GRPR[gene] and "single gene"[properties] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 721453	NM_005314.3(GRPR):c.17G>C (p.Cys6Ser)	GRPR (C6S)	Single nucleotide variant (missense variant)	GRPR-related disorder +1 more	GLikely benign
Select item 2350459	NM_005314.3(GRPR):c.79G>A (p.Asp27Asn)	GRPR (D27N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3051058	NM_005314.3(GRPR):c.110C>T (p.Pro37Leu)	GRPR (P37L)	Single nucleotide variant (missense variant)	GRPR-related disorder	GLikely benign
Select item 3102732	NM_005314.3(GRPR):c.200C>G (p.Thr67Arg)	GRPR (T67R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1297568	NM_005314.3(GRPR):c.242G>A (p.Ser81Asn)	GRPR (S81N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272012	NM_005314.3(GRPR):c.252G>T (p.Leu84Phe)	GRPR (L84F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102733	NM_005314.3(GRPR):c.259C>G (p.Leu87Val)	GRPR (L87V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309893	NM_005314.3(GRPR):c.286G>A (p.Val96Met)	GRPR (V96M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344739	NM_005314.3(GRPR):c.355A>G (p.Ile119Val)	GRPR (I119V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 790473	NM_005314.3(GRPR):c.396G>A (p.Thr132=)	GRPR	Single nucleotide variant (synonymous variant)	GRPR-related disorder +1 more	GBenign
Select item 2622311	NM_005314.3(GRPR):c.471C>G (p.Ile157Met)	GRPR (I157M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 753760	NM_005314.3(GRPR):c.504C>T (p.Ser168=)	GRPR	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 785695	NM_005314.3(GRPR):c.639T>C (p.Ala213=)	GRPR	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 780684	NM_005314.3(GRPR):c.658G>A (p.Val220Ile)	GRPR (V220I)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2612278	NM_005314.3(GRPR):c.691T>C (p.Tyr231His)	GRPR (Y231H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3053094	NM_005314.3(GRPR):c.784C>G (p.Leu262Val)	GRPR (L262V)	Single nucleotide variant (missense variant)	GRPR-related disorder	GLikely benign
Select item 2282171	NM_005314.3(GRPR):c.860G>T (p.Arg287Leu)	GRPR (R287L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2660062	NM_005314.3(GRPR):c.903T>C (p.Phe301=)	GRPR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 788755	NM_005314.3(GRPR):c.1011G>C (p.Leu337=)	GRPR	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3102731	NM_005314.3(GRPR):c.1040G>A (p.Arg347Gln)	GRPR (R347Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389415	NM_005314.3(GRPR):c.1067C>T (p.Thr356Ile)	GRPR (T356I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 748394	NM_005314.3(GRPR):c.1086G>A (p.Lys362=)	GRPR	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2256147	NM_005314.3(GRPR):c.1133T>A (p.Ile378Asn)	GRPR (I378N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2660063	NM_005314.3(GRPR):c.1140C>T (p.His380=)	GRPR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 745044	NM_005314.3(GRPR):c.1152C>G (p.Val384=)	GRPR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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Items: 25