List of variants in gene DLD reported as likely 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: 49

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HGVS	dbSNP	gnomAD frequency
NM_000108.5(DLD):c.338-81T>A	rs117252390	0.01669
NM_000108.5(DLD):c.875+124A>G	rs10238360	0.01383
NM_000108.5(DLD):c.198+253A>G	rs17154585	0.01287
NM_000108.5(DLD):c.876-253G>A	rs190908520	0.01008
NM_000108.5(DLD):c.685-153A>G	rs74333086	0.00988
NM_000108.5(DLD):c.438+43A>C	rs112595657	0.00986
NM_000108.5(DLD):c.*648G>A	rs57801571	0.00985
NM_000108.5(DLD):c.1237-102C>G	rs111661705	0.00985
NC_000007.14:g.107921300C>T	rs111877251	0.00983
NM_000108.5(DLD):c.1465-30G>T	rs78719279	0.00983
NM_000108.5(DLD):c.583-79T>C	rs113165651	0.00983
NM_000108.5(DLD):c.876-250T>C	rs183150245	0.00981
NM_000108.5(DLD):c.39+317G>C	rs75897288	0.00938
NM_000108.5(DLD):c.876-173G>A	rs112222905	0.00935
NM_000108.5(DLD):c.337+105A>G	rs2701043	0.00934
NM_000108.5(DLD):c.338-282G>A	rs75116491	0.00934
NM_000108.5(DLD):c.876-54C>G	rs116765230	0.00932
NM_000108.5(DLD):c.268-291C>T	rs113218317	0.00919
NM_000108.5(DLD):c.875+159C>A	rs75968761	0.00879
NM_000108.5(DLD):c.337+154A>C	rs149266807	0.00831
NM_000108.5(DLD):c.199-210A>T	rs111916412	0.00749
NM_000108.5(DLD):c.268-104G>A	rs114802532	0.00479
NM_000108.5(DLD):c.876-174C>T	rs113123129	0.00477
NM_000108.5(DLD):c.1375-232A>G	rs76408129	0.00449
NM_000108.5(DLD):c.*474T>C	rs16872391	0.00443
NM_000108.5(DLD):c.684+105G>C	rs115442960	0.00408
NM_000108.5(DLD):c.119-79T>G	rs189432944	0.00383
NM_000108.5(DLD):c.39+209C>T	rs115778377	0.00377
NM_000108.5(DLD):c.507C>T (p.Gly169=)	rs144351432	0.00224
NM_000108.5(DLD):c.826A>T (p.Thr276Ser)	rs148873419	0.00163
NM_000108.5(DLD):c.321A>G (p.Ala107=)	rs138398782	0.00022
NM_000108.5(DLD):c.1395T>C (p.Asn465=)	rs76313180	0.00021
NM_000108.5(DLD):c.282C>T (p.Asn94=)	rs144617361	0.00018
NM_000108.5(DLD):c.119-4G>A	rs376605135	0.00008
NM_000108.5(DLD):c.1452T>C (p.Cys484=)	rs760982359	0.00008
NM_000108.5(DLD):c.-42C>T	rs200830300	0.00003
NM_000108.5(DLD):c.-7C>G	rs761428885	0.00003
NM_000108.5(DLD):c.869A>G (p.Asp290Gly)	rs143555186	0.00003
NM_000108.5(DLD):c.1182C>T (p.Tyr394=)	rs757087726	0.00001
NM_000108.5(DLD):c.96G>C (p.Leu32=)	rs765623212	0.00001
NM_000108.5(DLD):c.*295del	rs139767397
NM_000108.5(DLD):c.*470G>T	rs111619940
NM_000108.5(DLD):c.-31G>A	rs374293887
NM_000108.5(DLD):c.118+191C>T	rs187885501
NM_000108.5(DLD):c.1236+204A>G	rs79008145
NM_000108.5(DLD):c.1236+7C>T	rs1554400485
NM_000108.5(DLD):c.199-6T>C	rs1584462430
NM_000108.5(DLD):c.267+117C>G	rs146985203
NM_000108.5(DLD):c.875+226T>G	rs77611523

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