"Illumina Laboratory Services, Illumina"[submitter] AND "TCF4-AS1"[gen - ClinVar

Format

Sort by

Choose Destination

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 167731	NM_001083962.2(TCF4):c.269A>G (p.Asn90Ser)	TCF4, TCF4-AS1 (N90S +4 more)	Single nucleotide variant (missense variant)	Pitt-Hopkins syndrome	GBenign FDA Recognized database
Select item 327306	NM_001083962.2(TCF4):c.212A>G (p.Tyr71Cys)	TCF4, TCF4-AS1 (Y71C +4 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 139402	NM_001083962.2(TCF4):c.208-8A>G	TCF4-AS1, TCF4	Single nucleotide variant (intron variant)	not specified +1 more	GBenign

Format

Sort by

Choose Destination

ClinVar