Related gene-specific medical variations for Gene (Select 101101775) - 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 3179182	NM_001004313.3(TMEM220):c.31G>A (p.Gly11Arg)	TMEM220, TMEM220-AS1 (G11R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2555712	NM_001004313.3(TMEM220):c.59C>A (p.Ala20Glu)	TMEM220, TMEM220-AS1 (A20E)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2296614	NM_001004313.3(TMEM220):c.62C>T (p.Ala21Val)	TMEM220, TMEM220-AS1 (A21V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2234393	NM_001004313.3(TMEM220):c.37A>T (p.Met13Leu)	TMEM220, TMEM220-AS1 (M13L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2206610	NM_001004313.3(TMEM220):c.10G>A (p.Ala4Thr)	TMEM220, TMEM220-AS1 (A4T)	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