List of variants in gene GNAS reported as likely benign for pituitary gland adenoma

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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: 33

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HGVS	dbSNP	gnomAD frequency
NM_080425.4(GNAS):c.1376C>G (p.Pro459Arg)	rs148033592	0.01117
NM_000516.7(GNAS):c.951C>T (p.Arg317=)	rs75561530	0.00680
NM_000516.7(GNAS):c.384G>A (p.Val128=)	rs3730166	0.00609
NM_000516.7(GNAS):c.366C>T (p.Pro122=)	rs35287986	0.00583
NM_080425.4(GNAS):c.1798C>G (p.Arg600Gly)	rs74897360	0.00538
NM_080425.4(GNAS):c.1221C>G (p.Thr407=)	rs200430001	0.00433
NM_080425.4(GNAS):c.484A>G (p.Met162Val)	rs138731520	0.00192
NM_016592.5(GNAS):c.537G>A (p.Pro179=)	rs181594534	0.00072
NM_080425.4(GNAS):c.1395A>C (p.Pro465=)	rs56213454	0.00027
NM_000516.7(GNAS):c.312+17T>C	rs78999525	0.00022
NM_000516.7(GNAS):c.530+11G>A	rs74474807	0.00017
NM_000516.7(GNAS):c.1038+17_1038+20del	rs773644530	0.00013
NM_000516.7(GNAS):c.213-11C>T	rs369370389	0.00013
NM_080425.4(GNAS):c.913T>C (p.Ser305Pro)	rs376517306	0.00008
NM_000516.7(GNAS):c.357G>A (p.Leu119=)	rs368741499	0.00006
NM_000516.7(GNAS):c.1039-4G>A	rs575570315	0.00005
NM_000516.7(GNAS):c.576G>T (p.Pro192=)	rs558915293	0.00005
NM_080425.4(GNAS):c.1462G>A (p.Ala488Thr)	rs552813440	0.00005
NM_000516.7(GNAS):c.684C>T (p.Arg228=)	rs147984566	0.00004
NM_000516.7(GNAS):c.936T>C (p.Phe312=)	rs764458531	0.00004
NM_080425.4(GNAS):c.958G>A (p.Asp320Asn)	rs201342585	0.00004
NM_000516.7(GNAS):c.1131C>T (p.Asn377=)	rs140075370	0.00003
NM_000516.7(GNAS):c.660-19C>T	rs370723643	0.00003
NM_000516.7(GNAS):c.111C>T (p.Tyr37=)	rs749235261	0.00001
NM_000516.7(GNAS):c.136C>T (p.Leu46=)	rs775009418	0.00001
NM_000516.7(GNAS):c.258-7A>C	rs1183884518	0.00001
NM_000516.7(GNAS):c.660-15C>A	rs755766644	0.00001
NM_000516.7(GNAS):c.738C>T (p.Phe246=)	rs772094317	0.00001
NM_000516.7(GNAS):c.432C>T (p.Pro144=)	rs11554266
NM_000516.7(GNAS):c.75G>A (p.Lys25=)	rs1326256762
NM_080425.4(GNAS):c.1276G>C (p.Ala426Pro)	rs767104257
NM_080425.4(GNAS):c.1428C>G (p.Ala476=)	rs559714658
NM_080425.4(GNAS):c.628G>C (p.Ala210Pro)	rs61749696

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