"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "TFRC"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2057180	NM_001128148.3(TFRC):c.2010C>T (p.Val670=)	TFRC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2654507	NM_001128148.3(TFRC):c.1818A>G (p.Glu606=)	TFRC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 732503	NM_001128148.3(TFRC):c.1038T>C (p.Phe346=)	TFRC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3026018	NM_001128148.3(TFRC):c.543C>T (p.Val181=)	TFRC	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1564859	NM_001128148.3(TFRC):c.396G>A (p.Ser132=)	TFRC	Single nucleotide variant (synonymous variant +1 more)	TFRC-related condition +1 more	GBenign/Likely benign
Select item 717697	NM_001128148.3(TFRC):c.312C>T (p.Thr104=)	TFRC	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign
Select item 1169927	NM_001128148.3(TFRC):c.162C>T (p.Ala54=)	TFRC	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign

ClinVar