MYC[gene] and "single gene"[properties] - ClinVar

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Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2658810	NM_002467.6(MYC):c.-263G>A	MYC	Single nucleotide variant (5 prime UTR variant)	not provided	GLikely benign
Select item 2658811	NM_002467.6(MYC):c.-96C>T	MYC	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 2658812	NM_002467.6(MYC):c.30+4A>T	MYC	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2658813	NM_002467.6(MYC):c.30+600C>T	MYC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2658814	NM_002467.6(MYC):c.31-172G>A	MYC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 722844	NM_002467.6(MYC):c.64T>C (p.Phe22Leu)	MYC (F21L +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 1679939	NM_002467.6(MYC):c.77A>G (p.Asn26Ser)	MYC (N25S +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 791168	NM_002467.6(MYC):c.144G>A (p.Gln48=)	MYC	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 12576	NM_002467.6(MYC):c.162G>C (p.Glu54Asp)	MYC (E54D +1 more)	Single nucleotide variant (missense variant)	Burkitt lymphoma	GPathogenic
Select item 376298	NM_002467.6(MYC):c.169C>T (p.Pro57Ser)	MYC (P57S +1 more)	Single nucleotide variant (missense variant)	Neoplasm	GLikely pathogenic
Select item 376459	NM_002467.6(MYC):c.173C>T (p.Pro58Leu)	MYC (P58L +1 more)	Single nucleotide variant (missense variant)	Malignant melanoma of skin +4 more	GLikely pathogenic
Select item 376299	NM_002467.6(MYC):c.176C>T (p.Ala59Val)	MYC (A59V +1 more)	Single nucleotide variant (missense variant)	Neoplasm	GLikely pathogenic
Select item 12574	NM_002467.6(MYC):c.214C>T (p.Pro72Ser)	MYC (P72S +1 more)	Single nucleotide variant (missense variant)	Burkitt lymphoma	GPathogenic
Select item 2658815	NM_002467.6(MYC):c.217A>G (p.Thr73Ala)	MYC (T72A +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GPathogenic OOncogenic
Select item 376458	NM_002467.6(MYC):c.217A>C (p.Thr73Pro)	MYC (T73P +1 more)	Single nucleotide variant (missense variant)	Carcinoma of esophagus +4 more	GLikely pathogenic
Select item 376300	NM_002467.6(MYC):c.218C>T (p.Thr73Ile)	MYC (T73I +1 more)	Single nucleotide variant (missense variant)	Neuroblastoma +5 more	GLikely pathogenic
Select item 12577	NM_002467.6(MYC):c.220C>G (p.Pro74Ala)	MYC (P74A +1 more)	Single nucleotide variant (missense variant)	Cholesteatoma of middle ear +1 more	Gother OLikely oncogenic
Select item 2413166	NM_002467.6(MYC):c.223C>A (p.Pro75Thr)	MYC (P74T +1 more)	Single nucleotide variant (missense variant)	Cholesteatoma of middle ear	Gother
Select item 376301	NM_002467.6(MYC):c.230C>T (p.Ser77Phe)	MYC (S77F +1 more)	Single nucleotide variant (missense variant)	Neoplasm	GLikely pathogenic
Select item 12575	NM_002467.6(MYC):c.302A>C (p.Asn101Thr)	MYC (N101T +1 more)	Single nucleotide variant (missense variant)	Neoplasm +1 more	GPathogenic/Likely pathogenic
Select item 2286886	NM_002467.6(MYC):c.409G>C (p.Glu137Gln)	MYC (E137Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3058659	NM_002467.6(MYC):c.438G>A (p.Gln146=)	MYC	Single nucleotide variant (synonymous variant)	MYC-related disorder	GLikely benign
Select item 929760	NM_002467.6(MYC):c.478G>A (p.Val160Ile)	MYC (V159I +1 more)	Single nucleotide variant (missense variant)	Premature ovarian failure	GUncertain significance
Select item 3297249	NM_002467.6(MYC):c.544G>A (p.Gly182Ser)	MYC (G181S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510151	NM_002467.6(MYC):c.671C>T (p.Ala224Val)	MYC (A223V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3057137	NM_002467.6(MYC):c.738G>A (p.Pro246=)	MYC	Single nucleotide variant (synonymous variant)	MYC-related disorder	GBenign
Select item 376302	NM_002467.6(MYC):c.778C>G (p.Pro260Ala)	MYC (P260A +1 more)	Single nucleotide variant (missense variant)	Neoplasm	GLikely pathogenic
Select item 2468497	NM_002467.6(MYC):c.909C>G (p.Ser303Arg)	MYC (S302R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 719682	NM_002467.6(MYC):c.1085C>T (p.Ser362Phe)	MYC (S361F +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 3257924	NM_002467.6(MYC):c.1177C>T (p.Arg393Cys)	MYC (R392C +1 more)	Single nucleotide variant (missense variant)	Neoplasm	OUncertain significance
Select item 3154445	NM_002467.6(MYC):c.1228A>G (p.Ile410Val)	MYC (I410V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3154448	NM_002467.6(MYC):c.1297G>C (p.Asp433His)	MYC (D432H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 810340	GRCh37/hg19 8q24.21(chr8:128750494-128753204)x3	MYC	Copy number gain	not provided	GLikely pathogenic

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Items: 33