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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 36

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HGVS	dbSNP	gnomAD frequency
NM_001918.5(DBT):c.1281+31T>G	rs115696850	0.03046
NM_001918.5(DBT):c.1281+273A>G	rs116767333	0.02690
NM_001918.5(DBT):c.251+105A>T	rs151132097	0.01958
NM_001918.5(DBT):c.1018-157C>A	rs114413482	0.01266
NM_001918.5(DBT):c.*5919A>G	rs115442245	0.01236
NM_001918.5(DBT):c.1281+6T>G	rs140115881	0.01022
NM_001918.5(DBT):c.1018-743G>A	rs74321712	0.01005
NM_001918.5(DBT):c.175+312T>C	rs79295393	0.00969
NM_001918.5(DBT):c.51+185A>G	rs3131838	0.00961
NC_000001.11:g.100249909G>C	rs41287254	0.00886
NM_001918.5(DBT):c.1281+248G>A	rs146214677	0.00873
NM_001918.5(DBT):c.724T>C (p.Ser242Pro)	rs146249007	0.00864
NM_001918.5(DBT):c.*8552A>T	rs543411196	0.00862
NM_001918.5(DBT):c.1018-464A>G	rs76174317	0.00861
NM_001918.5(DBT):c.555+96A>G	rs149618173	0.00612
NM_001918.5(DBT):c.51+202G>C	rs79737399	0.00539
NM_001918.5(DBT):c.*389A>G	rs142589460	0.00374
NM_001918.5(DBT):c.76T>C (p.Cys26Arg)	rs145674833	0.00302
NM_001918.5(DBT):c.1418A>G (p.Asn473Ser)	rs75525811	0.00196
NM_001918.5(DBT):c.753C>T (p.Asp251=)	rs79292123	0.00179
NM_001918.5(DBT):c.175+37G>A	rs76902654	0.00154
NM_001918.5(DBT):c.327C>T (p.Thr109=)	rs138796800	0.00078
NM_001918.5(DBT):c.37A>G (p.Asn13Asp)	rs140308307	0.00024
NM_001918.5(DBT):c.1210-8A>T	rs535837017	0.00023
NM_001918.5(DBT):c.556-7T>C	rs755448648	0.00009
NM_001918.5(DBT):c.9A>G (p.Ala3=)	rs772869478	0.00006
NM_001918.5(DBT):c.536G>A (p.Arg179His)	rs766629953	0.00004
NM_001918.5(DBT):c.1017+8A>G	rs541924732	0.00001
NM_001918.5(DBT):c.*1916dup	rs745306619
NM_001918.5(DBT):c.6902_6903del	rs71709231
NM_001918.5(DBT):c.*8554del	rs886044938
NM_001918.5(DBT):c.1210-10del	rs398123658
NM_001918.5(DBT):c.1210-10dup	rs398123658
NM_001918.5(DBT):c.1281+140dup	rs35150096
NM_001918.5(DBT):c.1281+156_1281+157del	rs35150096
NM_001918.5(DBT):c.1282-4C>A	rs1410431336

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