"Ambry Genetics"[submitter] AND "RASGRP3-AS1"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2606448	NM_001139488.2(RASGRP3):c.1592A>G (p.Asn531Ser)	RASGRP3, RASGRP3-AS1 (N531S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343946	NM_001139488.2(RASGRP3):c.1646G>A (p.Arg549Gln)	RASGRP3, RASGRP3-AS1 (R549Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214926	NM_001139488.2(RASGRP3):c.1694C>G (p.Ser565Trp)	RASGRP3, RASGRP3-AS1 (S565W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490498	NM_001139488.2(RASGRP3):c.1721T>C (p.Phe574Ser)	RASGRP3, RASGRP3-AS1 (F573S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151862	NM_001139488.2(RASGRP3):c.1780G>A (p.Val594Ile)	RASGRP3, RASGRP3-AS1 (V593I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151863	NM_001139488.2(RASGRP3):c.1792T>C (p.Ser598Pro)	RASGRP3, RASGRP3-AS1 (S597P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531126	NM_001139488.2(RASGRP3):c.1795C>T (p.Arg599Cys)	RASGRP3, RASGRP3-AS1 (R598C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539757	NM_001139488.2(RASGRP3):c.1931C>T (p.Ala644Val)	RASGRP3, RASGRP3-AS1 (A643V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487174	NM_001139488.2(RASGRP3):c.1951G>T (p.Ala651Ser)	RASGRP3, RASGRP3-AS1 (A651S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151864	NM_001139488.2(RASGRP3):c.1982A>G (p.His661Arg)	RASGRP3, RASGRP3-AS1 (H661R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457432	NM_001139488.2(RASGRP3):c.2005C>T (p.Arg669Trp)	RASGRP3, RASGRP3-AS1 (R668W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance