NM_014555.4:c.2783-511T>C

Variant names:

• chr11-2408423-A-G
• rs800344
• NM_014555.4:c.2783-511T>C

Variant summary

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

The NM_014555.4(TRPM5):​c.2783-511T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.868 in 152,280 control chromosomes in the GnomAD database, including 57,854 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 0.87 (57854 hom., cov: 34)
• Consequence: TRPM5 NM_014555.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.00400
• Publications: 3 publications found

Genes affected

TRPM5 (HGNC:14323): (transient receptor potential cation channel subfamily M member 5) This gene encodes a member of the transient receptor potential (TRP) protein family, which is a diverse group of proteins with structural features typical of ion channels. This protein plays an important role in taste transduction, and has characteristics of a calcium-activated, non-selective cation channel that carries Na+, K+, and Cs+ ions equally well, but not Ca(2+) ions. It is activated by lower concentrations of intracellular Ca(2+), and inhibited by higher concentrations. It is also a highly temperature-sensitive, heat activated channel showing a steep increase of inward currents at temperatures between 15 and 35 degrees Celsius. This gene is located within the Beckwith-Wiedemann syndrome critical region-1 on chromosome 11p15.5, and has been shown to be imprinted, with exclusive expression from the paternal allele. [provided by RefSeq, Oct 2010]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.03).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.921 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_014555.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	TRPM5	NM_014555.4	MANE Select	c.2783-511T>C		intron	N/A	NP_055370.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	TRPM5	ENST00000696290.1	MANE Select	c.2783-511T>C		intron	N/A	ENSP00000512529.1
	TRPM5	ENST00000533060.5	TSL:1	c.2783-511T>C		intron	N/A	ENSP00000434121.1
	TRPM5	ENST00000528453.1	TSL:1	c.2783-511T>C		intron	N/A	ENSP00000436809.1

Frequencies

GnomAD3 genomes AF: 0.868 AC: 132053 AN: 152162 Hom.: 57818 Cov.: 34

Gnomad AFR AF: 0.834

Gnomad AMI AF: 0.953

Gnomad AMR AF: 0.741

Gnomad ASJ AF: 0.919

Gnomad EAS AF: 0.609

Gnomad SAS AF: 0.813

Gnomad FIN AF: 0.926

Gnomad MID AF: 0.896

Gnomad NFE AF: 0.927

Gnomad OTH AF: 0.874

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

GnomAD4 genome AF: 0.868 AC: 132141 AN: 152280 Hom.: 57854 Cov.: 34 AF XY: 0.862 AC XY: 64161 AN XY: 74460

African (AFR) AF: 0.834 AC: 34654 AN: 41532

American (AMR) AF: 0.740 AC: 11316 AN: 15298

Ashkenazi Jewish (ASJ) AF: 0.919 AC: 3191 AN: 3472

East Asian (EAS) AF: 0.609 AC: 3157 AN: 5182

South Asian (SAS) AF: 0.814 AC: 3928 AN: 4828

European-Finnish (FIN) AF: 0.926 AC: 9838 AN: 10624

Middle Eastern (MID) AF: 0.888 AC: 261 AN: 294

European-Non Finnish (NFE) AF: 0.927 AC: 63076 AN: 68022

Other (OTH) AF: 0.875 AC: 1851 AN: 2116

Alfa AF: 0.904 Hom.: 116368

Bravo AF: 0.852

Asia WGS AF: 0.756 AC: 2628 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	2.9
DANN	Benign	0.41
PhyloP100		0.0040
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: rs800344; hg19: chr11-2429653;