List of variants in gene STIM1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001382567.1(STIM1):c.1302G>A (p.Glu434=)	rs116837894	0.00426
NM_001382567.1(STIM1):c.1664C>T (p.Ser555Phe)	rs141215990	0.00163
NM_001382567.1(STIM1):c.1634+287G>A	rs562406813	0.00157
NM_001382567.1(STIM1):c.114C>G (p.Ala38=)	rs150033189	0.00029
NM_001382567.1(STIM1):c.1128C>T (p.Ala376=)	rs200375470	0.00020
NM_001382567.1(STIM1):c.201A>G (p.Ala67=)	rs200194500	0.00015
NM_001382567.1(STIM1):c.570G>T (p.Leu190=)	rs200233698	0.00013
NM_001382567.1(STIM1):c.105C>T (p.Ser35=)	rs139540641	0.00012
NM_001382567.1(STIM1):c.1611A>G (p.Pro537=)	rs199512211	0.00003
NM_001382567.1(STIM1):c.1305C>T (p.Ile435=)	rs199801171	0.00001
NM_001382567.1(STIM1):c.1215A>G (p.Val405=)
NM_001382567.1(STIM1):c.1461C>T (p.Pro487=)	rs751169800
NM_001382567.1(STIM1):c.1525A>C (p.Thr509Pro)
NM_001382567.1(STIM1):c.1634+13C>A
NM_001382567.1(STIM1):c.198G>A (p.Glu66=)
NM_001382567.1(STIM1):c.516C>G (p.Thr172=)	rs2133104553
NM_001382567.1(STIM1):c.792-4C>A	rs200996329

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