rs16883343

Variant names:

• chr6-52995577-C-A
• rs16883343
• ENST00000365328.1:n.-43C>A

Your query was ambiguous. Multiple possible variants found:

• chr6-52995577-C-A
• chr6-52995577-C-G
• chr6-52995577-C-T

Variant summary

Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The ENST00000365328.1(7SK):​n.-43C>A variant causes a upstream gene change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0000198 in 151,886 control chromosomes in the GnomAD database, with no homozygous occurrence. 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 0.000020 (0 hom., cov: 33)
  • Exomes 𝑓: 0.0 (0 hom.)
  • Failed GnomAD Quality Control
• Consequence: 7SK ENST00000365328.1 upstream_gene
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -5.78
• Publications: 10 publications found

Genes affected

7SK (HGNC:):

RN7SK (HGNC:10037): (RNA component of 7SK nuclear ribonucleoprotein)

ACMG classification

Our verdict: Likely_benign. The variant received -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.79).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
RN7SK	NR_001445.2	n.-43C>A		upstream_gene_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
7SK	ENST00000365328.1	n.-43C>A		upstream_gene_variant		6
RN7SK	ENST00000636484.1	n.-44C>A		upstream_gene_variant		6

Frequencies

GnomAD3 genomes AF: 0.0000198 AC: 3 AN: 151886 Hom.: 0 Cov.: 33

Gnomad AFR AF: 0.0000483

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.00

Gnomad ASJ AF: 0.00

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.00

Gnomad FIN AF: 0.00

Gnomad MID AF: 0.00

Gnomad NFE AF: 0.0000147

Gnomad OTH AF: 0.00

GnomAD4 exome Data not reliable, filtered out with message: AC0 AF: 0.00 AC: 0 AN: 13924 Hom.: 0 Cov.: 0 AF XY: 0.00 AC XY: 0 AN XY: 6528

African (AFR) AF: 0.00 AC: 0 AN: 450

American (AMR) AF: 0.00 AC: 0 AN: 270

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 882

East Asian (EAS) AF: 0.00 AC: 0 AN: 3134

South Asian (SAS) AF: 0.00 AC: 0 AN: 106

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 228

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 94

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 7680

Other (OTH) AF: 0.00 AC: 0 AN: 1080

GnomAD4 genome AF: 0.0000198 AC: 3 AN: 151886 Hom.: 0 Cov.: 33 AF XY: 0.0000135 AC XY: 1 AN XY: 74178

African (AFR) AF: 0.0000483 AC: 2 AN: 41400

American (AMR) AF: 0.00 AC: 0 AN: 15254

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 3460

East Asian (EAS) AF: 0.00 AC: 0 AN: 5186

South Asian (SAS) AF: 0.00 AC: 0 AN: 4822

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 10592

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 316

European-Non Finnish (NFE) AF: 0.0000147 AC: 1 AN: 67856

Other (OTH) AF: 0.00 AC: 0 AN: 2090

Alfa AF: 0.00 Hom.: 1705

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.79
CADD	Benign	0.0010
DANN	Benign	0.54
PhyloP100		-5.8
PromoterAI		-0.018	Neutral

Splicing

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

Other links and lift over

dbSNP: rs16883343; hg19: chr6-52860375;