List of variants reported as likely benign for Hyperglycinuria; Neutral 1 amino acid transport defect; Iminoglycinuria by Fulgent Genetics, Fulgent Genetics

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Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_001003841.3(SLC6A19):c.966C>T (p.Tyr322=)	rs115133359	0.01389
NM_001003841.3(SLC6A19):c.555G>A (p.Thr185=)	rs115871703	0.00268
NM_001003841.3(SLC6A19):c.117G>A (p.Ala39=)	rs149830504	0.00197
NM_001003841.3(SLC6A19):c.775-4G>A	rs144753758	0.00158
NM_001003841.3(SLC6A19):c.1044C>T (p.Phe348=)	rs139103369	0.00073
NM_001003841.3(SLC6A19):c.558C>T (p.Ser186=)	rs140343487	0.00073
NM_001003841.3(SLC6A19):c.343+11C>T	rs146085736	0.00053
NM_001003841.3(SLC6A19):c.45C>G (p.Ile15Met)	rs138390777	0.00052
NM_001003841.3(SLC6A19):c.481+12C>G	rs370624507	0.00034
NM_001003841.3(SLC6A19):c.48G>A (p.Pro16=)	rs141911612	0.00034
NM_001003841.3(SLC6A19):c.887+8C>T	rs375506845	0.00034
NM_001003841.3(SLC6A19):c.162C>T (p.Asn54=)	rs139760936	0.00021
NM_001003841.3(SLC6A19):c.1539-20G>C	rs113981520	0.00017
NM_001003841.3(SLC6A19):c.684G>A (p.Thr228=)	rs148328575	0.00017
NM_001003841.3(SLC6A19):c.774+10C>T	rs372657226	0.00014
NM_001003841.3(SLC6A19):c.849C>T (p.Phe283=)	rs201416473	0.00011
NM_001003841.3(SLC6A19):c.195C>T (p.His65=)	rs143165913	0.00010
NM_001003841.3(SLC6A19):c.1302G>A (p.Gly434=)	rs544896068	0.00006
NM_001003841.3(SLC6A19):c.1284G>C (p.Gly428=)	rs750242948	0.00004
NM_001003841.3(SLC6A19):c.1596C>T (p.Val532=)	rs748088574	0.00004
NM_001003841.3(SLC6A19):c.1701+18C>T	rs112626901	0.00004
NM_001003841.3(SLC6A19):c.1173+20C>T	rs982302856	0.00003
NM_001003841.3(SLC6A19):c.1554C>T (p.Ile518=)	rs143414604	0.00003
NM_001003841.3(SLC6A19):c.1485C>T (p.Leu495=)	rs572012976	0.00001
NM_001003841.3(SLC6A19):c.1521C>T (p.Tyr507=)	rs1319482740	0.00001
NM_001003841.3(SLC6A19):c.453C>T (p.Ser151=)	rs756989097	0.00001
NM_001003841.3(SLC6A19):c.657C>T (p.Thr219=)	rs764090881	0.00001
NM_001003841.3(SLC6A19):c.1431C>T (p.Ser477=)	rs755478742
NM_001003841.3(SLC6A19):c.1599G>A (p.Thr533=)	rs112479136
NM_001003841.3(SLC6A19):c.202+12G>A	rs369314798

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