"PreventionGenetics, part of Exact Sciences"[submitter] AND "RASGRP1"[ - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2771966	NM_005739.4(RASGRP1):c.2229C>G (p.Leu743=)	RASGRP1	Single nucleotide variant (synonymous variant +1 more)	RASGRP1-related disorder +1 more	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 1169551	NM_005739.4(RASGRP1):c.1479A>G (p.Glu493=)	RASGRP1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1170545	NM_005739.4(RASGRP1):c.1446T>C (p.Tyr482=)	RASGRP1	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 1587495	NM_005739.4(RASGRP1):c.1410C>T (p.His470=)	RASGRP1	Single nucleotide variant (synonymous variant +1 more)	RASGRP1-related disorder +1 more	GLikely benign
Select item 1597148	NM_005739.4(RASGRP1):c.801G>A (p.Thr267=)	RASGRP1	Single nucleotide variant (synonymous variant)	RASGRP1-related disorder +1 more	GBenign/Likely benign
Select item 1667240	NM_005739.4(RASGRP1):c.756C>T (p.Asn252=)	RASGRP1	Single nucleotide variant (synonymous variant)	RASGRP1-related disorder +1 more	GLikely benign
Select item 1654852	NM_005739.4(RASGRP1):c.495T>C (p.His165=)	RASGRP1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 784309	NM_005739.4(RASGRP1):c.490T>A (p.Leu164Ile)	RASGRP1 (L164I)	Single nucleotide variant (missense variant)	RASGRP1-related disorder +1 more	GBenign