"RASGRP2-related disorder"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2049827	NM_001098671.2(RASGRP2):c.1797G>A (p.Thr599=)	RASGRP2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 627002	NM_001098671.2(RASGRP2):c.1490del (p.Phe497fs)	RASGRP2 (F352fs +1 more)	Deletion (frameshift variant)	not provided +2 more	GPathogenic/Likely pathogenic
Select item 501656	NM_001098671.2(RASGRP2):c.1466C>G (p.Ser489Cys)	RASGRP2 (S489C +1 more)	Single nucleotide variant (missense variant)	RASGRP2-related disorder +2 more	GLikely benign
Select item 3053141	NM_001098671.2(RASGRP2):c.1412+2T>C	RASGRP2	Single nucleotide variant (splice donor variant)	RASGRP2-related disorder	GLikely pathogenic
Select item 2064992	NM_001098671.2(RASGRP2):c.786C>T (p.His262=)	RASGRP2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 2716813	NM_001098671.2(RASGRP2):c.741C>T (p.Val247=)	RASGRP2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 750298	NM_001098671.2(RASGRP2):c.279C>T (p.Asn93=)	RASGRP2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign

ClinVar