rs7087400

Positions:

• chr10-90827423-A-G

Variant summary

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

The NM_019859.4(HTR7):​c.539+29710T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.379 in 152,044 control chromosomes in the GnomAD database, including 11,996 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 0.38 (11996 hom., cov: 32)
• Consequence: HTR7 NM_019859.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.831

Genes affected

HTR7 (HGNC:5302): (5-hydroxytryptamine receptor 7) The neurotransmitter, serotonin, is thought to play a role in various cognitive and behavioral functions. The serotonin receptor encoded by this gene belongs to the superfamily of G protein-coupled receptors and the gene is a candidate locus for involvement in autistic disorder and other neuropsychiatric disorders. Three splice variants have been identified which encode proteins that differ in the length of their carboxy terminal ends. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.87).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.559 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
HTR7	NM_019859.4	c.539+29710T>C		intron_variant		ENST00000336152.8	NP_062873.1
HTR7	NM_000872.5	c.539+29710T>C		intron_variant			NP_000863.1
HTR7	NM_019860.4	c.539+29710T>C		intron_variant			NP_062874.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
HTR7	ENST00000336152.8	c.539+29710T>C		intron_variant		1	NM_019859.4	ENSP00000337949
HTR7	ENST00000277874.10	c.539+29710T>C		intron_variant		1		ENSP00000277874	A1
HTR7	ENST00000371719.2	c.539+29710T>C		intron_variant		1		ENSP00000360784	P4

Frequencies

GnomAD3 genomes AF: 0.379 AC: 57548 AN: 151926 Hom.: 11978 Cov.: 32

Gnomad AFR AF: 0.566

Gnomad AMI AF: 0.143

Gnomad AMR AF: 0.357

Gnomad ASJ AF: 0.283

Gnomad EAS AF: 0.438

Gnomad SAS AF: 0.382

Gnomad FIN AF: 0.274

Gnomad MID AF: 0.342

Gnomad NFE AF: 0.290

Gnomad OTH AF: 0.364

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

GnomAD4 genome AF: 0.379 AC: 57608 AN: 152044 Hom.: 11996 Cov.: 32 AF XY: 0.378 AC XY: 28104 AN XY: 74336

Gnomad4 AFR AF: 0.565

Gnomad4 AMR AF: 0.357

Gnomad4 ASJ AF: 0.283

Gnomad4 EAS AF: 0.438

Gnomad4 SAS AF: 0.381

Gnomad4 FIN AF: 0.274

Gnomad4 NFE AF: 0.290

Gnomad4 OTH AF: 0.362

Alfa AF: 0.345 Hom.: 1191

Bravo AF: 0.393

Asia WGS AF: 0.405 AC: 1406 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
CADD	Benign	7.8
DANN	Benign	0.87

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: rs7087400; hg19: chr10-92587180;