List of variants in gene GCLC reported as benign for not provided

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_001498.4(GCLC):c.560+194G>A	rs553822	0.65518
NM_001498.4(GCLC):c.753+140dup	rs11385177	0.55074
NM_001498.4(GCLC):c.1395+83A>G	rs661603	0.52911
NM_001498.4(GCLC):c.561-110T>G	rs3736729	0.44155
NM_001498.4(GCLC):c.446+101G>A	rs2100375	0.27878
NM_001498.4(GCLC):c.1396-63G>A	rs2066511	0.24533
NM_001498.4(GCLC):c.446+233G>A	rs761141	0.20325
NM_001498.4(GCLC):c.1291-101G>A	rs524553	0.19789
NM_001498.4(GCLC):c.945+288T>C	rs9474576	0.19407
NM_001498.4(GCLC):c.1395+176C>T	rs2277108	0.19148
NM_001498.4(GCLC):c.1198-59T>A	rs1014852	0.18958
NM_001498.4(GCLC):c.1084+133A>G	rs1555903	0.17967
NM_001498.4(GCLC):c.945+196C>G	rs2235707	0.16567
NM_001498.4(GCLC):c.1703-19G>A	rs17885800	0.11413
NM_001498.4(GCLC):c.828+203G>A	rs16883912	0.11189
NM_001498.4(GCLC):c.1197+251T>C	rs12524494	0.09274
NM_001498.4(GCLC):c.1703-183C>G	rs16883893	0.09221
NC_000006.12:g.53545239G>A	rs17883901	0.06174
NM_001498.4(GCLC):c.234G>T (p.Leu78=)	rs2066508	0.02913
NM_001498.4(GCLC):c.1384C>T (p.Pro462Ser)	rs17883718	0.01172
NM_001498.4(GCLC):c.528A>G (p.Pro176=)	rs34307437	0.00956
NM_001498.4(GCLC):c.1524G>A (p.Thr508=)	rs17881359	0.00669
NM_001498.4(GCLC):c.1563C>T (p.Asp521=)	rs2066509	0.00368
NM_001498.4(GCLC):c.1478-16C>A	rs185146268	0.00306
NM_001498.4(GCLC):c.1478-6C>T	rs17880746	0.00218
NM_001498.4(GCLC):c.1703-11C>G	rs2066507	0.00201
NM_001498.4(GCLC):c.984A>T (p.Arg328=)	rs181411098	0.00010
NM_001498.4(GCLC):c.1632C>T (p.Asn544=)	rs913611013	0.00001
NM_001498.4(GCLC):c.*59AGCC[1]	rs1805189
NM_001498.4(GCLC):c.1581+26C>G	rs661346
NM_001498.4(GCLC):c.1703-45del	rs17880610
NM_001498.4(GCLC):c.560+325del	rs5876317
NM_001498.4(GCLC):c.561-222G>T	rs17884046
NM_001498.4(GCLC):c.829-116_829-115insGGTGGA	rs3830795

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