"BDNF-related condition"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

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Items: 37

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2636918	NM_001709.5(BDNF):c.691A>G (p.Ile231Val)	BDNF, BDNF-AS (I231V +4 more)	Single nucleotide variant (missense variant)	BDNF-related condition	GUncertain significance
Select item 2630210	NM_001709.5(BDNF):c.659T>C (p.Met220Thr)	BDNF, BDNF-AS (M220T +4 more)	Single nucleotide variant (missense variant)	BDNF-related condition	GUncertain significance
Select item 712726	NM_001709.5(BDNF):c.546C>T (p.Tyr182=)	BDNF, BDNF-AS	Single nucleotide variant (synonymous variant)	BDNF-related condition +1 more	GBenign/Likely benign
Select item 743862	NM_001709.5(BDNF):c.483C>T (p.Gly161=)	BDNF, BDNF-AS	Single nucleotide variant (synonymous variant)	BDNF-related condition +1 more	GLikely benign
Select item 3043298	NM_001709.5(BDNF):c.480G>A (p.Ser160=)	BDNF, BDNF-AS	Single nucleotide variant (synonymous variant)	BDNF-related condition	GLikely benign
Select item 3030169	NM_001709.5(BDNF):c.465T>C (p.Thr155=)	BDNF, BDNF-AS	Single nucleotide variant (synonymous variant)	BDNF-related condition	GLikely benign
Select item 2309743	NM_001709.5(BDNF):c.447G>A (p.Thr149=)	BDNF, BDNF-AS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +2 more	GLikely benign
Select item 2628764	NM_001709.5(BDNF):c.365T>C (p.Met122Thr)	BDNF, BDNF-AS (M122T +4 more)	Single nucleotide variant (missense variant)	BDNF-related condition	GUncertain significance
Select item 3045600	NM_001709.5(BDNF):c.309G>A (p.Glu103=)	BDNF, BDNF-AS	Single nucleotide variant (non-coding transcript variant +1 more)	BDNF-related condition	GLikely benign
Select item 1572707	NM_001709.5(BDNF):c.273G>A (p.Thr91=)	BDNF, BDNF-AS	Single nucleotide variant (non-coding transcript variant +1 more)	BDNF-related condition +1 more	GLikely benign
Select item 2759722	NM_001709.5(BDNF):c.258C>T (p.Asp86=)	BDNF, BDNF-AS	Single nucleotide variant (non-coding transcript variant +1 more)	BDNF-related condition +1 more	GLikely benign
Select item 3058922	NM_001709.5(BDNF):c.239A>G (p.Asn80Ser)	BDNF, BDNF-AS (N109S +4 more)	Single nucleotide variant (non-coding transcript variant +1 more)	BDNF-related condition	GUncertain significance
Select item 2628592	NM_001709.5(BDNF):c.226A>G (p.Lys76Glu)	BDNF, BDNF-AS (K105E +4 more)	Single nucleotide variant (non-coding transcript variant +1 more)	BDNF-related condition	GUncertain significance
Select item 2411940	NM_001709.5(BDNF):c.223C>G (p.Gln75Glu)	BDNF, BDNF-AS (Q157E +4 more)	Single nucleotide variant (non-coding transcript variant +1 more)	BDNF-related condition +1 more	GConflicting classifications of pathogenicity
Select item 3058089	NM_001709.5(BDNF):c.195C>T (p.His65=)	BDNF, BDNF-AS	Single nucleotide variant (synonymous variant +1 more)	BDNF-related condition	GLikely benign
Select item 3050887	NM_001709.5(BDNF):c.154G>A (p.Gly52Ser)	BDNF, BDNF-AS (G134S +4 more)	Single nucleotide variant (non-coding transcript variant +1 more)	BDNF-related condition	GUncertain significance
Select item 2636085	NM_001709.5(BDNF):c.136G>A (p.Val46Met)	BDNF, BDNF-AS (V128M +4 more)	Single nucleotide variant (non-coding transcript variant +1 more)	BDNF-related condition +1 more	GUncertain significance
Select item 3060439	NM_001709.5(BDNF):c.135C>T (p.Ser45=)	BDNF, BDNF-AS	Single nucleotide variant (non-coding transcript variant +1 more)	BDNF-related condition	GLikely benign
Select item 2634377	NM_001709.5(BDNF):c.113G>A (p.Arg38Gln)	BDNF, BDNF-AS (R120Q +4 more)	Single nucleotide variant (missense variant +1 more)	BDNF-related condition	GUncertain significance
Select item 3030850	NM_001709.5(BDNF):c.102C>T (p.Tyr34=)	BDNF, BDNF-AS	Single nucleotide variant (synonymous variant)	BDNF-related condition	GLikely benign
Select item 2634388	NM_001709.5(BDNF):c.92G>A (p.Gly31Asp)	BDNF, BDNF-AS (G113D +4 more)	Single nucleotide variant (missense variant)	BDNF-related condition	GUncertain significance
Select item 2631517	NM_001709.5(BDNF):c.5C>A (p.Thr2Asn)	BDNF, BDNF-AS (T10N +4 more)	Single nucleotide variant (missense variant)	BDNF-related condition	GUncertain significance
Select item 17696	NM_001709.5(BDNF):c.5C>T (p.Thr2Ile)	BDNF, BDNF-AS (T2I +4 more)	Single nucleotide variant (missense variant)	BDNF-related condition +3 more	GConflicting classifications of pathogenicity
Select item 2631964	NM_001709.5(BDNF):c.-21-15481C>A	BDNF, BDNF-AS (F73L)	Single nucleotide variant (missense variant +2 more)	BDNF-related condition	GUncertain significance
Select item 2635840	NM_001709.5(BDNF):c.-21-15487T>G	BDNF, BDNF-AS (N71K)	Single nucleotide variant (missense variant +2 more)	BDNF-related condition	GUncertain significance
Select item 2634443	NM_001709.5(BDNF):c.-21-15496C>G	BDNF, BDNF-AS (I68M)	Single nucleotide variant (missense variant +2 more)	BDNF-related condition	GUncertain significance
Select item 2633136	NM_001709.5(BDNF):c.-21-15533T>C	BDNF, BDNF-AS (V56A)	Single nucleotide variant (missense variant +2 more)	BDNF-related condition	GUncertain significance
Select item 3048025	NM_001709.5(BDNF):c.-21-15571A>G	BDNF, BDNF-AS	Single nucleotide variant (synonymous variant +2 more)	BDNF-related condition	GLikely benign
Select item 3030133	NM_001709.5(BDNF):c.-21-15592C>T	BDNF, BDNF-AS	Single nucleotide variant (synonymous variant +2 more)	BDNF-related condition	GLikely benign
Select item 1299836	NM_001709.5(BDNF):c.-21-15601_-21-15600del	BDNF, BDNF-AS (C34fs)	Deletion (frameshift variant +2 more)	BDNF-related condition	GLikely benign
Select item 3034836	NM_001709.5(BDNF):c.-21-15601A>G	BDNF, BDNF-AS	Single nucleotide variant (synonymous variant +2 more)	BDNF-related condition	GLikely benign
Select item 3046400	NM_001709.5(BDNF):c.-21-15610G>A	BDNF, BDNF-AS	Single nucleotide variant (synonymous variant +2 more)	BDNF-related condition	GLikely benign
Select item 2634288	NM_001709.5(BDNF):c.-21-15659_-21-15656dup	BDNF, BDNF-AS (L16fs)	Duplication (intron variant +2 more)	BDNF-related condition	GUncertain significance
Select item 3044706	NM_001143809.2(BDNF):c.66+8T>C	BDNF	Single nucleotide variant (intron variant)	BDNF-related condition	GLikely benign
Select item 1050281	NM_001143808.2(BDNF):c.-22+2T>G	BDNF (C20G)	Single nucleotide variant (missense variant +3 more)	BDNF-related condition	GUncertain significance
Select item 2635757	NM_001143809.2(BDNF):c.49G>A (p.Ala17Thr)	BDNF (A17T)	Single nucleotide variant (5 prime UTR variant +2 more)	BDNF-related condition	GUncertain significance
Select item 3050817	NM_001143809.2(BDNF):c.39G>C (p.Lys13Asn)	BDNF (K13N)	Single nucleotide variant (5 prime UTR variant +2 more)	BDNF-related condition	GLikely benign

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Items: 37