List of variants in gene TERT reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_198253.3(TERT):c.2287-5G>A	rs561426406	0.00005
NM_198253.3(TERT):c.553C>T (p.Arg185Trp)	rs770436206	0.00004
NM_198253.3(TERT):c.2072G>A (p.Arg691His)	rs202123213	0.00001
NM_198253.3(TERT):c.1094T>C (p.Phe365Ser)
NM_198253.3(TERT):c.2300C>G (p.Thr767Arg)
NM_198253.3(TERT):c.2833G>A (p.Asp945Asn)	rs1446074617

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