NM_000870.7:c.26+33697G>A

Variant names:

• chr5-148603292-C-T
• rs7711800
• NM_000870.7:c.26+33697G>A

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_000870.7(HTR4):​c.26+33697G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.501 in 151,584 control chromosomes in the GnomAD database, including 19,173 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 0.50 (19173 hom., cov: 31)
• Consequence: HTR4 NM_000870.7 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.326
• Publications: 5 publications found

Genes affected

HTR4 (HGNC:5299): (5-hydroxytryptamine receptor 4) This gene is a member of the family of serotonin receptors, which are G protein coupled receptors that stimulate cAMP production in response to serotonin (5-hydroxytryptamine). The gene product is a glycosylated transmembrane protein that functions in both the peripheral and central nervous system to modulate the release of various neurotransmitters. Multiple transcript variants encoding proteins with distinct C-terminal sequences have been described. [provided by RefSeq, May 2010]

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.99).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.533 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
HTR4	NM_000870.7	c.26+33697G>A		intron_variant	Intron 2 of 6	ENST00000377888.8	NP_000861.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
HTR4	ENST00000377888.8	c.26+33697G>A		intron_variant	Intron 2 of 6	1	NM_000870.7	ENSP00000367120.4

Frequencies

GnomAD3 genomes AF: 0.501 AC: 75910 AN: 151466 Hom.: 19145 Cov.: 31

Gnomad AFR AF: 0.538

Gnomad AMI AF: 0.561

Gnomad AMR AF: 0.535

Gnomad ASJ AF: 0.424

Gnomad EAS AF: 0.469

Gnomad SAS AF: 0.524

Gnomad FIN AF: 0.480

Gnomad MID AF: 0.354

Gnomad NFE AF: 0.480

Gnomad OTH AF: 0.481

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

GnomAD4 genome AF: 0.501 AC: 76003 AN: 151584 Hom.: 19173 Cov.: 31 AF XY: 0.499 AC XY: 36939 AN XY: 74072

African (AFR) AF: 0.539 AC: 22262 AN: 41328

American (AMR) AF: 0.536 AC: 8156 AN: 15226

Ashkenazi Jewish (ASJ) AF: 0.424 AC: 1469 AN: 3462

East Asian (EAS) AF: 0.468 AC: 2417 AN: 5160

South Asian (SAS) AF: 0.524 AC: 2526 AN: 4820

European-Finnish (FIN) AF: 0.480 AC: 5022 AN: 10472

Middle Eastern (MID) AF: 0.340 AC: 100 AN: 294

European-Non Finnish (NFE) AF: 0.480 AC: 32522 AN: 67812

Other (OTH) AF: 0.485 AC: 1020 AN: 2102

Alfa AF: 0.481 Hom.: 27399

Bravo AF: 0.508

Asia WGS AF: 0.512 AC: 1775 AN: 3470

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.99
CADD	Benign	0.31
DANN	Benign	0.44
PhyloP100		-0.33
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs7711800; hg19: chr5-147982855; COSMIC: COSV58792039;