"Baylor Genetics"[submitter] AND "MUC5B"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1030557	NM_002458.3(MUC5B):c.2725G>A (p.Asp909Asn)	MUC5B (D909N)	Single nucleotide variant (missense variant)	Interstitial lung disease 2	GUncertain significance
Select item 1033923	NM_002458.3(MUC5B):c.9005C>A (p.Thr3002Lys)	MUC5B-AS1, MUC5B (T3002K)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1033924	NM_002458.3(MUC5B):c.9355A>G (p.Thr3119Ala)	MUC5B, MUC5B-AS1 (T3119A)	Single nucleotide variant (missense variant)	Interstitial lung disease 2	GUncertain significance
Select item 1030558	NM_002458.3(MUC5B):c.9385C>T (p.Pro3129Ser)	MUC5B, MUC5B-AS1 (P3129S)	Single nucleotide variant (missense variant)	Interstitial lung disease 2	GUncertain significance
Select item 1033925	NM_002458.3(MUC5B):c.9849G>A (p.Thr3283=)	MUC5B, MUC5B-AS1	Single nucleotide variant (synonymous variant)	Interstitial lung disease 2	GUncertain significance
Select item 625559	GRCh37/hg19 11p15.5-15.3(chr11:193146-12643136)	C11orf40, C11orf42 +243 more	Copy number gain	Silver-Russell syndrome 1	GPathogenic

ClinVar