"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "RASGRP1"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2645158	NM_005739.4(RASGRP1):c.2121C>T (p.Pro707=)	RASGRP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2645159	NM_005739.4(RASGRP1):c.2097C>A (p.Ala699=)	RASGRP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1127206	NM_005739.4(RASGRP1):c.2042T>C (p.Ile681Thr)	RASGRP1 (I646T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1137779	NM_005739.4(RASGRP1):c.1632C>T (p.Phe544=)	RASGRP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 769409	NM_005739.4(RASGRP1):c.1548C>T (p.Leu516=)	RASGRP1	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 2645160	NM_005739.4(RASGRP1):c.849+8A>G	RASGRP1	Single nucleotide variant (intron variant)	not provided	GConflicting classifications of pathogenicity
Select item 916422	NM_005739.4(RASGRP1):c.843G>C (p.Val281=)	RASGRP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 807208	NM_005739.4(RASGRP1):c.319A>T (p.Ile107Phe)	RASGRP1 (I107F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar