ClinVar Miner

List of variants in gene ARHGEF16 reported as uncertain significance by Ambry Genetics

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Gene type:
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Total variants: 83
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HGVS dbSNP gnomAD frequency
NM_014448.4(ARHGEF16):c.355C>T (p.Arg119Trp) rs541615611 0.00060
NM_014448.4(ARHGEF16):c.1099G>T (p.Ala367Ser) rs147324873 0.00053
NM_014448.4(ARHGEF16):c.241C>G (p.Leu81Val) rs556522799 0.00034
NM_014448.4(ARHGEF16):c.1435T>C (p.Tyr479His) rs201584820 0.00023
NM_014448.4(ARHGEF16):c.1084A>G (p.Ile362Val) rs141425462 0.00012
NM_014448.4(ARHGEF16):c.1925C>T (p.Ala642Val) rs180731913 0.00011
NM_014448.4(ARHGEF16):c.52C>T (p.Arg18Cys) rs942176075 0.00011
NM_014448.4(ARHGEF16):c.919G>A (p.Val307Met) rs138148473 0.00011
NM_014448.4(ARHGEF16):c.1751A>G (p.Gln584Arg) rs201282947 0.00010
NM_014448.4(ARHGEF16):c.424G>A (p.Gly142Arg) rs777253808 0.00010
NM_014448.4(ARHGEF16):c.842A>G (p.Glu281Gly) rs760221421 0.00009
NM_014448.4(ARHGEF16):c.949C>T (p.Arg317Trp) rs140093908 0.00009
NM_014448.4(ARHGEF16):c.2020G>A (p.Gly674Arg) rs186738663 0.00008
NM_014448.4(ARHGEF16):c.569G>A (p.Arg190Gln) rs187419731 0.00008
NM_014448.4(ARHGEF16):c.719G>C (p.Ser240Thr) rs775696698 0.00008
NM_014448.4(ARHGEF16):c.1045C>T (p.Arg349Trp) rs1428821464 0.00007
NM_014448.4(ARHGEF16):c.1477C>T (p.Leu493Phe) rs777092820 0.00007
NM_014448.4(ARHGEF16):c.11G>A (p.Arg4Gln) rs1045272383 0.00005
NM_014448.4(ARHGEF16):c.709G>A (p.Glu237Lys) rs924346370 0.00005
NM_014448.4(ARHGEF16):c.116G>A (p.Arg39His) rs751723822 0.00004
NM_014448.4(ARHGEF16):c.770G>A (p.Arg257Gln) rs1012460755 0.00003
NM_014448.4(ARHGEF16):c.1838T>C (p.Val613Ala) rs1164678933 0.00002
NM_014448.4(ARHGEF16):c.2054G>A (p.Arg685His) rs534395921 0.00002
NM_014448.4(ARHGEF16):c.1553G>A (p.Arg518Gln) rs747219652 0.00001
NM_014448.4(ARHGEF16):c.1597G>A (p.Asp533Asn) rs373186673 0.00001
NM_014448.4(ARHGEF16):c.1606G>T (p.Val536Phe) rs567294084 0.00001
NM_014448.4(ARHGEF16):c.1790A>G (p.Gln597Arg) rs1639963488 0.00001
NM_014448.4(ARHGEF16):c.1877C>G (p.Ser626Cys) rs2521742875 0.00001
NM_014448.4(ARHGEF16):c.2059A>G (p.Ile687Val) rs1385359729 0.00001
NM_014448.4(ARHGEF16):c.463C>T (p.Arg155Trp) rs1453195678 0.00001
NM_014448.4(ARHGEF16):c.764G>C (p.Ser255Thr) rs894088724 0.00001
NM_014448.4(ARHGEF16):c.769C>T (p.Arg257Trp) rs1462238873 0.00001
NM_014448.4(ARHGEF16):c.811G>A (p.Glu271Lys) rs1267008760 0.00001
NM_014448.4(ARHGEF16):c.85G>C (p.Gly29Arg) rs547639596 0.00001
NM_014448.4(ARHGEF16):c.866T>C (p.Met289Thr) rs776340254 0.00001
NM_014448.4(ARHGEF16):c.884C>T (p.Ser295Leu) rs199607431 0.00001
NM_014448.4(ARHGEF16):c.893C>T (p.Ser298Phe) rs1639643574 0.00001
NM_014448.4(ARHGEF16):c.1030G>C (p.Glu344Gln) rs776606730
NM_014448.4(ARHGEF16):c.1046G>A (p.Arg349Gln) rs536938385
NM_014448.4(ARHGEF16):c.1093G>A (p.Glu365Lys)
NM_014448.4(ARHGEF16):c.1099G>A (p.Ala367Thr) rs147324873
NM_014448.4(ARHGEF16):c.1102G>C (p.Glu368Gln) rs2521695631
NM_014448.4(ARHGEF16):c.1165C>A (p.Gln389Lys)
NM_014448.4(ARHGEF16):c.1193T>C (p.Phe398Ser) rs774950266
NM_014448.4(ARHGEF16):c.1196G>A (p.Arg399Gln) rs1209365753
NM_014448.4(ARHGEF16):c.1212G>C (p.Glu404Asp)
NM_014448.4(ARHGEF16):c.1247T>C (p.Met416Thr) rs1639795771
NM_014448.4(ARHGEF16):c.1378A>C (p.Lys460Gln) rs750937556
NM_014448.4(ARHGEF16):c.1390C>A (p.Gln464Lys) rs2521713543
NM_014448.4(ARHGEF16):c.1432A>T (p.Met478Leu) rs2521714313
NM_014448.4(ARHGEF16):c.1496C>G (p.Ser499Cys) rs756061209
NM_014448.4(ARHGEF16):c.1513C>T (p.Arg505Cys)
NM_014448.4(ARHGEF16):c.1676T>A (p.Val559Glu) rs201085717
NM_014448.4(ARHGEF16):c.1676T>C (p.Val559Ala)
NM_014448.4(ARHGEF16):c.1699C>A (p.Leu567Ile) rs1489788224
NM_014448.4(ARHGEF16):c.1703C>A (p.Pro568His) rs749083124
NM_014448.4(ARHGEF16):c.1723C>T (p.Arg575Cys) rs143167978
NM_014448.4(ARHGEF16):c.1774G>C (p.Glu592Gln)
NM_014448.4(ARHGEF16):c.1783C>G (p.Gln595Glu) rs759695331
NM_014448.4(ARHGEF16):c.1792C>T (p.Leu598Phe)
NM_014448.4(ARHGEF16):c.181C>T (p.Arg61Trp)
NM_014448.4(ARHGEF16):c.1829G>A (p.Arg610Gln)
NM_014448.4(ARHGEF16):c.1841C>T (p.Ala614Val)
NM_014448.4(ARHGEF16):c.1843C>T (p.Leu615Phe)
NM_014448.4(ARHGEF16):c.2018A>T (p.Asp673Val) rs1640025714
NM_014448.4(ARHGEF16):c.2053C>G (p.Arg685Gly)
NM_014448.4(ARHGEF16):c.208C>T (p.Pro70Ser)
NM_014448.4(ARHGEF16):c.2111G>A (p.Arg704Gln)
NM_014448.4(ARHGEF16):c.227A>C (p.Glu76Ala)
NM_014448.4(ARHGEF16):c.296C>T (p.Ala99Val) rs1639453206
NM_014448.4(ARHGEF16):c.392C>A (p.Ser131Tyr) rs550096684
NM_014448.4(ARHGEF16):c.422C>T (p.Pro141Leu)
NM_014448.4(ARHGEF16):c.444C>G (p.Asn148Lys)
NM_014448.4(ARHGEF16):c.464G>A (p.Arg155Gln) rs1031473979
NM_014448.4(ARHGEF16):c.53G>A (p.Arg18His) rs1038152955
NM_014448.4(ARHGEF16):c.575C>T (p.Pro192Leu)
NM_014448.4(ARHGEF16):c.658C>G (p.Gln220Glu)
NM_014448.4(ARHGEF16):c.71G>A (p.Arg24Gln)
NM_014448.4(ARHGEF16):c.799C>T (p.Pro267Ser)
NM_014448.4(ARHGEF16):c.82G>A (p.Gly28Arg)
NM_014448.4(ARHGEF16):c.871G>A (p.Glu291Lys) rs1639641960
NM_014448.4(ARHGEF16):c.950G>T (p.Arg317Leu) rs1048897523
NM_014448.4(ARHGEF16):c.979C>T (p.His327Tyr)

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