"GeneDx"[submitter] AND "RASGRP2"[gene] - ClinVar

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Items: 38

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1293849	NM_001098671.2(RASGRP2):c.1772-150_1772-147del	RASGRP2	Deletion (intron variant)	not provided	GBenign
Select item 1286700	NM_001098671.2(RASGRP2):c.1772-148_1772-147del	RASGRP2	Deletion (intron variant)	not provided	GBenign
Select item 1226530	NM_001098671.2(RASGRP2):c.1772-147del	RASGRP2	Deletion (intron variant)	not provided	GBenign
Select item 1228532	NM_001098671.2(RASGRP2):c.1771+183C>T	RASGRP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 403363	NM_001098671.2(RASGRP2):c.1749C>A (p.Gly583=)	RASGRP2	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 284960	NM_001098671.2(RASGRP2):c.1592-3C>A	RASGRP2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1222996	NM_001098671.2(RASGRP2):c.1592-73A>G	RASGRP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277586	NM_001098671.2(RASGRP2):c.1592-230G>A	RASGRP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1209257	NM_001098671.2(RASGRP2):c.1592-231C>T	RASGRP2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1280627	NM_001098671.2(RASGRP2):c.1591+268C>T	RASGRP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1264749	NM_001098671.2(RASGRP2):c.1591+237G>A	RASGRP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1238902	NM_001098671.2(RASGRP2):c.1591+73G>A	RASGRP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228455	NM_001098671.2(RASGRP2):c.1591+37dup	RASGRP2	Duplication (intron variant)	not provided	GBenign
Select item 1203164	NM_001098671.2(RASGRP2):c.1591+37_1591+38dup	RASGRP2	Duplication (intron variant)	not provided	GLikely benign
Select item 1177728	NM_001098671.2(RASGRP2):c.1591+45_1591+48del	RASGRP2	Deletion (intron variant)	not provided	GBenign
Select item 1248539	NM_001098671.2(RASGRP2):c.1591+45T>G	RASGRP2	Single nucleotide variant (intron variant)	Platelet-type bleeding disorder 18 +1 more	GBenign
Select item 1247519	NM_001098671.2(RASGRP2):c.1413-222del	RASGRP2	Deletion (intron variant)	not provided	GBenign
Select item 2446127	NM_001098671.2(RASGRP2):c.1306C>T (p.Arg436Trp)	RASGRP2 (R291W +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1275299	NM_001098671.2(RASGRP2):c.1297-55A>C	RASGRP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1289252	NM_001098671.2(RASGRP2):c.1174-43T>C	RASGRP2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 403364	NM_001098671.2(RASGRP2):c.1173+12C>T	RASGRP2	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 1287361	NM_001098671.2(RASGRP2):c.1096-44T>C	RASGRP2	Single nucleotide variant (intron variant)	Platelet-type bleeding disorder 18 +1 more	GBenign
Select item 1273332	NM_001098671.2(RASGRP2):c.1096-92del	RASGRP2	Deletion (intron variant)	not provided	GBenign
Select item 1218730	NM_001098671.2(RASGRP2):c.1095+215G>A	RASGRP2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1245336	NM_001098671.2(RASGRP2):c.813+293C>T	RASGRP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1289771	NM_001098671.2(RASGRP2):c.813+204_813+205dup	RASGRP2	Duplication (intron variant)	not provided	GBenign
Select item 1209078	NM_001098671.2(RASGRP2):c.813+219del	RASGRP2	Deletion (intron variant)	not provided	GLikely benign
Select item 1231140	NM_001098671.2(RASGRP2):c.523-34A>G	RASGRP2	Single nucleotide variant (intron variant)	Platelet-type bleeding disorder 18 +1 more	GBenign
Select item 1174194	NM_001098671.2(RASGRP2):c.523-35C>T	RASGRP2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1253472	NM_001098671.2(RASGRP2):c.522+8C>T	RASGRP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1259868	NM_001098671.2(RASGRP2):c.372-45T>G	RASGRP2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1289148	NM_001098671.2(RASGRP2):c.372-164C>G	RASGRP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1219388	NM_001098671.2(RASGRP2):c.240-118C>G	RASGRP2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1214691	NM_001098671.2(RASGRP2):c.240-119G>A	RASGRP2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1239980	NM_001098671.2(RASGRP2):c.176+243G>A	RASGRP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1283513	NM_001098671.2(RASGRP2):c.176+44A>G	RASGRP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1265269	NM_001098671.2(RASGRP2):c.73+16G>A	RASGRP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 290751	NM_001098671.2(RASGRP2):c.17A>G (p.Asp6Gly)	LOC130005945, RASGRP2 (D6G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance

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Items: 38