"PreventionGenetics, part of Exact Sciences"[submitter] AND "GLS"[gene - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3054076	NM_014905.5(GLS):c.-212GCA[24]	GLS, LOC129935268	Microsatellite (5 prime UTR variant)	GLS-related condition	GLikely benign
Select item 3054034	NM_014905.5(GLS):c.-212GCA[23]	GLS, LOC129935268	Microsatellite (5 prime UTR variant)	GLS-related condition	GLikely benign
Select item 3047419	NM_014905.5(GLS):c.-212GCA[19]	GLS, LOC129935268	Microsatellite (5 prime UTR variant)	GLS-related condition	GLikely benign
Select item 3030444	NM_014905.5(GLS):c.-212GCA[26]	GLS, LOC129935268	Microsatellite (5 prime UTR variant)	GLS-related condition	GLikely benign
Select item 3054764	NM_014905.5(GLS):c.-212GCA[11]	GLS, LOC129935268	Microsatellite (5 prime UTR variant)	GLS-related condition	GLikely benign
Select item 3047867	NM_014905.5(GLS):c.-212GCA[12]	GLS, LOC129935268	Microsatellite (5 prime UTR variant)	GLS-related condition	GLikely benign
Select item 3047628	NM_014905.5(GLS):c.-212GCA[13]	GLS, LOC129935268	Microsatellite (5 prime UTR variant)	GLS-related condition	GLikely benign
Select item 3032445	NM_014905.5(GLS):c.-212GCA[9]	GLS, LOC129935268	Microsatellite (5 prime UTR variant)	GLS-related condition	GLikely benign
Select item 3031213	NM_014905.5(GLS):c.-212GCA[6]	GLS, LOC129935268	Microsatellite (5 prime UTR variant)	GLS-related condition	GLikely benign
Select item 3041394	NM_014905.5(GLS):c.125G>A (p.Gly42Glu)	GLS (G42E)	Single nucleotide variant (missense variant)	GLS-related condition	GLikely benign
Select item 3043984	NM_014905.5(GLS):c.228T>C (p.Pro76=)	GLS	Single nucleotide variant (synonymous variant)	GLS-related condition	GLikely benign
Select item 3032963	NM_014905.5(GLS):c.229T>G (p.Ser77Ala)	GLS (S77A)	Single nucleotide variant (missense variant)	GLS-related condition	GUncertain significance
Select item 3043609	NM_014905.5(GLS):c.266A>C (p.His89Pro)	GLS, LOC129935270 (H89P)	Single nucleotide variant (missense variant)	GLS-related condition	GBenign
Select item 2634709	NM_014905.5(GLS):c.286C>T (p.Pro96Ser)	GLS, LOC129935270 (P96S)	Single nucleotide variant (missense variant)	GLS-related condition	GUncertain significance
Select item 3054890	NM_014905.5(GLS):c.290C>T (p.Pro97Leu)	GLS, LOC129935270 (P97L)	Single nucleotide variant (missense variant)	GLS-related condition	GLikely benign
Select item 3024784	NM_014905.5(GLS):c.387-3T>C	GLS	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 3031672	NM_014905.5(GLS):c.388A>G (p.Lys130Glu)	GLS (K130E)	Single nucleotide variant (missense variant)	GLS-related condition	GUncertain significance
Select item 3049930	NM_014905.5(GLS):c.1039-5dup	GLS	Duplication (intron variant)	GLS-related condition	GLikely benign
Select item 2651767	NM_014905.5(GLS):c.1294G>T (p.Ala432Ser)	GLS (A432S)	Single nucleotide variant (missense variant)	GLS-related condition +1 more	GBenign
Select item 3050373	NM_014905.5(GLS):c.1650+8A>C	GLS	Single nucleotide variant (intron variant)	GLS-related condition	GBenign
Select item 3039095	NM_014905.5(GLS):c.1650+1093A>G	GLS	Single nucleotide variant (synonymous variant +1 more)	GLS-related condition	GLikely benign
Select item 2636710	NM_014905.5(GLS):c.1650+1116A>C	GLS (Q563P)	Single nucleotide variant (missense variant +1 more)	GLS-related condition	GUncertain significance
Select item 3051203	NM_014905.5(GLS):c.1651-10_1651-6del	GLS	Microsatellite (intron variant)	GLS-related condition	GLikely benign
Select item 2651769	NM_014905.5(GLS):c.1662G>A (p.Val554=)	GLS	Single nucleotide variant (synonymous variant)	GLS-related condition +1 more	GLikely benign
Select item 720765	NM_014905.5(GLS):c.1683A>C (p.Ala561=)	GLS	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3039072	NM_014905.5(GLS):c.1961A>G (p.Asn654Ser)	GLS (N654S)	Single nucleotide variant (missense variant)	GLS-related condition	GBenign

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Items: 26