C3715155[trait identifier] AND "Centogene AG - the Rare Disease Compan - 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 1333937	NM_005235.3(ERBB4):c.2443A>G (p.Ile815Val)	ERBB4 (I815V)	Single nucleotide variant (missense variant)	Amyotrophic lateral sclerosis type 19	GUncertain significance
Select item 1333938	NM_005235.3(ERBB4):c.508C>T (p.Pro170Ser)	ERBB4 (P170S)	Single nucleotide variant (missense variant)	Amyotrophic lateral sclerosis type 19	GUncertain significance