rs17706630

Variant names:

• chr17-3583848-G-A
• rs17706630
• NM_080704.4:c.1384-418C>T

Variant summary

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

The NM_080704.4(TRPV1):​c.1384-418C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.208 in 152,192 control chromosomes in the GnomAD database, including 3,615 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 (3615 hom., cov: 34)
• Consequence: TRPV1 NM_080704.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.07
• Publications: 4 publications found

Genes affected

TRPV1 (HGNC:12716): (transient receptor potential cation channel subfamily V member 1) Capsaicin, the main pungent ingredient in hot chili peppers, elicits a sensation of burning pain by selectively activating sensory neurons that convey information about noxious stimuli to the central nervous system. The protein encoded by this gene is a receptor for capsaicin and is a non-selective cation channel that is structurally related to members of the TRP family of ion channels. This receptor is also activated by increases in temperature in the noxious range, suggesting that it functions as a transducer of painful thermal stimuli in vivo. Four transcript variants encoding the same protein, but with different 5' UTR sequence, have been described for this gene. [provided by RefSeq, Jul 2008]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.81).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.25 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
TRPV1	NM_080704.4	c.1384-418C>T		intron_variant	Intron 9 of 16	ENST00000572705.2	NP_542435.2
TRPV1	NM_018727.5	c.1384-418C>T		intron_variant	Intron 8 of 15		NP_061197.4
TRPV1	NM_080705.4	c.1384-418C>T		intron_variant	Intron 8 of 15		NP_542436.2
TRPV1	NM_080706.3	c.1384-418C>T		intron_variant	Intron 7 of 14		NP_542437.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
TRPV1	ENST00000572705.2	c.1384-418C>T		intron_variant	Intron 9 of 16	1	NM_080704.4	ENSP00000459962.1

Frequencies

GnomAD3 genomes AF: 0.208 AC: 31620 AN: 152074 Hom.: 3615 Cov.: 34

Gnomad AFR AF: 0.117

Gnomad AMI AF: 0.226

Gnomad AMR AF: 0.257

Gnomad ASJ AF: 0.155

Gnomad EAS AF: 0.163

Gnomad SAS AF: 0.240

Gnomad FIN AF: 0.224

Gnomad MID AF: 0.212

Gnomad NFE AF: 0.253

Gnomad OTH AF: 0.230

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

GnomAD4 genome AF: 0.208 AC: 31618 AN: 152192 Hom.: 3615 Cov.: 34 AF XY: 0.207 AC XY: 15365 AN XY: 74396

African (AFR) AF: 0.117 AC: 4854 AN: 41544

American (AMR) AF: 0.257 AC: 3927 AN: 15280

Ashkenazi Jewish (ASJ) AF: 0.155 AC: 538 AN: 3466

East Asian (EAS) AF: 0.163 AC: 841 AN: 5172

South Asian (SAS) AF: 0.240 AC: 1158 AN: 4824

European-Finnish (FIN) AF: 0.224 AC: 2381 AN: 10608

Middle Eastern (MID) AF: 0.204 AC: 60 AN: 294

European-Non Finnish (NFE) AF: 0.253 AC: 17171 AN: 67978

Other (OTH) AF: 0.228 AC: 482 AN: 2114

Alfa AF: 0.235 Hom.: 13643

Bravo AF: 0.204

Asia WGS AF: 0.174 AC: 604 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.81
CADD	Benign	0.24
DANN	Benign	0.72
PhyloP100		-1.1
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: rs17706630; hg19: chr17-3487142;