Variants in gene ACADM with conflicting interpretations "likely pathogenic" and "uncertain significance"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 32

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000016.6(ACADM):c.1118T>C (p.Val373Ala)	rs373057729	0.00004
NM_000016.6(ACADM):c.388-3T>G	rs764942250	0.00004
NM_000016.6(ACADM):c.388-5G>A	rs759254037	0.00004
NM_000016.6(ACADM):c.50G>A (p.Arg17His)	rs17848070	0.00004
NM_000016.6(ACADM):c.216+5G>T	rs528788578	0.00003
NM_000016.6(ACADM):c.558T>A (p.Asn186Lys)	rs754359356	0.00003
NM_000016.6(ACADM):c.134A>G (p.Gln45Arg)	rs757434857	0.00002
NM_000016.6(ACADM):c.158G>A (p.Arg53His)	rs754938068	0.00002
NM_000016.6(ACADM):c.668T>C (p.Ile223Thr)	rs758111285	0.00002
NM_000016.6(ACADM):c.709-13A>G	rs746483754	0.00002
NM_000016.6(ACADM):c.1115C>A (p.Ala372Asp)	rs781424858	0.00001
NM_000016.6(ACADM):c.1257C>A (p.Tyr419Ter)	rs753928772	0.00001
NM_000016.6(ACADM):c.395C>G (p.Pro132Arg)	rs875989854	0.00001
NM_000016.6(ACADM):c.447G>T (p.Met149Ile)	rs121434277	0.00001
NM_000016.6(ACADM):c.503A>C (p.Asp168Ala)	rs745844469	0.00001
NM_000016.6(ACADM):c.599+5G>A	rs875989861	0.00001
NM_000016.6(ACADM):c.661G>A (p.Gly221Arg)	rs753627680	0.00001
NM_000016.6(ACADM):c.728G>A (p.Arg243Gln)	rs373852490	0.00001
NM_000016.6(ACADM):c.92G>A (p.Arg31His)	rs529894272	0.00001
NM_000016.6(ACADM):c.1046G>T (p.Arg349Leu)	rs760335676
NM_000016.6(ACADM):c.241G>A (p.Ala81Thr)	rs1448376709
NM_000016.6(ACADM):c.346T>G (p.Cys116Gly)	rs875989863
NM_000016.6(ACADM):c.353G>C (p.Gly118Ala)	rs1647188699
NM_000016.6(ACADM):c.388-19T>A	rs1553123252
NM_000016.6(ACADM):c.424AAG[2] (p.Lys144del)	rs875989857
NM_000016.6(ACADM):c.461T>G (p.Leu154Trp)	rs1553123263
NM_000016.6(ACADM):c.494C>T (p.Ala165Val)	rs1260394550
NM_000016.6(ACADM):c.536_568del (p.Lys179_Lys189del)	rs1553123869
NM_000016.6(ACADM):c.592G>A (p.Ala198Thr)	rs1647485086
NM_000016.6(ACADM):c.622G>T (p.Asp208Tyr)	rs983879715
NM_000016.6(ACADM):c.683C>A (p.Thr228Asn)	rs149678400
NM_000016.6(ACADM):c.946-6T>G	rs765793260

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.