"PreventionGenetics, part of Exact Sciences"[submitter] AND "ARFGAP2"[ - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3038983	NM_032389.6(ARFGAP2):c.*4G>A	ARFGAP2	Single nucleotide variant (3 prime UTR variant)	ARFGAP2-related condition	GBenign
Select item 3044117	NM_032389.6(ARFGAP2):c.1555G>A (p.Gly519Ser)	ARFGAP2 (G491S +2 more)	Single nucleotide variant (missense variant)	ARFGAP2-related condition	GLikely benign
Select item 3045169	NM_032389.6(ARFGAP2):c.1216C>T (p.Arg406Trp)	ARFGAP2 (R378W +2 more)	Single nucleotide variant (missense variant)	ARFGAP2-related condition	GBenign
Select item 3055789	NM_032389.6(ARFGAP2):c.1016G>A (p.Arg339His)	ARFGAP2 (R311H +2 more)	Single nucleotide variant (missense variant)	ARFGAP2-related condition	GBenign
Select item 3048473	NM_032389.6(ARFGAP2):c.1016G>T (p.Arg339Leu)	ARFGAP2 (R311L +2 more)	Single nucleotide variant (missense variant)	ARFGAP2-related condition	GLikely benign
Select item 3055614	NM_032389.6(ARFGAP2):c.809+6T>C	ARFGAP2	Single nucleotide variant (intron variant)	ARFGAP2-related condition	GBenign
Select item 3045780	NM_032389.6(ARFGAP2):c.798G>A (p.Ala266=)	ARFGAP2	Single nucleotide variant (synonymous variant)	ARFGAP2-related condition	GBenign
Select item 3037295	NM_032389.6(ARFGAP2):c.763C>T (p.Arg255Cys)	ARFGAP2 (R227C +2 more)	Single nucleotide variant (missense variant)	ARFGAP2-related condition	GBenign
Select item 3042168	NM_032389.6(ARFGAP2):c.674T>C (p.Leu225Pro)	ARFGAP2 (L197P +2 more)	Single nucleotide variant (missense variant)	ARFGAP2-related condition	GBenign
Select item 3050274	NM_032389.6(ARFGAP2):c.396+7G>A	ARFGAP2	Single nucleotide variant (intron variant)	ARFGAP2-related condition	GLikely benign
Select item 3033646	NM_032389.6(ARFGAP2):c.308A>G (p.Asn103Ser)	ARFGAP2 (N103S)	Single nucleotide variant (missense variant)	ARFGAP2-related condition	GLikely benign
Select item 3040603	NM_032389.6(ARFGAP2):c.265-10T>C	ARFGAP2	Single nucleotide variant (intron variant)	ARFGAP2-related condition	GLikely benign
Select item 3040288	NM_032389.6(ARFGAP2):c.191+6C>T	ARFGAP2	Single nucleotide variant (intron variant)	ARFGAP2-related condition	GLikely benign
Select item 3033986	NM_032389.6(ARFGAP2):c.-9G>A	ARFGAP2	Single nucleotide variant (5 prime UTR variant)	ARFGAP2-related condition	GLikely benign