List of variants in gene MMUT reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 36

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HGVS	dbSNP	gnomAD frequency
NM_000255.4(MMUT):c.1115T>C (p.Ile372Thr)	rs150968643	0.00050
NM_000255.4(MMUT):c.1417G>T (p.Ala473Ser)	rs188766510	0.00033
NM_000255.4(MMUT):c.878A>G (p.Gln293Arg)	rs138374956	0.00029
NM_000255.4(MMUT):c.284C>T (p.Pro95Leu)	rs190834116	0.00019
NM_000255.4(MMUT):c.781A>G (p.Ile261Val)	rs375054307	0.00019
NM_000255.4(MMUT):c.1332+3A>C	rs367641890	0.00018
NM_000255.4(MMUT):c.1763G>T (p.Arg588Leu)	rs141829043	0.00018
NM_000255.4(MMUT):c.1865T>C (p.Met622Thr)	rs201536536	0.00015
NM_000255.4(MMUT):c.1777G>C (p.Glu593Gln)	rs148285323	0.00013
NM_000255.4(MMUT):c.2087A>C (p.Asp696Ala)	rs759407117	0.00009
NM_000255.4(MMUT):c.1963C>T (p.Arg655Cys)	rs541001298	0.00007
NM_000255.4(MMUT):c.912G>A (p.Arg304=)	rs201311681	0.00006
NM_000255.4(MMUT):c.1630G>A (p.Gly544Arg)	rs78150750	0.00005
NM_000255.4(MMUT):c.1607C>T (p.Ala536Val)	rs369902876	0.00004
NM_000255.4(MMUT):c.2084C>T (p.Pro695Leu)	rs561197473	0.00004
NM_000255.4(MMUT):c.161A>G (p.Lys54Arg)	rs559152765	0.00002
NM_000255.4(MMUT):c.227G>A (p.Arg76Lys)	rs1252414363	0.00002
NM_000255.4(MMUT):c.431G>A (p.Arg144His)	rs776621768	0.00002
NM_000255.4(MMUT):c.1091A>C (p.Tyr364Ser)	rs563776413	0.00001
NM_000255.4(MMUT):c.1261G>A (p.Val421Met)	rs746763824	0.00001
NM_000255.4(MMUT):c.1400G>A (p.Arg467Gln)	rs147737629	0.00001
NM_000255.4(MMUT):c.1669C>T (p.Arg557Trp)	rs886061559	0.00001
NM_000255.4(MMUT):c.1828C>T (p.Arg610Cys)	rs770978452	0.00001
NM_000255.4(MMUT):c.1906A>G (p.Thr636Ala)	rs569669261	0.00001
NM_000255.4(MMUT):c.1970T>C (p.Val657Ala)	rs1767102899	0.00001
NM_000255.4(MMUT):c.2206C>T (p.Leu736Phe)	rs753461919	0.00001
NM_000255.4(MMUT):c.359A>G (p.Asn120Ser)	rs776108716	0.00001
NM_000255.4(MMUT):c.406G>A (p.Val136Ile)	rs1767739165	0.00001
NM_000255.4(MMUT):c.499G>A (p.Val167Met)	rs755709278	0.00001
NM_000255.4(MMUT):c.556A>G (p.Met186Val)	rs148331800	0.00001
NM_000255.4(MMUT):c.-35G>T	rs483352795
NM_000255.4(MMUT):c.1415C>T (p.Ala472Val)	rs747589392
NM_000255.4(MMUT):c.1421G>C (p.Arg474Pro)	rs368746965
NM_000255.4(MMUT):c.1670G>A (p.Arg557Gln)	rs756389945
NM_000255.4(MMUT):c.188C>T (p.Thr63Ile)	rs1767776360
NM_000255.4(MMUT):c.733A>G (p.Ile245Val)	rs754464973

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