MTNR1A[gene] and "single gene"[properties] - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1263722	NC_000004.12:g.186533547T>C	MTNR1A	Single nucleotide variant	not provided	GBenign
Select item 2357305	NM_005958.4(MTNR1A):c.1033G>A (p.Val345Ile)	MTNR1A (V345I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3216925	NM_005958.4(MTNR1A):c.976G>A (p.Asp326Asn)	MTNR1A (D326N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1252210	NM_005958.4(MTNR1A):c.945A>G (p.Thr315=)	MTNR1A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3216923	NM_005958.4(MTNR1A):c.930A>G (p.Ile310Met)	MTNR1A (I310M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1250542	NM_005958.4(MTNR1A):c.924A>G (p.Arg308=)	MTNR1A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3216919	NM_005958.4(MTNR1A):c.839G>C (p.Ser280Thr)	MTNR1A (S280T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216909	NM_005958.4(MTNR1A):c.698A>T (p.Asp233Val)	MTNR1A (D233V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 791529	NM_005958.4(MTNR1A):c.635T>C (p.Ile212Thr)	MTNR1A (I212T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2293602	NM_005958.4(MTNR1A):c.602T>A (p.Ile201Asn)	MTNR1A (I201N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 762676	NM_005958.4(MTNR1A):c.588C>T (p.Phe196=)	MTNR1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3296737	NM_005958.4(MTNR1A):c.506A>T (p.Gln169Leu)	MTNR1A (Q169L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216902	NM_005958.4(MTNR1A):c.474C>T (p.Ala158=)	MTNR1A	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 716546	NM_005958.4(MTNR1A):c.470C>T (p.Ala157Val)	MTNR1A (A157V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3216896	NM_005958.4(MTNR1A):c.442G>A (p.Val148Met)	MTNR1A (V148M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512982	NM_005958.4(MTNR1A):c.337G>A (p.Gly113Ser)	MTNR1A (G113S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231365	NM_005958.4(MTNR1A):c.274G>A (p.Gly92Arg)	MTNR1A (G92R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514471	NM_005958.4(MTNR1A):c.271A>T (p.Asn91Tyr)	MTNR1A (N91Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1181324	NM_005958.4(MTNR1A):c.185-154del	MTNR1A	Deletion (intron variant)	not provided	GBenign
Select item 2372611	NM_005958.4(MTNR1A):c.155T>C (p.Val52Ala)	MTNR1A (V52A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593996	NM_005958.4(MTNR1A):c.13G>C (p.Gly5Arg)	MTNR1A (G5R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254358	NM_005958.4(MTNR1A):c.6G>C (p.Gln2His)	MTNR1A (Q2H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 394745	GRCh37/hg19 4q35.2(chr4:187367725-187476383)x3	MTNR1A	Copy number gain	See cases	Gconflicting data from submitters

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Items: 23