ClinVar Miner

List of variants in gene MTR reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (961):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
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HGVS dbSNP
NM_000254.2(MTR):c.1067T>C (p.Leu356Ser) rs1286773616
NM_000254.2(MTR):c.1074T>C (p.Ser358=)
NM_000254.2(MTR):c.1129C>T (p.Arg377Cys)
NM_000254.2(MTR):c.1135A>G (p.Asn379Asp)
NM_000254.2(MTR):c.1522G>C (p.Glu508Gln)
NM_000254.2(MTR):c.1542A>T (p.Arg514Ser)
NM_000254.2(MTR):c.1575A>T (p.Lys525Asn) rs199700767
NM_000254.2(MTR):c.1862A>G (p.Asp621Gly) rs61736440
NM_000254.2(MTR):c.1954-6A>G rs1553321372
NM_000254.2(MTR):c.2014G>A (p.Glu672Lys) rs142774813
NM_000254.2(MTR):c.2165T>C (p.Leu722Pro) rs1553321807
NM_000254.2(MTR):c.2304+3A>C
NM_000254.2(MTR):c.2684A>C (p.Gln895Pro)
NM_000254.2(MTR):c.2758C>G (p.His920Asp) rs121913579
NM_000254.2(MTR):c.3140A>T (p.Tyr1047Phe)
NM_000254.2(MTR):c.3188A>G (p.Tyr1063Cys)
NM_000254.2(MTR):c.3227C>T (p.Thr1076Met)
NM_000254.2(MTR):c.3281G>A (p.Arg1094His)
NM_000254.2(MTR):c.3490C>T (p.Arg1164Cys)
NM_000254.2(MTR):c.349A>C (p.Met117Leu)
NM_000254.2(MTR):c.3514C>T (p.Arg1172Cys)
NM_000254.2(MTR):c.586A>G (p.Ile196Val)
NM_000254.2(MTR):c.866-10C>G rs368755647
NM_000254.2(MTR):c.899C>T (p.Thr300Met) rs201871910

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