably benign
R1470:Srcap	UTSW	7	127559727	unclassified	probably benign
R1761:Srcap	UTSW	7	127534845	missense	probably damaging	1.00
R1911:Srcap	UTSW	7	127534822	missense	probably damaging	0.99
R2483:Srcap	UTSW	7	127542147	missense	probably damaging	0.99
R2892:Srcap	UTSW	7	127539065	missense	probably damaging	0.99
R2893:Srcap	UTSW	7	127539065	missense	probably damaging	0.99
R3623:Srcap	UTSW	7	127542147	missense	probably damaging	0.99
R3976:Srcap	UTSW	7	127549239	missense	probably benign	0.18
R4001:Srcap	UTSW	7	127532167	missense	probably damaging	1.00
R4015:Srcap	UTSW	7	127525423	missense	probably benign	0.27
R4581:Srcap	UTSW	7	127558310	unclassified	probably benign
R4643:Srcap	UTSW	7	127541776	missense	probably damaging	1.00
R4644:Srcap	UTSW	7	127552598	missense	probably damaging	1.00
R4690:Srcap	UTSW	7	127538014	missense	probably damaging	1.00
R4693:Srcap	UTSW	7	127538544	missense	probably damaging	1.00
R4719:Srcap	UTSW	7	127541559	missense	probably benign	0.13
R4728:Srcap	UTSW	7	127540924	critical splice donor site	probably null
R4740:Srcap	UTSW	7	127549299	missense	probably damaging	1.00
R4752:Srcap	UTSW	7	127559000	unclassified	probably benign
R4834:Srcap	UTSW	7	127557610	critical splice donor site	probably null
R4837:Srcap	UTSW	7	127558962	unclassified	probably benign
R4884:Srcap	UTSW	7	127522017	missense	probably damaging	1.00
R4889:Srcap	UTSW	7	127538547	missense	possibly damaging	0.94
R5088:Srcap	UTSW	7	127541661	missense	probably benign	0.02
R5102:Srcap	UTSW	7	127530623	missense	probably damaging	1.00
R5358:Srcap	UTSW	7	127540320	missense	probably damaging	1.00
R5372:Srcap	UTSW	7	127557613	splice site	probably null
R5397:Srcap	UTSW	7	127553296	critical splice donor site	probably null
R5481:Srcap	UTSW	7	127532197	missense	probably damaging	1.00
R5566:Srcap	UTSW	7	127525303	missense	probably damaging	0.99
R5584:Srcap	UTSW	7	127528479	missense	probably damaging	1.00
R5693:Srcap	UTSW	7	127519816	missense	probably damaging	1.00
R5769:Srcap	UTSW	7	127559822	unclassified	probably benign
R5805:Srcap	UTSW	7	127542039	missense	possibly damaging	0.87
R5806:Srcap	UTSW	7	127559163	unclassified	probably benign
R5921:Srcap	UTSW	7	127558833	unclassified	probably benign
R5942:Srcap	UTSW	7	127538008	missense	probably damaging	1.00
R6014:Srcap	UTSW	7	127538750	missense	probably benign	0.01
R6057:Srcap	UTSW	7	127541356	missense	probably damaging	0.99
R6113:Srcap	UTSW	7	127560281	unclassified	probably benign
R6150:Srcap	UTSW	7	127534828	missense	probably damaging	1.00
R6212:Srcap	UTSW	7	127549689	missense	probably damaging	1.00
R6299:Srcap	UTSW	7	127530454	unclassified	probably benign
R6437:Srcap	UTSW	7	127528550	splice site	probably null
R6492:Srcap	UTSW	7	127522145	nonsense	probably null
R6537:Srcap	UTSW	7	127542220	missense	probably damaging	0.97
R6659:Srcap	UTSW	7	127542391	missense	probably damaging	1.00
R6713:Srcap	UTSW	7	127534917	missense	probably benign	0.28
R6717:Srcap	UTSW	7	127558310	unclassified	probably benign
R6941:Srcap	UTSW	7	127542597	missense	probably damaging	1.00
R7068:Srcap	UTSW	7	127541943	missense	probably benign	0.00
R7097:Srcap	UTSW	7	127539041	missense	probably damaging	1.00
R7394:Srcap	UTSW	7	127534828	missense	probably damaging	1.00
R7426:Srcap	UTSW	7	127538517	missense	possibly damaging	0.90
R7434:Srcap	UTSW	7	127560242	missense	unknown
R7559:Srcap	UTSW	7	127530550	missense	unknown
R7638:Srcap	UTSW	7	127538748	missense	probably benign	0.39
R7677:Srcap	UTSW	7	127559808	missense	unknown
R7715:Srcap	UTSW	7	127549288	missense	probably damaging	0.99
R7757:Srcap	UTSW	7	127530794	missense	probably damaging	0.99
R7811:Srcap	UTSW	7	127542049	missense	probably damaging	0.97
R7821:Srcap	UTSW	7	127530327	unclassified	probably benign
R7869:Srcap	UTSW	7	127539194	missense	possibly damaging	0.92
R7870:Srcap	UTSW	7	127560558	missense	unknown
R7941:Srcap	UTSW	7	127558290	unclassified	probably benign
R7994:Srcap	UTSW	7	127541758	missense	probably benign	0.00
R8035:Srcap	UTSW	7	127542612	missense	probably benign	0.05
R8066:Srcap	UTSW	7	127521632	missense	probably damaging	1.00
R8066:Srcap	UTSW	7	127540312	missense	possibly damaging	0.74
R8168:Srcap	UTSW	7	127542523	missense	probably damaging	1.00
R8194:Srcap	UTSW	7	127539197	missense	probably damaging	1.00
R8288:Srcap	UTSW	7	127531356	missense	probably damaging	1.00
R8307:Srcap	UTSW	7	127525369	missense	probably damaging	1.00
R8308:Srcap	UTSW	7	127553181	missense	possibly damaging	0.82
R8309:Srcap	UTSW	7	127549357	missense	probably damaging	0.98
R8311:Srcap	UTSW	7	127557797	missense	probably damaging	0.99
R8321:Srcap	UTSW	7	127540896	missense	probably damaging	1.00
R8365:Srcap	UTSW	7	127549697	missense	probably damaging	1.00
R8424:Srcap	UTSW	7	127542388	missense	probably benign	0.00
R8815:Srcap	UTSW	7	127558865	missense	unknown
R8817:Srcap	UTSW	7	127553223	missense	probably benign	0.23
R8924:Srcap	UTSW	7	127559032	missense	unknown
R8933:Srcap	UTSW	7	127552394	missense	probably damaging	1.00
R8961:Srcap	UTSW	7	127541929	missense	probably damaging	1.00
R9000:Srcap	UTSW	7	127531771	missense	possibly damaging	0.91
R9098:Srcap	UTSW	7	127552644	missense	probably damaging	0.99
R9124:Srcap	UTSW	7	127560702	missense	unknown
R9163:Srcap	UTSW	7	127521990	missense	unknown
R9332:Srcap	UTSW	7	127559640	missense	unknown
R9389:Srcap	UTSW	7	127542283	missense	probably damaging	1.00
R9464:Srcap	UTSW	7	127538101	missense	possibly damaging	0.95
R9467:Srcap	UTSW	7	127540359	missense	probably damaging	0.98
R9554:Srcap	UTSW	7	127552405	missense	probably damaging	1.00
R9596:Srcap	UTSW	7	127531864	missense	probably damaging	1.00
R9597:Srcap	UTSW	7	127522047	missense	possibly damaging	0.91
X0025:Srcap	UTSW	7	127560105	unclassified	probably benign

Predicted Primers

PCR Primer
(F):5'- TAGGACTCTCTGGAAGAAAAGC -3'
(R):5'- GCATGACAAAGATGAACCTGTG -3'

Sequencing Primer
(F):5'- CTCTCTGGAAGAAAAGCGGAAGC -3'
(R):5'- CATGACAAAGATGAACCTGTGAAAAG -3'

Posted On

2019-06-07