ADPRH[gene] and "single gene"[properties] - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3273553	NM_001125.4(ADPRH):c.308C>T (p.Ser103Leu)	ADPRH (S103L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3090204	NM_001125.4(ADPRH):c.399G>A (p.Met133Ile)	ADPRH (M133I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594057	NM_001125.4(ADPRH):c.415G>C (p.Gly139Arg)	ADPRH (G32R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294545	NM_001125.4(ADPRH):c.418C>T (p.Leu140Phe)	ADPRH (L140F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207238	NM_001125.4(ADPRH):c.479G>A (p.Arg160Gln)	ADPRH (R160Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496109	NM_001125.4(ADPRH):c.490C>G (p.His164Asp)	ADPRH (H164D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408302	NM_001125.4(ADPRH):c.706A>G (p.Ile236Val)	ADPRH (I129V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3090225	NM_001125.4(ADPRH):c.763G>C (p.Asp255His)	ADPRH (D255H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312205	NM_001125.4(ADPRH):c.790T>C (p.Ser264Pro)	ADPRH (S264P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461733	NM_001125.4(ADPRH):c.831T>G (p.Ile277Met)	ADPRH (I170M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612940	NM_001125.4(ADPRH):c.844G>A (p.Val282Ile)	ADPRH (V175I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3090240	NM_001125.4(ADPRH):c.873G>T (p.Glu291Asp)	ADPRH (E184D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3090243	NM_001125.4(ADPRH):c.877G>A (p.Ala293Thr)	ADPRH (A293T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273572	NM_001125.4(ADPRH):c.886G>A (p.Ala296Thr)	ADPRH (A296T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance