List of variants in gene combination LOC125446261, MLC1 reported as uncertain significance

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_015166.4(MLC1):c.230C>T (p.Pro77Leu)	rs145484765	0.00015
NM_015166.4(MLC1):c.223G>A (p.Val75Met)	rs148848827	0.00011
NM_015166.4(MLC1):c.229C>G (p.Pro77Ala)	rs1259479522	0.00002
NM_015166.4(MLC1):c.240G>A (p.Met80Ile)	rs281875310	0.00001
NM_015166.4(MLC1):c.260C>T (p.Ala87Val)	rs772086919	0.00001
NM_015166.4(MLC1):c.181T>A (p.Cys61Ser)	rs2518359057
NM_015166.4(MLC1):c.183C>A (p.Cys61Ter)	rs1436214826
NM_015166.4(MLC1):c.198G>A (p.Ser66=)	rs199991229
NM_015166.4(MLC1):c.235G>A (p.Glu79Lys)	rs1378938503
NM_015166.4(MLC1):c.247T>A (p.Leu83Met)	rs2518358338
NM_015166.4(MLC1):c.250C>G (p.Arg84Gly)
NM_015166.4(MLC1):c.255T>G (p.Cys85Trp)	rs2146932748
NM_015166.4(MLC1):c.256G>C (p.Ala86Pro)	rs2062186870
NM_015166.4(MLC1):c.257C>T (p.Ala86Val)	rs2518358168
NM_015166.4(MLC1):c.263G>C (p.Gly88Ala)

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