ClinVar Miner

List of variants studied for Cornelia de Lange syndrome 5 by Invitae

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 168
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HGVS dbSNP gnomAD frequency
NM_018486.3(HDAC8):c.159G>A (p.Gln53=) rs11093377 0.23437
NM_018486.3(HDAC8):c.438-15C>T rs72630048 0.05226
NM_018486.3(HDAC8):c.57C>T (p.Ile19=) rs145362166 0.00120
NM_018486.3(HDAC8):c.351G>T (p.Gly117=) rs199969298 0.00041
NM_018486.3(HDAC8):c.933G>A (p.Thr311=) rs183108231 0.00030
NM_018486.3(HDAC8):c.295+13C>T rs138424378 0.00018
NM_018486.3(HDAC8):c.164+19A>T rs188536186 0.00016
NM_018486.3(HDAC8):c.1111+9C>T rs368139150 0.00015
NM_018486.3(HDAC8):c.491G>A (p.Arg164Gln) rs148688742 0.00015
NM_018486.3(HDAC8):c.20C>G (p.Pro7Arg) rs147689487 0.00009
NM_018486.3(HDAC8):c.384C>T (p.Asp128=) rs1250641302 0.00008
NM_018486.3(HDAC8):c.169G>A (p.Val57Ile) rs200737947 0.00007
NM_018486.3(HDAC8):c.213C>T (p.His71=) rs782349794 0.00006
NM_018486.3(HDAC8):c.629-14C>T rs1164078285 0.00005
NM_018486.3(HDAC8):c.639C>T (p.Asp213=) rs142540077 0.00005
NM_018486.3(HDAC8):c.522C>T (p.Tyr174=) rs146015223 0.00004
NM_018486.3(HDAC8):c.834C>T (p.Asn278=) rs781878660 0.00004
NM_018486.3(HDAC8):c.206C>A (p.Thr69Asn) rs373083907 0.00003
NM_018486.3(HDAC8):c.372A>G (p.Gln124=) rs141306915 0.00003
NM_018486.3(HDAC8):c.915C>G (p.Gly305=) rs782121649 0.00003
NM_018486.3(HDAC8):c.984C>T (p.Ser328=) rs782234700 0.00003
NM_018486.3(HDAC8):c.1047G>A (p.Thr349=) rs782747900 0.00002
NM_018486.3(HDAC8):c.1082G>A (p.Arg361Gln) rs781862582 0.00002
NM_018486.3(HDAC8):c.111+20A>C rs782224300 0.00002
NM_018486.3(HDAC8):c.1111+16C>T rs1039038766 0.00002
NM_018486.3(HDAC8):c.198G>T (p.Glu66Asp) rs373199509 0.00002
NM_018486.3(HDAC8):c.22G>A (p.Ala8Thr) rs200093133 0.00002
NM_018486.3(HDAC8):c.281T>C (p.Ile94Thr) rs1452290404 0.00002
NM_018486.3(HDAC8):c.318A>G (p.Glu106=) rs1388554395 0.00002
NM_018486.3(HDAC8):c.429T>C (p.His143=) rs374885534 0.00002
NM_018486.3(HDAC8):c.516T>A (p.Ile172=) rs61752447 0.00002
NM_018486.3(HDAC8):c.561C>T (p.Asp187=) rs931276707 0.00002
NM_018486.3(HDAC8):c.756C>T (p.Tyr252=) rs368682006 0.00002
NM_018486.3(HDAC8):c.1052G>C (p.Ser351Thr) rs782558250 0.00001
NM_018486.3(HDAC8):c.1111+10G>T rs373892213 0.00001
NM_018486.3(HDAC8):c.135T>C (p.Ile45=) rs1556159779 0.00001
NM_018486.3(HDAC8):c.342T>C (p.Ala114=) rs1324464792 0.00001
NM_018486.3(HDAC8):c.357G>A (p.Thr119=) rs782021788 0.00001
NM_018486.3(HDAC8):c.438-17A>G rs782753936 0.00001
NM_018486.3(HDAC8):c.835A>G (p.Met279Val) rs1555993170 0.00001
NM_018486.3(HDAC8):c.910+17G>T rs782676451 0.00001
NM_018486.3(HDAC8):c.932C>T (p.Thr311Met) rs397515417 0.00001
NC_000023.10:g.(?_71681834)_(71681968_?)del
NC_000023.10:g.(?_71681834)_(71715138_?)dup
NM_018486.3(HDAC8):c.1005+2T>C rs2148039062
NM_018486.3(HDAC8):c.1005+5G>A
NM_018486.3(HDAC8):c.1006-4A>G
NM_018486.3(HDAC8):c.1019A>C (p.Tyr340Ser) rs1555949010
NM_018486.3(HDAC8):c.104C>T (p.Pro35Leu) rs782296225
NM_018486.3(HDAC8):c.1053C>T (p.Ser351=)
NM_018486.3(HDAC8):c.1058G>A (p.Arg353Gln)
NM_018486.3(HDAC8):c.1066C>T (p.Arg356Cys)
NM_018486.3(HDAC8):c.1068C>A (p.Arg356=)
NM_018486.3(HDAC8):c.1085T>C (p.Ile362Thr)
NM_018486.3(HDAC8):c.1104C>T (p.Tyr368=)
NM_018486.3(HDAC8):c.1105A>G (p.Ile369Val)
NM_018486.3(HDAC8):c.111+10G>A
NM_018486.3(HDAC8):c.111+14G>C rs2147618204
NM_018486.3(HDAC8):c.111+20A>G
NM_018486.3(HDAC8):c.111+6G>A
NM_018486.3(HDAC8):c.111+7G>A rs2147618283
NM_018486.3(HDAC8):c.1111+13C>T
NM_018486.3(HDAC8):c.1111+17del
NM_018486.3(HDAC8):c.1111G>A (p.Gly371Arg)
NM_018486.3(HDAC8):c.1112-10_1112-9del
NM_018486.3(HDAC8):c.1112-11C>G
NM_018486.3(HDAC8):c.1112-2A>G rs1131690790
NM_018486.3(HDAC8):c.1112-5T>G
NM_018486.3(HDAC8):c.1117C>A (p.Leu373Met)
NM_018486.3(HDAC8):c.111G>C (p.Arg37=)
NM_018486.3(HDAC8):c.112-11G>T
NM_018486.3(HDAC8):c.112-14G>A
NM_018486.3(HDAC8):c.112-17del rs3830710
NM_018486.3(HDAC8):c.112-18_112-17dup
NM_018486.3(HDAC8):c.112-29dup rs3830710
NM_018486.3(HDAC8):c.1126G>A (p.Val376Met)
NM_018486.3(HDAC8):c.11C>T (p.Pro4Leu)
NM_018486.3(HDAC8):c.12G>A (p.Pro4=)
NM_018486.3(HDAC8):c.141A>T (p.Ala47=)
NM_018486.3(HDAC8):c.164+2dup rs2147614590
NM_018486.3(HDAC8):c.164+4del rs2147614572
NM_018486.3(HDAC8):c.164+9T>C
NM_018486.3(HDAC8):c.165-11G>A
NM_018486.3(HDAC8):c.166A>G (p.Ile56Val)
NM_018486.3(HDAC8):c.20C>A (p.Pro7Gln)
NM_018486.3(HDAC8):c.21G>C (p.Pro7=) rs1603246257
NM_018486.3(HDAC8):c.225T>C (p.Tyr75=)
NM_018486.3(HDAC8):c.23C>A (p.Ala8Glu)
NM_018486.3(HDAC8):c.291G>A (p.Gly97=)
NM_018486.3(HDAC8):c.295+2T>G rs2051897517
NM_018486.3(HDAC8):c.296-13T>C
NM_018486.3(HDAC8):c.296-6C>T
NM_018486.3(HDAC8):c.29G>A (p.Ser10Asn) rs2147618964
NM_018486.3(HDAC8):c.306C>T (p.Cys102=)
NM_018486.3(HDAC8):c.310G>A (p.Ala104Thr)
NM_018486.3(HDAC8):c.31G>C (p.Gly11Arg)
NM_018486.3(HDAC8):c.330C>T (p.Asp110=) rs2051865907
NM_018486.3(HDAC8):c.349G>A (p.Gly117Arg)
NM_018486.3(HDAC8):c.356C>T (p.Thr119Met) rs587779380
NM_018486.3(HDAC8):c.381T>A (p.Ile127=)
NM_018486.3(HDAC8):c.383A>T (p.Asp128Val)
NM_018486.3(HDAC8):c.437+13C>G
NM_018486.3(HDAC8):c.437+16_437+19del
NM_018486.3(HDAC8):c.43G>A (p.Val15Ile)
NM_018486.3(HDAC8):c.440A>T (p.Asp147Val)
NM_018486.3(HDAC8):c.474T>C (p.Ala158=)
NM_018486.3(HDAC8):c.477C>T (p.Val159=)
NM_018486.3(HDAC8):c.487T>C (p.Leu163=)
NM_018486.3(HDAC8):c.491G>T (p.Arg164Leu)
NM_018486.3(HDAC8):c.499C>T (p.Arg167Trp)
NM_018486.3(HDAC8):c.500G>A (p.Arg167Gln)
NM_018486.3(HDAC8):c.502A>G (p.Lys168Glu) rs2148144312
NM_018486.3(HDAC8):c.510G>A (p.Glu170=)
NM_018486.3(HDAC8):c.522C>G (p.Tyr174Ter) rs146015223
NM_018486.3(HDAC8):c.525G>A (p.Val175=)
NM_018486.3(HDAC8):c.550+7C>T
NM_018486.3(HDAC8):c.550+9T>G
NM_018486.3(HDAC8):c.551-17G>A
NM_018486.3(HDAC8):c.558A>G (p.Glu186=) rs2148131646
NM_018486.3(HDAC8):c.587T>C (p.Met196Thr)
NM_018486.3(HDAC8):c.590C>A (p.Thr197Asn)
NM_018486.3(HDAC8):c.603C>T (p.His201=)
NM_018486.3(HDAC8):c.615A>G (p.Pro205=)
NM_018486.3(HDAC8):c.628+20G>A rs2148131378
NM_018486.3(HDAC8):c.628+7G>A
NM_018486.3(HDAC8):c.629-11C>G
NM_018486.3(HDAC8):c.629-16C>T
NM_018486.3(HDAC8):c.629-18T>C
NM_018486.3(HDAC8):c.640G>A (p.Val214Met)
NM_018486.3(HDAC8):c.657A>C (p.Leu219=)
NM_018486.3(HDAC8):c.666A>G (p.Gly222=)
NM_018486.3(HDAC8):c.667C>T (p.Arg223Trp) rs1556007534
NM_018486.3(HDAC8):c.669G>T (p.Arg223=)
NM_018486.3(HDAC8):c.66C>G (p.Pro22=)
NM_018486.3(HDAC8):c.66C>T (p.Pro22=)
NM_018486.3(HDAC8):c.683A>T (p.Asn228Ile) rs2148124551
NM_018486.3(HDAC8):c.68A>C (p.Glu23Ala) rs2147618656
NM_018486.3(HDAC8):c.717A>T (p.Lys239Asn)
NM_018486.3(HDAC8):c.731G>A (p.Cys244Tyr)
NM_018486.3(HDAC8):c.737+16_737+28del
NM_018486.3(HDAC8):c.737+3A>G
NM_018486.3(HDAC8):c.737+6G>A
NM_018486.3(HDAC8):c.738-17del
NM_018486.3(HDAC8):c.738-2A>G
NM_018486.3(HDAC8):c.738-4A>G rs782294776
NM_018486.3(HDAC8):c.747G>A (p.Lys249=)
NM_018486.3(HDAC8):c.748del (p.Glu250fs)
NM_018486.3(HDAC8):c.767A>T (p.Asn256Ile)
NM_018486.3(HDAC8):c.787C>T (p.Gln263Ter) rs886041838
NM_018486.3(HDAC8):c.822G>A (p.Met274Ile)
NM_018486.3(HDAC8):c.828C>T (p.Ser276=)
NM_018486.3(HDAC8):c.831T>A (p.Phe277Leu)
NM_018486.3(HDAC8):c.889G>C (p.Ala297Pro)
NM_018486.3(HDAC8):c.894A>G (p.Thr298=)
NM_018486.3(HDAC8):c.898A>C (p.Ile300Leu)
NM_018486.3(HDAC8):c.910+20A>G rs2148045760
NM_018486.3(HDAC8):c.911-13T>C
NM_018486.3(HDAC8):c.911-5G>C
NM_018486.3(HDAC8):c.914G>A (p.Gly305Asp) rs2148039310
NM_018486.3(HDAC8):c.925G>T (p.Ala309Ser)
NM_018486.3(HDAC8):c.927C>T (p.Ala309=)
NM_018486.3(HDAC8):c.930C>T (p.Asn310=)
NM_018486.3(HDAC8):c.951C>T (p.Tyr317=) rs1555991936
NM_018486.3(HDAC8):c.956C>T (p.Thr319Ile) rs2148039184
NM_018486.3(HDAC8):c.957C>T (p.Thr319=) rs782144834
NM_018486.3(HDAC8):c.958G>A (p.Gly320Arg) rs398122909
NM_018486.3(HDAC8):c.976A>G (p.Thr326Ala)
NM_018486.3(HDAC8):c.9_17dup (p.Pro7_Ala8insGluGluPro)

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