List of variants in gene ATP7A reported as likely benign for not provided

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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 14

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HGVS	dbSNP
NM_000052.7(ATP7A):c.1009G>A (p.Ala337Thr)	rs138039591
NM_000052.7(ATP7A):c.120+194A>G
NM_000052.7(ATP7A):c.1251G>T (p.Gly417=)
NM_000052.7(ATP7A):c.1543+9C>G
NM_000052.7(ATP7A):c.1722G>A (p.Thr574=)
NM_000052.7(ATP7A):c.1934G>A (p.Arg645Gln)	rs782729433
NM_000052.7(ATP7A):c.2903A>G (p.Glu968Gly)	rs138958687
NM_000052.7(ATP7A):c.3294+907C>T
NM_000052.7(ATP7A):c.3449T>C (p.Ile1150Thr)	rs201225704
NM_000052.7(ATP7A):c.3659-257G>C
NM_000052.7(ATP7A):c.4226+48A>G
NM_000052.7(ATP7A):c.4389T>C (p.Ser1463=)	rs371939448
NM_000052.7(ATP7A):c.610+108G>A
NM_000052.7(ATP7A):c.880A>T (p.Asn294Tyr)	rs150526992

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