List of variants in gene AFF4 reported as uncertain significance 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_014423.4(AFF4):c.2005C>T (p.Pro669Ser)	rs749188155	0.00002
NM_014423.4(AFF4):c.2491C>T (p.Arg831Trp)	rs374444704	0.00002
NM_014423.4(AFF4):c.2359A>G (p.Lys787Glu)	rs746518188	0.00001
GRCh37/hg19 5q31.1(chr5:132267870-132270633)x1
NM_014423.4(AFF4):c.1241C>T (p.Ser414Leu)
NM_014423.4(AFF4):c.1293C>T (p.His431=)	rs1760462005
NM_014423.4(AFF4):c.145T>C (p.Ser49Pro)
NM_014423.4(AFF4):c.1840AAG[1] (p.Lys615del)
NM_014423.4(AFF4):c.2140C>T (p.Leu714Phe)
NM_014423.4(AFF4):c.2260A>G (p.Lys754Glu)	rs752670107
NM_014423.4(AFF4):c.3343C>G (p.Gln1115Glu)

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