List of variants in gene GLDC reported as likely benign 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: 31

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HGVS	dbSNP	gnomAD frequency
NM_000170.3(GLDC):c.2748G>A (p.Leu916=)	rs139982267	0.00203
NM_000170.3(GLDC):c.40C>A (p.Arg14Ser)	rs182760732	0.00197
NM_000170.3(GLDC):c.2988G>C (p.Gln996His)	rs138640017	0.00112
NM_000170.3(GLDC):c.498T>C (p.Pro166=)	rs150193069	0.00110
NM_000170.3(GLDC):c.1401+9A>G	rs75555848	0.00097
NM_000170.3(GLDC):c.2328C>T (p.Leu776=)	rs149600380	0.00049
NM_000170.3(GLDC):c.1155+91C>T	rs779753406	0.00047
NM_000170.3(GLDC):c.45G>A (p.Gly15=)	rs577986419	0.00045
NM_000170.3(GLDC):c.2874C>T (p.Ser958=)	rs146339375	0.00028
NM_000170.3(GLDC):c.2126A>G (p.Asn709Ser)	rs150943866	0.00026
NM_000170.3(GLDC):c.1581-5C>T	rs184463452	0.00018
NM_000170.3(GLDC):c.2352C>T (p.Pro784=)	rs367781728	0.00017
NM_000170.3(GLDC):c.1926+6T>C	rs200007891	0.00011
NM_000170.3(GLDC):c.78G>C (p.Ser26=)	rs915226152	0.00006
NM_000170.3(GLDC):c.1446C>T (p.Asp482=)	rs201147701	0.00003
NM_000170.3(GLDC):c.84G>T (p.Pro28=)	rs1259938806	0.00003
NM_000170.3(GLDC):c.1359C>T (p.Ala453=)	rs766839627	0.00001
NM_000170.3(GLDC):c.1917G>A (p.Gly639=)	rs776998782	0.00001
NM_000170.3(GLDC):c.1941G>A (p.Pro647=)	rs1232468588	0.00001
NM_000170.3(GLDC):c.2793T>A (p.Ala931=)	rs367759326	0.00001
NM_000170.3(GLDC):c.63C>A (p.Arg21=)	rs372141443	0.00001
NM_000170.3(GLDC):c.96G>T (p.Pro32=)	rs1430526811	0.00001
NM_000170.3(GLDC):c.1167G>C (p.Ala389=)	rs199901045
NM_000170.3(GLDC):c.1262-4G>A	rs549797631
NM_000170.3(GLDC):c.1554G>C (p.Pro518=)	rs377219563
NM_000170.3(GLDC):c.190G>A (p.Ala64Thr)	rs141601131
NM_000170.3(GLDC):c.1927-4G>A	rs576723612
NM_000170.3(GLDC):c.2316-13_2316-12dup	rs3215923
NM_000170.3(GLDC):c.66G>C (p.Leu22=)	rs1337924090
NM_000170.3(GLDC):c.66G>T (p.Leu22=)	rs1337924090
NM_000170.3(GLDC):c.81G>A (p.Gly27=)	rs1457809070

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