List of variants in gene TCAP reported as likely benign for not specified

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: 20

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HGVS	dbSNP	gnomAD frequency
NM_003673.4(TCAP):c.316C>T (p.Arg106Cys)	rs45578741	0.00813
NM_003673.4(TCAP):c.32C>T (p.Ser11Leu)	rs45495192	0.00113
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_003673.3(TCAP):c.-13A>G	rs368175926	0.00010
NM_003673.4(TCAP):c.132C>T (p.Asp44=)	rs397516861	0.00006
NM_003673.4(TCAP):c.113G>T (p.Cys38Phe)	rs375310569	0.00005
NM_003673.3(TCAP):c.-18A>G	rs45550442	0.00004
NM_003673.4(TCAP):c.111-17C>T	rs567350904	0.00003
NM_003673.4(TCAP):c.267G>A (p.Leu89=)	rs1419129039	0.00002
NM_003673.4(TCAP):c.279C>T (p.Ile93=)	rs144149447	0.00002
NM_003673.4(TCAP):c.195C>G (p.Pro65=)	rs370118201	0.00001
NM_003673.4(TCAP):c.110+7G>A	rs886038533
NM_003673.4(TCAP):c.111-11C>T
NM_003673.4(TCAP):c.111-15dup	rs397516860
NM_003673.4(TCAP):c.192G>A (p.Ser64=)	rs771585295
NM_003673.4(TCAP):c.313G>A (p.Glu105Lys)	rs146906267
NM_003673.4(TCAP):c.346C>T (p.Leu116=)	rs876657586
NM_003673.4(TCAP):c.349C>T (p.Leu117=)	rs886038534
NM_003673.4(TCAP):c.34GAG[1] (p.Glu13del)	rs397516862

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