List of variants in gene AMT reported as likely benign 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000481.4(AMT):c.354G>A (p.Leu118=)	rs145194293	0.00072
NM_000481.4(AMT):c.152C>T (p.Ala51Val)	rs34812788	0.00024
NM_000481.4(AMT):c.363C>T (p.Asn121=)	rs367604855	0.00017
NM_000481.4(AMT):c.858C>A (p.Gly286=)	rs367726589	0.00014
NM_000481.4(AMT):c.195C>T (p.His65=)	rs145243292	0.00004
NM_000481.4(AMT):c.435C>T (p.Asn145=)	rs1318110345	0.00001
NM_000481.4(AMT):c.879G>C (p.Gly293=)	rs972670254	0.00001
NM_000481.4(AMT):c.891A>G (p.Arg297=)	rs763216113	0.00001
NM_000481.4(AMT):c.108A>C (p.Thr36=)	rs1179441264
NM_000481.4(AMT):c.259-6C>T	rs2049102970
NM_000481.4(AMT):c.552C>T (p.Gly184=)	rs771745221
NM_000481.4(AMT):c.705G>T (p.Val235=)	rs1324646911
NM_000481.4(AMT):c.714G>A (p.Ala238=)	rs772179698

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