List of variants in gene MMUT reported as uncertain significance by Counsyl

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_000255.4(MMUT):c.2197G>A (p.Val733Ile)	rs1183369398	0.00025
NM_000255.4(MMUT):c.277C>T (p.Arg93Cys)	rs746274670	0.00006
NM_000255.4(MMUT):c.1208G>A (p.Arg403Gln)	rs774457503	0.00003
NM_000255.4(MMUT):c.1669C>T (p.Arg557Trp)	rs886061559	0.00001
NM_000255.4(MMUT):c.2206C>T (p.Leu736Phe)	rs753461919	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.1156C>A (p.His386Asn)	rs1554159937
NM_000255.4(MMUT):c.1219A>T (p.Asn407Tyr)	rs576536579
NM_000255.4(MMUT):c.1679G>A (p.Cys560Tyr)	rs1238333040
NM_000255.4(MMUT):c.1790T>G (p.Ile597Arg)	rs1554158951
NM_000255.4(MMUT):c.1844C>G (p.Pro615Arg)	rs1554158777
NM_000255.4(MMUT):c.1850T>G (p.Leu617Arg)	rs1554158775
NM_000255.4(MMUT):c.260G>A (p.Gly87Glu)	rs1554160986
NM_000255.4(MMUT):c.41A>T (p.His14Leu)	rs886061561
NM_000255.4(MMUT):c.421G>A (p.Ala141Thr)	rs1554160730
NM_000255.4(MMUT):c.669_674dup (p.Glu224_Phe225insLeuGlu)	rs1554160637
NM_000255.4(MMUT):c.917C>T (p.Ser306Phe)	rs1085307929

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