List of variants in gene MMUT reported as likely benign for classic organic aciduria

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 24

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HGVS	dbSNP	gnomAD frequency
NM_000255.4(MMUT):c.1495G>A (p.Ala499Thr)	rs2229385	0.10476
NM_000255.4(MMUT):c.1992G>A (p.Ala664=)	rs144146728	0.00839
NM_000255.4(MMUT):c.1333-18T>G	rs111667453	0.00608
NM_000255.4(MMUT):c.1629C>T (p.Ser543=)	rs150642856	0.00479
NM_000255.4(MMUT):c.1083+20T>C	rs200148994	0.00356
NM_000255.4(MMUT):c.*34A>G	rs199933641	0.00345
NM_000255.4(MMUT):c.*101G>A	rs113025987	0.00315
NM_000255.4(MMUT):c.1444+13G>A	rs374285380	0.00061
NM_000255.4(MMUT):c.461G>A (p.Arg154His)	rs142068898	0.00028
NM_000255.4(MMUT):c.1084-12C>T	rs373027036	0.00016
NM_000255.4(MMUT):c.2124+16A>G	rs376257828	0.00014
NM_000255.4(MMUT):c.1676+10T>C	rs199886805	0.00009
NM_000255.4(MMUT):c.1956+17G>C	rs199735681	0.00006
NM_000255.4(MMUT):c.912-13G>A	rs542038574	0.00006
NM_000255.4(MMUT):c.756C>T (p.His252=)	rs376716145	0.00004
NM_000255.4(MMUT):c.123A>G (p.Pro41=)	rs753769272	0.00003
NM_000255.4(MMUT):c.1614C>T (p.Thr538=)	rs766999822	0.00003
NM_000255.4(MMUT):c.912-14C>T	rs200394018	0.00002
NM_000255.4(MMUT):c.1512A>G (p.Ala504=)	rs762792688	0.00001
NM_000255.4(MMUT):c.2046T>C (p.Val682=)	rs201456803	0.00001
NM_000255.4(MMUT):c.2082G>A (p.Arg694=)	rs752705830	0.00001
NM_000255.4(MMUT):c.423G>A (p.Ala141=)	rs547142339	0.00001
NM_000255.4(MMUT):c.954A>G (p.Glu318=)	rs1471303851	0.00001
NM_000255.4(MMUT):c.754-7del	rs750770186

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