List of variants in gene STRC reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_153700.2(STRC):c.5179G>C (p.Glu1727Gln)	rs141749062	0.00135
NM_153700.2(STRC):c.5200T>C (p.Trp1734Arg)	rs200770543	0.00124
NM_153700.2(STRC):c.4157T>C (p.Val1386Ala)	rs377674360	0.00081
NM_153700.2(STRC):c.4399G>A (p.Val1467Ile)	rs147447264	0.00064
NM_153700.2(STRC):c.4749G>T (p.Val1583=)	rs770417511	0.00048
NM_153700.2(STRC):c.4593T>C (p.Leu1531=)	rs201633242	0.00037
NM_153700.2(STRC):c.4546-13G>C	rs374896210	0.00026
NM_153700.2(STRC):c.4563G>A (p.Arg1521=)	rs140729822	0.00024
NM_153700.2(STRC):c.3555G>A (p.Leu1185=)	rs2597064	0.00014
NM_153700.2(STRC):c.4845C>T (p.Ser1615=)	rs184909019	0.00010
NM_153700.2(STRC):c.4260G>A (p.Lys1420=)	rs140545217	0.00008
NM_153700.2(STRC):c.4339G>A (p.Ala1447Thr)	rs140238012	0.00006
NM_153700.2(STRC):c.4903G>T (p.Val1635Phe)	rs2915791	0.00005
NM_153700.2(STRC):c.4237A>T (p.Thr1413Ser)	rs754834213	0.00003
NM_153700.2(STRC):c.3100-10C>T	rs727503450	0.00002
NM_153700.2(STRC):c.678A>T (p.Thr226=)	rs727503452	0.00002
NM_153700.2(STRC):c.4581G>A (p.Gln1527=)	rs1331991004	0.00001
NM_153700.2(STRC):c.4844+15G>A	rs749407115	0.00001
NM_153700.2(STRC):c.4904T>C (p.Val1635Ala)	rs1370498166	0.00001
NM_153700.2(STRC):c.2016A>G (p.Leu672=)	rs62018893
NM_153700.2(STRC):c.2172T>C (p.Val724=)	rs1308469405
NM_153700.2(STRC):c.3681+11G>A	rs796781098
NM_153700.2(STRC):c.4077G>A (p.Glu1359=)	rs1555447174
NM_153700.2(STRC):c.4702-3del	rs371263304
NM_153700.2(STRC):c.694A>G (p.Lys232Glu)	rs876657585

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