ClinVar Miner

List of variants in gene SPG7 reported as likely benign for not provided

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Total variants: 16
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HGVS dbSNP
NM_003119.4(SPG7):c.1053C>T (p.Pro351=)
NM_003119.4(SPG7):c.1324+3845T>C
NM_003119.4(SPG7):c.1324+3855T>C
NM_003119.4(SPG7):c.1324+3861del
NM_003119.4(SPG7):c.1324+3865G>C
NM_003119.4(SPG7):c.1324+3884C>G
NM_003119.4(SPG7):c.1457G>A (p.Arg486Gln) rs111475461
NM_003119.4(SPG7):c.2104-24del
NM_003119.4(SPG7):c.318G>A (p.Leu106=)
NM_003119.4(SPG7):c.376+105G>T
NM_003119.4(SPG7):c.376+140C>T
NM_003119.4(SPG7):c.758+294C>T
NM_003119.4(SPG7):c.758+316A>G
NM_003119.4(SPG7):c.861+196C>T
NM_003119.4(SPG7):c.987+216A>G
NM_003119.4(SPG7):c.987+57C>T

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