List of variants in gene SMARCAL1 reported as likely benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 31

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HGVS	dbSNP	gnomAD frequency
NM_014140.4(SMARCAL1):c.1129G>C (p.Glu377Gln)	rs2066518	0.03294
NM_014140.4(SMARCAL1):c.2626-268G>A	rs116315714	0.02507
NM_014140.4(SMARCAL1):c.127G>A (p.Ala43Thr)	rs2066524	0.01441
NM_014140.4(SMARCAL1):c.1096+28C>A	rs2066519	0.01195
NM_014140.4(SMARCAL1):c.2141+53_2141+54insC	rs199625205	0.01163
NM_014140.4(SMARCAL1):c.1710+256C>T	rs16856144	0.01032
NM_014140.4(SMARCAL1):c.2245-278A>C	rs142801547	0.00979
NM_014140.4(SMARCAL1):c.2528+36G>A	rs115145411	0.00979
NM_014140.4(SMARCAL1):c.423T>C (p.Tyr141=)	rs35907255	0.00906
NM_014140.4(SMARCAL1):c.811+103A>G	rs139574584	0.00860
NM_014140.4(SMARCAL1):c.901C>G (p.Pro301Ala)	rs146084305	0.00795
NM_014140.4(SMARCAL1):c.811+194T>A	rs144306591	0.00569
NM_014140.4(SMARCAL1):c.1645-246G>A	rs116559712	0.00518
NM_014140.4(SMARCAL1):c.1334+274G>A	rs141473566	0.00486
NM_014140.4(SMARCAL1):c.1645-132T>A	rs146596046	0.00447
NM_014140.4(SMARCAL1):c.2070+280G>A	rs111317170	0.00365
NM_014140.4(SMARCAL1):c.2141+55A>C	rs113194270	0.00330
NM_014140.4(SMARCAL1):c.2528+35C>T	rs116468485	0.00260
NM_014140.4(SMARCAL1):c.1212G>A (p.Ala404=)	rs2066525	0.00241
NM_014140.4(SMARCAL1):c.1271A>T (p.Asp424Val)	rs2066520	0.00215
NM_014140.4(SMARCAL1):c.1196C>T (p.Thr399Met)	rs139872089	0.00129
NM_014140.4(SMARCAL1):c.1908G>A (p.Leu636=)	rs375844575	0.00004
NM_014140.4(SMARCAL1):c.1148-282G>T	rs79653204
NM_014140.4(SMARCAL1):c.1334+8C>G	rs1574453912
NM_014140.4(SMARCAL1):c.1485+288T>C	rs16856111
NM_014140.4(SMARCAL1):c.1711-80C>T	rs140524986
NM_014140.4(SMARCAL1):c.1947C>T (p.Asp649=)	rs2066526
NM_014140.4(SMARCAL1):c.2245-192T>C
NM_014140.4(SMARCAL1):c.649A>C (p.Arg217=)
NM_014140.4(SMARCAL1):c.863-228C>A	rs73072258
NM_014140.4(SMARCAL1):c.863-228C>T	rs73072258

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