C11orf42[gene] and "single gene"[properties] - ClinVar - NCBI

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

Display options Sort by Location Download

Format

Tabular
Tabular (text)
UI List

Sort by

Location
Relevance
Gene
Variation

Choose Destination

File

Search results

Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3234623	NM_173525.3(C11orf42):c.552C>G (p.Leu184=)	C11orf42	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2219673	NM_173525.3(C11orf42):c.698T>C (p.Met233Thr)	C11orf42 (M233T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232850	NM_173525.3(C11orf42):c.737C>T (p.Thr246Ile)	C11orf42 (T246I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241100	NM_173525.3(C11orf42):c.779C>T (p.Thr260Met)	C11orf42 (T260M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

Display options Sort by Location Download

Format

Tabular
Tabular (text)
UI List

Sort by

Location
Relevance
Gene
Variation

Choose Destination

File