List of variants in gene MMUT reported as benign by GeneDx

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_000255.4(MMUT):c.-39-191A>G	rs9395493	0.59185
NM_000255.4(MMUT):c.386-247C>T	rs7767725	0.59047
NM_000255.4(MMUT):c.2011A>G (p.Ile671Val)	rs8589	0.58978
NM_000255.4(MMUT):c.911+246C>G	rs6915187	0.58575
NM_000255.4(MMUT):c.636G>A (p.Lys212=)	rs2229384	0.58567
NM_000255.3(MMUT):c.-198A>T	rs3729619	0.37031
NM_000255.4(MMUT):c.1083+57C>T	rs7769646	0.37023
NM_000255.4(MMUT):c.1595G>A (p.Arg532His)	rs1141321	0.30110
NM_000255.4(MMUT):c.1333-185A>G	rs4715130	0.30091
NM_000255.4(MMUT):c.1676+77A>C	rs9381786	0.21722
NM_000255.4(MMUT):c.912-110C>T	rs9369901	0.20713
NM_000255.4(MMUT):c.1561-282_1561-281del	rs57922774	0.11183
NM_000255.4(MMUT):c.1495G>A (p.Ala499Thr)	rs2229385	0.10476
NM_000255.4(MMUT):c.1084-195A>G	rs12190697	0.10266
NM_000255.4(MMUT):c.1333-278A>G	rs75427872	0.02063
NM_000255.4(MMUT):c.711A>G (p.Pro237=)	rs138085432	0.00930
NM_000255.4(MMUT):c.1992G>A (p.Ala664=)	rs144146728	0.00839
NM_000255.4(MMUT):c.*278A>G	rs182726681	0.00484
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.1084-50A>G	rs141825870	0.00203
NM_000255.4(MMUT):c.*201del	rs10713340
NM_000255.4(MMUT):c.*201dup	rs10713340
NM_000255.4(MMUT):c.1560+16_1560+17dup	rs56408395
NM_000255.4(MMUT):c.1560+16dup	rs56408395
NM_000255.4(MMUT):c.1594C>G (p.Arg532Gly)	rs764985110
NM_000255.4(MMUT):c.1677-164A>T	rs9463483
NM_000255.4(MMUT):c.1677-53A>G	rs9473557
NM_000255.4(MMUT):c.1808+66C>G	rs9473555
NM_000255.4(MMUT):c.1957-982del	rs35151510
NM_000255.4(MMUT):c.912-138C>T	rs9395492

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