Related gene-specific medical variations for Gene (Select 4256) - ClinVar - NCBI

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Links from Gene

Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2433745	NM_000900.5(MGP):c.62A>T (p.Glu21Val)	MGP (E21V +1 more)	Single nucleotide variant (missense variant)	Keutel syndrome	GUncertain significance
Select item 883398	NM_000900.5(MGP):c.*531T>C	LOC126861465, MGP	Single nucleotide variant (3 prime UTR variant)	Keutel syndrome	GUncertain significance
Select item 883397	NM_000900.5(MGP):c.*720C>A	LOC126861465, MGP	Single nucleotide variant (3 prime UTR variant)	Keutel syndrome	GUncertain significance
Select item 881047	NM_000900.5(MGP):c.*206A>G	LOC126861465, MGP	Single nucleotide variant (3 prime UTR variant)	Keutel syndrome +1 more	GBenign/Likely benign
Select item 377307	NM_000900.5(MGP):c.62-638G>C	MGP (E22D)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 307766	NM_000900.5(MGP):c.*251T>C	LOC126861465, MGP	Single nucleotide variant (3 prime UTR variant)	Keutel syndrome	GUncertain significance
Select item 307765	NM_000900.5(MGP):c.*315dup	LOC126861465, MGP	Duplication (3 prime UTR variant)	Keutel syndrome	GUncertain significance
Select item 307764	NM_000900.5(MGP):c.*339T>C	LOC126861465, MGP	Single nucleotide variant (3 prime UTR variant)	Keutel syndrome	GBenign
Select item 307763	NM_000900.5(MGP):c.*343G>A	LOC126861465, MGP	Single nucleotide variant (3 prime UTR variant)	Keutel syndrome +1 more	GBenign
Select item 307762	NM_000900.5(MGP):c.*455del	LOC126861465, MGP	Deletion (3 prime UTR variant)	Keutel syndrome	GUncertain significance
Select item 307761	NM_000900.5(MGP):c.*476T>C	LOC126861465, MGP	Single nucleotide variant (3 prime UTR variant)	Keutel syndrome	GUncertain significance
Select item 307760	NM_000900.5(MGP):c.*538C>G	LOC126861465, MGP	Single nucleotide variant (3 prime UTR variant)	Keutel syndrome	GLikely benign
Select item 307759	NM_000900.5(MGP):c.*552A>T	LOC126861465, MGP	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 307758	NM_000900.5(MGP):c.*604A>G	LOC126861465, MGP	Single nucleotide variant (3 prime UTR variant)	Keutel syndrome	GBenign
Select item 307757	NM_000900.5(MGP):c.*615A>G	LOC126861465, MGP	Single nucleotide variant (3 prime UTR variant)	Keutel syndrome	GBenign
Select item 307756	NM_000900.5(MGP):c.*755G>T	LOC126861465, MGP	Single nucleotide variant (3 prime UTR variant)	Keutel syndrome	GBenign