rs17139163

chr7-18399448-A-G

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_001321868.2(HDAC9):c.26-96814A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0183 in 152,306 control chromosomes in the GnomAD database, including 44 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 0.018 (44 hom., cov: 32)
• Consequence: HDAC9 NM_001321868.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.491

Genes affected

HDAC9 (HGNC:14065): (histone deacetylase 9) Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Histone acetylation/deacetylation alters chromosome structure and affects transcription factor access to DNA. The protein encoded by this gene has sequence homology to members of the histone deacetylase family. This gene is orthologous to the Xenopus and mouse MITR genes. The MITR protein lacks the histone deacetylase catalytic domain. It represses MEF2 activity through recruitment of multicomponent corepressor complexes that include CtBP and HDACs. This encoded protein may play a role in hematopoiesis. Multiple alternatively spliced transcripts have been described for this gene but the full-length nature of some of them has not been determined. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.47).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.0569 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
HDAC9	NM_001204144.3	c.26-59394A>G		intron_variant
HDAC9	NM_001321868.2	c.26-96814A>G		intron_variant
HDAC9	NM_001321869.2	c.26-96814A>G		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
HDAC9	ENST00000413509.6	c.-41-96814A>G		intron_variant		5
HDAC9	ENST00000417496.6	c.26-59394A>G		intron_variant		2
HDAC9	ENST00000433709.6	c.-42+4265A>G		intron_variant		3

Frequencies

GnomAD3 genomes AF: 0.0182 AC: 2774 AN: 152188 Hom.: 43 Cov.: 32

Gnomad AFR AF: 0.00553

Gnomad AMI AF: 0.0143

Gnomad AMR AF: 0.0186

Gnomad ASJ AF: 0.0161

Gnomad EAS AF: 0.0625

Gnomad SAS AF: 0.0298

Gnomad FIN AF: 0.0167

Gnomad MID AF: 0.0411

Gnomad NFE AF: 0.0220

Gnomad OTH AF: 0.0182

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

GnomAD4 genome AF: 0.0183 AC: 2781 AN: 152306 Hom.: 44 Cov.: 32 AF XY: 0.0186 AC XY: 1385 AN XY: 74498

Gnomad4 AFR AF: 0.00568

Gnomad4 AMR AF: 0.0186

Gnomad4 ASJ AF: 0.0161

Gnomad4 EAS AF: 0.0625

Gnomad4 SAS AF: 0.0298

Gnomad4 FIN AF: 0.0167

Gnomad4 NFE AF: 0.0220

Gnomad4 OTH AF: 0.0180

Alfa AF: 0.0207 Hom.: 4

Bravo AF: 0.0183

Asia WGS AF: 0.0330 AC: 113 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.47
Cadd	Benign	8.5
Dann	Benign	0.66

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs17139163; hg19: chr7-18439071;