List of variants in gene NDUFS1 reported as likely benign for not specified

Minimum submission review status:		Collection method:
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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: 17

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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.421-7A>G	rs192949406	0.00292
NM_005006.7(NDUFS1):c.1262+17A>G	rs144695826	0.00268
NM_005006.7(NDUFS1):c.153+9A>G	rs200675161	0.00048
NM_005006.7(NDUFS1):c.154-19T>C	rs757724566	0.00028
NM_005006.7(NDUFS1):c.1699A>G (p.Ile567Val)	rs147685849	0.00005
NM_005006.7(NDUFS1):c.1392+19T>C	rs770145746	0.00001
NM_005006.7(NDUFS1):c.1014G>A (p.Val338=)	rs763080348
NM_005006.7(NDUFS1):c.1668A>G (p.Thr556=)	rs1057521895
NM_005006.7(NDUFS1):c.1708+19A>G	rs1171270909
NM_005006.7(NDUFS1):c.253G>A (p.Ala85Thr)	rs774069983
NM_005006.7(NDUFS1):c.551+10T>G	rs1553506824
NM_005006.7(NDUFS1):c.636G>A (p.Lys212=)	rs1553506702
NM_005006.7(NDUFS1):c.738-20A>T	rs200128097
NM_005006.7(NDUFS1):c.933A>G (p.Lys311=)	rs1057523041
NM_005006.7(NDUFS1):c.966G>T (p.Ala322=)	rs1127566
NM_005006.7(NDUFS1):c.987+18dup	rs1212411871

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