Related gene-specific medical variations for Gene (Select 100873948) - 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: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3202093	NM_001142475.2(NREP):c.95A>T (p.Lys32Ile)	NREP, NREP-AS1 (K32I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202092	NM_001142475.2(NREP):c.69G>C (p.Arg23Ser)	NREP, NREP-AS1 (R23S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202091	NM_001142475.2(NREP):c.63G>T (p.Arg21Ser)	NREP, NREP-AS1 (R21S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401003	NM_001142475.2(NREP):c.35G>A (p.Arg12Gln)	NREP, NREP-AS1 (R12Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign

Display options Sort by Relevance Download

Format

Tabular
Tabular (text)
UI List

Sort by

Location
Relevance
Gene
Variation

Choose Destination

File