chr21-34985564-A-G

Variant names:

• chr21-34985564-A-G
• rs2014300
• NM_001754.5:c.58+63278T>C

Variant summary

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

The NM_001754.5(RUNX1):​c.58+63278T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.759 in 152,068 control chromosomes in the GnomAD database, including 45,483 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 0.76 (45483 hom., cov: 30)
• Consequence: RUNX1 NM_001754.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.67
• Publications: 43 publications found

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]

RUNX1 Gene-Disease associations (from GenCC):

• hereditary thrombocytopenia and hematologic cancer predisposition syndrome

  Inheritance: AD Classification: DEFINITIVE, SUPPORTIVE Submitted by: ClinGen, Orphanet
• hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1

  Inheritance: AD Classification: DEFINITIVE, STRONG Submitted by: Ambry Genetics, Genomics England PanelApp, G2P, Labcorp Genetics (formerly Invitae)
• acute myeloid leukemia

  Inheritance: AD Classification: STRONG Submitted by: Genomics England PanelApp

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.87).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.867 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001754.5. 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
	RUNX1	NM_001754.5	MANE Select	c.58+63278T>C		intron	N/A	NP_001745.2

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	RUNX1	ENST00000675419.1	MANE Select	c.58+63278T>C		intron	N/A	ENSP00000501943.1
	RUNX1	ENST00000300305.7	TSL:1	c.58+63278T>C		intron	N/A	ENSP00000300305.3
	RUNX1	ENST00000416754.1	TSL:1	c.58+63278T>C		intron	N/A	ENSP00000405158.1

Frequencies

GnomAD3 genomes AF: 0.760 AC: 115414 AN: 151952 Hom.: 45457 Cov.: 30

Gnomad AFR AF: 0.531

Gnomad AMI AF: 0.904

Gnomad AMR AF: 0.731

Gnomad ASJ AF: 0.814

Gnomad EAS AF: 0.889

Gnomad SAS AF: 0.863

Gnomad FIN AF: 0.900

Gnomad MID AF: 0.753

Gnomad NFE AF: 0.860

Gnomad OTH AF: 0.771

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

GnomAD4 genome AF: 0.759 AC: 115484 AN: 152068 Hom.: 45483 Cov.: 30 AF XY: 0.762 AC XY: 56623 AN XY: 74334

African (AFR) AF: 0.531 AC: 22005 AN: 41418

American (AMR) AF: 0.732 AC: 11193 AN: 15290

Ashkenazi Jewish (ASJ) AF: 0.814 AC: 2826 AN: 3472

East Asian (EAS) AF: 0.889 AC: 4592 AN: 5166

South Asian (SAS) AF: 0.863 AC: 4159 AN: 4822

European-Finnish (FIN) AF: 0.900 AC: 9532 AN: 10596

Middle Eastern (MID) AF: 0.748 AC: 220 AN: 294

European-Non Finnish (NFE) AF: 0.860 AC: 58503 AN: 67990

Other (OTH) AF: 0.773 AC: 1630 AN: 2108

Alfa AF: 0.831 Hom.: 175748

Bravo AF: 0.737

Asia WGS AF: 0.843 AC: 2932 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
CADD	Benign	6.0
DANN	Benign	0.60
PhyloP100		1.7

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: rs2014300; hg19: chr21-36357861;