ClinVar Miner

List of variants in gene CHUK reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 98
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HGVS dbSNP gnomAD frequency
NM_001278.5(CHUK):c.1341A>G (p.Gly447=) rs34458357 0.00369
NM_001278.5(CHUK):c.919A>G (p.Ile307Val) rs141877809 0.00201
NM_001278.5(CHUK):c.933+8T>G rs200843857 0.00134
NM_001278.5(CHUK):c.376A>T (p.Ser126Cys) rs34427437 0.00082
NM_001278.5(CHUK):c.2198A>G (p.Asn733Ser) rs151240721 0.00060
NM_001278.5(CHUK):c.339T>C (p.Cys113=) rs148215833 0.00056
NM_001278.5(CHUK):c.1679+10C>T rs369271354 0.00051
NM_001278.5(CHUK):c.1059A>C (p.Glu353Asp) rs373772425 0.00011
NM_001278.5(CHUK):c.1776C>T (p.His592=) rs149364994 0.00011
NM_001278.5(CHUK):c.1719C>T (p.His573=) rs371533046 0.00010
NM_001278.5(CHUK):c.1164T>C (p.Asp388=) rs201199767 0.00009
NM_001278.5(CHUK):c.1512A>C (p.Ser504=) rs200461553 0.00008
NM_001278.5(CHUK):c.264T>C (p.His88=) rs763477360 0.00006
NM_001278.5(CHUK):c.1269G>C (p.Leu423=) rs377555336 0.00004
NM_001278.5(CHUK):c.1570-14T>G rs772743813 0.00004
NM_001278.5(CHUK):c.1679+12C>T rs377222658 0.00004
NM_001278.5(CHUK):c.1680-18G>A rs374815060 0.00003
NM_001278.5(CHUK):c.106-10A>C rs201130944 0.00002
NM_001278.5(CHUK):c.1679+18T>G rs755747637 0.00002
NM_001278.5(CHUK):c.315+17G>C rs532237334 0.00002
NM_001278.5(CHUK):c.1170T>C (p.Ser390=) rs373844054 0.00001
NM_001278.5(CHUK):c.1410C>A (p.Ile470=) rs769565796 0.00001
NM_001278.5(CHUK):c.1530A>C (p.Ala510=) rs752542336 0.00001
NM_001278.5(CHUK):c.1569+18A>G rs1031792708 0.00001
NM_001278.5(CHUK):c.1729+16C>T rs751035306 0.00001
NM_001278.5(CHUK):c.2175T>C (p.His725=) rs1448076965 0.00001
NM_001278.5(CHUK):c.567C>T (p.Ala189=) rs748462224 0.00001
NM_001278.5(CHUK):c.582G>A (p.Glu194=) rs759472948 0.00001
NM_001278.5(CHUK):c.765T>C (p.Ser255=) rs1845918946 0.00001
NM_001278.5(CHUK):c.1028G>A (p.Arg343His)
NM_001278.5(CHUK):c.1053T>C (p.Ser351=)
NM_001278.5(CHUK):c.106-7T>G
NM_001278.5(CHUK):c.1128+16A>G
NM_001278.5(CHUK):c.1231+10G>T
NM_001278.5(CHUK):c.1231+12C>A
NM_001278.5(CHUK):c.1231+18A>G rs2134225431
NM_001278.5(CHUK):c.1232-10T>C
NM_001278.5(CHUK):c.1232-20T>C
NM_001278.5(CHUK):c.1267C>T (p.Leu423=)
NM_001278.5(CHUK):c.1302G>A (p.Val434=)
NM_001278.5(CHUK):c.1314A>G (p.Lys438=)
NM_001278.5(CHUK):c.132G>A (p.Lys44=)
NM_001278.5(CHUK):c.1355+15T>C
NM_001278.5(CHUK):c.1356-9G>A
NM_001278.5(CHUK):c.1401C>T (p.Asn467=)
NM_001278.5(CHUK):c.1425A>G (p.Gln475=)
NM_001278.5(CHUK):c.1443G>A (p.Glu481=)
NM_001278.5(CHUK):c.1485C>T (p.Ser495=) rs374991603
NM_001278.5(CHUK):c.1508-5T>C
NM_001278.5(CHUK):c.1569+14C>T
NM_001278.5(CHUK):c.1569+15G>A
NM_001278.5(CHUK):c.1680-19C>T
NM_001278.5(CHUK):c.1818T>C (p.Gly606=)
NM_001278.5(CHUK):c.1826+11T>G
NM_001278.5(CHUK):c.1827-14T>C
NM_001278.5(CHUK):c.1831T>C (p.Leu611=) rs2134207207
NM_001278.5(CHUK):c.1896C>T (p.Ile632=)
NM_001278.5(CHUK):c.1936A>C (p.Arg646=)
NM_001278.5(CHUK):c.1974+8A>G
NM_001278.5(CHUK):c.200+9A>G
NM_001278.5(CHUK):c.2001A>G (p.Val667=)
NM_001278.5(CHUK):c.201-5A>G
NM_001278.5(CHUK):c.201-8C>T
NM_001278.5(CHUK):c.2055G>A (p.Pro685=)
NM_001278.5(CHUK):c.2080C>T (p.Leu694=)
NM_001278.5(CHUK):c.2108+14G>C
NM_001278.5(CHUK):c.2108+18C>T
NM_001278.5(CHUK):c.2109-14C>T
NM_001278.5(CHUK):c.2109-17G>T
NM_001278.5(CHUK):c.2140T>C (p.Leu714=) rs1845183136
NM_001278.5(CHUK):c.2209-15C>T
NM_001278.5(CHUK):c.2209-8G>C
NM_001278.5(CHUK):c.277C>T (p.Leu93=)
NM_001278.5(CHUK):c.381T>C (p.Asp127=)
NM_001278.5(CHUK):c.385+10A>C
NM_001278.5(CHUK):c.385+14T>G
NM_001278.5(CHUK):c.386-18A>G
NM_001278.5(CHUK):c.450A>C (p.Ile150=)
NM_001278.5(CHUK):c.480A>T (p.Ile160=)
NM_001278.5(CHUK):c.543T>C (p.Phe181=)
NM_001278.5(CHUK):c.564+12T>C
NM_001278.5(CHUK):c.564+13T>C
NM_001278.5(CHUK):c.565-14T>C rs527912052
NM_001278.5(CHUK):c.636T>C (p.Phe212=)
NM_001278.5(CHUK):c.689+9T>C
NM_001278.5(CHUK):c.717A>G (p.Pro239=)
NM_001278.5(CHUK):c.759G>A (p.Arg253=)
NM_001278.5(CHUK):c.777T>C (p.Pro259=)
NM_001278.5(CHUK):c.797+15G>A
NM_001278.5(CHUK):c.798-13G>A
NM_001278.5(CHUK):c.798-16T>G
NM_001278.5(CHUK):c.798-19T>C rs747375856
NM_001278.5(CHUK):c.798-4C>G
NM_001278.5(CHUK):c.843T>C (p.Asn281=)
NM_001278.5(CHUK):c.876C>T (p.Asp292=)
NM_001278.5(CHUK):c.883T>C (p.Leu295=) rs1285995341
NM_001278.5(CHUK):c.921T>A (p.Ile307=)
NM_001278.5(CHUK):c.934-14T>C

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