ClinVar Miner

List of variants in gene HOMER2 reported as likely benign for not provided

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Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_004839.4(HOMER2):c.388-180_388-179insGTTTA rs397746891 0.00774
NM_004839.4(HOMER2):c.762+124G>A rs7183412 0.00706
NM_004839.4(HOMER2):c.764A>G (p.Glu255Gly) rs79448007 0.00523
NM_004839.4(HOMER2):c.*172C>T rs79958469 0.00436
NM_004839.4(HOMER2):c.363C>T (p.Ile121=) rs11629943 0.00181
NM_004839.4(HOMER2):c.638G>A (p.Arg213Gln) rs199601429 0.00131
NM_004839.4(HOMER2):c.643C>T (p.Arg215Cys) rs199835958 0.00103
NM_004839.4(HOMER2):c.234C>T (p.Ala78=) rs200280749 0.00101
NM_004839.4(HOMER2):c.762+35G>A rs201518346 0.00078
NM_004839.4(HOMER2):c.762+27C>G rs375281424 0.00073
NM_004839.4(HOMER2):c.387+41del rs3216752 0.00067
NM_004839.4(HOMER2):c.358A>G (p.Lys120Glu) rs76145073 0.00027
NM_004839.4(HOMER2):c.181A>G (p.Ile61Val) rs201330165 0.00024
NM_004839.4(HOMER2):c.93G>A (p.Ala31=) rs77711643 0.00024
NM_004839.4(HOMER2):c.539G>A (p.Arg180Gln) rs369968997 0.00021
NM_004839.4(HOMER2):c.89A>G (p.Gln30Arg) rs189123186 0.00011
NM_004839.4(HOMER2):c.295-15A>G rs373960234 0.00009
NM_004839.4(HOMER2):c.793A>G (p.Ile265Val) rs373795200 0.00008
NM_004839.4(HOMER2):c.388-17C>G rs372021638 0.00007
NM_004839.4(HOMER2):c.1023C>G (p.Thr341=) rs375487342 0.00006
NM_004839.4(HOMER2):c.402C>T (p.Asn134=) rs760018246 0.00005
NM_004839.4(HOMER2):c.495-19G>A rs375887599 0.00005
NM_004839.4(HOMER2):c.969C>T (p.Asp323=) rs758410534 0.00004
NM_004839.4(HOMER2):c.153C>T (p.Asp51=) rs761530407 0.00003
NM_004839.4(HOMER2):c.29G>A (p.Arg10Gln) rs560032927 0.00001
NM_004839.4(HOMER2):c.33G>A (p.Ala11=) rs201522712 0.00001
NM_004839.4(HOMER2):c.495-13C>A rs376932468 0.00001
NM_004839.4(HOMER2):c.525G>A (p.Glu175=) rs763908871 0.00001
NM_004839.4(HOMER2):c.707C>T (p.Thr236Met) rs532034212 0.00001
NM_004839.4(HOMER2):c.1023C>T (p.Thr341=)
NM_004839.4(HOMER2):c.163-12G>T
NM_004839.4(HOMER2):c.163-8T>G
NM_004839.4(HOMER2):c.214C>A (p.Gln72Lys)
NM_004839.4(HOMER2):c.294+19C>T
NM_004839.4(HOMER2):c.335T>C (p.Ile112Thr)
NM_004839.4(HOMER2):c.351G>A (p.Thr117=)
NM_004839.4(HOMER2):c.388-16C>T
NM_004839.4(HOMER2):c.432C>T (p.Ala144=)
NM_004839.4(HOMER2):c.495-14T>A rs199975432
NM_004839.4(HOMER2):c.495-15G>A
NM_004839.4(HOMER2):c.495-15_495-14delinsTC rs2151609262
NM_004839.4(HOMER2):c.495-16C>T
NM_004839.4(HOMER2):c.497C>T (p.Ala166Val)
NM_004839.4(HOMER2):c.499G>A (p.Ala167Thr)
NM_004839.4(HOMER2):c.5+15G>A
NM_004839.4(HOMER2):c.504C>T (p.Asn168=)
NM_004839.4(HOMER2):c.522C>T (p.Ile174=)
NM_004839.4(HOMER2):c.591G>A (p.Val197=)
NM_004839.4(HOMER2):c.6-19G>A
NM_004839.4(HOMER2):c.6-8T>C
NM_004839.4(HOMER2):c.6-9_6-8del
NM_004839.4(HOMER2):c.651+14A>G
NM_004839.4(HOMER2):c.651+19G>C rs1450320866
NM_004839.4(HOMER2):c.652-18G>A
NM_004839.4(HOMER2):c.66G>A (p.Lys22=)
NM_004839.4(HOMER2):c.711G>A (p.Gln237=)
NM_004839.4(HOMER2):c.727G>A (p.Glu243Lys)
NM_004839.4(HOMER2):c.762+17C>T
NM_004839.4(HOMER2):c.762+2T>A
NM_004839.4(HOMER2):c.795C>T (p.Ile265=)
NM_004839.4(HOMER2):c.844-43C>A rs144542599
NM_004839.4(HOMER2):c.915A>G (p.Lys305=)
NM_004839.4(HOMER2):c.967G>A (p.Asp323Asn)
NM_004839.4(HOMER2):c.974A>G (p.Lys325Arg)

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