chr19-43124678-A-G

Variant names:

• chr19-43124678-A-G
• rs10417319
• ENST00000635346.1:n.141-12839A>G

Variant summary

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

The ENST00000635346.1(PSG11-AS1):​n.141-12839A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.191 in 151,366 control chromosomes in the GnomAD database, including 3,107 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 0.19 (3107 hom., cov: 31)
• Consequence: PSG11-AS1 ENST00000635346.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.19
• Publications: 2 publications found

Genes affected

PSG11-AS1 (HGNC:56358): (PSG11, PSG2 and PSG5 antisense RNA 1)

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.232 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
PSG11-AS1	ENST00000635346.1	n.141-12839A>G		intron_variant	Intron 1 of 1	3
PSG11-AS1	ENST00000635495.1	n.322+22978A>G		intron_variant	Intron 2 of 2	5

Frequencies

GnomAD3 genomes AF: 0.191 AC: 28933 AN: 151248 Hom.: 3110 Cov.: 31

Gnomad AFR AF: 0.236

Gnomad AMI AF: 0.167

Gnomad AMR AF: 0.195

Gnomad ASJ AF: 0.185

Gnomad EAS AF: 0.00522

Gnomad SAS AF: 0.203

Gnomad FIN AF: 0.183

Gnomad MID AF: 0.187

Gnomad NFE AF: 0.179

Gnomad OTH AF: 0.181

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

GnomAD4 genome AF: 0.191 AC: 28942 AN: 151366 Hom.: 3107 Cov.: 31 AF XY: 0.191 AC XY: 14107 AN XY: 73940

African (AFR) AF: 0.236 AC: 9662 AN: 40958

American (AMR) AF: 0.194 AC: 2958 AN: 15210

Ashkenazi Jewish (ASJ) AF: 0.185 AC: 641 AN: 3466

East Asian (EAS) AF: 0.00523 AC: 27 AN: 5162

South Asian (SAS) AF: 0.202 AC: 969 AN: 4800

European-Finnish (FIN) AF: 0.183 AC: 1931 AN: 10550

Middle Eastern (MID) AF: 0.180 AC: 53 AN: 294

European-Non Finnish (NFE) AF: 0.179 AC: 12166 AN: 67906

Other (OTH) AF: 0.182 AC: 383 AN: 2110

Alfa AF: 0.191 Hom.: 540

Bravo AF: 0.195

Asia WGS AF: 0.126 AC: 439 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	0.80
DANN	Benign	0.43
PhyloP100		-1.2

Splicing

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

Other links and lift over

dbSNP: rs10417319; hg19: chr19-43628830;