rs9298190

Variant names:

• chr8-71932099-T-C
• rs9298190
• ENST00000457356.9:n.385-30824T>C

Variant summary

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

The ENST00000457356.9(MSC-AS1):​n.385-30824T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.364 in 151,856 control chromosomes in the GnomAD database, including 10,192 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 0.36 (10192 hom., cov: 32)
• Consequence: MSC-AS1 ENST00000457356.9 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.16
• Publications: 9 publications found

Genes affected

MSC-AS1 (HGNC:48724): (MSC antisense RNA 1)

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 (AFR) allele frequency at 95% confidence interval = 0.389 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000457356.9. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	MSC-AS1	NR_033651.1		n.308-30824T>C		intron	N/A
	MSC-AS1	NR_033652.1		n.777-30824T>C		intron	N/A

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	MSC-AS1	ENST00000457356.9	TSL:1	n.385-30824T>C		intron	N/A
	MSC-AS1	ENST00000518916.5	TSL:3	n.266-30824T>C		intron	N/A
	MSC-AS1	ENST00000519751.6	TSL:4	n.280-30824T>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.364 AC: 55273 AN: 151738 Hom.: 10181 Cov.: 32

Gnomad AFR AF: 0.394

Gnomad AMI AF: 0.356

Gnomad AMR AF: 0.318

Gnomad ASJ AF: 0.450

Gnomad EAS AF: 0.332

Gnomad SAS AF: 0.340

Gnomad FIN AF: 0.414

Gnomad MID AF: 0.472

Gnomad NFE AF: 0.348

Gnomad OTH AF: 0.368

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

GnomAD4 genome AF: 0.364 AC: 55318 AN: 151856 Hom.: 10192 Cov.: 32 AF XY: 0.366 AC XY: 27155 AN XY: 74234

African (AFR) AF: 0.394 AC: 16324 AN: 41430

American (AMR) AF: 0.317 AC: 4831 AN: 15224

Ashkenazi Jewish (ASJ) AF: 0.450 AC: 1560 AN: 3468

East Asian (EAS) AF: 0.332 AC: 1718 AN: 5174

South Asian (SAS) AF: 0.339 AC: 1633 AN: 4814

European-Finnish (FIN) AF: 0.414 AC: 4371 AN: 10564

Middle Eastern (MID) AF: 0.486 AC: 143 AN: 294

European-Non Finnish (NFE) AF: 0.348 AC: 23628 AN: 67862

Other (OTH) AF: 0.371 AC: 785 AN: 2114

Alfa AF: 0.349 Hom.: 6149

Bravo AF: 0.359

Asia WGS AF: 0.399 AC: 1386 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
CADD	Benign	5.1
DANN	Benign	0.78
PhyloP100		1.2
Mutation Taster		=100/0	polymorphism (auto)

Splicing

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

MaxEntScan Visualizer can be used to analyze the impact of this mutation on the neighboring sequence.

Other links and lift over

dbSNP: rs9298190;

hg19: chr8-72844334;