Related gene-specific medical variations for Gene (Select 163404) - ClinVar - NCBI

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

Display options Sort by Relevance Download

Format

Tabular
Tabular (text)
UI List

Sort by

Location
Relevance
Gene
Variation

Choose Destination

File

Links from Gene

Items: 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2531865	NM_001037317.2(PLPPR5):c.202C>T (p.Leu68Phe)	PLPPR5, PLPPR5-AS1 (L68F)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2407521	NM_001037317.2(PLPPR5):c.14C>T (p.Pro5Leu)	PLPPR5, PLPPR5-AS1 (P5L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385620	NM_001037317.2(PLPPR5):c.217G>T (p.Ala73Ser)	PLPPR5, PLPPR5-AS1 (A73S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance

Display options Sort by Relevance Download

Format

Tabular
Tabular (text)
UI List

Sort by

Location
Relevance
Gene
Variation

Choose Destination

File