"Database of Curated Mutations (DoCM)"[submitter] AND "B2M"[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 376370	NM_004048.4(B2M):c.1A>T (p.Met1Leu)	B2M (M1L)	Single nucleotide variant (missense variant +1 more)	Non-Hodgkin lymphoma +9 more	GLikely pathogenic
Select item 376369	NM_004048.4(B2M):c.1A>G (p.Met1Val)	B2M (M1V)	Single nucleotide variant (missense variant +1 more)	Small cell lung carcinoma +10 more	GLikely pathogenic OLikely oncogenic
Select item 376372	NM_004048.4(B2M):c.2T>G (p.Met1Arg)	B2M (M1R)	Single nucleotide variant (missense variant +1 more)	Squamous cell lung carcinoma +9 more	GLikely pathogenic
Select item 376371	NM_004048.4(B2M):c.2T>C (p.Met1Thr)	B2M (M1T)	Single nucleotide variant (missense variant +1 more)	Squamous cell lung carcinoma +9 more	GLikely pathogenic
Select item 376368	NM_004048.4(B2M):c.3G>A (p.Met1Ile)	B2M (M1I)	Single nucleotide variant (missense variant +1 more)	Non-Hodgkin lymphoma +9 more	GLikely pathogenic

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