List of variants in gene NDUFS1 reported by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_005006.7(NDUFS1):c.1251A>G (p.Arg417=)	rs1801318	0.34874
NM_005006.7(NDUFS1):c.414T>C (p.Asp138=)	rs11548670	0.05713
NM_005006.7(NDUFS1):c.1371G>A (p.Ser457=)	rs2230892	0.01121
NM_005006.7(NDUFS1):c.1291C>G (p.Leu431Val)	rs78042826	0.00353
NM_005006.7(NDUFS1):c.153+9A>G	rs200675161	0.00048
NM_005006.7(NDUFS1):c.873-9G>A	rs180899908	0.00048
NM_005006.7(NDUFS1):c.1516G>A (p.Val506Ile)	rs137889316	0.00034
NM_005006.7(NDUFS1):c.1029T>G (p.Gly343=)	rs72944827	0.00021
NM_005006.7(NDUFS1):c.1186G>A (p.Glu396Lys)	rs141724890	0.00009
NM_005006.7(NDUFS1):c.1235C>T (p.Pro412Leu)	rs751150787	0.00003
NM_005006.7(NDUFS1):c.154-10_154-9del	rs568965659
NM_005006.7(NDUFS1):c.154-11_154-9del	rs568965659
NM_005006.7(NDUFS1):c.154-12_154-9del	rs568965659
NM_005006.7(NDUFS1):c.154-9del	rs568965659
NM_005006.7(NDUFS1):c.966G>T (p.Ala322=)	rs1127566

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