ClinVar for MedGen (Select 347456) - ClinVar

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Items: 52

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1686708	NM_000516.7(GNAS):c.683G>A (p.Arg228His)	GNAS (R169H +5 more)	Single nucleotide variant (missense variant +1 more)	Pseudohypoparathyroidism type 1B +8 more	GUncertain significance
Select item 1647292	NM_000516.7(GNAS):c.660-19C>T	GNAS	Single nucleotide variant (intron variant)	Pseudohypoparathyroidism type 1C +8 more	GLikely benign
Select item 1639287	NM_000516.7(GNAS):c.213-11C>T	GNAS	Single nucleotide variant (intron variant)	Pseudohypoparathyroidism type 1C +8 more	GLikely benign
Select item 1637666	NM_000516.7(GNAS):c.312+17T>C	GNAS	Single nucleotide variant (intron variant)	Pseudohypoparathyroidism type 1C +8 more	GLikely benign
Select item 1629295	NM_000516.7(GNAS):c.530+11G>A	GNAS	Single nucleotide variant (intron variant)	Pseudohypoparathyroidism type 1C +9 more	GLikely benign
Select item 1628862	NM_000516.7(GNAS):c.660-15C>A	GNAS	Single nucleotide variant (intron variant)	not provided +8 more	GLikely benign
Select item 1626827	NM_000516.7(GNAS):c.258-7A>C	GNAS	Single nucleotide variant (intron variant)	McCune-Albright syndrome +8 more	GLikely benign
Select item 1601588	NM_000516.7(GNAS):c.1038+17_1038+20del	GNAS	Deletion (intron variant)	Progressive osseous heteroplasia +8 more	GBenign/Likely benign
Select item 1597362	NM_000516.7(GNAS):c.136C>T (p.Leu46=)	GNAS	Single nucleotide variant (intron variant +1 more)	Progressive osseous heteroplasia +8 more	GLikely benign
Select item 1596750	NM_000516.7(GNAS):c.1039-4G>A	GNAS	Single nucleotide variant (intron variant)	Progressive osseous heteroplasia +8 more	GLikely benign
Select item 1560162	NM_000516.7(GNAS):c.738C>T (p.Phe246=)	GNAS	Single nucleotide variant (synonymous variant +1 more)	not provided +8 more	GLikely benign
Select item 1431017	NM_000516.7(GNAS):c.367G>A (p.Glu123Lys)	GNAS (E109K +5 more)	Single nucleotide variant (missense variant +1 more)	not provided +8 more	GUncertain significance
Select item 1315968	NM_080425.4(GNAS):c.1275C>T (p.Phe425=)	GNAS (S363L)	Single nucleotide variant (genic upstream transcript variant +3 more)	not provided +8 more	GUncertain significance
Select item 1299925	NM_000516.7(GNAS):c.576G>T (p.Pro192=)	GNAS	Single nucleotide variant (synonymous variant +1 more)	not provided +8 more	GLikely benign
Select item 1284681	NM_000516.7(GNAS):c.357G>A (p.Leu119=)	GNAS	Single nucleotide variant (synonymous variant +1 more)	not provided +8 more	GBenign/Likely benign
Select item 1284589	NM_000516.7(GNAS):c.936T>C (p.Phe312=)	GNAS	Single nucleotide variant (synonymous variant +1 more)	McCune-Albright syndrome +8 more	GLikely benign
Select item 1284575	NM_016592.5(GNAS):c.537G>A (p.Pro179=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	McCune-Albright syndrome +8 more	GLikely benign
Select item 1217738	NM_000516.7(GNAS):c.91C>T (p.Gln31Ter)	GNAS (Q31*)	Single nucleotide variant (nonsense +1 more)	McCune-Albright syndrome +8 more	GPathogenic
Select item 1215279	NM_000516.7(GNAS):c.985G>A (p.Gly329Arg)	GNAS (G270R +5 more)	Single nucleotide variant (missense variant +1 more)	not provided +8 more	GUncertain significance
Select item 1205936	NM_080425.4(GNAS):c.1428C>G (p.Ala476=)	GNAS (P414R)	Single nucleotide variant (missense variant +2 more)	not provided +8 more	GBenign/Likely benign
Select item 1205909	NM_080425.4(GNAS):c.154G>A (p.Glu52Lys)	GNAS (E52K)	Single nucleotide variant (5 prime UTR variant +2 more)	Inborn genetic diseases +8 more	GConflicting classifications of pathogenicity
Select item 1203026	NM_080425.4(GNAS):c.1395A>C (p.Pro465=)	GNAS (Q403P)	Single nucleotide variant (missense variant +2 more)	not provided +8 more	GLikely benign
Select item 1098700	NM_080425.4(GNAS):c.1130G>T (p.Gly377Val)	GNAS (G315C +1 more)	Single nucleotide variant (missense variant +1 more)	Pseudohypoparathyroidism type 1C +8 more	GUncertain significance
Select item 1048823	NM_080425.4(GNAS):c.538C>T (p.Gln180Ter)	GNAS (Q180*)	Single nucleotide variant (synonymous variant +2 more)	McCune-Albright syndrome +7 more	GUncertain significance
Select item 931358	NM_080425.4(GNAS):c.1276G>C (p.Ala426Pro)	GNAS (A426P)	Single nucleotide variant (genic upstream transcript variant +3 more)	McCune-Albright syndrome +8 more	GConflicting classifications of pathogenicity
Select item 930718	NM_080425.4(GNAS):c.1323C>T (p.Pro441=)	GNAS (P379L)	Single nucleotide variant (missense variant +2 more)	McCune-Albright syndrome +7 more	GUncertain significance
Select item 871093	NM_000516.7(GNAS):c.348dup (p.Val117fs)	GNAS (V58fs +5 more)	Duplication (frameshift variant +1 more)	Pseudohypoparathyroidism type I A +8 more	GPathogenic
Select item 816910	NM_000516.7(GNAS):c.691C>T (p.Arg231Cys)	GNAS (R172C +5 more)	Single nucleotide variant (missense variant +1 more)	not provided +11 more	GPathogenic/Likely pathogenic
Select item 781570	NM_080425.4(GNAS):c.1221C>G (p.Thr407=)	GNAS (P345R)	Single nucleotide variant (missense variant +2 more)	Pseudohypoparathyroidism type 1B +8 more	GBenign/Likely benign
Select item 748266	NM_000516.7(GNAS):c.1131C>T (p.Asn377=)	GNAS	Single nucleotide variant (synonymous variant +1 more)	not provided +8 more	GLikely benign
Select item 744959	NM_000516.7(GNAS):c.684C>T (p.Arg228=)	GNAS	Single nucleotide variant (synonymous variant +1 more)	not provided +8 more	GLikely benign
Select item 729219	NM_000516.7(GNAS):c.384G>A (p.Val128=)	GNAS	Single nucleotide variant (synonymous variant +1 more)	not specified +9 more	GBenign/Likely benign
Select item 729218	NM_000516.7(GNAS):c.366C>T (p.Pro122=)	GNAS	Single nucleotide variant (synonymous variant +1 more)	not specified +10 more	GBenign/Likely benign
Select item 727640	NM_080425.4(GNAS):c.958G>A (p.Asp320Asn)	GNAS (D320N)	Single nucleotide variant (genic upstream transcript variant +3 more)	Pseudohypoparathyroidism type 1C +8 more	GLikely benign
Select item 722980	NM_000516.7(GNAS):c.951C>T (p.Arg317=)	GNAS	Single nucleotide variant (synonymous variant +1 more)	Pseudohypoparathyroidism type 1C +9 more	GBenign/Likely benign
Select item 719213	NM_080425.4(GNAS):c.913T>C (p.Ser305Pro)	GNAS (S305P)	Single nucleotide variant (synonymous variant +2 more)	Pseudohypoparathyroidism type 1C +8 more	GLikely benign
Select item 715266	NM_000516.7(GNAS):c.111C>T (p.Tyr37=)	GNAS	Single nucleotide variant (synonymous variant +1 more)	Pseudohypoparathyroidism type 1C +8 more	GLikely benign
Select item 715265	NM_000516.7(GNAS):c.75G>A (p.Lys25=)	GNAS	Single nucleotide variant (synonymous variant +1 more)	Pseudohypoparathyroidism type 1C +8 more	GLikely benign
Select item 489076	NM_080425.4(GNAS):c.98C>A (p.Ala33Asp)	GNAS (A33D)	Single nucleotide variant (5 prime UTR variant +2 more)	GNAS-related disorder +9 more	GUncertain significance
Select item 417936	NM_080425.4(GNAS):c.1455C>A (p.Ala485=)	GNAS (P423H)	Single nucleotide variant (missense variant +2 more)	McCune-Albright syndrome +8 more	GBenign
Select item 209158	NM_000516.7(GNAS):c.34C>T (p.Gln12Ter)	GNAS (Q12*)	Single nucleotide variant (nonsense +1 more)	not provided +11 more	GPathogenic
Select item 134496	NM_080425.4(GNAS):c.1462G>A (p.Ala488Thr)	GNAS (A488T)	Single nucleotide variant (genic upstream transcript variant +3 more)	Pseudohypoparathyroidism type 1B +7 more	GLikely benign
Select item 134493	NM_080425.4(GNAS):c.1798C>G (p.Arg600Gly)	GNAS (R600G)	Single nucleotide variant (synonymous variant +2 more)	Pseudohypoparathyroidism type 1B +8 more	GBenign/Likely benign
Select item 134491	NM_080425.4(GNAS):c.484A>G (p.Met162Val)	GNAS (M162V)	Single nucleotide variant (synonymous variant +2 more)	not provided +8 more	GBenign/Likely benign
Select item 134484	NM_080425.4(GNAS):c.628G>C (p.Ala210Pro)	GNAS (R147S +1 more)	Single nucleotide variant (missense variant +1 more)	Pseudohypoparathyroidism type 1B +8 more	GLikely benign
Select item 134480	NM_080425.4(GNAS):c.1376C>G (p.Pro459Arg)	GNAS (L397V +1 more)	Single nucleotide variant (missense variant +2 more)	Pseudohypoparathyroidism type 1B +8 more	GLikely benign
Select item 134479	NM_080425.4(GNAS):c.1307C>A (p.Ala436Asp)	GNAS (P374T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +8 more	GBenign
Select item 134475	NM_000516.7(GNAS):c.432C>T (p.Pro144=)	GNAS	Single nucleotide variant (synonymous variant +1 more)	Pseudohypoparathyroidism type 1B +8 more	GBenign/Likely benign
Select item 15938	NM_000516.7(GNAS):c.565_568del (p.Asp189fs)	GNAS (D130fs +5 more)	Deletion (frameshift variant +1 more)	not specified +12 more	GConflicting classifications of pathogenicity
Select item 15937	NM_000516.7(GNAS):c.601C>A (p.Arg201Ser)	GNAS (R201S +5 more)	Single nucleotide variant (missense variant +1 more)	PITUITARY TUMOR 3, GROWTH HORMONE-SECRETING, SOMATIC +2 more	GPathogenic
Select item 15934	NM_000516.7(GNAS):c.602G>A (p.Arg201His)	GNAS (R201H +5 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +4 more	GPathogenic OOncogenic
Select item 15933	NM_000516.7(GNAS):c.601C>T (p.Arg201Cys)	GNAS (R201C +5 more)	Single nucleotide variant (missense variant +1 more)	Pseudohypoparathyroidism type 1B +3 more	GPathogenic/Likely pathogenic OOncogenic

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Items: 52