List of variants in gene SLC17A8 reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_139319.3(SLC17A8):c.354+16T>C	rs77707755	0.00380
NM_139319.3(SLC17A8):c.1120G>T (p.Ala374Ser)	rs138307707	0.00078
NM_139319.3(SLC17A8):c.*6G>C	rs776625466	0.00004
NM_139319.3(SLC17A8):c.1537G>A (p.Glu513Lys)	rs767334253	0.00004
NM_139319.3(SLC17A8):c.1187-10C>T	rs768173927	0.00002
NM_139319.3(SLC17A8):c.1068A>G (p.Ser356=)
NM_139319.3(SLC17A8):c.1095C>T (p.Ile365=)
NM_139319.3(SLC17A8):c.1298-14dup	rs730880358
NM_139319.3(SLC17A8):c.1631AGA[1] (p.Lys545del)	rs141689561
NM_139319.3(SLC17A8):c.765C>T (p.Gly255=)

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