"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "TTC36-AS1" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 730490	NM_001197104.2(KMT2A):c.11147-5_11147-3del	KMT2A, TTC36-AS1	Microsatellite (non-coding transcript variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 376783	NM_001197104.2(KMT2A):c.11230C>T (p.Arg3744Ter)	KMT2A, TTC36-AS1 (R3744* +1 more)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 710751	NM_001197104.2(KMT2A):c.11292C>T (p.His3764=)	KMT2A, TTC36-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 806746	NM_001197104.2(KMT2A):c.11464C>T (p.Arg3822Cys)	TTC36-AS1, KMT2A (R3819C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 708736	NM_001197104.2(KMT2A):c.11505T>G (p.Gly3835=)	KMT2A, TTC36-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 1662686	NM_001197104.2(KMT2A):c.11586C>T (p.Ala3862=)	KMT2A, TTC36-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 720477	NM_001197104.2(KMT2A):c.11592C>T (p.Asn3864=)	KMT2A, TTC36-AS1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1176924	NM_001197104.2(KMT2A):c.11644-7T>C	KMT2A, TTC36-AS1	Single nucleotide variant (intron variant)	not provided	GUncertain significance

ClinVar