chr11-27672444-C-G

Variant names:

• chr11-27672444-C-G
• rs1401635
• NM_001709.5:c.-21-13859G>C

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_001709.5(BDNF):​c.-21-13859G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.727 in 151,966 control chromosomes in the GnomAD database, including 40,435 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.73 (40435 hom., cov: 30)
• Consequence: BDNF NM_001709.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0390
• Publications: 16 publications found

Genes affected

BDNF (HGNC:1033): (brain derived neurotrophic factor) This gene encodes a member of the nerve growth factor family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature protein. Binding of this protein to its cognate receptor promotes neuronal survival in the adult brain. Expression of this gene is reduced in Alzheimer's, Parkinson's, and Huntington's disease patients. This gene may play a role in the regulation of the stress response and in the biology of mood disorders. [provided by RefSeq, Nov 2015]

BDNF-AS (HGNC:20608): (BDNF antisense RNA)

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.926 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001709.5. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	BDNF	NM_001709.5	MANE Select	c.-21-13859G>C		intron	N/A	NP_001700.2
	BDNF	NM_001143810.2		c.225+1616G>C		intron	N/A	NP_001137282.1
	BDNF	NM_001143809.2		c.67-13859G>C		intron	N/A	NP_001137281.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	BDNF	ENST00000356660.9	TSL:1 MANE Select	c.-21-13859G>C		intron	N/A	ENSP00000349084.4
	BDNF	ENST00000438929.5	TSL:1	c.225+1616G>C		intron	N/A	ENSP00000414303.1
	BDNF	ENST00000395986.6	TSL:1	c.25-13859G>C		intron	N/A	ENSP00000379309.2

Frequencies

GnomAD3 genomes AF: 0.727 AC: 110408 AN: 151848 Hom.: 40413 Cov.: 30

Gnomad AFR AF: 0.756

Gnomad AMI AF: 0.794

Gnomad AMR AF: 0.757

Gnomad ASJ AF: 0.820

Gnomad EAS AF: 0.949

Gnomad SAS AF: 0.649

Gnomad FIN AF: 0.668

Gnomad MID AF: 0.785

Gnomad NFE AF: 0.694

Gnomad OTH AF: 0.736

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.727 AC: 110478 AN: 151966 Hom.: 40435 Cov.: 30 AF XY: 0.729 AC XY: 54115 AN XY: 74260

African (AFR) AF: 0.756 AC: 31349 AN: 41472

American (AMR) AF: 0.758 AC: 11554 AN: 15252

Ashkenazi Jewish (ASJ) AF: 0.820 AC: 2847 AN: 3470

East Asian (EAS) AF: 0.949 AC: 4900 AN: 5166

South Asian (SAS) AF: 0.648 AC: 3108 AN: 4798

European-Finnish (FIN) AF: 0.668 AC: 7047 AN: 10554

Middle Eastern (MID) AF: 0.803 AC: 236 AN: 294

European-Non Finnish (NFE) AF: 0.694 AC: 47164 AN: 67940

Other (OTH) AF: 0.735 AC: 1549 AN: 2108

Alfa AF: 0.717 Hom.: 4877

Bravo AF: 0.737

Asia WGS AF: 0.738 AC: 2566 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	1.5
DANN	Benign	0.38
PhyloP100		-0.039
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs1401635; hg19: chr11-27693991;