"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "LOC1268624 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2647425	NM_001005273.3(CHD3):c.841C>T (p.Arg281Cys)	CHD3, LOC126862484 (R281C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3025453	NM_001005273.3(CHD3):c.924G>A (p.Ser308=)	CHD3, LOC126862484	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3027216	NM_001005273.3(CHD3):c.1256G>A (p.Ser419Asn)	CHD3, LOC126862484 (S419N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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ClinVar