"PreventionGenetics, part of Exact Sciences"[submitter] AND "BHLHA9"[g - ClinVar

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

Format

Sort by

Choose Destination

Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 730614	NM_001164405.2(BHLHA9):c.33G>A (p.Thr11=)	BHLHA9	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1185322	NM_001164405.2(BHLHA9):c.237A>G (p.Leu79=)	BHLHA9	Single nucleotide variant (synonymous variant)	Camptosynpolydactyly, complex +3 more	GBenign
Select item 3031978	NM_001164405.2(BHLHA9):c.408C>T (p.Cys136=)	BHLHA9	Single nucleotide variant (synonymous variant)	BHLHA9-related condition	GLikely benign

Format

Sort by

Choose Destination