rs17464086

chr7-141781136-G-Achr7-141781136-G-C

Variant summary

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

The NM_016944.2(TAS2R4):c.*1748G>A variant causes a 3 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.457 in 151,970 control chromosomes in the GnomAD database, including 16,553 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 0.46 (16553 hom., cov: 32)
• Consequence: TAS2R4 NM_016944.2 3_prime_UTR
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.449

Genes affected

TAS2R4 (HGNC:14911): (taste 2 receptor member 4) This gene encodes a member of a family of candidate taste receptors that are members of the G protein-coupled receptor superfamily and that are specifically expressed by taste receptor cells of the tongue and palate epithelia. These apparently intronless genes encode a 7-transmembrane receptor protein, functioning as a bitter taste receptor. This gene is clustered with another 3 candidate taste receptor genes in chromosome 7 and is genetically linked to loci that influence bitter perception. [provided by RefSeq, Jul 2008]

SSBP1 (HGNC:11317): (single stranded DNA binding protein 1) SSBP1 is a housekeeping gene involved in mitochondrial biogenesis (Tiranti et al., 1995 [PubMed 7789991]). It is also a subunit of a single-stranded DNA (ssDNA)-binding complex involved in the maintenance of genome stability (Huang et al., 2009) [PubMed 19683501].[supplied by OMIM, Feb 2010]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.94).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.731 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
TAS2R4	NM_016944.2	c.*1748G>A		3_prime_UTR_variant	1/1	ENST00000247881.4

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
TAS2R4	ENST00000247881.4	c.*1748G>A		3_prime_UTR_variant	1/1		NM_016944.2	P1
SSBP1	ENST00000465582.5	c.*31-6587G>A		intron_variant		5		P1

Frequencies

GnomAD3 genomes AF: 0.457 AC: 69322 AN: 151852 Hom.: 16534 Cov.: 32

Gnomad AFR AF: 0.309

Gnomad AMI AF: 0.242

Gnomad AMR AF: 0.523

Gnomad ASJ AF: 0.470

Gnomad EAS AF: 0.752

Gnomad SAS AF: 0.593

Gnomad FIN AF: 0.483

Gnomad MID AF: 0.506

Gnomad NFE AF: 0.496

Gnomad OTH AF: 0.474

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

GnomAD4 genome AF: 0.457 AC: 69385 AN: 151970 Hom.: 16553 Cov.: 32 AF XY: 0.462 AC XY: 34306 AN XY: 74260

Gnomad4 AFR AF: 0.310

Gnomad4 AMR AF: 0.523

Gnomad4 ASJ AF: 0.470

Gnomad4 EAS AF: 0.751

Gnomad4 SAS AF: 0.593

Gnomad4 FIN AF: 0.483

Gnomad4 NFE AF: 0.496

Gnomad4 OTH AF: 0.478

Alfa AF: 0.465 Hom.: 1848

Bravo AF: 0.454

Asia WGS AF: 0.665 AC: 2309 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.94
Cadd	Benign	1.1
Dann	Benign	0.51

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs17464086; hg19: chr7-141480936;