"Illumina Laboratory Services, Illumina"[submitter] AND "TSHB"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 291984	NM_000549.5(TSHB):c.-13A>G	TSHB	Single nucleotide variant (5 prime UTR variant)	Isolated thyroid-stimulating hormone deficiency	GLikely benign
Select item 256640	NM_000549.5(TSHB):c.40A>G (p.Thr14Ala)	TSHB (T14A)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign
Select item 12687	NM_000549.5(TSHB):c.205C>T (p.Gln69Ter)	TSHB (Q24* +1 more)	Single nucleotide variant (nonsense)	TSHB-related condition +2 more	GPathogenic/Likely pathogenic
Select item 764732	NM_000549.5(TSHB):c.223A>G (p.Arg75Gly)	TSHB (R75G +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 291985	NM_000549.5(TSHB):c.256G>A (p.Gly86Arg)	TSHB (G86R +1 more)	Single nucleotide variant (missense variant)	Isolated thyroid-stimulating hormone deficiency	GUncertain significance
Select item 875322	NM_000549.5(TSHB):c.*64T>C	TSHB	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GConflicting classifications of pathogenicity

ClinVar