List of variants in gene FAM161A 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001201543.2(FAM161A):c.*1100T>C	rs78512710	0.00922
NM_001201543.2(FAM161A):c.1133T>G (p.Leu378Arg)	rs187695569	0.00389
NM_001201543.2(FAM161A):c.197C>T (p.Thr66Ile)	rs145199539	0.00372
NM_001201543.2(FAM161A):c.1153C>G (p.Gln385Glu)	rs139266382	0.00309
NM_001201543.2(FAM161A):c.2064T>C (p.Ile688=)	rs138464813	0.00145
NM_001201543.2(FAM161A):c.1309A>T (p.Arg437Ter)	rs200691042	0.00030
NM_001201543.2(FAM161A):c.494A>G (p.Gln165Arg)	rs201088869	0.00013
NM_001201543.2(FAM161A):c.1501del (p.Cys501fs)	rs767414973	0.00004
NM_001201543.2(FAM161A):c.685C>T (p.Arg229Ter)	rs267606794	0.00001
NM_001201543.2(FAM161A):c.1205C>G (p.Ser402Ter)	rs1553354522
NM_001201543.2(FAM161A):c.1212T>A (p.Cys404Ter)	rs4672457
NM_001201543.2(FAM161A):c.1355_1356del (p.Thr452fs)	rs397704718
NM_001201543.2(FAM161A):c.1567C>T (p.Arg523Ter)	rs202193201
NM_001201543.2(FAM161A):c.1602G>T (p.Lys534Asn)	rs367777806
NM_001201543.2(FAM161A):c.730del (p.Gln243_Met244insTer)	rs1167380267
NM_001201543.2(FAM161A):c.847C>T (p.Arg283Ter)	rs748847284

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