List of variants in gene SLC3A1 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 22

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HGVS	dbSNP	gnomAD frequency
NM_000341.4(SLC3A1):c.1381T>C (p.Tyr461His)	rs144162964	0.00044
NM_000341.4(SLC3A1):c.322A>G (p.Ile108Val)	rs138597262	0.00037
NM_000341.4(SLC3A1):c.680G>A (p.Arg227Gln)	rs142469446	0.00025
NM_000341.4(SLC3A1):c.1474G>A (p.Ala492Thr)	rs201989712	0.00014
NM_000341.4(SLC3A1):c.572A>G (p.Glu191Gly)	rs534054965	0.00010
NM_000341.4(SLC3A1):c.247C>T (p.Arg83Cys)	rs148946634	0.00007
NM_000341.4(SLC3A1):c.1613T>C (p.Val538Ala)	rs772556641	0.00006
NM_000341.4(SLC3A1):c.313A>G (p.Ile105Val)	rs200093674	0.00006
NM_000341.4(SLC3A1):c.569T>C (p.Met190Thr)	rs772817732	0.00005
NM_000341.4(SLC3A1):c.935G>C (p.Ser312Thr)	rs201325919	0.00005
NM_000341.4(SLC3A1):c.1334T>C (p.Ile445Thr)	rs187962930	0.00003
NM_000341.4(SLC3A1):c.1367G>A (p.Arg456His)	rs373852467	0.00002
NM_000341.4(SLC3A1):c.1085G>A (p.Arg362His)	rs121912697	0.00001
NM_000341.4(SLC3A1):c.1406T>G (p.Leu469Arg)	rs1469809535	0.00001
NM_000341.4(SLC3A1):c.508C>G (p.Leu170Val)	rs757439376	0.00001
NM_000341.4(SLC3A1):c.67G>A (p.Gly23Arg)	rs750919380	0.00001
NM_000341.4(SLC3A1):c.166G>A (p.Glu56Lys)	rs886056067
NM_000341.4(SLC3A1):c.24A>C (p.Arg8Ser)	rs376615998
NM_000341.4(SLC3A1):c.290T>C (p.Val97Ala)	rs147701210
NM_000341.4(SLC3A1):c.566C>A (p.Thr189Lys)	rs140317484
NM_000341.4(SLC3A1):c.685C>T (p.Arg229Trp)	rs758636942
NM_000341.4(SLC3A1):c.851A>T (p.Asp284Val)	rs933907652

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