rs6051727

Variant names:

• chr20-3306474-T-C
• rs6051727
• NM_001009984.3:c.1679-1931A>G

Variant summary

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

The NM_001009984.3(DNAAF9):​c.1679-1931A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.571 in 152,046 control chromosomes in the GnomAD database, including 24,904 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 0.57 (24904 hom., cov: 32)
• Consequence: DNAAF9 NM_001009984.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -4.58
• Publications: 6 publications found

Genes affected

DNAAF9 (HGNC:17721): (dynein axonemal assembly factor 9) This gene encodes an uncharacterized protein with a C-terminal coiled-coil region. The gene is located on chromosome 20p13 in a 1.8 Mb region linked to a spinocerebellar ataxia phenotype, but this gene does not appear to be a disease candidate. [provided by RefSeq, Dec 2011]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.96).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.587 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001009984.3. 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
	DNAAF9	NM_001009984.3	MANE Select	c.1679-1931A>G		intron	N/A	NP_001009984.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	DNAAF9	ENST00000252032.10	TSL:5 MANE Select	c.1679-1931A>G		intron	N/A	ENSP00000252032.9
	DNAAF9	ENST00000851200.1		c.1676-1931A>G		intron	N/A	ENSP00000521259.1
	DNAAF9	ENST00000953496.1		c.1679-1931A>G		intron	N/A	ENSP00000623555.1

Frequencies

GnomAD3 genomes AF: 0.572 AC: 86829 AN: 151928 Hom.: 24888 Cov.: 32

Gnomad AFR AF: 0.578

Gnomad AMI AF: 0.573

Gnomad AMR AF: 0.599

Gnomad ASJ AF: 0.575

Gnomad EAS AF: 0.562

Gnomad SAS AF: 0.456

Gnomad FIN AF: 0.600

Gnomad MID AF: 0.436

Gnomad NFE AF: 0.566

Gnomad OTH AF: 0.558

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

GnomAD4 genome AF: 0.571 AC: 86890 AN: 152046 Hom.: 24904 Cov.: 32 AF XY: 0.572 AC XY: 42503 AN XY: 74336

African (AFR) AF: 0.579 AC: 23994 AN: 41452

American (AMR) AF: 0.598 AC: 9135 AN: 15284

Ashkenazi Jewish (ASJ) AF: 0.575 AC: 1996 AN: 3472

East Asian (EAS) AF: 0.563 AC: 2911 AN: 5168

South Asian (SAS) AF: 0.455 AC: 2189 AN: 4814

European-Finnish (FIN) AF: 0.600 AC: 6351 AN: 10584

Middle Eastern (MID) AF: 0.428 AC: 125 AN: 292

European-Non Finnish (NFE) AF: 0.566 AC: 38495 AN: 67956

Other (OTH) AF: 0.554 AC: 1171 AN: 2112

Alfa AF: 0.568 Hom.: 76460

Bravo AF: 0.574

Asia WGS AF: 0.452 AC: 1573 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.96
CADD	Benign	0.0070
DANN	Benign	0.63
PhyloP100		-4.6
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

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

Other links and lift over

dbSNP: rs6051727; hg19: chr20-3287121;