"Ambry Genetics"[submitter] AND "CRHR2"[gene] - ClinVar

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Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3077423	NM_001883.5(CRHR2):c.1223C>T (p.Thr408Met)	CRHR2 (T435M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2301722	NM_001883.5(CRHR2):c.1180C>T (p.Pro394Ser)	CRHR2 (P393S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3269503	NM_001883.5(CRHR2):c.1134G>T (p.Gln378His)	CRHR2 (Q378H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3077422	NM_001883.5(CRHR2):c.1099C>T (p.Arg367Cys)	CRHR2 (R367C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2610342	NM_001883.5(CRHR2):c.1030A>G (p.Asn344Asp)	CRHR2, LOC126859981 (N371D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251868	NM_001883.5(CRHR2):c.1011G>C (p.Gln337His)	CRHR2, LOC126859981 (Q336H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3269504	NM_001883.5(CRHR2):c.978C>A (p.Phe326Leu)	CRHR2, LOC126859981 (F353L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383249	NM_001883.5(CRHR2):c.971T>C (p.Met324Thr)	CRHR2, LOC126859981 (M351T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220472	NM_001883.5(CRHR2):c.904A>G (p.Thr302Ala)	CRHR2 (T301A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355538	NM_001883.5(CRHR2):c.890C>T (p.Ser297Phe)	CRHR2 (S283F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597754	NM_001883.5(CRHR2):c.883C>T (p.Arg295Cys)	CRHR2 (R281C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077427	NM_001883.5(CRHR2):c.786C>G (p.Asp262Glu)	CRHR2 (D262E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511806	NM_001883.5(CRHR2):c.784G>A (p.Asp262Asn)	CRHR2 (D289N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3269505	NM_001883.5(CRHR2):c.753T>G (p.Asn251Lys)	CRHR2 (N237K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077426	NM_001883.5(CRHR2):c.743A>G (p.Tyr248Cys)	CRHR2 (Y248C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315857	NM_001883.5(CRHR2):c.709C>T (p.Pro237Ser)	CRHR2 (P223S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524015	NM_001883.5(CRHR2):c.698G>A (p.Cys233Tyr)	CRHR2 (C232Y +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264227	NM_001883.5(CRHR2):c.662G>A (p.Arg221His)	CRHR2 (R207H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289996	NM_001883.5(CRHR2):c.661C>T (p.Arg221Cys)	CRHR2 (R220C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3269502	NM_001883.5(CRHR2):c.583G>A (p.Val195Met)	CRHR2 (V195M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249581	NM_001883.5(CRHR2):c.580T>A (p.Phe194Ile)	CRHR2 (F180I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234652	NM_001883.5(CRHR2):c.577T>A (p.Tyr193Asn)	CRHR2 (Y179N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077425	NM_001883.5(CRHR2):c.414C>A (p.Phe138Leu)	CRHR2 (F124L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597682	NM_001883.5(CRHR2):c.343A>G (p.Ile115Val)	CRHR2 (I114V +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2312363	NM_001883.5(CRHR2):c.337T>C (p.Tyr113His)	CRHR2 (Y140H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369484	NM_001883.5(CRHR2):c.197A>C (p.Glu66Ala)	CRHR2 (E66A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549494	NM_001883.5(CRHR2):c.196G>A (p.Glu66Lys)	CRHR2 (E52K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241603	NM_001202475.1(CRHR2):c.108G>C (p.Gln36His)	CRHR2 (Q36H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 28