ClinVar Miner

List of variants in gene SBF2 reported as benign for not provided

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Total variants: 30
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HGVS dbSNP
GRCh37/hg19 11p15.4(chr11:10129950-10211233)x1
GRCh37/hg19 11p15.4(chr11:9938475-9942432)x1
GRCh37/hg19 11p15.4(chr11:9938475-9944824)x1
NM_030962.3(SBF2):c.1167+74C>T
NM_030962.3(SBF2):c.1173A>G (p.Ala391=) rs79470805
NM_030962.3(SBF2):c.1711-158dupG
NM_030962.3(SBF2):c.1711-84G>A
NM_030962.3(SBF2):c.3456-145T>C
NM_030962.3(SBF2):c.3653-233C>T
NM_030962.3(SBF2):c.3653-288G>A
NM_030962.3(SBF2):c.3978+152T>C
NM_030962.3(SBF2):c.3979-148T>C
NM_030962.3(SBF2):c.3979-173G>C
NM_030962.3(SBF2):c.4155+91T>C
NM_030962.3(SBF2):c.4156-183T>A
NM_030962.3(SBF2):c.4156-46C>T
NM_030962.3(SBF2):c.4443+224C>G
NM_030962.3(SBF2):c.4699-150G>T
NM_030962.3(SBF2):c.4932+216G>A
NM_030962.3(SBF2):c.4932+224C>T
NM_030962.3(SBF2):c.4932+65C>T
NM_030962.3(SBF2):c.4933-215G>A
NM_030962.3(SBF2):c.5038-57CAGT[3]
NM_030962.3(SBF2):c.514-53A>T
NM_030962.3(SBF2):c.5319+113delG
NM_030962.3(SBF2):c.5320-209A>G
NM_030962.3(SBF2):c.5451+102T>G
NM_030962.3(SBF2):c.5452-165C>G
NM_030962.3(SBF2):c.56-64G>A
NM_030962.3(SBF2):c.976-248T>C

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