List of variants in gene FAM161A reported by Institute of Human Genetics, Univ. Regensburg, Univ. Regensburg

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.1309A>T (p.Arg437Ter)	rs200691042	0.00030
NM_001201543.2(FAM161A):c.1270G>A (p.Val424Ile)	rs377666612	0.00014
NM_001201543.2(FAM161A):c.494A>G (p.Gln165Arg)	rs201088869	0.00013
NM_001201543.2(FAM161A):c.916C>T (p.Arg306Trp)	rs183615774	0.00009
NM_001201543.2(FAM161A):c.1501del (p.Cys501fs)	rs767414973	0.00004
NM_001201543.2(FAM161A):c.1568G>A (p.Arg523Gln)	rs767768523	0.00004
NM_001201543.2(FAM161A):c.1111G>T (p.Asp371Tyr)	rs752075492	0.00001
NM_001201543.2(FAM161A):c.1109del (p.Asn370fs)
NM_001201543.2(FAM161A):c.1230G>T (p.Arg410Ser)
NM_001201543.2(FAM161A):c.1355_1356del (p.Thr452fs)	rs397704718
NM_001201543.2(FAM161A):c.2034_2037del (p.Glu680fs)	rs748147923
NM_001201543.2(FAM161A):c.2121AGA[1] (p.Glu709del)	rs558080743
NM_001201543.2(FAM161A):c.332C>A (p.Ala111Glu)
NM_001201543.2(FAM161A):c.422+5G>T
NM_001201543.2(FAM161A):c.493C>T (p.Gln165Ter)
NM_001201543.2(FAM161A):c.730del (p.Gln243_Met244insTer)	rs1167380267

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