ClinVar Miner

List of variants in gene ERMARD reported as likely benign for not specified

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Gene type:
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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_018341.3(ERMARD):c.1899C>T (p.Tyr633=) rs61747673 0.00315
NM_018341.3(ERMARD):c.-13G>C rs182293452 0.00286
NM_018341.3(ERMARD):c.1695G>A (p.Thr565=) rs144899015 0.00274
NM_018341.3(ERMARD):c.265C>A (p.Gln89Lys) rs148450358 0.00270
NM_018341.3(ERMARD):c.1329T>C (p.Cys443=) rs76173501 0.00244
NM_018341.3(ERMARD):c.960G>A (p.Glu320=) rs149649895 0.00231
NM_018341.3(ERMARD):c.1513A>G (p.Thr505Ala) rs113995515 0.00158
NM_018341.3(ERMARD):c.1976G>T (p.Ser659Ile) rs117593791 0.00088
NM_018341.3(ERMARD):c.385C>T (p.Leu129=) rs141826774 0.00041
NM_018341.3(ERMARD):c.171G>C (p.Glu57Asp) rs187725532 0.00019
NM_018341.3(ERMARD):c.508-17A>C rs374621558 0.00006
NM_018341.3(ERMARD):c.364A>G (p.Ile122Val) rs374781539 0.00005
NM_018341.3(ERMARD):c.6+19C>T rs373555798 0.00005
NM_018341.3(ERMARD):c.1419T>C (p.Asn473=) rs570581453 0.00004
NM_018341.3(ERMARD):c.826G>A (p.Glu276Lys) rs573003364 0.00004
NM_018341.3(ERMARD):c.1234-16G>C rs371987913 0.00002
NM_018341.3(ERMARD):c.192C>T (p.Tyr64=) rs566808113 0.00001
NM_018341.3(ERMARD):c.900T>C (p.Thr300=) rs373839754 0.00001
NM_018341.3(ERMARD):c.1395-11_1395-10del rs538021384
NM_018341.3(ERMARD):c.1740-9del rs1554242528
NM_018341.3(ERMARD):c.1901C>T (p.Thr634Ile) rs552023965
NM_018341.3(ERMARD):c.897G>A (p.Glu299=) rs2128348267

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