List of variants in gene SACS reported as uncertain significance by Baylor Genetics

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_014363.6(SACS):c.8393C>A (p.Pro2798Gln)	rs140551762	0.00178
NM_014363.6(SACS):c.1278A>T (p.Leu426Phe)	rs138413501	0.00036
NM_014363.6(SACS):c.10008A>G (p.Lys3336=)	rs148971954	0.00031
NM_014363.6(SACS):c.2580A>G (p.Gln860=)	rs41283958	0.00031
NM_014363.6(SACS):c.10076C>T (p.Thr3359Ile)	rs368089670	0.00011
NM_014363.6(SACS):c.7394C>T (p.Ser2465Leu)	rs747676277	0.00008
NM_014363.6(SACS):c.11576G>A (p.Arg3859His)	rs149427669	0.00004
NM_014363.6(SACS):c.2597A>G (p.Lys866Arg)	rs761960824	0.00004
NM_014363.6(SACS):c.8192G>A (p.Arg2731His)	rs201127191	0.00004
NM_014363.6(SACS):c.10780A>T (p.Ile3594Leu)	rs994425261
NM_014363.6(SACS):c.1627G>A (p.Val543Met)	rs752705095
NM_014363.6(SACS):c.3427C>A (p.Gln1143Lys)	rs144267558
NM_014363.6(SACS):c.6941A>C (p.Asn2314Thr)	rs1868664491

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