ClinVar Miner

List of variants in gene MTR reported as benign for not specified

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Gene type:
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Total variants: 22
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HGVS dbSNP
NM_000254.2(MTR):c.1437C>T (p.Asp479=) rs115424814
NM_000254.2(MTR):c.2044-11G>T rs570088952
NM_000254.2(MTR):c.2044-9C>T rs531027742
NM_000254.2(MTR):c.2474-18T>A rs10925256
NM_000254.2(MTR):c.250-7G>A rs184332230
NM_000254.2(MTR):c.2594+15T>C rs1770449
NM_000254.2(MTR):c.2756A>G (p.Asp919Gly) rs1805087
NM_000254.2(MTR):c.3144A>G (p.Ala1048=) rs2229276
NM_000254.2(MTR):c.340-6C>T rs7526063
NM_000254.2(MTR):c.3474G>A (p.Leu1158=) rs142113735
NM_000254.2(MTR):c.3477C>T (p.Asp1159=) rs117061132
NM_000254.2(MTR):c.3491G>A (p.Arg1164His) rs61736326
NM_000254.2(MTR):c.3492C>A (p.Arg1164=) rs12070777
NM_000254.2(MTR):c.3496C>T (p.Leu1166=) rs12030699
NM_000254.2(MTR):c.3576C>T (p.Leu1192=) rs1131449
NM_000254.2(MTR):c.3599-10C>A rs41530146
NM_000254.2(MTR):c.3599-11G>A rs76731959
NM_000254.2(MTR):c.3599-18C>T rs116444161
NM_000254.2(MTR):c.3711+15G>T rs3820571
NM_000254.2(MTR):c.3712-8T>C rs12022937
NM_000254.2(MTR):c.858C>T (p.Pro286=) rs146019467
NM_000254.2(MTR):c.940G>A (p.Asp314Asn) rs2229274

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