List of variants in gene TCAP reported as uncertain significance by Eurofins NTD LLC (GA)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_003673.4(TCAP):c.353C>T (p.Ala118Val)	rs143233087	0.00092
NM_003673.4(TCAP):c.313G>C (p.Glu105Gln)	rs146906267	0.00051
NM_003673.4(TCAP):c.60C>G (p.Ala20=)	rs146502276	0.00034
NM_003673.4(TCAP):c.270G>A (p.Pro90=)	rs372538567	0.00017
NM_003673.4(TCAP):c.337C>T (p.Leu113Phe)	rs372312912	0.00014
NM_003673.4(TCAP):c.209G>A (p.Arg70Gln)	rs552865793	0.00012
NM_003673.4(TCAP):c.388C>T (p.Arg130Cys)	rs374886575	0.00009
NM_003673.4(TCAP):c.97C>T (p.Arg33Trp)	rs145524909	0.00009
NM_003673.4(TCAP):c.132C>T (p.Asp44=)	rs397516861	0.00006
NM_003673.4(TCAP):c.226C>T (p.Arg76Cys)	rs572836774	0.00006
NM_003673.4(TCAP):c.113G>T (p.Cys38Phe)	rs375310569	0.00005
NM_003673.4(TCAP):c.447C>T (p.Pro149=)	rs45614332	0.00004
NM_003673.4(TCAP):c.460C>T (p.Arg154Cys)	rs755539784	0.00004
NM_003673.4(TCAP):c.208C>T (p.Arg70Trp)	rs775636212	0.00003
NM_003673.4(TCAP):c.421C>G (p.Pro141Ala)	rs45509691	0.00002
NM_003673.4(TCAP):c.225C>T (p.Gly75=)	rs754744780	0.00001
NM_003673.4(TCAP):c.334C>T (p.Gln112Ter)	rs794729175	0.00001
NM_003673.4(TCAP):c.389G>A (p.Arg130His)	rs147503632	0.00001
NM_003673.4(TCAP):c.52C>T (p.Arg18Trp)	rs886038989	0.00001
NM_003673.4(TCAP):c.118C>T (p.Leu40=)	rs886043427
NM_003673.4(TCAP):c.169T>C (p.Cys57Arg)	rs886042772
NM_003673.4(TCAP):c.201G>A (p.Leu67=)	rs1567865110
NM_003673.4(TCAP):c.240G>T (p.Glu80Asp)	rs758101613
NM_003673.4(TCAP):c.313G>A (p.Glu105Lys)	rs146906267
NM_003673.4(TCAP):c.454C>G (p.Leu152Val)	rs1262032321
NM_003673.4(TCAP):c.460C>A (p.Arg154Ser)	rs755539784

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