"GeneDx"[submitter] AND "BTAF1"[gene] - ClinVar

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Search results

Items: 76

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1174183	NM_003972.3(BTAF1):c.14+299G>C	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1278473	NM_003972.3(BTAF1):c.15-104C>T	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1178514	NM_003972.3(BTAF1):c.139-60C>T	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1266434	NM_003972.3(BTAF1):c.254-206T>A	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1263341	NM_003972.3(BTAF1):c.254-127dup	BTAF1	Duplication (intron variant)	not provided	GBenign
Select item 1288738	NM_003972.3(BTAF1):c.254-123TG[20]	BTAF1	Microsatellite (intron variant)	not provided	GBenign
Select item 1247181	NM_003972.3(BTAF1):c.254-123TG[19]	BTAF1	Microsatellite (intron variant)	not provided	GBenign
Select item 1245501	NM_003972.3(BTAF1):c.254-123TG[17]	BTAF1	Microsatellite (intron variant)	not provided	GBenign
Select item 1265763	NM_003972.3(BTAF1):c.254-123TG[13]	BTAF1	Microsatellite (intron variant)	not provided	GBenign
Select item 1240855	NM_003972.3(BTAF1):c.254-123TG[10]	BTAF1	Microsatellite (intron variant)	not provided	GBenign
Select item 1234034	NM_003972.3(BTAF1):c.400+80C>T	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1243130	NM_003972.3(BTAF1):c.400+118G>A	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1247960	NM_003972.3(BTAF1):c.401-160T>A	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1252495	NM_003972.3(BTAF1):c.565-131A>G	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1290239	NM_003972.3(BTAF1):c.565-89T>G	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1291761	NM_003972.3(BTAF1):c.701+128T>G	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1248537	NM_003972.3(BTAF1):c.701+177A>G	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1241652	NM_003972.3(BTAF1):c.831+177T>C	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1268058	NM_003972.3(BTAF1):c.832-198A>G	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1283898	NM_003972.3(BTAF1):c.832-83G>C	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1181565	NM_003972.3(BTAF1):c.900+139C>T	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1287746	NM_003972.3(BTAF1):c.990+176G>T	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1265503	NM_003972.3(BTAF1):c.991-275T>C	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276078	NM_003972.3(BTAF1):c.991-66TG[13]	BTAF1	Microsatellite (intron variant)	not provided	GBenign
Select item 1264591	NM_003972.3(BTAF1):c.991-66TG[14]	BTAF1	Microsatellite (intron variant)	not provided	GBenign
Select item 1297985	NM_003972.3(BTAF1):c.991-45_991-38del	BTAF1	Deletion (intron variant)	not provided	GBenign
Select item 1247652	NM_003972.3(BTAF1):c.991-44TA[10]	BTAF1	Microsatellite (intron variant)	not provided	GBenign
Select item 1228961	NM_003972.3(BTAF1):c.991-44TA[13]	BTAF1	Microsatellite (intron variant)	not provided	GBenign
Select item 1240615	NM_003972.3(BTAF1):c.991-43A>G	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1286045	NM_003972.3(BTAF1):c.991-41A>G	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1178618	NM_003972.3(BTAF1):c.991-39A>G	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1268778	NM_003972.3(BTAF1):c.991-37A>G	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1283488	NM_003972.3(BTAF1):c.991-35A>G	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1244288	NM_003972.3(BTAF1):c.991-33A>G	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1259214	NM_003972.3(BTAF1):c.991-11T>C	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1232431	NM_003972.3(BTAF1):c.1263+233T>C	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1239590	NM_003972.3(BTAF1):c.1263+287C>T	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1252416	NM_003972.3(BTAF1):c.1264-228_1264-225del	BTAF1	Deletion (intron variant)	not provided	GBenign
Select item 1286203	NM_003972.3(BTAF1):c.1264-96A>G	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273202	NM_003972.3(BTAF1):c.1404+316G>T	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1281857	NM_003972.3(BTAF1):c.1529+243C>T	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1231643	NM_003972.3(BTAF1):c.1529+308G>A	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1261802	NM_003972.3(BTAF1):c.1530-304C>T	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1283430	NM_003972.3(BTAF1):c.1755+114T>C	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 782533	NM_003972.3(BTAF1):c.2620T>C (p.Leu874=)	BTAF1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1278733	NM_003972.3(BTAF1):c.2854+43T>G	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279658	NM_003972.3(BTAF1):c.2855-280AT[4]	BTAF1	Microsatellite (intron variant)	not provided	GBenign
Select item 1229398	NM_003972.3(BTAF1):c.3045+156G>A	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273214	NM_003972.3(BTAF1):c.3045+247A>G	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1247118	NM_003972.3(BTAF1):c.3200-222del	BTAF1	Deletion (intron variant)	not provided	GBenign
Select item 1255185	NM_003972.3(BTAF1):c.3200-195G>A	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1232262	NM_003972.3(BTAF1):c.3200-129G>A	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1289351	NM_003972.3(BTAF1):c.3309+142T>G	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1174252	NM_003972.3(BTAF1):c.3511+160T>G	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279399	NM_003972.3(BTAF1):c.3661-83G>A	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1227637	NM_003972.3(BTAF1):c.3672A>G (p.Pro1224=)	BTAF1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1282442	NM_003972.3(BTAF1):c.3813+64G>C	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1263638	NM_003972.3(BTAF1):c.3814-224C>T	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1238139	NM_003972.3(BTAF1):c.4104-62T>C	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236828	NM_003972.3(BTAF1):c.4181+50C>G	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1270353	NM_003972.3(BTAF1):c.4311+20T>A	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1284116	NM_003972.3(BTAF1):c.4584+6G>A	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1278481	NM_003972.3(BTAF1):c.4584+31G>T	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1250297	NM_003972.3(BTAF1):c.4584+136G>A	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1252763	NM_003972.3(BTAF1):c.4584+285G>A	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1222587	NM_003972.3(BTAF1):c.4585-329A>G	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1222124	NM_003972.3(BTAF1):c.4585-253G>A	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1259148	NM_003972.3(BTAF1):c.4585-144G>A	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1175382	NM_003972.3(BTAF1):c.4710+35A>G	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1287933	NM_003972.3(BTAF1):c.4711-271A>C	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282570	NM_003972.3(BTAF1):c.4711-208C>T	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1280473	NM_003972.3(BTAF1):c.4864-24_4864-17dup	BTAF1	Duplication (intron variant)	not provided	GBenign
Select item 1270903	NM_003972.3(BTAF1):c.5075+146C>A	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1290334	NM_003972.3(BTAF1):c.5076-193A>C	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276257	NM_003972.3(BTAF1):c.5235+49A>C	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1233685	NM_003972.3(BTAF1):c.5407-16G>T	BTAF1	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar

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Items: 76