List of variants in gene FAM89B reported by Ambry Genetics

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001098785.2(FAM89B):c.247C>T (p.Pro83Ser)	rs1857159080	0.00005
NM_001098785.2(FAM89B):c.205G>T (p.Ala69Ser)	rs987797650	0.00004
NM_001098785.2(FAM89B):c.212C>T (p.Ala71Val)	rs1249208835	0.00003
NM_001098785.2(FAM89B):c.408C>T (p.Ser136=)	rs374813667	0.00002
NM_001098785.2(FAM89B):c.444G>A (p.Ala148=)	rs1047423258	0.00002
NM_001098785.2(FAM89B):c.533A>C (p.Asp178Ala)	rs753891511	0.00002
NM_001098785.2(FAM89B):c.206C>T (p.Ala69Val)
NM_001098785.2(FAM89B):c.233C>T (p.Ala78Val)	rs905404078
NM_001098785.2(FAM89B):c.244C>A (p.Arg82Ser)
NM_001098785.2(FAM89B):c.370C>T (p.Leu124=)
NM_001098785.2(FAM89B):c.391T>C (p.Cys131Arg)	rs2496217756
NM_001098785.2(FAM89B):c.472G>A (p.Asp158Asn)	rs1488620917
NM_001098785.2(FAM89B):c.559A>G (p.Ile187Val)

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