ClinVar Miner

List of variants in gene BTK reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_000061.3(BTK):c.1899C>T (p.Cys633=) rs1135363 0.37760
NM_000061.3(BTK):c.*116A>C rs700 0.35507
NM_000061.3(BTK):c.840-262G>A rs67491067 0.34109
NM_000061.3(BTK):c.839+53A>C rs2746110 0.24705
NM_000061.3(BTK):c.241-175G>A rs3027629 0.23729
NM_000061.3(BTK):c.839+51C>A rs5951412 0.20859
NM_000061.3(BTK):c.776+78G>A rs2855259 0.16810
NM_000061.3(BTK):c.-30-198C>T rs73250683 0.15612
NM_000061.3(BTK):c.310-226G>A rs2301175 0.12108
NM_000061.3(BTK):c.588+172G>A rs3027641 0.11093
NM_000061.3(BTK):c.1350-176C>T rs3027643 0.08779
NM_000061.3(BTK):c.839+194G>C rs143542741 0.06044
NM_000061.3(BTK):c.310-124A>G rs3027632 0.02881
NM_001287344.2(BTK):c.72+3927C>T rs111262477 0.02280
NM_000061.3(BTK):c.954T>C (p.Ser318=) rs5991926 0.01964
NM_000061.3(BTK):c.141+11C>T rs138411530 0.00620
NM_000061.3(BTK):c.1631+71C>T rs2071223
NM_000061.3(BTK):c.1908+123del rs376521920
NM_000061.3(BTK):c.1908+142G>A rs184472722
NM_000061.3(BTK):c.1908+278dup rs60191867
NM_000061.3(BTK):c.1908+302C>T rs147512981
NM_000061.3(BTK):c.1909-149dup rs199950200
NM_000061.3(BTK):c.391+143dup rs193922127
NM_000061.3(BTK):c.391+251_391+253del rs373562379
NM_000061.3(BTK):c.391+251_391+257del rs79879307
NM_000061.3(BTK):c.839+41CT[7] rs200761404
NM_000061.3(BTK):c.839+53AT[8] rs199758498

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