ClinVar Miner

List of variants in gene MED13L reported as benign for not provided

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Total variants: 11
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HGVS dbSNP
GRCh37/hg19 12q24.21(chr12:116498873-116536921)x1
GRCh37/hg19 12q24.21(chr12:116498873-116621185)x1
GRCh37/hg19 12q24.21(chr12:116526507-116528428)x1
GRCh37/hg19 12q24.21(chr12:116526507-116536921)x1
GRCh37/hg19 12q24.21(chr12:116526663-116528428)x1
NM_015335.4(MED13L):c.1283A>G (p.His428Arg) rs144410580
NM_015335.4(MED13L):c.1904G>A (p.Ser635Asn) rs144457722
NM_015335.4(MED13L):c.2778C>T (p.Pro926=) rs144357346
NM_015335.4(MED13L):c.4767G>A (p.Ser1589=) rs573917510
NM_015335.4(MED13L):c.73-5del rs1593196291
NM_015335.4(MED13L):c.771C>T (p.Asp257=) rs148136300

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