ClinVar Miner

Variants in gene MARS1 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 10
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HGVS dbSNP gnomAD frequency
NM_004990.4(MARS1):c.2180G>A (p.Arg727Gln) rs113808165 0.00541
NM_004990.4(MARS1):c.1753+7A>G rs117914586 0.00435
NM_004990.4(MARS1):c.626G>A (p.Ser209Asn) rs141671963 0.00327
NM_004990.4(MARS1):c.2204+11G>A rs202080192 0.00239
NM_004990.4(MARS1):c.280-14C>T rs183195960 0.00223
NM_004990.4(MARS1):c.1812G>A (p.Gly604=) rs117633211 0.00083
NM_004990.4(MARS1):c.477C>T (p.Pro159=) rs117101415 0.00083
NM_004990.4(MARS1):c.1689C>T (p.Val563=) rs117833843 0.00071
NM_004990.4(MARS1):c.901C>T (p.Arg301Cys) rs139661803 0.00052
NM_004990.4(MARS1):c.873C>T (p.Ala291=) rs79531790

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