rs11970030

chr6-20929882-G-C

Variant summary

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

The NM_017774.3(CDKAL1):c.743-25537G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0955 in 152,146 control chromosomes in the GnomAD database, including 792 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 0.096 (792 hom., cov: 32)
• Consequence: CDKAL1 NM_017774.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.141

Genes affected

CDKAL1 (HGNC:21050): (CDK5 regulatory subunit associated protein 1 like 1) The protein encoded by this gene is a member of the methylthiotransferase family. The function of this gene is not known. Genome-wide association studies have linked single nucleotide polymorphisms in an intron of this gene with susceptibilty to type 2 diabetes. [provided by RefSeq, May 2010]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.12 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
CDKAL1	NM_017774.3	c.743-25537G>C		intron_variant		ENST00000274695.8

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
CDKAL1	ENST00000274695.8	c.743-25537G>C		intron_variant		1	NM_017774.3	P1
CDKAL1	ENST00000378610.1	c.743-25537G>C		intron_variant		2		P1

Frequencies

GnomAD3 genomes AF: 0.0955 AC: 14526 AN: 152028 Hom.: 791 Cov.: 32

Gnomad AFR AF: 0.0683

Gnomad AMI AF: 0.158

Gnomad AMR AF: 0.0682

Gnomad ASJ AF: 0.109

Gnomad EAS AF: 0.00616

Gnomad SAS AF: 0.0386

Gnomad FIN AF: 0.129

Gnomad MID AF: 0.0918

Gnomad NFE AF: 0.122

Gnomad OTH AF: 0.102

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

GnomAD4 genome AF: 0.0955 AC: 14531 AN: 152146 Hom.: 792 Cov.: 32 AF XY: 0.0929 AC XY: 6906 AN XY: 74370

Gnomad4 AFR AF: 0.0682

Gnomad4 AMR AF: 0.0680

Gnomad4 ASJ AF: 0.109

Gnomad4 EAS AF: 0.00637

Gnomad4 SAS AF: 0.0388

Gnomad4 FIN AF: 0.129

Gnomad4 NFE AF: 0.122

Gnomad4 OTH AF: 0.102

Alfa AF: 0.107 Hom.: 119

Bravo AF: 0.0910

Asia WGS AF: 0.0210 AC: 73 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
Cadd	Benign	2.0
Dann	Benign	0.68

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: rs11970030; hg19: chr6-20930113;