"Australian Red Cross Blood Service"[submitter] AND "RHD"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 619080	NM_016124.6(RHD):c.270G>C (p.Trp90Cys)	RHD, RSRP1 (W90C)	Single nucleotide variant (missense variant +2 more)	Weakened expression of D antigen	GAffects
Select item 1185564	NM_016124.6(RHD):c.277_278delinsGG (p.Leu93Gly)	RHD, RSRP1 (L93G)	Indel (missense variant +2 more)	weakened D expression by serology	GAffects
Select item 1300199	NM_016124.6(RHD):c.341G>C (p.Arg114Pro)	RHD, RSRP1 (R114P)	Single nucleotide variant (missense variant +2 more)	weakened D expression by serology	GAffects
Select item 253025	NM_016124.6(RHD):c.452G>A (p.Gly151Asp)	RHD, RSRP1 (G151D)	Single nucleotide variant (missense variant +2 more)	Blood group antigen abnormality	GAffects
Select item 1185596	NM_016124.6(RHD):c.709G>A (p.Ala237Thr)	RSRP1, RHD (A237T +1 more)	Single nucleotide variant (missense variant +1 more)	weakened D expression by serology	GAffects
Select item 1185597	NM_016124.6(RHD):c.[186G>T;410C>T455A>C602C>G604G>A733G>C]	RHD, RSRP1 (V245L +8 more)	Single nucleotide variant (missense variant +2 more)	altered RHD phenotype	GAffects
Select item 242592	NM_016124.6(RHD):c.1063G>A (p.Gly355Ser)	RSRP1, RHD (G355S +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	Anti-D isoimmunization affecting pregnancy +1 more	Grisk factor

ClinVar