List of variants in gene BCS1L reported by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001079866.2(BCS1L):c.1017T>C (p.Pro339=)	rs35843327	0.15996
NM_001079866.2(BCS1L):c.996C>T (p.Asn332=)	rs33946522	0.05607
NM_001079866.2(BCS1L):c.-49-530C>T	rs115162602	0.00544
NM_001079866.2(BCS1L):c.775T>A (p.Ser259Thr)	rs77729067	0.00132
NM_001079866.2(BCS1L):c.-50+458T>G	rs188224298	0.00056
NM_001079866.2(BCS1L):c.550C>T (p.Arg184Cys)	rs121908578	0.00011
NM_001079866.2(BCS1L):c.628G>A (p.Asp210Asn)	rs58447305

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