6-22306471-A-G

Variant names:

• chr6-22306471-A-G
• rs1341238
• ENST00000561912.3:n.570-10356A>G

Variant summary

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

The ENST00000561912.3(CASC15):​n.570-10356A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.614 in 152,058 control chromosomes in the GnomAD database, including 28,637 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 0.61 (28637 hom., cov: 33)
• Consequence: CASC15 ENST00000561912.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.12
• Publications: 2 publications found

Genes affected

CASC15 (HGNC:28245): (cancer susceptibility 15) This gene produces a long non-coding RNA that may regulate cell proliferation. This RNA is upregulated in hepatocellular carcinoma, where it is thought to function as an oncogene. However, some splice variants of this gene may function as a tumor suppressor in neuroblastoma and other tumor types. Circular RNA variants were observed at this gene. [provided by RefSeq, Dec 2017]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.763 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000561912.3. 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

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CASC15	ENST00000561912.3	TSL:5	n.570-10356A>G		intron	N/A
	CASC15	ENST00000651569.1		n.506-10356A>G		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.614 AC: 93270 AN: 151938 Hom.: 28597 Cov.: 33

Gnomad AFR AF: 0.644

Gnomad AMI AF: 0.588

Gnomad AMR AF: 0.638

Gnomad ASJ AF: 0.584

Gnomad EAS AF: 0.783

Gnomad SAS AF: 0.531

Gnomad FIN AF: 0.585

Gnomad MID AF: 0.642

Gnomad NFE AF: 0.589

Gnomad OTH AF: 0.624

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

GnomAD4 genome AF: 0.614 AC: 93366 AN: 152058 Hom.: 28637 Cov.: 33 AF XY: 0.616 AC XY: 45747 AN XY: 74310

African (AFR) AF: 0.644 AC: 26730 AN: 41488

American (AMR) AF: 0.639 AC: 9763 AN: 15290

Ashkenazi Jewish (ASJ) AF: 0.584 AC: 2027 AN: 3472

East Asian (EAS) AF: 0.783 AC: 4048 AN: 5168

South Asian (SAS) AF: 0.535 AC: 2582 AN: 4830

European-Finnish (FIN) AF: 0.585 AC: 6175 AN: 10564

Middle Eastern (MID) AF: 0.639 AC: 188 AN: 294

European-Non Finnish (NFE) AF: 0.589 AC: 39998 AN: 67938

Other (OTH) AF: 0.627 AC: 1321 AN: 2106

Alfa AF: 0.597 Hom.: 3392

Bravo AF: 0.618

Asia WGS AF: 0.666 AC: 2304 AN: 3464

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
CADD	Benign	0.32
DANN	Benign	0.53
PhyloP100		-1.1

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs1341238; hg19: chr6-22306700;