ARHGEF16[gene] and "single gene"[properties] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 68

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2511286	NM_014448.4(ARHGEF16):c.11G>A (p.Arg4Gln)	ARHGEF16 (R4Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596239	NM_014448.4(ARHGEF16):c.52C>T (p.Arg18Cys)	ARHGEF16 (R18C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468251	NM_014448.4(ARHGEF16):c.53G>A (p.Arg18His)	ARHGEF16 (R18H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490442	NM_014448.4(ARHGEF16):c.85G>C (p.Gly29Arg)	ARHGEF16 (G29R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407953	NM_014448.4(ARHGEF16):c.116G>A (p.Arg39His)	ARHGEF16 (R39H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313163	NM_014448.4(ARHGEF16):c.125C>T (p.Pro42Leu)	ARHGEF16 (P42L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2456197	NM_014448.4(ARHGEF16):c.241C>G (p.Leu81Val)	ARHGEF16 (L81V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129101	NM_014448.4(ARHGEF16):c.296C>T (p.Ala99Val)	ARHGEF16 (A99V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129102	NM_014448.4(ARHGEF16):c.355C>T (p.Arg119Trp)	ARHGEF16 (R119W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555473	NM_014448.4(ARHGEF16):c.392C>A (p.Ser131Tyr)	ARHGEF16 (S131Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488570	NM_014448.4(ARHGEF16):c.424G>A (p.Gly142Arg)	ARHGEF16 (G142R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461798	NM_014448.4(ARHGEF16):c.463C>T (p.Arg155Trp)	ARHGEF16 (R155W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350406	NM_014448.4(ARHGEF16):c.464G>A (p.Arg155Gln)	ARHGEF16 (R155Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217395	NM_014448.4(ARHGEF16):c.569G>A (p.Arg190Gln)	ARHGEF16 (R190Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313153	NM_014448.4(ARHGEF16):c.575C>T (p.Pro192Leu)	ARHGEF16 (P192L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129103	NM_014448.4(ARHGEF16):c.709G>A (p.Glu237Lys)	ARHGEF16 (E237K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129105	NM_014448.4(ARHGEF16):c.719G>C (p.Ser240Thr)	ARHGEF16 (S240T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129106	NM_014448.4(ARHGEF16):c.764G>C (p.Ser255Thr)	ARHGEF16 (S255T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129107	NM_014448.4(ARHGEF16):c.769C>T (p.Arg257Trp)	ARHGEF16 (R257W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466787	NM_014448.4(ARHGEF16):c.770G>A (p.Arg257Gln)	ARHGEF16 (R257Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313174	NM_014448.4(ARHGEF16):c.799C>T (p.Pro267Ser)	ARHGEF16 (P267S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129108	NM_014448.4(ARHGEF16):c.811G>A (p.Glu271Lys)	ARHGEF16 (E271K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541304	NM_014448.4(ARHGEF16):c.842A>G (p.Glu281Gly)	ARHGEF16 (E281G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2561344	NM_014448.4(ARHGEF16):c.866T>C (p.Met289Thr)	ARHGEF16 (M289T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129109	NM_014448.4(ARHGEF16):c.871G>A (p.Glu291Lys)	ARHGEF16 (E291K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209146	NM_014448.4(ARHGEF16):c.884C>T (p.Ser295Leu)	ARHGEF16 (S295L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524233	NM_014448.4(ARHGEF16):c.893C>T (p.Ser298Phe)	ARHGEF16 (S298F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591140	NM_014448.4(ARHGEF16):c.910A>G (p.Ser304Gly)	ARHGEF16 (S304G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2318697	NM_014448.4(ARHGEF16):c.919G>A (p.Val307Met)	ARHGEF16 (V307M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394019	NM_014448.4(ARHGEF16):c.949C>T (p.Arg317Trp)	ARHGEF16 (R317W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129111	NM_014448.4(ARHGEF16):c.950G>T (p.Arg317Leu)	ARHGEF16 (R317L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 782901	NM_014448.4(ARHGEF16):c.954G>A (p.Ala318=)	ARHGEF16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3129089	NM_014448.4(ARHGEF16):c.1030G>C (p.Glu344Gln)	ARHGEF16 (E344Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469784	NM_014448.4(ARHGEF16):c.1045C>T (p.Arg349Trp)	ARHGEF16 (R349W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517748	NM_014448.4(ARHGEF16):c.1046G>A (p.Arg349Gln)	ARHGEF16 (R349Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349902	NM_014448.4(ARHGEF16):c.1084A>G (p.Ile362Val)	ARHGEF16 (I362V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594629	NM_014448.4(ARHGEF16):c.1099G>A (p.Ala367Thr)	ARHGEF16 (A367T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350887	NM_014448.4(ARHGEF16):c.1099G>T (p.Ala367Ser)	ARHGEF16 (A367S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129090	NM_014448.4(ARHGEF16):c.1102G>C (p.Glu368Gln)	ARHGEF16 (E368Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237951	NM_014448.4(ARHGEF16):c.1193T>C (p.Phe398Ser)	ARHGEF16 (F398S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129091	NM_014448.4(ARHGEF16):c.1196G>A (p.Arg399Gln)	ARHGEF16 (R399Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611072	NM_014448.4(ARHGEF16):c.1247T>C (p.Met416Thr)	ARHGEF16 (M416T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129092	NM_014448.4(ARHGEF16):c.1378A>C (p.Lys460Gln)	ARHGEF16 (K460Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129093	NM_014448.4(ARHGEF16):c.1390C>A (p.Gln464Lys)	ARHGEF16 (Q464K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129094	NM_014448.4(ARHGEF16):c.1432A>T (p.Met478Leu)	ARHGEF16 (M478L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374341	NM_014448.4(ARHGEF16):c.1435T>C (p.Tyr479His)	ARHGEF16 (Y479H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538689	NM_014448.4(ARHGEF16):c.1477C>T (p.Leu493Phe)	ARHGEF16 (L493F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387847	NM_014448.4(ARHGEF16):c.1496C>G (p.Ser499Cys)	ARHGEF16 (S499C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219391	NM_014448.4(ARHGEF16):c.1553G>A (p.Arg518Gln)	ARHGEF16 (R518Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312965	NM_014448.4(ARHGEF16):c.1597G>A (p.Asp533Asn)	ARHGEF16 (D533N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311646	NM_014448.4(ARHGEF16):c.1606G>T (p.Val536Phe)	ARHGEF16 (V536F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 780210	NM_014448.4(ARHGEF16):c.1640T>C (p.Met547Thr)	ARHGEF16 (M547T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3129096	NM_014448.4(ARHGEF16):c.1676T>A (p.Val559Glu)	ARHGEF16 (V559E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258895	NM_014448.4(ARHGEF16):c.1699C>A (p.Leu567Ile)	ARHGEF16 (L567I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129097	NM_014448.4(ARHGEF16):c.1703C>A (p.Pro568His)	ARHGEF16 (P568H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521952	NM_014448.4(ARHGEF16):c.1723C>T (p.Arg575Cys)	ARHGEF16 (R575C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3025292	NM_014448.4(ARHGEF16):c.1735G>A (p.Val579Met)	ARHGEF16 (V579M)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2318810	NM_014448.4(ARHGEF16):c.1751A>G (p.Gln584Arg)	ARHGEF16 (Q584R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366253	NM_014448.4(ARHGEF16):c.1783C>G (p.Gln595Glu)	ARHGEF16 (Q595E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129099	NM_014448.4(ARHGEF16):c.1790A>G (p.Gln597Arg)	ARHGEF16 (Q597R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221051	NM_014448.4(ARHGEF16):c.1838T>C (p.Val613Ala)	ARHGEF16 (V613A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528083	NM_014448.4(ARHGEF16):c.1877C>G (p.Ser626Cys)	ARHGEF16 (S626C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 780211	NM_014448.4(ARHGEF16):c.1888+9G>A	ARHGEF16	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2405949	NM_014448.4(ARHGEF16):c.1925C>T (p.Ala642Val)	ARHGEF16 (A642V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533138	NM_014448.4(ARHGEF16):c.2018A>T (p.Asp673Val)	ARHGEF16 (D673V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379685	NM_014448.4(ARHGEF16):c.2020G>A (p.Gly674Arg)	ARHGEF16 (G674R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397225	NM_014448.4(ARHGEF16):c.2054G>A (p.Arg685His)	ARHGEF16 (R685H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243076	NM_014448.4(ARHGEF16):c.2059A>G (p.Ile687Val)	ARHGEF16 (I687V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 68