List of variants in gene MYC reported by Database of Curated Mutations (DoCM)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_002467.6(MYC):c.169C>T (p.Pro57Ser)	rs1057519849
NM_002467.6(MYC):c.173C>T (p.Pro58Leu)	rs1057519918
NM_002467.6(MYC):c.176C>T (p.Ala59Val)	rs775522201
NM_002467.6(MYC):c.217A>C (p.Thr73Pro)	rs750664148
NM_002467.6(MYC):c.218C>T (p.Thr73Ile)	rs756091827
NM_002467.6(MYC):c.230C>T (p.Ser77Phe)	rs1057519850
NM_002467.6(MYC):c.302A>C (p.Asn101Thr)	rs121918683
NM_002467.6(MYC):c.778C>G (p.Pro260Ala)	rs1057519851

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