"GeneDx"[submitter] AND "GGCX"[gene] - ClinVar

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Search results

Items: 39

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 337250	NM_000821.7(GGCX):c.*225G>A	GGCX	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 1220443	NM_000821.7(GGCX):c.*107dup	GGCX	Duplication (3 prime UTR variant)	not provided	GLikely benign
Select item 1210509	NM_000821.7(GGCX):c.*107del	GGCX	Deletion (3 prime UTR variant)	not provided	GLikely benign
Select item 337254	NM_000821.7(GGCX):c.*107T>G	GGCX	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1450284	NM_000821.7(GGCX):c.2110C>T (p.Arg704Ter)	GGCX (R647* +1 more)	Single nucleotide variant (nonsense)	not provided	GConflicting classifications of pathogenicity
Select item 1278677	NM_000821.7(GGCX):c.2085-21C>T	GGCX	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1233214	NM_000821.7(GGCX):c.2084+106T>G	GGCX	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 375657	NM_000821.7(GGCX):c.2084+45G>C	GGCX	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1800659	NM_000821.7(GGCX):c.1903C>G (p.Pro635Ala)	GGCX (P578A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 337261	NM_000821.7(GGCX):c.1889-17_1889-16del	GGCX	Deletion (intron variant)	Vitamin K-Dependent Clotting Factors +1 more	GBenign/Likely benign
Select item 3341038	NM_000821.7(GGCX):c.1454G>A (p.Arg485His)	GGCX (R428H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1240875	NM_000821.7(GGCX):c.1440-107TCT[2]	GGCX	Microsatellite (intron variant)	not provided	GBenign
Select item 337265	NM_000821.7(GGCX):c.1242C>T (p.Thr414=)	GGCX	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 337266	NM_000821.7(GGCX):c.1218C>T (p.Arg406=)	GGCX	Single nucleotide variant (synonymous variant)	Vitamin K-dependent clotting factors, combined deficiency of, type 1 +1 more	GBenign
Select item 1241950	NM_000821.7(GGCX):c.1155+50C>T	GGCX	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 337268	NM_000821.7(GGCX):c.974G>A (p.Arg325Gln)	GGCX (R325Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 3340370	NM_000821.7(GGCX):c.890-109_890-107del	GGCX	Microsatellite (intron variant)	not provided	GLikely benign
Select item 1278150	NM_000821.7(GGCX):c.890-212G>A	GGCX	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 16206	NM_000821.7(GGCX):c.763G>A (p.Val255Met)	GGCX (V255M +1 more)	Single nucleotide variant (missense variant)	not provided	GPathogenic/Likely pathogenic
Select item 1282061	NM_000821.7(GGCX):c.726-178CAA[11]	GGCX	Microsatellite (intron variant)	not provided	GBenign
Select item 1255241	NM_000821.7(GGCX):c.726-178CAA[15]	GGCX	Microsatellite (intron variant)	not provided	GBenign
Select item 1251547	NM_000821.7(GGCX):c.726-178CAA[13]	GGCX	Microsatellite (intron variant)	not provided	GBenign
Select item 1241255	NM_000821.7(GGCX):c.726-178CAA[12]	GGCX	Microsatellite (intron variant)	not provided	GBenign
Select item 1241080	NM_000821.7(GGCX):c.726-178CAA[14]	GGCX	Microsatellite (intron variant)	not provided	GBenign
Select item 1199995	NM_000821.7(GGCX):c.725+20G>T	GGCX	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign
Select item 1221805	NM_000821.7(GGCX):c.618+177A>C	GGCX	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1270946	NM_000821.7(GGCX):c.618+154del	GGCX	Deletion (intron variant)	not provided	GBenign
Select item 1190779	NM_000821.7(GGCX):c.618+89C>T	GGCX	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 337275	NM_000821.7(GGCX):c.339C>T (p.Asp113=)	GGCX	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1233191	NM_000821.7(GGCX):c.214+197dup	GGCX	Duplication (intron variant)	not provided	GBenign
Select item 1215721	NM_000821.7(GGCX):c.214+116A>G	GGCX	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1281979	NM_000821.7(GGCX):c.44-32G>A	GGCX	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277970	NM_000821.7(GGCX):c.44-67A>T	GGCX	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1220260	NM_000821.7(GGCX):c.44-118_44-105dup	GGCX	Duplication (intron variant)	not provided	GLikely benign
Select item 1183323	NM_000821.7(GGCX):c.44-162G>T	GGCX	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1237610	NM_000821.7(GGCX):c.43+107del	GGCX	Deletion (intron variant)	not provided	GBenign
Select item 1182965	NM_000821.7(GGCX):c.43+106del	GGCX	Deletion (intron variant)	not provided	GBenign
Select item 1214343	NM_000821.7(GGCX):c.43+33T>A	GGCX	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1289081	NC_000002.12:g.85561615C>A	GGCX, LOC129934217	Single nucleotide variant	not provided	GBenign

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Items: 39