rs9974986

Positions:

• chr21-34968519-T-C

Variant summary

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

The NM_001754.5(RUNX1):​c.59-75556A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.62 in 151,930 control chromosomes in the GnomAD database, including 29,712 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 0.62 (29712 hom., cov: 30)
• Consequence: RUNX1 NM_001754.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.844

Genes affected

RUNX1 (HGNC:10471): (RUNX family transcription factor 1) Core binding factor (CBF) is a heterodimeric transcription factor that binds to the core element of many enhancers and promoters. The protein encoded by this gene represents the alpha subunit of CBF and is thought to be involved in the development of normal hematopoiesis. Chromosomal translocations involving this gene are well-documented and have been associated with several types of leukemia. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.85).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.683 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
RUNX1	NM_001754.5	c.59-75556A>G		intron_variant		ENST00000675419.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
RUNX1	ENST00000675419.1	c.59-75556A>G		intron_variant			NM_001754.5	A1

Frequencies

GnomAD3 genomes AF: 0.621 AC: 94227 AN: 151812 Hom.: 29705 Cov.: 30

Gnomad AFR AF: 0.535

Gnomad AMI AF: 0.786

Gnomad AMR AF: 0.695

Gnomad ASJ AF: 0.641

Gnomad EAS AF: 0.442

Gnomad SAS AF: 0.645

Gnomad FIN AF: 0.665

Gnomad MID AF: 0.674

Gnomad NFE AF: 0.657

Gnomad OTH AF: 0.648

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

GnomAD4 genome AF: 0.620 AC: 94263 AN: 151930 Hom.: 29712 Cov.: 30 AF XY: 0.623 AC XY: 46289 AN XY: 74250

Gnomad4 AFR AF: 0.534

Gnomad4 AMR AF: 0.694

Gnomad4 ASJ AF: 0.641

Gnomad4 EAS AF: 0.442

Gnomad4 SAS AF: 0.645

Gnomad4 FIN AF: 0.665

Gnomad4 NFE AF: 0.657

Gnomad4 OTH AF: 0.644

Alfa AF: 0.648 Hom.: 14524

Bravo AF: 0.618

Asia WGS AF: 0.488 AC: 1700 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
CADD	Benign	9.1
DANN	Benign	0.80

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

Publications

LitVar

Other links and lift over

dbSNP: rs9974986; hg19: chr21-36340816;