6-136974197-A-G

Variant summary

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

The ENST00000414680.1(RPL35AP3):n.21T>C variant causes a non coding transcript exon change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.801 in 271,808 control chromosomes in the GnomAD database, including 87,773 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 0.76 (44668 hom., cov: 33)
  • Exomes 𝑓: 0.85 (43105 hom.)
• Consequence: RPL35AP3 ENST00000414680.1 non_coding_transcript_exon
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.869

Genes affected

RPL35AP3 (HGNC:21117): (ribosomal protein L35a pseudogene 3)

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 (AFR) allele frequency at 95% confidence interval = 0.816 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
RPL35AP3	ENST00000414680.1	n.21T>C		non_coding_transcript_exon_variant	1/1

Frequencies

GnomAD3 genomes AF: 0.765 AC: 116168 AN: 151882 Hom.: 44637 Cov.: 33

Gnomad AFR AF: 0.824

Gnomad AMI AF: 0.699

Gnomad AMR AF: 0.803

Gnomad ASJ AF: 0.763

Gnomad EAS AF: 0.824

Gnomad SAS AF: 0.734

Gnomad FIN AF: 0.765

Gnomad MID AF: 0.732

Gnomad NFE AF: 0.719

Gnomad OTH AF: 0.759

GnomAD4 exome AF: 0.847 AC: 101434 AN: 119808 Hom.: 43105 Cov.: 0 AF XY: 0.847 AC XY: 58834 AN XY: 69498

Gnomad4 AFR exome AF: 0.874

Gnomad4 AMR exome AF: 0.880

Gnomad4 ASJ exome AF: 0.875

Gnomad4 EAS exome AF: 0.869

Gnomad4 SAS exome AF: 0.865

Gnomad4 FIN exome AF: 0.782

Gnomad4 NFE exome AF: 0.854

Gnomad4 OTH exome AF: 0.868

GnomAD4 genome AF: 0.765 AC: 116246 AN: 152000 Hom.: 44668 Cov.: 33 AF XY: 0.768 AC XY: 57043 AN XY: 74272

Gnomad4 AFR AF: 0.824

Gnomad4 AMR AF: 0.803

Gnomad4 ASJ AF: 0.763

Gnomad4 EAS AF: 0.824

Gnomad4 SAS AF: 0.733

Gnomad4 FIN AF: 0.765

Gnomad4 NFE AF: 0.719

Gnomad4 OTH AF: 0.760

Alfa AF: 0.750 Hom.: 9891

Bravo AF: 0.770

Asia WGS AF: 0.768 AC: 2673 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	0.82
Dann	Benign	0.16

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs2040034; hg19: chr6-137295334;