chr17-45574056-T-C

Position:

• chr17-45574056-T-C

Variant summary

Our verdict is Likely benign. Variant got -4 ACMG points: 0P and 4B. BP4_Strong

The ENST00000686949.1(ENSG00000291175):​n.134+10516A>G variant causes a intron, non coding transcript change involving the alteration of a non-conserved nucleotide. 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 0.43 (2178 hom., cov: 53)
  • Failed GnomAD Quality Control
• Consequence: ENST00000686949.1 intron, non_coding_transcript
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.795

Genes affected

(HGNC:):

ACMG classification

Verdict is Likely_benign. Variant got -4 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
	ENST00000686949.1	n.134+10516A>G		intron_variant, non_coding_transcript_variant
	ENST00000701132.1	n.31+10516A>G		intron_variant, non_coding_transcript_variant

Frequencies

GnomAD3 genomes AF: 0.00 AC: 65342 AN: 151076 Hom.: 2180 Cov.: 53 FAILED QC

Gnomad AFR AF: 0.326

Gnomad AMI AF: 0.513

Gnomad AMR AF: 0.444

Gnomad ASJ AF: 0.506

Gnomad EAS AF: 0.316

Gnomad SAS AF: 0.466

Gnomad FIN AF: 0.427

Gnomad MID AF: 0.503

Gnomad NFE AF: 0.495

Gnomad OTH AF: 0.468

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

GnomAD4 genome Data not reliable, filtered out with message: InbreedingCoeff AF: 0.432 AC: 65356 AN: 151194 Hom.: 2178 Cov.: 53 AF XY: 0.429 AC XY: 31648 AN XY: 73838

Gnomad4 AFR AF: 0.326

Gnomad4 AMR AF: 0.444

Gnomad4 ASJ AF: 0.506

Gnomad4 EAS AF: 0.316

Gnomad4 SAS AF: 0.466

Gnomad4 FIN AF: 0.427

Gnomad4 NFE AF: 0.495

Gnomad4 OTH AF: 0.467

Alfa AF: 0.454 Hom.: 295

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	0.84
DANN	Benign	0.23

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs2693363; hg19: chr17-43651422;