Related gene-specific medical variations for Gene (Select 196513) - 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: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3341601	NM_152640.5(DCP1B):c.93C>A (p.Ile31=)	CACNA1C, DCP1B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3080575	NM_152640.5(DCP1B):c.7G>C (p.Ala3Pro)	CACNA1C, DCP1B (A3P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080573	NM_152640.5(DCP1B):c.212G>A (p.Gly71Glu)	CACNA1C, DCP1B (G71E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2570815	NM_152640.5(DCP1B):c.294T>G (p.Pro98=)	CACNA1C, DCP1B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2283727	NM_152640.5(DCP1B):c.80A>G (p.Tyr27Cys)	CACNA1C, DCP1B (Y27C)	Single nucleotide variant (missense 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