ClinVar for Gene (Select 221935) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3316961	NM_152744.4(SDK1):c.4972A>T (p.Thr1658Ser)	SDK1 (T145S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316960	NM_152744.4(SDK1):c.1040T>A (p.Leu347His)	SDK1 (L347H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316959	NM_152744.4(SDK1):c.3281A>G (p.Tyr1094Cys)	SDK1 (Y1094C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316958	NM_152744.4(SDK1):c.2679G>A (p.Pro893=)	SDK1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3316957	NM_152744.4(SDK1):c.1220G>T (p.Gly407Val)	SDK1 (G407V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3316956	NM_152744.4(SDK1):c.751A>G (p.Thr251Ala)	SDK1 (T251A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3316955	NM_152744.4(SDK1):c.5483C>T (p.Ala1828Val)	SDK1 (A1828V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316954	NM_152744.4(SDK1):c.4217G>A (p.Gly1406Asp)	LOC105375131, SDK1 (G1406D)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3316953	NM_152744.4(SDK1):c.4616T>C (p.Val1539Ala)	SDK1 (V26A +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3316952	NM_152744.4(SDK1):c.3137C>A (p.Ala1046Asp)	SDK1 (A1046D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316950	NM_152744.4(SDK1):c.1431T>G (p.Asn477Lys)	SDK1 (N477K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316949	NM_152744.4(SDK1):c.2188G>T (p.Val730Leu)	SDK1 (V730L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316948	NM_152744.4(SDK1):c.6539C>T (p.Ala2180Val)	SDK1 (A2180V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3316947	NM_152744.4(SDK1):c.6171C>G (p.Asp2057Glu)	SDK1 (D2057E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316946	NM_152744.4(SDK1):c.5416A>G (p.Ser1806Gly)	SDK1 (S1806G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316945	NM_152744.4(SDK1):c.2767A>G (p.Ile923Val)	SDK1 (I923V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316944	NM_152744.4(SDK1):c.5871C>A (p.Ser1957Arg)	SDK1 (S1957R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316943	NM_152744.4(SDK1):c.2209C>T (p.Arg737Cys)	SDK1 (R737C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316942	NM_152744.4(SDK1):c.4331C>T (p.Pro1444Leu)	SDK1 (P1444L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3316941	NM_152744.4(SDK1):c.4741C>A (p.Pro1581Thr)	SDK1 (P1581T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316939	NM_152744.4(SDK1):c.1627G>A (p.Val543Ile)	LOC126859931, SDK1 (V543I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316938	NM_152744.4(SDK1):c.1177G>A (p.Glu393Lys)	SDK1 (E393K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316937	NM_152744.4(SDK1):c.6563C>T (p.Thr2188Met)	SDK1 (T2188M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3316936	NM_152744.4(SDK1):c.2807C>T (p.Thr936Met)	SDK1 (T936M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316935	NM_152744.4(SDK1):c.4321G>A (p.Asp1441Asn)	SDK1 (D1441N)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3316934	NM_152744.4(SDK1):c.1035A>C (p.Arg345Ser)	SDK1 (R345S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316933	NM_152744.4(SDK1):c.2842G>A (p.Val948Ile)	SDK1 (V948I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316932	NM_152744.4(SDK1):c.2539G>T (p.Ala847Ser)	SDK1 (A847S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316931	NM_152744.4(SDK1):c.1592T>C (p.Met531Thr)	LOC126859931, SDK1 (M531T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316930	NM_152744.4(SDK1):c.3730G>A (p.Glu1244Lys)	SDK1 (E1244K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316928	NM_152744.4(SDK1):c.714A>T (p.Ile238=)	SDK1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3316927	NM_152744.4(SDK1):c.5443T>C (p.Ser1815Pro)	SDK1 (S302P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316926	NM_152744.4(SDK1):c.3062A>T (p.His1021Leu)	SDK1 (H1021L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316925	NM_152744.4(SDK1):c.1252C>T (p.Leu418Phe)	SDK1 (L418F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316924	NM_152744.4(SDK1):c.2441C>G (p.Pro814Arg)	SDK1 (P814R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316923	NM_152744.4(SDK1):c.4486C>T (p.Arg1496Trp)	SDK1 (R1496W)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3316922	NM_152744.4(SDK1):c.5866C>T (p.Arg1956Trp)	SDK1 (R1956W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158996	NM_152744.4(SDK1):c.8G>C (p.Arg3Pro)	SDK1, SDK1-AS1 (R3P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158994	NM_152744.4(SDK1):c.781G>A (p.Val261Met)	SDK1 (V261M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158993	NM_152744.4(SDK1):c.772G>A (p.Ala258Thr)	SDK1 (A258T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158992	NM_152744.4(SDK1):c.686G>T (p.Gly229Val)	SDK1 (G229V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158991	NM_152744.4(SDK1):c.671C>T (p.Thr224Ile)	SDK1 (T224I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158990	NM_152744.4(SDK1):c.6511G>A (p.Glu2171Lys)	SDK1 (E2171K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3158989	NM_152744.4(SDK1):c.6487C>T (p.Arg2163Cys)	SDK1 (R650C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158988	NM_152744.4(SDK1):c.6460A>C (p.Asn2154His)	SDK1 (N641H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158987	NM_152744.4(SDK1):c.6212T>G (p.Leu2071Arg)	SDK1 (L2071R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158986	NM_152744.4(SDK1):c.616C>A (p.Arg206Ser)	SDK1 (R206S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158985	NM_152744.4(SDK1):c.6058A>C (p.Ile2020Leu)	SDK1 (I507L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158984	NM_152744.4(SDK1):c.5981C>T (p.Thr1994Met)	SDK1 (T481M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158983	NM_152744.4(SDK1):c.5962G>C (p.Glu1988Gln)	SDK1 (E1988Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158982	NM_152744.4(SDK1):c.5749G>C (p.Glu1917Gln)	SDK1 (E1917Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158981	NM_152744.4(SDK1):c.5708C>T (p.Pro1903Leu)	SDK1 (P390L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158980	NM_152744.4(SDK1):c.5684C>T (p.Thr1895Ile)	SDK1 (T1895I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158979	NM_152744.4(SDK1):c.5665G>C (p.Glu1889Gln)	SDK1 (E376Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158978	NM_152744.4(SDK1):c.5618T>A (p.Val1873Glu)	SDK1 (V1873E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158977	NM_152744.4(SDK1):c.5404C>T (p.Pro1802Ser)	SDK1 (P1802S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158976	NM_152744.4(SDK1):c.5387G>A (p.Arg1796His)	SDK1 (R1796H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158975	NM_152744.4(SDK1):c.5347G>A (p.Ala1783Thr)	SDK1 (A270T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158974	NM_152744.4(SDK1):c.529G>A (p.Ala177Thr)	SDK1 (A177T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158973	NM_152744.4(SDK1):c.5092G>A (p.Glu1698Lys)	SDK1 (E1698K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158972	NM_152744.4(SDK1):c.5074G>A (p.Val1692Met)	SDK1 (V1692M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158971	NM_152744.4(SDK1):c.503G>A (p.Arg168His)	SDK1 (R168H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158970	NM_152744.4(SDK1):c.4994C>T (p.Thr1665Ile)	SDK1 (T152I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158969	NM_152744.4(SDK1):c.4979C>T (p.Thr1660Met)	SDK1 (T147M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158968	NM_152744.4(SDK1):c.4762A>G (p.Thr1588Ala)	SDK1 (T1588A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158967	NM_152744.4(SDK1):c.4646A>G (p.Tyr1549Cys)	SDK1 (Y36C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158966	NM_152744.4(SDK1):c.4580A>C (p.Tyr1527Ser)	SDK1 (Y1527S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158965	NM_152744.4(SDK1):c.4558C>T (p.Pro1520Ser)	SDK1 (P1520S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158964	NM_152744.4(SDK1):c.4478G>A (p.Arg1493His)	SDK1 (R1493H)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3158962	NM_152744.4(SDK1):c.4162G>A (p.Glu1388Lys)	LOC105375131, SDK1 (E1388K)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3158961	NM_152744.4(SDK1):c.4130C>T (p.Ala1377Val)	LOC105375131, SDK1 (A1377V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3158960	NM_152744.4(SDK1):c.4125C>T (p.Asp1375=)	LOC105375131, SDK1	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GLikely benign
Select item 3158959	NM_152744.4(SDK1):c.404A>T (p.Glu135Val)	SDK1 (E135V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158958	NM_152744.4(SDK1):c.3712A>C (p.Thr1238Pro)	SDK1 (T1238P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158957	NM_152744.4(SDK1):c.3685G>A (p.Val1229Ile)	SDK1 (V1229I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3158956	NM_152744.4(SDK1):c.3649C>T (p.Arg1217Cys)	SDK1 (R1217C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158955	NM_152744.4(SDK1):c.3467C>T (p.Pro1156Leu)	SDK1 (P1156L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158954	NM_152744.4(SDK1):c.3411C>A (p.Asn1137Lys)	SDK1 (N1137K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158953	NM_152744.4(SDK1):c.3278G>T (p.Gly1093Val)	SDK1 (G1093V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158952	NM_152744.4(SDK1):c.3262C>T (p.Leu1088Phe)	SDK1 (L1088F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158951	NM_152744.4(SDK1):c.3232A>C (p.Ile1078Leu)	SDK1 (I1078L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158950	NM_152744.4(SDK1):c.3163C>G (p.Leu1055Val)	SDK1 (L1055V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158949	NM_152744.4(SDK1):c.3019A>C (p.Ile1007Leu)	SDK1 (I1007L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158948	NM_152744.4(SDK1):c.2779T>C (p.Phe927Leu)	SDK1 (F927L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158947	NM_152744.4(SDK1):c.2764A>G (p.Thr922Ala)	SDK1 (T922A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158946	NM_152744.4(SDK1):c.2654C>T (p.Thr885Ile)	SDK1 (T885I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158945	NM_152744.4(SDK1):c.2626G>A (p.Val876Met)	SDK1 (V876M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158944	NM_152744.4(SDK1):c.254C>T (p.Ala85Val)	SDK1, SDK1-AS1 (A85V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158943	NM_152744.4(SDK1):c.2404C>T (p.Arg802Cys)	SDK1 (R802C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158942	NM_152744.4(SDK1):c.225G>C (p.Lys75Asn)	SDK1, SDK1-AS1 (K75N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158941	NM_152744.4(SDK1):c.2155T>C (p.Ser719Pro)	SDK1 (S719P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158940	NM_152744.4(SDK1):c.2075G>A (p.Arg692Gln)	SDK1 (R692Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158939	NM_152744.4(SDK1):c.2074C>T (p.Arg692Trp)	SDK1 (R692W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158938	NM_152744.4(SDK1):c.2019C>A (p.Asn673Lys)	SDK1 (N673K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158937	NM_152744.4(SDK1):c.1844C>T (p.Ala615Val)	SDK1 (A615V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3158936	NM_152744.4(SDK1):c.1729G>A (p.Val577Ile)	SDK1 (V577I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158934	NM_152744.4(SDK1):c.1387G>A (p.Glu463Lys)	SDK1 (E463K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158933	NM_152744.4(SDK1):c.1351G>C (p.Glu451Gln)	SDK1 (E451Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158932	NM_152744.4(SDK1):c.1337A>C (p.Gln446Pro)	SDK1 (Q446P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158931	NM_152744.4(SDK1):c.1192G>C (p.Ala398Pro)	SDK1 (A398P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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