List of variants in gene MMUT reported as uncertain significance by Natera, Inc.

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: 34

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HGVS	dbSNP	gnomAD frequency
NM_000255.4(MMUT):c.1125G>A (p.Met375Ile)	rs148091558	0.00163
NM_000255.4(MMUT):c.393G>A (p.Gln131=)	rs145682249	0.00116
NM_000255.4(MMUT):c.836A>G (p.Tyr279Cys)	rs2228282	0.00058
NM_000255.4(MMUT):c.1115T>C (p.Ile372Thr)	rs150968643	0.00050
NM_000255.4(MMUT):c.2196C>T (p.Ala732=)	rs201963242	0.00034
NM_000255.4(MMUT):c.878A>G (p.Gln293Arg)	rs138374956	0.00029
NM_000255.4(MMUT):c.1008G>A (p.Met336Ile)	rs150095448	0.00024
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.1421G>A (p.Arg474Gln)	rs368746965	0.00010
NM_000255.4(MMUT):c.2087A>C (p.Asp696Ala)	rs759407117	0.00009
NM_000255.4(MMUT):c.2084C>T (p.Pro695Leu)	rs561197473	0.00004
NM_000255.4(MMUT):c.598A>G (p.Ile200Val)	rs772104231	0.00003
NM_000255.4(MMUT):c.1031C>G (p.Ser344Cys)	rs762281578	0.00002
NM_000255.4(MMUT):c.1355T>A (p.Met452Lys)	rs760718889	0.00002
NM_000255.4(MMUT):c.1532G>A (p.Arg511Gln)	rs776065390	0.00002
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.1261G>A (p.Val421Met)	rs746763824	0.00001
NM_000255.4(MMUT):c.1400G>A (p.Arg467Gln)	rs147737629	0.00001
NM_000255.4(MMUT):c.1476C>T (p.Tyr492=)	rs779301267	0.00001
NM_000255.4(MMUT):c.1494C>T (p.Asp498=)	rs752651149	0.00001
NM_000255.4(MMUT):c.1659G>A (p.Val553=)	rs764316430	0.00001
NM_000255.4(MMUT):c.2082G>A (p.Arg694=)	rs752705830	0.00001
NM_000255.4(MMUT):c.241T>A (p.Leu81Ile)	rs150841850	0.00001
NM_000255.4(MMUT):c.406G>A (p.Val136Ile)	rs1767739165	0.00001
NM_000255.4(MMUT):c.422C>T (p.Ala141Val)	rs565348836	0.00001
NM_000255.4(MMUT):c.53A>G (p.Gln18Arg)	rs372601759	0.00001
NM_000255.4(MMUT):c.656A>G (p.Asn219Ser)	rs950211877	0.00001
NM_000255.4(MMUT):c.1499T>C (p.Val500Ala)	rs766908649
NM_000255.4(MMUT):c.754C>T (p.His252Tyr)	rs796052010

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