List of variants in gene AFG3L2 reported as uncertain significance for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_006796.3(AFG3L2):c.536A>G (p.Tyr179Cys)	rs368594369	0.00016
NM_006796.3(AFG3L2):c.1762G>A (p.Ala588Thr)	rs374828650	0.00005
NM_006796.3(AFG3L2):c.530A>G (p.Asn177Ser)	rs371921200	0.00005
NM_006796.3(AFG3L2):c.292+2T>C	rs779805236	0.00003
NM_006796.3(AFG3L2):c.376C>T (p.His126Tyr)	rs752336670	0.00003
NM_006796.3(AFG3L2):c.1040C>G (p.Thr347Ser)	rs1191222406
NM_006796.3(AFG3L2):c.1064C>T (p.Thr355Met)	rs1057522195
NM_006796.3(AFG3L2):c.1167C>T (p.Val389=)	rs1282576516
NM_006796.3(AFG3L2):c.1780-9A>C
NM_006796.3(AFG3L2):c.1838A>C (p.Gln613Pro)
NM_006796.3(AFG3L2):c.1984G>T (p.Val662Phe)	rs1555670564
NM_006796.3(AFG3L2):c.2062C>G (p.Pro688Ala)	rs797045221
NM_006796.3(AFG3L2):c.2140G>A (p.Ala714Thr)

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