List of variants in gene TANC2 reported by University of Washington Center for Mendelian Genomics, University of Washington

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_001394998.1(TANC2):c.2486G>A (p.Arg829His)	rs775421108	0.00004
NM_001394998.1(TANC2):c.2500C>T (p.Arg834Cys)	rs1282488329	0.00001
NM_001394998.1(TANC2):c.1441+1G>A	rs2045256930
NM_001394998.1(TANC2):c.2571_2572dup (p.Cys858fs)	rs2046750269
NM_001394998.1(TANC2):c.2603C>T (p.Ala868Val)	rs2047545401
NM_001394998.1(TANC2):c.4080del (p.Glu1361fs)	rs2048834387
NM_001394998.1(TANC2):c.4268+2T>G	rs2048929422
NM_001394998.1(TANC2):c.4450C>T (p.Gln1484Ter)	rs780968730
NM_001394998.1(TANC2):c.4657del (p.Arg1553fs)	rs2048988947
NM_001394998.1(TANC2):c.4699C>T (p.Gln1567Ter)	rs764041869
NM_001394998.1(TANC2):c.4701del (p.Gln1567fs)	rs2048990416
NM_001394998.1(TANC2):c.4965_4968del (p.Gln1656fs)	rs2048999762
NM_001394998.1(TANC2):c.5318A>G (p.His1773Arg)	rs2049010059
NM_001394998.1(TANC2):c.5571_5596dup (p.Phe1866delinsCysIleProLysValTer)	rs2049017627
NM_001394998.1(TANC2):c.769+1G>A	rs1419550439
NM_025185.3(TANC2):c.1589_1590delGA	rs2046598826

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