chr4-15384242-C-T

Position:

• chr4-15384242-C-T

Variant summary

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

The NR_125911.1(C1QTNF7-AS1):​n.86+43587G>A variant causes a intron, non coding transcript change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.48 in 152,086 control chromosomes in the GnomAD database, including 19,166 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 0.48 (19166 hom., cov: 32)
• Consequence: C1QTNF7-AS1 NR_125911.1 intron, non_coding_transcript
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.625

Genes affected

C1QTNF7 (HGNC:14342): (C1q and TNF related 7) Predicted to enable identical protein binding activity. Predicted to be located in extracellular space. Predicted to be part of collagen trimer. [provided by Alliance of Genome Resources, Apr 2022]

C1QTNF7-AS1 (HGNC:40683): (C1QTNF7 antisense RNA 1)

(HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.685 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
C1QTNF7-AS1	NR_125911.1	n.86+43587G>A		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
C1QTNF7-AS1	ENST00000502344.5	n.86+43587G>A		intron_variant, non_coding_transcript_variant		3
	ENST00000515495.1	n.105-21719G>A		intron_variant, non_coding_transcript_variant		3

Frequencies

GnomAD3 genomes AF: 0.480 AC: 72946 AN: 151968 Hom.: 19133 Cov.: 32

Gnomad AFR AF: 0.691

Gnomad AMI AF: 0.627

Gnomad AMR AF: 0.524

Gnomad ASJ AF: 0.369

Gnomad EAS AF: 0.491

Gnomad SAS AF: 0.462

Gnomad FIN AF: 0.401

Gnomad MID AF: 0.282

Gnomad NFE AF: 0.361

Gnomad OTH AF: 0.418

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

GnomAD4 genome AF: 0.480 AC: 73034 AN: 152086 Hom.: 19166 Cov.: 32 AF XY: 0.484 AC XY: 35971 AN XY: 74330

Gnomad4 AFR AF: 0.691

Gnomad4 AMR AF: 0.525

Gnomad4 ASJ AF: 0.369

Gnomad4 EAS AF: 0.492

Gnomad4 SAS AF: 0.461

Gnomad4 FIN AF: 0.401

Gnomad4 NFE AF: 0.361

Gnomad4 OTH AF: 0.415

Alfa AF: 0.399 Hom.: 6032

Bravo AF: 0.497

Asia WGS AF: 0.488 AC: 1695 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
CADD	Benign	1.1
DANN	Benign	0.42

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: rs4629443; hg19: chr4-15385866;