"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "MAPK15"[ge - 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 2658905	NM_139021.3(MAPK15):c.106G>A (p.Gly36Ser)	MAPK15 (G36S)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2658906	NM_139021.3(MAPK15):c.1117G>C (p.Ala373Pro)	MAPK15 (A373P)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3024737	NM_139021.3(MAPK15):c.1154G>A (p.Gly385Asp)	MAPK15 (G385D)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3024645	GRCh37/hg19 8q23.3-24.3(chr8:113392581-146364022)x3	LY6E, LY6H +173 more	Copy number gain	not provided	GPathogenic

Display options Sort by Location Download

Format

Tabular
Tabular (text)
UI List

Sort by

Location
Relevance
Gene
Variation

Choose Destination

File