6-36677244-A-G

Variant names:

• chr6-36677244-A-G
• rs3829968
• NM_001291549.3:c.-141-452A>G

Variant summary

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

The NM_001291549.3(CDKN1A):​c.-141-452A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.141 in 152,068 control chromosomes in the GnomAD database, including 1,845 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 0.14 (1845 hom., cov: 32)
• Consequence: CDKN1A NM_001291549.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.887
• Publications: 5 publications found

Genes affected

CDKN1A (HGNC:1784): (cyclin dependent kinase inhibitor 1A) This gene encodes a potent cyclin-dependent kinase inhibitor. The encoded protein binds to and inhibits the activity of cyclin-cyclin-dependent kinase2 or -cyclin-dependent kinase4 complexes, and thus functions as a regulator of cell cycle progression at G1. The expression of this gene is tightly controlled by the tumor suppressor protein p53, through which this protein mediates the p53-dependent cell cycle G1 phase arrest in response to a variety of stress stimuli. This protein can interact with proliferating cell nuclear antigen, a DNA polymerase accessory factor, and plays a regulatory role in S phase DNA replication and DNA damage repair. This protein was reported to be specifically cleaved by CASP3-like caspases, which thus leads to a dramatic activation of cyclin-dependent kinase2, and may be instrumental in the execution of apoptosis following caspase activation. Mice that lack this gene have the ability to regenerate damaged or missing tissue. Multiple alternatively spliced variants have been found for this gene. [provided by RefSeq, Sep 2015]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.223 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001291549.3. 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
	CDKN1A	NM_001291549.3		c.-141-452A>G		intron	N/A	NP_001278478.1
	CDKN1A	NM_001374509.1		c.-49-544A>G		intron	N/A	NP_001361438.1
	CDKN1A	NM_001374510.1		c.34+674A>G		intron	N/A	NP_001361439.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CDKN1A	ENST00000448526.6	TSL:3	c.-37-658A>G		intron	N/A	ENSP00000409259.3
	CDKN1A	ENST00000615513.4	TSL:2	c.-6+720A>G		intron	N/A	ENSP00000482768.1
	CDKN1A	ENST00000459970.1	TSL:5	n.44-544A>G		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.141 AC: 21428 AN: 151950 Hom.: 1829 Cov.: 32

Gnomad AFR AF: 0.226

Gnomad AMI AF: 0.0681

Gnomad AMR AF: 0.112

Gnomad ASJ AF: 0.196

Gnomad EAS AF: 0.109

Gnomad SAS AF: 0.0512

Gnomad FIN AF: 0.137

Gnomad MID AF: 0.137

Gnomad NFE AF: 0.104

Gnomad OTH AF: 0.136

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

GnomAD4 genome AF: 0.141 AC: 21480 AN: 152068 Hom.: 1845 Cov.: 32 AF XY: 0.144 AC XY: 10681 AN XY: 74330

African (AFR) AF: 0.226 AC: 9389 AN: 41454

American (AMR) AF: 0.112 AC: 1708 AN: 15292

Ashkenazi Jewish (ASJ) AF: 0.196 AC: 679 AN: 3470

East Asian (EAS) AF: 0.109 AC: 562 AN: 5176

South Asian (SAS) AF: 0.0509 AC: 245 AN: 4818

European-Finnish (FIN) AF: 0.137 AC: 1453 AN: 10576

Middle Eastern (MID) AF: 0.134 AC: 39 AN: 292

European-Non Finnish (NFE) AF: 0.104 AC: 7058 AN: 67970

Other (OTH) AF: 0.135 AC: 285 AN: 2110

Alfa AF: 0.134 Hom.: 208

Bravo AF: 0.145

Asia WGS AF: 0.0800 AC: 278 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	1.0
DANN	Benign	0.72
PhyloP100		-0.89

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: rs3829968; hg19: chr6-36645021;