"Invitae"[submitter] AND "NRK"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 723211	NM_198465.4(NRK):c.1104C>T (p.His368=)	NRK	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 727510	NM_198465.4(NRK):c.1313G>A (p.Arg438Gln)	NRK (R438Q)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 754464	NM_198465.4(NRK):c.1992C>A (p.Thr664=)	NRK	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 782826	NM_198465.4(NRK):c.2365C>T (p.Pro789Ser)	NRK (P789S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 781556	NM_198465.4(NRK):c.3392A>G (p.Asn1131Ser)	NRK (N1131S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 712402	NM_198465.4(NRK):c.3838T>C (p.Leu1280=)	NRK	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 727874	NM_198465.4(NRK):c.4154T>C (p.Val1385Ala)	NRK (V1385A)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 748568	NM_198465.4(NRK):c.4707A>G (p.Thr1569=)	NRK	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

ClinVar