"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "PHF2"[gene - ClinVar

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

Format

Sort by

Choose Destination

Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 733486	NM_005392.4(PHF2):c.1935C>T (p.Leu645=)	PHF2	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2659315	NM_005392.4(PHF2):c.2349-2312_2349-2310del	PHF2	Deletion (intron variant)	not provided	GLikely benign
Select item 2659316	NM_005392.4(PHF2):c.2976C>A (p.Thr992=)	PHF2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

Format

Sort by

Choose Destination