List of variants in gene NARS2 reported by CeGaT Center for Human Genetics Tuebingen

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_024678.6(NARS2):c.1289+7A>G	rs201591441	0.00236
NM_024678.6(NARS2):c.25C>T (p.Arg9Trp)	rs141907023	0.00153
NM_024678.6(NARS2):c.369C>T (p.Ala123=)	rs151326892	0.00118
NM_024678.6(NARS2):c.1082A>G (p.Asn361Ser)	rs150355410	0.00054
NM_024678.6(NARS2):c.1262+6G>A	rs185461968	0.00037
NM_024678.6(NARS2):c.492T>C (p.Ala164=)	rs369110182	0.00021
NM_024678.6(NARS2):c.1027-1412A>G
NM_024678.6(NARS2):c.1027-1444C>G
NM_024678.6(NARS2):c.1096G>A (p.Val366Ile)	rs765813020
NM_024678.6(NARS2):c.1290-36A>G
NM_024678.6(NARS2):c.392A>G (p.Lys131Arg)
NM_024678.6(NARS2):c.636T>C (p.Asn212=)
NM_024678.6(NARS2):c.791C>G (p.Ser264Cys)
NM_024678.6(NARS2):c.87C>T (p.Ser29=)

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