List of variants in gene TYK2 reported by CeGaT Center for Human Genetics Tuebingen

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: 28

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HGVS	dbSNP	gnomAD frequency
NM_003331.5(TYK2):c.1953C>T (p.Ile651=)	rs12720355	0.01009
NM_003331.5(TYK2):c.157G>A (p.Ala53Thr)	rs55762744	0.00716
NM_003331.5(TYK2):c.2783C>T (p.Ala928Val)	rs35018800	0.00499
NM_003331.5(TYK2):c.3330G>A (p.Glu1110=)	rs114073289	0.00353
NM_003331.5(TYK2):c.1869C>T (p.Asp623=)	rs140078545	0.00110
NM_003331.5(TYK2):c.2250C>T (p.Gly750=)	rs138652649	0.00093
NM_003331.5(TYK2):c.648G>A (p.Pro216=)	rs142642403	0.00030
NM_003331.5(TYK2):c.2670G>C (p.Thr890=)	rs144332908	0.00026
NM_003331.5(TYK2):c.810C>T (p.Phe270=)	rs56107150	0.00021
NM_003331.5(TYK2):c.1236G>A (p.Ala412=)	rs56212434	0.00015
NM_003331.5(TYK2):c.662G>A (p.Arg221Gln)	rs747608147	0.00006
NM_003331.5(TYK2):c.1362C>G (p.Pro454=)	rs374268170	0.00004
NM_003331.5(TYK2):c.1501C>T (p.Arg501Trp)	rs756944840	0.00004
NM_003331.5(TYK2):c.1821C>G (p.Arg607=)	rs773859320	0.00004
NM_003331.5(TYK2):c.2814C>G (p.Pro938=)	rs763629813	0.00004
NM_003331.5(TYK2):c.353G>A (p.Arg118Gln)	rs369530676	0.00002
NM_003331.5(TYK2):c.1297T>C (p.Tyr433His)	rs764428779	0.00001
NM_003331.5(TYK2):c.2602C>T (p.Arg868Trp)	rs762311335	0.00001
NM_003331.5(TYK2):c.2983A>G (p.Ile995Val)	rs764232789	0.00001
NM_003331.5(TYK2):c.1285G>A (p.Asp429Asn)	rs758589580
NM_003331.5(TYK2):c.2036G>C (p.Arg679Pro)	rs200247986
NM_003331.5(TYK2):c.2393G>A (p.Trp798Ter)	rs2145184643
NM_003331.5(TYK2):c.2909-1G>A	rs1599328119
NM_003331.5(TYK2):c.2994C>A (p.Ala998=)	rs1555716215
NM_003331.5(TYK2):c.466-1G>A	rs2145259879
NM_003331.5(TYK2):c.647del (p.Pro216fs)	rs1555719963
NM_003331.5(TYK2):c.777_778delinsTT (p.Tyr259_Leu260=)	rs1555719851
NM_003331.5(TYK2):c.844C>T (p.Leu282=)	rs753449931

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