"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "TTC21A"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1335506	NM_001366900.1(TTC21A):c.842C>T (p.Thr281Ile)	TTC21A (T240I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2653684	NM_001366900.1(TTC21A):c.1284C>T (p.His428=)	TTC21A	Single nucleotide variant (synonymous variant +1 more)	TTC21A-related condition +1 more	GBenign/Likely benign
Select item 3025327	NM_001366900.1(TTC21A):c.1948C>A (p.Pro650Thr)	TTC21A (P609T +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2498927	NM_001366900.1(TTC21A):c.2135+3A>G	TTC21A	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3024797	NM_001366900.1(TTC21A):c.2939C>T (p.Ala980Val)	TTC21A (A939V +3 more)	Single nucleotide variant (missense variant +1 more)	TTC21A-related condition +1 more	GBenign
Select item 2578938	NM_001366900.1(TTC21A):c.3360G>A (p.Arg1120=)	TTC21A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1879575	NM_001366900.1(TTC21A):c.3850G>A (p.Glu1284Lys)	TTC21A (E1243K +3 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign

ClinVar