rs1362999

Variant names:

• chr10-35463622-T-C
• rs1362999
• NM_145012.6:c.155-19782T>C

Your query was ambiguous. Multiple possible variants found:

• chr10-35463622-T-C
• chr10-35463622-T-G

Variant summary

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

The NM_145012.6(CCNY):​c.155-19782T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.427 in 152,042 control chromosomes in the GnomAD database, including 14,855 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 0.43 (14855 hom., cov: 33)
• Consequence: CCNY NM_145012.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -4.11
• Publications: 4 publications found

Genes affected

CCNY (HGNC:23354): (cyclin Y) Cyclins, such as CCNY, control cell division cycles and regulate cyclin-dependent kinases (e.g., CDC2; MIM 116940) (Li et al., 2009 [PubMed 18060517]).[supplied by OMIM, May 2009]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.584 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CCNY	NM_145012.6	c.155-19782T>C		intron_variant	Intron 1 of 9	ENST00000374704.8	NP_659449.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CCNY	ENST00000374704.8	c.155-19782T>C		intron_variant	Intron 1 of 9	1	NM_145012.6	ENSP00000363836.4

Frequencies

GnomAD3 genomes AF: 0.426 AC: 64778 AN: 151924 Hom.: 14818 Cov.: 33

Gnomad AFR AF: 0.590

Gnomad AMI AF: 0.341

Gnomad AMR AF: 0.432

Gnomad ASJ AF: 0.448

Gnomad EAS AF: 0.400

Gnomad SAS AF: 0.340

Gnomad FIN AF: 0.300

Gnomad MID AF: 0.396

Gnomad NFE AF: 0.353

Gnomad OTH AF: 0.447

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

GnomAD4 genome AF: 0.427 AC: 64878 AN: 152042 Hom.: 14855 Cov.: 33 AF XY: 0.422 AC XY: 31376 AN XY: 74344

African (AFR) AF: 0.591 AC: 24490 AN: 41468

American (AMR) AF: 0.433 AC: 6611 AN: 15280

Ashkenazi Jewish (ASJ) AF: 0.448 AC: 1553 AN: 3466

East Asian (EAS) AF: 0.400 AC: 2071 AN: 5172

South Asian (SAS) AF: 0.340 AC: 1636 AN: 4810

European-Finnish (FIN) AF: 0.300 AC: 3172 AN: 10566

Middle Eastern (MID) AF: 0.391 AC: 115 AN: 294

European-Non Finnish (NFE) AF: 0.353 AC: 23976 AN: 67970

Other (OTH) AF: 0.448 AC: 944 AN: 2106

Alfa AF: 0.408 Hom.: 1717

Bravo AF: 0.448

Asia WGS AF: 0.404 AC: 1407 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	0.12
DANN	Benign	0.56
PhyloP100		-4.1
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: rs1362999; hg19: chr10-35752550;