10-90834586-C-T

Position:

• chr10-90834586-C-T

Variant summary

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

The NM_019859.4(HTR7):​c.539+22547G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.213 in 151,970 control chromosomes in the GnomAD database, including 4,447 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 0.21 (4447 hom., cov: 32)
• Consequence: HTR7 NM_019859.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0460

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=-0.83).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.376 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
HTR7	NM_019859.4	c.539+22547G>A		intron_variant		ENST00000336152.8	NP_062873.1
HTR7	NM_000872.5	c.539+22547G>A		intron_variant			NP_000863.1
HTR7	NM_019860.4	c.539+22547G>A		intron_variant			NP_062874.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
HTR7	ENST00000336152.8	c.539+22547G>A		intron_variant		1	NM_019859.4	ENSP00000337949.3
HTR7	ENST00000277874.10	c.539+22547G>A		intron_variant		1		ENSP00000277874.6
HTR7	ENST00000371719.2	c.539+22547G>A		intron_variant		1		ENSP00000360784.2

Frequencies

GnomAD3 genomes AF: 0.213 AC: 32327 AN: 151852 Hom.: 4438 Cov.: 32

Gnomad AFR AF: 0.382

Gnomad AMI AF: 0.0954

Gnomad AMR AF: 0.225

Gnomad ASJ AF: 0.162

Gnomad EAS AF: 0.279

Gnomad SAS AF: 0.233

Gnomad FIN AF: 0.122

Gnomad MID AF: 0.180

Gnomad NFE AF: 0.119

Gnomad OTH AF: 0.226

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

GnomAD4 genome AF: 0.213 AC: 32358 AN: 151970 Hom.: 4447 Cov.: 32 AF XY: 0.214 AC XY: 15914 AN XY: 74296

Gnomad4 AFR AF: 0.381

Gnomad4 AMR AF: 0.225

Gnomad4 ASJ AF: 0.162

Gnomad4 EAS AF: 0.279

Gnomad4 SAS AF: 0.233

Gnomad4 FIN AF: 0.122

Gnomad4 NFE AF: 0.119

Gnomad4 OTH AF: 0.224

Alfa AF: 0.178 Hom.: 614

Bravo AF: 0.231

Asia WGS AF: 0.239 AC: 829 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.83
CADD	Benign	4.1
DANN	Benign	0.78

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: rs1935349; hg19: chr10-92594343;