ClinVar Miner

List of variants in gene TMEM127 reported as likely benign for Hereditary Paraganglioma-Pheochromocytoma Syndromes

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Total variants: 37
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HGVS dbSNP
NM_017849.3(TMEM127):c.102C>T (p.Ala34=) rs781643869
NM_017849.3(TMEM127):c.12C>T (p.Pro4=) rs1406470818
NM_017849.3(TMEM127):c.136A>G (p.Thr46Ala) rs144659242
NM_017849.3(TMEM127):c.210C>T (p.Asp70=) rs1553437721
NM_017849.3(TMEM127):c.213G>A (p.Val71=) rs777169152
NM_017849.3(TMEM127):c.267A>G (p.Thr89=) rs773384410
NM_017849.3(TMEM127):c.270G>T (p.Val90=) rs748896126
NM_017849.3(TMEM127):c.288C>T (p.Ile96=) rs758726687
NM_017849.3(TMEM127):c.313C>T (p.Leu105=) rs754465684
NM_017849.3(TMEM127):c.324C>T (p.Leu108=) rs148381232
NM_017849.3(TMEM127):c.330T>C (p.Ala110=) rs1157106593
NM_017849.3(TMEM127):c.384C>T (p.Arg128=) rs755188175
NM_017849.3(TMEM127):c.393C>T (p.Phe131=) rs756680897
NM_017849.3(TMEM127):c.394G>A (p.Ala132Thr) rs750870974
NM_017849.3(TMEM127):c.402C>A (p.Ile134=) rs1553436974
NM_017849.3(TMEM127):c.411T>A (p.Val137=) rs760099422
NM_017849.3(TMEM127):c.426C>T (p.Thr142=) rs552787569
NM_017849.3(TMEM127):c.519C>T (p.Phe173=) rs758676810
NM_017849.3(TMEM127):c.522C>T (p.Ala174=) rs367951215
NM_017849.3(TMEM127):c.573G>A (p.Thr191=) rs147816248
NM_017849.3(TMEM127):c.651C>T (p.Asn217=) rs759801591
NM_017849.3(TMEM127):c.663G>A (p.Pro221=) rs377760956
NM_017849.3(TMEM127):c.666G>A (p.Ala222=) rs772481029
NM_017849.3(TMEM127):c.672T>C (p.Tyr224=) rs201935270
NM_017849.3(TMEM127):c.81G>A (p.Pro27=) rs1553437743
NM_017849.4(TMEM127):c.196C>T (p.Leu66=) rs1211097710
NM_017849.4(TMEM127):c.214T>C (p.Leu72=) rs1573977624
NM_017849.4(TMEM127):c.327C>T (p.Ser109=) rs773650718
NM_017849.4(TMEM127):c.354G>A (p.Pro118=) rs1392614291
NM_017849.4(TMEM127):c.39C>T (p.Arg13=) rs1060503975
NM_017849.4(TMEM127):c.409+9T>C rs1573970006
NM_017849.4(TMEM127):c.410-7C>T rs375440877
NM_017849.4(TMEM127):c.444T>C (p.Tyr148=) rs768545721
NM_017849.4(TMEM127):c.468C>A (p.Ala156=) rs749579854
NM_017849.4(TMEM127):c.507C>A (p.Val169=) rs1573969264
NM_017849.4(TMEM127):c.636A>G (p.Ser212=) rs1573969010
NM_017849.4(TMEM127):c.67C>T (p.Leu23=) rs749807415

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