MEG3[gene] and "single gene"[properties] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 48

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 162014	NC_000014.9:g.100824888_100829190delins100833642_100833702	MEG3	Indel	Paternal uniparental disomy of chromosome 14	GPathogenic
Select item 3040216	NR_046473.1(MEG3):n.578G>A	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GLikely benign
Select item 3059566	NR_046473.1(MEG3):n.679G>C	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GBenign
Select item 2644539	NR_046473.1(MEG3):n.936-391G>T	MEG3	Single nucleotide variant (non-coding transcript variant)	not provided	GLikely benign
Select item 3054634	NR_046473.1(MEG3):n.936-366G>A	MEG3	Single nucleotide variant (non-coding transcript variant +1 more)	MEG3-related disorder	GLikely benign
Select item 2644540	NC_000014.9:g.100831954T>G	MEG3	Single nucleotide variant	not provided	GBenign
Select item 2636776	NR_046473.1(MEG3):n.1050-1536G>T	MEG3	Single nucleotide variant (intron variant)	MEG3-related disorder	GUncertain significance
Select item 3239017	NC_000014.9:g.100835004G>A	MEG3	Single nucleotide variant	not provided	GBenign
Select item 2644541	NC_000014.9:g.100835277del	MEG3	Deletion	not provided	GLikely benign
Select item 2644542	NC_000014.9:g.100835512T>C	MEG3	Single nucleotide variant	not provided	GUncertain significance
Select item 2644543	NC_000014.9:g.100835704G>A	MEG3	Single nucleotide variant	not provided	GLikely benign
Select item 3043544	NR_046473.1(MEG3):n.1050-132C>A	MEG3	Single nucleotide variant (intron variant)	MEG3-related disorder	GLikely benign
Select item 3034727	NR_046473.1(MEG3):n.1153G>A	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GLikely benign
Select item 3042001	NR_046473.1(MEG3):n.1165G>A	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GLikely benign
Select item 3056262	NR_046473.1(MEG3):n.1184-7G>C	MEG3	Single nucleotide variant (intron variant)	MEG3-related disorder	GBenign
Select item 3044287	NR_046473.1(MEG3):n.1296dup	MEG3	Duplication (non-coding transcript variant)	MEG3-related disorder	GBenign
Select item 3046639	NR_046473.1(MEG3):n.1460G>A	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GLikely benign
Select item 3055213	NR_046473.1(MEG3):n.1700C>T	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GLikely benign
Select item 3053082	NR_046473.1(MEG3):n.2250_2251del	MEG3	Deletion (non-coding transcript variant)	MEG3-related disorder	GLikely benign
Select item 3035435	NR_046473.1(MEG3):n.3109del	MEG3	Deletion (non-coding transcript variant)	MEG3-related disorder	GLikely benign
Select item 3053362	NR_046473.1(MEG3):n.3629G>A	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GLikely benign
Select item 3052746	NR_046473.1(MEG3):n.4204C>T	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GLikely benign
Select item 3056329	NR_046473.1(MEG3):n.4210A>G	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GBenign
Select item 3056978	NR_046473.1(MEG3):n.4528A>C	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GBenign
Select item 3053740	NR_046473.1(MEG3):n.4628A>G	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GLikely benign
Select item 3057216	NR_046473.1(MEG3):n.4715A>G	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GBenign
Select item 3250900	NR_190994.1(MEG3):n.4927A>G	MEG3	Single nucleotide variant (non-coding transcript variant)	not provided	GBenign
Select item 3040103	NR_046473.1(MEG3):n.4868G>A	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GLikely benign
Select item 3046670	NR_046473.1(MEG3):n.5431A>T	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GLikely benign
Select item 3041128	NR_046473.1(MEG3):n.5439C>T	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GLikely benign
Select item 3035333	NR_046473.1(MEG3):n.5994_6001del	MEG3	Deletion (non-coding transcript variant)	MEG3-related disorder	GLikely benign
Select item 3045089	NR_046473.1(MEG3):n.6629C>T	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GLikely benign
Select item 3034698	NR_046473.1(MEG3):n.6706G>T	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GLikely benign
Select item 3060854	NR_046473.1(MEG3):n.6838G>A	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GBenign
Select item 3055484	NR_046473.1(MEG3):n.7358C>G	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GBenign
Select item 3041445	NR_046473.1(MEG3):n.7371T>G	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GBenign
Select item 3045679	NR_046473.1(MEG3):n.7405G>A	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GBenign
Select item 3039480	NR_046473.1(MEG3):n.7884A>G	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GBenign
Select item 3053291	NR_046473.1(MEG3):n.8115C>T	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GBenign
Select item 3044961	NR_046473.1(MEG3):n.8133T>C	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GBenign
Select item 3060897	NR_046473.1(MEG3):n.8471A>G	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GBenign
Select item 2644544	NR_046473.1(MEG3):n.9148A>G	MEG3	Single nucleotide variant (non-coding transcript variant)	not provided	GLikely benign
Select item 2644545	NC_000014.9:g.100856066T>C	MEG3	Single nucleotide variant (genic downstream transcript variant)	not provided	GBenign
Select item 2644546	NC_000014.9:g.100858254G>A	MEG3	Single nucleotide variant (genic downstream transcript variant)	not provided	GBenign
Select item 2644547	NC_000014.9:g.100858307C>T	MEG3	Single nucleotide variant (genic downstream transcript variant)	not provided	GLikely benign
Select item 2644548	NC_000014.9:g.100859188G>C	MEG3	Single nucleotide variant (genic downstream transcript variant)	not provided	GBenign
Select item 3044354	NC_000014.9:g.100860746G>C	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GBenign
Select item 3037629	NC_000014.9:g.100860980G>A	MEG3	Single nucleotide variant (non-coding transcript variant)	MEG3-related disorder	GBenign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 48