rs17647719

Positions:

• chr15-51276007-A-G

Variant summary

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

The NM_000103.4(CYP19A1):​c.-38-33057T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.146 in 152,184 control chromosomes in the GnomAD database, including 2,795 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 0.15 (2795 hom., cov: 32)
• Consequence: CYP19A1 NM_000103.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.671

Genes affected

CYP19A1 (HGNC:2594): (cytochrome P450 family 19 subfamily A member 1) This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and catalyzes the last steps of estrogen biosynthesis. Mutations in this gene can result in either increased or decreased aromatase activity; the associated phenotypes suggest that estrogen functions both as a sex steroid hormone and in growth or differentiation. Alternative promoter use and alternative splicing results in multiple transcript variants that have different tissue specificities. [provided by RefSeq, Dec 2016]

MIR4713HG (HGNC:53124): (MIR4713 host gene)

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.84).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.322 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
CYP19A1	NM_000103.4	c.-38-33057T>C		intron_variant		ENST00000396402.6	NP_000094.2
MIR4713HG	NR_146310.1	n.195-1976A>G		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
CYP19A1	ENST00000396402.6	c.-38-33057T>C		intron_variant		1	NM_000103.4	ENSP00000379683	P1
MIR4713HG	ENST00000559909.1	n.195-1976A>G		intron_variant, non_coding_transcript_variant		4

Frequencies

GnomAD3 genomes AF: 0.146 AC: 22186 AN: 152066 Hom.: 2780 Cov.: 32

Gnomad AFR AF: 0.326

Gnomad AMI AF: 0.00439

Gnomad AMR AF: 0.118

Gnomad ASJ AF: 0.0677

Gnomad EAS AF: 0.250

Gnomad SAS AF: 0.233

Gnomad FIN AF: 0.0794

Gnomad MID AF: 0.0918

Gnomad NFE AF: 0.0462

Gnomad OTH AF: 0.110

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

GnomAD4 genome AF: 0.146 AC: 22257 AN: 152184 Hom.: 2795 Cov.: 32 AF XY: 0.150 AC XY: 11134 AN XY: 74412

Gnomad4 AFR AF: 0.326

Gnomad4 AMR AF: 0.118

Gnomad4 ASJ AF: 0.0677

Gnomad4 EAS AF: 0.250

Gnomad4 SAS AF: 0.231

Gnomad4 FIN AF: 0.0794

Gnomad4 NFE AF: 0.0462

Gnomad4 OTH AF: 0.118

Alfa AF: 0.106 Hom.: 342

Bravo AF: 0.155

Asia WGS AF: 0.288 AC: 1003 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.84
CADD	Benign	1.1
DANN	Benign	0.61

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

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

Publications

LitVar

Other links and lift over

dbSNP: rs17647719; hg19: chr15-51568204;