Related gene-specific medical variations for Gene (Select 131831) - ClinVar - NCBI

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

Links from Gene

Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3276373	NM_152394.5(ERICH6):c.176A>T (p.Glu59Val)	ERICH6, ERICH6-AS1 (E59V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3257586	NM_152394.5(ERICH6):c.96A>G (p.Glu32=)	ERICH6, ERICH6-AS1 +1 more	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 3090254	NM_152394.5(ERICH6):c.264C>A (p.Asp88Glu)	ERICH6, ERICH6-AS1 (D88E)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3090253	NM_152394.5(ERICH6):c.229T>G (p.Tyr77Asp)	ERICH6, ERICH6-AS1 (Y77D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2288406	NM_152394.5(ERICH6):c.83A>T (p.Glu28Val)	ERICH6, ERICH6-AS1 +1 more (E28V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2273808	NM_152394.5(ERICH6):c.308G>C (p.Ser103Thr)	ERICH6, ERICH6-AS1 (S103T)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2255627	NM_152394.5(ERICH6):c.37C>A (p.Pro13Thr)	ERICH6, ERICH6-AS1 +1 more (P13T)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2250134	NM_152394.5(ERICH6):c.19C>T (p.Pro7Ser)	ERICH6, ERICH6-AS1 (P7S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance